Patent Application
20050187187
The present invention relates to novel glycosaminoglycans and also to their pharmaceutically acceptable addition salts, and more precisely to carboxyl-reduced and chemoselectively O-sulfated derivatives of chondroitin sulfate, isolated or as a mixture, to the use thereof as a medicinal product and to the pharmaceutical compositions containing them.
Glycoaminoglycans (GAGs) are essentially made up of alternating uronic acid-amino sugar (or vice versa) units of the type such as those encountered in the oligosaccharide or polysaccharide chains of biologically active natural GAGs such as heparin, heparan sulfate, dermatan sulfate, chondroitins, chondroitin sulfates or hyaluronic acid.
The uronic acid units correspond more specially to the D-glucoronic or L-iduronic acid structure and the amino sugar units to the D-galactosamine structure.
The natural GAGs exhibit therapeutic activities as thrombin inhibitors. They therefore exhibit antithrombotic and anticoagulant activity and are used in cardiovascular pathologies in which there is a risk of thrombosis.
Sulfated derivatives of chondroitin sulfate are described for their anticoagulant properties in patent application FR 2584728.
Moreover, O-persulfated derivatives of chondroitin sulfate have been described and studied for their properties in rheumatoid arthritis in international application WO 92/13541-A1.
The applicant has developed a novel process using a carboxyl-reduction step and a sulfatation (sulfating) step for obtaining novel chondroitin sulfate derivatives exhibiting advantageous properties for treating or preventing disorders which display an increased activity of at least one of the matrix metalloproteinases.
The carboxyl-reduced and chemoselectively O-sulfated derivatives of chondroitin sulfate of formula (I) have a very regular polymeric structure with degrees of purity of the order of 90%. Reproducible and unexpected biological properties result therefrom.
In the pathological condition of osteoarthritis, the degradation of aggrecan, the main proteoglycan of cartilage in the joints, represents a very early and crucial event. The pathological loss of aggrecan is caused by proteolytic cleavages in its interglobular domain. Amino acid sequence analyses of the proteoglycan metabolites isolated from the synovial fluid of patients suffering from joint damage, from osteoarthritis or from an inflammatory disorder of the joints, have shown that proteolytic cleavage exists between the amino acids Glu373 and Ala374 in the interglobular domain of human aggrecan (Lohmander, et al., Arthritis Rheum., 36: 1214-1222 (1993)). The proteolytic activity responsible for this cleavage is called “aggrecanase” and can be attributed to the metalloproteinase (MP) or matrix metalloproteinase (MMP) superfamily.
Zinc is an essential element in the catalytically active center of metalloproteinases. MMPs cleave collagen, laminin, proteoglycans, elastin or gelatin under physiological conditions. They therefore play an important role in bone tissue and connective tissue. A large number of different MMP inhibitors are known (see, for example, EP 0 606 046; WO 94/28889). However, the known MMP inhibitors frequently have a significant disadvantage. They lack specificity for any particular class of MMP. On the contrary, most MMP inhibitors simultaneously inhibit a plurality of MMPs.
Consequently, a need exists for MMP inhibitors that have more narrowly defined specificities in order to more effectively treat or prevent specific disorders.
A subject of the invention is most particularly the carboxyl-reduced and sulfated derivatives of chondroitin sulfate of formula (I):
in which R1, R2, R3 and R4, which may be identical or different, represent H or SO3M, it being understood that at least one of the substituents R1, R2, R3 and R4 represents a group SO3M, n is an integer of between 0 and 200, M is an alkali metal, said derivatives being in the form of an isolated compound or in the form of mixtures, and also the diastereoisomers thereof.
In particular, a subject of the invention is the carboxyl-reduced derivatives of chondroitin sulfate according to formula (I), wherein M is chosen from sodium, calcium, magnesium and potassium, and in particular sodium.
Preferably, in formula (I), n is an integer of between 100 and 200.
A subject of the invention is more particularly the carboxyl-reduced derivatives of chondroitin sulfate as described above, wherein R1, R2, R3 and R4 represent SO3Na.
A subject of the invention is more particularly the carboxyl-reduced derivatives of chondroitin sulfate as described above, wherein R1, R2 and R4 represent SO3Na and R3 represents H.
A subject of the invention is more particularly the carboxyl-reduced derivatives of chondroitin sulfate as described above, wherein R1 represents H or SO3Na, R2 represents SO3Na and R3 and R4 represent H.
A subject of the invention is more particularly the carboxyl-reduced derivatives of chondroitin sulfate as described above, wherein R1 represents H or SO3Na, R2 and R3 represent SO3Na and R4 represents H.
These polysaccharides thus comprise an even number of saccharides.
In general, the mixtures of polysaccharides according to the invention can be prepared, firstly, by carboxyl-reduction of chondroitin sulfate or of its derivatives, followed by chemoselective sulfatation, or conversely by sulfatation followed by carboxyl-reduction.
A subject of the invention is therefore the process for preparing carboxyl-reduced and sulfated derivatives of chondroitin sulfate as defined above, using the following steps:
The following reaction scheme illustrates the present invention:
Alternatively, the carboxyl-reduced, chemoselectively O-sulfated derivatives of chondroitin sulfate can be obtained by sulfatation of a quaternary ammonium salt of chondroitin sulfate in organic medium by means of a complex of sulfuric anhydride with an organic base such as pyridine or trimethylamine, followed by carboxyl-reduction by means of a carbodiimide derivative such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, in the presence of a reducing agent such as sodium borohydride, or by means of an ester derivative, such as the methyl ester, in the presence of a reducing agent such as sodium borohydride.
The persulfated or 6-O-sulfated, carboxyl-reduced derivative of chondroitin sulfate can then be trans-salified with a quaternary ammonium salt and then optionally sulfated on the hydroxyl function in the 6′-position thus generated, by the action of a complex of sulfuric anhydride with an organic base such as pyridine or trimethylamine.
A subject of the invention is therefore also a process for preparing the carboxyl-reduced derivatives of chondroitin sulfate as defined above by successively carrying out the following steps:
The following reaction scheme illustrates the present invention:
The processes according to the present invention are characterized by the strong chemoselectivity of the carboxyl-reduction and sulfatation reactions. The products which result therefrom are notably homogeneous and result in true polymers. The carboxyl-reduced chondroitin sulfate derivatives have purities of the order of 90%. This homogeneity is determined by NMR and infrared structural analysis.
Reproducible and unexpected biological properties result therefrom.
The persulfatation reactions are preferably carried out in organic medium by means of a complex of sulfuric anhydride with an organic base such as pyridine or trimethylamine. They are generally followed by a salification reaction, for example by the action of sodium acetate.
In general, the carboxyl-reduced or non-carboxyl-reduced derivative of chondroitin sulfate can be trans-salified with a quaternary ammonium salt and then chemoselectively O-sulfated on the hydroxyls in the 6- and 6′-positions only, or persulfated by reaction with a complex of sulfuric anhydride with an organic base such as pyridine or trimethylamine.
For optimal chemoselectivity of the reactions' for persulfatation of the carboxyl-reduced or non-carboxyl-reduced chondroitin sulfate, it is preferable to use a benzethonium salt in the presence of 10 to 30 equivalents of pyridine-sulfuric anhydride complex per hydroxyl function to be sulfated. For the same reason, the reactions should preferably be carried out at temperatures of between −15 and 70° C.
During the persulfatation of the benzethonium salt of the carboxyl-reduced chondroitin sulfate (compound of formula (I) with R1═H/R2═SO3Na or R1═SO3Na/R2═H and R3═R4═H), the procedure is preferably carried out at temperatures of between 50 and 70° C. This is illustrated in example 1.
For optimal chemoselectivity of the 6,6′-O-sulfatation of the carboxyl-reduced chondroitin sulfate benzethonium salt (compound of formula (I) with R1═H/R2═SO3Na, R1═SO3Na/R2═H and R3═R4═H), the procedure is carried out in the presence of 5 to 15 equivalents of pyridine-sulfuric anhydride complex, at temperatures of between −15 and 5° C. This is illustrated in example 2.
The persulfatation of the chondroitin sulfate benzethonium salt is, for its part, carried out at temperatures of between 50 and 70° C. This is illustrated in example 3.
Similarly, for optimal chemoselectivity of the 6-O-sulfatation of the chondroitin sulfate benzethonium salt, it is preferable to carry out the reaction in the presence of 5 to 15 equivalents of pyridine-sulfuric anhydride complex, at temperatures of between −15 and 5° C. Even more preferably, the reaction should be carried out in the presence of approximately 10 equivalents of pyridine-sulfuric anhydride complex, at a temperature in the region of 0° C. This is illustrated in example 4.
During the (re)sulfatation of the persulfated, carboxyl-reduced derivative of the chondroitin sulfate benzethonium salt (compound of formula (I) with R1 ═R2═R4═SO3Na and R3═H), the procedure is preferably carried out in the presence of 10 to 30 equivalents of pyridine-sulfuric anhydride complex, at temperatures in the region of 20° C. This is illustrated in example 5.
For optimal chemoselectivity of the 6′-O-sulfatation of the 6-O-sulfated, carboxyl-reduced chondroitin sulfate benzethonium salt (compound of formula (I) with R1═H/SO3Na R2═SO3Na and R3═R4═H), it is preferable to carry out the reaction in the presence of 5 to 15 equivalents of pyridine-sulfuric anhydride complex, at temperatures of between −15 and 5° C. Even more preferably, the reaction should be carried out in the presence of approximately 10 equivalents of pyridine-sulfuric anhydride complex at a temperature in the region of −10° C. This is illustrated in example 6.
The carboxyl-reduced derivatives of chondroitin sulfate can be obtained by carboxyl-reduction of chondroitin sulfate or of its derivatives, according to the operating conditions described, for example, by R. L. Taylor and H. E. Conrad, Biochemistry, 11 (8), 1383-1388, (1972). The chondroitin sulfate is reacted with a soluble carbodiimide derivative in aqueous phase, such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, so as to form an activated adduct, which is reduced with a reducing agent such as sodium borohydride.
The term “derivatives (compounds) of chondroitin sulfate” is intended to mean in particular the chondroitin sulfate sodium salt, the chondroitin sulfate benzethonium salt, the sulfated derivatives of chondroitin sulfate, and also the sulfated derivatives of chondroitin sulfate benzethonium salts.
According to an alternative method, the carboxyl-reduced derivatives of chondroitin sulfate can also be obtained by carboxyl-reduction of an ester of chondroitin sulfate or of its chemoselectively O-sulfated derivatives.
By way of example, methyl esters of chondroitin sulfate or of its chemoselectively O-sulfated derivatives can be used and can be reduced by means of a reducing agent such as sodium borohydride.
The reaction with the carbodiimide derivative is preferably carried out in the presence of 5 to 20 equivalents of reactant and at a pH of between 4 and 5. Even more preferably, the reaction with the carbodiimide derivative is carried out in the presence of 7 to 13 equivalents of reactant and at a pH of between 4.3 and 4.9.
The reduction per se is carried out with a reducing agent known to those skilled in the art, and in particular with an alkali metal borohydride. By way of example, it is possible to use sodium borohydride.
The reduction per se of the activated adduct of the chondroitin sulfate derivative is carried out with 10 to 300 equivalents of alkali metal borohydride at a temperature of between 10 and 70° C. More preferably, the reduction of the abovementioned adduct is carried out in the presence of alkali metal borohydride at a temperature of between 10 and 30° C.
Most particularly, a subject of the invention is the process using the following steps:
Alternatively, a subject of the invention is most particularly the process using the following steps:
When it is desired to obtain isolated derivatives from the mixture of carboxyl-reduced derivatives of chondroitin sulfate as obtained according to the process described above, the following process should then be applied to the mixture:
The sodium hydrogen carbonate solution is preferably a solution of 0.1 to 1 mol/l. Even more preferably, the separation is carried out at a concentration of 1 mol/l. The detection is carried out by refractometry.
A subject of the invention is also the carboxyl-reduced and chemoselectively O-sulfated derivatives of chondroitin sulfate, isolated or as a mixture as defined above, which can be obtained according to the process(es) as defined above.
The polysaccharides of formula (I), isolated or as mixtures, can be used as medicinal products.
These polysaccharides exhibit in particular strong inhibitory activity on certain matrix metalloproteases. These inhibitors are particularly indicated for the treatment of pathological states where a large increase in matrix metalloproteinase activity is noted.
The pathological states to which the present invention refers involve an increase in the activity of at least one of the following matrix metalloproteinases: neutrophil elastase, matrisilyn (MMP-7), aggrecanase, hADAMTS1 and gelatinase A (MMP-2).
The compounds can therefore be used for preventing and treating diseases such as degenerative joint disorders (such as osteoarthritis), spondylosis, chondrolysis associated with joint trauma or prolonged joint immobilizations (often following an injury to the meniscus or patella or the rupture of ligaments), disorders related to injuries (healing), periodontal disorders, chronic disorders of the locomotor system (such as chronic or acute inflammatory, immunological or metabolic forms of arthritis), arthropathies, or disorders related to bone metabolism.
A subject of the invention is also the pharmaceutical compositions containing the compounds of formula (I), isolated or as a mixture, and also one or more pharmaceutically acceptable excipients, vehicles or additives.
Another aspect of the invention is a process for preparing the pharmaceutical compositions containing the compounds of formula (I), wherein an amount corresponding to a desired dose of a compound of formula (I) is mixed with one or more pharmaceutically acceptable excipients, vehicles, additives.
The compounds of formula (I) can be administered via various routes. They may include, without being limited, subcutaneous, intraarticular, intraperitoneal or intravenous injections.
The administration may also be rectal, oral, by inhalation, or else transdermal.
In the case of solutions for injection (for example in the form of an ampoule), the doses may range from 5 μg to approximately 200 mg of compound of formula (I), and preferably from 10 μg to 40 mg.
The daily dose indicated for the treatment of an adult patient weighing approximately 70 kg is from 10 μg to 500 mg of active ingredients, generally from 20 mg to approximately 100 mg. However, depending on the circumstances, higher or lower daily doses may be appropriate.
These doses can be administered once a day in the form of a single dosage unit.
Alternatively, the doses can be administered in a plurality of smaller doses, given repeatedly at defined intervals over time.
The following examples illustrate the invention without, however, limiting it.
Chondroitin Sulfate
The chondroitin sulfate used for preparing the compounds illustrating this invention has a molecular mass of 85.2 kDalton. It is produced from fish cartilage and consists of a mixture of chondroitin A and chondroitin C in 50/50 proportions. Its chemical structure can be described by formula (I) with the groups R1═SO3M and R2═R3═R4═H or R1═H, R2═SO3M, R3═R4═H.
a) Preparation of the Carboxyl-Reduced Chondroitin Sulfate Sodium Salt
1 g of chondroitin sulfate sodium salt is dissolved, at a temperature in the region of 20° C., in 150 ml of water.
The pH of the solution is adjusted to a value of 4.7±0.1 by adding a 0.1 N hydrochloric acid solution. 3.45 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride are added and the mixture obtained is stirred while maintaining the pH at a value of 4.7±0.1 by adding a 0.1 N hydrochloric acid solution. When the pH is stabilized at a value in the region of 4.7, 1.8 g of sodium borohydride are added in small portions. The reaction medium is stirred for approximately 20 hours at a temperature in the region of 20° C. After cooling to a temperature in the region of 10° C., the reaction medium is neutralized by adding concentrated hydrochloric acid (10 N) to a pH in the region of 7. 600 ml of a 10% sodium acetate solution in methanol are added. The solid obtained is filtered, and then dissolved in 50 ml of water. 150 ml of a 10% sodium acetate solution in methanol are added to the solution obtained. The solid obtained is filtered, and then dissolved in 50 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 26 hours. The content of the membranes is lyophilized to give 0.682 g of carboxyl-reduced chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 73%.
Proton spectrum in D2O, 400 MHz, T=333 K (δ in ppm—mixture of chondroitins A and C): 2.0 (3H, s), 3.30 (1H, m), between 3.4 and 3.65 (4H, m), between 3.7 and 4.05 (3H+1/2H, m), 4.18 (2H, s), between 4.4 and 4.6 (2H, m), 4.81 (1/2H, s)
b) Preparation of the Carboxyl-Reduced Chondroitin Sulfate Benzethonium Salt
A solution of 1.6 g of benzethonium chloride in 12 ml of water is added to the solution of 0.685 g of carboxyl-reduced chondroitin sulfate sodium salt in 10 ml of water. The suspension obtained is filtered. The cake is washed with water and then dried at 40° C. under reduced pressure (6 kPa) to give 1.25 g of carboxyl-reduced chondroitin sulfate benzethonium salt in the form of a cream solid. The yield obtained is 96%.
c) Preparation of the Carboxyl-Reduced and Persulfated Chondroitin Sulfate Sodium Salt
0.2 g of carboxyl-reduced chondroitin sulfate benzethonium salt is dissolved, at a temperature in the region of 60° C. and under an inert atmosphere, in 6 ml of anhydrous dimethylformamide. When dissolution is complete, a solution of 2.08 g of pyridine-sulfuric anhydride complex in 15 ml of anhydrous dimethylformamide is added to the above solution. After stirring for 1 hour 30 min at a temperature in the region of 60° C., the reaction medium is cooled to a temperature in the region of 10° C. 6 ml of water and then 0.90 ml of a 10% sodium acetate solution in methanol are added. The suspension obtained is filtered. The cake is dissolved in 30 ml of water and is then precipitated by adding 90 ml of a 10% sodium acetate solution in methanol. The suspension obtained is filtered. The cake is washed with methanol (twice 5 ml) and then dissolved in 50 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 30 hours. The content of the membrane is lyophilized to give 0.148 g of carboxyl-reduced and persulfated chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 74%.
Proton spectrum in D2O, 400 MHz, T=298 K (δ in ppm—mixture of chondroitins A and C): 2.05 (3H, s), 3.85 (1H, m), between 3.92 and 4.05 (3H, m), between 4.12 and 4.3 (5H, m), 4.58 (1H, s), 4.65 (1H, s), 4.75 (1H, m), 4.95 (1H, s), 5.0 (1H, s).
a) Preparation of the Carboxyl-Reduced Chondroitin Sulfate Sodium Salt.
The carboxyl-reduced chondroitin sulfate sodium salt is prepared according to Example 1-a.
b) Preparation of the Carboxyl-Reduced Chondroitin Sulfate Benzethonium Salt.
The carboxyl-reduced chondroitin sulfate benzethonium salt is prepared according to example 1-b.
c) Preparation of the Carboxyl-Reduced and 6,6′-O-sulfated Chondroitin Sulfate Sodium Salt
0.13 g of carboxyl-reduced chondroitin sulfate benzethonium salt is dissolved, at a temperature in the region of 20° C. and under an inert atmosphere, in 10 ml of anhydrous dimethylformamide. When dissolution is complete, a solution of 0.2 g of pyridine-sulfuric anhydride complex in 5 ml of anhydrous dimethylformamide is added to the above solution, at a temperature in the region of −10° C. After stirring for 2 hours 30 min at a temperature in the region of −10° C., 2 ml of water and then 60 ml of a 10% sodium acetate solution in methanol are added. The suspension obtained is stirred for 30 minutes, left to sediment overnight, and then filtered. The cake is washed with 5 ml of methanol, dissolved in 20 ml of water, and then precipitated by adding 60 ml of a 10% sodium acetate solution in methanol. The suspension obtained is filtered. The cake is washed with methanol (twice 5 ml) and then dissolved in 10 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 5 days. The content of the membrane is lyophilized to give 0.074 g of carboxyl-reduced and 6,6′-O-sulfated chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 83%.
Proton spectrum in D2O, 400 MHz, T=333 K (δ in ppm—mixture of 4 chondroitins, possibly sulfated in the C4 position (Gal 2N6S), possibly epimerized in the C5 position (Glu6S)): 2.0 (3H, s), 3.30 (1H, m), between 3.5 and 4.25 (11H, m), between 4.4 and 4.7 (2H, m), between 4.75 and 4.92 (1/2H).
a) Preparation of the Chondroitin Sulfate Benzethonium Salt.
A solution of 113 g of benzethonium chloride in 560 ml of water is added to the solution of 50 g of chondroitin sulfate sodium salt in 715 ml of water. The suspension obtained is stirred for 1 hour at a temperature in the region of 20° C. and then left to sediment overnight. The supernatant is removed by settling out and then replaced with the same volume of water. The suspension is again stirred for one hour and then left to sediment. The operation described above is repeated 3 times. The suspension is then filtered. The cake is washed with water and then dried at 40° C. under reduced pressure (6 kPa) to give 123.4 g of chondroitin sulfate benzethonium salt in the form of a white solid. The yield obtained is 94%.
b) Preparation of the Persulfated Chondroitin Sulfate Sodium Salt
5 g of chondroitin sulfate benzethonium salt are dissolved, at a temperature in the region of 60° C. and under an inert atmosphere, in 100 ml of anhydrous dimethylformamide. When dissolution is complete, a solution of 26.5 g of pyridine-sulfuric anhydride complex in 250 ml of anhydrous dimethylformamide is added to the above solution. After stirring for 1 hour 30 min at a temperature in the region of 60° C., the reaction medium is cooled to a temperature in the region of 10° C. 100 ml of water and then 1350 ml of a 10% sodium acetate solution in methanol are added. The suspension obtained is filtered. The cake is washed with methanol (50 ml), dissolved in 400 ml of water, and then precipitated by adding 1200 ml of a 10% sodium acetate solution in methanol. The suspension obtained is filtered. The cake is washed with methanol (20 ml) and then dissolved in 200 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 4 days. The content of the membrane is lyophilized to give 2 g of persulfated chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 66%.
Proton spectrum in D2O, 400 MHz, T=298 K (δ in ppm—mixture of chondroitins A and C): 2.05 (3H, s), 4.0 (3H, m), 4.1 (1H, s), 4.23 (2H, m), 4.4 (2H, m), 4.7 (1H, m), 4.82 (1H, d, J=3 Hz), 4.87 (1H, s), 4.95 (1H, s).
c) Preparation of the Persulfated, Carboxyl-Reduced Chondroitin Sulfate Sodium Salt
0.5 g of persulfated chondroitin sulfate sodium salt are dissolved, at a temperature in the region of 20° C., in 45 ml of water. The pH of the solution is adjusted to a value of 4.7±0.1 by adding a 0.1 N hydrochloric acid solution. 1.1 g of 1-ethyl-3-(3-dimethylamino-propyl)carbodiimide hydrochloride are added and the mixture obtained is stirred while maintaining the pH at a value of 4.7±0.1 by adding a 0.1 N hydrochloric acid solution. When the pH is stabilized at a value in the region of 4.7, 4.44 g of sodium borohydride are added in small portions. The reaction medium is stirred for approximately 20 hours at a temperature in the region of 20° C. After cooling to a temperature in the region of 10° C., the reaction medium is neutralized by adding concentrated hydrochloric acid (10 N) to a pH in the region of 7. The reaction medium is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 65 hours. 600 ml of a 10% sodium acetate solution in methanol are added to the content of the membranes. The solid obtained is filtered, and then dissolved in 200 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 28 hours. The content of the membranes is lyophilized to give 0.28 g of persulfated, carboxyl-reduced chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 59%.
Proton spectrum in D2O, 400 MHz, T=323 K (δ in ppm—mixture of chondroitins A and C): 2.0 (3H, s), 3.65 (3H, m), 3.89 (3H, m), 3.96 (1H, m), 4.05 (1H, s), 4.2 (2H, s), 4.7 (2H, m), 4.89 (1H, s), 4.93 (1H, s).
a) Preparation of the Chondroitin Sulfate Benzethonium Salt
The chondroitin sulfate benzethonium salt is prepared according to example 3-a.
b) Preparation of the 6-O-sulfated Chondroitin Sulfate Sodium Salt
10 g of chondroitin sulfate benzethonium salt are dissolved, at a temperature in the region of 0° C. and under an inert atmosphere, in 200 ml of anhydrous dimethylformamide. When dissolution is complete, a solution of 10.6 g of pyridine-sulfuric anhydride complex in 100 ml of anhydrous dimethylformamide is added to the above solution. After stirring for 2 hours 30 min at a temperature in the region of 0° C., 150 ml of water and then 1600 ml of a 10% sodium acetate solution in methanol are added. The suspension obtained is filtered. The cake is dissolved in 500 ml of water and then precipitated by adding 1500 ml of a 10% sodium acetate solution in methanol. The suspension obtained is filtered. The cake is washed with methanol (20 ml), and then dissolved in 200 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 24 hours. The content of the membrane is lyophilized to give 2.89 g of 6-O-sulfated chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 69%.
Proton spectrum in D2O, 400 MHz, T=323 K (δ in ppm—mixture of chondroitins A and C): 2.0 (3H, s), 3.35 (1H, m), 3.55 (1H, m), between 3.62 and 4.38 (3H+1/2H, m), between 3.4 and 4.1 (2H, m), 4.2 (2H, m), 4.45 (1H, m), 4.55 (1H, m), 4.78 (1/2H, s).
c) Preparation of the 6-O-sulfated, Carboxyl-Reduced Chondroitin Sulfate Sodium Salt
2 g of 6-O-sulfated chondroitin sulfate sodium salt are dissolved, at a temperature in the region of 20° C., in 250 ml of water. The pH of the solution is adjusted to a value of 4.7±0.1 by adding a 0.1 N hydrochloric acid solution. 6.5 g of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride are added and the mixture obtained is stirred while maintaining the pH at a value of 4.7±0.1 by adding a 0.1 N hydrochloric acid solution. When the pH is stabilized at a value in the region of 4.7, 25.8 g of sodium borohydride are added in small portions. The reaction medium is stirred for approximately 20 hours at a temperature in the region of 20° C. After cooling to a temperature in the region of 10° C., the reaction medium is neutralized by adding concentrated hydrochloric acid (10 N) to a pH in the region of 7. The reaction medium is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 50 hours. 1530 ml of a 10% sodium acetate solution in methanol are added to the content of the membranes. The solid obtained is filtered, washed with methanol, and then dissolved in 100 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 24 hours. The content of the membranes is lyophilized to give 0.758 g of 6-O-sulfated, carboxyl-reduced chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 41%.
Proton spectrum in D2O, 400 MHz, T=298 K (δ in ppm—mixture of chondroitins A and C (1/3 4-OSO3H, 2/3 6-OSO3H)): 2.0 (3H, s), 3.30 (1H, m), between 3.4 and 3.90 (7H+1/3H, m), between 3.92 and 4.05 (2H, m), 4.19 (4/3H, s), between 4.4 and 4.6 (2H, m), 4.88 (1/3H, s).
a) Preparation of the Persulfated, Carboxyl-Reduced Chondroitin Sulfate Benzethonium Salt
A solution of 0.9 g of benzethonium chloride in 15 ml of water is added to the solution of 0.4 g of persulfated, carboxyl-reduced chondroitin sulfate sodium salt (prepared according to example 3) in 15 ml of water. The suspension obtained is stirred for 1 hour at a temperature in the region of 20° C., left to sediment overnight, and then filtered. The cake is washed with water (6 times 50 ml), dried in a dessicator under vacuum, and then at 80° C. under reduced pressure (6 kPa), to give 0.95 g of persulfated, carboxyl-reduced chondroitin sulfate benzethonium salt in the form of a white solid. The yield obtained is 80%.
b) Preparation of the Carboxyl-Reduced and Persulfated Chondroitin Sulfate Sodium Salt
0.95 g of persulfated, carboxyl-reduced chondroitin sulfate benzethonium salt are dissolved, at a temperature in the region of 20° C. and under an inert atmosphere, in 10 ml of anhydrous dimethylformamide. When dissolution is complete, a solution of 1.27 g of pyridine-sulfuric anhydride complex in 5 ml of anhydrous dimethylformamide is added to the above solution. After stirring for 2 hours 30 min at a temperature in the region of 20° C., the reaction medium is cooled to a temperature in the region of 10° C. 7 ml of water and then 60 ml of a 10% sodium acetate solution in methanol are added. The suspension obtained is filtered. The cake is dissolved in 50 ml of water. The suspension obtained is filtered. The filtrate is precipitated by adding 120 ml of a 10% sodium acetate solution in methanol. The suspension obtained is filtered. The cake is dissolved in 10 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 26 hours. The content of the membrane is lyophilized to give 0.17 g of carboxyl-reduced and persulfated chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 48%.
Proton spectrum in D2O, 400 MHz, T=298 K (δ in ppm—mixture of chondroitins A and C): 2.05 (3H, s), 3.85 (1H, m), between 3.92 and 4.05 (3H, m), between 4.12 and 4.3 (5H, m), 4.58 (1H, s), 4.65 (1H, s), 4.75 (1H, m), 4.95 (1H, s), 5.0 (1H, s).
a) Preparation of the 6-O-sulfated, Carboxyl-Reduced Chondroitin Sulfate Benzethonium Salt
A solution of 1.9 g of benzethonium chloride in 30 ml of water is added to the solution of 0.8 g of 6-O-sulfated, carboxyl-reduced chondroitin sulfate sodium salt (prepared according to example 4) in 30 ml of water. The suspension obtained is stirred for 1 hour at a temperature in the region of 20° C., left to sediment overnight, and then filtered. The cake is washed with water (5 times 25 ml), dried in a desiccator under vacuum, and then at 60° C. under reduced pressure (6 kPa), to give 1.64 g of 6-O-sulfated, carboxyl-reduced chondroitin sulfate benzethonium salt in the form of a white solid. The yield obtained is 96%.
b) Preparation of the Carboxyl-Reduced and 6,6′-O-sulfated Chondroitin Sulfate Sodium Salt
0.5 g of 6-O-sulfated, carboxyl-reduced chondroitin sulfate benzethonium salt is dissolved, at a temperature in the region of 20° C. and under an inert atmosphere, in 8 ml of anhydrous dimethylformamide. When dissolution is complete, a solution of 0.65 g of pyridine-sulfuric anhydride complex in 4 ml of anhydrous dimethylformamide is added to the above solution, at a temperature in the region of −10° C. The reaction medium is stirred at a temperature in the region of −10° C. for 2 hours 30 min. 5 ml of water and then 80 ml of a 10% sodium acetate solution in methanol are added. The suspension obtained is filtered. The cake is washed with methanol, dissolved in 20 ml of water, and then precipitated by adding 60 ml of a 10% sodium acetate solution in methanol. The suspension obtained is filtered. The cake is dissolved in 10 ml of water. The solution obtained is loaded into a PM 3500 cellulose ester membrane and dialyzed, changing the water baths regularly for 26 hours. The content of the membrane is lyophilized to give 0.22 g of carboxyl-reduced and 6,6′-O-sulfated chondroitin sulfate sodium salt in the form of a white lyophilized material. The yield obtained is 79%.
Proton spectrum in D2O, 400 MHz, T=333 K (δ in ppm—mixture of 4 chondroitins, possibly sulfated in the C4 position (Gal 2N6S), possibly epimerized in the C5 position (Glu6S)): 2.0 (3H, s), 3.30 (1H, m), between 3.5 and 4.25 (11H, m), between 4.4 and 4.7 (2H, m), between 4.75 and 4.92 (1/2H).
Pharmacological Test
Effect of the carboxyl-reduced derivatives on the aggrecanase in synovial fluids or on preparations of recombinant ADAMTS protein.
The analysis is carried out on 96-well plates. Before the analysis, serial dilutions of the assay compounds are prepared in an aqueous solution.
Digestion:
In each well, a fixed volume of synovial fluid or aggrecanase activity generating a known increase, between 1.0 and 1.4 absorbance units (405 nm), under the conditions of the analysis, is mixed with 3 μl of solution of compound from the respective dilution step. Dulbecco's modified Eagle's medium (DMEM) is added to each well to give a final volume of 300 μl. The plate is then incubated for 1 hour at 37° C. in a carbon dioxide atmosphere.
After the addition of 5 μl of a solution of 1 μg/μl of recombinant substrate Agglmut in DMEM to each well (substrate as described by Bartnik E. et al., EP 785274, 1997), the reagent mixture is incubated for 4 hours at 37° C. under a carbon dioxide atmosphere.
Preparation of the Analytical Plate:
In a first step, the microplate is coated with 100 μl per well of a commercial goat anti-mouse IgG antibody for 1 hour at ambient temperature (5 μg/ml in a phosphate buffered saline solution, pH 7.4 [PBS buffer]). After washing with the PBS buffer containing 0.1% of Tween-20 (washing buffer), the wells are blocked by means of a step consisting of a one hour incubation with 100 μl per well of 5% bovine serum albumin in a PBS buffer containing 0.05% of Tween-20. Following another rinse with the washing buffer, each well is incubated with 100 μl of a solution, diluted to 1:1000, of BC-3 antibody in a PBS buffer containing 0.05% of Tween 20 and 0.5% of bovine serum albumin, at ambient temperature for one hour. This antibody recognizes the typical aggrecanase cleavage fragments (Hughes C. E. et al., Biochem. J. 305 (3), 799-804, 1995).
Assay Procedure:
After another rinse of the analytical plate with the washing buffer, the complete set of mixtures originating from the preceding digestion is transferred to this plate, well by well, and incubated at ambient temperature for one hour. The plate is again washed as above. Next, 100 μl of the second antibody (anti-human IgG antibody labeled with peroxidase, 1:1000 in PBS containing 0.5% of BSA and 0.05% of Tween-20) are added to each well, with subsequent incubation at ambient temperature again for one hour. After a final rinse with the washing buffer, the color development is initiated by adding 100 μl of ABTS substrate solution (2 mg/ml, 2,2′-azinobis (3-ethylbenzothiazolinesulfonic acid) in 40 mM of sodium citrate plus 60 mM of disodium hydrogen phosphate, adjusted to a pH of 4.4 by adding acetic acid; 0.25 μl of 35% hydrogen peroxide added per ml immediately before measurement). The measurement is carried out by means of the screen mode using detection at 405 nm relative to a reference filter (620 nm) with automatic readings at 5-second intervals. The development is stopped as soon as the maximum signal (405 nm) in the absorbance range of 1.0 to 1.4 is reached.
Table 1
% inhibition of conversion of the substrate by activity of the aggrecanase in the supernatant.
The estimated IC50 of the product of example 1 is of the order of 0.004 μg/ml
Inhibition of Factor Xa
For the calibration, a standard sample of low molecular weight heparin (Enoxaparin) was used as reference.
The serial dilutions of the assay compound are prepared in a 0.046 M Tris buffer, pH 8.4, containing 0.15 M NaCl, 0.007 M EDTA, 0.1% of Tween 80 and 0.12 IU/ml of human antithrombin III. The samples of 50 μl of the respective dilutions are incubated with 50 μl of bovine factor Xa (13.6 U/ml) at 37° C. for 80 seconds. Next, 50 μl of chromogenic substrate, 1.1 mM S-2765, are added. The absorbance at 405 nm is measured in a photometer. The activity of the deblocked factor Xa is indicated by the emission of p-nitroaniline from the substrate.
Compared to the reference heparin compound (100 U/mg), the glycosamonoglycans present a factor Xa, with much lower inhibitory activity:
Commercial ELISA kits (such as those provided, for example, by the company Amersham Biosciences, kits RPN2617 and RPN2620) were used, respectively, to determine the inhibitory activity with respect to the MMP-2 and MMP-7 enzymes. The concentrations of the enzymes are, respectively, 800 ng/ml for MMP-2. The tests were carried out in accordance with the manufacturer's recommendations, by performing a series of dilutions of the compound to be studied in a PBS buffer, pH 7.5. The MMP-2 enzymes were inhibited in a concentration-dependent manner.
Estimated IC50: 0.4 μg/ml
| Number | Date | Country | Kind |
|---|---|---|---|
| 0314988 | Dec 2003 | FR | national |
This application claims the benefit of U.S. Provisional Application No. 60/618,662 filed Oct. 12, 2004 and benefit of priority from French Patent Application No. 03 14988 filed Dec. 19, 2003, both of which are incorporated herein by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 60618662 | Oct 2004 | US |
