GB2386067A

GB2386067A - Long-acting parasiticidal composition with improved bioavailability comprising an avermectin or milbemycin, plus a salicylanilide & a polymeric species

Info

Publication number: GB2386067A
Application number: GB0204713A
Authority: GB
Inventors: William Blakely; Lillian Cromie; Sean Duffy
Original assignee: Norbrook Laboratories Ltd
Current assignee: Norbrook Laboratories Ltd
Priority date: 2002-02-28
Filing date: 2002-02-28
Publication date: 2003-09-10
Also published as: GB0204713D0; AU2003205858A1; AR038853A1; WO2003072112A1

Abstract

An injectable composition prepared for treating animals suffering from parasites, which parasites are known to be susceptible to at least one of the avermectins, milbemycins or salicylanilides, comprises a first parasiticidal agent selected from amongst the avermectins and the milbemycins, together with another parasiticidal agent selected from the salicylanilides in an amount such that the injectable composition delivers at least about 2.5 mg salicylanilide per kilogram live weight of the animal to be treated, in a physiologically tolerable solvent system suitable for injection, and an amount of a polymeric species that is effective to improve bioavailability of the salicylanilide parasiticidal agent over a period of treatment. H preferably comprises ivermectin in an amount of from 0.1 to 10%(w/v), a solvent selected from the group consisting of glycerol formal, propylene glycol, polyethylene glycol and combinations thereof, and a salicylanilide such as closantel. The polymeric species is preferably selected from the group consisting of polyvinylpyrrolidone and polyoxypropylene/polyoxyethylene block copolymers. The polymeric species improves the bioavailability of the salicylanilide as determined by blood plasma levels.

Description

Long-Acting Iniectable Parasiticidal Composition Field of the Invention.

This invention relates to injectable parasiticidal compositions, especially combination products for veterinary use, based on for example an avermectin or milbemycin together with another parasiticidal agent. Such combination products exhibit efficacy across a broader spectrum of parasites than is observed with the use of a single parasiticidal agent alone.

Background of the Invention Warm-blooded animals are subject to attack by parasites, and man has long sought to combat such parasites afflicting domestic companion animals, farmed livestock and exotic animals, to alleviate suffering and for commercial gain. The manner of attack by the parasites, and the identification of a sensitive stage in the life cycle of the parasite, may influence greatly the choice of combating agent.

Thus percutaneous treatments using topically applied preparations such as lotions, paints, creams, gels, dusting powders,"pour-ons"and dips are commonly suitable for ectoparasites, but combating endoparasites requires careful selection of the method of administration and the delivery system. Oral drenches, pastes, boluses, tablets, and granules for incorporating into feed mixes are known methods capable of being used by the animal husbandrymen, but other methods which are intended to avoid use of the gastrointestinal route are typically administered by qualified practitioners. Such other methods include use of aerosols, and parenteral drug compositions which are selectively prepared as solution or suspension or micronised powder formulations intended for subcutaneous, intracutaneous, and intramuscular injection according to the intended delivery regime. These last methods require special care in formulation to avoid irritation at the site of injection or possible adverse allergic or pyrogenic reactions.

Injectable formulations are typically prepared using aqueous or nonaqueous ("solvent") vehicles. The latter class may comprise physiologically tolerable alcohols, glycols, esters, a limited range of organic aromatic solvents, and vegetable oils and extracts or modified forms thereof. In selecting vehicles, the skilled person has to consider a number of issues including, solubility of the

intended active ingredient (s), the affinity of the drug to certain vehicles, whether it will affect any essential auxiliaries, pH, stability over time, viscosity, and naturally the risk of any toxic effect upon the animal to be treated. Therefore, formulation of a parasiticide is a complex task.

Traditional parasiticides include chemical agents such as the benzimidazoles, and carbamates, and plant extracts such as the pyrethroids, which tend to be used to combat ectoparasites such as ticks and mites.

The avermectins are very potent antiparasitic agents which are useful against a broad spectrum of endoparasites and ectoparasites in mammals as well as having agricultural uses against various parasites found in and on crops and soil. The basic avermectin compounds are isolated from the fermentation broth of the soil micro-organism Streptomyces avermitilis and these compounds are described in US patent US 4 310 519. Furthermore, derivatives of these basic avermectin compounds have been prepared by a variety of chemical means.

Some of the avermectin group of compounds contain a 22, 23-double bond and others contain a disaccharide at the 13-position which consists of a-Loleandrosyl-a-L-oleandrosyl group. One or both saccharide units can be removed forming a monosaccharide or an aglycone (where both saccharides are removed) as described in US patent US 4206205. The aglycone derivatives possess a hydroxy group at the 13 position which may be removed to form the 13-doxy compound as described in the patents US 4 171 314 and US 4 173 571. Acylation of hydroxy groups on the avermectin compounds and derivatives can be carried out as described in US 4 201 861.

The milbemycin series of compounds, disclosed in US 3 950 360, are structurally similar to the avermectin family in that they contain the sixteen membered macrocyclic ring. However, they do not contain the disaccharide subunit and there are differences in the substituent groups.

Ivermectin, disclosed in US 4 199 569, is prepared by the selective reduction of the 22,23 double bond of the avermectin compounds. Ivermectin is a mixture of 22,23-dihydro Avermectin 81 a and B1 b in a ratio of at least 80: 20.

Ivermectin is an especially preferred active component in pesticidal compositions, and there is extensive literature on its activity, demonstrating its efficacy against internal and external parasites, and its ability to interfere in the life cycle of certain parasites. The Merck Index (1996) cites several references including J. C. Chabala et al, J. Med. Chem. 23,1134 (1980); J. R. Egerton et al, Brit. Vet. J. 136,88 (1980); W. C. Campbell etal, Science 221,823-828 (1983) to mention but a few.

Formulation of ivermectin for the purposes of delivery in a variety of presentations, e. g. as an oral drench, pour-on, parenteral formulations, granules for adding to feed, and syringeable pastes. has proved highly challenging and numerous patents have been published on its use. Ivermectin exhibits a lipophilic character but it can be solvate in aqueous systems, and various patents describe special solvent systems for use in its formulation. Thus reference may be made at least to EP 0 045 655, and EP 0 146 414 for example.

Although ivermectin is surprisingly effective, and has enjoyed a long period of commercial success, there remains a keen interest in exploiting ivermectin against a wider range of parasites and in overcoming tolerance by some parasites which demands higher amounts of ivermectin to be delivered. Taking into account the fact that a significant volume of use of ivermectin is in protecting and treating animals intended for human consumption, there are constraints on the residual amount of ivermectin in the carcass of such an animal. Therefore, high loading of ivermectin, even if technically feasible, in a delivery system are not necessarily the optimum solution.

Combination formulations are also desirable taking account of acquired tolerance or resistance in pests to prolonged usage of other more traditional parasiticidal agents. This phenomenon is well documented, e. g. in relation to worming compositions. Synergistic effects or complementary effects of combined parasiticidal agents have been observed as a route to combating the aforesaid tolerance problem. Synergistic anthelmintic compositions are discussed in WO 94/28887, which focuses on substituted mono-and bisphenols, salicylanilides, benzene sulphonamides, halogenated benzimidazoles, benzimidazoles, and benzimidazol carbamates.

The salicylanilides, tend to be effective against fungal attack, but the chemically modified derivative closantel is an effective worming agent. Closantel is described in US 4 005 218 and in the literature, e. g. J. Guerrero et al, J. Parasitol. 68,616, (1983); H. Van den Bossche et ai, Arch. lnt. Physio. Biochim, 87, 851 (1979) ; H. J. Kane et at, Mol. Biochem. Parasitol. 1, 347 (1980).

The opportunity to combine the use of avermectins with other parasiticidal agents has been explored already. Thus one finds that skin-absorbable pour-on formulations containing triclabendazole, optionally containing an avermectin, tetramisole or levamisole have been proposed in WO 0061068. An injectable formulation containing closantel together with an avermectin or milbemycin has been proposed in WO 95/05812. Formulations of the pour-on and injectable type are discussed in WO 01/60380, which comprise use of a pyrrolidone solvent and a bridging solvent such as a xylene, optionally including a further solubility agent such as propylene glycol caprylic acids and esters or peanut oil. This special solvent system is needed to address the difficulties of formulating differing parasiticidal agents such as closantel and ivermectin together.

Salicylanilide derivatives such as closantel provide useful control over a range of parasites and are especially useful against liver fluke. The avermectin group of anti-parasitic compounds of which ivermectin is the best known example, provide complementary protection against many other parasites such as roundworms. Therefore, there are advantages to be gained if a combination of these drugs could be provided in a form that can be conveniently administered to livestock and which will provide effective control of parasitic infection.

For ivermectin and closantel the established dose rate for injection of livestock is of the order of 200/-lg/kg (ivermectin) and 2.5mg/kg (closantel).

Provision of a satisfactory aqueous formulation is problematical because the optimum pH for each drug is different. An acidic system providing the optimum pH for ivermectin, whereas closantel requires an alkaline medium for satisfactory dissolution.

Accordingly non-aqueous or essentially non-aqueous formulations were investigated. Ivermectin can be prepared in non-aqueous or low water content

systems that are suitable for injection. Glycerol formal, propylene glycol, polyethylene glycol, pyrrolidone, and related solvents have been used in various formulations, singly or in combination. Patent publication WO 95/05812 discloses closantel and ivermectin solutions for injection using some of the solvents established as suitable for ivermectin (glycerol formal, polyethylene glycol, propylene glycol and water). However the effectiveness of the formulations, in terms of bioavailability of the active parasiticidal agents, described in that patent application were not disclosed.

The results of our research into the efficacy of such formulations are summarised in Table 1 presented hereinbelow.

In order to evaluate formulations of the type described in the reference WO 95/05812, administration of an ivermectin/closantel combination product as disclosed therein, at a dosage corresponding to 2.5 mg/kg closantel was carried out according to established industry practices. However, this failed to produce blood plasma levels of closantel greater than 20 ppm (Examples 1 and 2 in Table 1 reported hereinafter). According to typical experience, it was anticipated that a higher amount of closantel would have a favourable effect on the blood plasma levels. Increasing the closantel concentration in such formulations was readily achieved, allowing higher dosing of closantel in the combination product. Despite these attempts at higher dosing, administration of closantel at 5 mg/kg did not increase blood plasma levels at all and even at the exceptionally high dosing level of 7.5 mg/kg the blood plasma levels only increased to 31 ppm (Examples 3 and 4 in Table 1). Therefore the proposed formulations available from following the teachings of the reference WO 95/05812 surprisingly failed to deliver the expected solution to the problem of obtaining a satisfactory combination product.

Objects of the Invention Accordingly, it is an object of the present invention to provide improved veterinary pharmaceutical preparations. In particular it is an object of the invention to provide a composition having activity against a broad range of endo-and ectoparasites including flukes. It is a further object of this invention to provide preparations which are suitable for administration by injection. A still further object of the invention is to provide a veterinary pharmaceutical product combining

ivermectin and closantel in an effective formulation enabling enhanced bioavailability of closantel in excess of the observed prior art levels.

Summary of the Invention Surprisingly it has been found that the inclusion of a significant amount of a polymeric moiety, especially polyvinylpyrrolidone (PVP) has a dramatic effect on the bioavailability of salicylanilides such as closantel in parasiticidal formulations.

Lutrol, (a polyoxypropylene/polyoxyethylene block copolymer, known as a polymeric surfactant) also showed some benefit in this respect but not as demonstrably effective as the PVP.

Accordingly, the invention enables the provision of injectable parasiticidal compositions, especially combination products, based on for example an avermectin or milbemycin together with another parasiticidal agent of the salicylanilide type with effective bioavailability of the parasiticidal agents.

Thus according to one aspect of the invention, an injectable parasiticidal composition prepared for treating animals, comprises a first parasiticidal agent selected from amongst the avermectins and the milbemycins, typically in an amount of from 0. 1 to 10% (w/v), together with another parasiticidal agent selected from the salicylanilides in an amount such that the injectable composition delivers at least about 2. 5 mg salicylanilide per kilogram live weight of the animal to be treated, in a physiologically tolerable solvent system suitable for injection, characterised in that the composition comprises an amount of a polymeric species that is effective to improve bioavailability of the salicylanilide parasiticidal agent over a period of treatment.

A preferred injectable composition comprises ivermectin in an amount of from 0. 1 to 10% (w/v), along with closantel in an amount sufficient to provide the required dosage amount.

Preferably, the polymeric species is selected from a polyvinylpyrrolidone (PVP) or a polyoxypropylene/polyoxyethylene block copolymer, the former being especially preferred.

Polyvinylpyrrolidone is available in powder form of various molecular weights (Mw circa 10, 000 up to 55, 000, and above : Aldrich Catalogue 2000-2001)

for pharmaceutical use and is generally adopted as a dispersing and suspending agent (Merck Index). Thus it is surprising that it offers the observed beneficial effect for two reasons. Firstly, its normal use is in preparing the formulation, but here it is unnecessary, because the actives are readily introduced to the solvent system without such an aid, indeed our findings in this respect bears out the findings of the earlier patent applicant (Phoenix-W 01/60380) in terms of making a stable formulation. Secondly, a person experienced in this art would predict that macromolecules may have an adverse effect on bioavailability when present in a preparation due to interaction between the macromolecule and the drug component, leading to the so-called"drug binding"impairing bioavailability.

Therefore, hitherto on the basis of the present state of the art, prior to the present work, it could not have predicted that PVP would have a beneficial effect with respect to inhibiting depletion of effective amounts of closantel from blood after injection. Thus PVP is surprisingly found to be effective in the manufacture of an injectable parasiticidal composition comprising closantel having long acting efficacy, such that the amount of PVP used enables the desired period of efficacy to be designed into the formulation to provide a controllable period of effective treatment with a predictable depletion period permitting slaughter for human consumption of the treated animal if required.

A suitable solvent system comprises glycerol formal (GF), or a mixture of propylene glycol (PG) and GF, or a mixture of a polyethylene glycol (PEG) and GF.

A range of PEG solvents according to molecular weight is commercially available, and any of those, or others that may yet be made available, may be chosen for convenience provided that the PEG is presented or rendered available as a liquid during formulation. Typically, PEG 200 to 1500 are readily to hand from commercial sources, and thus can be used for the purposes herein, but PEG 200 to PEG 600 are usefully employed in this invention. A preferred solvent system consists of PEG 200 with GF.

Thus according to the invention, it is now possible to obtain in a single injectable formulation, an avermectin, preferably ivermectin, and a salicylanilide, preferably closantel, which is effective to deliver closantel when administered to

the animal such that an effective plasma concentration of is readily achieved closantel over a period of treatment.

The potential ranges of the preferred parasiticidal agents useful in such formulations are: Ivermectin - from 0. 1 to 10% w/v, preferably 1 to 5 % w/v; Closantel-from 1 to 30% w/v, preferably 1 to 15 % w/v.

The quantity of polymeric species, especially polyvinylpyrrolidone, required to be effective depends on the desired salicylanilide activity of the mixture but typically at least 11 % PVP is required to permit the higher effective amounts of e. g. closantel desired to be achieved, and good results are demonstrated at levels of 15% or more. With regard to relative ratio of polymeric component to closantel, it has been demonstrated that good bioavailability of closantel is achieved when a ratio of greater than 1.44 : 1 is established in the formulation.

Modes for Carrying Out the Invention Formulation Examples-Solvent Systems A: In the preparation of a 0. 5% w/v ivermectin parenteral solution the composition was as follows : Ivermectin 0. 5% w/v Closantel (as Na salt) 12. 5%w/v PVP (K12) 18. 0% w/v Glycerol Formal q. s. ad 1 00% v/v B: In the preparation of a 0. 5% w/v ivermectin parenteral solution the composition was as follows :

Ivermectin 0. 5% w/v Closantel (as Na salt) 12. 5% w/v PVP (K12) 18. 0% w/v Propylene Glycol 40% w/v Glycerol Formal q. s. ad 100% v/v

C : In the preparation of a 0. 5% w/v ivermectin parenteral solution the composition was as follows : Ivermectin 0. 5% w/v Closantel (as Na salt) 12. 5%w/v PVP (K12) 18. 0% w/v Polyethylene Glycol 200 40% w/v Glycerol Formal q. s. ad 100% v/v General Method of Formulation : These formulations were made up following usual industry practice. Thus PVP is initially dissolved in the PEG 200 and half the volume of glycerol formal.

Then the closantel is introduced with stirring as required. Finally the ivermectin is added, and dissolved, and the remainder of the solvent is added to the final desired volume. The solution is sterilised by membrane filtration and packaged aseptically.

Test Results: Performance Examples 1 to 7 describe the trials of prior art proposals in comparison with formulations according to the invention.

Test Example 1: 2.5 mg/kg closantel in a formulation of 0.5% ivermectin in glycerol formal.

Test Example 2: 2.5 mg/kg closantel in a formulation of 0.5% ivermectin in glycerol formal and polyethylene glycol 200.

Test Example 3: 5 mg/kg closantel in a formulation of 0.5% ivermectin in glycerol formal with polyethylene glycol 200.

Test Example 4: 7.5 mg/kg closantel in a formulation of 0.5% ivermectin in glycerol formal with polyethylene glycol 200.

Test Example 5 : 5 mg/kg closantel in a formulation of 0.5% ivermectin in glycerol formal, and containing PVP.

Test Example 6: 5 mg/kg closantel in a formulation of 0.5% ivermectin in glycerol formal with propylene glycol, and containing PVP.

Test Example 7: 5 mg/kg closantel in a formulation of 0.5% ivermectin in glycerol formal with polyethylene glycol 200, and containing PVP.

The results of bioavailability with respect to closantel are presented in the Table 1 hereinafter.

Table 1 Example Solvent Ivermectin Closantel PVP Closantel Closantel System Content Content Content Dose Maximum (% w/v) (% w/v) (% w/v) (mg/kg) Plasma level (ppm) 1 GF 0.5 6. 25-2. 5 14.8 2 PEG/GF 0.5 6. 25-2. 5 19.3 3 PEG/GF 0.5 25 - 5 18.6 4 PEG/GF 0.5 18. 75-7. 5 31.3 5 GF 0.5 12.5 18 5 52.8 6 PG/GF 0.5 12.5 18 5 48.3 7 PEG/GF 0.5 12.5 18 5 57.8

GF = Glycerol Formal PEG = Polyethylene Glycol PG = Propylene Glycol In formulations using two solvents the first mentioned solvent is added at 40% With the second added to make up the required volume.

Industrial Applicability In view of the aforesaid advantages and properties of the compositions described herein, the invention will be usefully applied in the field of veterinary medicine in particular for combating endoparasites and ectoparasites typically afflicting livestock such as bovines, equines, ovines and caprines.

Claims

CLAIMS 1. An injectable parasiticidal composition prepared for treating animals, comprises a first parasiticidal agent selected from amongst the avermectins and the milbemycins, together with another parasiticidal agent selected from the salicylanilides in an amount such that the injectable composition delivers at least about 2.5 mg salicylanilide per kilogram live weight of the animal to be treated, in a physiologically tolerable solvent system suitable for injection, wherein the composition comprises an amount of a polymeric species that is effective to improve bioavailability of the salicylanilide parasiticidal agent over a period of treatment.
2. A composition as claimed in claim 1, wherein the polymeric species is selected from the group consisting of polyvinylpyrrolidones (PVP).
3. A composition as claimed in claim 1, wherein the polymeric species is selected from the group consisting of polyoxypropylene/polyoxyethylene block copolymers.
4. A composition according to any one of claims 1 to 3, wherein the salicylanilide is closantel.
5. A composition according to any one of claims 1 to 3, wherein the first anti- parasitic agent is selected from the group consisting of avermectins.
6. A composition according to any one of claims 1 to 3, wherein the first anti- parasitic agent is selected from the group consisting of milbemycins.
7. A composition according to claim 4, wherein the first anti-parasitic agent is ivermectin present in an amount in the range 0.1 to 10% (w/v).
8. A composition according to claim 4, wherein closantel is present in an amount of 1 to 30% (w/v).
9. A composition according to any one of claims 1 to 3, wherein the solvent is selected from the group consisting of propylene glycol (PG), polyethylene glycols (PEG), glycerol formal, and water individually or in combination.

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10. A composition according to any one of claims 1 to 3, wherein the polymeric species is present in an amount in the range of from 1 % to 35% and above.
11. A composition according to claim 4, wherein the polymeric species is PVP present in an amount of at least 11 %.
12. A composition according to any one of the Formulation Examples or Test Examples 5,6, or 7 hereinbefore.