Long emission wavelength chemiluminescent compounds and their use in test assays

BACKGROUND OF THE INVENTION
1. Technical Field:
The present invention relates to a new class of chemiluminescent, aromatic ring-fused acridinium compounds (AFAC) which emit green or yellow light upon simple chemical treatments. This invention also relates to conjugates formed from AFAC and binding partners, e.g. biological molecules, and test assays utilizing the conjugates. Furthermore the invention relates to test assays in which the detection and/or quantitation of two or more substances or analytes in a test sample can be carried out simultaneously due to the discernable and non-interfering light emission characteristics of two or more chemiluminescent conjugates.
2. Technical Review:
Chemiluminescent compounds that emit light with separated wavelength maxima and minimally overlapping but correctable emission spectra can be very useful in analytical assays, particularly in industrial assays, and in clinical diagnostic assays for multi-substance, e.g. multi-analyte, determinations. Such compounds can be used to tag or label binding partners, e.g. biological molecules, such as antigens, antibodies, and nucleic acids to form conjugates or tracers that are capable of producing mutually non-interfering, or minimally over-lapping light emission signals or spectra, that allow the simultaneous detection and/or quantitation of multiple substances in a test sample. For example, simultaneous determinations of serum levels of luteinizing hormone (LH) and follicle stimulating hormone (FSH) from one patient sample is possible, and is demonstrated below, utilizing two chemiluminescent compounds having light emission spectra which span about 100-250 nm for a spectral region with signal intensity above 5% of peak height, but differing in their emission maxima so that the signals are discernable. In one example the emission maxim of two chemiluminescent signals differ by about 60 nm and preferably by 80 nm or more. A further example where simultaneous determinations is possible according to the methods described herein, is in the assay of amplified nucleic acid sequences, e.g. oncogenes associated with malignant transformation. See EP-A-0 481 704 (U.S. Pat. No. 5,407,798) and references cited therein) which is commonly assigned and incorporated herein by reference. In such assays, the inclusion of a parallel, internal reference material for a known, different target sequence in the same working vessel or reaction medium as a positive control is recognized as important to assay performance, for example, to safeguard false negative results. In other assay formats, the inclusion of a known control substance will also serve to assess assay performance.
The economical benefit and the experimental necessity of determining and/or quantitating two or more substances, e.g. analytes, in a test sample were the two main underlying motives in the development of a multiple-tracer assay system of the present invention. It was further envisioned that an ideal multiple-tracer system would emit multiple-wavelength signals under identical chemical conditions. It was recognized that it would be less desirable and more cumbersome to combine two chemiluminescent tracers in a multiple-analyte assay system that required two different sets of signal generating mechanisms, conditions and timings as would be in the case of utilizing two different classes of chemiluminescent compounds such as acridinium compounds pairing with luminol series or with stable dioxetanes, which involve the use of other chemicals or enzymes to generate the signal. Furthermore the two or more different chemiluminescent compounds or conjugates must have emission efficiency differing by not more than one order of magnitude.
A still further fundamental requirement was the adequate stability of the chemiluminescent compounds in aqueous media or environment, which will withstand the shipping conditions for commercial products when placed in kit form.
These goals have been achieved by developing stable chemiluminescent analogues within the same general class that exhibit bathochromic shifts in their emission maxima, and emit light with comparable efficiency under identical chemical treatments.
Chemiluminescent acridinium compounds which are shown herein to emit blue light upon treatment with hydrogen peroxide and metal hydroxide have been well documented. U.S. Pat. Nos. 4,745,181, 4,918,192, 5,110,932, 5,227,489 and 5,241,070 describe stable polysubstituted-aryl acridinium esters; all of which are commonly assigned and incorporated herein by reference. Such acridinium compounds shall be referred to generally herein as "reference acridinium esters" or "acridinium esters". Such compounds as indicated include an acridinium ring system and, depending on the use of such compounds, further include an appropriate functional group(s), e.g. for attaching the label to a substance to form conjugates for use in a test assay, including the assays of the present invention.
Batmanghelich, et al, EP-A-0 478 626 (priority GB 2233450A (Jun. 24, 1989)), described the use of acridinium compounds of varying light emission, i.e. fast and slow durations to prepare different tracer conjugates, to achieve a "substantially simultaneous" quantitation of two or more different analytes. This approach, however, has several major drawbacks. First, one of the acridinium esters includes electron-withdrawing substituents on the phenolic moiety in order to achieve very short duration of light emission, i.e. complete emission or emission maxima in one second. This type of compound, e.g. a ortho-dihalogenated aryl acridinium ester, however, may suffer from lack of stability in aqueous environment. Second, light emission kinetics must be carefully examined to permit accurate correction in order to distinguish the light emission contributed individually by the two tracers during the overlapping period of light emission. The described method relies on the measurement of photons emitted in two separate time windows for sequential integration of light intensity. Unless the light emission overlap is relatively small, such correction could be a potential source for poor assay precision, particularly for detection of two analytes having widely different concentrations. The requirement for smaller light emission overlap would in turn demand the availability of a pair of chemiluminescent compounds, one having very short and the other very long duration of light emission; and would lead to compounds which either have stability problems or render the dual-analyte assay unpractical due to excessively prolonged signal-collection time. Where the signal collection time is extended, an advantage of performing two assays in a single test sample would be lost.
Batmanghelich et al also described acridinium compounds of different light emission spectra to prepare different tracer conjugates. The approach was to extend the electronic conjugation of the acridinium nucleus to obtain 3-(4-Carboxybutadienyl)-acridinium ester (compound 2b) with bathochromic shift of about 80 nm in the emission maximum as compared to the parent acridinium ester (compound 2a). Extension of electronic conjugation of the acridinium nucleus does not necessarily lead to major bathochromic shift in the emission maximum which is practically needed to construct a dual-analyte immunoassays and a possible reduction in emission efficiency. No teaching was made of benzacridinium chemiluminescent compounds or conjugates for use in such assays. Experimental data for 3-Carboxybutadienyl-acridinium ester is provided herein.
McCapra et al, U.S. Pat. Nos. 5,281,712, 5,283,334, 5,284,951, 5,284,952, 5,290,936, 5,321,136 and EP-A-0 322 926, suggested a "chemiluminescent moiety" consisting of heterocyclic ring or ring system with ester, amide linkages attached to one of the carbon atoms on the ring or ring system. These chemiluminescent compounds were said to include benz�a!acridinium, benz�b!acridinium, and benz�c!acridinium but the synthesis and structure of these compounds or conjugates was not described. Neither emission wavelength maxima, nor light emission efficiency of said compounds were predicted; nor were the use of at least two chemiluminescent compounds or conjugates in an assay method, nor the utility of such compounds when used in assays based on their emission spectra described.
The synthesis of substituted acridine compounds have been described by Dombrowski et al in EP-A-0 369 344.
Dombrowski provided an alternative method of preparing a substituted N-arylisation that leads to the key intermediate of substituted acridine-9-carboxylic acid. The method taught involved the use of a properly substituted Triphenyl Bismuth Diacetate reacting with isatin or substituted isatin to form the desired substituted N-arylisation product which then undergoes the well-known base catalyzed rearrangement. See J.Martinet and A. Dansette: Bull. Soc. Chim. Fr. 45, 101 (1929) to give the key intermediate acridine-9-carboxylic acid. However, this approach has several drawbacks. First, the formation of the desired Triphenyl Bismuth Diacetate needed in this approach is a lengthy synthesis. For instance, the synthesis of simple, unsubstituted triphenylbismuth diacetate requires four steps involving the reactions of the following sequence: PhBr.fwdarw.PhMgBr.fwdarw.Ph.sub.3 Bi.fwdarw.Ph.sub.3 BiCl.sub.2 .fwdarw.Ph.sub.3 Bi(OAc).sub.2. See J. V. Supniewski and R. Adams: J. Am. Chem. Soc., 48, 507 (1926). Secondly, many functional groups that are required at the desired position(s) of the benzene ring are not compatible with the nature of this reaction. For example, in the step of forming Grignard reagent PhMgBr, any reactive carbonyl groups in the benzene ring would react intermolecularly to form the complex, unwanted mixture. Lastly, this process requires the use of a Bismuth salt and Bismuth is a heavy metal belonging to the same periodic group VA as arsenic and antimony. Therefore, a more efficient process involving the use of less toxic reactants(s) is warranted.
The nomenclature of benz�a!acridinium and benz�b!acridinium utilized in this disclosure is based on Rule 21.5 of Definitive Rules for Nomenclature of Organic Chemistry, Ed. International Union of Pure and Applied Chemistry in the 1957 REPORT OF THE COMMISSION ON THE NOMENCLATURE OF ORGANIC CHEMISTRY.
According to the example given on Benz�a!anthracene, the compound arising from fusing benzene ring to the peripheral sides of the acridinium nucleus (structure below) should therefore be named according to whether side a, b, or c of the acridinium nucleus is fused with the benzene ring. ##STR1##
The following abbreviations are utilized in the disclosure:
1. ABAC: angular benz�a!acridinium compound
2. AFAC: aromatic ring fused acridinium compound
3. EtO: ethoxy
4. DMAE: dimethyl acridinium ester
5. DIPAE: diisopropyl acridinium ester
6. LBAC: linear benz�b!acridinium compound
7. LEAC: longer emission acridinium compound
8. LEAE: longer emission acridinium ester
9. MeO: methoxy
10. NSE: N-sulfoethyl
11. NSP N-sulfopropyl
12. PCT: percent cross talk
13. PMP: paramagnetic particles
14. QAE: quaternary ammonium ethoxy
15. RLU: relative light units
16. EC-AE: electronically conjugated acridinium ester
17. NOS-AE: non-ortho-substituted acridinium ester
18. pCE-AE: para-carboxyethyl acridinium ester
SUMMARY OF THE INVENTION
A method is described for detection and/or quantitation of at least two substances in a test sample comprising simultaneously detecting the emission signals of at least two chemiluminescent conjugates; each chemiluminescent conjugate being associated with a substance sought to be detected and/or quantitated in the test sample. The emission signals of each of the chemiluminescent conjugates are discernable by their spectral emissions, so that the substances may be detected and/or quantitated.
A chemiluminescent compound for use in the assays of the present invention is described by the formula: ##STR2## where W is carbon; alternatively, C.sub.7, W, C.sub.9 or C.sub.10 can be replaced with --N.dbd.;
or W can be omitted and C.sub.7 connected to C.sub.9, and C.sub.7, C.sub.9 or C.sub.10 can be replaced with --O--, --S--, --NH-- or --NR--;
Y is a branched or straight chained alkyl containing optionally up to 20 carbon atoms, halogenated or unhalogenated, or a polysubstituted aryl moiety of the formula: ##STR3## R.sub.1 is an alkyl, alkenyl, alkynyl or aralkyl containing optionally up to 20 heteroatoms;
R.sub.2, R.sub.3, R.sub.9 and R.sub.10 are identical or different groups selected from hydrogen, substituted or unsubstituted aryl (ArR or Ar), halide, amino, hydroxyl, nitro, sulfonate, --R, --CN, --COOH, --SCN, --OR, --SR, --SSR, --C(O)R, --C(O)OR, --C(O)NHR, or --NHC(O)R;
R.sub.2 includes a single or multiple substituent at C.sub.1-4 ;
R.sub.2 can also be a fused aromatic ring with or without heteroatoms;
R.sub.3 includes a single or multiple substituent at C.sub.7, W, C.sub.9 or C.sub.10 ;
A is a counter ion including CH.sub.3 SO.sub.4.sup.-, FSO.sub.3.sup.-, CF.sub.3 SO.sub.4.sup.-, C.sub.4 F.sub.9 SO.sub.3.sup.-, CH.sub.3 C.sub.6 H.sub.4 SO.sub.3.sup.- and halide;
X is a heteroatom including nitrogen, oxygen or sulfur, such that when X is oxygen or sulfur Z is omitted, when X is nitrogen then Z is --SO.sub.2 --Y', and Y' is equal to Y, and where the substituents to Y and Y' do not have to be the same;
R.sub.4 and R.sub.8 are alkyl, alkenyl, alkynyl, alkoxyl, alkylthiol, amido,
R.sub.5 and R.sub.7 are any of R.sub.3, R.sub.9 and R.sub.10 defined above;
R.sub.6 .dbd.--R.sub.11 --R.sub.12,
where R.sub.11 is not required but optionally can be branched or straight-chained alkyl, substituted or unsubstituted aryl or aralkyl containing optionally up to 20 heteroatoms,
and R.sub.12 is a leaving group or an electrophilic functional group attached with a leaving group or --Q--R--Nu, --Q--R(I).sub.n Nu, --Q--Nu, --R--Nu or --Nu, n is a number of at least 1, Nu is a nucleophilic group, Q is a functional linkage, I is an ionic or ionizable group;
R.sub.5 and R.sub.6, and R.sub.6 and R.sub.7 are interchangeable; and
R is alkyl, alkenyl, alkynyl, aryl or aralkyl containing optionally up to 20 heteroatoms.
A chemiluminescent compound or conjugate is characterized in that upon chemical treatment the compound or conjugate emits a blue-green, green, yellow, orange and red-orange light having a discernable emission spectra peak or maximum. In one embodiment, i.e. compound, the emission maxima is greater than or equal to 480 nm and in a preferred embodiment greater than or equal to 515 nm.
An amplification method is described for target sequences, including one or more nucleic acid sequences, in a test sample comprising providing a test sample suspected of containing one or more target sequences, adding an internal reference to said test sample, amplifying the target sequences, providing at least two chemiluminescent conjugates, each chemiluminescent conjugate being associated with target sequences and the internal reference, and simultaneously detecting and/or quantitating amplified target sequences and the internal reference by emissions of the chemiluminescent conjugates.
Accordingly, it is a primary object of the invention to provide a method for the simultaneous detection and/or quantitation of at least two substances in a test sample by use of at least two different chemiluminescent compounds or conjugates each having discernable emission spectra.
Another object of the invention is to provide an assay method for the simultaneous detection and/or quantitation of an analyte and an internal standard or control in a single test medium or transfer tube.
Still another object of the invention is to increase the efficiency of automated analyzers by providing for the simultaneous performance of two assays on a test sample in a single reaction medium or transfer tube.
A further object of the invention is to provide methods for synthesis of chemiluminescent compounds and intermediate products which may be used to synthesize such chemiluminescent compounds.
A still further object of the invention is to provide a simpler and alternative method for the preparations of the substituted N-aryl-isatins and N-aryl-benzisatins which lead to the preparation of the corresponding key intermediates of acridine-9-carboxylic acid and substituted benz�b!acridine-12-carboxylic acid.
An object of the invention is to provide chemiluminescent, aromatic ring-fused acridinium compounds (AFAC) that emit green or yellow light.
Another object of the invention is to provide chemiluminescent, aromatic ring-fused acridinium compounds (AFAC) that emit green or yellow light with wavelength maxima or peaks greater than or equal to 515 nm.
Still another object of the invention is to provide a simultaneous dual chemiluminescent label assay.
A further object of the invention is to provide hydrophilic AFAC which carries one or more ionic and/or ionizable groups with or without, additionally, the reactive functional groups useful for forming covalent linkages with other micro- or macromolecules or encapsulation inside liposomes.
An object of this invention is to provide AFAC conjugates formed between AFAC directly or indirectly with binding partners, e.g. biological molecules.
Another object of this invention is to provide test assays involving the use of acridinium ester and AFAC conjugates.
Still another object of the invention is to provide multianalyte assays in which the determination of two or more analytes or substances or combination thereof present in the sample as a mixture, can be carried out simultaneously in the same reaction medium or transfer tube due to the mutually non-interfering, or minimally over-lapping but correctable light signals produced by the same chemical treatments of two or more different chemiluminescent tracers or compounds.
A further object of the present invention is to provide test kits for performing dual chemiluminescent label test assays.
An object of the present invention is to provide test kits having two or more chemiluminescent reagents for simultaneously assaying at least two substances in a test sample.
Another object of the invention is to provide intermediate compounds to be utilized in the synthesis of labels for use in analytical assays.
Still another object of the present invention is to provide chemiluminescent compounds having light emission spectra which span about 100-250 nm, for a spectral region with signal intensity above 5% of peak height.
These and other objects in view, as will be apparent to those skilled in the art, the invention resides in the combination of elements set forth in the specification and covered by the claims appended hereto.

BRIEF DESCRIPTION OF DRAWINGS
The foregoing and other objects and advantages of the invention will be appreciated more fully from the following further description thereof with reference to the accompanying drawings wherein
FIGS. 1A-1P illustrate the structures of representative acridinium esters, ABAC, and LBAC's.
FIGS. 2A-2C illustrate the synthesis of p-methylphenyl 3-aldo-acridine-9-carboxylate, benzyloxycarbonylbut-2-enyltriphenylphoshoran, p-Methylphenyl 3-(4'carboxy)-trans, trans-butadienyl-10-methyl-acridinium-9-carboxylate trifluoroacetate(3-Carboxylbutadienyl-AE,EC-AC).
FIGS. 3A-3E illustrate emission spectra of acridinium esters and ABAC of the present invention as follows:
FIG. 3A is an emission spectrum of DMAE-Bz (50 .mu.g in 0.5 ml of acetonitrile);
FIG. 3B is an emission spectrum of 3-MeO-DMAE-Bz (50 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.422 nm;
FIG. 3C is an emission spectrum of DIPAE-Bz (20 .mu.g in 0.5 ml in acetonitrile) peak.apprxeq.428 nm;
FIG. 3D is an emission spectrum for 3-QAE-DMAE-NHS (40 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.426 nm; and
FIG. 3E is an emission spectrum of angular benz�a! acridinium ester (2 mg in 0.2 ml of DMF) peak.apprxeq.440 nm.
FIGS. 4A-4J illustrate emission spectra of LBAC of the present invention as follows:
FIG. 4A is an emission spectrum of LEAE-Bz (50 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.520 nm;
FIG. 4B is an emission spectrum of DIP-LEAE-Bz (50 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.520 nm;
FIG. 4C is an emission spectrum of 3-EtO-LEAE-Bz (50 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.508 nm;
FIG. 4D is an emission spectrum of 3-QAE-LEAE-Bz (100 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.544 nm;
FIG. 4E is an emission spectrum of 2-MeO-LEAE-Bz (30 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.550 nm;
FIG. 4F is an emission spectrum of LEAC-Bz (50 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.520 nm;
FIG. 4G is an emission spectrum of 2-QAE-LEAE-NHS (70 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.550 nm;
FIG. 4H is an emission spectrum of NSP-LEAE-Bz (15 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.516 nm;
FIG. 4I is an emission spectrum of 2-MeO-NSE-LEAE-NHS (50 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.546 nm; and
FIG. 4J is an emission spectrum of 2-MeO-LEAE-Imidate (100 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.550 nm.
FIGS. 5A-5B illustrate emission spectra of non-ortho-substituted acridinium esters as follows:
FIG. 5A is an emission spectrum of 3-Carboxybutadienyl-AE (150 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.464 nm; and
FIG. 5B is an emission of p-carboxyethyl-AE (25 .mu.g in 0.5 ml of acetonitrile) peak.apprxeq.430 nm.
FIGS. 6A-6E illustrate emission spectra of mixed acridinium esters and LBAC of the present invention as follows:
FIG. 6A is an emission spectrum of mixed DMAE-Bz (10 .mu.g) and LEAE-Bz (50 .mu.g in 0.5 ml of acetonitrile);
FIG. 6B is an emission spectrum of mixed DMAE-Bz (100 .mu.g) and 2-MeO-LEAE-Bz (25 .mu.g in 0.5 ml of acetonitrile);
FIG. 6C is an emission spectrum of mixed 3-MeO-DMAE-Bz (50 .mu.g) and 2-MeO-LEAE-Bz (30 .mu.g in 0.5 ml of acetonitrile); and
FIG. 6D is an emission spectrum of mixed 3-MeO-DMAE-Bz (5 .mu.g) and 2-QAE-LEAE-NHS (105 .mu.g) in 0.5 ml of acetonitrile).
FIG. 6E is an emission spectrum of mixed DMAE (3 .mu.g) and 3-Carboxybutadienyl)-AE(25 .mu.g) in 0.5 ml of acetonitrile.
FIGS. 7A-7E illustrate transmittance curves of various optical filters as follows:
FIG. 7A is a transmittance curve of a BG-38 optical filter;
FIG. 7B is a transmittance curve of a corion P70-450 optical filter;
FIG. 7C is a transmittance curve of a corion LL500 optical filter;
FIG. 7D is a transmittance curve of a corion laminated CS550/CS600 optical filter; and
FIG. 7E is a transmittance curve of a corion LL520 optical filter.
FIGS. 8A-8D illustrate the stability profiles of the emission properties (%RLU) of various AE's under heat stressing in various pH buffer solutions (0.2 m PO.sub.4, 0.1% BSA solution at 37.degree. C.) over time as follows:
FIG. 8A illustrates the stability profiles of the emission properties (%RLU) of various AE's under heat stressing in a pH 9.0 buffer solution over time;
FIG. 8B illustrates the stability profiles of the emission properties (%RLU) of various AE's under heat stressing in a pH 8.5 buffer solution over time;
FIG. 8C illustrates the stability profiles of the emission properties (%RLU) of various AE's under heat stressing in a pH 8 buffer solution; and
FIG. 8D illustrates the stability profiles of the emission properties (%RLU) of various AE's under heat stressing in a pH 7.4 buffer solution.
FIGS. 9A-9D illustrate HPLC profiles of various AE's before and after being heat stressed at 37.degree. C. at pH 8.0 for 24 hours as follows:
FIGS. 9A-9B illustrate the HPLC profiles of 3-Carboxybutadienyl-AE before (FIG. 9A) and after (FIG. 9B) being heat stressed; and
FIGS. 9C-9D illustrate the HPLC profiles of LEAE before (FIG. 9C) and after (FIG. 9D) being heat stressed.
FIG. 10 illustrates the area of overlap between the transmittance curve of an optical filter (Corion LL500) and the emission spectra of DMAE-Bz.
FIG. 11 illustrates the area of overlap between the transmittance curve of an optical filter (Corion P70-450) and the emission spectra of LEAE-Bz.
FIG. 12 illustrates normalized spectral energy densities for DMAE and 3-Carboxybutadienyl-AE.
FIG. 13 illustrates a schematic arrangement of the primary components of a dual luminometer system.
FIG. 14 illustrates spectral energy densities of DMAE and 3-Carboxybutadienyl-AE after passing through a cut-off filter of 410 nm.
FIG. 15 illustrates spectral energy densities of DMAE and 3-Carboxybutadienyl-AE after passing through a cut-off filter of 532 nm.
FIG. 16 illustrates FSH standard curve assays read on a dual PMT luminometer.
FIG. 17 illustrates LH standard curve assays read on a dual PMT luminometer.

DESCRIPTION OF PREFERRED EMBODIMENT
The AFAC of present invention comprise linear benz�b!acridinium (LBAC), furanoacridinium, thiophenoacridinium, pyrroacridinium compounds and pyridoacridinium compounds. By virtue of the specific position of the aromatic ring fused to the acridinium nucleus LBAC was unexpectedly found to generate a chemiluminescent emission signal with much greater bathochromic shift than the angular benz�a!acridinium compounds (ABAC), and to the corresponding "reference acridinium esters", i.e. DMAE-Bz, DIPAE-Bz, 3-MeO-DMAE-Bz, p-carboxyethyl-AE and 3-Carboxybutadienyl-AE.
The general structure of AFAC is represented by Formula ##STR4##
The general structures of linear benz�b!acridinium compounds and the isomeric, furano-, thiopheno-, pyrro- and pyrido- acridinium compounds are shown by the Formulas II, III A-III C, and IV A-IV D respectively. ##STR5##
One subclass of the AFAC contains reactive functional group(s), in addition to the fundamental chemiluminescent compound with properties described above, to enable formation, i.e., by covalent linkage, with binding partners, and particularly with biological molecules, to produce conjugates useful as non-isotopic tracers in binding assays or as a key integral part of a multianalyte assay system. Another subclass of the AFAC contains one or more ionic and/or ionizable groups which enhance the solubility of the compounds in aqueous media and/or allow them to be encapsulated inside liposomes with low leakage. Such hydrophilic LBAC can also be modified to carry additional reactive functional groups to allow forming conjugates with other micro or macromolecules.
Preferred LBAC, Furanoacridinium compounds, Thiophenoacridinium compounds, Pyrroacridinium compounds and Pyridoacridinium compounds having the above-mentioned characteristics and being suitable for above-described utilities include chemiluminescent compounds represented by the above Formulas I, II, III A-III C, and IV A-IV D respectively, where:
W is a carbon, Formula I becomes the LBAC class of chemiluminescent compounds as represented by Formula II; or W can be omitted and C.sub.7 connected to C.sub.9 and one of C.sub.7, C.sub.9 or C.sub.10 can be replaced with --O--, --S--, --NH--, or --NR-- to form a 5-membered aromatic ring fused linearly to the acridinium nucleus as shown in Formula III A-C; or C.sub.7, W, C.sub.9, or C.sub.10 can be replaced with --N.dbd. to form a 6-membered pyrido ring fused linearly to the acridinium nucleus as shown in Formula IV A-D;
R.sub.1 is an alkyl, alkenyl, alkynyl, or aralkyl containing optionally up to 20 heteroatoms, preferably nitrogen, oxygen, halogen, phosphorus or sulfur.
R.sub.2, R.sub.3, R.sub.9 and R.sub.10 are identical or different groups selected from hydrogen, substituted or unsubstituted aryl (ArR or Ar), halide, amino, hydroxyl, nitro, sulfonate, --R, --CN, --CO.sub.2 H, --SCN, --OR, --SR, --SSR, --C(O)R, --C(O)OR, --(O)NHR, or --NHC(O)R.
R is alkyl, alkenyl, alkynyl, aryl, or aralkyl, containing optionally up to 20 heteroatoms.
R.sub.2 includes a single or multiple substituent(s) at C.sub.1-4. R.sub.3 includes a single or multiple substituent(s) at C.sub.7, W, C.sub.9 or C.sub.10 .
R.sub.2 can be also a fused aromatic ring with or without heteroatoms.
A-- is a counter ion including CH.sub.3 SO.sub.4 --, FSO.sub.3 --, CF.sub.3 SO.sub.4 --, C.sub.4 F.sub.9 SO.sub.3 --, CH.sub.3 C.sub.6 H.sub.4 SO.sub.3 --, and halide.
X is a heteroatom including nitrogen, oxygen, or sulfur, when X is oxygen or sulfur Z is omitted, when X is nitrogen then Z is --SO.sub.2 --Y'.
Y is a branched or straight chained alkyl containing optionally up to 20 carbon atoms, halogenated or unhalogenated, or a polysubstituted aryl moiety of Formula V: ##STR6## Y' is equal to Y, and the substituents to Y and Y' do not have to be the same.
R.sub.4, and R.sub.8 are alkyl, alkenyl, alkynyl, alkoxyl, alkylthio, amido, groups positioned to ensure better stability of AFAC in aqueous media or environment. The stability of AFAC rendering them suitable for commercialization is attributed to the steric effect, electronic effect, or a combination thereof resulting from the presence of these two groups. R.sub.5 and R.sub.7 are as recited for R.sub.3, R.sub.9, and R.sub.10 in Formula I. For conjugating AFAC to biological molecules, R.sub.6 can be a leaving group, an electrophilic group, or an electrophilic functional group attached with a leaving group, or functional groups which can be readily converted into such reactive groups, directly attached or connected via a spacer to the ring. A "spacer" is defined as branched or straight-chained alkyl, substituted or unsubstituted aryl or aralkyl, optionally containing up to 0-20 heteroatams. Examples of such functional groups include: ##STR7## --N.dbd.C.dbd.S, --N.dbd.C.dbd.O, --N.sub.2 +U--, --N.sub.3, --COOH, --U, or --SO.sub.2 U, where U is a halide.
Alternatively, R.sub.6 can be a protected or unprotected nucleophilic functional group directly attached or connected via a spacer to Y. Thus R.sub.6 .dbd.--Q--R--Nu, --Q--R(I)n--Nu, --Q--Nu, --R--Nu, or --Nu, where R is defined as above.
Q is a functional linkage arising from the covalent coupling between two functional groups each of which resides originally as substituents on Y and R or Nu, respectively. The introduction of Q in the construct of R.sub.6 represents a modular concept which allows the attachment of R--Nu, R(I)n--Nu or Nu directly to a preformed AFAC. Examples of Q include:
--C(O)--, --C(O)NH--, --NHC(O)--, --NHC(O)O--, --NH--, --O--, --S--, --NHC(O)NH--, --NHC(S)NH--, --C(.dbd.N+H.sub.2)NH--, --SO.sub.2 --, --SO.sub.3 --,
(I)n is an ionic or ionizable group including but not limited to quaternary ammonium,
--COOH, --SO.sub.3 H, --SO.sub.4 H, --PO.sub.3 H.sub.2, and --PO.sub.4 H.sub.2, where n is a number of at least 1.
The presence of the ionic or ionizable group(s) will enhance the hydrophilicity of AFAC and compatibility for its usage in aqueous media. The choice and positioning of such ionic or ionizable groups have the advantage of enhancing the binding of the biological molecule/AFAC conjugate to the corresponding binding partners of said biological molecule.
Nu is a nucleophilic group on the compound that will facilitate conjugation of compound with biological molecules which may lack nucleophilic group for coupling, but may have electrophilic group or its readily converted precursor. Examples of the protected nucleophilic functional groups or groupings include:
t-Butyloxycarbonylamino and 3-(2-pyridinyldithio)-propionyl (PDP). ##STR8## t-Butyloxycarbonyl (t-Boc) is the protective group on amino which can be removed by acid, e.g. trifluoroacetic acid, treatment. The S-2-pyridinyl group in PDP is a protective moiety which can be removed to generate free --SH group upon treatment with dithiothreotol (DTT) at suitable pH. The usage of these protective groups of --NH.sub.2 and --SH nucleophilic groups is known to those skilled in the arts of organic chemistry. Examples of the unprotected nucleophilic functional groups include: amino, thiol, hydroxyl, active methylene adjacent to a strong electron-withdrawing group, organic metallic moieties. Examples of such a nucleophilic R.sub.6 grouping, its conjugation to biological molecules, and the conjugate utilities have been disclosed in EP-A-0 361 817 which is commonly assigned and incorporated herein by reference.
To provide more hydrophilic compounds that can be encapsulated inside liposomes for the purpose of constructing signal-enhancing lumisomes, R.sub.2, R.sub.3 or R.sub.6 can be strongly ionizable groups directly attached or more suitably connected via spacer to the aromatic rings. Examples of strongly ionizable groups include: phosphate, phosphonate, sulfate, and sulfonate. Examples of such a R.sub.6 grouping, the incorporation of the hydrophilic chemiluminescent molecules into liposomes and the utility of the resulting lumisomes have been disclosed in EP-A-0 361 817 (priority U.S. Ser. No. 226,639 (Aug. 1, 1988)) which is commonly assigned and incorporated herein by reference. Similarly, to provide hydrophilic AFAC that can be conjugated with biological molecules directly, R.sub.2 and/or R.sub.3 can be an ionic or strongly ionizable groups directly attached or more suitably connected via spacer to the aromatic-ring fused acridinium nucleus, and R.sub.6 can be a reactive functional group-containing side chain as recited above. The positions of R.sub.2, R.sub.3, R.sub.5 and R.sub.6, and R.sub.6 and R.sub.7 substituents in all AFAC are interchangeable.
One of the possible precursors to AFAC should be AFAC with the R.sub.6 substituent being hydrogen or R, with R defined as above.
When X is nitrogen, Y can be a branched or straight chained alkyl of 1 to 20 carbon atoms or a moiety equal to Formula V above with all the possible substituents as recited, and Z is represented by the following Formula VI:
Z.dbd.--SO2--Y' (Formula VI)
where Y' is a branched or straight chained alkyl of 1 to 20 carbon atoms, halogenated or unhalogenated, or a moiety equal to the Formula V shown above with all the possible substitutents as recited. The substituents to both Y and Y' do not necessarily have to be the same.
Preferred aromatic ring-fused acridinium compounds (AFAC) are as described above. More preferentially, they are the LBAC series with the following substituents: R.sub.1 is a methyl, sulfopropyl or sulfoethyl group; R.sub.9, R.sub.10 are hydrogen, methoxy or halogen; R.sub.2 is a hydrogen, 2-MeO, 2-quarternaryammoniumalkoxy, 3-MeO, 3-EtO, 3-quarternaryammoniumalkoxy, or 3-carboxyalkyloxy group; R.sub.3, R.sub.5 and R.sub.7 are hydrogen; when X is oxygen or sulfur, R.sub.4 and R.sub.8 are methyl, ethyl, isopropyl groups; R.sub.6 is one of the following groups attached to the 4-position of Formula V, carboxylate, N-succinimidyloxycarbonyl, benzyloxycarbonyl, N-aminoalkylcarbamoyl, Sulfomethylcarbamoyl, N-�N-(2-amino-3-S-(3'-sulfopropyl)-thiopropionyl)-2-aminoethyl!carbamoyl, N-7-(1,3-disulfonaphthalenyl)carbamoyl, N-�1-carboxyl-2-(3-sulfopropylthio!ethyl)carbamoyl, N-(2-sulfonyloxyethyl)carbamoyl, N-(2-phosphonoethyl)carbamoyl, N-(2-phosphonoxyethyl)carbamoyl and alkoxyiminoethyl; when X is nitrogen, Y represents Formula V with R.sub.5 and R.sub.7 being hydrogen and R.sub.6 being carboxylate, N-succinimidyloxycarbonyl, N-succinimidyloxycarbonylalkyl, benzyloxycarbonyl, or N-aminoalkylcarbamoyl; Z represents Formula VI with Y' being an alkyl or phenyl.
Intermediate compounds which may be utilized to synthesize the chemiluminescent compounds of the present invention include:
An intermediate of the formula: ##STR9## where w is carbon; alternatively, C.sub.7, W, C.sub.9 or C.sub.10 can be replaced with --N.dbd.;
or W can be omitted and C.sub.7 connected to C.sub.9, and C.sub.7, C.sub.9 or C.sub.10 can be replaced with --O--, --S--, --NH--or --NR--;
R.sub.2, R.sub.3, R.sub.9 and R.sub.10 are identical or different groups selected from hydrogen, substituted or unsubstituted aryl (ArR or Ar), halide, amino, hydroxyl, nitro, sulfonate, --R, --N, --COOH, --SCN, --R, --OR, --SR, --SSR, --C(O)R, --C(O)OR, --(O)NHR, or --NHC(O)R;
R.sub.2 includes a single or multiple substituent at C.sub.1-4 ;
R.sub.3 includes a single or multiple substituent at C.sub.7, W, C.sub.9 and C.sub.10 ;
R.sub.2 can also be a fused aromatic ring with or without heteroatoms; and
R is alkyl, alkenyl, alkynyl, aryl or aralkyl containing optionally up to 20 heteroatoms.
An intermediate of the formula: ##STR10## where W is carbon; alternatively, C.sub.7, W, C.sub.9 or C.sub.10 can be replaced with --N.dbd.;
or W can be omitted and C.sub.7 connected to C.sub.9, and C.sub.7, C.sub.9 or C.sub.10 can be replaced with --O--, --S--, --NH--or --NR--;
Y is a branched or straight chained alkyl containing optionally up to 20 carbon atoms, halogenated or unhalogenated, or a polysubstituted aryl moiety of the formula: ##STR11## R.sub.2, R.sub.3, R.sub.9 and R.sub.10 are identical or different groups selected from hydrogen, substituted or unsubstituted aryl (ArR or Ar), halide, amino, hydroxyl, nitro, sulforate, --R, --N, --COOH, --SCN, --OR, --SR, --SSR, --C(O)R, --C(O)OR, --(O)NHR, or --NHC(O)R;
R.sub.2 includes a single or multiple substituent at C.sub.1-4 ;
R.sub.3 includes a single or multiple substituent at C.sub.7, W, C.sub.9 or C.sub.10 ;
R.sub.2 can also be a fused aromatic ring with or without heteroatoms;
X is a heteroatom including nitrogen, oxygen or sulfur, such that when X is oxygen or sulfur Z is omitted, when X is nitrogen then Z is --S0.sub.2 --Y', Y' is equal to Y and the substituents to Y and Y' do not have to be the same;
R.sub.4 and R.sub.8 are alkyl, alkenyl, alkynyl, alkoxyl, alkylthiol, amido;
R.sub.5 and R.sub.7 are any of R.sub.3, R.sub.9 and R.sub.10 defined above;
R.sub.6 .dbd.--R.sub.11 --R.sub.12,
where R.sub.11 is not required but optionally can be branched or straight-chained alkyl, substituted or unsubstituted aryl or aralkyl containing optionally up to 20 heteroatoms;
and R.sub.12 is a leaving group or an electrophilic functional group attached with a leaving group or --Q--R--Nu, --Q--R(I).sub.n Nu, --Q--Nu, --R--Nu or Nu where n is a number of at least 1, Nu is a nucleophilic group, Q is a functional linkage, I is an ionic or ionizable group;
R.sub.5 and R.sub.6, and R.sub.6 and R.sub.7 are interchangeable; and
R is alkyl, alkenyl, alkynyl, aryl or aralkyl containing optionally up to 20 heteroatoms.
Another embodiment of the present invention is an alternative process of forming substituted N-arylisatin and N-arylbenzisatin comprising reacting a compound of formula IXa or IXb: ##STR12## wherein R.sub.13, R.sub.14, R.sub.15, R.sub.16, R.sub.17, and R.sub.18 are identical or different groups selected from hydrogen, substituted amino, hydroxyl, nitro, sulfonate, --R, --CN, --COOH, --SCN, --OR, --SR, --SSR, --C(O)R, --C(O)OR, --C(O)NHR, or --NHC(O)R, and R is alkyl, alkenyl, alkynyl, aryl or aralkyl containing optionally up to 20 heteroatoms, with a compound of formula X: ##STR13## wherein R.sub.19 is halogen, and R.sub.20 is defined as R.sub.13 through R.sub.18. The above reaction is performed in the presence of a base, preferably sodium hydride, which serves to deprotonate the nitrogen attached to the isatins or benzisatins, and a metal or metal salt catalyst, preferably copper halide to produce an N-arylated isatin (Formula XI) or N-arylated benzisatin (Formula XII). ##STR14##
Heating is normally needed to speed up the reaction. A temperature range of 170.degree.-185.degree. C. is preferred. Both N-arylated isatin and N-arylated benzisatin can be treated with strong base, preferably potassium hydroxide solution, and heated to produce a substituted acridine-9-carboxylic acid (Formula XIII) or substituted benz�b!acridine-12-carboxylic acid (Formula XIV), respectively. ##STR15##
The following examples describe the synthesis of the preferred compounds and intermediates of the present invention, the structures of which are shown in FIG. 1. The examples are intended to illustrate and not to limit the invention and may be used as a guide by those skilled in the art to synthesize compounds having alternate substitutents than those shown in the examples.
Example 1
Preparation of (4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 5-Methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (LEAE-Bz)
3-Anilino-2-naphthoic Acid
A mixture of 3-hydroxy-2-naphthoic acid (Aldrich cat. # H4600-7) (376 g, 2.0 mol) and aniline (376 ml, 4.1 mol) was heated at 170.degree. C. with stirring under nitrogen for 16 hours. The resulting mixture, when hot, was poured into 1N HCl (2.5 ml), heated to 100.degree. C., and stirred at this temperature for 5 minutes. The mixture, when hot, was filtrated and the solid was washed with 0.2N HCl (600 ml). The wet material was boiled and mechanically stirred with 0.5N sodium carbonate solution (6.0 ml) for 10 minutes, cooled and filtered. The reddish filtrate was treated dropwise with 5N HCl with stirring to .about.pH 7. The resulting yellow precipitate was collected, washed with small amount of water and crystallized from ethanol (400 ml) to give 3-anilino-2-naphthoic acid (36 g, 7%). Rf 0.6 (silica gel, EM Art. 5715, 20% methanol/chloroform). MS (EI): m/z 264 (M).
12-Chloro-benz�b!acridine
A mixture of 3-anilino-2-naphthoic acid (10.0 g, 37.98 mmol) and phosphorous oxychloride (35.4 ml, 379.8 mmol) was refluxed at 150.degree. C. under nitrogen with stirring for 2 hours. The resulting purple mixture was cooled and evaporated under reduced pressure to dryness. The content was added with stirring to a mixture of chloroform/ice/conc. ammonium hydroxide (200 ml/200 g/200 ml). The chloroform layer was separated and dried over calcium chloride. Removal of the solvent under reduced pressure gave -12-chlorobenz-�b!acridine (9.4 g, 95%). Rf 0.8 (silica gel, hexane/ethyl acetate 2:1). MS (EI): m/z 263 (M).
12-Cyano-benz�b!acridine
A mixture of -12-chloro-benz�b!acridine (2.3 g, 8.68 mmol), potassium cyanide (620 mg, 9.55 mmol) and copper(I) cyanide (391 mg, 4.43 mmol) in anhydrous methanol (16 ml) was bubbled with nitrogen for 1 minute and then kept in a sealed tube. The mixture was heated at 160.degree. C. with stirring for 4.5 hours and cooled. The red-brown mixture was evaporated and the residue was flash-chromatographed (W.C. still et al: J. Org. Chem., 43, 2923, (1978)) on a silica column (Baker silica gel, Cat# 7024-1) packed with hexane and eluted with 10% ethyl acetate-hexane, yielding red 12-cyano-benz�b!acridine (1.54 g, 70%). Rf 0.7 (silica gel, hexane/ethyl acetate 2:1). MS (FAB, Thioglycerol Matrix): m/z 255 (M+1).
Benz�b!acridine-12-carboxylic Acid Hydrochloride
A mixture of 12-cyano-benz�b!acridine (557 mg, 2.19 mmol) and tetrabutylammonium bromide (71 mg, 0.22 mmol) in 50% sulfuric acid (v/v, 50 ml) was heated at 160.degree.-170.degree. C. under nitrogen with stirring for 44 hours and cooled. The resulting mixture was poured into ice-water (500 ml); the purple precipitate was collected and washed with water. The wet material was dissolved with warming in 2N NaOH (100 ml) and then filtered. The filtrate was acidified in an ice-water bath with concentrated HCl to pH 3-4, giving purple benz�b!acridine-12-carboxylic acid hydrochloride (510 mg, 75%). Rf 0.4 (silica gel, chloroform/methanol/water 65:25:4). MS (FAB, Thioglycerol Matrix): m/z 274 (M+1).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl Benz�b!acridine-12-carboxylate
A suspension of benz�b!acridine-12-carboxylic acid hydrochloride (370 mg, 1.2 mmol) in anhydrous pyridine (50 ml) was warmed at 60.degree. C. for 5 minutes. The slightly cloudy solution was then cooled to 0.degree. C. and treated with p-toluenesulfonyl chloride (388 mg, 2.33 mmol) at 0.degree. C. for 10 minutes and at room temperature for another 15 minutes to give the first reaction mixture. This reaction mixture was further treated with benzyl 2,6-dimethyl-4-hydroxybenzoate, see U.S. Pat. No. 4,745,181, (694 mg, 2.71 mmol) to give the second reaction mixture, which was stirred at room temperature under nitrogen for 40 hours, and then evaporated under reduced pressure to dryness. The residue was flash-chromatographed on a silica column packed with hexane and eluted with 50% ether-hexane to give orange-red (4-benzyloxycarbonyl-2,6-dimethyl)phenyl benz�b!acridine-12-carboxylate (450 mg), 74%). Rf 0.6 (silica gel, 20% ethyl acetate/toluene). MS (FAB, Thioglycerol Matrix): m/z 512 (M+1).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 5-Methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (LEAE-Bz)
To a solution of (4-benzyloxycarbonyl-2,6-dimethyl)phenyl benz�b!acridine-9-carboxylate (115 mg, 0.23 mmol) in anhydrous methylene chloride (5 ml) was added methyl fluorosulfonate (0.128 ml, 2.25 mmol). The solution was stirred at room temperature under nitrogen for 20 hours, and then treated with anhydrous ether (10 ml). The resulting precipitate was collected and washed with ether (100 ml), giving dark-brown (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 5-methyl-benz�b!acridinium-12-carboxylate fluorosulfonate (136 mg, 97%). MS (FAB, Thioglycerol Matrix): m/z 526 (M).
Example 2
Preparation of (2,6-Dimethyl-4-N-succinimidyloxycarbonyl)phenyl 5-Methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (LEAE-NHS)
(4-Carboxy-2,6-dimethyl)phenyl Benz�b!acridine-12-carboxylate Hydrobromide
A solution of (4-benzyloxycarbonyl-2,6-dimethyl)phenyl benz�b!acridine-12-carboxylate (198 mg, 0.39 mmol), prepared in Example 1, in 30% hydrogen bromide-acetic acid (5 ml) was stirred at 55.degree.-60.degree. C. under nitrogen for 4 hours. The mixture was treated with anhydrous ether (20 ml); the precipitate was collected and washed with ether (100 ml) to give (4-carboxy-2,6-dimethyl)phenyl benz�b!acridine-12-carboxylate hydrobromide quantitatively. Rf 0.4 (silica gel, 5% methanol/chloroform). MS (EI): m/z 421 (M).
(2,6-Dimethyl-4-N-succinimidyloxycarbonyl)phenyl Benz�b!acridine-12-carboxylate
To a solution of (4-carboxy-2,6-dimethyl)phenyl benz�b!acridine-12-carboxylate hydrobromide (108 mg, 0.22 mmol) in anhydrous N,N-dimethylformamide (5 ml) was added at 0.degree. C. dicyclohexylcarbodiimide (111 mg, 0.54 mmol). After stirring at this temperature for 30 minutes, N-hydroxysuccinimide (62 mg, 0.54 mmol) was added. The solution was stirred under nitrogen at 0.degree. C. for 10 minutes and then at room temperature for 24 hours. The resulting mixture was treated with acetic acid (3 drops) and evaporated to dryness under reduced pressure. The residue was extracted with chloroform and the chloroform extract was evaporated under reduced pressure to dryness. The residue was flash-chromatographed on a silica column packed and eluted with ether to give (2,6-dimethyl-4-N-succinimidyloxycarbonyl)phenyl benz�b!acridine-12-carboxylate (20 mg, 18%). Rf 0.6 (silica gel, 20%). MS (EI): m/z 518 (M).
(2,6-Dimethyl-4-N-succinimidyloxycarbonyl)phenyl 5-Methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (LEAE-NHS)
To a solution of (2,6-dimethyl-4-N-succinimidyloxycarbonyl)phenyl benz�b!acridine-12-carboxylate (14 mg, 0.026 mmol) in anhydrous methylene chloride (1 ml) was added methyl fluorosulfonate (0.021 ml, 0.26 mmol). The resulting brown solution was stirred at room temperature under nitrogen for 20 hours, and then treated with anhydrous ether (1 ml). The precipitate was collected and washed with ether (40 ml), yielding (2,6-dimethyl-4-N-succinimidyloxycarbonyl)phenyl 5-methylbenz�b!acridinium-12-carboxylate-fluorosulfonate (11 mg, 65%). MS (FAB, Thioglycerol Matrix): m/z 533 (M)
Example 3
Preparation of (4-Benzyloxycarbonyl-2,6-diisopropyl)phenyl 5-Methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (DIP-LEAE-Bz)
3,5-Diisopropyl-4-hydroxybenzoic acid
This acid was prepared according to the procedure of W. H. Meek et al. J. Chemical and Engineering Data, 14(3), 388, (1969). To a solution of 2,6-diisopropylphenol (Aldrich cat. # D12660-8) (37.0 ml, 0.20 mol) in anhydrous N,N-dimethylacetamide (150 ml) was added sodium methoxide (16.2 g, 0.30 mol). Carbon dioxide was passed through the mixture throughout the subsequent reaction period. The mixture was heated with stirring and the solvent was slowly distilled out during 2 hours of the period until the pot temperature reached to 180.degree. C. The mixture was allowed to continue stirring at 180.degree. C. for another 1.5 hours and then cooled to 90.degree. C. The flow of carbon dioxide was discontinued and water (400 ml) was added. The mixture, after further cooled to room temperature, was washed with toluene (4.times.60 ml) and then treated with conc. hydrochloric acid in an ice-water bath to pH 3. The resulting mixture was extracted with diethyl ether (2.times.150 ml); the ether extract was washed with brine (100 ml) and dried over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure gave 3,5-diisopropyl-4-hydroxybenzoic acid (10.4 g, 23%). Rf 0.5 (silica gel, 50% diethyl ether/hexane). MS (CI, CH4): m/z 223 M+1).
Benzyl 3,5-Diisopropyl-4-hydroxybenzoate
To a solution of 3,5-diisopropyl-4-hydroxybenzoic acid (1.223 g, 5.50 mmol) in methanol (25 ml) was added potassium hydroxide (308 mg, 5.50 mmol) in water (5 ml). The resulting solution was stirred at room temperature under nitrogen for 1 hour, and then evaporated completely to dryness under reduced pressure. This potassium salt was dissolved in anhydrous acetonitrile (30 ml) and N,N-dimethylformamide (15 ml), and treated with dibenzo-18-crown-6 (198 mg, 0.55 mmol). After 30 minutes of stirring at 80.degree. C. under nitrogen, the solution was further treated with benzyl bromide (0.712 ml, 6.05 mmol). The stirring was continued at 80.degree. C. under nitrogen for 4 hours. The resulting mixture, after cooling, was filtrated. The filtrate was evaporated under reduced pressure to dryness. The residue was flash-chromatographed on a silica column packed with hexane and eluted with 20% ethyl acetate/hexane, yielding crystalline benzyl, 3,5-diisopropyl-4-hydroxybenzoate (1.35 g, 79%). Rf 0.6 (silica gel, 20% ethyl acetate/toluene). MS(EI). m/z 312 (M).
(4-Benzyloxycarbonyl-2,6-diisopropyl)phenyl Benz�b!acridine-12-carboxylate
A suspension of benz�b!acridine-12-carboxylic acid hydrochloride from Example 1 (200 mg, 0.65 mmol) in anhydrous pyridine (30 ml) was warmed at 60.degree. C. for 5 minutes. The slightly cloudy solution was then cooled to 0.degree. C. and treated with p-toluenesulfonyl chloride (247 mg, 1.29 mmol). The solution was stirred at 0.degree. C. for 40 minutes and room temperature for another 10 minutes, and benzyl 2,6-diisopropyl-4-hydroxybenzoate (202 mg, 0.65 mmol) was added. This reaction mixture was allowed to continue stirring at room temperature under nitrogen for 20 hours, and then evaporated under reduced pressure to dryness. The residue was flash-chromatographed on a silica column packed with hexane and eluted with 25% ether-hexane to give orange (4-benzyloxycarbonyl-2,6-diisopropyl)phenyl benz�b!acridine-12-carboxylate (187 mg, 51%). Rf 0.6 (silica gel, 20% ethyl acetate/toluene). MS(CI, CH4): m/z 570 (M+3).
(4-Benzyloxycarbonyl-2,6-diisopropyl)phenyl 5-Methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (DIP-LEAE-Bz)
To a solution of (4-Benzyloxycarbonyl-2,6-diisopropyl)phenyl benz�b!acridine-12-carboxylate (50 mg, 0.088 mmol) in anhydrous methylene chloride (3 ml) was added methyl fluorosulfonate (0.072 ml, 0.088 mmol). The brown solution was stirred at room temperature under nitrogen for 24 hours, and then treated with anhydrous ether (4 ml). The resulting precipitate was collected and washed with ether (10 ml), giving dark-brown (4-benzyloxycarbonyl-2,6-diisopropyl)phenyl 5-Methyl-benz�b!acridinium-12-carboxylate fluorosulfonate (39 mg, 64%). MS (FAB, Thioglycerol Matrix): m/z 582 (M).
Example 4
Preparation of N-(4-Methoxyphenyl-N-�3-(benzyloxycarbonyl)phenylsulfonyl! 5-Methyl-benz�b!acridinium-12-carboxamide Fluorosulfonate (LEAC-Bz)
3-�N-(4-Methoxyphenyl)sulfamido!benzoic acid
To a solution of 3-(chlorosulfonyl)benzoic acid (Kodak cat. #1188655) (4.4 g, 20.00 mmol) and triethylamine (2.78 ml, 20.00 mmol) in anhydrous methylene chloride (40 ml) was added at 0.degree. C. 4-anisidine (2.46 g, 20.00 mmol). After 10 minutes of stirring at 0.degree. C., a large quantity of precipitate formed from the solution. The mixture was allowed to continue stirring at room temperature under nitrogen for 2 hours. After filtration, the collected off-white solid was washed with water (50 ml) and then with ether (50 ml), giving 3-�N-(4-methoxyphenyl)sulfamido!benzoic acid (4.50 g, 74%). Rf 0.5 (silica gel, chloroform/methanol/water 65:25:4). MS(CI, CH4): m/z 308 (M+1).
Benzyl 3-�N-(4-Methoxyphenyl)sulfamido!benzoate
To a solution of 3-�N-(4-methoxyphenyl)sulfamido!benzoic acid (2.00 g, 6.52 mmol) in N,N-dimethylformamide (20 ml) was added a solution of sodium hydroxide (260.6 mg, 6.52 mmol) in water (5 ml). The resulting solution was stirred at room temperature under nitrogen for 1 hour, and then evaporated completely to dryness under reduced pressure. This sodium salt was dissolved in anhydrous acetonitrile (40 ml) and N,N-dimethylformamide (20 mL), and treated with dibenzo-18-crown-6 (235 mg, 0.65 mmol). After 30 minutes of stirring at 80.degree. C. under nitrogen, the solution was further treated with benzyl bromide (0.852 ml, 7.27 mmol). The stirring was continued at 80.degree. C. under nitrogen for 4 hours. The resulting mixture, after cooling, was filtrated. The white solid was washed with small amount of acetonitrile. The combined acetonitrile filtrate was evaporated under reduced pressure to dryness. The reside was flash-chromatographed on a silica column packed with hexane and eluted with 15% ethyl acetate/hexane, yielding crystalline benzyl 3-�N-(4-methoxyphenyl)sulfamido!benzoate (2.00 g, 77%). Rf 0.5 (silica gel, 20% ethyl acetate/toluene). MS(CI, CH4): m/z 397 (M+1).
N-(4-Methoxyphenyl)-N-�3-(benzyloxycarbonyl)phenylsulfonyl! Benz�b!acridine-12-carboxamide
A suspension of benz�b!acridine-12-carboxylic acid hydrochloride (200 mg, 0.65 mmol) in anhydrous pyridine (30 ml) was warmed at 60.degree. C. for 5 minutes. The slightly cloudy solution was then cooled to 0.degree. C., and treated with p-toluenesulfonyl chloride (247 mg, 1.29 mmol). The solution was stirred at 0.degree. C. for 40 minutes and room temperature for another 10 minutes, and benzyl 3-�N-(4-methoxyphenyl)sulfamido!benzoate (257 mg, 0.65 mmol) was added. This reaction mixture was allowed to continue stirring at room temperature under nitrogen for 20 hours, and then was evaporated under reduced pressure to dryness. The residue was flash-chromatographed on a silica column packed with hexane and eluted with 25% hexane-ether to give orange N-(4-methoxyphenyl)-N-�3-(benzyloxycarbonyl)phenylsulfonyl! benz�b!acridine-12-carboxamide (177 mg, 68%). Rf 0.4 (silica gel, 20% ethyl acetate/toluene). MS(CI, CH4): m/z 653 (M+1).
N-(4-Methoxyphenyl)-N-�3-(benzyloxycarbonyl)phenylsulfonyl!5-Methyl-benz�b!acridinium-12-carboxamide Fluorosulfonate (LEAC-Bz)
To a solution of N-(4-methoxyphenyl)-N-�3-(benzyloxycarbonyl)phenylsulfonyl! benz�b!acridine-12-carboxamide (50 mg, 0.077 mmol) in anhydrous methylene chloride (3 ml) was added methyl fluorosulfonate (0.062 ml, 0.77 mmol). The dark-brown solution was stirred at room temperature under nitrogen for 20 hours, and treated with anhydrous ether (10 ml). The resulting precipitate was collected and washed with ether (10 ml), giving blue-black N-(4-methoxyphenyl)-N-�3-(benzyloxycarbonyl)phenylsulfonyl! 5-methyl-benz�b!acridinium-12-carboxamide fluorosulfonate (38 mg, 65%). MS (FAB, Thioglycerol Matrix): m/z 667 (M).
Example 5
Preparation of (4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-Ethoxy-5-methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (3-EtO-LEAE-Bz) Benzo�5.6!isatin
Benzo�5,6!isatin was prepared according to the procedure of A. Etienne and A. Staehelin, Bull. Soc. Chim. France., 6, 743, (1954).
3-Hydroxy-benz�b!acridine-12-carboxylic Acid.
A mixture of benzo�5,6!isatin (500 mg, 2.54 mmol) and potassium hydroxide (996 mg, 17.78 mmol) in water (2 ml) and n-butanol (2 ml) was heated with stirring to 100.degree. C. to give a homogeneous solution, followed by addition of resorcinol (1.95 g, 17.78 mmol). After the solution was further heated to 140.degree. C. and the solvents were slowly blown away with nitrogen during a 30-minute period, another 2 ml of water and 1 ml of n-butanol were added. The temperature of the solution was maintained at 140.degree. C. while blowing of nitrogen continued for a total of 2 hours. The gummy mixture was cooled and dissolved in 100 ml of water; the solution was acidified with concentrated hydrochloric acid in an ice-water bath to pH 2. The resulting precipitate was collected, washed with water, and flash-chromatographed on a silica column packed with chloroform and eluted with 20% methanol-chloroform followed by chloroform-methanol-water (65:25:4) to give 3-hydroxy-benz�b!acridine-12-carboxylic acid (210 mg, 29%). Rf 0.3 (silica gel, chloroform/methanol/water 65:25:4). MS (FAB, Thioglycerol Matrix): m/z 290 (M+1).
Ethyl 3-Ethoxy-benz�b!acridine-12-carboxylate
To a mixture of 3-hydroxy-benz�b!acridine-12-carboxylic acid (90 mg, 0.28 mmol) and cesium carbonate (451 mg, 1.38 mmol) in methyl sulfoxide (3.5 ml) was added bromoethane (207 .mu.l, 2.77 mmol). The mixture was stirred under nitrogen at 25.degree. C. for 4 hours, and treated with water (10 ml). The mixture was adjusted to pH 5 with 5% HCl; the resulting precipitate was collected and washed with water. The crude product was purified on a silica column packed with chloroform and eluted with 5% methanol-chloroform to give ethyl 3-ethoxy-benz�b!acridinium-12-carboxylate (36 mg, 38%). Rf 0.5 (silica gel, diethyl ether/hexane 3:1). MS (FAB, Thioglycerol Matrix): m/z 346 (M+1).
3-Ethoxy-benz�b!acridinium-12-carboxylic Acid Hydrochloride
A solution of ethyl 3-ethoxy-benz�b!acridinium-12-carboxylate (35 mg, 0.10 mmol) in 16% sodium hydroxide (1 ml) and methanol (3 ml) was stirred under nitrogen at 25.degree. C. for 2 days and at 40.degree. C. for additional 4 hours, and then evaporated to dryness under reduced pressure. The residue was suspended in water (20 ml) and adjusted to pH 3 in an ice-water bath with concentrated HCl. The precipitate was collected and washed with water to give 3-ethoxybenz�b!acridine-1 2-carboxylic acid hydrochloride (30 mg, 83%). Rf 0.8 (silica gel, chloroform/methanol/water 65:25:4). MS (CI, CH4): m/z 318 (M+1).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-Ethoxy-benz�b!acridine-12-carboxylate
A slightly-cloudy solution of 3-ethoxy-benz�b!acridine-12-carboxylic acid hydrochloride (19 mg, 0.054 mmol) in pyridine (1 ml) and N,N'-dimethylpropyleneurea (DMPU, 1.5 ml) was cooled at 0.degree. C. and p-toluenesulfonyl chloride (21 mg, 0.11 mmol) was added. After 20 minutes of stirring, benzyl 3,5-dimethyl-4-hydroxybenzoate (14 mg, 0.055 mmol) and N,N'-dimethylaminopyridine (1 mg) were added. The mixture was stirred at 25.degree. C. under nitrogen for 20 hours and then evaporated under reduced pressure to dryness. The residue was treated with water (5 ml) and extracted with ether (5.times.5 ml). The combined ether layer was washed with water (1.times.10 ml), brine (1.times.10 ml) and dried over magnesium sulfate. Removal of the solvent under reduced pressure gave a crude mixture, which was separated on a preparative-TLC plate (2 mm silica gel, EM Art. 5717) by developing with ether/hexane (3:2). The major orange band was collected and extracted with 10% methanol/ether. Removal of the solvents under reduced pressure gave orange (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 3-ethoxy-benz�b!acridine-12-carboxylate (5 mg, 17%). Rf 0.6 (silica gel, diethyl ether/hexane). MS (FAB, Thioglycerol Matrix): m/z 556 (M+1).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-Ethoxy-5-methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (3-EtO-LEAE-Bz)
To a solution of (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 3-ethoxy-benz�b!acridine-12-carboxylate (9 mg, 0.0162 mmol) in methylene chloride (1 ml) was added methyl fluorosulfonate (13.1, 0.162 mmol). The solution was stirred at 25.degree. C. under nitrogen for 36 hours and then treated with diethyl ether (10 ml). The precipitate was collected and washed with diethyl ether (20 ml), giving (4-benzyloxycarbonyl-2,6-dimethyl)phenyl-3-ethoxy-5-methyl benz�b!acridinium-12-carboxylate fluorosulfonate (3-EtO-LEAE-Bz , 7 mg 65%) MS (CI, CH4): m/z 570 (M+2).
Example 6
Preparation of (4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-(N,N-Diethyl-N-methyl-ammonium)ethoxy-5-methyl-benz�b!acridinium-12-carboxylate Difluorosulfonate (3-QAE-LEAE-Bz)
N,N-Diethylaminoethyl 3-(N,N-Diethylamino)ethoxy-benz�b!acridine-12-carboxylate
A solution of 3-hydroxy-benz�b!acridine-12-carboxylic acid (415 mg, 1.28 mmol) in methyl sulfoxide (12 ml) was treated with cesium carbonate (5 g, 15.4 mmol) at 25.degree. C. for 10 minutes and diethylamminoethyl bromide hydrobromide (1.5 g, 6.4 mmol) was added. The mixture was stirred at 25.degree. C. under nitrogen for 4 hours and then quenched with water (100 ml). The precipitate was collected and washed with water (50 ml). The crude product was separated on 4 preparative-TLC plates (2 mm silica gel) by developing with 20% methanol/chloroform. The orange band was collected and extracted with 10% methanol/chloroform. Removal of the solvents under reduced pressure gave N,N-diethylaminoethyl 3-(N,N-diethylamino)ethoxy-benz�b!acridine-12-carboxylate (73 mg, 12%). Rf 0.6 (silica gel, 20% methanol/chloroform). MS (CI, CH4): m/z 488 (M+1).
3-(N,N-Diethylamino)ethoxy-benz�b!acridine-12-carboxylic acid hydrochloride
A solution of N,N-diethylaminoethyl 3-(N,N-diethylamino)ethoxy-benz�b!acridine-12-carboxylate (60 mg, 0.123 mmol) in 4N sodium hydroxide (4 ml) and methanol (12 ml) was stirred at 65.degree. C. under nitrogen for 16 hours, and then evaporated under reduced pressure to dryness. The residue was dissolved in water (10 ml); the solution was carefully acidified in an ice-water bath with concentrated HCl to pH 4. The resulting precipitate was collected and washed with diethyl ether (5 ml) to give 3-(N,N-diethylamino)ethoxy-benz�b!acridine-12-carboxylic acid hydrochloride (32 mg, 61%). Rf 0.3 (silica gel, chloroform/methanol/water 65:25:4).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-(N,N-Diethylamino ethoxy-benz�b!acridine-12-carboxylate
A mixture of 3-(N,N-diethylamino)ethoxybenz�b!acridine-12-carboxylic acid hydrochloride (29 mg, 0.069 mmol) and p-toluenesulfonyl chloride (29 mg, 0.152 mmol) in pyridine (12 ml) was stirred at 80.degree. C. for 5 minutes. The resulting homogeneous solution was cooled to 25.degree. C. and further treated with benzyl 4-hydroxy-3,5-dimethylbenzoate (20 mg, 0.078 mmol). After stirring at 25.degree. C. under nitrogen for 16 hours, the solvent was removed under reduced pressure. The residue was purified on a preparative-TLC plate (2 mm silica gel) developed with 15% methanol/chloroform. The orange band was collected and extracted with 10% methanol/chloroform. Evaporation of the solvents under reduced pressure gave (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 3-(N,N-diethylamino)ethoxy-benz�b!acridine-12-carboxylate (17 mg, 39%). Rf 0.6 (silica gel, 10% methanol/chloroform). MS (FAB, Glycerol Matrix): m/z 627 (M+1).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-(N,N-Diethyl-N-methyl-ammonium)ethoxy-5-methyl-benz�b!acridinium-12-carboxylate Difluorosulfonate (3-OAE-LEAE-Bz)
A solution of (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 3-(N,N-diethylamino)ethoxy-benz�b!acridine-12-carboxylate (13 mg, 0.0208 mmol) in methylene chloride (1.9 ml) was treated with methyl fluorosulfonate (25 .mu.l, 0.308 mmol). After 15 hours of stirring under nitrogen at 25.degree. C., the reaction mixture was slowly added to diethyl ether (5 ml). The precipitate was collected and washed with ether (10 ml) to give (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 3-(N,N-diethyl-N-methyl-ammonium)ethoxy-5-methyl benz�b!acridinium-12-carboxylate difluorosulfonate (3-QAE-LEAE-BZ, 9 mg, 53%). MS (FAB, Glycerol Matrix): m/z 659 (M+3).
Example 7
Preparation of (4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 2-Methoxy-5-methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (2-MeO-LEAE-Bz)
3-(4-Methoxy)anilino-2-naphthoic Acid
A mixture of p-anisidine (84.7 g, 687.7 mmol) and 3-hydroxy-2-naphthoic acid (64.7 g, 343.9 mmol) was mechanically stirred at 160.degree. C. under nitrogen for 22 hours. After cooling to 130.degree. C., the mixture was treated with hot 1N hydrochloric acid (1000 ml), stirred at 130.degree. C. for 10 minutes, and filtrated, when hot. The resulting cake was stirred with hot 0.5N sodium carbonate (2200 ml) for 15 minutes and filtrated when hot. The filtrate was cooled and acidified to pH 6.5 with concentrated HCl in an ice-water bath. The precipitate was collected and washed with methanol (150 ml), yielding 3-(4-methoxy)anilino-2-naphthoic acid (14.8 g, 15%). Rf 0.6 (silica gel, 10% methanol/chloroform). MS (CI, CH4): m/z 294 (M+1).
12-Chloro-2-methoxy-benz�b!acridine
A mixture of 3-(4-methoxy)anilino-2-naphthoic acid (15.4 g, 49.44 mmol) and phosphorousoxy chloride (46 ml, 494.4 mmol) was refluxed at 120.degree. C. under nitrogen for 3.5 hours, and then evaporated under reduced pressure to dryness. The residue was taken into a mixed solvent containing chloroform (500 ml)/ice (450 g)/ammonium hydroxide (450 ml). The resulting two layers were separated. The aqueous layer was extracted with chloroform (3.times.250 ml). The combined chloroform layer was dried over calcium chloride and evaporated to dryness under reduced pressure, yielding 12-chloro-2-methoxy-benz�b!acridine (12.5 g, 86%). Rf 0.8 (silica gel, 60% diethyl ether/hexane). MS (CI, CH4): m/z 294 (M+1).
12-Cyano-2-methoxy-benz�b!acridine A mixture of -12-chloro-2-methoxy-benz�b!acridine (562 mg, 1.905 mmol), potassium cyanide (136 mg, 2.096 mmol) and copper(I) cyanide (86 mg, 0.953 mmol) in methanol (3.7 ml) was stirred at 170.degree. C. in a sealed-tube for 4.5 hours. The resulting mixture was filtrated, and the solid was washed with chloroform/methanol (2:1, 10 ml). The combined filtrate was evaporated under reduced pressure to give a residue, which was flash-chromatographed on a silica column packed with chloroform and eluted with 1% methanol/chloroform to yield -12-cyano-2-methoxy-benz�b!acridine (477 mg, 88%). Rf 0.6 (silica gel, 1% methanol/chloroform). MS (CI, CH4): m/z 285 (M+1).
2-Hydroxy-benz�b!acridine-12-carboxylic acid hydrosulfate
A mixture of -12-cyano-2-methoxy-benz�b!acridine (8.3 g, 29.1 mmol) and 50% sulfuric acid (v/v, 280 ml) was mechanically stirred under nitrogen at 160.degree. C. for 48 hours. The resulting mixture was cooled and poured into ice-water (1800 ml). The precipitate was collected, washed with water (200 ml), and flash-chromatographed on a silica column packed with chloroform and eluted with 20% methanol/chloroform followed by chloroform/methanol/water (65:25:4) to give 2-hydroxy-benz�b!acridine-12-carboxylic acid hydrosulfate (4.8 g, 43%). Rf 0.4 (silica gel, chloroform/methanol/water 65:25:4).
Methyl 2-Methoxy-benz�b!acridine-12-carboxylate
To a solution of 2-hydroxy-benz�b!acridine-12-carboxylic acid hydrochloride (186 mg, 0.572 mmol) in methyl sulfoxide (4 ml) were added cesium carbonate (746 mg, 2.29 mmol) and iodomethane (143 .mu.l, 2.29 mmol). The resulting mixture was stirred at 25.degree. C. under nitrogen for 4 hours and then treated with water (50 ml). The mixture was acidified in an ice-water bath with concentrated HCl to pH 6. The resulting precipitate was collected, washed with water (5 ml) and air-dried. The crude mixture was purified on 4 preparative-TLC plates (2 mm silica gel) developed with diethyl ether/hexane (5:1); the major orange band was collected and extracted with 10% methanol/chloroform. Removal of the solvents under reduced pressure gave methyl 2-methoxy-benz�b!acridine-12-carboxylate (35 mg, 17%). Rf 0.8 (silica gel, diethyl ether/hexane 5:1).
2-Methoxy-benz�b!acridine-12-carboxylic Acid
A solution of methyl 2-methoxy-benz�b!acridine-12-carboxylate (35 mg, 0.10 mmol) in 4N sodium hydroxide (3 ml) and methanol (9 ml) was stirred at 65.degree. C. for 15 hours. The resulting mixture was evaporated under reduced pressure to dryness. The residue was dissolved in water (40 ml); the aqueous solution was acidified to pH 5 with concentrated HCl in an ice-water bath. The precipitate was collected and washed with water (5 ml), yielding 2-methoxybenz�b!acridine-12-carboxylic acid (20 mg, 59%). Rf 0.5 (silica gel, chloroform/methanol/water 65:25:4). MS (CI, CH4: m/z 304 (M+1).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 2-Methoxybenz�b!acridine-12-carboxylate
A solution of 2-methoxy-benz�b!acridine-12-carboxylic acid (18 mg, 0.0529 mmol) in pyridine (5 ml) was treated with p-toluenesulfonyl chloride (20 mg, 0.106 mmol) at 25.degree. C. for 15 minutes and then benzyl 3,5-dimethyl-4-hydroxybenzoate (27 mg, 0.106 mmol) was added. After 15 hours of stirring at 25.degree. C. under nitrogen, the reaction mixture was evaporated under reduced pressure to remove the pyridine. The residue was purified on a preparative-TLC (2 mm silica gel) developed with diethyl ether/hexane (3:2). The orange band was collected and extracted with 5% methanol/chloroform. Removal of the solvents under reduced pressure gave (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 2-methoxy-benz�b!acridine-12-carboxylate (2.7 mg, 9%). Rf 0.5 (silica gel, 60% diethyl ether/hexane).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 2-Methoxy-5-methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (2-MeO-LEAE-Bz)
A solution of 4-benzyloxycarbonyl-2,6-dimethyl)phenyl 2-methoxy-benz�b!acridine-12-carboxylate (2.5 mg, 0.0046 mmol) in methylene chloride (1 ml) was treated with methyl fluorosulfonate (3.7 .mu.l, 0.56 mmol) at 25.degree. C. with stirring under nitrogen for 15 hours. The reaction mixture was added to anhydrous diethyl ether (4 ml). The resulting precipitate was collected and washed with diethyl ether (5 ml) to afford (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 2-methoxy-5-methyl-benz�b!acridinium-12-carboxylate fluorosulfonate (2-MeO-LEAE-Bz) (1.5 mg, 49%). MS (FAB, Thioglycerol Matrix): m/z 556(M).
Example 8
Preparation of (2,6-Dimethyl-4-succinimidyloxycarbonyl)phenyl 5-Methyl-2-(trimethylammonium)ethoxy-benz�b!acridinium-12-carboxylate Difluorosulfonate (2-QAE-LEAE-NHS)
N,N-Dimethylaminoethyl 2-(N,N-Dimethylamino)ethoxy-benz�b!acridine-12-carboxylate
To a solution of 2-hydroxy-benz�b!acridine-12-carboxylic acid hydrochloride (360 mg, 1.108 mmol) in methyl sulfoxide (11 ml) were added cesium carbonate (3.61 g, 11.08 mmol) and N,N-dimethylaminoethyl bromide hydrobromide (1.03 g, 4.432 mmol). After 15 hours of stirring at 60.degree. C. under nitrogen, the reaction mixture was diluted with methyl sulfoxide (20 ml) and filtered to remove the insoluble impurities. The filtrate was concentrated under reduced pressure to a small volume, which was separated on a preparative-TLC plate (2 mm silica gel) by developing with chloroform/methanol/water (47:48:5). The desired orange band was collected and extracted with 25% methanol/chloroform. Removal of the solvents under reduced pressure gave N,N-dimethylaminoethyl 2-(N,N-dimethylamino)ethoxy-benz�b!acridine-12-carboxylate (86 mg, 18%). Rf 0.6 (silica gel, chloroform/methanol/water 65:25:4). MS (FAB, Glycerol Matrix): m/z 432 (M+1).
2-(N,N-Dimethylamino)ethoxy-benz�b!acridine-12-carboxylic acid
A solution of N,N-dimethylaminoethyl 2-(N,N-dimethylamino)ethoxy-benz�b!acridine-12-carboxylate (86 mg, 0.20 mmol ) in 4N sodium hydroxide (7.3 ml) and methanol (22 ml) was stirred at 65.degree. C. for 1 hour and at 35.degree. C. for 15 hours. The reaction mixture was evaporated under reduced pressure to dryness. The residue was washed with water (5 ml) and air-dried, yielding 2-(N,N-dimethylamino)ethoxy-benz�b!acridine-12-carboxylic acid (23 mg, 32%). Rf 0.3 (silica gel, chloroform/methanol/water 65:25:4). MS (FAB, Glycerol Matrix): m/z 361 (M+1).
Succinimidyl 3,5-Dimethyl-4-hydroxy-benzoate
A solution of 3,5-dimethyl-4-hydroxybenzoic acid (5.0 g, 30.0 mmol) in N,N -dimethylformamide (150 ml) was cooled to 0.degree. C. and treated with N-hydroxysuccinimide (3.45 g, 30.0 mmol) and 1,3-dicyclohexylcarbodiimide (6.81 g, 33.0 mmol). The solution was stirred under nitrogen at 0.degree. C. for 2 hours and then at 25.degree. C. for 16 hours. The resulting mixture was stirred with 0.5 ml of acetic acid for 15 minutes, and then filtered to remove the insoluble urea. The filtrate was evaporated under reduced pressure to dryness. The dried material was washed with diethyl ether (100 ml) and suspended in boiling ethyl acetate (200 ml). The suspension, when hot, was filtered to remove insoluble impurities. The filtrate was concentrated and suspended in hot ethyl acetate/methylene chloride (1:1, 200 ml) and cooled to give an off-white powder in 2.91 g (37%). Rf 0.6 (silica gel, diethyl ether). (2,6-Dimethyl-4-succinimidyloxycarbonyl)phenyl 2-(N,N-Dimethylamino)ethoxy-benz�b!acridine-12-carboxylate
A solution of 2-(N,N-dimethylamino)ethoxybenz�b!acridine-12-carboxylic acid (30 mg, 0.0833 mmol) in pyridine (4 ml) was treated with p-toluenesulfonyl chloride (31.8 mg, 0.166 mmol) at 25.degree. C. for 10 minutes, followed by addition of succinimidyl 3,5-dimethyl-4-hydroxybenzoate (32 mg, 0.0833 mmol). After 15 hours of stirring at 25.degree. C. under nitrogen, the solution was diluted with chloroform (10 ml), quickly washed with water (3.times.4 ml) and evaporated under reduced pressure to dryness. The residue was purified on two preparative-TLC plates (lmm silica gel) developed with 10% methanol/chloroform. The desired orange band was collected and extracted with 10% methanol/chloroform. Removal of the solvents under reduced pressure gave (2,6-dimethyl-4-succinimidyloxycarbonyl)phenyl 2-(N,N-dimethylamino)ethoxy-benz�b!acridine-12-carboxylate (7 mg, 14%). Rf 0.8 (silica gel, 10% methanol/chloroform). MS (FAB, Thioglycerol Matrix): m/z 606 (M+1).
(2,6-Dimethyl-4-succinimidyloxycarbonyl)phenyl 5-Methyl-2-(trimethylammonium)ethoxy-benz�b!acridinium-12-carboxylate Difluorosulfonate (2-OAE-LEAE-NHS)
A solution of 2, 6-dimethyl-4-N-succinimidyloxycarbonyl)phenyl 2-(N,N-dimethyl amino)ethoxy-benz�b!acridine carboxylate (1.9 mg, 0.0031 mmol) in anhydrous methylene chloride (4 ml) was treated with methyl fluorosulfonate (3.8 .mu.l, 0.0465 mmol). The solution was allowed to stir at 25.degree. C. under nitrogen for 16 hours. The resulting precipitate was collected and washed with diethyl ether (2 ml) to give (2,6-dimethyl-4-succinimidyloxycarbonyl)phenyl 5-methyl-2-(trimethylammonium)ethoxy-benz�b!acridinium-12-carboxylate difluorosulfonate (2-QAE-LEAE-NHS) (1.0 mg, 39%).
Example 9
Preparation of (4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 5-(3-Sulfopropyl)-benz�b!acridinium-12-carboxylate (NSP-LEAE-Bz)
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 5-(3-Sulfopropyl)-benz�b!acridinium-12-carboxylate (NSP-LEAE-Bz)
A mixture of (4-benzylcarboxyl-2,6-dimethyl)phenyl benz�b!acridine-12-carboxylate from Example 1 (30 mg, 0.0587 mmol) and 1,3-propane sulton (600 mg, 4.9 mmol) was flushed with nitrogen and kept in a sealed tube. The tube was heated with stirring at 180.degree. C. for 5 hours and then cooled. The resulting mixture was purified by reverse-phase preparative-HPLC on a C-18 column (YMC SH-344-15, S-15, 128), eluted under gradient condition with 25% to 40% acetonitrile in 0.05M aqueous trifluoroacetic acid from 0 to 20 minutes, 40% to 90% over 5 minutes, and maintaining 90% acetonitrile for another 10 minutes. The fraction with retention time of 17 minutes was collected and evaporated under reduced pressure to give 3.2 mg of the title compound (NSP-LEAE-Bz). MS (FAB, Glycerol Matrix): m/z 634 (M+1).
Example 10
Preparation of (2,6-Dimethyl-4-N-succinimidyloxycarbonyl)phenyl 2-Methoxy-5-(2-sulfoethyl)benz�b!acridinium-12-carboxylate (2-MeO-NSE-LEAE-NHS)
(2,6-Dimethyl-4-N-succinimidyloxycarbonyl)phenyl 2-Methoxy-benz�b!acridinium-12-carboxylate
A mixture of 2-methoxy-benz�b!acridine-12-carboxylic acid from Example 7 (208 mg, 0.6118 mmol) in pyridine (20 ml) was treated with p-toluenesulfonyl chloride (233 mg, 1.2235 mmol) at 25.degree. C. for 10 minutes, followed by addition of succinimidyl 3,5-dimethyl-4-hydroxy-benzoate (161 mg, 0.6118 mmol). After 24 hours of stirring under nitrogen at 25.degree. C., the pyridine was removed by evaporation under reduced pressure. The resulting mixture was flash-chromatographed on a silica column packed and eluted with diethyl ether. The crude product collected was further purified on a Chromatotron plate (1 mm silica gel) by elution with diethyl ether to yield 80 mg (24%) of the pure product. Rf 0.8 (silica gel, ethyl acetate/hexane 2:1). MS (FAB, Thioglycerol Matrix): 549 (M+1).
2,6-Dimethyl-4-N-succinimidyloxycarbonyl)phenyl 2-Methoxy-5-(2-sulfoethyl)-benz �b!acridinium-12-carboxylate (2-MeO-NSE-LEAE-NHS)
A mixture of (2,6-dimethyl-4-N-succinimidyloxycarbonyl)phenyl 2-methoxy-benz�b!acridine-12-carboxylate (23 mg, 0.04197 mmol) and ethylenesulfonyl chloride (prepared according to the procedure of C. S. Rondestredt Jr., J. Amer. Chem. Soc., 76, 1926 (1954)) (378 .mu.l, 4.197 mmol) was stirred at 25.degree. C. under nitrogen for 63 hours. The resulting mixture was purified by reverse-phase preparative-HPLC on a C-18 column, eluted under gradient condition with 35% acetonitrile in 0.05M aqueous trifluoroacetic acid from 0 to 10 minutes, 35% to 80% from 10 to 30 minutes, 80% to 90% from 30 to 35 minutes, and remaining 90% for another 5 minutes. The fraction with retention time of 25 minutes was collected and evaporated under reduced pressure to give 2.2 mg (8%) of the title compound (2-MeO-NSE-LEAE-NHS). MS (FAB, Thioglycerol Matrix): m/z 657 (M+1).
Example 11
Preparation of �2,6-Dimethyl-4-(2-methoxyiminoethyl)!phenyl 2-Methoxy-5-methyl-benz�b!acridinium-12-carboxylate Dichloride (2-MeO-LEAE-Imidate)
(4-Cyanoethyl-2,6-dimethyl)phenyl 2-Methoxy-benz�b!acridine-12-carboxylate
A suspension of 2-methoxy-benz�b!acridine-12-carboxylic acid from Example 7 (100 mg, 0.2941 mmol) in pyridine (15 ml) was treated with p-toluenesulfonyl chloride (112 mg, 0.5882 mmol) at 0.degree. C. for 40 minutes, followed by addition of triethylamine (164 .mu.l. 1.1789 mmol) and 4-cyanoethyl-2,6-dimethyl-phenol (prepared according to the procedure of E. Jexova et al, CS 158810, Jul. 15, 1975; CA 84(13):898299)(51 mg, 0.2914 mmol). After 18 hours of stirring at 25.degree. C. under nitrogen, the reaction solution was evaporated under reduced pressure to remove the pyridine. The residue was purified on 4 preparative-TLC plates (2 mm silica gel) developed twice with ethyl acetate/hexane (3:4). The major orange band was collected and extracted with methanol/chloroform (1:30). Removal of the solvents under reduced pressure gave the title compound (75 mg, 55%). Rf 0.5 (silica gel, ethyl acetate/hexane 2:3). MS (FAB, Thioglycerol Matrix): m/z 461 M+1).
(4-Cyanoethyl-2-6-dimethyl)phenyl 2-Methoxy-5-methyl benz�b!acridinium-12-carboxylate Fluorosulfonate
A solution of (4-cyanoethyl-2,6-dimethyl)phenyl 2-methoxy-benz�b!acridine-12-carboxylate (20 mg, 0.04338 mmol) in methylene chloride (1 ml) was treated with methyl flurosulfonate (17.5 .mu.l, 0.2169 mmol) at 25.degree. C. with stirring under nitrogen for 18 hours. The reaction mixture was added to anhydrous diethyl ether (5 ml). The resulting precipitate was collected and purified by reverse-phase preparative-HPLC on a C-18 column, eluted under gradient condition with 40% to 80% acetonitrile in 0.05M aqueous trifluoroacetic acid from 0 to 30 minutes, and remaining 80% acetonitrile for another 40 minutes. The fraction with retention time of 24 minutes was collected and evaporated under reduced pressure to give the product (15.7 mg 65%). MS (FAB, Thioglycerol Matrix): m/z 475 (M).
�2, 6-Dimethyl-4-(2-methoxyiminoethyl)!phenyl 2-methoxy-5-methyl benz�b!acridinium-12-carboxylate Dichloride (2-MeO-LEAE-Imidate)
A solution of (4-cyanoethyl-2,6-dimethyl)phenyl 2-Methoxy-5-methyl benz�b!acridinium-12-carboxylate fluorosulfonate (4 mg, 0.00697 mmol) in anhydrous methanol (0.5 ml) was treated with anhydrous hydrogen chloride (gas) at 0.degree. C. for 10 minutes. The reaction solution was then reduced by blowing with nitrogen to a small volume; and the concentrate was added to anhydrous diethyl ether (3 ml). The resulting precipitate was collected and washed with diethyl ether (5 ml), yielding the title compound (2-MeO-LEAE-Imidate) (1.5 mg, 37%).
PREPARATION OF THE ANALOGS OF ACRIDINIUM ESTER.
Example 12
Preparation of (4-Benzyloxycarbonyl-2,6-diisopropyl)phenyl 10-Methyl-acridinium-9-carboxylate Fluorosulfonate (DIPAE-BZ)
(4-Benzyloxycarbonyl-2,6-diisopropyl)phenyl Acridine-9-carboxylate
A mixture of acridine-9-carboxylic acid hydrochloride (74 mg, 0.33 mmol) in thionyl chloride (3 ml, 41.1 mmol) was refluxed at 110.degree. C. under nitrogen for 2 hours. After cooling, the solution was evaporated under reduced pressure to dryness. The solid was washed with anhydrous diethyl ether (5 ml) to give acridine-9-carbonyl chloride hydrochloride. This acid chloride was dissolved in anhydrous pyridine (4 ml), followed by addition of benzyl 3,5-diisopropyl-4-hydroxy-benzoate (102 mg, 0.33 mmol) and 4-N,N-dimethylamino-pyridine (16 mg, 0.13 mmol). After 16 hours of stirring at 25.degree. C. under nitrogen, the solution was evaporated under reduced pressure to dryness. The residue was purified on a Chromatotron plate (1 mm silica gel) by elution with 20% diethyl ether/hexane to yield (4-benzyloxycarbonyl-2,6-diisopropyl)phenyl acridine-9-carboxylate (64 mg, 38%). Rf 0.6 (silica gel, 20% ethyl acetate/toluene). MS(EI): m/z 517(M).
(4-Benzyloxycarbonyl-2,6-diisopropyl)phenyl 10-Methyl-acridinium-9-carboxylate Fluorosulfonate (DIPAE-BZ)
A solution of (4-benzyloxycarbonyl-2,6-diisopropyl)phenyl acridine-9-carboxylate (62 mg, 0.120 mmol) in anhydrous methylene chloride (3 ml) was treated with methyl fluorosulfonate (97 .mu.l, 1.198 mmol). After 21 hours of stirring at 25.degree. C. under nitrogen, the solution was treated with anhydrous diethyl ether (10 ml). The resulting precipitate was collected, washed with diethyl ether (20 ml) and crystallized from acetonitrile/diethyl ether to give (4-benzyloxycarbonyl-2,6-diisopropyl)phenyl 10-methylacridinium-9-carboxylate fluorosulfonate (DIPAE-BZ) (20 mg, 26%).
Example 13
Preparation of (4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-Methoxy-10-methyl-acridinium-9-carboxylate Fluorosulfonate (3-MeO-DMAE-Bz)
Methyl 3-Methoxy-acridine-9-carboxylate
To a solution of 3-hydroxy-acridine-9-carboxylic acid (2 g, 8.368 mmol) in methyl sulfoxide (50 ml) was added at 25.degree. C. cesium carbonate (10.9 g, 33.47 mmol), followed by slow addition of iodomethane (2.08 ml, 33.47 mmol). After 2 hours of stirring at 25.degree. C. under nitrogen, the mixture was poured into water (500 ml). The precipitate was collected, washed with water (200 ml) and air-dried. The resulting mixture was flash-chromatographed on silica column packed with chloroform and eluted with 1% methanol/chloroform, followed by 2% methanol/chloroform, to give the crude product. This crude product was further purified on six preparative-TLC plates (2 mm silica gel) by elution with 5% methanol/chloroform. The major band was collected and extracted with 5% methanol/chloroform. Removal of the solvents under reduced pressure gave methyl 3-methoxy-acridine-9-carboxylate (1.05 g, 47%). Rf 0.7 (silica gel, 5% methanol/chloroform).
3-Methoxy-acridine-9-carboxylic Acid Hydrochloride
A solution of methyl 3-methoxy-acridine-9-carboxylate (900 mg, 3.37 mmol) in 4N sodium hydroxide (10 ml) and methanol (30 ml) was stirred at 65.degree. C. under nitrogen for 14 hours, cooled and evaporated under reduced pressure to dryness. The solid was dissolved in water (100 ml); the aqueous solution was washed with diethyl ether (4.times.50 ml) and acidified in an ice-water bath with concentrated HCl to pH 3. The resulting precipitate was collected, washed with water (200 ml) and air-dried, to give 3-methoxy-acridine-9-carboxylic acid hydrochloride (710 mg, 73%). Rf 0.6 (silica gel, chloroform/methanol/water 65:25:4).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-Methoxy-acridine-9-carboxylate
To a suspension of 3-methoxy-acridine-9-carboxylic acid hydrochloride (150 mg, 0.519 mmol) in pyridine (25 ml) was added at 0.degree. C. p-toluenesulfonyl chloride (198 mg, 1.038 mmol). After stirred for 10 minutes, the suspension turned homogeneous; and then benzyl 3,5-dimethyl-4-hydroxybenzoate (132 mg, 0.519 mmol) was added. The solution was stirred at 65.degree. C. under nitrogen for 2 hours and at 25.degree. C. for additional 20 hours, and evaporated under reduced pressure to dryness. The residue was suspended in chloroform (100 ml), washed with 5% ammonium hydroxide (4.times.50 ml), water (2.times.50 ml), brine (1.times.50 ml) and dried over anhydrous magnesium sulfate. Removal of the chloroform under reduced pressure gave a crude mixture, which was purified on 2 preparative-TLC plates (2 mm silica gel) developed with toluene/ethyl acetate (4:1). The major band was collected and extracted with 10% methanol/chloroform. Evaporation of the solvents under reduced pressure yielded (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 3-methoxy-acridine-9-carboxylate. Rf 0.7 (silica gel, 20% ethyl acetate/toluene). MS: (CI CH.sub.4) m/z 492 (M+1).
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 3-Methoxy-10-methyl-acridinium-9-carboxylate Fluorosulfonate (3-MeO-DMAE-Bz)
A solution of (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 3-methoxy-acridine-9-carboxylate (45 mg, 0.0916 mmol) in anhydrous methylene chloride (2 ml) was treated with fluoromethyl sulfonate (74 .mu.l, 0.916 mmol). After 19 hours of stirring at 25.degree. C. under nitrogen, the solution was treated with anhydrous diethyl ether (6 ml). The resulting precipitate was collected and washed with diethyl ether (20 ml), yielding (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 3-methoxy-10-methyl-acridinium-9-carboxylate fluorosulfonate (3-MeO-DMAE-Bz) (41 mg, 74%). MS (FAB, Thioglycerol Matrix): m/z 506 (M).
Example 14
Synthesis of an ABAC
The preparations of an angular benz�a!acridinium ester, (4-benzyloxycarbonyl-2,6-dimethyl)phenyl 5-methyl-benz�a!acridinium-12-carboxylate methosulfate and the intermediates are given below:
Benz�a!acridine-12-carboxylic acid:
The procedure is essentially that reported by Martinet, J. and Dansette, A. in Bull. Soc. Chim., Fr., 45, 101 (1929).
N--Phenyl-.beta.-naphthylamine (22.9 g, 0.1 mol) (Aldrich, Cat# 17,805-5) was mixed with diethylketomalonate (18 g, 0.1 mol) (Aldrich, Cat# D9,740-1) in 5 ml of acetic acid and heated in an oil bath at 150.degree. C. for 45 mins. The reaction mixture solidified upon cooling. The solid was transferred to a fritted funnel, washed thoroughly with ethyl alcohol, and dried in a desiccator under vacuum to give ethyl phenyl-1-benzo-4,5-dioxindol-3-carboxylate: mp 169.degree.-170.degree. C. A portion of this first intermediate (7 g, 0.02 mol) was further treated with 100 ml of 10% KOH, heated at reflux for 90 minutes and left at room temperature overnight. To this second reaction mixture was added 200 ml of 1N HCl. The resulting yellow precipitate was filtered, washed with boiling ethanol, dried to give 2.1 g (33.8%) of the title compound. MS (CI, CH4): m/z 274 (M+1).
Benz�a!acridine-12-carbonyl chloride:
To benz�a!acridine-12-carboxylic acid (1 g, 3.66 mmol) obtained above was added 10 ml of thionyl chloride. The mixture was heated at 95.degree. C. for 3 hours, cooled, treated with 50 ml of benzene, and stored at 4.degree. C. overnight. The precipitates were collected by filtration, washed with benzene, then ethyl ether, and dried in a desiccator under vacuum to give 300 mg (28%) of the acid chloride.
(4-Benzyloxycarbonyl-2,6-dimethyl)phenyl 5-methyl-benz�a!acridinium-12-carboxylate methosulfate:
A solution of 4-benzyloxycarbonyl-2,6-dimethylphenol (0.27 g, 1 mmol) in 10 ml of dry pyridine was treated with 32 mg, 0.26 mmol of 4-dimethylaminopyridine (Aldrich, Cat.# 10,770-0). To this solution was added benz�a!acridine-12-carbonyl chloride prepared above. The solution was heated at 100.degree. C. for 3 hours and evaporated to give a residue which was purified on 3 preparative TLC plates (EM Cat# 5717) developed with 5% methanol in toluene/ethyl acetate (4:1) mixture. A fluorescent band with Rf slightly below that of the starting phenol was stripped, eluted with 5% methanol in chloroform, and the eluent evaporated to give 433 mg of yellow intermediate, (4-benzyloxycarbonyl-2,6-dimethyl)phenyl benz�a!acridine-12-carboxylate.
This intermediate was dissolved in 20 ml of trichloromethane, treated with 4 ml of dimethyl sulfate and heated at 85.degree. C. for 48 hours and cooled. The yellow precipitate was filtered and washed with ether to give 222 mg (37%) of the desired product. MS (FAB Thioglycerol Matrix): m/z 526 (M)).
Example 15
Synthesis of p-Methylphenyl 3-(4'-carboxy)trans, trans-butadienyl-10-methyl-acridinium-9-carboxylate trifluoroacetate (3-Carboxybutadienyl-AE, an EC-AE)
3-(1.3-Dioxolan-2-yl)bromobenzene
A solution of 3-bromobenzaldehyde (15.87 g, 85.78 mmol), 1,2-ethyleneglycol (8.01 g, 128.7 mmol) and p-toluenesulfonic acid hydrate (100 mg ) in benzene (200 ml) was refluxed at 110.degree. C. under nitrogen for 3 hours, and the water formed in the reaction was collected through a Dean Stark trap. The resulting solution was cooled to room temperature, and washed with 10% sodium hydroxide (2.times.100 ml), water (4.times.100 ml) and brine (1.times.100 ml), and dried over magnesium sulfate. Removal of the solvent under reduced pressure gave the title compound as an oily material (16.8 g, 86%).
N-�3-(1.3-Dioxolan-2-yl)phenyl!isatin
A solution of isatin (5.0 g, 34.0 mmol) in anhydrous N. N-dimethyl formamide (150 ml) was treated with sodium hydride (60% dispersion, 1.632 g, 40.8 mmol) with stirring at room temperature for 20 minutes until the formation of hydrogen gas ceased. To the mixture was added cupric iodide (12.9 g, 68.0 g) followed by 3-(1,3-dioxolan-2-yl)bromobenzene (15.57 g, 68.0 mmol). After 8 hours of stirring at 150.degree. C. under nitrogen, the brown mixture was cooled to room temperature, and then treated with chloroform (750 ml). The resulting mixture was filtered to remove the precipitate. The filtrate was evaporated under reduced pressure to dryness to afford a brown solid.
3-(1,3-Dioxolan-2-yl)acridine-9-carboxylic acid
About two-thirds of the above crude product was refluxed in 150 ml of 10% aqueous potassium hydroxide at 120.degree. C. for 8 hours. After cooling to room temperature, the mixture was filtered. The filter cake was washed with 100 ml of water. The combined filtrate was cooled in an ice-water bath and adjusted with concentrated hydrochloric acid to pH 2-3. The precipitate was washed with water (2.times.100 ml) followed by diethyl ether (2.times.150 ml). The resulting material was dried under vacuum at 50.degree. C. for 2 hours to give a yellow product (3.5 g, 52% yield for the two steps based on isatin). The product was essentially homogeneous on TLC. .sup.1 H NMR (DMSO-d6): .delta.ppm 4.04 (2H, m), 4.15 (2H, m), 6.03 (1H, s), 7.73 (1H, d, J=8.9 Hz), 7.75 (1H, dt, J1=6.6 Hz, J2=1.0 Hz), 7.93 (1H, dt, J1=6.6 Hz, J2=1.0 Hz), 8.09 (1H, br. d, J=8.5 Hz), 8.11 (1H, br. d, J=9.0 Hz), 8.23 (1H, d, J=8.9 Hz), 8.24 (1H, s). .sup.13 C NMR (DEPT, DMSO-d6): .delta.ppm 65.2 (t), 102.3 (d), 121.1 (s) 121.2 (s), 125.36 (d), 125.43 (d), 125.8 (d), 127.2 (d), 127.6 (d), 129.4 (d), 131.0 (d), 139.0 (s), 140.7 (s), 147.6 (s), 148.3 (s), 168.2 (s).
3-Aldo-acridine-9-carboxylic acid
A mixture of 3-(1,3-dioxolan-2-yl)acridine-9-carboxylic acid (1.85 g, 6.27 mmol) in 50 ml of 80% aqueous acetic acid was heated with stirring at 65.degree. C. After 6 hours, another 20 ml of 80% aqueous acetic acid was added, and the mixture was heated for additional 4 hours. The resulting mixture was cooled to room temperature, and treated with 500 ml of diethyl ether. The resulting precipitate was collected and washed with diethyl ether (5.times.100 ml). The yellow material was dried over P.sub.2 O.sub.5 under vacuum overnight, yielding 1.55 g (98% yield) of the product.
p-Methylphenyl 3-aldo-acridine-9-carboxylate
A suspension of 3-aldo-acridine-9-carboxylic acid (950 mg, 3.78 mmol) in 100 ml of anhydrous pyridine was stirred at 60.degree. C. for 10 minutes and then cooled to room temperature. The suspension was treated with p-toluenesulfonyl chloride (1.438 g, 7.57 mmol) at room temperature for 10 minutes to form a light-brown homogeneous solution. To the solution was then added p-cresol (382 mg, 3.78 mmol), and the solution was stirred at room temperature under nitrogen for 40 hours. The resulting solution was evaporated under reduced pressure to dryness. The residue was dissolved in 200 ml of chloroform which was washed with 5% aqueous NaOH (2.times.100 ml), water (4.times.100 ml) and dried over sodium sulfate. Removal of the solvent under reduced pressure gave a brownish residue. This residue was separated on a flash column (silica, F 4 cm.times.45 cm), eluted with 4 liters of 50% diethyl ether/hexane to obtain the desired product (250 mg, 19% yield). Rf: 0.5 (20% ether/hexane). .sup.1 H NMR (CDCl.sub.3): .delta.ppm 2.42 (3H, s), 7.32 (4H, s), 7.74 (1H, dt, J1=7.9 Hz, J2=1.2 Hz), 7.91 (1H, dt, J1=7.4 Hz, J2=1.3 Hz), 8.09 (1H, dd, J1=9.1 Hz, J2=1.6 Hz), 8.24 (1H, br. d, J=8.7 Hz), 8.30 (1H, d, J=9.1 Hz), 8.35 (1H, d, J=8.8 Hz), 8.75 (1H, d, J=1.2 Hz), 10.29 (1H, d, J=0.6 Hz). 13C NMR (CDCl3, DEPT): .delta.ppm 21.0 (q), 121.0 (d), 122.9 (d), 123.4 (s), 124.9 (s), 125.0 (s), 126.4 (d), 129.0 (d), 130.4 (d), 131.2 (d), 136.4 (s), 136.8 (s), 137.3 (d), 137.6 (s), 148.0 (s), 148.1 (s), 149.4 (s), 165.5 (s), 191.7 (d).
Benzyl Crotonate
A solution of crotonic acid (5.0 g, 58.1 mmol) and potassium hydroxide (3.254 g, 58.1 mmol) in 50 ml of water was stirred at room temperature for 5 minutes, and then the water was removed under reduced pressure. The resulting white solid was further dried under vacuum at 60.degree. C. for 1 hour to produce sodium crotonate. This salt was suspended in anhydrous N,N-dimethylformamide (200 ml) and heated at 70.degree. C. for 10 minutes. After cooling to room temperature, 9.9 35 g (58.1 mmol) of benzyl bromide was added. The mixture was heated at 70.degree. C. with stirring under nitrogen for 3 hours. Removal of the solvent under reduced pressure gave an oily material, which was separated on a flash column (silica, F4.times.45 cm) by elution with 4 liters of 5% diethyl ether/hexane. The desired product was obtained as a oil (7.9 g, 77% yield). .sup.1 H NMR (CDCl.sub.3): .delta.ppm 1.86 (3H, dd, J1=6.9 Hz, J2=1.7 Hz), 5.17 (2H, s), 5.88 (1H, dd, J1=15.6 Hz, J2=1.7 Hz), 7.03 (1H, m), 7.34 (5H, m). .sup.13 C NMR (CDCl3): .delta.ppm 18.0 (q), 65.9 (t), 122.4 (d), 128.1 (d), 128.5 (d), 136.1 (s), 145.1 (d), 166.3 (s).
Benzyl 4-bromo-but-2-enate
To a solution of benzyl crotonate (4.0 g, 22.73 mmol) in anhydrous carbon tetrachloride (20 ml) was added N-bromosuccinimide (4.045 g, 22.7 mmol). The resulting suspension was refluxed at 100.degree. C. under nitrogen for 20 minutes. After cooling to room temperature, the solid was removed by filtration. The filtrate was evaporated under reduced pressure to dryness. The oily residue was separated on a flash column (silica, F 4.times.40 cm), packed with hexane. The column was eluted with 4 liters of 4% ethyl acetate. The desired product was obtained as an oil (510 mg, 9% yield). Rf: 0.4 (10% ether/hexane) .sup.1 H NMR (CDCl.sub.3): .delta.ppm 3.99 (2H, dd, J1=7.4 Hz, J2=1.3 Hz), 5.19 (2H, s), 6.07 (1H, dt, J1=15.3 Hz, J2=1.1 Hz), 7.04 (1H, m), 7.36 (5H, m). .sup.13 C NMR (CDCl3): .delta.ppm 29.0 (t), 66.5 (t), 124.2 (d), 128.2 (d), 128.3 (d), 128.5 (d), 135.8 (s), 142.2 (d), 165.2 (s).
Benzyloxycarbonylprop-1-enyl triphenylphosphorane bromide
A solution of benzyl 4-bromo-but-2-enate (430 mg, 1.68 mmol) and triphenylphosphine (661 mg, 2.52 mmol) in benzene (3 ml) was stirred at room temperature under nitrogen for 20 hours. The resulting white solid was collected through filtration and washed with benzene (3.times.2 ml), and dried at 100.degree. C. under vacuum to give the title compound (510 mg, 59% yield). .sup.1 H NMR (CD.sub.3 OD): .delta.ppm 4.60 (2H, m, slowly disappeared due to deuterium exchange), 5.13 (2H, s), 6.16 (1H, dd, J1=15.3 Hz, J2=1.1 Hz), 6.81 (1H, m), 7.33 (5H, m), 7.78 (12 H, m), 7.90 (3H, m). .sup.13 C NMR (CD3OD): .delta.ppm 67.6 (t), 68.1 (t), 118.3 (s), 118.8 (s), 119.4 (s), 120.0 (s), 129.3 (d), 129.4 (d), 129.5 (d), 129.6 (d), 129.7 (d), 131.4 (d), 131.5 (d), 131.7 (d), 134.7 (d), 134.85 (d), 134.94 (d), 135.1 (d), 135.2 (d), 135.3 (d), 136.5 (d), 136.6 (d), 136.69 (d), 136.73 (d), 155.7 (s); 165.8 (s).
3-(Benzyloxycarbonyl)prop-1-enyl triphenylphosphorane
A suspension of benzyloxycarbonylbut-2-enyl triphenylphosphorane bromide (188 mg, 0.364 mmol) in anhydrous tetrahydrofuran (10 ml) was treated with sodium hydride (60% dispersion, 14.6 mg, 0.364 mmol) with stirring at room temperature under nitrogen for 15 hours. The resulting yellow mixture was evaporated under reduced pressure to dryness to form the above title reagent as a yellow solid, which was used immediately for the next step of the reaction.
p-Methylphenyl 3-(4'-benzyloxycarbonyl)-trans, trans-butadienyl-acridine-9-carboxylate
3-(Benzyloxycarbonyl)prop-1-enylidene triphenylphosphorane was suspended in dry benzene (10 ml), which was freshly distilled from calcium hydride, followed by addition of p-methylphenyl 3-aldo-acridine-9-carboxylate (88 mg, 0.280 mmol). The mixture was refluxed at 100.degree. C. with stirring under nitrogen for 17 hours, to give a homogeneous solution, which was evaporated under reduced pressure to dryness. The resulting residue was divided into roughly four equal portions. Each portion was then applied on a reverse phase column (YMC, Wilmington, NC, 30.times.500 mm, ODS-A, S-10, 120 .ANG.) mounted on a Beckman Prep 60 ADD-ON HPLC system (Columbia, Md.). The product was eluted at 25 ml/min in step-gradient by mixing H.sub.2 O (solvent A) and Acetonitrile (solvent B) in the following manner: at 30% B for 10 min, 30% to 60% B in 5 min, 60% to 100% B in 40 min and at 100% B for 25 min. The same fractions (retention time: 68.4 min, monitored at 260 nm) from four separations were pooled and the solvents were removed under reduced pressure to give the light-brown product (45 mg, 32% yield). .sup.1 H NMR (CDCl.sub.3): .delta.ppm 2.43 (3H, s), 5.25 (2H, s), 6.17 (1H, d, J=15.3 Hz), 7.15 (1H, d). MS (Positive Ion Electrospray): m/z 500 (M+1).
p-Methylphenyl 3-(4'-benzyloxycarbonyl)-trans, trans-butadienyl-10-methyl-acridinium-9-carboxylate fluorosulfonate
A solution of p-methylphenyl 3-(4'-benzyloxycarbonyl)butadienyl-acridine-9-carboxylate (16 mg, 0.0321 mmol) in 1.5 ml of anhydrous methylene chloride was treated with methyl fluorosulfonate (25.9 ml, 0.321 mmol). The solution was stirred at room temperature under nitrogen for 17 hours. The resulting yellow suspension was treated with 5 ml of anhydrous diethyl ether. The solid was collected, washed with diethyl ether (4.times.5 ml) and then applied on the same RP HPLC system described above. The product was eluted at 25 ml/min in step-gradient by mixing 0.05% TFA/H.sub.2 O (solvent A) and 0.05% TFA/Acetonitrile (solvent B) in the following manner: at 40% B for 10 min and 40% to 100% B in 30 min. The purified product (retention time at 19 min, monitored at 260 nm) was obtained (6 mg, 31% yield). .sup.1 H NMR (CD.sub.3 CN): .delta.ppm 2.43 (3H, s), 5.1 (3H, s), 5.25 (2H, s), 6.35 (1H, s), 7.3-7.4 (1H, m), 7.51 (1H, dd), 7.58 (1H, dd), 8.02 (1H, dd), 8.13 (1H, d), 8.33 (1H, d), 8.39 (1H, d), 8.43 (1H, dd), 8.71 (1H, d), 8.87 (1H, s). MS (Positive Ion Electrospray): m/z 514 (M).
p-Methylphenyl 3-(4'-carboxy)-trans, trans-butadienyl-10-methyl-acridinium-9-carboxylate trifluoroacetate
A solution of p-methylphenyl 3-(4'-benzyloxycarbonyl)butadienyl-10-methyl-acridinium-9-carboxylate fluorosulfonate (5 mg) in the mixed trifluoroacetic acid and methyl sulfide (0.3 ml each) was stirred at room temperature under nitrogen for 22 hours. The solution was then quenched with water (0.5 ml) and extracted with ethyl acetate. The organic layer was evaporated under reduced pressure to dryness. The residue was purified on a reverse phase column (Beckman Ultrasphere column, 10.times.250 mm, ODS, particle size 10 m) mounted on a Beckman Analytical HPLC System (System Gold). The product was eluted at 4 ml/min in step-gradient by mixing 0.05% TFA/H.sub.2 O (solvent A) and 0.05% TFA/Acetonitrile (solvent B) in the following manner: at 30% B for 5 min and 30% to 100% B in 40 min. The desired product (retention time at 18.4 min, monitored at 260 nm) was isolated as a yellow solid (3.4 mg). .sup.1 H NMR (CD.sub.3 CN): .delta.ppm 2.43 (3H, s), 4.8 (3H, s), 6.32 (1H, d), 7.39 (1H, d), 7.47 and 7.42 (4H, q), 7.55 (1H, dd), 7.63 (1H, dd), 8.08 (1H, dd), 8.27 (1H, d), 8.44 (1H, dd), 8.47 (1H, d), 8.49 (1H, d), 8.55 (1H, s), 8.61 (1H, d). MS (Positive Ion Electrospray): m/z 424 (M).
Example 16
Synthesis of p-carboxyethylphenyl 10-methylacridinium-9-carboxylate trifluoroacetate (pCE-AE)
The starting material p-(N-succinimidyloxycarbonylethyl)phenyl 10-methyl-acridinium-9-carboxylate fluorosulfonate was customer-synthesized by LC Services Corporation (Woburn, Mass.) following the procedure described by Weeks, et.al. �Clinical chemistry, 29, 1474-1479, (1983)!. p-(N-succinimidyloxycarbonylethyl)phenyl 10-methyl-acridinium-9-carboxylate fluorosulfonate (13 mg) was dissolved in 1.5 ml of DMF and equal volume of water. To this was added 1 ml of 2N HCl and the resulting solution was stirred at room temperature for 18 hours. The reaction mixture was separated on a reverse phase column (YMC, Wilmington, N.C., 20.times.250 mm, ODS-A, S-5, 120 .ANG.) mounted on a Beckman Prep 60 ADD-ON HPLC System. The product was eluted at 10 ml/min in step-gradient by mixing 0.05% TFA/H.sub.2 O (solvent A) and Acetonitrile (solvent B) in the following manner: at 30% B for 20 min, 30% to 60% B in 5 min and at 60% B for 25 min. The desired product (retention time at 20 min, monitored at 260 nm) was isolated as yellow solid (6 mg). .sup.1 H NMR (CD.sub.3 CN): .delta.ppm 2.70 (2H, t), 3.01(2H, t), 4.86 (3H, s), 7.50 (4H, m), 8.12 (2H, m), 5.53 (6H, m), 8.67 (1H, s), 8.70 (1H, s). MS (Positive Ion Electrospray): m/z 386 (M).
Example 17
Synthesis of (4'-Carboxy-2',6'-dimethyl)phenyl 5-methyl-benz�b!acridinium-12-carboxylate Trifluoroacetate. (LEAE-COOH)
A solution of crude (4'-Benzyloxycarbonyl-2',6'-dimethyl)phenyl 5-methyl-benz�b!acridinium-12-carboxylate Fluorosulfonate (210 mg) in 10 ml of 30% HBr/ACOH was stirred at 50.degree. C. for 3 hours. The reaction mixture was cooled down to room temperature, blown with nitrogen to remove the excess amount of HBr and the residue mixed with 30 ml of ether to give purple precipitate. The precipitate was applied on a reverse phase column (YMC, Wilmington, N.C., 30.times.500 mm, ODS-A, S-10, 120 .ANG.) mounted on a Beckman Prep 60 ADD-ON HPLC system. The product was eluted at 25 ml/min in step-gradient by mixing 0.05% TFA/H.sub.2 O (solvent A) and 0.05% TFA/Acetonitrile (solvent B) in the following manner: at 8% B for 5 min, 8% to 25% B in 5 min, 25% to 50% B in 25 min, 50% to 100% B in 5 min and at 100% B for 35 min. The desired peak (retention time: 67 min, monitored at 260 nm) was collected and the solvents removed under the vacuum to give the product as purple solid (16 mg). MS (Positive Ion Electrospray): m/z 436 (M).
Example 18
Alternative synthesis of benz�b!acridine-12-carboxylic acid
N-phenyl benz�5,6!isatin.
To the reaction flask containing benzo�5,6!isatin (6 g, 50.7 mmol) in 180 ml of DMF was added NaH (2.43 g, 60.8 mmol) and the reaction was stirred at room temperature for about 50 min until the formation of the hydrogen gas ceased. To the resulting solution were added iodobenzene (15.5 g, 76.1 mmol) and CuI (21.2 g, 111.5 mmol). The reaction mixture was then stirred at 170.degree. C. overnight. The reaction mixture was chromatographed on the flash column, eluted with ether/toluene (5% increasing to 10%) to give the desired product (4.28 g, yield 31%). Rf: 0.5, 15% ether/hexane.
Benz�b!acridine carboxylic acid.
A suspension of N-phenyl benz�5,6!isatin (4.28 g, 15.7 mmol) in 150 ml of 10% KOH was purged with nitrogen and then stirred at 115.degree. C. for an hour. The reaction was cooled down to room temperature, diluted with additional 400 ml of water and acidified by the addition of concentrated HCl to give a purple precipitate. The precipitate was collected, washed with large amount of water and dried to give the product as purple solid. (4.28 g, yield 88.2%). This product was also used for the synthesis of the identical intermediate, (4-benzyloxycarbonyl-2,6-dimethyl)phenyl benz�b!acridine-12-carboxylate, as described in Example 1.
Example 19
Alternative Synthesis of 2-methoxybenz�b!acridine-12-carboxylic acid
N-(4'-methoxy)phenyl benz�5,6!isatin.
To the reaction flask containing benzoisatin (5 g, 25.4 mmol) in 170 ml of DMF was added NaH (1.22 g, 30.4 mmol) and then the reaction was stirred at room temperature for about 40 min until the formation of the hydrogen gas ceased. To the resulting solution were added iodoanisol (11.868 g, 50.8 mmol) and CuI (10.623 g, 55.8 mmol). The reaction mixture was then stirred at 170.degree. C. overnight. The reaction mixture was evaporated to remove the solvent and redissolved in 600 ml of EtOAc. The resulting mixture was washed with 5% HCl and water, filtered, evaporated and then chromatographed on the flash column, eluted with ether/toluene (6% increasing to 12%) to give the desired product (1.99 g, yield 26%). Rf: 0.6, 15% ether/toluen. MS (CI, CH.sub.4): m/z 304 (M+1).
2-methoxy-benz�b!acridine-12-carboxylic acid.
A mixture of N-(4'-methoxy)phenyl benz�5,6!isatin (1.24 g, 4.09 mmol) in 160 ml of 10% KOH was stirred at 120.degree. C. for 35 min. The reaction was then diluted in additional 150 ml of water and acidified in the ice bath by the addition of concentrated HCl to give a purple precipitate. The precipitate was collected, washed with large amount of water and dried to give 1.11 g of product (yield 79.9%). MS(CI, CH.sub.4) : m/z 304 (M+1).
Example 20
Alternative synthesis of 2-(N,N-dimethylamino)ethoxy-benz�b!acridine-12-carboxylic acid
p-N,N-dimethylaminoethoxy 4-iodobenzene.
To an iced cooled solution of 2-dimethylamino ethylchloride hydrochloride (10.48 g, 72.72 mmol) in 30 ml of water, a solution of NaOH (3.49 g, 87.26 mmol) in 20 ml of water was added. After 30 min stirring, the reaction was saturated with NaCl for 15 min and extracted with toluene (5.times.50 ml). The toluene fractions were combined and dried over KOH pellets. In a separate flask, a mixture of KOH (4.07 g, 72.72 mmol) and 4-indophenol (16 g, 72.72 mmol) in 48 ml of anhydrous ethanol was stirred at room temperature for 1.5 hours and evaporated under vacuo to give the 4-iodophenoxide salt as a greenish oily residue. The above dimethylaminoethyl chloride in toluene solution was then added to the 4-iodophenoxide residue and the mixture refluxed with stirring at 120.degree. C. for 21 hours. The reaction mixture was cooled down and filtered. The filtrate was evaporated and the residue redissolved in 200 ml of ether. After filtration, the filtrate was bubbled with HCl gas to give a copious white precipitate, which was then filtered and dried to give the p-N,N-dimethylaminoethoxy 4-iodobenzene hydrogen chloride as white solid (11 g, yield 46.2%).
p-N,N-dimethylaminoethoxy 4-iodobenzene hydrogen chloride (11 g, 33.6 mmol) was dissolved in 300 ml of water. The solution was neutralized with NaOH and saturated with NaCl. The mixture was then extracted with toluene (100 ml.times.4) and the combined extract was washed with brine and dried over MgSO.sub.4. The solution was filtered and evaporated to give 6.5 g of p-N,N-dimethylaminoethoxy 4-iodobenzene.(yield 66.5%). .sup.1 H NMR (CDCl.sub.3): .delta.ppm 2.32 (6H,s), 2.71 (2H, t, J=7.2 Hz), 4.01 (2H,t,J=7.2 Hz), 6.69 (2H,d,J=8.0 Hz), 7.53 (2H,d,J=8.0 Hz).
N-(p-N,N-dimethylaminoethoxy)phenyl benz�5,6!isatin.
To the reaction flask containing benzo�5,6!isatin (4 g, 20.3 mmol) in 120 ml of DMF was added 0.974 g of NaH. The reaction solution was stirred at room temperature for 20 min and p-N,N-dimethylaminoethoxy 4-iodobenzene (6.5 g, 22.3 mmol) and CuI (8.5 g, 44.7 mmol) were added into the resulting solution. The reaction mixture was stirred at 170.degree. C. to 175.degree. C. for 20 hours and then evaporated to remove the DMF. The residue was triturated with mixture of toluene and MeOH (1:1), filtered and the filtrate concentrated. The concentrate was chromatographed on the flash column, eluted with methanol/toluene (500 ml 0%, 1000 ml 10%, 1000 ml 20%, 1000 ml 25%, 1000 ml 30%, 1000 ml 35%, 3000 ml 40%). The desired product was obtained as white solid (2389 mg, yield 32.7%). Rf: 0.4, 30% methanol/toluene. MS (FAB, Thioglycerol Matrix): m/z 361 M+1).
2-(N,N-dimethylamino)ethoxy benz�b!acridine carboxylic acid.
The suspension of N-(p-N,N-dimethylaminoethoxy)phenyl benz�b!isatin (104 mg, 0.28 mmol) in 30 ml of 10% KOH was stirred at 115.degree. C. to 128.degree. C. for 25 min. The reaction mixture was cooled down to room temperature and neutralized to pH 6.5 by the addition of HCl to produce a yellow precipitate. The precipitate was collected, washed with ether and dried to give 51 mg of product. (yield 51%). This product was also used for the synthesis of the identical intermediate, (2,6-dimethyl-4-succinimidyloxycarbonyl)phenyl 2-(N,N-dimethylamino)ethoxy-benz�b!acridine-12-carboxylate, as described in Example 8.
PREPARATION OF CONJUGATES:
In the chemiluminescent compounds of the present invention, preferably at the R.sub.6 position, depending on which coupling moiety is selected, the AFAC label can be reacted directly with the specific binding partner, ligand, or hapten either in an aqueous or an organic medium.
It is understood that alternate positions of the chemiluminescent compound may have a coupling moiety to be reacted with a binding partner to form a conjugate.
The chemiluminescent labels can include an appropriate leaving group or an electrophilic functional group attached with a leaving group or functional groups which can be readily converted into such reactive groups, directly attached or connected via a spacer for attaching a substance to form a conjugate to be utilized in a test assay. An example of preparing the LEAE-anti-TSH conjugate is provided below.
PREPARATION OF LEAE-ANTI-TSH CONJUGATE:
A solution of a monoclonal anti-TSH antibody (2 mg, 0.013 umol) in 1.36 ml of 0.1M phosphate buffer, pH 8.0 was treated with a solution of LEAE-NHS (43 ug, 0.067 umole) in 240 ul of acetonitrile at room temperature for one hour. The conjugation reaction was stopped by adding a solution of lysine (10 mg) in 0.5 ml of 0.1M phosphate buffer, pH 8. The LEAE-conjugated anti-TSH was purified by passing the reaction mixture through a Sephadex G-25 column (1.times.20 cm) packed and eluted with 10 mM Phosphate, pH 8. The elution was monitored at 280 nm with a ISCO UV detector. The desired conjugate was collected when the first void volume peak was eluted out.
Preparation of Oligonucleotide conjugate:
A method for conjugating binding parties, haptens, or ligands of luminescent labels to polynucleotides is described in EP-A-O 537 994 (U.S. Pat. No. 5,622,825), which is commonly assigned and incorporated herein by reference.
LIGHT EMISSION SPECTRA:
The light emission spectra of LBAC's and the reference acridinium esters were determined by a Fast Spectral Scanning System (FSSS) of Photo Research (a division of Kollmorgen Corp) of Burbank, Calif., U.S.A. The experiment was carried out in a dark room. Each sample was dissolved in HPLC grade acetonitrile at the concentration of 1 mg/ml or higher and diluted with the same solvent to obtain the sample solution in the concentration specified. A typical determination utilized 10 to 100 ug of each compound, with the exception of the angular benz�a!acridinium ester (2 mg), and 3-Carboxybutadienyl-AE (150 .mu.g) separately or mixed together in 0.5 ml acetonitrile contained in 13.times.100 mm borosilicate test tube. The tube was placed on a tube rack raised to a proper height. The FSSS optical head was placed in front of the tube at close distance and with its lens focused on the liquid in the tube. The sample solution was first treated with 0.35 ml of the Flashing Reagent #1 (Ciba Corning Diagnostics) containing 0.1N HNO.sub.3 and 0.1% H.sub.2 O.sub.2. The room was then darkened, and 0.35 ml of the Flashing Reagent #2 (Ciba Corning Diagnostics) containing 0.25N NaOH and 0.2% ARQUAD was added to the reaction mixture immediately, see U.S. Pat. No. 4,927,769 which is commonly assigned and incorporated herein by reference. The light which was generated instantaneously following the addition of the Reagent #2 was recorded by FSSS for 4 seconds except for 2-MeO-LEAE-Imidate which was recorded for 30 seconds starting from split second before the Reagent #2 was added. The results of the various determinations are summarized in Table I.
TABLE I______________________________________ Emission Max Range*Compound Quantity .sup..about. (nm) (nm)______________________________________ 1. DMAE-Bz 20 ug 426-428 410-510 2. 3-MeO-DMAE-Bz 50 ug 422 395-520 3. DIPAE-Bz 20 ug 426 405-520 4. ABAC 2 mg 436-440 410-530 5. LEAE-Bz 50 ug 520-524 490-670 6. DIP-LEAE-Bz 50 ug 520 485-670 7. 2-MeO-LEAE-Bz 30 ug 550 510-700 8. 3-EtO-LEAE-Bz 50 ug 508 470-660 9. 3-QAE-LEAE-Bz 100 ug 544 470-68010. 2-QAE-LEAE-NHS 70 ug 550 510-70011. LEAC-Bz 50 ug 520 485-67012. NSP-LEAE-Bz 15 ug 516 482-65513. 2-MeO-NSE- 50 ug 546 500-700 LEAE-NHS14. 2-MeO-LEAE- 100 ug 550 500-710 Imidate15. 3-Carboxybuta- 150 ug 464 415-585 dienyl-AE16. P-Carboxyethyl- 25 ug 430 410-520 AE______________________________________ .sup..about. The emission maximum for each compound could vary by 0-4 nm between different determinations. *Range is set for spectral region with signal intensity of above 5% of peak height. The ABAC is (4Benzyloxycarbonyl-2,6-dimethyl)phenyl 5methyl-benz�a!acridinium12-carboxylate methosulfate.
Recorded emission spectra are shown in FIGS. 3A-3E, 4A-4J, 5A-5B, and 6A-6E. FIGS. 3A-3E, 4A-4J, and 5A-5B show individual emission spectra of chemiluminescent compounds including an acridinium ring system and compounds including a benzacridinium ring system. The difference of the emission maxima between acridinium esters and LBAC's were found to range between 80-128 nm, while that between acridinium esters and the ABAC was about 8-14 nm and that between p-carboxyethyl-AE and 3-Carboxybutadienyl-AE was 34 nm. As shown in FIGS. 6A-6D, when the acridinium esters and LBAC's were mixed in a tube and flashed simultaneously, the resulting combined emission spectra showed the ideal summed up spectral profile, indicative of the non-interfering nature of these two groups of chemiluminescent emission signals. It is understood that these data may vary depending on the instrumentation utilized and the components of the instrumentation, particularly the filters. The major portions of the original constituting spectra which remained unchanged were indeed non-overlapping. These important physical characteristics fulfill the prerequisite for two or more subclasses of chemiluminescent compounds to be utilized in test assays for detecting and/or quantitating at least two substances in a test sample, and particularly to multianalyte clinical diagnostic assays. In the preferred method a benzacridinium compound is utilized as one component of the assay method and more specifically an Nalkylated benzacridinium compound.
As noted above, a luminometer for detecting and/or quantitating at least two chemiluminescent emission spectra is described in U.S. Ser. No. 08/035,341.
LIGHT EMITTING EFFICIENCY:
The light emitting efficiency of LBAC's, ABAC, DMAE-Bz (ortho-substituted AE derivatives) and 3-Carboxybutadienyl-AE and p-carboxyethyl-AE (non ortho-substituted AE derivatives) was determined on a Berthold luminometer (MLA-I) (Ciba Corning Diagnostics Corp.) fitted with a BG-38 filter with wavelength transmission range of about 320 to 650 nm at transmission efficiency of 20 to 97%. (FIG. 7A). Alternate filters may be incorporated in luminometers to expand the range of transmission efficiency.
Each sample was prepared in acetonitrile solution at 1 mg/ml, serially diluted to 10 ug/ml in acetonitrile and further on to 1 ng/ml, 0.1 ng/ml and 0.01 ng/ml in 10 mM phosphate buffer with 0.15M NaCl, 0.1% BSA. 0.05% NaN.sub.3, pH8.
To determine the light emitting efficiency, 25 ul of blank (the buffer matrix) or each sample were flashed by injecting 0.35 ml each of the Flashing Reagents #1 and #2 sequentially. Light emission was integrated for 2 seconds and results as means of duplicate determination are given in Table II.
TABLE II__________________________________________________________________________Compound Total Counts (RLU's)/2 sec(counter Molecular amount flashed (pg) RLU's/mol*ion) Weight 0.25 pg 2.5 pg 25.0 pg (1 .times. E20)__________________________________________________________________________DMAE-Bz 587 76,477 769,477 6,786,57 1.8(CH.sub.3 SO.sub.4 .sup.-)DIPAE-Bz 631 82,115 845,660 6,041,380 2.1(FSO.sub.3 .sup.-)3-MeO-DMAE-Bz 605 -- 54,760 523,380 0.13(FSO.sub.3 .sup.-)ABAC 613 -- 23,600 143,400 0.058(CH.sub.3 SO.sub.4 .sup.-)LEAE-Bz 625 105,857 1,037,943 9,037,063 2.6(FSO.sub.3 .sup.-)DIP-LEAE-Bz 681 29,930 240,610 2,413,320 0.66(FSO.sub.3 .sup.-)LEAC-Bz 766 79,873 767,553 6,312,163 2.4(FSO.sub.3 .sup.-)3-EtO-LEAE-Bz 669 93,635 883,785 6,364,935 2.4(FSO.sub.3 .sup.-)3-QAE-LEAE-Bz 854 16,765 107,540 1,005,855 0.37(FSO.sub.3 .sup.-)2-MeO-LEAE-Bz 655 27,810 223,995 2,140,890 0.59(FSO.sub.3 .sup.-)2-QAE-LEAE-NHS 854 ND.sup..about. ND.sup..about. ND.sup..about. ND.sup..about.(FSO.sub.3 .sup.-)NSP-LEAE-Bz 633 22,715 212,485 2,250,520 0.542-MeO-NSE- 646 14,853 145,403 1,503,100 0.38LEAE-NHS2-MeO-LEAE- 578 ND.sup..about. ND.sup..about. ND.sup..about. ND.sup..about.Imidate (2 Cl.sup..about.)3-Carboxybuta- 537 -- -- 554,285 0.12dienyl-AEp-Carboxyethyl- 499 -- 715,555 5,607,245 1.4AE__________________________________________________________________________ *counts/mol calculated from quantity of 2.5 pg, except for 3Carboxybutadienyl AE which was calculated at 25 pg. The ABAC is (4Benzyloxycarbonyl-2,6-dimethyl) phenyl 5methyl-benz�a!acridinium12-carboxylate methosulfate. .sup..about. ND = not determined prior to the establishment of final purity of the compound.
From the data shown in Table II, the light emitting efficiency of the LBAC's was comparable to that of DMAE-Bz within the range of 0.21 to 1.39 fold, depending on the substitutents on the benzacridinium nucleus and the phenoxy group. The light emitting efficiency of 3-Carboxybutadienyl-AE, an EC-AE, was 12-15 fold lower than non EC-AEs, e.g., p-carboxyethyl-AE and DMAE-Bz. It should be noted these determinations were based on 2-second signal collection and have not taken into account the flashing kinetics of the individual compounds, e.g. some compounds may take greater that 2 seconds to release most of their signals, the sensitivity of the photomultiplying tube, and the transmission efficiency of the optical filter(s) at different points of the spectral range. The LEAC findings, however, were totally unexpected in view of the much lower light emitting efficiency of the isomeric ABAC. This level of light emitting efficiency renders LEAC's useful in sensitive binding assays, including multi-analyte assays. In contrast, the low quantum yield of EC-AE's would likely pose a problem if such compounds were utilized in multi-analyte assays requiring medium to high sensitivity; particularly because of the emission overlap between EC-AE and non-EC-AE's, see Table I.
KINETIC STUDY ON LIGHT EMISSION:
Due to the electronic and/or steric effects of different substituents on the phenoxy moiety, the acridinium and benzacridinium nucleus, it was anticipated that not all the DMAE analogs, ABAC, NOS-AE, and LEAC's would have the same flashing rates under identical conditions. In other words, within 2 seconds of signal collection time different compounds were expected to release different percentages of total releasable signals. A time course study over a period of up to 10 seconds was conducted to determine these percentages, by flashing the compounds and normalizing all the signals collected for different lengths of time to that of 10 seconds. The results are summarized in Table III.
TABLE III______________________________________ Percent signal released over different lengths of timeCompounds 10.0 s 6.0 s 4.0 s 2.0 s 1.0 s 0.5 s______________________________________DMAE-Bz 100% 99% 96% 80% 48% 10%DIPAE-Bz 100% 98% 97% 89% 64% 14%3-MeO-DMAE-Bz 100% 80% 70% 57% 49% 26%ABAC 100% 89% 73% 52% 20% 3%LEAE-Bz 100% 98% 97% 88% 71% 27%DIP-LEAE-Bz 100% 80% 67% 47% 26% 4%LEAC-Bz 100% 102% 98% 93% 82% 73%3-EtO-LEAE-Bz 100% 95% 93% 85% 78% 45%3-QAE-LEAE-Bz 100% 91% 88% 84% 75% 34%2-MeO-LEAE-Bz 100% 92% 83% 65% 42% 16%2-QAE-LEAE-NHS 100% 88% 76% 59% 37% 9%NSP-LEAE-Bz 100% 95% 96% 91% 72% 14%2-MeO-NSE- 100% 96% 90% 79% 58% 22%LEAE-NHS2-MeO-LEAE- 100% 76% 59% 40% 23% 6%Imidate3-Carboxybuta- 100% 94% 91% 88% 79% 39%dienyl-AEp-Carboxy- 100% 96% 95% 93% 90% 47%ethyl-AE______________________________________ The ABAC is (4Benzyloxycarbonyl-2,6-dimetyl)phenyl 5methyl-benz�a!acridinium12-carboxylate methosulfate.
As shown by the data of TABLE III, particularly at the 0.5 and 1 second intervals, the flashing kinetics varied widely for different DMAE analogs, ABAC and LEAC's. These data on release percentages should be utilized in comparing the light emission efficiency of the compounds for developing various assay utilizing the chemiluminescent compounds.
MUTUALLY NON-INTERFERING LIGHT EMISSION:
Beside exhibiting discernable mutually non-interfering nature of their light emission spectra as mentioned above, DMAE and LEAE in the form of protein conjugates also demonstrated no mutual interactions in their light emissions during flashing as shown by no decrease or increase of the combined Relative Light Units (RLU) registered.
The testing was carried out as follows:
DMAE-anti-TSH and LEAE-anti-TSH were diluted in 10 mM phosphate buffer with 0.15M NaCl, 0.1% BSA, 0.05% NaN.sub.3, pH 8 at two concentrations, such that 25 ul of the solutions would give about 200,000 and 1,000,000 RLU's, respectively, when they were flashed in the same manner on the Berthold luminometer equipped as described above. The light emission of each sample (25 ul) was measured separately and then the same volume of each were combined and measured again. In single sample determinations, an additional equal volume of the buffer was added to maintain the same sample volume as in the combined sample determinations. Results of the testing are summarized in Table IV.
TABLE IV______________________________________Single sample determination* Combined sample determination*(RLU) (RLU)DMAE-anti-TSH LEAE-anti-TSH Theoretical Found (%)______________________________________860,617 1,017,200 1,877,817 1,835,350 (98%)173,200 191,820 365,029 362,293 (99%)______________________________________ *Each value, was the mean of triplicate determinations. (RLU Relative light units)
The results in Table IV show that the two tracers of different emission spectra were absolutely non-interfering between each other in their light emission. This characteristic further ensures their utility in multi-analyte binding assays. The LEAE of the preferred method is a N-alkylated benzacridinium compound.
STABILITY of CONJUGATED LBAC'S:
LBAC-Anti-TSH conjugates were prepared and tested for their stability in aqueous media. DMAE-anti-TSH conjugate was also tested side by side. The retention of chemiluminescent activity as a function of temperature at various pH's (using citrate-phosphate buffer containing 0.1% BSA) was monitored over 7 day period. Proper concentrations of the above conjugates (0.8-1.4.times.10.sup.6 RLU's/25 ul) were placed in two sets of different buffers (pH 7.4, 8.0, 8.5, and 9.0). One set was kept at 4.degree.-8.degree. C. as a control, while the other was subjected to 37.degree. C. The buffered samples (25 ul) were flashed periodically as described above. The results are summarized in Table V.
TABLE V______________________________________Relative Stability* of ConjugatespH Compds 1 day 3 days 5 days 7 days______________________________________7.4 I 93% 98% 91% 95% II 66% 56% 51% 44% III 67% 78% 77% 80% IV 89% 94% 101% 96% V 66% 46%8.0 I 99% 104% 96% 98% II 106% 106% 80% 83% III 79% 69% 68% 71% IV 102% 114% 140% 138% V 45% 13%8.5 I 92% 102% 89% 81% II 111% 97% 110% 82% III 81% 76% 78% 86% IV 134% 142% 150% 156%9.0 I 90% 95% 70% 71% III 94% 68% 51% 71% IV 133% 140% 149% 130%______________________________________ Compounds I-V are DMAEanti-TSH, LEAEanti-TSH, 2MeO-LEAE antiTSH, 3EtO-LEAE-anti-TSH, and Nonortho-substituted AEanti-TSH, respectively. Th stability data for Nonortho-substituted AEanti-TSH were equivalent to tha reported earlier in U.S. Pat. No. 4,745,181. *Relative Stability is defined by expressing the percentage chemiluminescent activity of 37.degree. C. samples relative to that of th corresponding 4-8.degree. C. samples. For example, at pH 8, after 7 days of storage, the DMAEanti-TSH and LEAEanti-TSH 37.degree. C. samples retained 87% and 83% activity, respectively, in comparison. with the corresponding 4.degree. C. samples, while the nonortho-substituted acridinium ester retained only 13% activity in comparison with the corresponding 4.degree. C. sample.
The stability study summarized in Table V demonstrates that the stabilizing effect of ortho-substitution on the phenoxy ring not only applies to the class of acridinium esters, it also benefits the LBAC's series to about the same extent with regard to maintaining their chemiluminescent activity in aqueous media at or near pH 8 under prolonged heat-stress conditions as required for commercial binding assay products. Listed in great contrast is the stability data of the non-ortho-substituted acridinium ester conjugate at pH 8. A non-ortho-substituted LEAC would likely also have poor stability in aqueous media.
STABILITY OF NON-CONJUGATED DMAE, NOS-AE's AND LEAE
To further assess the stability of LEAE relative to DMAE, 3-Carboxybutadienyl-AE and p-Carboxyethyl-AE in their non-conjugated forms, the four compounds were subjected to 37.degree. C. heat stress in 0.2M phosphate buffers containing 0.1% BSA, with pH of 7.4, 8.0, 8.5, or 9.0 to compare their stability in terms of remaining chemiluminescent activity. both LEAE and LMAE are used in their de-benzylated (carboxylic) forms (see example 17, and U.S. Pat. No. 5,227,489, respectively) in order to mach with the other two NOS-AE's. All the compounds were first solubilized in acetonitrile/water mixture to give concentration of 1 mg/ml and further diluted about 1.times.10.sup.5 to 1.times.10.sup.6 folds with individual buffers stated above to reach the working concentration range of 5-8.times.10.sup.6 RLU/25 ul. The sample solutions in different pH's were all kept in polypropylene containers stored in 37.degree. C. chamber. Aliquots of sample solutions (25 ul) were withdrawn and flashed periodically as described above. The results are represented in FIG. 8 (Panel A-D). Compared to the corresponding reference counts determined at Day 0, when stressed at 37.degree. C., DMAE took a very slow decline in counts over 7-day period in all pH's tested and appeared to be the most stable with the acceptable total loss of counts between 12-20% only. LEAE took a different profile of good stability, with 35-48% loss in day 1, but then maintained essentially no loss at pH 8-9, or further 10% loss at pH 7.4 for the rest of 7-day period. This stability profile of LEAE could be attributed to a one-time quenching phenomenon that was completed within one day and caused the loss of about 1/3-1/2 of the total activity when the LEAE was diluted to the working concentration. This quenching phenomenon, in effect, reduces the quantum yield of LEAE to that comparable to DMAE and should have no impact on LEAE's usefulness in commercial product. On the other hand, both p-carboxyethyl-AE and 3-Carboxybutadienyl-AE were shown to be very unstable with more than 70% loss in 2 days of heat stress and approaching about 85-100% loss at the end of 7 days under all pH's tested.
The stability of LEAE and 3-Carboxybutadienyl-AE solutions was also examined based on their HPLC profiles before and after being heated at 37.degree. C. for 24 hr. HPLC analysis was carried out on a Reverse Phase column (Bondclone C18, 3.9.times.300 mm, P/N OOH-2117-CO, Phenomenex, Torrance, Calif.), mounted on a Beckman Analytical HPC system (System Gold). The samples (about 20-50 ug each) were dissolved in 300 ul of 1:2 mixture of MeOH and 50 mM phosphate, pH 8.0. About 50-80 ul of the sample solution was injected and eluted at 1 ml/min in step gradient by mixing 0.05% TFA/H.sub.2 O (solvent A) and 0.05% TFA/Acetonitrile (solvent B) in the following manner: at 30% B for 5 min. and increasing form 30% to 100% B in 40 min. The chromatograms shown in FIG. 9 (Panel A-D) demonstrated that 3-Carboxybutadienyl-AE in pH 8 buffer decomposed nearly completely in 24 hr. at 37.degree. C. Under these conditions, the compound which gave a retention time of 17 min originally changed to two new major products with much longer retention times of 25.1 min and 33.6 min, respectively. In the absence of a proper means to maintain its stability, the fast speed of decomposition will render 3-Carboxybutadienyl-AE unusable in a commercial binding assay product.
On the other hand, LEAE sample under the same conditions was shown to be mostly intact after 24 hr. of heat stressing, with retention time of about 21 min.
This HPLC analysis further confirmed the big difference in the stability of LEAE vs. 3-Carboxybutadienyl-AE. The former is undoubtedly acceptable for commercial products, while the latter is hardly useful for being extremely labile.
SIGNAL-TO-NOISE IN BINDING ASSAYS:
LEAE-anti-TSH was employed as tracer in a TSH assay. Performance was assessed by determining signal-to-noise (S/N) ratio. The performance of DMAE-antiTSH was also compared side by side. The assay was configured as follows:
100 microliters of either of the above conjugates was incubated for two hours at room temperature with 100 ul of a TSH standard (Ciba Corning Diagnostics Corp., Medfield, Mass.). Incubations were done separately with five standards containing either 0, 0.5, 1.0, 16 or 100 uIu/ml of TSH. A second incubation was then performed by adding 500 ul of MAGIC.RTM. magnetic particle immobilized with sheep anti-TSH (Ciba Corning Diagnostics Corp.) to the above mixture, then waiting for 30 minutes at room temperature.
A wash was done first by magnetically separating the particles from the solution, decanting the solution, then adding 500 ul of water, followed by another magnetic separation. The washed particles were resuspended in 100 ul of water. Flashing and counting were done according to the above-described procedures. The results are provided in Table VI using ratios of the counts with a TSH standard containing TSH versus the zero TSH standard.
TABLE VI______________________________________ S/N at various StandardsConjugate 0.4 uIu/ml 1.0 uIu/ml 16 uIu/ml 100 uIu/ml______________________________________DMAE-anti-TSH 10.0 20.9 202.3 669.4LEAE-anti-TSH 5.4 8.4 87.4 282.6______________________________________
The results given in Table VI indicate that LEAE conjugate can be utilized in an immunoassay format to provide a dose-response curve and, therefore, allows the development of useful assays.
DUAL-ANALYTE SIMULTANEOUS IMMUNOASSAY:
Instrumentation:
One embodiment of a Dual-PMT Luminometer (DPL) utilized to demonstrate the hardware of DPL includes at least two photo multiplier tube (PMT) assemblies, an injection pump for Flashing Reagent #2, and a cube-shape light tight chamber designed for holding a disposable cuvette. At two opposite sides of the chamber, two cylindrical PMT tube assemblies are separately attached such that light of two different spectral ranges generated inside the cuvette can be individually registered by the PMT assemblies. The top of the cuvette-holding chamber is hinged to allow the cuvette to be manually inserted and removed. In addition, the top also has a fixed probe attached for the purpose of injecting the Flashing Reagent #2 into the cuvette. Within each PMT assembly an optical filter selected for particular spectral range, and is inserted between the cuvette and the PMT tube.
Alternate embodiments and configurations of DPLs may be designed for semi-automated and automated detection of two or more chemiluminescent compounds or conjugates in a test sample. A luminometer as a component on an automated analyzer is described in EP-A-0 502 638 noted above.
Essential to the discrimination or discernability of two or more emitted light spectra are the choices of a plurality of optical filters with proper wavelength cutoffs.
Filters of this type are widely available from commercial vendors and may be modified, i.e. by lamination or specifically manufactured to be incorporated in a PMT assembly for detection and/or quantitation of spectral signals of the conjugates. Careful selection of filters will enhance the ability to discern emission signals and with appropriate correction may allow multiple signals with the emission overlap to be discerned.
For the purpose of running a simultaneous LH/FSH dual-immunoassay as disclosed below, a long pass filter (P/N LL-500 of Corion, Holliston, Mass.) and a short pass filter (P/N P70-450 also of Corion) were chosen to match with the two different spectral ranges of light generated from a pair of tracers, LEAE-anti-LH and DMAE-anti-FSH, which were prepared in the same manner as described above for LEAE-anti-TSH and DMAE-antiTSH, respectively. The transmittance curves for the two filters are shown in FIGS. 7B and 7C. The choice of the optical filters should take into consideration the requirements on maximal signal transmittance and minimal signal cross-talk. Optical filters with more desirable transmittance profile and cut-off may be selected to maximize the transmission of light emitted from the tracers and/or to fit better with the emission spectral ranges of particular chemiluminescent compounds so as to improve the Percent Cross Talk (PCT) as described below. For example Corion's laminated CS550/CS600 filter (FIG. 7D) was found to be a better replacement for filter P70-450 as the short pass filter matching with the long pass filter LL-500 for the determination of the pair of DMAE and LEAE tracers. Not only was the registered RLU's for DMAE tracer found to increase by more than 2 fold as a result of this filter's use, the Percentage Cross Talks, as shown in Table VII, were also greatly improved. Furthermore, as more LEAE derivatives with even longer emission maxima were developed, e.g. 2-MeO-LEAE, long pass filters such as LL-520 (FIG. 7E) would be a better choice than filter LL-500 for enabling further reduction of the PCT.
For system controlling, which generally includes the basic functions of parameter setting, execution and registration of flashing, signal correction as described below as a function of filters used and the chemiluminescent compounds utilized, and data display, a personal computer unit containing proper software is utilized and connected to the DPL.
PERCENTAGE CROSS-TALKS (PCT's) DETERMINATION:
As mentioned above the two optical filters installed in two separate PMT assemblies on the DPL were intended to gate the emitted lights of two different spectral ranges: the long pass filter is to match with the longer emission from LEAE tracer and the short pass filter with the shorter emission from DMAE tracer. However, as illustrated by FIGS. 10 and 11, because of the minor overlap between the transmittance curves and the emission spectra of the cross-matching pairs, light signals generated by one tracer can be picked up by the primary PMT intended for it but also in small percentage by the secondary PMT intended for the other tracer, and vice versa. That portion of signal of one tracer, that can be registered by the secondary PMT, must be quantitated separately in term of percentage for each tracer prior to their use in a dual-analyte immunoassay, in order that the apparent RLU's can be corrected and the pure signal of each tracer detected by each PMT assembly be obtained when the two tracers were flashed simultaneously in the same tube.
Table VII shows the determined PCT's of several pairs of tracers. Anti-FSH-DMAE and anti-LH-LEAE were used in the simultaneous LH/FSH dual-analyte assay described below. Other pairs of tracers were included to demonstrate that through the selection of acridinium and benzacridinium compounds of wider separation in their emission maxima and proper choice of optical filters, minimal PCT's ideal for multi-analyte assay can be realized. The PCT's were obtained by dividing the minor signal from the secondary PMT by the major signal from the primary PMT in each case, and multiplying the results by 100%.
The concentrations of the samples were randomly selected such that the primary signals fell in the range of 100,000 to 1,500,000 RLU's per 25 ul sample. Each determination was made by sequentially pipeting 25 ul of one tracer solution, 300 ul of Flashing Reagent #1 into the cuvette, vortexing the resulting solution briefly, inserting the cuvette into the PMT housing, and performing the flashing by injecting 300 ul of Flashing Reagent #2 through the key-board control.
TABLE VII______________________________________Determination of Percent Cross-Talk (PCT) Long Pass Signals Short Pass SignalsSample (RLU's) (RLU's) PCT (%)______________________________________SET (I)*:LH tracer 538 688diluent 444 396Anti-LH-LEAE 6.25 E5 4.18 E4 6.7 5.78 E5 3.91 E4 6.8 6.19 E5 4.18 E4 6.8 Aver. 6.8FSH tracer 242 288diluent 268 340Anti-FSH-DMAE 2.32 E4 1.59 E5 14.5 2.42 E4 1.65 E5 14.7 2.60 E4 1.75 E5 14.8 Aver. 14.7SET (II) :Anti-LH-LEAE 1.27 E6 5.52 E4 4.4 1.25 E6 5.40 E4 4.3 Ave. 4.4Anti-FSH-DMAE 4.62 E4 4.28 E5 10.8 4.60 E4 4.23 E5 10.9 Ave. 10.9SET (III)+:Buffer .sup..about. 348 278 350 284Anti-TSH-2-MeO- 9.90 E5 1.29 E4 1.3LEAE 9.88 E5 1.29 E4 1.3 Ave. 1.3Anti-FSH-DMAE 1.17 E4 3.77 E5 3.1 1.17 E4 3.81 E5 3.1 Ave. 3.1SET (IV)#:Buffer .sup..about. 187 608 182 429Anti-TSH-2-MeO- 2.12 E5 6.26 E3 2.9LEAE 2.0 E5 5.95 E3 2.9 Aver. 2.9Anti-TSH-DMAE 2.93 E4 5.39 E5 5.4 3.12 E4 5.83 E5 5.4 Aver. 5.4______________________________________ *Optical filters mounted on the DPL: LL500 & P70450. Optical filters mounted on the DPL: LL500 & Laminated CS550/CS-600. +Optical filters mounted on the DPL: LL520 & Laminated CS550/CS-600. #Optical filters mounted on the DPL: LL520 & P70450. .sup..about. The buffer was 10 mM PBS/0.1% BSA/0.05% NaN.sub.3, pH 8.0.
The constancy of the PCT over a wide range of RLU's is critical in the multi-analyte assay signal correction. Table VIII shows that when the laminated CS550/CS600 filter and LL520 filter were used to gate the short pass and long pass signals, respectively, the PCT for anti-TSH-DMAE has the mean of 2.96% with standard deviation of 0.16% over RLU range of 10,000 to 7,000,000 counts or broader, while the PCT for anti-CKMB-LEAE has the mean of 4.79% with standard deviation of 0.23% over RLU range of 50,000 to 7,000,000 counts or broader.
TABLE VIII______________________________________Constancy of Percent Cross-Talk Short Pass Signal Long Pass Signal PCT Mean/SDSample (RLU's) (RLU's) (%) (%)______________________________________Anti-TSH-DMAE 6,689,796 217,010 3.24 6,545,872 212,956 3.25 6,645,674 210,262 3.16 1,469,500 43,710 2.97 1,469,770 45,004 3.06 1,450,042 43,492 3.00 303,944 8,922 2.81* 302,876 8,788 2.78* 287,632 8,928 2.98* 59,468 2,106 2.95* 58,816 2,072 2.93* 60,314 1,996 2.73* 12,298 692 2.77* 11,956 692 2.86* 12,420 716 2.96* 2.96/0.16Buffer Diluent 738 496 702 320Anti-CKMB-LEAE 320,758 6,663,484 4.81 315,344 6,497,756 4.85 320,224 6,528,242 4.91 61,374 1,350,584 4.54 61,514 1,329,548 4.63 60,036 1,330,152 4.51 13,044 264,526 4.71* 11,968 244,106 4.67* 12,324 245,542 4.78* 3,312 56,120 4.84* 3,586 54,906 5.45* 3,220 53,928 4.87* 4.79/0.23Buffer Diluent 652 372 622 346______________________________________ *Correction was made in consideration of the additional signal contribute by the buffer and system noise.
EQUATIONS FOR CORRECTING THE APPARENT RLU's DUE TO CROSS-TALKS IN DUAL-TRACER DETERMINATION:
When DMAE and LEAE derivatives or tracers are mixed and flashed simultaneously, the observed long and short pass signals can be broken down as follows:
S(s)=S(DMAE)+S'(LEAE)+b1 (1)
S(l)=S(LEAE)+S'(DMAE)+b2 (2)
Where, S(s) and S(l) are the observed short and long pass signals, respectively; S(DMAE) and S(LEAE) are the portions of signals due to DMAE and LEAE in the observed short and long pass signals, respectively. They will also be referred to as the corrected DMAE and LEAE signals; S' (DMAE) and S' (LEAE) are portions of the long and short pass signals due to DMAE and LEAE cross-talking, respectively; b1 and b2 are the combined signals due to assay components and system noise in the absence of DMAE and LEAE tracers, respectively.
Since the PCT's (represented by k1 and k2 below) are constants for any particular DMAE and LEAE tracers, there exist the following relationships:
S'(DMAE)=k1.times.S(DMAE) (3)
S'(LEAE)=k2.times.S(LEAE) (4)
Where k1, k2 are the PCT's for the DMAE and LEAE tracers, respectively.
Substitute equation (4) into (1):
S(s)=S(DMAE)+k2.times.S(LEAE)+b1
or
S(DMAE)=S(s)-k2.times.S(LEAE)-b1 (5)
Substitute equations (5) into (3) and (3) into (2): ##EQU1##
Equations (5) and (6) will yield the corrected short pass signal due to DMAE tracer and long pass signal due to LEAE tracer, respectively. For the purpose of demonstrating the feasibility of conducting a simultaneous LH/FSH dual-analyte assay, the determination of the combined matrix and system noises, b1 and b2 was found not to be significant. They were therefore both assigned a 0 value in the signal corrections for the following examples of the dual-analyte assays.
The following analysis was completed to determine the viability of using DMAE and 3-Carboxybutadienyl-AE, together in a dual label application. Given that the viability of such an application is determined by the amount of cross-talk, and cross-talk is negatively effected by overlap of the spectral energy densities (S.E.D.) of the esters, the substantial overlap for these two esters may make their use impractical. The following analysis predicts the minimum total cross-talk (and the associated light attenuation) across two optical paths for optimally selected "theoretical" filters.
After optimizing the selection of the optical filters, the minimum total cross-talk (defined below), for this combination of esters was calculated to be 14%. This represents the contributions of both esters, where the optimal percent cross-talk of DMAE into the 3-Carboxybutadienyl-AE channel was 9% and the optimal percent cross-talk of 3-Carboxybutadienyl-AE into the DMAE channel was 11%. Although one of these values may be further reduced, this is not possible without increasing the cross-talk of the other. When considering this trade-off, a total cross-talk of 14% represents a minimum for these two esters.
The light attenuation associated the optimal cross-talk values were 76% and 86% for the DMAE, respectively.
It is important to note that the results of this optimization analysis represent a best case scenario. Due the the difficulty of constructing an optimization algorithm using commercially available filters, theoretical filters were used to facilitate the analysis. These filters have exemplary properties which are not typical of those which are available commercially. As such, both the cross-talk and loss values are overly optimistic.
A total cross-talk of 14% is unacceptable for most dual label assays. This is because of variability and the role it play when correcting RLU readings for the cross-talk phenomenon. When there is a large mismatch in the RLU levels measured across two channels, variability in the larger signal, in association with a large cross-talk value, leads to variability in the smaller. This in turn leads to large errors in the "true" RLU results. For example, given a seven fold increase in the light levels read in the c-AE channel relative to the DMAE channel, and assuming the C.V.'s are 3% in both channels, the C.V. of the corrected RLU's associated with DMAE would be approximately 16.5%. This elevated C.V. of the corrected DMAE signal is due to the variation in the RLU's added to the DMAE channel from the elevated signal in the 3-Carboxybutadienyl-AE channel and the cross-talk phenomenon. The same analogy holds if the 3-Carboxybutadienyl-AE channel is elevated relative to the DMAE channel.
To effectively implement a dual label assay, the emission spectra of the two esters should be as narrow as possible and preferably have minimal if no overlap. In the event that the overlap is present, the design of a detection system requires the use of optical filters to separate signals. As is evident from FIG. 12, the S.E.D. for the DMAE and 3-Carboxybutadienyl-AE overlap substantially. The peak of the two spectra are at roughly 430 and 470 nm, respectively, and the 3-Carboxybutadienyl-AE is broader than DMAE given that both are normalized in the figure.
FIG. 13 shows a schematic of a typical optical system including the cuvette (containing the assay with both A.E.'s present), and two optical paths (often called channels), where an optical path includes a filter and detector selected to optimize collection efficiency and minimize cross-talk. The purpose of filter 1 is to remove components of the light from the 3-Carboxybutadienyl-AE. similarly, the purpose of filter 2 is to remove components of the light from the DMAE. Unfortunately, in addition to excluding the light from the unwanted ester, the filters also attenuate the desired signal resulting in "losses".
Once the filters have been selected, both the percent cross-talk and losses may be evaluated where PMT quantum efficiency effects, geometry, and scattering phenomena are neglected. FIGS. 14 and 15 show the signals from both the DMAE and 3-Carboxybutadienyl-AE (entering PMT1 and PMT2) after passing through filters 1 and 2, respectively. Filter 1 allows signals of wavelength shorter than 430 nm to pass while filter 2 allows wavelengths longer than 532 nm to pass. As discussed below, the choice of these wavelengths yields the optimal cross-talk for the system. It is clear from the figures that after filtering, the DMAE is the dominant signal in optical path 1 and the 3-Carboxybutadienyl-AE in the dominant signal in optical path 2.
The total detectable light of each ester is represented by the shaded areas "under" the filtered S.E.D. curves. After filtering it is clear that much of the original signal is lost, where the losses are approximated by, ##EQU2##
There, .function..sub.1 and .function..sub.2 are the filters in both paths and S.sub.DMAE and S.sub.3-Carboxybutadienyl-AE represent the spectral energy densities of the esters. In simpler terms, the losses are simply one minus the ratio of the filtered light (represented by area 1 and area 3 in FIGS. 14 and 15) to the original light (represented by the areas under the S.E.D. curves in FIG. 12.
The percent cross-talk for DMAE into optical path 2 (X.sub.DMAE,2), is defined as the amount of signal measured in path 2 (where the filter is selected to exclude the DMAE), divided by the amount of signal measured in path 1 (the path with the filter designed to pass DMAE and attenuate 3-Carboxybutadienyl-AE). A similar analogy holds for the percent cross-talk for 3-Carboxybutadienyl-AE into optical path 1. These ratios are defined as follows, ##EQU3##
For example, given the optimal choice of filters (shown in FIGS. 14 and 15), X.sub.DMAE,2 is determined by dividing area 4 by area 1, similarly, X.sub.3-Carboxybutadieny-AE,1 is determined by dividing area 2 by area 3. These values are 9% and 11% respectively.
THE OPTIMIZATION ALGORITHM:
As mentioned, the minimum total cross-talk was determined by optimizing the filter selection for the system. As evaluating every combination of commercially available filters is impractical, "theoretical" filters were constructed. These filters were assumed to have 100% transmission when trying to pass light and 0% transmission in cut-off regions. Both the assumption of 100% transmission and the sharp transition to 0% transmission lead to conservative estimates of cross-talk and optimistic estimates of losses.
As may be evident, moving the location of the filters (hence cut-offs) changes the resulting cross-talk and loss values. It is the freedom to move these cut-offs which allows the minimization of cross-talk. To optimize filter selection and minimize cross-talk the following methodology was followed:
the filters were iteratively moved in the following ranges in 2 nm steps,
430.ltoreq.filter 1 cutoff.ltoreq.480 nm
500.ltoreq.filter 2 cutoff.ltoreq.550 nm (filter 1 was restricted to wavelengths longer than 430 nm to avoid the noise floor for 3-Carboxybutadienyl-AE and filter 2 was restricted to wavelength shorter than 550 to avoid the noise flow for DMAE).
cross-talk values and losses were calculated for all combinations of filter 1 and filter 2 cut-offs within these limits.
the total cross-talk (X.sub.tot) was calculated for each combination of filters where, ##EQU4## the combination of filters which led to the minimum value of X.sub.tot was defined to be optimum.
As mentioned above, after evaluating all combinations of filters (within the limits stated) the minimum total cross-talk was found to be 14% for this combination of esters, where X.sub.DMAE,2 and X.sub.3-Carboxybutadienyl-AE,1 were found to be 9% and 11% respectively. This minimum corresponded to a filter 1 cut-off at 430 nm and the filter 2 cut-off at 532 nm.
SIMULTANEOUS IMMUNOASSAY FOR LUTEINIZING HORMONE (LH) AND FOLLICLE STIMULATING HORMONE (FSH):
One objective of the invention is to provide a method for simultaneously detecting and/or quantitating two or more substances or analytes in a single sample through the utilization of two different chemiluminescent labels or conjugates.
In an example of one embodiment, the assay system utilizes a DMAE labelled FSH antibody and a LEAE labelled LH antibody. The following examples demonstrate that LH and FSH standard curves and sample recovery are identical within the limits of experimental error when each analyte is assayed as a single analyte by introduction of one chemiluminescent tracer into the assay system, or in a dual analyte system which employs two chemiluminescent tracers. The examples further show that tracers prepared from a pair of a DMAE and a LEAC can be utilized in a simultaneous assay of two substances for which a corresponding binding partner, e.g. antibody, is available.
Example 21
Single FSH assay using Dual-Analyte Immunoassay System
The Magic Lite FSH kit components and protocol (Ciba Corning Diagnostics) were modified such that the assay could be performed as a single or dual analyte assay depending on the tracer selection. A solid phase consisting of paramagnetic particles (PMP) coupled to anti-FSH antibodies and PMP coupled to anti-LH antibodies was prepared by removing the buffer diluent from the Magic Lite FSH kit solid phase and resuspending these particles in Magic Lite LH kit solid phase (Ciba Corning Diagnostics Corp.). The kit tracer, anti-FSH-DMAE, was diluted 1:2 in Magic Lite LH kit tracer buffer. Standards for calibration contained both FSH and LH. Standards were prepared by spiking known concentrations of purified human FSH and human LH into a horse serum basepool. Nominal standard values were 0, 0.9, 2.2, 4.4, 8.8, 21.9, 43.8, 87.5, 140.0, 201.0 mIu/ml of FSH. Nominal LH concentrations were 0, 1.0, 2.5, 5.0, 10.0, 25.0, 50.0, 100.0, 160.0, 230.0 mIu/ml LH. Samples for analysis were prepared by spiking a human serum pool with varying concentrations of both purified human FSH and human LH. Additionally, serum based multi-constituent calibrators containing human FSH and human LH were used as samples.
To perform the assay, 50 ul of each standard or sample and 200 ul of diluted FSH tracer were vortex mixed and incubated for 30 minutes at room temperature. 500 ul of the combined anti-FSH/anti-LH solid phase was added, vortex mixed and incubated for 30 minutes at room temperature. The reacted solid phase was magnetically separated for 3 minutes in a Magic Lite rack (Ciba Corning Diagnostics Corp.), see European Patent 136126, and the supernatant decanted. The reacted solid phase was next washed with 1.0 ml of distilled water, separated for 3 minutes. The supernatant was decanted, and 100 ul of distilled water added. Each sample was manually transferred to a cuvette, and counted for 5 seconds on the DPL described above. The results (in RLU's) obtained from the short pass (DMAE) channel were used to calculate FSH concentration in each sample. Concentrations were calculated by using 10-point calibration with a spline data reduction routine. Each standard and sample was assayed in replicates of three. RLU's and % CVC for this assay are shown in Table IX under the heading FSH single-analyte assay. FSH sample recovery is shown in Table X under the heading FSH single-analyte assay. The FSH standard curve presented as % B/Bmax vs log FSH concentration is shown in FIG. 16 labelled as FSH single-analyte assay.
Example 22
Single LH Assay using Dual-analyte Immunoassay System
The solid phase reagent, standards, and samples described in Example 21 were used to perform an LH assay. The anti-FSH-DMAE tracer was replaced with an anti-LH-LEAE tracer which was diluted 1:2 in Magic Lite FSH kit tracer diluent. The assay methodology described in Example 21 was applied to this assay, except that the RLU results obtained from the Long pass (LEAE) channel were used to calculate LH sample concentrations.
The assay was calibrated using nine of the standards described in Example 21, excluding the 1.0 mIu/ml LH standard. Results for this assay are shown in Table XI and Table XII under the heading LH single-analyte assay. The standard curve is shown in FIG. 17 labelled as LH single-analyte assay.
Example 23
Simultaneous LH/FSH Assay using Dual-analyte Immunoassay System
Solid phase reagent, standards, and samples described in Examples 21 and 22 were used to perform a dual label LH/FSH assay in a single tube. The tracer consisted of the Magic Lite FSH kit tracer, anti-FSH-DMAE diluted 1:2 in the anti-LH-LEAE tracer. The assay methodology was the same as that described in Example 21. The raw RLU's from each channel was mathematically corrected for cross-talk prior to concentration calculations. Corrected RLU's and concentrations resulting from these corrected RLU's are shown in Tables IX-XII, and are labelled as dual-analyte assay. Mean sample recovery for single analyte vs. dual analyte assays are compared by t-test in Tables X and XII. The FSH and LH standard curves are shown in FIGS. 16 and 17 and labelled as FSH and LH dual-analyte assay, respectively.
Assays and Assay Formats
The present invention relates to chemiluminescent compounds and more particularly, the use of two or more chemiluminescent conjugates to simultaneously detect two or more substances in a test sample. The disclosure teaches the use of benzacridinium compounds and preferably N-alkylated benzacridinium compounds in such assays.
A test substance includes any component(s) or analytes sought to be detected and/or quantitated in a test sample, including but not limited to, more than one component of a single structure, e.g. more than one portion of a nucleic acid sequence or different loci of a chromosome, genome or molecule, where the components or analytes may be of biological or industrial origin, such as nucleic acids, proteins, ligands, haptens or other materials or compounds to which an appropriate assay method can be formatted. It is understood that the test sample and/or substance may need to be pretreated to render it assayable by a test method. The test substances and quantities thereof sought to be detected may limit the types of assays which can be performed because of, for example, sensitivity concerns, but not the use of chemiluminescent labels for detection. Various internal standards or controls may be added to a test sample for detection and/or quantitation to assess the performance of the assay. Diagnostic assays exemplified by immunoassays, hybridization assays and amplification assays have increasingly incorporated chemiluminescent labels in their formats. Designs and formats of such assays are well known by those skilled in the art and extensively published in the technical and patent literature, for example, an assay format may require the separation of a reaction product or unreacted agent to a transfer tube for detection and/or quantitation. Such separation techniques may be useful for competitive assays, solid phase assays or to limit interferents.
In one embodiment of the invention, two or more chemiluminescent conjugates are utilized as labels in an amplification assay. Representative amplification assays include but should not be limited to polymerase chain reaction (PCR), autocatalytic replication of recombinant RNA and amplification of midivariant DNA or RNA. See EP-A-O 481 704 (priority U.S. Ser. No. 598,269 (Oct. 16, 1990)) which is commonly assigned and incorporated herein by reference. Such methods, as taught in the technical and patent may be made adaptable to incorporate chemiluminescent labels, and particularly two or more chemiluminescent labels for detection of target sequences of interest. The advantage of using a multi-label method is to detect and/or quantitate a plurality of target sequences or one or more target sequences and an internal standard. An example of such a method includes providing a test sample suspected of containing one or more target sequences, amplifying the target sequences, providing at least two chemiluminescent conjugates, each chemiluminescent conjugate being associated with a target sequence(s) and simultaneously detecting and/or quantifying amplified target sequences by emissions of at least two chemiluminescent conjugates. In another step of this method an internal reference, control or control system may be added to the assay to insure assay performance and results. The internal reference may be amplified as well as the target sequences.
The use of chemiluminescent labels for such assays serves to demonstrate the utility of this invention.
The chemiluminescent compounds of this invention are adapted to be packaged in kit form for commercial sale. The chemiluminescent labels of these kits may be conjugated to appropriate substances or materials which are specific to the substances sought to be detected in the test samples. Appropriate functional groups may be added to the chemiluminescent compounds for use in various assays and other applications. Examples of assays for which the methods of the present invention may be utilized include but should not be limited to: assays including at least two antibodies of different specifities; assays including at least two antigens; assays including at least one antigen and at least one antibody; and assays for molecules indicative of cancer, infectious diseases, genetic abnormalities, genetic disposition, genetic assessment and to monitor medicinal therapy.
It is to be understood that various other modifications will be apparent to and can readily be made by those skilled in the art, given the disclosure herein, without departing from the scope and materials of this invention. It is not, however, intended that the scope of the claims appended hereto be limited to the description as set forth herein, but rather that the claims be construed as encompassing all features of patentable novelty which reside in the present invention, including all features which would be treated as equivalents thereof by those skilled in the art to which the invention pertains. It is also noted that the examples given therein are intended to illustrate, and not to limit the invention.
TABLE IX______________________________________MEAN RLU's and % CVCFOR MODIFIED MAGIC LITE FSH ASSAYS FSH RESULTS FSH SINGLE DUAL ANALYTE ASSAY ANALYTE ASSAY*SAMPLE (VALUE) MEAN RLU % CVC MEAN RLU % CVC______________________________________S1 (0) 1336 4.3 610 6.7S2 (0.9) 1891 5 1309 14.4S3 (2.2) 3202 10.9 2375 6.7S4 (4.4) 5155 9.4 4189 3.9S5 (8.8) 9005 2.6 7702 2.4S6 (21.9) 19637 5.5 16942 5.2S7 (43.8) 35491 0.7 30563 4S8 (87.5) 56844 1.7 51969 5S9 (140.0) 74850 0.9 66499 0.5S10 (201.0) 87531 0.8 77003 0.5SAMPLE 1 9962 7.3 8417 2.8SAMPLE 2 16779 4.9 14777 0.8SAMPLE 3 29683 13 28721 4.5SAMPLE 4 62549 2.2 55878 2.4SAMPLE 5 93019 1.1 84182 3.3SAMPLE 6 103290 3 93297 1.2LOW MULTI-CAL 1756 9 1160 9.8HIGH MULTI-CAL 80308 2.4 71082 0.6TOTAL COUNTS 564200 571392______________________________________ *corrected RLU
TABLE X__________________________________________________________________________FSH SAMPLE RECOVERY: SINGLE ANALYTE ASSAY VS. DUAL ANALYTE ASSAY FSH SINGLE FSH DUAL CRITICAL ANALYTE ASSAY ANALYTE ASSAY T-VALUESAMPLE MIU/ML % CVD MIU/ML % CVD T-VALUE 95% C.I.__________________________________________________________________________SAMPLE 1 9.923 8.6 9.737 3.2 0.36 .+-.4.30SAMPLE 2 18.291 5.7 18.668 1 -0.62 .+-.4.30SAMPLE 3 35.235 15.1 40.708 5.3 -1.65 .+-.4.30SAMPLE 4 101.951 3.5 98.877 4.2 0.98 .+-.3.18SAMPLE 5 >> >>SAMPLE 6 >> >>MULTI-CAL LOW 0.693 30.8 0.697 20.1 -0.2 .+-.3.18MULTI-CAL HIGH 163.132 5.4 163.812 1.4 -0.13 .+-.4.30__________________________________________________________________________
TABLE XI______________________________________MEAN RLU'S AND % CVCFOR MODIFIED MAGIC LITE LH ASSAYS LH RESULTS LH SINGLE DUAL ANALYTE ANALYTE ASSAY ASSAY*SAMPLE (VALUE) MEAN RLU % CVC MEAN RLU % CVC______________________________________S1 (0) 17,883 14.2 18,477 10.6S3 (2.5) 24,310 1.9 22,818 2.7S4 (5.0) 27,007 6.5 25,118 11.9S5 (10.0) 34,713 11.6 28,934 6.2S6 (25.0) 42,440 4.6 41,543 5.3S7 (50.0) 65,787 2.9 71,140 6.2S8 (100.0) 115,760 6.8 113,694 1.9S9 (160.0) 161,767 4.4 164,225 4.4S10 (230.0) 223,569 4.8 205,347 4.5SAMPLE 4 42,157 2.8 40,519 8.2SAMPLE 5 82,934 4.3 83,592 5.5SAMPLE 6 110,502 2.8 113,285 1.9MULTI-CAL HIGH 86,189 3.5 90,451 2.9TOTAL COUNTS 2,250,526 2,322,672______________________________________ *CORRECTED RLU
TABLE XII__________________________________________________________________________LH SAMPLE RECOVERY: SINGLE ANALYTE ASSAY VS. DUAL ASSAY LH RESULTS LH SINGLE DUAL ANALYTE CRITICAL ANALYTE ASSAY ASSAY* T-VALUESAMPLE MIU/ML % CVD MIU/ML % CVD T-VALUE 95% C.I.__________________________________________________________________________SAMPLE 4 21.347 7 22.342 15.3 -0.46 .+-.4.30SAMPLE 5 67.392 5.7 64.829 7.5 0.72 .+-.3.18SAMPLE 6 97.375 3.6 97.984 2.5 -0.25 .+-.3.18MULTI-CAL HIGH 70.906 4.5 72.153 4 -0.5 .+-.3.18__________________________________________________________________________

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5281712	McCapra	Jan 1994
5283334	McCapra	Feb 1994
5284951	McCapra	Feb 1994
5284952	Ranakrishnan	Feb 1994
5290936	Beheshti	Mar 1994
5321136	McCapra	Jun 1994
5338847	McCapra	Aug 1994
5340714	Katsilometes	Aug 1994
5393469	Akhavan-Tafti	Feb 1995
5395752	Law et al.	Mar 1995
5447687	Lewis et al.	Sep 1995
5449556	Law et al.	Sep 1995
5468646	Mattingly et al.	Nov 1995
5527684	Mabile et al.	Jun 1996
5656207	Woodhead et al.	Aug 1997
5702887	Law et al.	Dec 1997

Number	Date	Country
136 126	Jun 1985	EPX
194 132	Sep 1986	EPX
219 309	Apr 1987	EPX
233 053	Sep 1987	EPX
0263657	Apr 1988	EPX
273115	Jul 1988	EPX
296 136	Dec 1988	EPX
0322926	May 1989	EPX
353 971	Feb 1990	EPX
361 817	Apr 1990	EPX
369 344	May 1990	EPX
478 626	Jan 1991	EPX
421 788	Apr 1991	EPX
481 704	Apr 1992	EPX
0304202	Jul 1992	EPX
502 638	Sep 1992	EPX
537 994	Apr 1993	EPX
0377729	Aug 1993	EPX
506 055	Aug 1937	GBX
2026159	Jan 1980	GBX
5 045 929	Nov 1980	GBX
2 163 553	Feb 1986	GBX
2233450	Jan 1991	GBX
WO8901157	Feb 1989	WOX
WO8910552	Nov 1989	WOX
WO9000164	Jan 1990	WOX
9000168	Jan 1990	WOX
WO9100511	Jan 1991	WOX
9208722	May 1992	WOX
9212255	Jul 1992	WOX
9213264	Aug 1992	WOX

Long emission wavelength chemiluminescent compounds and their use in test assays

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US Referenced Citations (37)

Foreign Referenced Citations (31)

Non-Patent Literature Citations (25)

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