EP0581846A1

EP0581846A1 - Sulfate polysaccharides, preparation method, pharmaceutical composition and utilization

Info

Publication number: EP0581846A1
Application number: EP92910133A
Authority: EP
Inventors: Jean-Pierre Baron; André BRUN; Hendrik Hemker; André Uzan
Original assignee: Rhone Poulenc Rorer SA
Current assignee: Aventis Pharma SA
Priority date: 1991-04-23
Filing date: 1992-04-21
Publication date: 1994-02-09
Also published as: FR2675806B1; NZ242431A; JPH06506968A; EP0511075A1; MX9201846A; IE921287A1; CA2108363A1; AU1748592A; ZA922874B; FR2675806A1; WO1992018544A1

Abstract

L'invention concerne de nouveaux mélanges d'oligosaccharides sulfatés présentant la structure générale des oligosaccharides constitutifs de l'héparine, ayant une masse moléculaire moyenne de 6U0,6kD, une polydispersité proche de 1, et la capacité d'inhiber la génération de thrombine. L'invention concerne également leur préparation et des compositions pharmaceutiques les contenant.The invention relates to new mixtures of sulfated oligosaccharides having the general structure of the heparin-constituting oligosaccharides, having an average molecular weight of 6U0.6kD, a polydispersity close to 1, and the ability to inhibit the generation of thrombin. The invention also relates to their preparation and to pharmaceutical compositions containing them.

Description

SULPHATED POLYSACCHARIDES. PREPARATION PROCESS. PHARMACEUTICAL COMPOSITION AND USE

The present invention relates to the field of low molecular weight polysaccharides. More particularly, it relates to oosaccharide compositions exhibiting excellent pharmacological and antifhrombotic properties.

Generally speaking, antithrombotic treatments use two main categories of agents, namely anticoagulants and antiplatelet agents. Among the anticoagulant agents, the anti-vitamin K compounds constitute a very important family. These compounds being active orally, they are used in many indications. However, their use is still limited by certain drawbacks and in particular the risks of hemorrhage they cause - and the difficulty of adapting the dosage to a long-term treatment. Heparin is the second category of anticoagulant agents. They are biological substances of extraction from the family of glycosaminoglycans composed of oligosaccharides having chain lengths and varying degrees of sulfation. Heparin is used in various types of thrombosis, in particular in the treatment or prevention of venous thrombosis, possibly associated with other therapies.

The disadvantage of heparins lies in their high anticoagulant activity which can cause bleeding, and in their sensitivity to certain serum factors, such as pf4, which requires the use of relatively large doses. Furthermore, heparins are very heterogeneous products. It is therefore difficult to assess their mechanism of action, to assess the contribution of each of the components in the overall activity of heparin, and, therefore, to increase the antimrombotic activity without increasing the side effects. .

A first solution to the drawbacks mentioned above has been provided by low molecular weight heparins. These heparins are obtained by fragmentation (depolymerization) of the oligosaccharide chains using chemical or enzymatic agents. In particular, depolymerization has been described by treatment of a heparin ester in the presence of a strong base (EP 40144). It can also be carried out by treatment of heparin in the presence of nitrous acid, or by the action of a heparinase (EP 64452). These different processes lead to mixtures of oligosaccharides having the general structure of the polysaccharides constituting heparin, but having a lower weight average molecular weight. Particularly, research has mainly focused on mixtures derived from heparin having very short oligosaccharide chains. Thus, patent EP 27089 indicates that mixtures of oligosaccharides derived from heparin not containing more than 8 saccharide units have a specific antithrombotic activity greater than heparin. In the same way, hexasaccharides were prepared and their antithrombotic properties studied (EP 64452). Mention may also be made of the more recent patents EP. 84999 and EP 301 618 on polysaccharides such as hexa-, penta- and tetrasaccharides derived from heparin.

However, the products described to date have not made it possible to solve the problems encountered with heparins in a completely satisfactory manner. In particular, the correlation between the average molecular weight of the products and their side effects could not be confirmed in vivo.

The applicant has now shown that it is possible to obtain, from native or depolymerized heparins, mixtures of oligosaccharides having markedly improved antithrombin properties, and consequently, better therapeutic potentials. Unexpectedly, the Applicant has indeed shown that a large part of the antithrombotic activity of heparin is contained in a narrow and homogeneous fraction.

The present invention more specifically results from the identification of monodispersed heparin fractions and having an average molecular weight close to 6 kD, possessed a high antithrombin activity.

As illustrated in the examples, it is therefore possible to obtain mixtures having a particularly high antithrombotic activity by calibrating the molecular mass and reducing the polydispersity.

An object of the invention resides in a mixture of sulfated oligosaccharides having the general structure of the oligosaccharides constituting heparin, characterized in that it has a weight-average molecular mass of 6 + 0.6 kD and a near polydispersity of 1, and in that it has the capacity to inhibit the generation of thrombin.

The polydispersity corresponds to the ratio of the average molecular weight of the mixture to its number average molecular weight. She reports on the molecular homogeneity of the mixture. The closer this value is to 1, the more homogeneous the mixture.

In addition to their antithrombin properties, the mixtures of the invention have particularly advantageous phaπnacokinetic properties. Thus, compared with native heparin and its depolymerized forms, the mixtures of the invention have a lower sensitivity to serum factors such as ρf4, which increases their therapeutic potential.

Other advantages of the mixtures of the invention render in particular in the reduction of certain undesirable side effects, such as: - the thrombocytopenic effect. One of the drawbacks of known mixtures derived from heparin stems from the drop in the number of platelets that they can cause. This undesirable effect is greatly reduced when the mixtures of the invention are used.

- immunogenic reactions. When such reactions are too large, it is clear that the therapeutic efficacy of the products is reduced. The low immunogenicity of the mixtures of the invention constitutes another of their

• very interesting pharmacological characteristics.

Furthermore, other advantages of the mixtures of the invention lie in particular in their excellent bioavailability and plasma half-life. The properties set out above allow particularly effective pharmaoological use, in particular in the prophylaxis and treatment of venous or arterial thromboses. In addition, they should make it possible to use larger doses in vivo without increasing the risk of bleeding. In a preferred embodiment, the mixtures of the invention are more particularly fractions of depolymerized heparin.

As indicated previously, the depolymerized heparin can be obtained by any chemical, enzymatic or other technique known to those skilled in the art making it possible to fragment the oligosaccharide chains of heparin. In particular, the methods described in patents EP 40144, EP 64452, EP 37319 or

EP 337327 are suitable for the invention.

Even more preferably, the mixtures of the invention consist of oligosaccharides having a 2-Q-sulfo 4 enopyranosuronic acid at one of their ends. A particularly advantageous mixture consists of a fraction of heparin depolymerized by the action of a base on a heparin ester.

The antithrombin activity of the mixtures of the invention can be demonstrated in a test in which the generation of thrombin is triggered in the presence of human thromboplasm (extrinsic route) or by contact (intrinsic route). Such a test has been described previously (Hemker et aL, Thromb. Haemostas. 56, 9-17,

1986).

This activity can be expressed quantitatively, by the amount of product necessary for the inhibition of 25% of the generation of thrombin. In this way, the increase in activity of the mixtures of the invention appears clearly since, in vitro, their specific antithrombin activity is, surprisingly, increased by a factor greater than 100% compared to l heparin used at the start - In view of the particularly advantageous pharmacokinetic properties of the mixtures of the invention, this increase in specific activity is even greater in vivo. More particularly, the mixtures of the invention make it possible, in a teist performed on plasma poor in platelets, to inhibit 25% of the generation of thrombin at concentrations below 300 ng ml.

Another subject of the invention relates to a process for the preparation of a mixture as defined above, characterized in that a heparin or a heparin depolymerized by gel-filtration is fractionated.

The process of the invention involves several parameters, the control of which makes it possible to calibrate the molecular mass of the final mixture, and to fix its polydispersity. These parameters are in particular the ionic strength of the eluent and the nature of the support used. More preferably, the fractionation is characterized in that the steps consisting in (i) putting the starting heparin or depolymerized heparin in solution in the eluent are carried out successively (ii) passing the solution thus obtained to through at least one column containing the solid support for gei-filtration previously balanced with the same eluent, and (iii) recovering the fractions of desired molecular weight.

In a particular embodiment of the invention, it is preferred to use as starting heparin a depolymerized heparin.

Even more preferably, use is made of a heparin depolymerized by the action of a base on a heparin ester. In particular, the depolymerization can be carried out in an aqueous medium or in an inert organic solvent, under the action an organic or inorganic base such as for example sodium or potassium hydroxide, an alkaline carbonate or a tertiary amine (triethylamine, triethylene diamine, etc.). The action of the base on the ester makes it possible to carry out a partial and controlled depolymerization of the heparin without altering its general structure.

More generally, the depolymerization conditions described in patent EP 40144 can be used in the present invention.

As eluent which can be used in the process of the invention, mention may be made of different types of saline solutions, such as sodium chloride solutions. However, the applicant has shown that, in order to obtain fractions having the best properties, it is particularly advantageous to carry out the fractionation using an eluent chosen from phosphate buffers, such as in particular potassium phosphate, sodium phosphate or NH ₄ H2PO ₄ . It is also possible to use NaClO ₄ or NH .NOg solutions which make it possible to obtain mixtures having excellent characteristics.

The concentration of the eluent and therefore its ionic strength are adapted to the desired final mixture. In particular, the concentration of the eluent is advantageously less than 1M, and even more preferably between 0.1 and 0.5 M. When using a phosphate buffer, it is particularly advantageous to operate at concentrations close to 0.2 M.

In the second step of the process of the invention, the support used is generally chosen as a function of the average molecular weight of the starting mixture (native heparin, depolymerized, etc.), of the desired final product, and of the behavior of the mixture of departure in the eluent used. Advantageously, a polyacrylamide-agarose type gel is used as support. By way of example, mention may be made of the gels AcA 54, AcA 202, Sephadex G25 or G50, or even Biogel P30 which give good results.

In a first particularly advantageous embodiment of the method of the invention, during the second fractionation step, the solid support is distributed in several columns arranged in series. This variant of the invention makes it possible to use large final amounts of support for gel-filtration, without the drawbacks of the prior art, namely-essentially the packing phenomena. In this way, the separation is much clearer, including in the high molecular weights, in a single operation of fractionation, and the supports are more easily regenerable.

The number of columns used is adapted by those skilled in the art according to the volume and the nature of the gel used, so as to obtain the best balance between the effectiveness of the separation and the harmful effect due to the packing of the gel. For practical reasons of implementation, it is generally preferred to use in the second step of the process a number of columns less than 20.

By way of illustration, 40 liters of AcA 202 gel can be divided into 10 columns of 4 liters.

In another particularly advantageous embodiment of the method of the invention, at least two types of support are used in the second stage of the fractionation, having -different separation characteristics. This variant of the invention makes it possible to obtain a final fractionation of better quality.

By way of example, the fractionation can be carried out on the following sequence of gels: AcA 202 - AcA 54 - AcA 202.

For a better implementation of the invention, it is important to use high amounts of gel, so as to achieve a sharper separation and to obtain greater homogeneity. However, taking into account the fairly slow flow rates used for this kind of gel-filtration, the volume of gel must be adapted to the quantity of product to be separated, so as to obtain the best balance between separation and the effect of longitudinal diffusion.

Advantageously, in the process of the invention, the starting heparin (g) / gel volume (1) ratio is less than 2, and even more preferably between 0.5 and 1.5. The invention also relates to a process for the preparation of mixtures of weakly dispersed oligosaccharides and of calibrated molecular weight by fractionation by gel-filtration on solid support of heparin or depolymerized heparin, characterized in that the solid support is divided into several columns arranged in series. Another subject of the invention relates to a pharmaceutical composition having as active ingredient a mixture as defined above. Such a composition can be used particularly advantageously in the prophylaxis or the treatment or prevention of thrombotic accidents. More specifically, it can be used: - in the prevention of venous thrombosis in risk situations, - in the prevention of arterial thrombotic accidents, in particular in the case of myocardial infarction,

- in the post-operative regime, in the prevention of venous thromboses • in surgical patients, or, - in the prevention of thromboses in the surgical equipment.

The present invention will be more fully described with the aid of the following examples, which should be considered as illustrative and not limiting.

Example 1: Preparation of mixtures according to the invention.

- Depolymerization of heparin To a solution of 10 g of sodium heparinate in 100 ml of water is added a solution of 25 g of benzethonium chloride in 125 ml of water. The product obtained at room temperature is filtered, washed with water and then dried. 15 g of benzethonium heparinate thus obtained are dissolved in 75 ml of methylene chloride, to which 15 ml of benzyl chloride are added. The solution is heated to a temperature between 25 and 35 ° C for 25 hours. 90 ml of a 10% solution of sodium acetate in methanol are then added, filtered, washed with methanol and dried. 10 g of heparin benzyl ester obtained under the conditions described above in the form of the sodium salt are dissolved in 250 ml of water. To this solution, heated to approximately 60 ° C., 0.9 g of soda is added. The temperature is maintained for 1 hour 30 minutes at approximately 60 ° C, and the reaction mixture is then cooled to around 20 ° C and neutralized by addition of dilute hydrochloric acid. The concentration of the medium is then adjusted to 10% sodium chloride, and the product is precipitated in 750 ml of methanol, filtered and dried.

- Several glass columns are used for the fractionation: (a) 1 column with a diameter of 95 mm and a height of 2 m containing 14 liters of AcA 202 gel (gel in the form of polyacrylamide-agarose beads, with a diameter between 60 and 140 μm),

(b) 1 column with a diameter of 50 mm and a height of 2 m containing 4 liters of AcA 54 gel (gel in the form of polyacrylamide-agarose beads, with a diameter between 60 and 140 μm),

(c) 2 columns with a diameter of 50 mm and a height of 1 m containing 2 liters of AcA 202 gel.

A solution containing 20 g of heparin depolymerized under the conditions described above is placed at the head of column (a) and eluted with a phase mobile consisting of a 0.33M NaCl solution, at a flow rate of 210 ml / hour.

The fractions are collected at the end of column (a) and loaded at the head of column (b). The elution is carried out with the. same solution, and the fractions collected are passed successively on the 2 columns (c). This treatment makes it possible to efficiently separate and recover at the outlet of column (c) a fraction having the following characteristics:

Molecular Weight: 6100 +/- 200

Polydispersity: 1.01

Example Z:

- 10 columns with an internal diameter of 2.5 cm and a height of 50 cm each containing approximately 0.25 liters of AcA 202 gel are connected in series,

- A solution containing 2 g of heparin depolymerized under the conditions of example 1 is loaded at the top of the device and eluted with a 0.2 M aqueous solution of H2PO4 at a flow rate of 0.42 ml / min. - from 9 p.m., 113 fractions of 12.6 ml are collected.

The characteristics of these fractions are given in Table 1, in which the average molecular weight was determined by refractometry.

Example:

The procedure is as in Example 2: - 10 columns with an internal diameter of 10 cm and a height of 50 cm each containing 3 to 4 liters of AcA 202 gel are connected in series,

- A solution containing 30 g of heparin depolymerized under the conditions of Example 1 is loaded at the top of the device and eluted with a 0.2 M aqueous solution of KH2PO4 at a flow rate of 6.8 ml / min. Fractions are obtained having the desired polydispersity characteristics.

Ex m le 4:

The antithrombin activity of the mixtures of the invention is measured on plasma stimulated by human thromboplastin (extrinsic route) or by contact (phospholipids + kaoline: intrinsic route) under the conditions described above (see Hemker et al. Cited above). The activity is estimated by the decrease the peak of the thrombin generation curve compared to a control carried out in the presence of buffer only. The results are expressed by the IC25: concentration necessary to obtain 25% inhibition of the generation of thrombin.

Protocol:

To a volume of plasma is added 1/4 volume of 50 mM Tris-HCl buffer, 0.1 M NaCl, pH 7.35 with 0.5 mg ml of bovine albumin, containing different concentrations of samples to be tested. After a 5 min incubation. at 37 ° C, the generation of thrombin is triggered by the addition of 1/4 of volume of diluted thromboplastin 1:40 in 0.1 M CaC12 (extrinsic system) or by 6 μM of phospholipids (20% phosphatidyl serine, 80 % phosphatidyl choline) and 0.15 mg / ml of kaoline in 0.1 M CaCl 2 (intrinsic system). The generation of thrombin is obtained by measuring at regular intervals (15-30 sec.) The amydolitic activity on the substrate S2238, chromogenic substrate at 405 nM specific for thrombin. Different concentrations of the samples are tested, in order to obtain 25% of control ihnibition.

Results:

On platelet-poor plasma

1) extrinsic starting depolymerized heparin: CI25 = 450 ng / ml

Mixture prepared in Example 1: CI25 = 200 ng ml

Activity gain: 125%

2) intrinsic way

Starting depolymerized heparin: CI25 = 550 ng / ml Mixture prepared in Example 1: CI25 = 250 ng / ml

Activity gain: 120%

On platelet-rich plasma:

Starting depolymerized heparin: CI25 = 1100 ng / ml Mixture prepared in Example 1: CI25 = 500 ng / ml Under the same conditions, native heparin (not depolymerized, not fractionated) has no inhibitory activity at 2500 ng / ml.

TABLE 1

N ^β MOLECULAR MASS FRACTION MEDIUM POLYDISPERSITY

14-17 10712 1.027

18-20 8400 1.013

21-22 7,519 1.010

23-24 6,986 1,011

26-27 6365 1.008

28-31 5874 1.009

32-35 5295 1.011

36-40 4761 1.012

42-46 4192 1.013

48-53 3,608 1,016

56-61 2988 1.019

64-70 2359 1.023

75-80 1,758 1.029

83-85 1476 1.028

88-94 1,176 1.027

Claims

1. Mixture of sulfated oligosaccharides having the general structure of the oligosaccharides constituting heparin, characterized in that it has an average molecular mass of 6 ± 0.6 kD and a polydispersity close to 1, and in that it has the ability to inhibit the generation of thrombin.

2. Mixture according to claim 1 characterized in that it is a fraction of depolymerized heparin.

3. Mixture according to claim 2 characterized in that it consists of oligosaccharides having a 2-β-sulfo 4 enopyranosuronic acid at one of their ends.

4. Mixture according to claim 3 characterized in that it is a fraction of heparin depolymerized by the action of a base on a heparin ester.

5. Mixture according to any one of claims 1 to 4 characterized in that, in a test on plasma low in platelets stimulated by human thromboplastin or by contact, it has the capacity to inhibit 25% of the generation of thrombin at concentrations below 400 ng / ml.

6. Method for preparing a mixture according to one of claims 1 to 4 characterized in that Ton fractionates a hepiririn or a heparin depolymerized by gel-filtration.

7. Method according to claim 6 characterized in that the fractionation successively comprises the steps consisting in (i) putting the starting heparin or depolymerized heparin in solution in the eluent, (ii) passing the solution thus obtained through at least one column containing the solid support for gel-filtration, previously equilibrated with the same eluent, and (iϋ) recovering the fractions of desired molecular weight.

8. Method according to claim 7 characterized in that a depolymerized heparin is used.

9. Method according to claim 8 characterized in that one uses a heparin depolymerized by the action of a base on a heparin ester.

10. Method according to claim 7 characterized in that the eluent is constituted by a phosphate buffer, preferably a sodium phosphate or potassium phosphate buffer, or by solutions of NaCK> 4 or NH4NO3 ..

11. Method according to claim 7 characterized in that, after the second stage of the fractionation, the support is distributed in several columns arranged in series.

12. Method according to claim 11 characterized in that a number of columns less than 20 is used.

13. Method according to claim 7 characterized in that the second step is carried out successively using at least 2 types of support, having different separation characteristics.

14. Method according to any one of claims 7, 11, 12 and 13 characterized in that the support used is a gel of polyacrylamide-agarose type.

15. The process as claimed in claim 14, characterized in that the starting heparin (g) / gel volume (1) ratio is less than 2, and preferably between 0.5 and 1.5.

16. Method for preparing a mixture of weakly dispersed oligosaccharides and having a calibrated molecular weight by fractionation by gel-filtration on a solid support of heparin or depolymerized heparin, characterized in that the solid support is distributed in several columns available in series.

17. Pharmaceutical composition having as active ingredient a mixture of oligosaccharides according to any one of claims 1 to 5.

18. Pharmaceutical composition according to claim 17 intended for the treatment and prevention of venous and arterial thromboses.

19. Pharmaceutical composition according to claim 17 intended for the prevention of arterial thrombotic accidents, in particular in the case of myocardial infarction,

20. The pharmaceutical composition according to claim 17 intended for a use in post-operative regime, in the prevention of venous thrombosis in surgical patients.

21. Use of a mixture of oligosaccharides according to any one of claims 1 to 5 in the prevention of thromboses in surgical equipment.