Patent Application
20210402011
The present invention relates to a novel compound for detecting HNO in biological systems. More particularly, the present invention relates to a compound of formula (I), process for preparation thereof and use of compound of formula (I) for detecting HNO in biological systems. The present invention further relates to a kit comprising compound of formula (I).
Nitroxyl (HNO) is an elusive chemical species that has been shown to possess intriguing biological properties. For example, nitroxyl has been implicated in the mechanism of cyanamide's inhibitory effect on aldehyde dehydrogenase in treating alcohol abuse as well as reversing experimental heart failure.
Despite HNO having been described in the chemical literature for decades, there are surprising gaps in the literature that complicate the rational exploitation of its pharmacological properties. A number of studies have suggested that it may confer important biological functions in various physiological processes. For example, HNO also known to interact with bio-thiols in aldehyde dehydrogenase, leading to the inhibition of the enzyme's activity. HNO could mediate relaxation of resistant-like arteries by activating voltage-dependent K+ channel. Also, nitroxyl (HNO) is involved in the regulating cardiovascular functions and may provide useful tools for treating cardiovascular diseases such as heart failure. The role of HNO in different biological processes still remains largely unknown.
HNO is a new candidate heart failure drug therapy, has been shown to enhance overall cardiovascular function in both healthy and failing hearts, at least in part, by increasing Ca2+ re-uptake into the CSR and SERCA2a, that regulates intracellular Ca2+—handling and thus plays a critical role in initiating cardiac contraction and relaxation. HNO can increase systolic force and decrease diastolic pressure in both normal and failing canine hearts through upregulating the calcitonin gene-related peptide. Thus, more and more observations suggest that HNO may provide a powerful therapeutic agent for heart failure cure.
Several methodologies based on various analytical techniques (e.g., colorimetric methods, EPR, HPLC, mass spectrometry and electrochemical analysis) for the detection of HNO are available in the literature. Such methodologies are either time-consuming or involve the destruction of cells and tissues and are thus not ideally suited to in vivo tracking and detection of HNO. In this context, reagents that show fluorescence ON response on detection of HNO are used as an imaging reagent as well as for studying biospecies in living samples. Such reagents also allow high sensitivity and spatiotemporal resolution. Among the various reagents that show such a response, phosphine-based reagents have received considerable attention. King and co-workers were first to report the reaction of HNO with organic phosphines to produce the corresponding phosphine oxide and azaylide [J. Am. Chem. Soc., 2011, 133 (30), pp 11675-11685]. Since then, chemodosimetric probe molecules have been exploited in this reaction for specific detection of HNO using fluorophores like rhodamine, coumarine, napthalimide, and BODIPY. This reaction has also been exploited in developing FRET-based receptors for HNO. Most of these receptors show a luminescence response within the visible region of the spectrum.
Article titled “Development of green to near-infrared turn-on fluorescent probes for the multicolour imaging of nitroxyl in living systems” by B Dong published in J. Mater. Chem. B, 2016, 4, 1263-1269 reports three novel turn-on probes (NP-1-3) based on structurally related dyes with different emission colors as fluorescent scaffolds for detecting HNO in biological systems. The probes exhibit high sensitivity, excellent selectivity, desirable performance at physiological pH and low cytotoxicity.
Article titled “A fluorescent probe for specific detection of cysteine in the lipid dense region of cells” by Firoj Ali et al. published in Chem. Commun., 2015, 51, 16932-16935 reports a new cysteine (Cys) specific chemodosimetric reagent (ER-F) is used in imaging of endogenous Cys localized in the lipid dense region of the live Hct116 cells and the release of Cys within HepG2 cells from a drug following a biochemical transformation.
Article titled “A Near-Infrared Fluorescent Probe for Detection of Nitroxyl in Living Cells” by LIU Ping et al. published in Chinese Journal of Analytical Chemistry; 2015, 43 (12), pp 1829-1836 reports a near-infrared (NIR) metal-free fluorescent probe, ER-JN, designed and synthesized for the detection of intracellular HNO level in simulated physiological conditions and living cells. The as-prepared probe exhibited high sensitivity, good selectivity and low cytotoxicity and applied to fluorescent bio-imaging of HNO in simulated physiological conditions. When used in detection of HNO, quantum yield of the probe increased from 0.01 to 0.35. The linear range was 0.50 μM, with the detection limit of 0.03 μM (S/N=3).
Article titled “Resorufin based fluorescence ‘turn-on’ chemodosimeter probe for nitroxyl (HNO)” by K N Bobba et al. published in RSC Adv., 2015, 5, 84543-84546 reports a cellular responsive, highly selective fluorogenic and chromogenic chemodosimeter probe for HNO. This new probe showed ˜30 fold fluorescence enhancement in the presence of HNO and is sensitive to HNO at concentrations as low as 0.02 μM. Further, it is capable of detecting HNO levels in cellular milieus as well as in live specimens e.g. C. elegans.
Article titled “A near-infrared fluorescent probe for the selective detection of HNO in living cells and in vivo” by P Liu et al. published in Analyst, 2015, 140, pp 4576-4583 reports a near-infrared (NIR) metal-free fluorescent probe Cyto-JN for the detection of nitroxyl (HNO) in living cells and in vivo. The metal-free Cyto-JN is composed of two moieties: the Aza-BODIPY fluorophore and the HNO recognition unit, the diphenylphosphinobenzoyl group. Cyto-JN can react with HNO in a 1:1 stoichiometry, which may bring great benefit to the detection efficiency of bioassays.
Article titled “A highly sensitive and reductant-resistant fluorescent probe for nitroxyl in aqueous solution and serum” by G J Mao et al. published in Chem. Commun., 2014, 50, 5790-5792 reports a novel coumarin-based fluorescent probe, P-CM, for quantitative detection of nitroxyl (HNO). P-CM exhibits a selective response to HNO over other biological reductants and was also applied for quantitative detection of HNO in bovine serum with satisfactory results.
Article titled “A two-photon fluorescent turn-on probe for nitroxyl (HNO) and its bioimaging application in living tissues” by K Zheng et al. published in Chem. Commun., 2015, 51, 5754-5757 reports synthesis of two-photon fluorescent probe for specific detection of nitroxyl. They have demonstrated that the probe GCTPOC-1 is suitable for fluorescence imaging of HNO not only in living cells, but also in living tissues using two-photon fluorescence microscopy. The phosphine-based derivative for two-photon imaging of exogenous HNO in HeLa cells following excitation at 780 nm (λMon=512 nm). Despite such efforts, examples of probes for the targeted detection/scavenging of HNO in specific organelles are rather uncommon, and thus, there is ample scope for the development of such reagents. Despite its many attractions, one of the drawbacks of employing optical microscopy is that it has a practical resolution limit of around 250 nm.
Luminescence-based methods are popular and powerful tool for detecting biologically active species in living cells due to its simplicity, excellent sensitivity, and well-defined spatiotemporal resolutions. The HNO fluorescent probes developed in previous studies were mostly based on the reduction of (1) Cu(II) to Cu(I), or (2) nitroxide to hydroxylamine using HNO. These probes were shown to be capable of detecting HNO in living cells. However, it was also noted that the probes might be interfered by other biologically abundant reductants in the living cells, such as glutathione and ascorbate. Furthermore, example of a reagent that could be used for monitoring of intracellular SERCA2a activity has eluded till date. Such a reagent would have a direct relevance for developing an efficient imaging reagent for HNO and as well as inhabiting SERCA2a activity induced by HNO, which would have serious implication in clinical diagnostic field.
Therefore, there is a need to design an appropriate reagent for detection and quantification of HNO under physiological as well as in biological samples for diagnostic application has significance. Accordingly, the present invention provides a compound which allow for sensitive and selective detection of HNO.
The main objective of the present invention is to provide a novel compound of formula (I).
Another objective of the present invention is to provide a process for the preparation of compound of formula (I).
Yet another objective of the present invention is to provide use of compound of formula (I) for the detection of HNO in biological systems.
Still another objective of the present invention is to provide a kit for the detection of HNO comprising at least compound of formula (I).
Accordingly, the present invention provides a compound of formula (I);
In another embodiment, the present invention provides a process for the preparation of compound of formula (I) comprising the steps of:
In preferred embodiment, said solvent is dichloromethane (CH2Cl2).
In another preferred embodiment, said process is carried out under nitrogen atmosphere.
In yet another embodiment, the present invention provides use of compound of formula (I) for the detection of UNO in biological systems.
In another embodiment, the present invention provides a fluorescent OFF-ON based molecular probe ER-HNO for the specific detection of HNO under physiological condition with excellent sensitivity.
In preferred embodiment, the compound of formula (I) is used as imaging reagent for HNO detection in live HCT116 cells or RAW 264.7 cells.
In one embodiment, the present invention provides a method of detection of HNO in biological systems using compound of formula (I).
In still another embodiment, the present invention provides a kit for the detection of HNO comprising at least compound of formula (I).
The invention will now be described in detail in connection with certain preferred and optional embodiments, so that various aspects thereof may be more fully understood and appreciated.
The terms “compound of formula (I)”, “ER-HNO”, “ER-HNO” and “Probe ER-HNO” are used interchangeably in the specification; however they have the same meaning.
In the view of above, the present invention provides a compound of formula (I);
The IUPAC name of compound of formula (I) is (E)-4-(2-(5,5-difluoro-1,7,9-trimethyl-10-phenyl-5H-5l4,6l4-dipyrrolo[1,2-c:2′,1′-f][1,3,2]diazaborinin-3-yl)vinyl)phenyl 2-(diphenylphosphanyl)benzoate.
In another embodiment, the present invention provides a process for preparation of compound of formula (I) comprising the steps of:
In preferred embodiment, said solvent is dichloromethane (CH2Cl2).
In another preferred embodiment, said process is carried out under nitrogen atmosphere.
The process for the preparation of probe ER-HNO is as shown scheme 1;
In yet another embodiment, the present invention provides use of compound of formula (I) for the detection of HNO in biological systems.
In preferred embodiment, the present invention provides a fluorescent OFF-ON based molecular probe ER-HNO for the specific detection of HNO under physiological condition with excellent sensitivity.
In another preferred embodiment, the present invention provides use of compound of formula (I) as imaging reagent for HNO detection in live HCT116 cells or RAW 264.7 cells.
The compound of formula (I) exhibits high selectivity, good sensitivity and low cytotoxicity in the detection of HNO. Besides, the compound of formula (I) shows perfect endoplasmic localization in living cells. It is observed that the compound of formula (I) can detect HNO without interference from other analytes.
In one embodiment, the present invention provides a method of detection of HNO in biological systems using compound of formula (I).
The spectroscopic properties of ER-HNO in aq. PBS buffer medium under physiological pH medium. No significant difference is observed in the electronic spectra of ER-HNO and ER-S. In order to check the response of ER-HNO probe (10 uM) with in presence of 20 mole equivalent of various ROS and RNS (HNO, HOCl, H2O2, —OH, TBHP, NO3−, NO2−, benzoyl peroxide, S2− and ascorbate) emission spectra are recorded in aq. PBS buffer medium are shown in
The probe ER-HNO itself shows a weak emission spectrum (Φ=0.002, for λExt=530 nm) in aq-PBS buffer medium. An enhancement in emission signal are observed at λMax=586 nm (Φ=0.105, for λExt=530 nm) with gradual increasing [HNO] (
The interferences studies also confirmed the emission response of ER-HNO in presence of HNO, remain unchanged even in presence of excess amount of other analytes, used for the studies (
An MTT assay confirmed the non-toxic nature of probe ER-HNO towards live Hct116. Therefore, ER-HNO is tested as an imaging reagent for the detection of HNO in Hct116 colon cancer. The cells are incubated with probe ER-HNO (1 μM) for 15 min at 37° C. in acetonitrile-PBS buffer (0.2:99.8, v/v) at pH 7.2 and no intracellular fluorescence is observed. CLSM images for cells that are further incubated with HNO (20 μM) showed a strong intracellular fluorescence (
From CLSM images as shown in
The SERCA2 is monitored using ER-HNO using Western blot experiment. The
The toxicity of the probe molecule toward live RAW 264.7 macrophages cells and cytotoxicity assays confirmed the low toxicity of the probe. The results encouraged to explore the use of the probe as an imaging reagent for the intracellular detection of HNO in these macrophage cells. Cells in DMEM culture media are incubated with ER-HNO (1.0 μM) for 15 min at 37° C. and subsequently viewed under confocal laser scanning microscope (CLSM) using a 530 nm laser as an excitation source. No intracellular fluorescence is observed until these pretreated cells are also exposed to AS, then a strong intracellular fluorescence was observed under CLSM (
As for the CLSM experiments, RAW macrophage cells incubated with ER-HNO (1 μM) for 15 min at 37° C. in acetonitrile-PBS buffer (0.2:99.8, v/v) at pH 7.2 displayed no intracellular fluorescence. In contrast, cells incubated with ER-HNO (1 μM) and then treated with Angeli's salt (Na2N2O3) for 30 min, showed strong intracellular fluorescence (
In still another embodiment, the present invention provides a kit for the detection of HNO comprising at least compound of formula (I).
The following examples, which include preferred embodiments, will serve to illustrate the practice of this invention, it is being understood that the particulars shown are by way of example and for purpose of illustrative discussion of preferred embodiments of the invention.
Examples Following examples are given by way of illustration therefore should not be construed to limit the scope of the invention.
Under N2 atmosphere, to a solution of 2-(diphenylphosphino) benzoic acid (100 mg, 0.32 mmol) in dry CH2Cl2, DCC (80 mg, 0.39 mmol) was added and stirred at 0° C. for 2 hr. To this, Compound ER-S (150 mg, 0.35 mmol) and DMAP (20 mg, 0.16 mmol) were added and it was stirred at 27° C. for 6 hr. Reaction was monitored by TLC. Then the mixture was concentrated under vacuum, and the crude product was purified by silica gel column chromatography by using 5% ethyl acetate in PET ether medium to give the compound ER-HNO. Yield 38%. 1H NMR (CDCl3, 400 MHz, 5 ppm): 7.73 (2H, d, J 6.7), 7.68 (5H, dd, J 12.4, 7.4), 7.63 (2H, d, J 5.4), 7.56 (3H, d, J 8.5), 7.51 (5H, t, J 8.6), 7.47 (5H, d, J 5.6), 7.32 (2H, J 4.9), 7.19 (1H, d, J 16.3), 6.92 (1H, d, J 8.3), 6.60 (1H, s), 6.03 (1H, s), 2.62 (3H, s), 1.44 (3H, s), 1.41 (3H, s). 13C NMR (CDCl3, 125 MHz): 190.99, 164.54, 155.27, 155.06, 153.99, 153.80, 142.51, 141.53, 137.30, 134.76, 134.53, 134.15, 133.94, 133.68, 133.48, 133.16, 132.88, 132.35, 131.94, 131.85, 131.75, 131.44, 131.11, 130.98, 128.91, 128.67, 128.60, 128.48, 128.41, 122.42, 116.15, 25.98.
Stock solution of probe ER-HNO (1×10−4M) was prepared in HPLC grade acetonitrile. All the analytes stock solution (1×10−2M) was prepared in aqueous HEPES buffer (10 mM) medium at pH 7.2. 500 μL of this stock solution of probe ER-HNO was added to 4.5 ml of PBS (10 mM) aqueous buffer medium having solution pH 7.2 to make the effective ER-HNO concentration of (1×10−5) M. This solution was used for all the photophysical studies. All the photophysical studies were performed in aq. PBS: CH3CN medium (9:1, v/v) at pH7.2. All emission studies were done using λExt=530 nm with an emission slit width of 2/2 nm, unless and otherwise mentioned.
For confocal studies, Hct116 cells (3×105) were seeded on cover slips placed in 6 well plates. After 24 hours, Hct116 cells were treated with ER-HNO (1 μM) for 30 minutes at 37° C. in a 5% CO2 air environment. Cells were then washed thrice with Phosphate Buffer (1×PBS) and fixed with 4% PFA for 20 minutes and washed again with IX PBS. Nail paint was used to seal the cover slips mounted on the glass slides for each well plates. Again Hct116 cells were pre-treated with ER-HNO (1 μM) for 15 minutes, then Hct116 cells were further expose to Angeli's salt (HNO donor), then cells were washed thrice with media and followed by incubation with ER-HNO (1 μM) for another 15 minutes under same conditions. Cells were again washed with 1×PBS buffer and fixed with 4% PFA for 20 minutes and washed again with 1×PBS. Confocal laser scanning microscopic (CLSM) images were acquired in Olympus Fluoview Microscope with λExt/λMon=530/573 nm.
RAW 264.7 cells were seeded on cover slips placed in 6 well plates. After 24 hours cells washed with DMEM medium then cells were treated with ER-HNO (1 μM) for 25 minutes. Cells were then washed thrice with culture medium and further treated with Angeli's salt (HNO donor) of different concentration for 30 min. After that cells were washed again with Phosphate Buffer Saline (3×PBS). Then cells were fixed with 4% PFA for 10 min. Again cells were washed thrice and then cover slips mounted using mounting medium. Nail paints was used to seal the coverslips mounted on the glass slides. Images were acquired by using Olympus FluoView FV-1000 Confocal Microscope.
HCT116 cells were cultured in DMEM medium containing 10% Fetal Bovine Serum (FBS) supplemented with 100 Units of Penicillin Streptomycin antibiotics. Cells were treated with Angeli's salt 10 uM, ER-HNO 30 μM or both for 24 hrs. Prior to the treatment processes, DMEM medium was treated with N-Ethylmalemide (NEM) 1 mM and this medium was used to culture the cells. Post 24 hrs cells harvested and whole cell lysate proteins extracted. 40 ug of the proteins were resolved in SDS PAGE gel and transferred into PVDF membrane using Western Blot methods. The blot was over-night blocked with 5% Bovine Serum Albumin (BSA) at 4° C. 1:4000 dilution of SERCA2 antibody was to probe the blot for 2 hrs at room-temperature (RT). After three washes with 1×TBST, 1:4000 dilution of anti-rabbit HRP conjugated antibody was used to probe the blot for 1 hr at RT. After three washes with IX TBST, the blot was developed using auto-radiography in X-ray film.
For DCFDA staining, HCT116 cells were cultured in DMEM medium containing 5 mM glucose supplemented with 10% FBS and 100 Units of antibiotics. Prior to the treatment processes, DMEM medium with 1% FBS was treated with N-Ethylmalemide (NEM) 1 mM and this medium was used to culture the cells further. Cells were treated with Angeli's salt 10 uM, L 30 uM or both for 2 hrs. After treatment cells were harvested by trypsinization and washed with complete DMEM media by centrifugation. Pellet was suspended in 1 ml of PBS buffer. 10 μM DCFDA (Sigma) was added to cells followed by incubation at 37° C. 5% CO2 incubator for 45 mins. DCFDA stained cells were analyzed in BD FACS Canto II using FITC channel. For Annexin V staining cultured HCT116 cells were harvested after trypsinization and washed with 1×PBS buffer. 500 ul of Annexin V binding buffer was used to re-suspend the cells. 5 ul of Annexin-V FITC antibody added to the re-suspended cell and incubated in dark for 5 mins. Antibody stained cells were then analyzed using BD Calibur FACs in FITC channel. The flow cytometry experiment confirmed that probe ER-HNO is capable of reducing RNS & ROS level induced by HNO [
RAW 264.7 cells were seeded on Coverslips (22 mm×22 mm, 170±5 μm square Cover glasses) placed in 6-well plates in DMEM culture medium containing (10% FBS and 1% penicillin-streptomycin) for 24 h at 37° C. 5% CO2. After 24 h when 70% confluency was achieved the cells were washed with DMEM culture medium then cells were treated with ER-HNO probe (1 μM) for 30 min. Cells were then washed thrice with culture medium and further treated with different Angeli's salt (AS) for 30 min. Then cells were washed again with phosphate buffer saline (3×PBS). After carrying out the Live cell uptake of the ER-HNO probe and the small molecule, the cells were fixed with 4% PFA for 15 min and then washed thrice with PBS and two times and then the coverslips were mounted using the Mounting medium (Vectashield h-1000). The coverslips were then sealed using nail varnish, and the sample was then imaged. Because SIM relies on the cell morphology, the cells were examined with a light microscope and then imaged using SIM.
The in vitro cytotoxicity of ER-HNO on RAW 264.7 cells were determined by conventional MTT (3-(4, 5-Dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide) assay. RAW 264.7 cells (5×103) were seeded in each well of a 96 well plate and cultured in a 37° C. incubator supplied with 5% CO2. Cells were maintained in DMEM medium, supplemented with 10% Foetal Bovine Serum and 100 Units of Penicillin Streptomycin antibiotics. After 24 hours the cells were treated with different concentrations of the ER-HNO in triplicates for 24 hours. After the treatment, cells were added with 0.5 μg/ml of MTT reagent. The plate was then incubated for 4 hours at 37° C. 100 μl of Isopropyl Alcohol was added to each well. Optical density was measured at 570 nm using Multiskan Go (Thermo Scientific) to find the concentration of the cell inhibition. IC50 value has been calculated to be 90 μM.
The formula used for the calculation of the MTT assay for evaluation of the cell viability was as follows:
Cell viability (%)=(Means of absorbance value of treated group/Means of absorbance value of untreated control)×100.
Imaging of Artemia nauplii by luminescence was performed using a fluorescence microscope with a 20×, 0.4 NA microscope objective (Olympus), coupled to an intensified CCD camera. The Artemia nauplii were imaged in both bright-field and epifluorescence geometries. The latter was enabled by a fluorescence filter set. The illumination intensity was about 10 W/mm2. Artemia nauplii in incubated by ER-HNO (1 μM) for 30 minutes showed no fluorescence, however on exposure to HNO, strong fluorescence was observed by fluorescence microscopy (
| Number | Date | Country | Kind |
|---|---|---|---|
| 201611041925 | Dec 2016 | IN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IN2017/050571 | 12/5/2017 | WO | 00 |
