US20120253029A1

US20120253029A1 - Process for the preparation of highly o-sulfated epimerized derivatives of k5 polysaccharide and intermediates therein

Info

Publication number: US20120253029A1
Application number: US13/465,495
Authority: US
Inventors: Pasqua Anna Oreste; Giorgio Zoppetti
Original assignee: Glycores 2000 Srl
Current assignee: Glycores 2000 Srl
Priority date: 2002-06-18
Filing date: 2012-05-07
Publication date: 2012-10-04
Also published as: US9346893B2; US20140316129A1

Abstract

A new method is described for the oversulfation of epiK5-N-sulfate to obtain an epiK5-amine-O-oversulfate with very high sulfation degree which, by subsequent N-sulfation, provides new epiK5-N,O-oversulfate-derivatives with a sulfation degree of at least 4, basically free of activity on the coagulation parameters and useful in the cosmetic or pharmaceutical field. Also described are new low molecular weight epiK5-N-sulfates useful as intermediates in the preparation of the corresponding LMW-epiK5-N,O-oversulfate-derivatives.

Description

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of application Ser. No. 12/895,894 filed on Oct. 1, 2010, allowed; which is a continuation of application Ser. No. 10/518,302, filed on May 31, 2005, now U.S. Pat. No. 7,838,644; which is the national stage of Application No. PCT/IB2003/002338, filed on Jun. 17, 2003; claiming priority benefit of the Italian applications MI2002A001245, MI2002A001246 and MI2002A001854, filed on 18 Jun. 2002, 18 Jun. 2002 and 27 Aug. 2002, respectively.
This application also is a continuation-in-part of application Ser. No. 12/120,167, filed on May 13, 2008, pending; which is a continuation-in-part of application Ser. No. 10/518,303, filed on May 31, 2005, abandoned; which is the national stage of Application No. PCT/IB2003/002339, filed on Jun. 17, 2003; claiming priority benefit of the Italian applications MI2002A001245, MI2002A001246 and MI2002A001854, filed on 18 Jun. 2002, 18 Jun. 2002, and 27 Aug. 2002, respectively; and which is also a continuation-in-part of application Ser. No. 10/582,687, now U.S. Pat. No. 7,812,151, filed on Jun. 16, 2006, which is the national stage of Application No. PCT/IB2004/004128, filed on Dec. 15, 2004; claiming priority benefit of the Italian application MI2003A002498, filed on 17 Dec. 2003.

FIELD OF THE INVENTION

The present invention concerns new derivatives of K5 polysaccharide with a very high degree of sulfation, a process for their preparation, highly O-sulfated new intermediates useful in their synthesis and pharmaceutical compositions containing said derivatives of K5 polysaccharide as active ingredients substantially free of activity on coagulation.
In particular, the invention refers to a process for the preparation of epiK5-N,O-oversulfates starting with a K5 polysaccharide, previously N-deacetylated, N-sulfated and C5-epimerized at least 20% (epiK5-N-sulfate), through O-oversulfation in suitable conditions and subsequent N-sulfation, to said epiK5-N,O-oversulfates of antiangiogenic and antiviral activity and to new low molecular weight epiK5-N-sulfate intermediates.

BACKGROUND OF THE INVENTION

The glycosaminoglycans such as heparin, heparan sulfate, dermatan sulfate, chondroitin sulfate and hyaluronic acid are biopolymers that are industrially extracted from various animal organs.
In particular, heparin, mainly obtained by extraction from pig intestinal mucosa or from bovine lung, is a polydispersed copolymer with a molecular weight distribution from approximately 3,000 to approximately 30,000 D consisting of a mixture of chains essentially consisting of a uronic acid (glucuronic acid or iduronic acid) and of an amino sugar (glucosamine) linked by α-1→4 or β-1→4 bonds. In heparin, the uronic unit can be O-sulfated in position 2 and the glucosamine unit is N-acetylated or N-sulfated, 6-O-sulfated, and 3-O-sulfated in approximately 0.5% of the present glucosamine units.
The properties and natural biosynthesis of heparin in mammals have been described by Lindahl et al., 1986 in Lane, D. and Lindahl, U. (Editors) “Heparin. Chemical and Biological Properties; Clinical Applications”, Edward Arnold, London, Pages 159-190, by Lindahl, U, Feingold D. S, and Roden L, 1986 TIBS, 11, 221-225 and by Conrad H. E. “Heparin Binding Proteins”, Chapter 2: Structure of Heparinoids. Academic Press, 1998. The biosynthesis of heparin occurs starting with its precursor N-acetylheparosan consisting of a chain mixture consisting of the repetitive disaccharide unit glucuronyl-β-1→4-N-acetylglucosamine. Said precursor undergoes enzymatic modifications which partially hydrolyze the N-acetyl group, substituting it with an SO₃ ⁻ group, epimerize the carboxyl in position 5 of a part of the glucuronic units converting them into iduronic units and introduce O-sulfate groups to get a product which, once extracted industrially, has approximately double the number of sulfate groups in respect of the carboxyl ones per disaccharide unit. These enzymatic modifications lead, among others, to the formation of the pentasaccharide region binding to antithrombin III (ATIII), called active pentasaccharide, which is the structure necessary for the high affinity binding of heparin to the ATIII and fundamental for anticoagulant and antithrombotic activity of the heparin itself. This pentasaccharide, present inside only some of the chains which form heparin, contains a glucosamine unit sulfated in position 3 and a glucuronic acid spaced out between disaccharides containing iduronic acids.
In nature, the formation of the active pentasaccharide is made possible by the epimerization reaction of the carboxyl of a part of the glucuronic units into iduronic units by the glucuronyl-C5-epimerase (C5-epimerization) and by suitable sulfation which also leads to the introduction of a sulfate group onto the hydroxyl in position 3 of the glucosamine. More particularly, in nature the formation of the active pentasaccharide is made possible by the fact that the C5-epimerization occurs in clusters, i.e. on portions of chains, and extensively, which results in a product that contains more iduronic units than glucuronic ones. Commercial heparin, in fact, contains approximately 70% of iduronic units and 30% of glucuronic units.
Alongside the main anticoagulant and antithrombotic activities, heparin also exercises antilipemic, antiproliferative, antiviral, antitumor and antimetastatic activities, but its use as a drug is hindered by the side effects due to the anticoagulant action which can cause bleeding.

PRIOR ART

It is known that the capsular K5 polysaccharide isolated from Escherichia coli, described by Vann W. F. et al., in European Journal of Biochemistry, 1981, 116, 359-364 (“Vann 1981”), consists of a mixture of chains consisting of the repetitive disaccharide unit glucuronyl-β-1→4-N-acetylglucosamine and therefore shows the same repetitive sequence (A)
of the N-acetylheparosan precursor of heparin. The capsular K5 polysaccharide, referred to hereafter as “K5 polysaccharide” or more simply “K5”, was chemically modified by Lormeau et al. as described in U.S. Pat. No. 5,550,116 and by Casu et al. as described in Carbohydrate Research, 1994, 263, 271-284. K5-O-sulfates having antitumor, antimetastatic, antiviral, in particular anti-HIV activities are described in EP 333243 and WO 98/34958. The K5 was also modified chemically and enzymatically in order to obtain products having the same type of in vitro biological activity on coagulation as that of heparin as extracted from animal organs (extractive heparin).
The attainment of the products having an activity on coagulation of the same type as that of extractive heparin occurs by processes which imitate that occurring in nature and envisage the entire key step of C5-epimerization with D-glucuronyl C5 epimerase.
The processes described in IT 1230785, WO 92/17507, WO 96/14425 and WO 97/43317 utilize K5 as the starting material. K5 originating from fermentation is subjected to N-deacetylation followed by N-sulfation and on the K5-N-sulfate thus obtained C5-epimerization with C5-epimerase in solution, obtained either by chromatography of a solution of microsomal enzymes from mouse mastocytoma (IT 1230 785) or from bovine liver (WO 92/17507, WO 96/14425 and WO 97/43317), is performed.
The D-glucuronyl C5 epimerase from bovine liver was purified by Campbell, P. et al. in J. Biol. Chem., 1994, 269/43, 26953-26958 (“Campbell 1994”) who also supplied its composition in amino acids and described its use in solution for the transformation of a K5-N-sulfate into the corresponding 30% epimerized product, demonstrating the formation of iduronic acid by HPLC method after a total nitrous depolymerization to disaccharide.
The document WO 98/48006 describes the DNA sequence which codes for the D-glucuronyl C5 epimerase and a recombinant D-glucuronyl C5 epimerase, obtained from a recombinant expression vector containing said DNA, afterwards purified by Campbell et al. as shown by Jin-Ping L. et al. in J. Biol Chem. 2001, 276, 20069-20077 (“Jin-Ping 2001”).
The complete C5-epimerase sequence was described by Crawford B. E. et al. in J. Biol. Chem., 2001, 276 (24), 21538-21543 (Crawford 2001).
Beside the key step of C5-epimerization, and immediately after said epimerization, the most recent processes include an oversulfation step of the epiK5-N-sulfate, followed by controlled desulfation of the intermediate oversulfated product thus obtained, giving rise to N-desulfated products as it happens in the case of LMW-heparin (Naggi et al. Carbohydrate Research, 2001, 336, 283-290).
The document WO 98/42754 and the corresponding U.S. Pat. No. 6,197,943 disclose the preparation of glycosaminoglycans having high antithrombotic activity in vitro, containing at least 20% of iduronic units sulfated in position 2 and not sulfated in position 3 and at least 30% of sulfaminoglucosaminic units sulfated in position 3 and in position 6, and having a sulfates/carboxyls molar ratio ranging from 2.0 to 3.5, starting from an oversulfated substrate, and describes the oversulfation reaction for preparing said oversulfated substrate. These documents cite oversulfated, optionally epimerized K5 polysaccharide among the possible substrate, but it is difficult to infer the real structure and sulfation pattern of said oversulfated glycosaminoglycan substrate when said substrate is an oversulfated, optionally epimerized epiK5 polysaccharide. By reproducing the disclosed oversulfation reaction using an N-deacetylated/N-sulfated and C5-epimerized K5 polysaccharide as starting material, it has been ascertained that the obtained oversulfated substrate has a sulfation degree of about 2.5 and a glucosamine 3-O-sulfate content of about 30%.
The document WO 01/72848 describes a method for the preparation of N-deacetylated N-sulfated derivatives of K5 polysaccharide, at least 40% epimerized to iduronic acid in respect of the total the uronic acids, having a molecular weight from 2,000 to 30,000, containing from 25 to 50% of high affinity chains for ATIII and having an anticoagulant and antithrombotic activity expressed as HCII/anti-Xa ratio from 1.5 to 4. Said document describes the oversulfation of a 40-60% epimerized K5-N-sulfate and shows that the product obtained, whose ¹³C-NMR is illustrated, has a sulfate group content per disaccharide unit of 2-3.5. Repeating the aforesaid oversulfation under the described conditions and examining the ¹³C-NMR it was ascertained that the product obtained is actually a free amine whose 6-O-sulfate content is 80-95%, that of 3-O-sulfate on the amino sugar is 30%, but whose sulfation degree is at most 3.2. It was also observed that in the conditions of oversulfation described in WO 01/72848 a degree of sulfation higher than 3.2 was not obtained. The document US 2002/0062019 describes a process for the preparation of epiK5-N,O-sulfates, active in the control of coagulation, having a degree of sulfation from 2.3 to 2.9 and a molecular weight from 2,000 to 30,000, or from 4,000 to 8,000, or from 18,000 to 30,000. The aforesaid process involves the steps: (p-a) an N-deacetylation of K5 polysaccharide and an N-sulfation of the resulting K5-amine, (p-b) an epimerization of K5-N-sulfate, (p-c) an O-oversulfation of epiK5-N-sulfate, (p-d) a partial O-desulfation, (p-e) a selective 6-O-sulfation, (p-f) a N-sulfation of the product thus obtained, whatever product obtained at the end of one of steps (p-b)-(p-f) being optionally submitted to a depolymerization. Said document describes an epiK5N,O-sulfate having a molecular weight of 7,400, obtained by the aforesaid steps (p-a)-(p-f) followed by a nitrous depolymerization at the end of step (p-f), with a degree of sulfation from 2.3 to 2.9.
The same document also describes a fraction of K5 with a molecular weight of approximately 5,000 which can also be subjected to steps (p-a)-(p-f).
In order to standardize the terminology and render the text more comprehensible, in the present description conventional terms or expressions will be used, in the singular or plural. In particular:

- by “K5” or “K5 polysaccharide” is meant the capsular polysaccharide from Escherichia coli obtained by fermentation, i.e. a chain mixture consisting of disaccharide units (A) optionally containing a double bond at the non-reducing end as shown above, whenever prepared and purified according to the methods described in literature, in particular according to Vann 1981, according to Manzoni M. et al., Journal of Bioactive Compatible Polymers, 1996, 11, 301-311 (“Manzoni 1996”) or according to the method described in WO 01/72848 and in WO 02/068447; it is obvious for a person skilled in the art that what is shown hereafter can be applied to any N-acetylheparosan;
- by “C5-epimerase” is meant the D-glucuronyl C-5 epimerase, extractive or recombinant, in any case prepared, isolated and purified, in particular as described in Campbell 1994, in WO 98/48006, in Jin-Ping L. et al. in J. Biol Chem. 2001, 276, 20069-20077 (Jin-Ping 2001”) or in Crawford 2001;
- by K5-amine is meant at least 95% N-deacetylated K5, but in which N-acetyl groups are undetectable with a normal NMR apparatus;
- by “K5-N-sulfate” is meant at least 95% N-deacetylated and N-sulfate K5, normally 100%, since N-acetyl groups are undetectable with a normal NMR apparatus, as described hereafter;
- by “epiK5”, within the nomenclature of the glycosaminoglycans described herein, is meant the K5 polysaccharide and its derivatives in which 20-60% of the glucuronic units is C5-epimerized to iduronic units, the preparation of epiK5 itself still being unknown;
- by “epiK5-N-sulfate” is meant K5-N-sulfate in which 20-60% of the glucuronic units is C5-epimerized to iduronic units;
- by “epiK5-amine-O-oversulfate” is meant an epiK5-amine-O-sulfate with a sulfation degree of at least 3.4;
- by “epiK5-N,O-oversulfate” is meant an epiK5-amine-O-sulfate completely N-sulfated with a sulfation degree of at least 4;

In addition:

- the conventional terms and expressions herein defined above refer to a K5 as isolated after fermentation, generally with a molecular weight distribution from approximately 1,500 to approximately 50,000 with a mean molecular weight of 10,000-25,000, advantageously of 15,000-25,000;
- the conventional terms and expressions defined herein above, when preceded by the acronym “LMW” (low molecular weight), for example LMW-K5-N-sulfate, LMW-epiK5-N-sulfate, indicate low molecular weight products, obtained by fractionation or by depolymerization of K5-N-sulfate and consisting of or derived from K5-N-sulfates having a mean molecular weight from approximately 1,500 to approximately 12,000, calculated on a 100% N-sulfated product;
- the conventional terms and expressions as defined herein above, when followed by “-derivative” indicate as a whole both the derivatives from native K5 and those of low molecular weight; more particularly, the suffix “-derivative”, which follows the conventional terms and expressions as defined herein above, (a) when added to “epiK5-N-sulfate” globally designates epiK5-N-sulfates deriving from native K5 polysaccharide and fragments of said epiK5-N-sulfates obtained by its depolymerization; (b) when added to “epiK5-amine-O-oversulfate” or to epiK5-amine-N,O-oversulfate”, globally and respectively designates epiK5-amine-O-oversulfates and epiK5-amine-N,O-oversulfates deriving from epiK5-N-sulfate-derivatives; and (c) its absence means that said epiK5-N-sulfates, epiK5-amine-O-oversulfates or epiK5-amine-O-oversulfates either are derived from native K5 polysaccharide or are low molecular weight products but, in this case, the chemical name is preceded by “LMW” as defined above;
- by the term “approximately”, referring to the molecular weight, is meant the molecular weight measured by viscosimetry±the theoretical weight of a disaccharide unit, including the weight of the sodium, calculated as 461 in the case of an epiK5-N-sulfate-derivative and 806 in the case of an epiK5-N,O-oversulfated-derivative with a sulfation degree of 4.35;
- by the expression “mixture of chains in which at least 90% of said chains have the formula . . . .” indicates that 90% of said chains has a number of repetitive disaccharide units within the range of the given integers and the remaining 10% of chains may be outside said range, the chemical structure essentially being that of the given repetitive disaccharide unit;
- by the expression “preponderant species”, is meant the compound which, in the mixture constituting the LMW-epiK5-N-sulfate, the LMW-epiK5-amine-O-oversulfate or the LMW-epiK5-N,O-oversulfate, is the most represented type, determined by the peak of the curve of the molecular weight measured by HPLC;
- unless otherwise specifically stated, by “degree of sulfation” is meant the ratio SO₃ ⁻/COO⁻, expressible also as the number of sulfate groups per disaccharide unit, measured with the conductimetric method described by Casu B. et al. in Carbohydrate Research, 1975, 39, 168-176 (Casu 1975), the same utilized in WO 01/72848;
- by “conditions of O-oversulfation” is meant an extreme O-sulfation performed, for example, according to the Method C described by B. Casu et al. in Carbohydrate Research, 1994, 263, 271-284 (Casu 1994);
- by the term “alkyl” is meant a linear or branched alkyl, whereas “tetrabutylammonium” denotes the tetra-n-butylammonium group.

SUMMARY OF THE INVENTION

It has now surprisingly been found that, unlike that which occurs with the processes described in IT 1230785, WO 92/17507, WO 96/14425, WO 97/43317, WO 01/72848 and US 2002/0062019, starting with an epiK5-N-sulfate it is possible to obtain an epiK5-amine-O-oversulfate with a greater degree of sulfation than every other epiK5-amine-O-sulfate described in literature, for example in WO 01/72848, by preparing a tertiary or quaternary organic base salt of said epiK5-N-sulfate taking care to let the reaction mixture to stand for a time period of 30-60 minutes maintaining the pH at approximately 7 with the same organic base and then treating the salt obtained with an O-sulfation agent in the conditions of O-oversulfation. Said epiK5-amine-O-oversulfates with a very high degree of sulfation are characterized by a high content, at least 40%, advantageously from 50% to 80%, in glucosamine 3-O-sulfate, not obtainable according to the known oversulfation methods.
Subjecting the epiK5-amine-O-oversulfates thus obtained to N-sulfation, new epiK5-N,O-oversulfates are obtained which, unlike the products described in IT 1230785, WO 92/17507, WO 96/14425, WO 97/43317, WO 01/72848 and US 2002/0062019, are free of activity on coagulation and useful for the preparation of medicines, particularly pharmaceutical compositions of antiangiogenic and antiviral activity or of cosmetic compositions.
By depolymerization with nitrous acid of said epiK5-N,O-oversulfates new LMW-epiK5-N,O-oversulfates are obtained, free of activity on coagulation and with antiangiogenic and antiviral activity.
In preparing N,O-sulfate N-deacetylated derivatives of K5 polysaccharide, at least 40% epimerized of iduronic acid in respect of the total of the uronic acids and having low molecular weight according to the method described in WO 01/72848, it was ascertained that the depolymerization of the product of high molecular weight obtained at the end of the final N-sulfation step of the process can give varying results since it generally produces some depolymerized products showing much lower activity, than that of the high molecular weight products from which they arise, on all the coagulation parameters. It is assumed this takes place because degradation with nitrous acid is influenced by the presence of the sulfate groups. In particular the sulfates in position 3 of the glucosamine result in heterogeneous products, as described by Nagasawa et al. in Thrombosis Research, 1992, 65, 463-467 (Nagasawa 1992).
It has now been found that subjecting an epiK5-N-sulfate, free of NH₂and acetyl groups and having an iduronic acid content of 20-60%, advantageously 40-60%, preferably around 50% in respect of the total of uronic acids, to depolymerization, for example to nitrous depolymerization, LMW-epiK5-N-sulfates free of NH₂and acetyl groups are obtained which constitute new valuable intermediates for the preparation of LMW-epiK5-N,O-oversulfates having a high degree of activity on different biological parameters, with or without activity on coagulation parameters.
In particular, it was found that it is possible to depolymerize an epiK5-N-sulfate in order to obtain new LMW-epiK5-N-sulfates of mean molecular weight of from approximately 2,000 to approximately 4,000, more particularly specific LMW-epiK5-N-sulfates consisting of mixtures in which the predominant compound is a decasaccharide or a dodecasaccharide or a tetradecasaccharide. Also these LMW-epiK5-N-sulfates, otherwise unobtainable, have interesting biological properties and are useful intermediates for the preparation of LMW-epiK5-N,O-oversulfated having antiviral and/or antiangiogenic activity and, surprisingly, substantially free of activity on coagulation.
LMW-epiK5-N-sulfates which are free of NH₂and of acetyl groups are novel glycosaminoglycans.
By subjecting a LMW-epiK5-N-sulfate to the aforesaid method of salt formation with a tertiary or quaternary organic base, taking care to let the reaction mixture to stand for a time period of 30-60 minutes while maintaining the pH at approximately 7 with the same organic base and then treating the obtained salt with an O-sulfation agent under the conditions of O-oversulfation, new LMW-epiK5-amine-O-oversulfates are obtained. By subjecting the LMW-epiK5-amine-O-oversulfate to N-sulfation, new N-sulfated and O-oversulfated derivatives (LMW-epiK5-N,O-oversulfates) are obtained, substantially free of activity on coagulation and exhibiting antiviral and/or antiangiogenic activity, useful for the preparation of pharmaceutical or cosmetic compositions.
These LMW-epiK5-N-sulfates are obtained starting from a K5-N-sulfate by an epimerization reaction using an isolated and purified recombinant C5-epimerase, immobilized on a solid support, at a temperature of approximately 30° C. and at a pH of approximately 7 for 12-24 hours in the presence of a bivalent cation selected among calcium, magnesium, barium and manganese and a subsequent nitrous depolymerization reaction of the epimerized product thus obtained, or vice versa.
Surprisingly, from observations made on the course of the epimerization reaction in the aforesaid conditions, it is possible to assume that, contrary to that occurs in nature in the biosynthesis of heparin, ordinary and not “cluster” type C5-epimerization of the substrate occurs every 2 glucuronic acid units which leads to epi-K5-N-sulfate-derivatives characterized by a repetitive tetrasaccharide unit consisting of two glucosamine units separated by a glucuronic unit and followed by an iduronic unit or vice versa.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 shows the ¹³C-NMR spectrum of the epiK5-amine-O-oversulfate of Example 6 which is characterized by a content in glucosamine 3-O-sulfate of 70%.

DETAILED DESCRIPTION

Thus, according to one of its aspects, the present invention provides a process for the preparation of epiK5-N,O-oversulfate-derivatives, which comprises
(a) treating an epiK5-N-sulfate-derivative, in acidic form, with a tertiary or quaternary organic base, letting the reaction mixture to stand for a time period of 30-60 minutes at a pH of approximately 7 by addition of said base and isolating its salt with said organic base;
(b) treating said salt of the epiK5-N-sulfate-derivative with an O-sulfation reagent in the conditions of O-oversulfation;
(c) treating the epi-K5-amine-O-oversulfate-derivative thus obtained with a reagent of N-sulfation and isolating the epiK5-N,O-oversulfate-derivative thus obtained.
Generally, the epiK5-N,O-oversulfate-derivative is isolated in sodium salt form and optionally said sodium salt is transformed into another chemically or pharmaceutically acceptable salt.
In this context, the term “chemically acceptable” refers to a cation usable in chemical synthesis, such as the sodium, ammonium, tetraalkylammonium ion, or for the purification of the product, whereas “pharmaceutically acceptable” is self-explanatory.
Advantageous cations are those derived from alkaline metals, alkaline-earth metals, ammonium, tetra(C₁-C₄)alkylammonium, aluminum and zinc. Preferred cations are the sodium, calcium and tetrabutylammonium ions.
According to an advantageous embodiment, step (a) is carried out by passing a solution of the sodium salt of epiK5-N-sulfate-derivative having a mean molecular weight from approximately 1,000 to approximately 25,000, advantageously from approximately 1,500 to approximately 25,000, i.e. of K5 polysaccharide, previously N-deacetylated, N-sulfated preferably 100%, 20-60% C5-epimerized and optionally depolymerized with nitrous acid, through an acid ionic exchange resin, for example of the type IR-120 H⁺, collecting the eluate, containing the starting epiK5-N-sulfate-derivative in acidic form and also including the washing water of the resin, and neutralizing the eluate with tertiary or quaternary organic base, preferably with an aqueous solution of tetrabutylammonium (TBA) hydroxide. The solution is left to stand for 1 hour, maintaining its pH at 7 by addition of the same base, and the tertiary amine or quaternary ammonium salt of said epiK5-N-sulfate-derivative thus obtained is isolated by lyophilization.
In step (b), the O-oversulfation occurs by treating the salt thus obtained with an excess of O-sulfating agent and working at a temperature from 20 to 70° C. for a time period of up to 24 hours in an aprotic polar solvent according to the known technique.
Advantageously, said tertiary or quaternary organic base salt, preferably the TBA salt, of the epiK5-N-sulfate-derivative, i.e. of K5 polysaccharide, previously N-deacetylated, N-sulfated preferably 100%, and 20-60% C5-epimerized and optionally depolymerized with nitrous acid, having a mean molecular weight from approximately 1,000 to approximately 25,000, advantageously from approximately 1,500 to approximately 25,000 as isolated in step (a), is dissolved in dimethyl formamide and treated with 2-10 moles of an O-sulfation reagent for every free hydroxyl at a temperature of 40-60° C. for 10-20 hours. As an O-sulfation reagent is advantageously used the pyridine.SO₃adduct in a quantity of 2.5-5 moles, preferably 2.5-4 moles per free hydroxyl per disaccharide and the reaction is advantageously carried out at 50-60° C., preferably at 55° C., overnight. The product obtained upon termination of the reaction, is isolated by addition of 0.1-1 volume of water and neutralization, preferably with sodium hydroxide, precipitation with a saturated sodium chloride solution in acetone, filtration and possible ultrafiltration.
The product thus obtained is generally the sodium salt of an epiK5-amine-O-oversulfate-derivative having a glucosamine-3-O-sulfate content of at least 40%, preferably from 50% to 80% and an iduronic acid content of 20-60% of the total of the uronic acids, having a mean molecular weight from approximately 3,500 to approximately 40,000, advantageously from approximately 4,500 to approximately 40,000 and a sulfation degree of at least 3.4, advantageously of at least 3.5, more advantageously from 3.55 to 4, preferably from 3.55 to 3.8. The sodium salt thus obtained can be converted into another salt. By way of example an exchange with the calcium ion can be performed working with ultrafiltration membranes.
In Step©, the epiK5-amine-O-oversulfate-derivative with a very high degree of sulfation is N-sulfated using the known N-sulfation methods in literature.
In practice, the N-sulfation is performed by treating an aqueous solution containing the epiK5-amine-O-oversulfated-derivative originating from step (b) with sodium carbonate and an agent of N-sulfation, for example a tri(C₁-C₄)alkylamine.SO₃or pyridine.SO₃adduct, maintaining the mixture at 30-50° C. for 8-24 hours and isolating the desired epiK5-N,O-oversulfate-derivative, for example by diafiltration. Optionally the step of N-sulfation is repeated until obtaining more than 95% substitution, preferably complete.
The new epiK5-N,O-oversulfate-derivatives thus obtained are generally in their sodium salt form. Said sodium salt can be converted into another chemically or pharmaceutically acceptable salt. Particularly advantageous salts are those of alkaline metals, alkaline-earth metals, of ammonium, tetra(C₁-C₄)alkylammonium, aluminum and zinc. Preferred are the salts of sodium, calcium and tetrabutylammonium.
The starting epiK5-N-sulfates subjected to step (a) of the process of the present invention are derived from a K5 polysaccharide, previously N-deacetylated, N-sulfated virtually 100%, and 20-60% C5-epimerized, advantageously 40-60%, and optionally depolymerized with nitrous acid, having a mean molecular weight from approximately 1,000 to approximately 25,000, advantageously from approximately 1,500 to approximately 25,000. Preferably, said starting material is an epi-K5-N-sulfate having a mean molecular weight between 10,000 and 25,000 or a LMW-epiK5-N-sulfate having a mean molecular weight from approximately 1,000 to approximately 12,000, advantageously from approximately 1,000 to approximately 10,000, preferably between approximately 1,500 and approximately 8,000.
The epiK5-N-sulfates, prepared by C5-epimerization of K5-N-sulfates, are well known in literature and widely described for example in WO 92/17507, WO 01/72848, WO 98/14425, WO 97/43317 or US 2002/0062019. Their preparation by C-5 epimerization of the glucuronic unit of K5-N-sulfate with a D-glucuronyl C5 epimerase was described in documents cited herein above.
A LMW-epiK5-N-sulfate having an iduronic unit content of approximately 20%, obtained by N-deacetylation, N-sulfation and C5-epimerization of a fraction of K5 having a mean molecular weight of 5,000 is described in WO 92/17507. However such described LMW-epiK5-N-sulfate contains a considerable amount, at least 30%, of acetyl groups.
An epiK5-N-sulfate with an iduronic acid content of 40-60%, particularly advantageous as a starting material, is that obtained by epimerization of a K5-N-sulfate virtually free of acetyl groups, in turn prepared from particularly pure K5, in particular not containing lipophilic substances, described in WO 02/068477. According to a preferential embodiment, a K5-N-sulfate obtained from a K5 free of lipophilic substances like that described in WO 02/068477 is used for the epimerization and the C5 epimerization is performed with a D-glucuronyl C5-epimerase that is isolated, purified and immobilized on a solid support, at a pH of approximately 7, at a temperature of approximately 30° C. and for a time period of 12-24 hours in the presence of at least one bivalent ion selected among calcium, magnesium, barium and manganese
The LMW-epiK5-N-sulfates having a higher content of iduronic units, in particular 40-60%, preferably 50-55%, are new, particularly advantageous products as starting materials in the preparation of LMW-epiK5-N,O-oversulfate-derivatives.
The LMW-epiK5-N-sulfates as shown above are prepared by a process characterized in that a K5-N-sulfate is subjected, in any one order,
(i) to C5-epimerization with a D-glucuronyl C5-epimerase that is isolated, purified and in solution or immobilized on a solid support, at a pH of approximately 7, at a temperature of approximately 30° C. and for a time period of 12-24 hours in the presence of at least one bivalent ion selected among calcium, magnesium, barium and manganese; and
(ii) to a nitrous depolymerization optionally followed by reduction, normally with sodium borohydride.
The expression “in any order” shows that the process can be indifferently carried out both in the direction (i)-(ii), i.e. in the sequence shown above, as well as in reverse direction, i.e. also in the direction (ii)-(i), subjecting the K5-N-sulfate at first to the nitrous depolymerization reaction, optionally followed by reduction with sodium borohydride, and afterwards to C5-epimerization in the aforesaid conditions. The preferred order is in the direction 1→2. The sequence (ii)-(i) is preferably utilized starting with LMW-K5-N-sulfates having a mean molecular weight of more than 4,000, preferably starting with approximately 6,000. For example, one can determine the amount of sodium nitrite which, starting with 1 g of epiK5-N-sulfate, allows the attainment of a LMW-epiK5-N-sulfate with a molecular weight of more than 4,000, in particular of at least 6,000, so as to obtain useful intermediates for the preparation of LMWepiK5-N,O-oversulfates. In fact, in this case, in step (ii) the percentage of optimum epimerization is obtained.
According to a preferential aspect of the invention, the C5-epimerase is immobilized on an inert solid support.
The C5-epimerase, preferably recombinant, isolated and purified for example according to Campbell 1994, WO 98/48006, Jin-Ping 2001 or Crawford 2001, is immobilized on an inert support in the presence of the substrate, i.e. in the presence of starting K5-N-sulfate-derivative or in the presence of LMW-K5-N-sulfate, advantageously having a mean molecular weight of more than 4,000, preferably of at least 6,000. The immobilization is performed according to conventional methods, for example as described in WO 01/72848.
The C-5 epimerization reaction is carried out by recirculating 20-1,000 ml of a 25 mM HEPES solution at a pH of approximately 7 containing 0.001-10 g of substrate (K5-N-sulfate or LMW-K5-N-sulfate, preferably with a molecular weight of more than 4,000, in particular of at least 6,000) and a cation selected among calcium, magnesium, barium and manganese at a concentration of between 10 and 60 mM through a column containing from 1.2×10⁷to 3×10¹¹cpm of the immobilized enzyme, maintaining the pH at approximately 7 at approximately 30° C., at a flow of 30-220 ml/hour for a time period of 12-24 hours, advantageously 15-24 hours.
Preferably said solution is recirculated at a flow of approximately 200 ml/hour overnight (15-20 hours). The product obtained is purified and separated according to known methods, for example by ultrafiltration and precipitation with ethanol. The product thus obtained is either consisting of epiK5-N-sulfate (and in such case is dissolved in water and subjected to depolymerization) or LMW-epiK5-N-sulfate (in such case it constitutes the end product). The percentage of epimerization, in practice the amount of iduronic units as regards the glucuronic ones, is calculated using ¹H-NMR according to the method described in WO 96/4425.
The nitrous depolymerization reaction is carried out according to known methods used for the depolymerization of heparin, for example according to the method described in EP 37319, in WO 82/03627 or according to the method for the depolymerization of a K5-N-sulfate described in EP 544592, but starting from a K5-N-sulfate or an epiK5-N-sulfate containing from 0 to no more than 10%, preferably no more than 5%, of acetyl groups. Preferably, the depolymerization, performed with sodium nitrite and hydrochloric acid on an epiK5-N-sulfate virtually free of acetyl groups, is followed by in situ reduction with sodium borohydride.
In practice, a cold aqueous solution of epiK5-N-sulfate is brought to acid pH (approximately 2) with hydrochloric acid and, still cold, treated with sodium nitrite maintaining the temperature (approximately 4° C.) and the pH (approximately 2) constant and, upon termination of depolymerization (approximately 15-30 minutes) the solution is neutralized with sodium hydroxide and treated, still at approximately 4° C., with an aqueous solution of sodium borohydride. Upon termination of the reduction (approximately 4 hours) the excess sodium borohydride is destroyed with hydrochloric acid, the solution is neutralized with sodium hydroxide and the depolymerized (and reduced) product is isolated according to known methods, for example by straightforward precipitation with ethanol or acetone. The product obtained upon termination of depolymerization can be either a LMW-epiK5-N-sulfate (in such case it constitutes the end product) or a LMW-K5-N-sulfate (and in such case is directly subjected to C5-epimerization as shown herein above, after isolation or also in solution without being previously isolated, in particular when it has a mean molecular weight of more than 4,000, preferably of at least 6,000, or is utilized to prepare antiangiogenic and antiviral LMW-K5-N,O-oversulfates). By appropriately controlling the depolymerization reaction, in particular using different amounts of sodium nitrite, are obtained LMW-K5-N-sulfates or LMW-epiK5-N-sulfates having a mean molecular weight in the entire interval from approximately 1,500 to approximately 12,000, advantageously from approximately 1,500 to approximately 10,000, preferably from approximately 1,500 to approximately 7,500, calculated at the ¹³C-NMR spectrum through the integration of the signal attributed to the C2 of 2,5-anhydromannitol with that of the anomeric carbon of the glucosamine inside the polysaccharide chain. According to a general manner of procedure, starting for example from 1 g of epiK5-N-sulfate, the starting product is dissolved in 100-200 ml of deionized water and thermostated at 4° C. Then an amount of sodium nitrite is added so as to obtain the desired mean molecular weight, for example from approximately 2,000 to approximately 4,000. Therefore, starting from an epiK5-N-sulfate having a molecular weight of 20,000 measured with the HPLC method equipped with a BioRad BioSil 250 column and using a heparin standard of known molecular weight, the preparation of such LMW-epiK5-N-sulfate will require the addition of 330 to 480 mg of sodium nitrite dissolved in a 0.2% aqueous solution to the solution containing the epiK5-N-sulfate kept at 4° C., and previously brought to pH 2.2 through the addition of 1 N HCl. It is left to react under slow agitation for 20-40 minutes at 4° C., then it is neutralized with 1 N NaOH. The product obtained is brought to room temperature and treated with reducing agent such as for example sodium borohydride (250-500 mg dissolved in 50-100 ml of water) and left to react for 4-8 hours. The excess sodium borohydride is eliminated by bringing the pH to 5-5.5 with 0.1 N HCl and letting to stand for a further 2-4 hours. In the end the solution is neutralized with 0.1 N NaOH and the product is recovered by precipitation with acetone or ethanol after concentrating the product by evaporation at reduced pressure.
Similarly, the amount of sodium nitrite can be determined which, starting from 1 g of K5-N-sulfate or epiK5-N-sulfate, allows the attainment of a LMW-K5-N-sulfate or a LMW-epiK5-N-sulfate with a mean molecular weight from approximately 4,000 to approximately 12,000, advantageously from approximately 4,000 to approximately 7,500, in particular of 6,000-7,500.
The LMW-epiK5-N-sulfate thus obtained, with an iduronic acid content from 20% to 60%, advantageously from 40% to 60%, preferably of 50-55% and virtually free of NH₂and N-acetyl groups, having a mean molecular weight from approximately 1,500 to approximately 12,000, advantageously from approximately 1,500 to approximately 10,000, preferably from approximately 1,500 to approximately 7,500 and their chemically or pharmaceutically acceptable salts are new products useful as particularly interesting starting materials in the preparation of LMW epiK5-N,O-oversulfates, but are also themselves useful as active ingredients of pharmaceutical or cosmetic compositions and represent an additional aspect of the present invention.
Advantageously, the starting materials in the preparation of the epiK5-N,O-oversulfate-derivatives of the present invention are epiK5-N-sulfate-derivatives consisting of a mixture of chains in which at least 90% of said chains have the formula
in which the uronic units are 20-60% consisting of iduronic acid, n is an integer from 2 to 100, advantageously from 3 to 100 and the corresponding cation is chemically or pharmaceutically acceptable. More advantageously, said starting epiK5-N-sulfate-derivatives consist of a chain mixture in which at least 90% of said chains have the formula I in which the uronic units are 40-60% consisting of iduronic acid, n is an integer from 2 to 100, advantageously from 3 to 100 and the corresponding cation is chemically acceptable. Preferred starting materials are LMW-epiK5-N-sulfates as shown above, consisting of a chain mixture in which at least 90% of said chains have the formula I in which the uronic units are 20-60% advantageously 40-60%, preferably 50-55%, those of iduronic acid, n is an integer from 2 to 20, advantageously from 3 to 15 and the corresponding cation is chemically acceptable.
In practice, said preferred LMW-epiK5-N-sulfates consist of a mixture of chains in which at least 90% of said chains have the formula I′
in which 20-60%, advantageously 40-60%, preferably 50-55% of the uronic units are those of iduronic acid, q is an integer from 2 to 20, advantageously from 3 to 15, and the corresponding cation is chemically or pharmaceutically acceptable.
In this context, the term “chemically” refers to a cation usable in chemical synthesis, such as sodium, ammonium, tetra(C₁-C₄)alkylammonium ions, or for the purification of the product. Advantageous cations are those derived from alkaline metals, alkaline-earth metals, ammonium, tetra(C₁-C₄)alkylammonium, aluminum and zinc. Preferred cations are the sodium, calcium and tetrabutylammonium ions.
Particularly interesting are the LMW-epiK5-N-sulfates consisting of a mixture of chains in which at least 90% of said chains have the formula I′ herein above, obtained by nitrous depolymerization of the corresponding epiK5-N-sulfates shown above and subsequent possible reduction for example with sodium borohydride. Among these, are preferred the LMW-epiK5-N-sulfates consisting of a mixture of chains in which the preponderant species has the formula I′a
in which the uronic units are 60-40% consisting of glucuronic acid and 40% to 60% of iduronic acid, p is an integer from 4 to 8. The mean molecular weight of these products is from approximately 2000 to approximately 4000 and the corresponding cation is chemically or pharmaceutically acceptable.
The origin of these epiK5-N-sulfates from a step of nitrous depolymerization involves, at the reducing end of the majority of the chains in said chain mixture, the presence of a 2,5-anhydromannose unit or, in the case of reduction with for example sodium borohydride, of 2,5-anhydromannitol of structure (a)
in which X represents a formyl group or a hydroxymethyl group. Therefore, the reducing end of the majority (60-70% of the chains) is actually represented by the structure (b)
in which X is as defined above.
The presence of the structure (a) does not have any influence on the chemical characteristics of the epiK5-N-sulfates and their derivatives since any sulfation would lead to a possible introduction of one or two sulfate groups which would not however significantly move the sulfation degree of the O-sulfated derivatives. It is however preferable that the nitrous depolymerization is followed by reduction for example with sodium borohydride since, according to the process of the present invention, said LMW-epiK5-N-sulfates are subjected to sulfation and acylation reactions whose influence, of the 2,5-anhydromannose radical of structure (a), is unknown on the formyl group in which X represents formyl. Besides, the presence of structure (a) does not influence the biological activity of the products, as demonstrated by Østergaard P. B. et al. in Thrombosis Research, 1987, 45, 739-749 (Østergaard 1987) for the heparins of low molecular weight.
Particularly advantageous LMW-epiK5-N-sulfates according to the present invention are consisting of chain mixtures in which the preponderant species is a compound of formula I′b
in which X is formyl or, preferably, hydroxymethyl, m is 4, 5 or 6, the corresponding cation is one chemically or pharmaceutically acceptable ion and the glucuronic and iduronic units are present alternately, starting with a glucuronic or iduronic unit. In such case the glucuronic/iduronic ratio is from 45/55 to 55/45, i.e. approximately 50/50.
The use of the C5-epimerase, preferably recombinant, preferably immobilized on a solid support under the conditions shown above therefore allows an epimerization of K5-N-sulfate-derivatives into epiK5-N-sulfate-derivatives in a regular manner and not a “cluster” epimerization as it occurs in nature.
Thus, according to another of its aspects, the present invention provides the use of the isolated and purified C5-epimerase, for the conversion of a K5-N-sulfate-derivative into a corresponding epiK5-N-sulfate-derivative characterized by a repetitive tetrasaccharide unit consisting of two glucosamine units separated by a glucuronic unit and followed by an iduronic unit or separated by an iduronic unit and followed by a glucuronic unit.
Said epimerization occurs optimally if carried out on a K5-N-sulfate-derivative having a mean molecular weight of more than 4,000, preferably from 6,000 to 7,500.
According to the present invention, the starting epiK5-N-sulfate-derivatives, preferably 100% N-sulfated (in particular the epiK5-N-sulfate-derivatives consisting of mixture of chains in which at least 90% of said chains have the formula I or I′ or in which the preponderant species has the formula I′a or I′b where X is hydroxymethyl), are subjected to the aforesaid steps (a) and (b), upon termination of which are isolated the corresponding, new epiK5-amine-O-oversulfate-derivatives, in which the amine is not substituted, normally in sodium salt form, which can be transformed into another chemically or pharmaceutically acceptable salt. Particularly advantageous salts are those of alkaline metals, alkaline-earth metals, ammonium, tetra(C₁-C₄)alkylammonium, aluminum and zinc and, among these, the salts of sodium, calcium and tetrabutylammonium are preferred.
Thus, according to another of its aspects, the present invention provides new epiK5-amine-O-oversulfate-derivatives and their chemically or pharmaceutically acceptable salts, obtainable by a process which comprises
(a) treating an epiK5-N-sulfate-derivative, in acidic form, with a tertiary or quaternary organic base, letting the reaction mixture to stand for a time period of 30-60 minutes at a pH of approximately 7 and isolating the corresponding organic base salt of said epiK5-N-sulfate;
(b) treating said tertiary amine or quaternary ammonium salt of said epiK5-N-sulfate-derivative with an O-sulfation agent in the conditions of O-oversulfation and isolating the epiK5-amine-O-oversulfate-derivative.
The process consisting of steps (a) and (b) above, which produces epiK5-amine-O-oversulfate-derivatives having a glucosamine 3-O-sulfate content of at least 40%, represents a further embodiment of the present invention. According to this advantageous process, the complete formation of the tertiary amine or quaternary ammonium salt of the epiK5-N-sulfate-derivative of step (a) allows a deeper oversulfation in subsequent step (b) with consequent obtainment of epiK5-amine-O-oversulfate-derivatives containing a very high content, from 40% to 80%, in glucosamine-3-O-sulfate groups, with a sulfation degree higher than 3.4, preferably from 3.55 to 3.8, heretofore impossible to be attained.
Thus it is a further object of the present invention to provide a process for the preparation of epiK5-amine-O-oversulfate-derivatives having a glucosamine 3-O-sulfate content of at least 40%, which comprises
(a) treating an epiK5-N-sulfate-derivative, in acidic form, with a tertiary or quaternary organic base, letting the reaction mixture to stand for a time period of 30-60 minutes at a pH of approximately 7 and isolating the corresponding organic base salt of said epiK5-N-sulfate; and
(b) treating said tertiary amine or quaternary ammonium salt of said epiK5-N-sulfate-derivative with an O-sulfation agent in the conditions of O-oversulfation and isolating the epiK5-amine-O-oversulfate-derivative.
As, set forth above, the epiK5-amine-O-oversulfate-derivatives obtained at the end of the process are normally isolated as sodium salt, said salt being converted into another chemically or pharmaceutically acceptable salt, as described above and also below, for example by making an exchange with the calcium ion working with ultrafiltration membranes, or also by passing an aqueous solution of the sodium salt on a column containing a cationic exchange resin such as Amberlite® IR-120⁺ and treating the eluate with an inorganic or organic base for example with the hydroxide of another alkaline or alkali-earth metal or with a tertiary or quaternary organic base such as tributylamine, pyridine, or tetrabutylammonium hydroxide.
Using, as advantageous starting materials of step (a), epiK5-N-sulfate-derivatives consisting of a mixture of chains in which at least 90% of said chains has the aforesaid formula I, in which the uronic units are 20-60% consisting of iduronic acid, n is a integer from 3 to 100 and the corresponding cation is chemically or pharmaceutically acceptable, at the end of step (b) an epiK5-amine-O-oversulfate-derivative is obtained consisting of a mixture of chains in which at least 90% of said chains have the formula II
in which the uronic units are 20-60% consisting of iduronic acid, n is an integer from 2 to 100, preferably from 3 to 100, R, R′ and R″ are hydrogen or SO₃ ⁻, for a sulfation degree of at least 3.4, advantageously of at least 3.5, more advantageously from 3.55 to 4, preferably from 3.55 to 3.8 and the corresponding cation is chemically or pharmaceutically acceptable.
These epiK5-amine-O-oversulfate-derivatives with a very high degree of sulfation are new products useful as intermediates in the preparation of their N-sulfate or N—(C₂-C₄)acylated derivatives substantially free of activity on the coagulation parameters, but having other interesting pharmacological properties.
Advantageous epiK5-amine-O-oversulfate-derivatives with a very high degree of sulfation consist of a mixture of chains in which at least 90% of said chains have the formula II in which the uronic units are 40-60% consisting of iduronic acid, n is an integer from 2 to 100, preferably from 3 to 100, with a mean molecular weight from approximately 2,000 to approximately 40,000, advantageously from approximately 4,500 to approximately 40,000, R is at least 40%, preferably 50-80% SO₃ ⁻, R′ and R″ are both SO₃ ⁻ or one is hydrogen and the other is 5-10% SO₃ ⁻ in monosulfate glucuronic acid and 10-15% SO₃ ⁻ in monosulfate iduronic acid, the degree of sulfation is more than 3.4, advantageously of at least 3.5, more advantageously from 3.55 to 4, preferably from 3.55 to 3.8, and the corresponding cation is chemically or pharmaceutically acceptable.
Preferred epiK5-amine-O-oversulfate-derivatives with a very high degree of sulfation are LMW-epiK5-amine-O-oversulfates consisting of a mixture of chains in which at least 90% of said chains have the formula II in which 40-60%, preferably 50-55%, of the uronic units are those of iduronic acid, R is at least 40%, advantageously 50-80%, preferably approximately 65% SO₃ ⁻, R′ and R″ are both SO₃ ⁻ or one is hydrogen and the other is 5-10% SO₃ ⁻ in glucuronic acid and 10-15% SO₃ ⁻ in iduronic acid, n is an integer from 2 to 20, advantageously from 3 to 15, with a mean molecular weight from approximately 4,000 to approximately 8,000 and the corresponding cation is chemically or pharmaceutically acceptable.
In practice, said preferred LMW-epiK5-amine-O-oversulfates are consisting of a mixture of chains in which at least 90% of said chains have the formula II′
in which the uronic units are 20-60% consisting of iduronic acid, q is an integer from 2 to 20, advantageously from 3 to 15, R, R′ and R″ are hydrogen or SO₃ ⁻, for a sulfation degree of at least 3.4, advantageously of at least 3.5, more advantageously from 3.55 to 4, preferably from 3.55 to 3.8, and the corresponding cation is a chemically or pharmaceutically acceptable ion.
Among these LMW-epiK5-amine-O-oversulfates are preferred those consisting of a mixture of chains in which the preponderant species has the formula II′ a
in which the uronic units are 20-60% consisting of iduronic acid, p is an integer from 4 to 8, R, R′ and R″ are as defined above, the degree of sulfation is at least 3.4, advantageously of at least 3.5, more advantageously from 3.55 to 4, preferably from 3.55 to 3.8 and the corresponding cation is chemically or pharmaceutically acceptable.
The origin of the new LMW-epiK5-amine-O-oversulfates from LMW-epiK5-sulfates obtained by nitrous depolymerization and subsequent reduction with, for example, sodium borohydride, involves, at the reducing end of the majority of the chains in said chain mixture, the presence of a 2,5-anhydromannitol sulfated unit of structure (a′)
in which R represents hydrogen or SO₃ ⁻.
Thus, the reducing end of the majority of the chains in said chain mixture is represented by the structure (b′)
in which the uronic unit can be glucuronic or iduronic.
Among the aforesaid new LMW-epiK5-amine-O-oversulfates, are preferred those consisting of chain mixtures in which the preponderant species is a compound of formula II′b
in which the uronic units are 40-60% consisting of iduronic acid, m is 4, 5 or 6, R, R′ and R″ are hydrogen or SO₃ ⁻, X″ is OH or OSO₃ ⁻, for a sulfation degree of at least 3.4, advantageously of at least 3.5, more advantageously from 3.55 to 4, preferably from 3.55 to 3.8, the iduronic units being present alternately, starting with a glucuronic or iduronic unit, and the corresponding cation is a chemically or pharmaceutically acceptable ion.
All these epiK5-amine-O-oversulfate-derivatives with a very high degree of sulfation are new products which are useful intermediates for the preparation of the new N-substituted epiK5-amine-O-oversulfate-derivatives and therefore represent an additional aspect of the present invention.
In particular, according to another of its aspects, the invention concerns the use of the aforesaid epiK5-amine-O-oversulfate-derivatives with a very high degree of sulfation for the preparation of new N-substituted, in particular N-sulfated or N-acylated, epiK5-amine-O-oversulfate-derivatives.
At the end of Step© of the process of the present invention, consisting of an N-sulfation of the epiK5-amine-O-oversulfate-derivatives obtained at the end of step (b) (in particular the epiK5-amine-O-oversulfate-derivatives consisting of chain mixtures in which at least 90% of said chains have the formula II or II′ or in which the preponderant species has the formula II′a or II′b), epiK5-N,O-oversulfate-derivatives are obtained whose iduronic acid content is 20-60% of the total of the uronic acids and whose sulfation degree is at least 4, preferably from 4 to 4.6.
Thus, according to another of its aspects, the present invention provides new N-deacetylated derivatives of K5 polysaccharide, O-sulfated and N-sulfated, C5-epimerized to iduronic acid in at least 20% of the total of the uronic units, having a mean molecular weight from approximately 2,000 to approximately 45,000, a sulfation degree of at least 4, said derivatives being substantially inactive on the coagulation parameters.
Similarly to that stated above, said new derivatives are, as a whole, denoted by the general term “epiK5-N,O-oversulfate-derivatives”, independently of their molecular weight.
In particular, the mean molecular weight is between approximately 2,000 to approximately 45,000 since said derivatives originate either from an epi-K5-N-sulfate obtained by N-deacetylation and N-sulfation of K5 by fermentation or by the nitrous depolymerization of the latter. By controlling said nitrous depolymerization it is possible to obtain low molecular weight derivatives in virtually all the aforesaid interval. However, for use of the derivatives of the present invention as pharmaceutical or cosmetic products it is advantageous to prepare low molecular weight derivatives, with a mean molecular weight from approximately 2,000 to approximately 16,000, advantageously from approximately 3,500 to approximately 13,000 with a molecular weight distribution of between approximately 1,000 and approximately 15,000, preferably from approximately 4,500 to approximately 9,000, with a molecular weight distribution from approximately 2,000 to approximately 10,000, or of high molecular weight derivatives, originating from the unfractionated K5, with a mean molecular weight of between approximately 20,000 and approximately 45,000, with a molecular weight distribution from approximately 2,000 to approximately 70,000.
In the epiK5-N,O-oversulfate-derivatives of the present invention the degree of sulfation is very high, preferably from 4 to 4.6, the nitrogen of the glucosamine being virtually 100% sulfated. Besides, the epiK5-N,O-oversulfate-derivatives are 100% 6-O-sulfated and 50-80% 3-O-sulfated in their glucosamine units, 5-10% 3-O-monosulfated in glucuronic units, 10-15% O-monosulfated in iduronic units and 2.3-di-O-sulfated in the remaining uronic units, considering that the degree of sulfation is at least 4.
Advantageous epiK5-N,O-oversulfate-derivatives according to the present invention are obtained through epiK5-amine-O-oversulfate-derivatives in turn prepared from epiK5-N-sulfate-derivatives consisting of a chain mixture in which at least 90% of said chains has the aforesaid formula I, in which the uronic units are 20-60% consisting of iduronic acid, n is an integer from 2 to 100, advantageously from 3 to 100 and the corresponding cation is chemically or pharmaceutically acceptable.
In such case, the new epiK5-N,O-oversulfate-derivatives are consisting of chain mixtures in which at least 90% of said chains have the formula III
in which the uronic units are 20-60% consisting of iduronic acid, n is an integer from 2 to 100, preferably from 3 to 100, R, R′ and R″ are hydrogen or SO₃ ⁻, Z is SO₃ ⁻, the degree of sulfation is at least 4, preferably from 4 to 4.6 and the corresponding cation is chemically or pharmaceutically acceptable.
Said cations are advantageously those of alkaline metals, alkaline-earth metals, ammonium, tetra(C₁-C₄)alkylammonium, aluminum and zinc and, among these, preferably the salts of sodium, calcium and tetrabutylammonium.
Among the aforesaid new epiK5-amine-N,O-oversulfate-derivatives, those consisting of chain mixtures in which at least 90% of said chains has the aforesaid formula III in which R is SO₃ ⁻ in 50%-80%, preferably in approximately 65% of said chains and the degree of sulfation is at least 4, advantageously is from 4 to 4.6, preferably from 4 to 4.3.
Advantageous epiK5-N,O-oversulfate-derivatives with a very high degree of sulfation are consisting of a chain mixture in which at least 90% of said chains have the formula III, in which Z is SO₃ ⁻, the uronic units are 40-60% consisting of iduronic acid, n is an integer from 2 to 100, preferably from 3 to 100, with a mean molecular weight from approximately 2,000 to approximately 45,000, advantageously from approximately 4,500 to approximately 45,000, R is at least 40%, preferably 50-80% SO₃ ⁻, R′ and R″ are both SO₃ ⁻ or one is hydrogen and the other is 5-10% SO₃ ⁻ in monosulfate glucuronic acid and 10-15% SO₃ ⁻ in monosulfate iduronic acid, the degree of sulfation is at least 4, from 4 to 4.6 and the corresponding cation is chemically or pharmaceutically acceptable.
Preferred epiK5-N,O-oversulfate-derivatives are LMW-epiK5-N,O-oversulfates consisting of a chain mixture in which at least 90% of said chains have the formula III in which the uronic units are 40-60% comprised, preferably 50-55%, of iduronic acid, R is at least 40%, advantageously 50-80%, preferably approximately 65% SO₃ ⁻, R′ and R″ are both SO₃ ⁻ or one is hydrogen and the other is 5-10% SO₃ ⁻ in glucuronic acid and 10-15% SO₃ ⁻ in iduronic acid, Z is 100% SO₃ ⁻ or (C₂-C₄)acyl, n is an integer from 2 to 20, preferably from 3 to 15, with a mean molecular weight from approximately 4,000 to approximately 8,500 and the corresponding cation is chemically or pharmaceutically acceptable.
In practice, said preferred epiK5-N,O-oversulfate-derivatives with a very high degree of sulfation are consisting of a mixture of chains in which at least 90% of said chains have the formula III′
in which the uronic units are 20-60% consisting of iduronic acid, q is an integer from 2 to 20, advantageously from 3 to 15, R, R′ and R″ represent hydrogen or an SO₃ ⁻ group, Z is SO₃ ⁻, for a sulfation degree of at least 4, preferably from 4 to 4.6 and the corresponding cation is one chemically or pharmaceutically acceptable ion.
Particularly interesting are chain mixtures of formula III′ in which 40-60%, preferably 50-55% of the uronic units are those of iduronic acid, R is at least 40%, advantageously 50-80%, preferably approximately 65% SO₃ ⁻, R′ and R″ are both SO₃ ⁻ or one is hydrogen and the other is 5-10% SO₃ ⁻ in glucuronic acid and 10-15% SO₃ ⁻ in iduronic acid, n is an integer from 2 to 20, advantageously from 3 to 15, with a mean molecular weight from approximately 2,000 to approximately 16,000, advantageously from approximately 3,500 to approximately 13,000, preferably from approximately 4,500 to approximately 9,000 and the corresponding cation is chemically or pharmaceutically acceptable.
Among these LMW-epiK5-N,O-oversulfates, are advantageous those consisting of a mixture of chains in which the preponderant species has the formula III′ a
in which the uronic units are 20-60% consisting of iduronic acid, p is an integer from 4 to 8, Z is SO₃ ⁻, R, R′ and R″ are hydrogen or SO₃ ⁻, for a sulfation degree of at least 4, preferably from 4 to 4.6 and the corresponding cation is chemically or pharmaceutically acceptable.
The origin of the new LMW-epiK5-N,O-oversulfates from LMW-epiK5-sulfates obtained by nitrous depolymerization and subsequent reduction with, for example, sodium borohydride involves, at the reducing end of the majority of the chains in said chain mixture, the presence of a sulfated 2,5-anhydromannitol unit of structure (a′) as shown above, in which R represents hydrogen or SO₃ ⁻.
Thus, the reducing end of the majority of the chains in said chain mixture is represented by the structure (b″)
in which Z represents SO₃ ⁻ and the uronic unit can be glucuronic or iduronic.
Among the aforesaid new LMW-epiK5-N,O-oversulfates, are preferred those consisting of mixtures in which the preponderant species is a compound of formula III′b
in which R, R′ and R″ are hydrogen or SO₃ ⁻, Z is SO₃ ⁻, X″ is OH or OSO₃ ⁻, m is 4, 5 or 6, for a sulfation degree of at least 4, preferably from 4 to 4.6, the uronic units are present alternately, starting with a glucuronic or iduronic unit, and the corresponding cation is a chemically or pharmaceutically acceptable ion. Said cations are advantageously those of alkaline metals, alkaline-earth metals, ammonium, tetra(C₁-C₄)alkylammonium, aluminum and zinc and preferably, among these, the sodium, calcium and tetrabutylammonium ions.
If an epiK5-N-sulfate is used as a starting epiK5-N-sulfate-derivative of the process of the present invention, i.e. a native K5 polysaccharide, previously N-deacetylated, N-sulfated normally to 100%, 20-60% C5-epimerized and not depolymerized, at the end of step (c) an epiK5-N,O-oversulfate is isolated which can be subjected to nitrous depolymerization and possible, subsequent reduction with, for example, sodium borohydride to obtain the corresponding LMW-epiK5-N,O-oversulfate having the same degree of sulfation. In particular, LMW-epiK5-N,O-oversulfates are obtained consisting of a chain mixture in which at least 90% of said chains have the formula III′ or III′ a, in which the uronic units are 20-60% consisting of iduronic acid, q, R, R′ R″ and Z have the meaning defined above, for a sulfation degree of at least 4, preferably from 4 to 4.6 and the corresponding cation is a chemically or pharmaceutically acceptable ion. In such case, the origin of these LMW-epiK5-N,O-oversulfates from a depolymerization reaction and possible, subsequent reduction with, for example, sodium borohydride involves, at the reducing end of the majority of the chains in said chain mixture, the presence of a 2,5-anhydromanno unit of structure (a″)
in which X is formyl or hydroxymethyl and R represents hydrogen or SO₃ ⁻.
The new epiK5-N,O-oversulfate-derivatives, especially in their salt form, are highly anionic products able to capture the free radicals and are utilizable in the cosmetics industry as adjuvants against hair loss or to prepare “anti-ageing” creams and, in the pharmaceutical industry, as products for the treatment of dermatitis. Besides, the epiK5-N,O-oversulfate-derivatives of the present invention, in particular the LMW-epiK5-N,O-oversulfates possess antiangiogenic and antiviral activity and therefore constitute active ingredients for the preparation of medicines.
Thus, according to one of its additional aspects, the present invention provides pharmaceutical compositions including, as one of their active ingredients, a pharmacologically active amount of an epiK5-N,O-oversulfate-derivative as shown above or of one of its pharmaceutically acceptable salts, in mixture with a pharmaceutical excipient.
In the pharmaceutical compositions of the present invention for oral, subcutaneous, intravenous, transdermal or topical administration, the active ingredients are preferably administered in the form of dosage units, in mixture with the classic pharmaceutical excipients or vehicles.
The posology can vary widely depending on the age, weight, and the health condition of the patient. This posology includes the administration of a dose from 1 to 1000 mg, advantageously from 10 to 750 mg, preferably 250 to 500 mg from one to three times a day by intravenous, subcutaneous, oral, transdermal or topical administration.
The pharmaceutical compositions of the present invention are formulated with the classic excipients suitable for different ways of administration. Particularly advantageous are the formulations in the form of creams, ointments, liniments, gels, foams, balsams, vaginal pessaries, suppositories, solutions or suspensions suitable for local administration.
Advantageously, the compositions of the present invention include, as one of its active ingredients, an epiK5-N,O-oversulfate-derivative obtainable starting from an epiK5-N-sulfate-derivative according to steps (a), (b) and (c) of the process described above, or starting from an epiK5-N-sulfate not depolymerized, according to steps (a), (b) and (c) of the process described above, with possible subsequent nitrous depolymerization after step (c), or one of its pharmaceutically acceptable salts, in mixture with a pharmaceutical excipient. Advantageously, said epiK5-N,O-oversulfate-derivative consists of a chain mixture in which at least 90% of said chains have the formula III or III′ or in which the preponderant species is a compound of formula III′a or III′b. Preferred active ingredient is a LMW-epiK5-N,O-oversulfate having a sulfation degree of at least 4, preferably from 4 to 4.6, advantageously having a mean molecular weight from approximately 3,500 to approximately 11,000, more advantageously from approximately 3,500 to approximately 5,200 and substantially free of N-acetyl groups.
Finally, according to another of its aspects, the present invention provides a cosmetic composition including an effective amount of an epiK5-N,O-oversulfate-derivative or one of its pharmaceutically acceptable salts, in mixture with a cosmetic excipient.
A salt selected from the group consisting of salts of sodium, potassium, calcium, magnesium, aluminum and zinc of the epiK5-N,O-oversulfate derivatives, in particular those consisting of chain mixtures in which at least 90% of said chains have the formula III or III′ or in which the preponderant species has the formula III′a or III′b, is an effective active ingredient of the pharmaceutical or cosmetic compositions of the present invention.
The following examples illustrate the invention without however limiting it.

Preparation I

Preparation of K5 Polysaccharide from Escherichia coli

At first fermentation is carried out in an Erlenmeyer flask using the following medium:


Fat-free soya meal	2	g/l
K₂HPO₄	9.7	g/l
KH₂PO₄	2	g/l
MgCl₂	0.11	g/l
Sodium citrate	0.5	g/l
Ammonium sulfate	1.0	g/l
Glucose	2	g/l
Spring water	1000	ml

pH = 7.3

The medium is sterilized at 120° C. for 20 minutes. The glucose is prepared separately in solution form which is sterilized at 120° C. for 30 minutes and added sterilely to the medium. The Erlenmeyer flask is inoculated with a suspension of E. coli cells Bi 8337/41 (O10:K5:H4) originating from a slant kept in Triptic soy agar, and incubated at 37° C. for 24 hours under controlled agitation (160 rpm, 6 cm stroke). The bacterial growth is measured by counting the cells using a microscope. In a subsequent operation, a 14 l Chemap-Braun fermenter containing the same medium as above, is 0.1% inoculated with the culture of the Erlenmeyer flask as above and fermentation is performed by aeration of 1 vvm, (vvm=volume of air per volume of liquid per minute) 400 rpm agitation and temperature of 37° C. for 18 hours. During fermentation the pH, the oxygen, the glucose residue, K5 polysaccharide produced and bacterial growth are measured. At the end of fermentation the temperature is brought to 80° C. for 10 minutes. The cells are separated from the medium through centrifugation at 10,000 rpm and the supernatant is ultrafiltered using an SS 316 (MST) module fitted with PES membrane with nominal cut-off of 800 and 10,000 D to reduce the volume to 1/5. K5 polysaccharide is then precipitated by addition of 4 volumes of acetone at 4° C. and left to settle overnight at 4° C. Finally it is recovered by centrifugation at 10,000 rpm for 20 minutes or filtration. Deproteinization of the solid obtained is carried out by using a type II protease from Aspergillus orizae in a buffer of 0.1 M NaCl and 0.15 M EDTA at pH 8 containing SDS (0.5% sodium dodecyl sulfate) (10 mg/l of filtrate) at 37° C. for 90 minutes. The solution obtained is ultrafiltered on model SS 316 with membrane at a nominal cut-off of 10,000 D with 2 extractions with 1M NaCl and washed with water until disappearance of absorbance in the ultrafiltrate. K5 polysaccharide is then precipitated with acetone and a yield of 850 mg per liter of fermenter is obtained. The purity of the polysaccharide obtained is measured through the determination of the uronic acids (carbazole method), proton and carbon 13 NMR, UV and protein content. The purity is more than 80%.

The polysaccharide obtained is composed of two fractions of different molecular weight, respectively 30,000 and 5,000 D as emerges from the determination by HPLC using a Pharmacia 75 HR column and a single fraction with a retention time of approximately 9 minutes using two seriate columns of Bio-sil SEC 250 (Bio Rad) and Na₂SO₄as mobile phase at room temperature and a flow of 0.5 ml/minute. The measurement is performed against a standard curve obtained with fractions of heparin of known molecular weight.
The ¹H-NMR spectrum of the purified K5 thus obtained shows different signals attributable to methyls of lipophilic substances.

Preparation II

Purification of K5

In 100 ml of a saturated aqueous solution of sodium chloride and thermostated at 4° C. is dissolved 1 g of K5 obtained at the end of PREPARATION I and to the solution thus obtained are added 3 volumes of cold isopropanol. The saline concentration of the solution is brought to 3 M by addition of the calculated amount of a saturated sodium chloride solution and the solution obtained is left in a cold environment (approximately 4° C.) overnight. The precipitate which forms is separated by centrifugation at 10,000 rpm for 20 minutes and the purity of the product is checked by dialysis overnight and subsequent examination of the ¹H-NMR spectrum, from which signals in the region under 1.5 ppm must be absent. Optionally, the operation of dissolution in water saturated with NaCl and precipitation with isopropanol is repeated. The precipitate is dissolved in water and ultrafiltered on a Miniplate Millipore membrane 10,000 D cut off until disappearance of the salts. Thus a K5 having a purity of at least 99% is obtained from whose ¹H-NMR spectrum no traces of lipophilic impurities result in the region under 1.5 ppm.

Preparation III

Preparation of a K5-N-Sulfate

(i) N-Deacetylation

Ten grams of pure K5 polysaccharide prepared as described in PREPARATION II are dissolved in 1000 ml of 2N sodium hydroxide and the solution thus prepared is left at 60° C. for 24 hours. The solution is brought to room temperature then to neutral pH (pH 7) with 6N hydrochloric acid.

(i) N-Sulfation

To the solution containing the deacetylated K5, kept at 40° C., are added 16 g of sodium carbonate and afterwards and in 4 hours, 16 g of pyridine.SO₃ ⁻. At the end of the reaction, after 24 hours, the solution is brought to room temperature, then to pH 6.5-7 with a 5% solution of hydrochloric acid. The product is purified from salts by diafiltration using a 1,000 D helically wound membrane (prepscale cartridge-Millipore). The process is terminated when the conductivity of the permeate is less than 1000 μS, preferably less than 100 μS. The intradialysis is reduced until a 10% concentration of the polysaccharide is obtained using the same in concentration dialysis system. The concentrated solution is dried by lyophilization. Upon ¹³C-NMR spectrum analysis N-acetyl or NH₂residues do not appear.

Preparation IV

LMW-K5-N-Sulfate

The product obtained as described in Example 1, steps (i) and (ii), of WO 02/068477 is depolymerized by the degradation method with nitrous acid and subsequent reduction of the aldehyde which forms. 1 g of K5-N-sulfate is dissolved in 200 ml of cold distilled water, the pH is brought to 2.2 with 1N HCl and 480 mg of sodium nitrite dissolved in 240 ml of cold distilled water are added. The solution is then maintained for 30 minutes at 4° C. At the end of the reaction the solution is brought to pH 7 with 1 M NaOH and then to room temperature. The solution is then added with 450 mg. of NaBH₄and left to react for 4 hours. The excess NaBH₄is eliminated with HCl bringing the pH to 5-6. The product, neutralized with 0.1 M NaOH, is recovered by precipitation with 3 volumes of acetone at 4° C., filtration with filtering funnel and dried at 40° C. in a vacuum oven. 900 mg of LMW-K5-N-sulfate are obtained with a mean molecular weight of approximately 2,000, consisting of a chain mixture in which the preponderant species is a compound of formula I′b in which m is 4 and the uronic units are those of glucuronic acid.

Example 1

LMW-EpiK5-N-Sulfate

Sequence (i)→(ii)

(i) Epimerization to EpiK5-N-Sulfate

Ten grams of K5-N-sulfate obtained as described in Example 1, steps (i) and (ii), of WO 02/068477, from whose ¹H-NMR spectrum, signals concerning acetyl groups or NH₂do not appear, are dissolved in 600 ml of 25 mM HEPES buffer at pH 7, containing CaCl2 at a concentration of 50 mM and the solution thus obtained is made to recirculate through a 50 ml column filled with Sepharose 4B resin containing 5 g of recombinant C5-epimerase (WO 96/14425) immobilized as described in Example 1 of WO 01/72848. The reaction is carried out at 30° C. at pH 7 with a flow of 200 ml/h for 24 hours. The product obtained is purified by ultrafiltration and precipitation with ethanol. Thus an epiK5-N-sulfate is obtained whose iduronic acid content is 54%.
(ii) Depolymerization of epiK5-N-Sulfate
To a solution of 1 g of the product thus obtained, in 25 ml of distilled water cooled to 4° C. and brought to pH 2.2 with 1N HCL, are added 230 mg of sodium nitrite dissolved in 115 ml of cold distilled water. The solution is then maintained for 30 minutes at 4° C. At the end of the reaction the solution is brought to room temperature and the pH to 7 with 0.1 M NaOH. The solution is then added with 450 mg. of NaBH4 and left to react for 4 hours. The product is recovered by precipitation with 3 volumes of acetone at 4° C., filtration with filtering funnel and dried at 40° C. in a vacuum oven. 900 mg of LMW-epiK5-N-sulfate are obtained with an iduronic acid content of 54% and a molecular weight distribution from 1,000 to 4,000, measured with HPLC method.

Example 2

LMW-EpiK5-N-Sulfate

Sequence (ii)→(i)

(ii) Depolymerization of K5-N-Sulfate

2 g of K5-N-sulfate, obtained as described in Example 1, steps (i) and (ii), of WO 02/068477, is depolymerized as described in PREPARATION I, using 100 mg of sodium nitrite and 300 mg of sodium borohydride. An amount of 1.8 g of LMW-K5-N-sulfate with a mean molecular weight of 5,000 is obtained.

(i) Epimerization of LMW-K5-N-Sulfate

1 g of LMW-K5 N-sulfate obtained in step (ii) herein above is treated as described in step (i) of the Example 1. An epimerized product is obtained with an iduronic acid/glucuronic acid ratio of 44/56 against a ratio of 0/100 of the starting product, with a molecular weight distribution from 2,000 to 10,000 and with a mean molecular weight of 5,000 D. The yield, calculated by measuring the content of uronic acids against a standard with the carbazole method (Bitter and Muir, Anal. Biochem. 1971, 39, 88-92) is 90%.

Example 3

LMW-EpiK5-N-Sulfate

Sequence (i)→(ii)

(i) Epimerization of K5-N-Sulfate

A 2 g amount of K5 N-sulfate, obtained as described in Example 1, steps (i) and (ii), of WO 02/068477, is dissolved in 120 ml of 25 mM HEPES buffer, pH 7, containing 50 mM CaCl₂. The solution obtained is made to recirculate through a 50 ml column filled with the resin containing the immobilized enzyme obtained as described in WO 96/14425. This operation is carried out at 30° C. with a flow of 200 ml/h for 24 hours. The product obtained is purified through ultrafiltration on a 1000 D membrane and passing over an IR 120 H⁺ ionic exchange column, neutralizing the eluate with 1N NaOH. The sample is recovered by precipitation with ethanol or acetone. An epimerized product is obtained with an iduronic acid/glucuronic acid ratio of 55/45 against a ratio of 0/100 of the starting product. The percentage of epimerization was calculated with ¹H-NMR according to the method described in WO 96/14425. The yield, calculated by measuring the content of uronic acids against a standard with the carbazole method (Bitter and Muir Anal. Biochem. 39, 88-92-1971) is 90%.
(ii) Depolymerization of epi-K5-N-Sulfate
One gram of product obtained in step (a) is depolymerized by the degradation method with nitrous acid and subsequent reduction of the aldehyde which forms. In particular one continues by dissolving the product in 25 ml of cold distilled water brought to pH 2.2 with 1N HCl and adding it with 230 mg of sodium nitrite dissolved in 115 ml of cold distilled water. The solution is then maintained for 30 minutes at 4° C. At the end of the reaction the solution is brought to room temperature and the pH to 7 with 0.1 M NaOH. The solution is then added with 450 mg. of NaBH₄and left to react for 4 hours. The product is recovered by precipitation with 3 volumes of acetone at 4° C., filtration with filtering funnel and dried at 40° C. in a vacuum oven. A yield of 900 mg of LMW-epiK5-N-sulfate having with a molecular weight distribution measured by HPLC method which ranges from 1,000 to 4,000 and with a glucuronic unit content of 45% and an iduronic unit content of 55% is obtained.

Example 4

EpiK5-N,O-Oversulfate

(a) Tetrabutylammonium Salt of EpiK5-N-Sulfate

A solution in 40 ml of water of 400 mg of epiK5-N-sulfate, as obtained at the end of step (i) of the Example 1, is thermostated at 4° C., then passed over IR 120⁺ ionic exchange resin preconditioned with water at 4° C. The eluate obtained, consisting of 100 ml of a solution at pH 1.94, is neutralized with a 15% solution of tetrabutylammonium hydroxide and left at room temperature for one hour, maintaining the pH at 7 by addition of 15% tetrabutylammonium hydroxide and finally is lyophilized. Thus, 805 mg of tetrabutylammonium salt of epiK5-N-sulfate are obtained.

(b) Epi-K5-Amine-O-Oversulfate

A solution containing 805 mg of the salt thus obtained in 30 ml of dimethyl formamide is set at 55° C. and treated with 30 ml of dimethyl formamide containing 2.26 g of pyridine.SO₃adduct. The reaction at 55° C. is continued overnight then 60 ml of water are added to the mixture. After neutralization with 1N NaOH, the product is precipitated with 3 volumes of acetone saturated with NaCl and set at 4° C. overnight. The precipitate is recovered by filtration on guch G4 and then ultrafiltered with 1000 D TFF Millipore system and dried at reduced pressure. Thus, 550 mg of epi-K5-amine-O-oversulfated are obtained having a content of iduronic acid of 54%, of glucosamine-6-O-sulfate of 100%, of glucosamine 3-O-sulfate of 60%, of monosulfate glucuronic acid of 10%, of monosulfate iduronic acid of 15%, the rest of the uronic units being disulfated, with a sulfation degree of 3.55.

(c) EpiK5-Amine-O-Oversulfate-N-Sulfate

To a solution of 250 mg of the epi-K5-amine-O-oversulfate obtained in step (b) in 15 ml of water are added 400 mg of sodium carbonate, then to the mixture thus obtained are added 400 mg of pyridine.SO₃adduct in solid form a little at a time in 4 hours. The reaction mixture is kept at 55° C. overnight, then is stopped bringing the pH to 7 with 0.1N HCl. After ultrafiltration on a 1000 D membrane are added 3 volumes of acetone saturated with sodium chloride and the precipitate is recovered by centrifugation at 5000 rpm for 5′. Thus 244 mg of epiK5-N,O-oversulfate are obtained whose sulfation degree, measured with conductimetric method according to Casu et al. 1975, is 4.25. By the analysis of the ¹H-RMN spectrum it results that the epiK5-N,O-oversulfate thus obtained has an iduronic acid content of 54%, 6-O-sulfate of 100%, N-sulfate of 100%, glucosamine 3-O-sulfate of 60%, monosulfate glucuronic acid of 10%, monosulfate iduronic acid of 15%, the rest of the uronic units being disulfated. From the ¹H-NMR spectrum is therefore calculated a sulfation degree of 4.35 which, considering the margins of error of the methods, corresponds to the sulfation degree of epiK5-amine-O-oversulfated obtained upon termination of step (b), 100% N-sulfated. It is therefore assumed that, beyond a certain percentage of sulfate groups, the strong anionic nature of the product can lead to an underestimation of the degree of sulfation determined with the conductimetric method.

Example 5

LMW-EpiK5-Amine-O-Oversulfate

(a) Depolymerized-LMW-EpiK5-N-Sulfate

(a1) Starting K5-N-Sulfate
A solution of 8 g of 95% pure K5 polysaccharide in 800 ml of 2N NaOH is heated to 60° C. for 24 hours. After cooling, the solution is brought to pH 7 by 6N HCl. To the thus neutralized solution, at first 12.8 g of sodium carbonate, then, portionwise in 4 hours, 12.8 g of pyridine.SO₃adduct in solid form are added. The reaction mixture is kept at 40° C. for 24 hours. After elimination of the salts by ultrafiltration on membrane Millipore Prepscale TFF 1000 D cut-off, the obtained product is recovered by precipitation with 3 volumes of acetone. Thus, 8 g of K5-N-sulfate are obtained. Its ¹H-NMR spectrum shows a 100% N-sulfation (absence of signals due to NH₂and acetyl groups).
(a2) Depolymerized-LMW-Epi-K5-N-Sulfate. Sequence (i)→(ii)
(i) Epimerization.
The 8 g of K5 N-sulfate thus obtained are dissolved in 200 ml of 0.25M Hepes pH 7 buffer containing 50 mM CaCl₂and treated in solution with 9.6×10¹⁰cpm of recombinant C5-epimerase at 30° C. for 24 hours at pH 7. At the end of the reaction, the sample is purified by elimination of the salts by ultrafiltration on Millipore Prepscale TFF 1000 D cut-off membrane and, then, precipitated with 3 volumes of acetone. Thus, 7.5 g of epiK5-N-sulfate are obtained. Its epimerization percentage, in practice the amount of iduronic units in respect of the glucuronic ones, calculated by ¹H-NMR according to the method described in WO 96/4425, is 52%.
(ii) Depolymerization.
The 7.5 g of epiK5-N-sulfate thus obtained are dissolved in 150 ml water and the solution is thermostated at 4° C., then the pH is brought to 2.2 by previously cooled 1M HCl. To the solution, 431.2 mg of sodium nitrite, corresponding to 21.56 ml of a 2% solution of sodium nitrite in water, are added. The pH is brought to 2.2 again and the reaction mixture is kept at 4° C. for 20 minutes under stirring. After neutralization to pH 7.0 with 6N HCl, 1.35 g of sodium borohydride are added to the solution. The reduction is carried out by keeping the reaction mixture at room temperature for 4 hours, then the excess of reducing agent is destroyed by bringing the pH to 5 with 1N HCl, stirring until disappearance of effervescence. The pH is brought to 7-7.2 again with 1M NaOH. The depolymerized product is recovered by ultrafiltration with Millipore TFF 1,000 D cut-off membrane and subsequent precipitation with 3 volumes of acetone. Thus, 7 g of depolymerized-LMW-K5-N-sulfate are obtained. The mean molecular weight of this product, calculated via HPLC, is 6,000.

(b) LMW-EpiK5-Amine-O-Oversulfate

(b1) Tetrabutylammonium Salt of the Depolymerized-LMW-EpiK5-N-Sulfate.
A solution of 7 g of depolymerized-LMW-K5-N-sulfate obtained at the end of step (a) in 350 ml water is passed through a column of IR-120 H⁺. The pH of the eluate is 2.91. The percolated solution is brought to pH 7 with a 15% solution of tetrabutylammonium hydroxide (42.2 ml) and kept one hour at room temperature with controls in order to maintain the pH at a value of 7. After concentration on rotavapor of the tetrabutylammonium salt, the sample is frozen and lyophilized. Thus, 10.9 g of tetrabutylammonium salt of the depolymerized-LMW-epiK5-N-sulfate are obtained.
(b2) O-oversulfation.
The tetrabutylammonium salt thus obtained is dissolved in 158 ml of dimethyl formamide, then 28.8 g of pyridine.SO₃dissolved in 158 ml of DMF are added and the reaction mixture is kept at 45° C. for 18 hours. A volume of 316 ml water are added to stop the reaction and the pH is brought to 7 with 30% NaOH. The depolymerized-LMW-epiK5-amine-O-oversulfate is recovered by precipitation with 3 volumes of acetone saturated with NaCl (1.896 liters) and subsequent diafiltration on Millipore TFF 1,000 D membrane until elimination of the salts. The depolymerized-LMW-epiK5-amine-O-oversulfate has a mean molecular weight of 6,000.

Example 6

EpiK5-Amine-O-Oversulfate

(a) Tetrabutylammonium Salt of EpiK5-N-Sulfate

A solution in 40 ml of water of 400 mg of epiK5-N-sulfate was thermostated at 4° C., then passed over Amberlite® IR 120⁺ ionic exchange resin preconditioned with water at 4° C. The obtained eluate, consisting of 100 ml of a solution at pH 1.94 containing epiK5-N-sulfate in acidic form, was neutralized (pH 7) with a 15% solution of tetrabutylammonium (TBA) hydroxide and left at room temperature for one hour, maintaining the pH at 7 by addition of 15% tetrabutylammonium hydroxide, and finally was lyophilized to give the TBA salt of epiK5-N-sulfate (TBA. epiK5-N-sulfate);

(b) EpiK5-Amine-O-Oversulfate

A solution containing the TBA.epiK5-N-sulfate thus obtained in 30 ml of dimethylformamide was set at 55° C. and treated with 30 ml of dimethylformamide containing 2.26 g of pyridine.SO₃adduct. The reaction at 55° C. was continued overnight, then 60 ml of water were added to the mixture. After neutralization with 1N NaOH, the product was precipitated with 3 volumes of acetone saturated with NaCl and set at 4° C. overnight. The precipitate was recovered by filtration on guch G4, then ultrafiltered with 1000 D TFF Millipore system and dried at reduced pressure to give epiK5-amine-O-oversulfate. This product has the following sulfation profile:
Glucosamine 6-O-sulfate content: 100%;
Glucosamine 3-O-sulfate content: 70%;
Glucosamine N-sulfate content: 0%
Glucuronic acid 3-O-sulfate content: 0%;
Non-sulfated uronic acids: 0%
Iduronic acid 3-O-sulfate content: 10%;
Uronic acid 2,3-sulfate content: 90%;
Sulfation degree: 3.6.
The ¹³C-NMR spectrum of this epiK5-amine-O-oversulfate is shown in FIG. 1.

Claims

1. A process for the preparation of epiK5-amine-O-oversulfate-derivatives having a glucosamine 3-O-sulfate content of at least 40%, which comprises

(a) treating an epiK5-N-sulfate-derivative, in acidic form, with a tertiary or quaternary organic base, letting the reaction mixture to stand for a time period of 30-60 minutes at a pH of approximately 7 and isolating the corresponding organic base salt of said epiK5-N-sulfate; and

(b) treating said tertiary amine or quaternary ammonium salt of said epiK5-N-sulfate-derivative with an O-sulfation agent in the conditions of O-oversulfation and isolating the epiK5-amine-O-oversulfate-derivative.

2. The process of claim 1, wherein said epiK5-amine-O-oversulfate-derivative is isolated in form of sodium salt and optionally converted into another chemically or pharmaceutically acceptable salt.

3. The process of claim 1, wherein said other chemically or pharmaceutically acceptable salt is a member selected from the group consisting of alkaline-earth metals, ammonium, tetra(C₁-C₄)alkylammonium, aluminum and zinc salts.

4. The process of claim 1, wherein an epiK5-N-sulfate-derivative having a mean molecular weight from approximately 1,000 to approximately 25,000 is used as starting material.

5. The process of claim 4, wherein said starting epiK5-N-sulfate-derivative has a mean molecular weight from approximately 1,000 to approximately 12,000.

6. The process of claim 4, wherein said starting epiK5-N-sulfate-derivative has a mean molecular weight from approximately 1,500 to approximately 25,000.

7. The process of claim 6, wherein said epiK5-N-sulfate-derivative has a mean molecular weight from approximately 10,000 to approximately 25,000.

8. The process of claim 1, wherein said epiK5-N-sulfate-derivative is a LMW-epiK5-N-sulfate having a content in iduronic acid of from 40% to 60% and a mean molecular weight from approximately 1,500 to approximately 12,000.

9. The process of claim 8, wherein said LMW-epiK5-N-sulfate has a mean molecular weight of from approximately 1,500 to approximately 10,000.

10. The process of claim 9, wherein said LMW-epiK5-N-sulfate has a mean molecular weight of from approximately 1,500 to approximately 7,500.

11. The process of claim 1, wherein an epiK5-N-sulfate-derivative consisting of a mixture of chains in which at least 90% of said chains have the formula I

in which 20-60% of the uronic units are those of iduronic acid, n is an integer from 2 to 100 and the corresponding cation is chemically or pharmaceutically acceptable, is used as starting material.

12. The process of claim 11 wherein said starting material consists of a mixture of chains in which at least 90% of said chains have the formula I, in which 40-60% of the uronic units are those of iduronic acid.

13. The process of claim 12 wherein, in formula I, n is an integer from 3 to 100.

14. A LMW-epiK5-N-sulfate free of NH₂and acetyl groups having a content in iduronic acid of from 20% to 60% and a mean molecular weight of from approximately 1,000 to approximately 12,000.

15. The LMW-epiK5-N-sulfate of claim 14 having a content in iduronic acid of from 40% to 60% and a molecular weight of from approximately 1,500 to approximately 10,000.

16. The LMW-epiK5-N-sulfate of claim 15 having a mean molecular weight of from approximately 1,500 to approximately 7,500.