NO175135B - Frozen, aqueous dispersion for pharmaceutical or veterinary use as carrier - Google Patents

Description

This invention relates to a frozen, aqueous dispersion for use as a carrier for pharmaceutical or veterinary medicinal purposes. The dispersion includes a biodegradable amphipathic copolymer, and in particular such a copolymer which is rapidly self-dispersible in water so that a stable dispersion is formed.

Such copolymers are useful in the production of preparations with continuous release of drugs, and are particularly useful in the production of such mixtures where the drug is sensitive to denaturation or degradation by exposure to organic solvents, non-neutral pH or elevated temperature, e.g. many polypeptide drugs. The copolymers described herein allow the preparation of continuous release preparations of these drugs under conditions whereby non-neutral pH and elevated temperature are avoided, and under such conditions that exposure to organic solvents is avoided or reduced to a minimal level in solvent mixtures containing only a small proportion of organic solvent.

It is to be understood that in this specification the term "self-dispersible", when applied to a copolymer, means a copolymer which disperses to form a stable dispersion when added to water, without the addition of any surfactant or other additive. In this context, a "stable" dispersion is one which does not agglomerate or precipitate to any significant extent within the time normally required to process the copolymer into a sustained release formulation, e.g. 24 hours.

US Patent Nos. 3,773,919 and 3,887,699 describe the use of biodegradable polymers, particularly polylactide and poly(lactide-co-glycolide), in the manufacture of sustained-release pharmaceutical compositions, and although their disclosure includes certain polypeptide- drugs, we have found that the manufacturing conditions, which involve a temperature of at least 130°C, are such that they almost completely cleave many polypeptide drugs, so that satisfactory continuous-release preparations are not achievable using the technology from these US - patent documents.

Furthermore, European Patent Publication No. 58481 indicates that the copolymers described in the above-mentioned US patents, even if they are processed differently, e.g. to avoid cleavage of the polypeptide drug, cannot be used to obtain satisfactory preparations with continuous release of polypeptides. Furthermore, the release profile was rather biphasic and discontinuous, in that an initial release period resulting from surface leaching of the polypeptide was followed by a prolonged "dead-phase" in which nothing or very little was released, and this in turn was followed by the main release of the polypeptide with the consequence that the copolymer matrix absorbed water and was biodegraded.

However, EP 58481 disclosed that satisfactory continuous release preparations of certain polypeptides could be formed using polylactide or poly(lactide-co-glycolide) with generally lower molecular weights than those disclosed in the aforementioned US patents, and at lower temperatures, but it was still necessary during the processing to use organic solvents, against which many polypeptides are unstable.

European patent publication no. 92918 describes the use of biodegradable amphipathic copolymers of the general type used in the present invention, in the production of preparations with continuous release. However, the copolymers described there are not self-dispersible in water to form stable dispersions, but require the use of organic solvents, which, as indicated above, can be denaturing for polypeptides in the subsequent processing into sustained release preparations.

In the present invention, a biodegradable copolymer is used which is self-dispersible in water, and which can therefore be used in the production of preparations with continuous release of drugs without resorting to the use of high temperatures or non-neutral pH, and, for water-soluble drugs such as polypeptides, without exposing the drug to the use of organic solvents during manufacture. Such copolymers may be self-dispersible as originally synthesized, or copolymers which are not inherently self-dispersible may be made so by the methods described herein.

The biodegradable amphipathic copolymers used in the invention are also useful for the production of injectable preparations with delayed continuous release of drugs which, unlike polypeptides, have a low molecular weight and low water solubility. For such drugs, the copolymers described here act as very effective dispersants, and they can provide colloidal suspensions that can be administered by injection to provide delayed continuous release of lipophilic drugs.

Moreover, the dispersion of biodegradable amphipathic copolymers according to this invention can be used to prepare drug mixtures which can be directed to targets in particular organs of the human or animal body. It is known that particles or microspheres of different sizes are collected in different organs of the body after intravenous injection, depending on the size of the injected particles (for an overview, see Tomlinson, "Microsphere Delivery Systems For Drug Targeting And Controlled Release" in Int. Pharm. Tech. and Prod. Mfr., 4, (3), pp. 49-57, 1983). For example, particles smaller than 50 nm can pass through the fenestrations in the liver endothelium and become localized, perhaps by lymphatic transport,

in the spleen, bone marrow and possibly tumor tissue. Intravenous, intra-arterial or intraperitoneal injection of particles of approximately 0.1 to 2.0 nm leads to rapid removal of particles from the blood stream by the macrophages in the reticuloendothelial system, with possible localization of these in the lyosomes of the Kuppfer cells in the liver. Intravenous delivery of particles over 7-12 nm leads to mechanical filtration in the lungs, while particles between 2 and 12 nm will be trapped within the capillary network, not only in the lungs, but also in the liver and spleen. Intra-arterial delivery of particles larger than 12 um causes them to block the first capillary layer they encounter. Dispersions according to this invention can be produced with regulated particle size, which can be targeted at organs in the manner described above.

Scheme 1 provides a schematic illustration of the processes involved in this invention.

The frozen, aqueous dispersion according to the invention is characterized in that it contains a self-dispersible form of an amphipathic, non-crosslinked linear, branched or grafted block copolymer having a minimum weight-average molecular weight of 1000, in which the hydrophobic component is biodegradable or hydrolytically unstable and the hydrophilic component may or may not be biodegradable or hydrolytically unstable, prepared by dissolving such copolymer in the non-self-dispersible form in a water-miscible solvent which either has a low boiling point or is freeze-dryable , agitate said solution vigorously while adding an excess of water, and freeze the resulting dispersion.

The self-dispersible copolymer described above can also be prepared by freeze-drying a freeze-dried stable aqueous dispersion of a pharmaceutically or veterinary acceptable amphipathic, non-crosslinked linear, branched or grafted block copolymer having a minimum weight average molecular weight of 1000, in which the hydrophobic component is biodegradable or hydrolytically unstable under such conditions, and the hydrophilic component may or may not be biodegradable or hydrolytically unstable under such conditions.

When reference is made here to an "aqueous dispersion", it is understood that this comprises a dispersion in water alone, or in water containing a small proportion, e.g. up to 10%, of a water-miscible organic solvent.

The copolymers which can be used as starting materials in the above process are those described in European Patent Publication No. 92918 which is referred to above.

The frozen, stable aqueous dispersion according to the invention can be obtained by dissolving the copolymer described immediately above in its non-self-dispersible form, as originally synthesized, in a minimal amount of a water-miscible solvent, which either has a low boiling point, e.g. e.g. below 100°C, e.g. methanol or ethanol, or can be freeze-dried, e.g. dioxane or acetic acid, vigorously agitate said solution while slowly adding an excess of water to form an extremely fine, stable aqueous dispersion, and then freeze said dispersion.

The present invention can be utilized to produce a solid copolymer/drug powder material by freeze-drying a frozen, stable aqueous dispersion of the copolymer and the drug.

The frozen, stable aqueous dispersion according to the invention can be obtained when the drug is water-soluble, e.g. a polypeptide, by dispersing the self-dispersible copolymer in water, buffering the dispersion to physiological or neutral pH, mixing the buffered dispersion with an aqueous solution of the water-soluble drug, and freezing the resulting copolymer/drug dispersion.

Special water-soluble polypeptides that can be used in this invention are e.g. oxytocin, vasopressin, adrenocorticotrophic hormone (ACTH), epidermal growth factor (EGF), transforming growth factor antagonists, prolactin, luliberin or luteinizing hormone-releasing hormone (LH-RH), LH-RH agonists or antagonists, growth hormone, triggering growth hormone factor, insulin, somatostatin, bombesin antagonists, glucagon, interferon, gastrin, tetragastrin, pentagastrin, urogastron, secretin, calcitonin, enkephalins, endorphins, angiotensins, renin, bradykinin, bacitracins, polymyxins, colistins, tyrocidin, gramicidins, and synthetic analogues and modifications and pharmaceutically active fragments thereof, monoclonal antibodies and soluble vaccines.

When the drug is water-soluble, the frozen, stable aqueous dispersion can be obtained by dissolving the drug in the self-dispersible copolymer in a minimum amount of a water-miscible organic solvent, e.g. dioxane, acetic acid, acetonitrile, methanol or ethanol, slowly add an excess of water to the vigorously agitated solution to form a fine, stable dispersion, and then freeze the dispersion.

Any drug with low water solubility is suitable for use with the dispersion according to the invention.

Alternatively, one of the freeze-drying processes can be avoided by using the copolymer in its non-self-dispersible form, dissolving it in a water-miscible organic solvent, precipitating it as a fine dispersion by slowly adding an excess of water under vigorous agitation, adding a solution of a drug, either in water, if the drug is water-soluble, or in a water-miscible organic solvent or in a mixture thereof with water if the drug is water-insoluble, to the copolymer dispersion, and then freezing and freeze-drying the total mixture.

Certain pharmaceutically or veterinary acceptable amphipathic, non-crosslinked linear, branched or grafted block copolymers, having a minimum weight average molecular weight of 1000, in which the hydrophobic component is biodegradable or hydrolytically unstable under normal physiological conditions, and in which the hydrophilic component may or may not be biodegradable or hydrolytically unstable under such conditions, are self-dispersible in water as synthesized. These are copolymers that contain a large hydrophilic proportion,

i.e. more than 50%, in relation to the hydrophobic part, or copolymers in which the hydrophobic part has a low molecular weight, e.g. a M w of less than 5000.

Moreover, the structure of the copolymer, and the nature of the individual hydrophilic and hydrophobic polymers therein, regulate the degree of self-dispersibility in water for the copolymer obtained therefrom. Thus, e.g. polylactide-grafted polyvinylpyrrolidone (PVP) self-dispersible when it contains 50% or more of PVP, although the polylactide may have a relatively high molecular weight, e.g. a Mw of more than 30,000; and polylactide/polyethylene glycol 1900

(equal amounts) is self-dispersible. However, polylactide/polyethylene glycol 5000 (equal amounts) is difficult to self-dispersible, and above this molecular weight the copolymers are not immediately self-dispersible in water, but must initially have the addition of a small part of an organic solvent, which can then be removed by evaporation or freeze drying.

As indicated above, dispersions according to this invention are useful in the preparation of preparations with delayed continuous release of drugs. As described above, a mixture of a copolymer and a drug can be prepared under such conditions that the drug is not exposed to high temperature, non-neutral pH, high concentrations of organic solvent or organic solvent at elevated temperature, and such copolymer-drug mixtures can be processed into suitable pharmaceutical or veterinary medicinal mixtures by conventional methods, e.g. by compression molding at low temperatures (many can be conveniently compression molded at about 60°C, well below the cleavage temperature of most drugs, including polypeptide drugs which are among those most susceptible to cleavage at high temperatures) to form implantable depot mixtures, such as e.g. described in European Patent Publications Nos. 58481 and 92918, which provide a delayed continuous release of the drug. Alternatively, for water-insoluble drugs, the copolymer-drug mixture can be simply dispersed in sterile water to provide a fine aqueous dispersion that can be used as a sustained-release injectable formulation, or, if the particle size is appropriately controlled, an admixture that targets a special organ, as described above.

The particle size of such an aqueous dispersion can be controlled within fairly narrow limits by controlling the particle size of the copolymer used. This is achieved during the preparation of the self-dispersible form of the copolymer used, and is achieved by suitably adjusting the rate of addition of water to the solution of copolymer in the freeze-dryable, water-miscible solvent, and regulating the agitation rate during this process. The particle size in the thus obtained dispersion can be measured in a conventional way, e.g. by optical microscopy, Coulter counters or nanosorters.

Useful co-excipients in the preparation of preparations with delayed continuous release of polypeptides during use

of the above-described copolymer/drug mixtures, are low- or high-molecular weight water-soluble polymers that are compatible, or partially compatible with these, such as gelatin, polyvinylpyrrolidone, dextran, polyethylene glycols, sodium alginate and water-soluble, synthetic, non-therapeutic polypeptides. Such co-excipients provide additional hydrophilic areas,

or pores, in the polymer matrix, and also stabilize the tertiary structure of the polypeptide by chain entanglement, which is achievable because they are compatible or partially compatible with the polypeptide.

Example 1

2 g of a biodegradable copolymer of type AB comprising 25% by weight of a methoxy polyethylene glycol with a molecular weight of 5900 (component A) and 75% by weight of poly(D,L-lactide) (component B) were dissolved in glacial acetic acid (2 ml) , and the solution was vigorously stirred while distilled water (21 mL) was added slowly to form an extremely fine dispersion. The dispersion was frozen, and freeze-dried at 0.01 mm Hg (13.3 Pa) for 24 hours to give a dry powder copolymer.

When adding the dry powder to water, below

stirring, it was redispersed to form a very fine dispersion.

Example 2

The dry powder copolymer from e.g. 1 (0.5 g) was dispersed under vigorous stirring in distilled water (5 ml) containing sodium azide (0.01%), and the dispersion was buffered to pH 8 with 0.1N sodium hydroxide. Bovine serum albumin (BSA)

(0.125 g) was dissolved in distilled water (1.0 ml) and <14>C-methylated BSA (10 µl of a 5 uCi per ml solution in 0.01 M sodium phosphate buffer) was added, the BSA solution was added to the copolymer dispersion, the mixture was frozen and then lyophilized at 0.01 mm Hg (13.3 Pa) for 24 hours.

The lyophilized product was cast at 60-70° to give 1 cm square discs with thicknesses of 0.2 cm, 0.09 cm and 0.04 cm. Each of the different slices was individually immersed in 2 ml of phosphate-buffered saline (pH 7.4) containing 0.02% sodium azide, at 37°C. After intervals, the medium was removed and replaced with frit buffer, and the released radioactivity in the removed medium was assessed.

Example 3

2.5 g of a poly(D,L-lactide-co-glycolide) graft(polyvinyl-pyrrolidone) copolymer containing 50% by weight of poly(D,L-lactide-co-glycolide) comprising equimolar amounts of lactide and glycolide, and 50% by weight of polyvinylpyrrolidone was dissolved in glacial acetic acid (5 mL) and stirred vigorously while distilled water (20 mL) was added slowly to form a very fine dispersion, which was then frozen and freeze-dried at 0, 1 mm Hg (13.3 Pa) for 24 hours, to give a dry powder copolymer.

Upon addition of the dry powder copolymer to water, with stirring, it redispersed almost immediately to form a very fine dispersion.

Example 4

2.0 g of a biodegradable block copolymer of the ABA type comprising 80% by weight of poly(D,L-lactide) (component A) and 20% by weight of polyethylene glycol of molecular weight 2000 (component B) was added to absolute ethanol ( 3 ml) and stirred vigorously while water (1.5 ml) was added slowly to form an extremely fine dispersion. A further 15 ml of water was added, with vigorous stirring, to give a dilute dispersion of the copolymer, which was then buffered to pH 8 by the addition of 0.1 N sodium hydroxide.

Bovine serum albumin (BSA) (0.5 g) was dissolved in water

(5 ml) and <14>C-methylated BSA (70 µl of a 5 uCi/ml solution in

0.01 M sodium phosphate) was added. The BSA solution was then mixed with the copolymer dispersion, frozen and freeze-dried at 0.01

mm Hg (13.3 Pa) for 30 hours.

The lyophilized powder was cast at 60°C to give. square slices of 1 cm and with thicknesses of 0.36 cm, 0.16 cm and 0.06 cm. Each of the different discs was then individually immersed in 2 ml of phosphate-buffered saline, pH 7.4, at 37°C. After intervals, the medium was withdrawn and replaced with fresh buffer, and the released radioactivity in the withdrawn medium was assessed.

Example 5

Purified methoxy polyethylene glycol of molecular weight 1900, vigorously stirred at 160°C for 1 hour at 0.1 mm Hg (13.3 Pa) (10 g), and freshly prepared vigorously dried D,L-lacti.d (10 g) were stirred under nitrogen at 160°C, tin(II) octoate (tin(II)-2-ethylhexanoate)

(50 µl) was added and the mixture was held at 160°C for 3 hours to give a straw colored, slightly viscous liquid which solidified on cooling. The solid product (0.5 g) was added to distilled water (5 ml) and stirred at 37°C for 18 hours, after which time a very fine dispersion or colloidal suspension was formed, which appeared completely clear, except a very faint blue

haze when held up to the light.

In contrast to braid, a simple mixture of the same methoxy polyethylene glycol (0.25 g) and poly(D,L-lactic acid) did not give

(0.25 g) in distilled water (5 ml) some dispersion after stirring

at 37°C for a similar period, but the polyester remained as a semi-solid, non-dispersed phase.

Example 6

An AB block copolymer of poly(d,1-lactide) and methoxy polyethylene glycol containing 50 wt% polyester and 50 wt% polyether was prepared by ring-opening polymerization of d,1-lactide in the presence of methoxypolyethylene glycol 5000 at 160°C

using an organotin catalyst.

100 mg of the block copolymer and 10 mg of an anti-estrogen, ICI 189150, which has very low aqueous solubility, were dissolved

in 0.4 ml of glacial acetic acid, and 2 ml of water was added slowly with vigorous stirring to give a colloidal suspension of drug/polymer in the acetic acid/water mixture. The mixture was frozen and lyophilized at 0.01 mm Hg (13.3 Pa) for 24 hours to give a solid lyophilized product.

By adding 0.9% sodium chloride solution in water, the freeze-dried product was redispersed to give a stable dispersion suitable for injection.

Claims (1)

Frozen, aqueous dispersion for use as a carrier for pharmaceutical or veterinary medicinal purposes, characterized in that it contains a self-dispersible form of an amphipathic, non-crosslinked linear, branched or grafted block copolymer having a minimum weight-average molecular weight of 1000, in which the hydrophobic component is biodegradable or hydrolytically unstable and the hydrophilic component may or may not be biodegradable or hydrolytically unstable, prepared by dissolving such copolymer in the non-self-dispersible form in a water-miscible solvent which either has a low boiling point or is freeze-dryable, vigorously agitating said solution while adding an excess of water, and freeze the resulting dispersion.