Fluorocyclosaccharide drug delivery systems

Abstract

Novel fluorine-containing cyclic saccharide compounds, in particular fluorocyclodextrin compounds, and drug inclusion complexes of these compounds, as well as methods for preparation of the novel fluorine-containing cyclic saccharide compounds, including fluorocyclodextrins, and drug inclusion complexes of the compounds. In addition, methods for following the disposition and fate in vivo of drug inclusion complexes of the invention.

Description

This invention relates to novel fluorine-containing cyclic saccharide compounds, in particular fluorocyclodextrin compounds, and to drug inclusion complexes of these compounds. The invention also relates to methods for preparation of the novel fluorine-containing cyclic saccharide compounds, including fluorocyclodextrins, and drug inclusion complexes of the compounds. The invention further relates to methods for following the disposition and fate in vivo of drug inclusion complexes of the invention.

BACKGROUND OF THE INVENTION

Site-specific drug delivery and trans-membrane drug delivery represent substantial challenges in the development and efficacious use of drugs. In addition, many drugs are susceptible to chemical and/or biochemical degradation on their way to their site of pharmacological action. Failure to deliver the drug for whatever reason will result in decreased efficacy. If the drug cannot reach the site of action in adequate concentrations, increased toxicity due to the requirement for larger and/or more frequent doses may seriously affect the therapeutic outcome.

BRIEF DESCRIPTION OF DRAWINGS

The invention, as exemplified by preferred embodiments, is described with reference to the accompanying drawings in which:

FIG. 1 shows .sup.19 F NMR spectrum of mouse liver after 6-F.sub.3 .beta.CD administration.

FIG. 2 shows .sup.19 F NMR spectrum of mouse blood after 6-F.sub.3 .beta.CD administration.

FIG. 3 shows .sup.19 F NMR spectrum of mouse urine after 6-F.sub.3 .beta.CD administration.

FIG. 4 shows .sup.19 F NMR spectrum of 6-F.sub.3 .beta.CD.

FIG. 5 shows .sup.19 F NMR spectrum of flutamide.

FIG. 6 shows .sup.19 F NMR spectrum of inclusion complex of flutamide with 6-F.sub.3 .beta.CD.

FIG. 7 shows .sup.19 F NMR spectrum of flurbiprofen.

FIG. 8 shows .sup.19 F NMR spectrum of inclusion complex of flurbiprofen with 6-F.sub.3 .beta.CD.

FIG. 9 shows .sup.19 F NMR spectrum of inclusion complex of flurbiprofen with 6-F.sub.3 .beta.CD plus parent flurbiprofen.

FIG. 10 shows IR spectrum of 6-F.sub.3 .beta.CD.

FIG. 11 shows IR spectrum of physical mixture (1:1) of 6-F.sub.3 .beta.CD and trifluridine.

FIG. 12 shows IR spectrum of an inclusion complex of 6-F.sub.3 .beta.CD and trifluridine.

FIG. 13 shows IR spectrum of trifluridine.

DESCRIPTION OF THE INVENTION

In accordance with the present invention, a novel group of fluorine-containing cyclic saccharides are provided, including fluorocyclodextrins. These compounds permit new applicability for .sup.19 F MRS techniques in a clinically useful method.

When the compounds of the invention are used as drug carriers, there is a difference in the .sup.19 F chemical shift between the free carrier molecule and the cyclic saccharide-drug inclusion complex. This provides a novel method for determining the integrity of the complex with any drug, and is not limited to drugs which themselves contain F, as in Lincoln's system.

The change in .sup.19 F MRS chemical shift between the drug-occupied or complexed carrier and the free carrier can be used to differentiate and measure the free and complexed species. The invention provides a novel method for measuring the integrity of inclusion complexes in vivo by a method which is non-invasive and does not involve the administration of radioactive compounds to the subject.

In accordance with one aspect of the invention, methods are provided for the synthesis of fluorine-containing cyclic saccharides, including fluorocyclodextrins, and for the preparation of drug inclusion complexes employing these compounds.

A variety of cyclic saccharides are known which can form inclusion complexes with a range of chemicals/drugs/biochemicals. One type of cyclic saccharides are cyclodextrins (reference 12--the references referred to herein are listed in pages 31-36) (reference 45) (reference 46). .beta.-Cyclodextrin (.beta.-CD) ##STR1## has seven 1,4-linked glycopyranose sub-units that form a toroida "basket" with an inner cavity diameter of approximately 5-7 .ANG.. The primary hydroxyls (at C-6) are at the narrow end of the torus and the secondary hydroxyls (C-2 and C-3) are at the mouth (wide end), with the OH groups at C-2 pointing toward the cavity, while the OH groups at C-3 point outward. Thus, the outer surface becomes distinctly hydrophilic. The inner "basket" is hydrophobic, with a structure of carbon atoms and ether-oxygen atoms; this inner structure supports drug inclusion complex formation, in part through non-specific interactions (e.g. Van der Weals forces) between the drug and cyclodextrin (reference 13).

.alpha.-cyclodextrin (.alpha.-CD) is similar to .beta.-CD, except that .alpha.-CD has only 6 sub-units. .gamma.-cyclodextrin (.gamma.-CD) has 8 sub-units and .delta.-cyclodextrin (.delta.-CD) has 9 sub-units (see Endo et al, "Purification and Characterization of .eta.-Cyclodextrin," The 7th International Cyclodextrins Symposium, Tokyo (Apr. 25-28, 1994). Although .beta.-CD has an ideal cavity size for the inclusion of a variety of drugs, it has two disadvantages: 1) it is nephrotoxic and 2) it has lower water solubility than either .alpha.-CD or .gamma.-CD. It has been shown that derivatization of the primary and/or secondary hydroxyl groups can both increase its solubility and decrease its irritant properties (references 13-15).

When drugs and cyclodextrins form inclusion complexes, H-bonding and non-specific forces change in both drug and carrier molecules, giving rise to changes in the chemical shifts of nuclear magnetic resonances; if either or both molecules have fluorine in their structures, this gives rise to changes in .sup.19 F Magnetic Resonance Spectroscopy (MRS) chemical shifts.

Several fluorine-containing drugs, including flurbiprofen, have been successfully incorporated into .beta.-CD and derivatized .beta.-CD's as inclusion complexes (reference 13). Lincoln et al. have used .sup.19 F MRS to study the incorporation of model fluorine-containing drugs and biochemicals into cyclodextrin inclusion complexes (references 23-27); they have found .sup.19 F MRS to a useful technique to study chiral molecular recognition (references 26,17), stability/dissociation constants and drug-cyclodextrin stoichiometry in inclusion complexes, and cis/trans geometric effects (reference 23) in inclusion complexes. Their studies demonstrated and indeed were based on inclusion-complex-induced changes in the .sup.19 F MRS chemical shifts of fluorine atoms on the fluorine-containing drug. These changes are due to changes in H-bonding and to non-specific forces experienced by the drug upon inclusion complex formation.

.sup.19 F NMR or Magnetic Resonance Spectroscopy (MRS) spectroscopy is a powerful tool for the study of cyclodextrin-drug complexes, having the advantages of high sensitivity and simple spectra. To date, however, these studies have been limited to complexes involving F-containing drugs.

Other cyclic saccharides can be used, e.g., cyclic saccharides with sugars other than glucose.

The present invention is exemplified with reference to fluorine-containing cyclodextrin compounds, but the invention broadly relates to any fluorine-containing cyclic saccharide compound. The fluorine atoms can be attached to cyclic saccharides in a manner analogous to the mechanisms for attachment disclosed herein for cyclodextrin compounds and by other means, which are known by those skilled in the art and which can be practiced without any undue experimentation. Such fluorine-containing cyclic saccharide compounds will exhibit properties which are similar to the properties exhibited by the fluorine-containing compounds disclosed herein.

For example, suitable cyclic saccharides include cycloisomaltooligosaccharides (CI-7, CI-8 and CI-9, below) disclosed in Oguma et al, "Novel Cyclic Sugars, Cycloisomaltooligosaccharides, and Cycloisomaltooligosaccharide Synthase," The 7th International Cyclodextrins Symposium, Tokyo (Apr. 25-28, 1994). ##STR2##

Likewise, suitable cyclic saccharides also include Maltosyl cyclodextrins as disclosed in Mikuni et al, "Continuous Production of Maltosyl Cyclodextrins Using Immobilized Pullulanase on Novel Ceramic Carrier," The 7th International Cyclodextrins Symposium, Tokyo (Apr. 25-28, 1994). Such Maltosyl cyclodextrins are synthesized by enzyme reaction of pullulanase from maltose and cyclodextrings such as .alpha.-CD, .beta.-CD and .gamma.-CD.

In addition, trimaltosyl-.beta.-CD's disclosed in Okada et al, "Structural Determination of Positional Isomers of Multi-Branched Cyclomalto-Oligosaccharides (Cyclodextrins) by Enzymatic Degradation," The 7th International Cyclodextrins Symposium, Tokyo (Apr. 25-28, 1994) can be used as the cyclic saccharide according to the present invention.

The cyclodextrins of the invention can also be in the form of a molecular tube as disclosed in Li et al, "Synthesis of Tubular Polymers of Cyclodextrins by Using a Polymer Chain as Matrix," The 7th International Cyclodextrins Symposium, Tokyo (Apr.25-28, 1994).

Preferred cyclic saccharides according to the present invention are .beta.-cyclodextrins.

The fluorination achieved in the fluoro-cyclic saccharides of the invention provides a signal, suitable for location of the carrier in a whole animal or in a patient, so that the location of drug delivery can be determined in vivo, using known Magnetic Resonance Imaging (MRI) techniques. By using known MRS techniques, one can follow the breakdown of the drug inclusion complexes containing the cyclic saccharides of the invention either in tissue samples taken from a subject or in whole body studies on a subject and thereby determine the rate of drug delivery and drug release to the body or its tissues.

The techniques of whole body, in vivo, in situ MRI have become routine in medical diagnosis of biochemical and anatomical lesions, and in studies of bioenergetics and xenobiotic transformations. Although MRS and MRI are applied primarily to proton (.sup.1 H) studies, the virtual absence of any fluorine in mammalian soft tissue and the high sensitivity of .sup.19 F (second only to .sup.1 H) make .sup.19 F MRS and .sup.19 F MRI unique and powerful tools for the investigation of biotransformation, biodistribution and excretion of fluorinated substances.

The advantages with .sup.19 F NMR spectra are that they are clean (few overlapping signals), easily recognizable by F--H coupling, relatively easy to interpret and not masked by a huge water signal, which is a characteristic of in vivo proton MRS.

Table 2 demonstrates the change in .sup.19 F chemical shift between compounds of the invention in their free state and in drug inclusion complex form. The inclusion complex of trifluridine and 6-F.sub.3 .beta.CD appears to show no change in .sup.19 F chemical shift in comparison to the parent compound, i.e., trifluridine and 6-F.sup.3 .beta.CD. It is believed that this is because trifluridine and related nucleosides are too small to achieve a considerable interaction in the cavity of .beta.-CD (Hoffman et al., (1970), Biochem., V. 9, p. 3542) and therefore, on dilution with the NMR solvent, D.sub.2 O, the drug readily dissociates and the complex is lost.

Table 2 shows significant changes in the .sup.19 F chemical shift for flutamide/6-F.sub.3 .beta.CD inclusion complex and flurbiprofen/6-F.sub.3 .beta.CD inclusion complex.

The invention provides a method for determining in tissue samples or in a patient whether administered drug inclusion complex remains intact or has broken down to deliver free drug by examination of the .sup.19 F chemical shift in the signal obtained from the tissue or from the patient.

In order to prepare the fluorine-containing cyclic saccharide according to the present invention, a cyclic saccharide is reacted with a fluorine-containing compound. The fluorine-containing compound can generally be any compound which is suitable for either adding a fluorine atom to the cyclic saccharide or adding a moiety which contains a fluorine atom to the cyclic saccharide. This reaction can generally be conducted at any temperature from about room temperature up to about 100.degree. C.

The following are representations of suitable processes for making fluorine-containing cyclic saccharides according to the present invention: ##STR3##

As described above, the present invention broadly relates to fluorine-containing cyclic saccharide compounds, any of which can readily be tested for its usefulness in providing the properties described herein by employing routine experimentation.

The following are representative examples of compounds in accordance with the present invention:

(i) Fluorine Substituent at the Primary Carbon Center ##STR4## wherein: 1. R.dbd.R.sup.1 .dbd.F. 2. R.dbd.CH.sub.2 F, one or more R.sup.1 .dbd.CH.sub.2 OH, the remaining R.sup.1 .dbd.CH.sub.2 F; i.e. for .beta.-CD, R.sup.1 =x CH.sub.2 OH, (6-x) CH.sub.2 F, x=0-6. 3. R.dbd.CH.sub.2 F, one or more R.sup.1 .dbd.CO.sub.2 H, the remaining R.sup.1 .dbd.CH.sub.2 F; i.e. for .beta.-CD, R.sup.1 =x CO.sub.2 H, (6-x) CH.sub.2 F, x=0-6. 4. R.dbd.CH.sub.2 F, one or more R.sup.1 .dbd.CH.sub.2 R.sup.2 (where R.sup.2 .dbd.NH.sub.2 or N.sub.3), the remaining R.sup.1 .dbd.CH.sub.2 F; i.e. for .beta.-CD, R.sup.1 =-x CH.sub.2 R.sup.2 (where R.sup.2 .dbd.NH.sub.2 or N.sub.3), (6-x) CH.sub.2 F, x=0-6. 5. R.dbd.CH.sub.2 F, one or more R.sup.1 .dbd.CH.sub.2 OR.sup.2 (where R.sup.2 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), the remaining R.sup.1 .dbd.CH.sub.2 F; i.e. for .beta.-CD, R.sup.1 =x CH.sub.2 OR.sup.2 (where R.sup.2 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), (6-x) CH.sub.2 F, x=0-6. 6. R is CH.sub.2 OCH.sub.2 CF.sub.3, CH.sub.2 NHC.sub.6 H.sub.4 F, or other moieties which contain fluorine. Also, in 2-5 above, the carboxy, amino, or carbohydrate moiety can be used to build an amino acid, peptide or carbohydrate antigen in order to realize specificity through molecular recognition (i.e., receptor, antibody-antigen complex, etc.) or for enhancing solubility or complex formation. (ii) Fluorine Substituent at a Secondary Carbon Center ##STR5## (a) Gluco Configuration 1. R.dbd.CH.sub.2 OH, R.sup.1 .dbd.F, R.sup.2 .dbd.OH, R.sup.3 .dbd.H. 2. R.sup.1 .dbd.F, R.sup.2 .dbd.OH, R.sup.3 .dbd.H, at least one R.dbd.CO.sub.2 H, the remaining R=CH.sub.2 OH; i.e. for .beta.-CD, R=x CO.sub.2 H, (7-x) CH.sub.2 OH, x=0-7. 3. R.sup.1 .dbd.F, R.sup.2 .dbd.OH, R.sup.3 .dbd.H, at least one R.dbd.CH.sub.2 R.sup.4 (where R.sup.4 .dbd.NH.sub.2 or N.sub.3), the remaining R.dbd.CH.sub.2 OH, i.e. for .beta.-CD, R=-x CH.sub.2 R.sup.4 (where R.sup.4 .dbd.NH.sub.2 or N.sub.3), (7-x) CH.sub.2 OH, x=0-7. 4. R.sup.1 .dbd.F, R.sup.2 .dbd.OH, R.sup.3 .dbd.H, at least one R.dbd.CH.sub.2 R.sup.5 (where R.sup.5 =sugar moiety i. e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CH.sub.2 R.sup.5 (where R.sup.5 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), (7-x) CH.sub.2 OH, x=0-7. Also, in 2-4 above, the carboxy, amino, or carbohydrate moiety can be used to build an amino acid, peptide or carbohydrate antigen in order to realize specificity through molecular recognition (i.e., receptor, antibody-antigen complex, etc.) or for enhancing solubility or complex formation. (b) Manno Configuration 1. R.dbd.CH.sub.2 OH, R.sup.1 .dbd.F, R.sup.2 .dbd.H, R.sup.3 .dbd.OH. 2. R.sup.1 .dbd.F, R.sup.2 .dbd.H, R.sup.3 .dbd.OH, at least one R.dbd.CO.sub.2 H, the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CO.sub.2 H, (7-x) CH.sub.2 OH, x=0-7. 3. R.sup.1 .dbd.F, R.sup.2 .dbd.H, R.sup.3 .dbd.OH, at least one R.dbd.CH.sub.2 R.sup.4 (where R.sup.4 .dbd.NH.sub.2 or N.sub.3), the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CH.sub.2 R.sup.4 where R.sup.4 .dbd.NH.sub.2 or N.sub.3), (7-x) CH.sub.2 OH, x=0-7. 4. R.sup.1 .dbd.F, R.sup.2 .dbd.H, R.sup.3 .dbd.OH, at least one R.dbd.CH.sub.2 OR.sup.5 (where R.sup.5 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CH.sub.2 OR.sup.5 (where R.sup.5 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), (7-x) CH.sub.2 OH, x=0-7. Also, in 2-4 above, the carboxy, amino, or carbohydrate moiety can be used to build an amino acid, peptide or carbohydrate antigen in order to realize specificity through molecular recognition (i.e., receptor, antibody-antigen complex, etc.) or for enhancing solubility or complex formation. (iii) Fluorine Substituent at a Single Secondary Carbon Center ##STR6## (a) Gluco Configuration 1. R.dbd.OH, R.sup.1 .dbd.H. (b) Manno Configuration 1. R.dbd.H, R.sup.1 .dbd.OH.

The desired number of fluorine atoms in the fluorine-containing cyclic saccharide molecule depends on the drug being incorporated and the purpose for which the complex is being used. When the drug contains no fluorine atoms, it is generally desirable to include the maximum number of effective fluorine atoms. For example, a fluorine-containing cyclic saccharide molecule could include 21 fluorine atoms, which would provide a very large signal from the fluorine-containing cyclic saccharide when conducting .sup.19 F analysis. In instances where the drug contains one or more fluorine atom, it is desirable to provide a 1:1 ratio, i.e., the total number of fluorine atoms in the drug molecule(s) in a complex is equal to the total number of fluorine atoms in the cyclic saccharide molecule in the complex. With such a formulation, equal signals are received from the drug and from the cyclic saccharide, providing clearer signals for analyzing the drug and the cyclic saccharide both before and after release of the drug from the cyclic saccharide. If the cyclic saccharide contains more fluorine atoms than the drug in the complex, a correspondingly stronger signal is received for the cyclic saccharide, and there is a corresponding decrease in sensitivity with respect to the fate of the drug. It is preferred that the one or more fluorine atoms per molecule of cyclic saccharide be symmetrically positioned.

In accordance with the present invention, the fluorine-containing cyclic saccharide is then mixed with one or more equivalents of drug to form the inclusion complex. This step can be conducted at room temperature and/or the temperature can be elevated to accelerate the formation of the complex. As discussed above, the present invention is widely applicable to many different types of drugs, and each can be readily tested for its usefulness according to the present invention by routine experimentation.

Examples of suitable drugs for inclusion in accordance with the present invention include mitoxantrone (Novantrone).RTM., taxol, progesterone, testosterone, ibuprofen, hydrocortisone, digitoxin, digoxin, diazepam, and peptides. The drugs may also be fluorinated (i.e. as a second marker or for NOE experiments, e.g., fluorinated analogs of mitoxantrone, taxol, progesterone, testosterone, ibuprofen, hydrocortisone, digitoxin, digoxin, diazepam, and peptides), fluorinated amino acids and peptides, F.sub.3 TDR, fluorouracil and fluorinated pyridoxyl analogs.

The ratio of fluorine-containing cyclic saccharide to the drug is typically 1:1 (on a molar basis), however, there may be instances where more than one drug molecule can be complexed by a single cyclic saccharide. Thus, the preferred ratio can readily be determined experimentally for each combination of fluorine-containing cyclic saccharide and drug.

Doses are determined in accordance with established medical techniques by routine experimentation.

The present invention also relates to pharmaceutical formulation and methods of making the same, comprising one or more inclusion complex according to the invention together with a suitable complex carrier or excipient. The selection of a complex carrier and/or excipient and the formation of pharmaceutical formulations can be carried out in accordance with well-known procedures.

The pharmaceutical compensition according to the present invention, which include a drug and a fluorine-containing cyclic saccharide according to the present invention, are suitable for treating disease states.

The inclusion complexes according to the present invention can be administered by any suitable route of administration. Such routes of administration include all of the routes well known in the art, such as, oral, parenteral, transdermal, nasal, rectal, e.g., as tablets, capsules, injectable solutions, eye-drops, etc.

The fluorine-containing cyclic saccharides in accordance with the present invention can be employed in any procedure in which the corresponding non-fluorine-containing cyclic saccharides can be employed. For example, the fluorine-containing cyclodextrins according to the present invention can be used in any circumstance in which cyclodextrins can be employed.

The present invention further relates to a process for providing site specific delivery of a drug to a patient, comprising administering to a patient a complex as disclosed herein.

The present invention further relates to a process for analyzing in vivo the location and time of drug association from a complex according to the present invention by performing .sup.19 F MRS on a patient to whom such a complex has been administered.

The present invention further relates to a process for analyzing in vivo the activity of a drug, the process comprising administering to a patient a complex as disclosed herein and performing .sup.19 F MRS on the patient.

The present invention also relates to a process for determining the location of a tumor in a patient by administering a complex as disclosed herein to the patient and performing .sup.19 F MRS on the patient.

The present invention provides a process for treating tissue extracted from a living being, comprising administering to the tissue a complex as disclosed therein.

EXAMPLES

Compounds were characterized by elemental analysis and by .sup.1 H, .sup.13 C and .sup.19 F NMR spectroscopy.

NMR Spectroscopy

A Bruker AM-300 (7.05 Tesla, 282.39 Mhz) and a Bruker CXP-100 (2.35 Telsa, 94.26 Mhz, 40 cm. bore) spectrometer were used for .sup.19 F NMR spectroscopy. The CXP-100 spectrometer was used with a 20 mm diameter, three turn horizontal coil. The biodistribution and excretion study of Example 4 was performed on the CXP-100 spectrometer, while .sup.1 H, .sup.13 C and .sup.19 F NMR spectra for synthesized compounds, blood, urine and extracts of liver were obtained using the Bruker AM-300 instrument. The .sup.19 F NMR were acquired over a spectral width of 70.0 ppm (between +60.0 and -10.0 ppm). The number of scans varied from 2.5 k to 45 k scans depending on the size of biological samples. An aqueous solution of chromium acetate (90 .mu.L; 0.1M) was used as a relaxation agent to enhance the S/N ratio. Exponential line broadening of 0-40 Hz was imposed on the data prior to Fourier transformation. An aqueous solution of potassium fluoride (5 .mu.L; 0.2M) was used as an internal standard during acquisition of .sup.19 F NMR spectra while .sup.1 H and .sup.13 C NMR spectra were locked on deuterium. D.sub.2 O was used as a solvent for samples of blood, urine and liver extract) which appeared at .delta.4.68 ppm (.sup.1 H NMR spectra) with respect to tetramethylsilane. The resolution limits for .sup.1 H, .sup.13 C and .sup.19 F were observed between 0.5-1.1, 2.0-3.0 and 1.3-20.0 Hz, respectively. The chemical shifts are reported in .delta. ppm.

Example 1

Synthesis of Fluorinated Cyclodextrins

A. Anhydrous .beta.-cyclodextrin (.beta.CD; 4.0 g) dried overnight over refluxing methanol in a hi-vac system was dissolved in anhydrous 2,2,2-trifluoroethanol, that had been presaturated with HCl gas; the mixture was heated at 70.degree. C. for 24 h. A TLC examination of the mixture at this time showed the formation of two major products and complete disappearance of .beta.-CD. Usual workup and purification of this mixture on a silica gel column yielded two products:

1. Heptakis �6.0-(2,2,2-trifluoroethyl)!-.beta.-cyclodextrin (6-F.sub.3 .beta.CD)

Yield, 35.5%, mp. 122.degree.-124.degree. C.; .sup.1 H NMR (D.sub.2 O) .delta.4.94 (d, J.sub.7.1 =3.5 H.sub.2, 1H, H-1), 4.18-3.94 (m, 2H, CH.sub.2 CF.sub.3), 3.76 (d, J gem=12.0 Hz of d, J.sub.5,6 =2.0 Hz, 1H of H-6), 3.72-3.56 (m, 3H, H-5, H-6 and H-3), 3.49 (d, J.sub.1,2 =3.5 Hz of d, J.sub.3,2 =9.5 H.sub.2, 1H, H-2) and 3.32 (dd, J.sub.5,4 =J.sub.3,4 =9.5 H.sub.2, 1H, H-4) ppm; .sup.19 F NMR (D.sub.2 O+CF.sub.3 COOH)-.delta.1.60 (t, J.sub.H,F =8.9 Hz, CF.sub.3); .sup.13 C NMR (D.sub.2 O) .delta.124.56 (q, J.sub.F,C =277.2 Hz, CF.sub.3), 99.56 (C-1), 73.36 (C-3), 72.96 (C-5), 71.75 (C-2), 70.00 (C-4), 65.08 (q, J.sub.F,C =34.9 Hz, CH.sub.2 CF.sub.3) ppm; anal calcd. for C.sub.56 H.sub.77 O.sub.42 F.sub.21 91/2 H.sub.2 O (1880.2); C, 35.70; H, 5,14; found; C, 35.67; H, 4.85%

B. Because of limited steric access and the need to maintain free 1.degree. and 2.degree. hydroxyls at C-6 and C-2 respectively, a modification of the synthetic process is required for heptakis (3-fluoro-3-deoxy)-.beta.-cyclodexrin (3-F.beta.CD). Two alternate synthetic processes follow.

1. Direct fluorination of 3-OH Group

This involves replacement of free-OH group at C-3 of .beta.-CD using strong fluorinating reagents such as diethylaminosulfur trifluoride (DAST) (reference 28) or antimony pentafluoride (SbF.sub.5) (reference 29). Anhydrous 2,6-disubstituted .beta.-CD is dissolved in an optimum quantity of anhydrous aprotic solvent and this solution is added to a precooled solution of DAST or SbF.sub.5. The progress of the reaction is monitored on analytical TLC plates. This 2,6-disubstituted-3-F-intermediate, obtained after usual purification procedures is subjected to deprotection (reference 30) to obtain 3-F.beta.CD.

2. Replacement of a Protective Group

This technique involves the synthesis of 2,6-disubstituted-3-O-methane sulfonyl (or trifluoromethane-sulfonyl)-.beta.-CD, followed by its replacement with fluoride ion. 2,6-Disubstituted-3-O-methane sulfonyl (trifluoromethane sulfonyl)-.beta.-CD is reacted with fluoride to yield 2,6-Disubstituted-3-fluoro-.beta.-CD which on deprotection yields the desired 3-fluoro-.beta.-cyclodextrin (3-F.beta.CD).

Example 2

6-F.sub.3 .beta.CD/Trifluridine Inclusion Complex

This inclusion complex was prepared by a modification of the kneading method of Shimada et al. (reference 34). Trifluridine or trifluoromethyl-2'-deoxyuridine is an antiviral nucleoside.

Equimolar amounts of trifluridine (8.65 mg) and 6-F.sub.3 .beta.CD (50 mg) were kneaded in a mechanical ball mill, together with a small amount of water. After 10 minutes, the resulting paste was diluted with 5 volumes of water, filtered through a 0.45.mu. Millipore filter and then lyophilized (reference 34). The resulting residue was very hydroscopic and required storage in a dry chamber.

Formation of the complex was confirmed by Differential Scanning Calorimetry (DSC) analysis. DSC was performed on the inclusion complex on an aluminum pad with lid, using a chamber gas purge (N.sub.2 ; 20 Ml min.sup.1); the temperature was raised at a rate of 5.degree. C. min.sup.-1. Trifluridine, 6-F.sub.3 .beta.CD and a physical mixture (not a complex) of the two were analyzed as well, using identical conditions. DCS data are shown in Table 1 and confirm the formation of an inclusion complex.

In addition, infrared spectra were recorded for three of the materials, trifluridine, 6-F.sub.3 .beta.CD and their inclusion complex, and .sup.19 F MRS studies were performed. The IR Spectra are shown in FIGS. 10 to 13. The results of the .sup.19 F MRS studies are shown in Table 2.

As will be understood by those skilled in the art, this procedure may be employed to form inclusion complexes of 6-F.sub.3 .beta.CD with a variety of drugs, including trifluridine, flurbiprofen and flutamide.

TABLE 1______________________________________DSC data for 6-F.sub.3 .beta.-CD, trifluridine and the6-F.sub.3 .beta.-CD/trifluridine inclusion complexCOMPOUND mmmH (J/g) Temperature .degree.C.______________________________________6-F.sub.3 .beta.CD 81.92 123.32trifluridine -105.30 190.90 +50.55 203.60inclusion +30.21 60.58 -39.53 87.71 -17.19 131.04______________________________________ TABLE 2______________________________________.sup.19 F NMR Chemical Shifts of 6-F.sub.3 .beta.-CD and their inclusionComplexes DEUTERATEDCOMPOUND .sup.19 F NMR SOLVENT______________________________________6-F.sub.3 .beta.CD 2.07 (triplet) CD.sub.3 OD (FIG. 1)Trifluoridine 12.17 (singlet) D.sub.2 O(F.sub.3 TdR)inclusion complex F.sub.3 TdR 12.17 (singlet) D.sub.2 Oof F.sub.3 TdR with 6-F.sub.3 .beta.CD 1.60 (triplet)6-F.sub.3 .beta.CDFlutamide 15.86 (singlet) CD.sub.3 OD (FIG. 2)inclusion complex Flutamide 15.79 CD.sub.3 OD (FIG. 3)of Flutamide with (singlet)6-F.sub.3 .beta.CD 6-F.sub.3 .beta.CD 2.05 (triplet)Flurbiprotein -42.53 (triplet) CD.sub.3 OD (FIG. 4)inclusion complex Fluribiprotein -42.61 CD.sub.3 OD (FIG. 5)of Flurbiprotein (triplet)6-F.sub.3 .beta.CD 6-F.sub.3 .beta.CD 2.05 (triplet)______________________________________ All the chemical shifts are in comparison with sodium trifluoroacetic aci (TFA) used as internal standard.

As will be understood by those skilled in the art, the same process may be employed to prepare inclusion complexes of 3-F.beta.CD.

Example 3

Synthesis of Heptakis (6-Fluoro-6-Deoxy)-.beta.-Cyclodextrin (6-F.beta.CD)

A.1. Direct fluorination of 6-OH group

This involves reaction of free OH group using strong fluorinating agents such as diethylaminosulfur trifluoride (DAST) (reference 28), antimony pentafluoride (SbF.sub.5) (reference 29) or hydrogen fluoride (reference 36). In a typical reaction, .beta.-CD is taken in an appropriate solvent and treated with the fluorinating agent in an appropriate reaction vessel. The reaction conditions vary with the nature of fluorinating reagent. The crude reaction mixture is subjected to column chromatography to obtain the pure product.

A.2. Replacement of a protective/halo group at C-6

This involves the substitution of heptakis 6-O-alkyl/aryl sulfonyl .beta.-CD (references 37,38) or of a heptakis (6-halo-6-deoxy)-.beta.-CD (references 39,40) with a) metal fluorides (AgF, AgF.sub.2, KF etc.) or b) DAST or c) HF/dioxane.

B. Synthesis of heptakis (3-fluoro-3-deoxy)-.beta.-cyclodextrin (3-F.beta.CD) and heptakis (2-fluoro-2-deoxy)-.beta.-cyclodextrin (2-F.beta.CD) B.1. Replacement of a protective group

This involves substitution of a protective group at C-3 (to obtain 3-F.beta.-CD) (reference 41) with a proper fluorinating agent as described in section A.1.

B.2. Opening of an epoxy linkage between C-2 and C-3 of .beta.-CD

This involves the reaction of heptakis (2,3-epoxy)-.beta.cyclodextrin (reference 42) with a desired fluorinating agent. The fluorinating agents include AgF.sub.2, borontrifluoride etherate and hydrogen fluoride. The reaction is done in an appropriate anhydrous solvent. This reaction gives a mixture of fluorinated cyclodextrins which is purified on an alumina column.

B.3. Reaction of free OH group at C-2

This involves reaction of Per 3,6-anhydro-.beta.-CD (reference 43) with a fluorinating agent either directly or via formation of heptakis (2-halo-3,6-anhydro)-.beta.-CD (reference 44) followed by opening of anhydro linkage by alkaline hydrolysis to yield heptakis 2-(fluoro-2-deoxy)-.beta.-cyclodextrin.

Example 4

Biodistribution Studies

6-F.sub.3 .beta.CD (90 mg/ml in water) was administered to a BALB/C mouse by intravenous injection through the tail vein, at a dose of 13.5 mg 6-F.sub.3 .beta.CD per mouse. The mouse was placed in a beaker layered with filter paper to absorb the urine excreted during the experiment. 15 minutes after administration of the drug complex, blood was collected by cardiac puncture, the mouse was sacrificed by euthanasia in dry ice and the desired organs were collected by dissection. All samples were immediately frozen and held frozen until NMR studies.

The biodistribution of 6-F.sub.3 .beta.CD at 15 minutes after a single intravenous dose is shown in Table 3.

TABLE 3______________________________________ Organ % Dose______________________________________ liver 4.09 kidney 1.87 intestine 0.72 tail 2.14 blood 62.59 urine 40.96______________________________________

After intravenous injection of 6-F.sub.3 .beta.CD, metabolic degradation over the first fifteen minutes accounts for far less than 5% of the administered dose.

FIGS. 1, 2 and 3 show .sup.19 F NMR spectrum of mouse intact liver, blood and urine respectively at 15 minutes after intravenous administration of 6-F.sub.3 .beta.CD.

Example 5

6-F.sub.3 .beta.CD/Flutamide Inclusion Complex

An inclusion complex of 6-F.sub.3 .beta.CD and flutamide, a non-steroidal fluorine-containing nitrophenyl propamide used for its anti-androgen effects in prostate cancer chemotherapy, was prepared as described in Example 2.

.sup.19 F MRS studies were performed. The results are shown in FIGS. 4, 5 and 6 and in Table 2.

Example 6

6-F.sub.3 .beta.CD Flurbiprofen Complex

An inclusion complex of 6-F.sub.3 .beta.CD and flurbiprofen, a propionic acid-based, fluorine-containing, non-steroidal anti-inflammatory drug, was prepared as described in Example 2.

.sup.19 F MRS studies were performed and the results are shown in FIGS. 7, 8 and 9 and Table 2.

References

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Claims

1. A cyclic oligosaccharide compound wherein the saccharide monomers are in pyranoside form, said compound comprising at least two fluorine atoms, each attached to said cyclic oligosaccharide or to a substituent such that no greater than three atoms are positioned between said fluorine atom and said cyclic structure.

2. A compound as recited in claim 1, wherein said cyclic oligosaccharide is a cyclodextrin.

3. A compound as recited in claim 2, wherein said cyclodextrin is selected from the group consisting of .alpha.-CD, .beta.-CD and .gamma.-CD.

4. A compound as recited in claim 2, selected from the group consisting of:

heptakis-6-fluoro-6-deoxy-.beta.-cyclodextrin,

heptakis-3-fluoro-3-deoxy-.beta.-cyclodextrin,

heptakis-6-fluoro-3-deoxy-.beta.-cycloaltrin,

6-monotrifluoroethylthio-6-deoxy-.beta.-cyclodextrin, and

heptakis-trifluoroethyl-.beta.-cyclodextrin.

5. A compound as recited in claim 2, selected from the group consisting of:

(a) compounds having the formula: ##STR7## wherein (i) R.dbd.R.sup.1 .dbd.F;

(ii) R.dbd.CH.sub.2 F, one or more R.sup.1 .dbd.CH.sub.2 OH, the remaining R.sup.1 .dbd.CH.sub.2 F; i.e. for .beta.-CD, R.sup.1 =x CH.sub.2 OH, (6-x) CH.sub.2 F, x=0-6;

(iii) R.dbd.CH.sub.2 F, one or more R.sup.1 .dbd.CO.sub.2 H, the remaining R.sup.1 .dbd.CH.sub.2 F; i.e. for .beta.-CD, R.sup.1 =x CO.sub.2 H, (6-x) CH.sub.2 F, x=0-6;

(iv) R.dbd.CH.sub.2 F, one or more R.sup.1 .dbd.CH.sub.2 R.sup.2 (where R.sup.2 .dbd.NH.sub.2 or N.sub.3), the remaining R.sup.1 .dbd.CH.sub.2 F; i.e. for .beta.-CD, R.sup.1 =x CH.sub.2 R.sup.2 (where R.sup.2 .dbd.NH.sub.2 or N.sub.3), (6-x) CH.sub.2 F, x=0-6;

(v) R.dbd.CH.sub.2 F, one or more R.sup.1 .dbd.CH.sub.2 OR.sup.2 (where R.sup.2 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), the remaining R.sup.1 .dbd.CH.sub.2 F; i.e. for .beta.-CD, R.sup.1 =x CH.sub.2 OR.sup.2 (where R.sup.2 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), (6-x) CH.sub.2 F, x=0-6;

(vi) R is CH.sub.2 OCH.sub.2 CF.sub.3, or CH.sub.2 NHC.sub.6 H.sub.4 F, or other moieties which contain fluorine, each R.sup.1 each R.sup.1 equals F, CH.sub.2 OH, CH.sub.2 F, CH.sub.2 R.sup.2 or CH.sub.2 OR.sup.2 (where R.sup.2 is as defined above);

(b) compounds having the formula: ##STR8## wherein: (i) R.dbd.CH.sub.2 OH, R.sup.1 .dbd.F, R.sup.2 .dbd.OH, R.sup.3 .dbd.H;

(ii) R.sup.1 .dbd.F, R.sup.2 .dbd.OH, R.sup.3 .dbd.H, at least one R.dbd.CO.sub.2 H, the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CO.sub.2 H, (7-x) CH.sub.2 OH, x=0-7;

(iii) R.sup.1 .dbd.F, R.sup.2 .dbd.OH, R.sup.3 .dbd.H, at least one R.dbd.CH.sub.2 R.sup.4 (where R.sup.4 .dbd.NH.sub.2 or N.sub.3), the remaining R.dbd.CH.sub.2 OH, i.e. for .beta.-CD, R=x CH.sub.2 R.sup.4 (where R.sup.4 .dbd.NH.sub.2 or N.sub.3), (7-x) CH.sub.2 OH, x=0-7;

(iv) R.sup.1 .dbd.F, R.sup.2 .dbd.OH, R.sup.3 .dbd.H, at least one R.dbd.CH.sub.2 R.sup.5 (where R.sup.5 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CH.sub.2 R.sup.5 (where R.sup.5 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), (7-x) CH.sub.2 OH, x=0-7;

(v) R.dbd.CH.sub.2 OH, R.sup.1 .dbd.F, R.sup.2 .dbd.H, R.sup.3 .dbd.OH;

(vi) R.sup.1 .dbd.F, R.sup.2 .dbd.H, R.sup.3 .dbd.OH, at least one R.dbd.CO.sub.2 H, the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CO.sub.2 H, (7-x) CH.sub.2 OH, x=0-7;

(vii) R.sup.1 .dbd.F, R.sup.2 .dbd.H, R.sup.3 .dbd.OH, at least one R.dbd.CH.sub.2 R.sup.4 (where R.sup.4 .dbd.NH.sub.2 or N.sub.3), the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CH.sub.2 R.sup.4 (where R.sup.4 .dbd.NH.sub.2 or N.sub.3), (7-x) CH.sub.2 OH, x=0-7;

(viii) R.sup.1 .dbd.F, R.sup.2 .dbd.H, R.sup.3 .dbd.OH, at least one R.dbd.CH.sub.2 OR.sup.5 (where R.sup.5 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), the remaining R.dbd.CH.sub.2 OH; i.e. for .beta.-CD, R=x CH.sub.2 OR.sup.5 (where R.sup.5 =sugar moiety i.e. Glc, GlcNAc, Gal, GalNAc, Fuc, Neu5Ac, or other suitable sugar moieties), (7-x) CH.sub.2 OH, x=0-7;

(c) compounds having the formula: ##STR9## wherein: (i) R.dbd.OH, R.sup.1 .dbd.H;

(ii) R.dbd.H, R.sup.1 .dbd.OH.

6. A complex comprising a fluorine-containing cyclic oligosaccharide as recited in claim 1 and a drug.

7. A complex as recited in claim 6, wherein said drug is selected from the group consisting of mitoxantrone, taxol, progesterone, testosterone, ibuprofen, hydrocortisone, digitoxin, digoxin, diazepam, and peptides, fluorinated analogs of mitoxantrone, taxol, progesterone, testosterone, ibuprofen, hydrocortisone, digitoxin, digoxin, diazepam, and peptides, fluorinated amino acids and peptides, F.sub.3 TDR, fluorouracil and fluorinated pyridoxyl analogs.

8. A complex as recited in claim 6, wherein said cyclic oligosaccharide is a cyclodextrin.

9. A pharmaceutical composition comprising complex as recited in claim 6 together with a suitable complex carrier or excipient.

10. A process of making a fluorine-containing oligosaccharide compound of claim 1 wherein the saccharide monomers are in pyranoside form, comprising reacting a fluorine containing compound with a cyclic oligosaccharide to form said fluorine-containing oligosaccharide compound, said fluorine atom thereby becoming attached to said cyclic oligosaccharide or to a substituent such that no greater than three atoms are positions between said fluorine atom and said cyclic oligosaccharide.

11. A process as recited in claim 10, wherein said cyclic oligosaccharide is a cyclodextrin.

12. A process as recited in claim 10, wherein said process comprises at least one process step selected from the group consisting of: ##STR10## ##STR11## ##STR12## ##STR13## (5) reacting .beta.-CD with 2,2,2-trifluoroethanol; (6) reacting .beta.-CD with diethylaminosulfur trifluoride;

(7) reacting .beta.-CD with antimony pentafluoride;

(8) reacting cyclodextrin with hydrogen fluoride;

(9) reacting cyclodextrin with a metal fluoride selected from the group consisting of AgF, AgF.sub.2 and KF;

(10) reacting cyclodextrin with BF.sub.3 etherate.

13. A process for making a complex comprising a fluorine-containing cyclic oligosaccharide as recited in claim 1 and a drug, the process comprising mixing a fluorine-containing oligosaccharide as recited in claim 1 with a drug.

14. A process as recited in claim 13, wherein said cyclic oligosaccharide is a cyclodextrin.

15. A process for providing site specific delivery of a drug to a patient, comprising administering to a patient in need of treatment with said drug a complex as recited in claim 6.

16. A process as recited in claim 15, wherein said cyclic oligosaccharide is a cyclodextrin.

17. A process for analyzing in vivo the location and time of drug release from a complex as recited in claim 6, said process comprising administering said complex to a patient and performing .sup.19 F MRS on said patient.

18. A process for analyzing in vivo activity of a drug, said process comprising administering to a patient a complex as recited in claim 6, and performing .sup.19 F MRS on said patient.

19. A method for determining the location of tumor in a patient using .sup.19 F MRI comprising administering a complex as recited in claim 6.

20. A method of analyzing tissue extracted from a living being comprising treating said tissue with a complex as recited in claim 6 and subsequently analyzing said tissue using .sup.19 F MRS.

21. A complex comprising the cyclic oligosaccharide compound of claim 1 and at least one additional compound selected from the group consisting of an amino acid, a peptide and a carbohydrate antigen.

22. A complex comprising a fluorine-containing cyclic oligosaccharide compound as recited in claim 2 and a drug.

23. A complex comprising a fluorine-containing cyclic oligosaccharide compound as recited in claim 3 and a drug.

24. A complex comprising a fluorine-containing cyclic oligosaccharide compound as recited in claim 4 and a drug.

25. A complex comprising a fluorine-containing cyclic oligosaccharide compound as recited in claim 5 and a drug.