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WO1993015727A1 - Antimalarial synergistic compositions containing benflumetol - Google Patents

Antimalarial synergistic compositions containing benflumetol Download PDF

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Publication number
WO1993015727A1
WO1993015727A1 PCT/EP1993/000163 EP9300163W WO9315727A1 WO 1993015727 A1 WO1993015727 A1 WO 1993015727A1 EP 9300163 W EP9300163 W EP 9300163W WO 9315727 A1 WO9315727 A1 WO 9315727A1
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WO
WIPO (PCT)
Prior art keywords
effective amount
benflumetol
synergistically effective
quinine
pharmaceutical composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP1993/000163
Other languages
French (fr)
Inventor
Anton Alexander Poltera
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Ciba Geigy AG
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Filing date
Publication date
Priority to EP93902246A priority Critical patent/EP0583439B1/en
Priority to DE69323941T priority patent/DE69323941T2/en
Priority to RU93058291A priority patent/RU2118158C1/en
Priority to HU9303152A priority patent/HU220605B1/en
Priority to FI934360A priority patent/FI934360A7/en
Priority to SG1996001151A priority patent/SG45193A1/en
Priority to AU33522/93A priority patent/AU668376B2/en
Priority to PL93300806A priority patent/PL172590B1/en
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Priority to JP51371093A priority patent/JP3560970B2/en
Publication of WO1993015727A1 publication Critical patent/WO1993015727A1/en
Priority to NO933271A priority patent/NO304409B1/en
Anticipated expiration legal-status Critical
Priority to GR990401168T priority patent/GR3030086T3/en
Ceased legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/49—Cinchonan derivatives, e.g. quinine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A61P33/06—Antimalarials
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present invention relates to a synergistic antimalarial composition, methods of trea ⁇ ting malaria by administering that composition, and to a process for the preparation of that synergistic antimalarial composition.
  • Drug resistant malaria is a serious clinical and public health problem.
  • the malaria parasite Plasmodium falciparum has developed the versatility of evading the effects of standard drugs such as chloroquine either by genetic mutation or by non-genetic adaption methods.
  • standard drugs such as chloroquine either by genetic mutation or by non-genetic adaption methods.
  • the spread of Plasmodium falciparum resistant to chloroquine and other antimalarial drugs is a major challenge to health care programms in tropical and subtropical countries. Therefore, novel pharmaceutical compositions which diminish the resistance against malarial parasites, are needed for successful therapy.
  • compositions containing the agent benflumetol have been re ⁇ ported in Chemical Abstracts 97:28538 h and 101:136941u.
  • Other compositions contain combinations of known antimalarial agents.
  • the combination of amodiaquine and tetracycline have been used in the clinic [Suphat Noeypatimanond, et al. (1983), Treatment of Plasmodium falciparum malaria with a combination of amodiaquine and tetracycline in central Thailand, Trans. R. Soc. Trop. Med. and Hyg. 73 (3), 338-340].
  • compositions containing the agent benflumetol in combination with the agent quinine or a derivative thereof have improved antimalarial activity and are more active than compositions containing only the individual component benflumetol, or alternatively, quinine derivatives.
  • composition defines a mixture comprising the combination of a compound of the formula I with at least one compound of the group (II).
  • This mixture either consists of a dry preparation of the active components (I) and (IT) such as a lyophilisate or preferably contains additives suitable for the manufacture of a dosage form such as tablets, capsules or suppositories.
  • synergistic action defines the increase of efficacy of the composition above the efficacy level of at least one individual active component (I) or (II) at the given dose.
  • the efficacy of all active components present in the pharmaceutical composition is increased.
  • the synergistic effect is most desirable as it enables the use of a lower dosage of an individual component and/or improvement of activity above the activity levels of the individual components.
  • the synergism of the claimed composition is proved by experimental results from in-vitro and in-vivo models.
  • the results show that the activity of the component according to formula I is raised as compared to the activity of benflumetol (I) in an individual dosage form and that the activity of the component (II) is also being raised.
  • Synergistic action against malaria of the composition according to the present invention permits the combined application of different drug regimens during therapy by the admini ⁇ stration of one dosage form such as one or two tablets per day.
  • the active component (I) mentioned above, wherein Bu denotes n-butyl, is known under the name benflumetol, see C.A.R.N. 82186-77-4.
  • Pharmaceutical compositions containing benflumetol individually and their activity against malaria are also known, see the abstracts according to CA. 97:28538h and 101:136941.
  • the preparation of benflumetol has been disclosed in the Published Chinese Patent Application 88/076666.X.
  • the active components selected from the group (II) consisting of quinine, mefloquine, halofantrine, primaquine and pyronaridine are known active agents useful in malaria therapy.
  • a pharmaceutically acceptable salt of quinine is, for example, the acid addition salt with one or two equivalents of a monobasic inorganic or organic acid or the acid addition salt with a dibasic inorganic or organic acid.
  • Such acid addition salt is, for example, the hydrohalide salt, e.g. the hydrochloride, hydrobromide or hydroiodide salt, the dihydrohalide salt, e.g. the dihydrochloride, dihydrobromide, or dihydroiodide salt, the hydrogensulfate or sulfate salt, the hydrogencarbonate or carbonate salt, the ethylcarbonate, formate, acetate, gluconate or tannate salt of quinine.
  • the hydrohalide salt e.g. the hydrochloride, hydrobromide or hydroiodide salt
  • the dihydrohalide salt e.g. the dihydrochloride, dihydrobromide, or dihydroiodide salt
  • a pharmaceutically acceptable derivate of quinine is, for example, the structurally related quinidine, cinchonine or cinchonidine derivative thereof.
  • Those derivatives are preferably present in the composition as acid addition salt, e.g. as hydrogenhalide or dihydrogenhalide salt, e.g. as hydrochloride or dihydrochloride.
  • Mefloquine (CAS Reg.No. 53230-10-7) is preferably present in the composition as hydrochloride acid addition salt (CAS Reg. No. 51773-92-3). Reference is made to the entry No. 1381-v at page 513 of Martindale, The Extra Pharmacopoeia, Twenty-ninth Ed., The Pharmaceutical Press London 1989.
  • Halofantrine (CAS Reg.Nos. 69756-53-2 and 66051-63-6) is preferably present in the composition as hydrochloride acid addition salt (CAS Reg. No. 36167-63-2). Reference is made to the entry No. 16829-p at page 512 of Martindale, The Extra Pharmacopoeia (loc.cit.).
  • Chloroquine, 7-chloro-4-[4-diethylamino-l-methyl-n-butylamino]-quinoline is a known antimalarial agent from the 4-aminoquinoline group and is preferably present in the composition in the form of its diphosphate or sulfate salt. Reference is made to entry No. 2163 at page 334 of the Merck Index, Eleventh Edition.
  • Primaquine 8-(4-Amino-l-methyl-n-butylamino)-6-methoxy-quinoline, is a known antimalarial agent from the 8-aminoquinoline group and is represented by the following structural formula:
  • Pyronaridine is a known antimalarial agent represented by the following structural formula:
  • a pharmaceutical composition suitable for synergistic action of the active components against malaria which comprises the combination of a synergistically effective amount of benflumetol (I) with a synergistically effective amount of at least one compound selected from the group (TI) consisting of quinine, mefloquine and halofantrine, or a pharmaceutically acceptable salt or derivative thereof having antimalarial efficacy.
  • a synergistically effective amount of benflumetol (I) with a synergistically effective amount of at least one compound selected from the group (TI) consisting of quinine, mefloquine and halofantrine, or a pharmaceutically acceptable salt or derivative thereof having antimalarial efficacy.
  • composition suitable for synergistic action of the active components against malaria which comprises the combination of a synergistically effective compound of benflumetol (I) with a synergistically effective amount of a pharmaceutically acceptable acid addition salt of quinine.
  • compositions according to the present invention are preferably present in the composition according to the present invention.
  • the additives are used for the preparation of preferably enteral or parenteral dosage forms according to conventional formulation methods.
  • suitable additives include inert diluents or fillers, thereby forming solid or liquid dosage forms such as tablets, powders, capsules, syrups and the like.
  • suitable additives include inert diluents or fillers, thereby forming solid or liquid dosage forms such as tablets, powders, capsules, syrups and the like.
  • the pharmaceutical compositions can, if desired, contain additional ingredients such as flavourings, binders, excipients and the like.
  • tablets containing various solid additives such as starch, dextrin, alginic acid and certain complex silicates, together with binding agents such as polyvinylpyrrolidone, sucrose, gelatin and acacia.
  • binding agents such as polyvinylpyrrolidone, sucrose, gelatin and acacia.
  • lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often useful for tabletting purposes.
  • Solid compositions of a similar type may also be employed as fillers in soft and hard gelatin capsules, preferred materials therefore include lactose or milk sugar and high molecular weight polyethylene glycols.
  • the mixture of the compounds can for example be administered in a gelatin capsule.
  • Such formulation could be based on a suitable refined edible oil such as sunflower oil, corn oil, peanut oil, coconut oil or til oil.
  • the active components (I) and (II) are formulated in a single unit dosage form such as tablets or capsules.
  • the active components (I) and (II) may also be formulated into two individual dosage forms contained within one administration system (kit of parts), which are simultaneously or consecutively administered. The same route of administration is possible, e.g. admini ⁇ stration of two individual dosage forms contained within one kit of parts.
  • One tablet or capsule containing component (I) and, consecutively, a second dosage form containing component (II) is administered.
  • An individual dose regimen may be developed especially during clinical treatment, e.g. by administering after the first occurrence of malaria a tablet or capsule containing a high dose of the active component (I) or, correspondingly, multi ⁇ plying lower doses in the beginning of malaria attacks, and administering also a tablet or capsule containing a lower dose of the active component (II).
  • dosage forms containing a lower dose of component (I) and a higher dose of compo ⁇ nent (II) are administered.
  • Different dosage forms present in one kit-of-parts may also be administered simultaneously or consecutively, e.g. by administration of a tablet containing component (I) and a suppository containing component (II).
  • the dosage range may also be varied according to the dose regimens given above.
  • compositions according to the present invention in therapy against malaria are evident from in-vitro and in-vivo results from experiments carried out in established test models.
  • the ability of the composition to act as an effective and long-acting antimalarial agent even against strains of P.berghei known to be extremely resistant against other antimalarial agents reflects the usefulness of the present invention.
  • the present invention also relates to a method of treatment against malaria which com ⁇ prises administering to a patient after the outbreak of malaria the above-mentioned pharmaceutical composition comprising the combined active components (I) and (II).
  • the composition is administered to the patient for a period of time of at least four days, preferably five or more days.
  • the term method of treatment also comprises prophylactic administration of the compo ⁇ sition to healthy patients to prevent the outbreak of the disease in high-risk areas of contamination, especially in regions between the tropics of Capricorn and cancer.
  • the dose of the active component benflumetol (I) as contained in the pharmaceutical composition may vary within wide limits and depends on the condition of the patient and the time period elapsed after the outbreak of the disease. Based on in-vivo data from model experiments as reported below in the Examples, it is established that the daily dose of benflumetol is between about 0.2-50.0 mg/kg, preferably 0.2-10.0 mg/kg and especially about 0.2-5.0 mg/kg. This daily dose can be raised considerably upon need in view of the low toxicity and high tolerability of benflumetol. It is also estimated that the daily dose of component (II) in the composition, is between 0.2 and 50 mg/kg, preferably 0.3-5.0 mg kg and especially between about 0.4-3.0 mg/kg.
  • the dose ratio of component (I) to component (II) may also vary within wide limits. Synergism will be especially efficient if benflumetol is administered in equal weight amounts or, preferably, in excess amounts as compared to the weight amounts of component (II) administered. Accordingly, the weight amount of benflumetol may vary from one to ten parts for each part component (II), administered. Preferably, three to seven parts and especially five to six parts of benflumetol are administered for each part of component (II).
  • the dose amounts given and dose ratios refer to daily administrations.
  • the invention also relates to a process for the preparation of the pharmaceutical composi ⁇ tion suitable for synergistic action of the active components against malaria which com ⁇ prises combining an effective amount of a compound of formula I with an effective amount of the component (II) and formulating this combination of active components under optional addition of pharmaceutically acceptable additives to a suitable dosage form.
  • novel pharmaceutical compositions contain, for example, from 10 % to 80 %, prefer ⁇ ably from 20 % to 60 %, of the combination of the active components.
  • Pharmaceutical compositions according to the invention are suitable for enteral administration and are, for example, formulated into oral dosage unit forms, such as drag ⁇ es, tablets, capsules or suppositories. These are manufactured in a manner known per se, for example by means of conventional mixing, granulating, confectioning, dissolving or lyophilising processes.
  • pharmaceutical preparations for oral administration can be obtained by combi ⁇ ning the active ingredient with solid carriers, optionally granulating a resulting mixture, and processing the mixture or granulate, if desired or necessary, after the addition of suitable adjuncts, to form tablets or drag ⁇ e cores.
  • the active components (I) and (II) are milled either individually or together to particle sizes from about 10 ⁇ to about 400 ⁇ , preferably 20 ⁇ to 200 ⁇ . At least 90 % of the crystals of the active components are present in these ranges.
  • Micronisation is preferably effected by known methods using an ultrasonics disintergrator, e.g. of the Branson Sonifier type as described e.g. in J. Pharm. Sci. 53 (9), 1040-1045 (1965), or by stirring a suspension with a high-speed agitator, for example with a stirrer of the Homorex type (supplied by Brogli & Co., Basel).
  • an ultrasonics disintergrator e.g. of the Branson Sonifier type as described e.g. in J. Pharm. Sci. 53 (9), 1040-1045 (1965)
  • stirring a suspension with a high-speed agitator for example with a stirrer of the Homorex type (supplied by Brogli & Co., Basel).
  • micronisation is effected at about 500 to 10,000 rpm (rotations per minute) by dissolving or suspending the combination of the active components in an organic solvent, e.g.
  • methanol, ethanol or propylene glycol precipitating it in microcrystalline form at ca. 0°-5°C in water or an aqueous salt solution, e.g. 2 % sodium chloride solution which may additionally contain a protective colloid such as gelatin or a cellulose ether, e.g. methyl cellulose or hydroxypropyl methyl cellulose, in low concentration (0.1-1 %), and filtering the resultant stirred suspension.
  • the filter cake is dried at low temperature, e.g. ca. 0°-5°C, under vacuum (e.g. below 50 mbar, preferably at 0.5 mbar). The subsequent drying can be effected at ca. 50°-90°C.
  • the crystals thus obtained are then formulated to granulates, preferably by wet granulation which is carried out according to standard methods.
  • the pharmaceutical composition is preferably prepared by compressing a granular formulation which is obtained, for example, by sieving and, if desired, by comminuting the drug, with or without the excipients, compacting with another solvent such as ethanol or water, removing the solvent or drying, with or without the addition of lubricants or glidants such as magnesium stearate or TWEEN, comminuting the granules and sieving once more.
  • the granules can be compressed to tablet cores in a conventional tabletting machine, for example an EKO Korsch eccentric tabletting machine, at a pressure of ca. 10 kN.
  • Coating can be effected by applying an aqueous-ethanolic solution in which, for example, poly ⁇ ethylene glycol and saccharose is dissolved or dispersed.
  • Drag ⁇ e cores are provided with suitable coatings that may be resistant to gastric juices, there being used, inter alia, concentrated sugar solutions that may contain gum arabic, talc, polyvinylpyrrolidone or polyethylene glycol. Colorings, flavorings or pigments may be added to the syrups,tablets or drag ⁇ e coatings, for example for identification purposes, masking taste or to indicate different doses of active ingredient.
  • T e dry-filled capsules may contain the active components in the form of a granulate, for example in admixture with fillers, such as lactose, binders, such as starches, and/or glidants, such as talc or magnesium stearate, and optionally stabilisers.
  • the active ingredient is preferably dissolved or suspended in suitable liquids, such as fatty oils, paraffin oil or liquid polyethylene glycols, to which stabilisers may also be added.
  • Suitable for enteral administration are also suppositories that consist of the combination of the active ingredients and a suppository base.
  • Suitable as suppository bases are, for example, natural or synthetic triglycerides, paraffins, polyethylene glycols or higher alkanols. It is also possible to use gelatin rectal capsules that contain a combination of the active ingredient and a base material; suitable base materials are, for example, liquid triglycerides, polyethylene glycols or paraffin hydrocarbons.
  • Quinine dihydrochloride crystals are passed through a 100 mesh size sieve.
  • Benflumetol crystals are passed through a 60 mesh size sieve and mixed with the quinine solid, starch and dextrin. This mixture is passed 3 times through a 40 mesh size sieve.
  • Tween®-80 is added to the paste of starch which is mixed with the above formulation. This mixture is granulated by way of wet-granulation, passed through a 40 mesh size sieve, dried at reduced pressure at 50-60°C. The Mg-stearate is added, and the tablets are pressed.

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Abstract

The invention relates to a synergistic antimalarial composition which comprises the antimalarial agent benflumetol and also an antimalarial agent from the quinine group such as quinine. The composition can be formulated into solid dosage forms such as tablets and is useful for the treatment of drug resistant malaria.

Description

ANTIMALARIAL SYNERGISTIC COMPOSITIONS CONTAINING BENFLUMETOL
The present invention relates to a synergistic antimalarial composition, methods of trea¬ ting malaria by administering that composition, and to a process for the preparation of that synergistic antimalarial composition.
Drug resistant malaria is a serious clinical and public health problem. The malaria parasite Plasmodium falciparum has developed the versatility of evading the effects of standard drugs such as chloroquine either by genetic mutation or by non-genetic adaption methods. The spread of Plasmodium falciparum resistant to chloroquine and other antimalarial drugs is a major challenge to health care programms in tropical and subtropical countries. Therefore, novel pharmaceutical compositions which diminish the resistance against malarial parasites, are needed for successful therapy.
The antimalarial effect of compositions containing the agent benflumetol has been re¬ ported in Chemical Abstracts 97:28538 h and 101:136941u. Other compositions contain combinations of known antimalarial agents. For example, the combination of amodiaquine and tetracycline have been used in the clinic [Suphat Noeypatimanond, et al. (1983), Treatment of Plasmodium falciparum malaria with a combination of amodiaquine and tetracycline in central Thailand, Trans. R. Soc. Trop. Med. and Hyg. 73 (3), 338-340]. Another antimalarial combination (FANS ED, mefloquine, pyrimethamine and sulphadoxine) has been launched on the market [Tropical Diseases Research, Seventh Programme Report, Chapter 2; Malaria, UNDP World BankAVΗO. Published by WHO, 1985].
The use of combinations of artemisinine, its derivatives and other antimalarial compounds, such as quinine, has been published in the German Patent Application P 37 15 378. Also the synergistic effect of a combination of artemisinine and primaquine is known (Wan Yaode, Cang Qizhong, Pharmacy Bulletin, Vol. 16, No. 1, 1981).
Combinations of the antimalarial agents artemether, arteether, artemisinine, dihydro- artemisinine, or artesunate with quinidine or with mefloquine have been disclosed in the European Patent Application 362 810.
Motivation for the present invention has been drawn from the need in therapy for an im¬ proved antimalarial composition of higher activity and lower resistance against malarial parasites such as Plasmodium falciparum.
It has now been found that pharmaceutical compositions containing the agent benflumetol in combination with the agent quinine or a derivative thereof have improved antimalarial activity and are more active than compositions containing only the individual component benflumetol, or alternatively, quinine derivatives.
The following invention relates to a pharmaceutical composition suitable for synergistic action of the active components against malaria comprising a synergistically effective amount of a compound of the formula:
Figure imgf000004_0001
combined with a synergistically effective amount of at least one compound selected from the group (II) consisting of quinine, mefloquine, halofantrine, chloroquine, primaquine and pyronaridine or a pharmaceutically acceptable salt or derivative thereof having antimalarial efficacy.
The general definitions and terms used in this specification of the invention preferably have the following meanings:
The term pharmaceutical composition defines a mixture comprising the combination of a compound of the formula I with at least one compound of the group (II). This mixture either consists of a dry preparation of the active components (I) and (IT) such as a lyophilisate or preferably contains additives suitable for the manufacture of a dosage form such as tablets, capsules or suppositories.
The term synergistic action defines the increase of efficacy of the composition above the efficacy level of at least one individual active component (I) or (II) at the given dose. Preferably, the efficacy of all active components present in the pharmaceutical composition is increased. The synergistic effect is most desirable as it enables the use of a lower dosage of an individual component and/or improvement of activity above the activity levels of the individual components.
The synergism of the claimed composition is proved by experimental results from in-vitro and in-vivo models. The results show that the activity of the component according to formula I is raised as compared to the activity of benflumetol (I) in an individual dosage form and that the activity of the component (II) is also being raised.
Synergistic action against malaria of the composition according to the present invention permits the combined application of different drug regimens during therapy by the admini¬ stration of one dosage form such as one or two tablets per day.
The application of a dosage form comprising the active component benflumetol (I) allows permanent action against malaria. This is evident from tests carried out in different stand¬ ard in-vitro and in-vivo pharmacological models. The presence in the same dosage form of the second active component (II) allows immediate and fast action against protozoa after the outbreak of the disease.
The active component (I) mentioned above, wherein Bu denotes n-butyl, is known under the name benflumetol, see C.A.R.N. 82186-77-4. Pharmaceutical compositions containing benflumetol individually and their activity against malaria are also known, see the abstracts according to CA. 97:28538h and 101:136941. The preparation of benflumetol has been disclosed in the Published Chinese Patent Application 88/076666.X.
The active components selected from the group (II) consisting of quinine, mefloquine, halofantrine, primaquine and pyronaridine are known active agents useful in malaria therapy.
A pharmaceutically acceptable salt of quinine is, for example, the acid addition salt with one or two equivalents of a monobasic inorganic or organic acid or the acid addition salt with a dibasic inorganic or organic acid. Such acid addition salt is, for example, the hydrohalide salt, e.g. the hydrochloride, hydrobromide or hydroiodide salt, the dihydrohalide salt, e.g. the dihydrochloride, dihydrobromide, or dihydroiodide salt, the hydrogensulfate or sulfate salt, the hydrogencarbonate or carbonate salt, the ethylcarbonate, formate, acetate, gluconate or tannate salt of quinine.
A pharmaceutically acceptable derivate of quinine is, for example, the structurally related quinidine, cinchonine or cinchonidine derivative thereof. Those derivatives are preferably present in the composition as acid addition salt, e.g. as hydrogenhalide or dihydrogenhalide salt, e.g. as hydrochloride or dihydrochloride.
Quinine and the above-mentioned salts and derivatives thereof are known antimalarial agents. Reference is made to the Merck Index published by Merck & Co., Inc. Tenth Edition (1983), and the various entries at pages 1164-1166.
Mefloquine (CAS Reg.No. 53230-10-7) is preferably present in the composition as hydrochloride acid addition salt (CAS Reg. No. 51773-92-3). Reference is made to the entry No. 1381-v at page 513 of Martindale, The Extra Pharmacopoeia, Twenty-ninth Ed., The Pharmaceutical Press London 1989.
Halofantrine (CAS Reg.Nos. 69756-53-2 and 66051-63-6) is preferably present in the composition as hydrochloride acid addition salt (CAS Reg. No. 36167-63-2). Reference is made to the entry No. 16829-p at page 512 of Martindale, The Extra Pharmacopoeia (loc.cit.).
Chloroquine, 7-chloro-4-[4-diethylamino-l-methyl-n-butylamino]-quinoline is a known antimalarial agent from the 4-aminoquinoline group and is preferably present in the composition in the form of its diphosphate or sulfate salt. Reference is made to entry No. 2163 at page 334 of the Merck Index, Eleventh Edition.
Primaquine, 8-(4-Amino-l-methyl-n-butylamino)-6-methoxy-quinoline, is a known antimalarial agent from the 8-aminoquinoline group and is represented by the following structural formula:
Figure imgf000007_0001
The antimalarial efficacy of this compound is also reported in Chapter 34, Parasite Chemotherapy, E.B.Roche et al., Principles of Medicinal Chemistry, W.O.Foye (Editor), Lea & Febiger, Philadelphia/London 1989.
Pyronaridine is a known antimalarial agent represented by the following structural formula:
Figure imgf000007_0002
The synthesis of this compound is reported in Acta Pharmaceutica Sinica 15: 630-632 (1980). The antimalarial efficacy of this compound is also reported in Practical Chemotherapy of Malaria, Report of a WHO Scientific Group, Technical Report Series 805, Geneva 1990, see Chapter 8.5, pages 122-124.
Preferred is a pharmaceutical composition suitable for synergistic action of the active components against malaria which comprises the combination of a synergistically effective amount of benflumetol (I) with a synergistically effective amount of at least one compound selected from the group (TI) consisting of quinine, mefloquine and halofantrine, or a pharmaceutically acceptable salt or derivative thereof having antimalarial efficacy.
Especially preferred is a pharmaceutical composition suitable for synergistic action of the active components against malaria which comprises the combination of a synergistically effective compound of benflumetol (I) with a synergistically effective amount of a pharmaceutically acceptable acid addition salt of quinine.
Pharmaceutically acceptable additives are preferably present in the composition according to the present invention. The additives are used for the preparation of preferably enteral or parenteral dosage forms according to conventional formulation methods.
For oral administration suitable additives include inert diluents or fillers, thereby forming solid or liquid dosage forms such as tablets, powders, capsules, syrups and the like. The pharmaceutical compositions can, if desired, contain additional ingredients such as flavourings, binders, excipients and the like.
For example, tablets containing various solid additives such as starch, dextrin, alginic acid and certain complex silicates, together with binding agents such as polyvinylpyrrolidone, sucrose, gelatin and acacia. Additionally, lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often useful for tabletting purposes. Solid compositions of a similar type may also be employed as fillers in soft and hard gelatin capsules, preferred materials therefore include lactose or milk sugar and high molecular weight polyethylene glycols.
For other oral dosage forms the mixture of the compounds can for example be administered in a gelatin capsule. Such formulation could be based on a suitable refined edible oil such as sunflower oil, corn oil, peanut oil, coconut oil or til oil.
In a preferred embodiment of the present invention, the active components (I) and (II) are formulated in a single unit dosage form such as tablets or capsules.
The active components (I) and (II) may also be formulated into two individual dosage forms contained within one administration system (kit of parts), which are simultaneously or consecutively administered. The same route of administration is possible, e.g. admini¬ stration of two individual dosage forms contained within one kit of parts. One tablet or capsule containing component (I) and, consecutively, a second dosage form containing component (II) is administered. An individual dose regimen may be developed especially during clinical treatment, e.g. by administering after the first occurrence of malaria a tablet or capsule containing a high dose of the active component (I) or, correspondingly, multi¬ plying lower doses in the beginning of malaria attacks, and administering also a tablet or capsule containing a lower dose of the active component (II). In the course of treatment, dosage forms containing a lower dose of component (I) and a higher dose of compo¬ nent (II) are administered. Different dosage forms present in one kit-of-parts may also be administered simultaneously or consecutively, e.g. by administration of a tablet containing component (I) and a suppository containing component (II). The dosage range may also be varied according to the dose regimens given above.
The usefulness of the pharmaceutical composition according to the present invention in therapy against malaria is evident from in-vitro and in-vivo results from experiments carried out in established test models. The ability of the composition to act as an effective and long-acting antimalarial agent even against strains of P.berghei known to be extremely resistant against other antimalarial agents reflects the usefulness of the present invention.
The present invention also relates to a method of treatment against malaria which com¬ prises administering to a patient after the outbreak of malaria the above-mentioned pharmaceutical composition comprising the combined active components (I) and (II). The composition is administered to the patient for a period of time of at least four days, preferably five or more days.
The term method of treatment also comprises prophylactic administration of the compo¬ sition to healthy patients to prevent the outbreak of the disease in high-risk areas of contamination, especially in regions between the tropics of Capricorn and cancer.
The dose of the active component benflumetol (I) as contained in the pharmaceutical composition may vary within wide limits and depends on the condition of the patient and the time period elapsed after the outbreak of the disease. Based on in-vivo data from model experiments as reported below in the Examples, it is established that the daily dose of benflumetol is between about 0.2-50.0 mg/kg, preferably 0.2-10.0 mg/kg and especially about 0.2-5.0 mg/kg. This daily dose can be raised considerably upon need in view of the low toxicity and high tolerability of benflumetol. It is also estimated that the daily dose of component (II) in the composition, is between 0.2 and 50 mg/kg, preferably 0.3-5.0 mg kg and especially between about 0.4-3.0 mg/kg.
The dose ratio of component (I) to component (II) may also vary within wide limits. Synergism will be especially efficient if benflumetol is administered in equal weight amounts or, preferably, in excess amounts as compared to the weight amounts of component (II) administered. Accordingly, the weight amount of benflumetol may vary from one to ten parts for each part component (II), administered. Preferably, three to seven parts and especially five to six parts of benflumetol are administered for each part of component (II). The dose amounts given and dose ratios refer to daily administrations.
The invention also relates to a process for the preparation of the pharmaceutical composi¬ tion suitable for synergistic action of the active components against malaria which com¬ prises combining an effective amount of a compound of formula I with an effective amount of the component (II) and formulating this combination of active components under optional addition of pharmaceutically acceptable additives to a suitable dosage form.
The novel pharmaceutical compositions contain, for example, from 10 % to 80 %, prefer¬ ably from 20 % to 60 %, of the combination of the active components. Pharmaceutical compositions according to the invention are suitable for enteral administration and are, for example, formulated into oral dosage unit forms, such as dragόes, tablets, capsules or suppositories. These are manufactured in a manner known per se, for example by means of conventional mixing, granulating, confectioning, dissolving or lyophilising processes. For example, pharmaceutical preparations for oral administration can be obtained by combi¬ ning the active ingredient with solid carriers, optionally granulating a resulting mixture, and processing the mixture or granulate, if desired or necessary, after the addition of suitable adjuncts, to form tablets or dragόe cores.
In a preferred embodiment of the process, the active components (I) and (II) are milled either individually or together to particle sizes from about 10 μ to about 400 μ, preferably 20 μ to 200 μ. At least 90 % of the crystals of the active components are present in these ranges.
Particles of this size are obtained by conventional comminution methods, e.g. grinding in an air jet mill, ball mill or vibrator mill. Micronisation is preferably effected by known methods using an ultrasonics disintergrator, e.g. of the Branson Sonifier type as described e.g. in J. Pharm. Sci. 53 (9), 1040-1045 (1965), or by stirring a suspension with a high-speed agitator, for example with a stirrer of the Homorex type (supplied by Brogli & Co., Basel). In these preferred methods, micronisation is effected at about 500 to 10,000 rpm (rotations per minute) by dissolving or suspending the combination of the active components in an organic solvent, e.g. methanol, ethanol or propylene glycol, and precipitating it in microcrystalline form at ca. 0°-5°C in water or an aqueous salt solution, e.g. 2 % sodium chloride solution which may additionally contain a protective colloid such as gelatin or a cellulose ether, e.g. methyl cellulose or hydroxypropyl methyl cellulose, in low concentration (0.1-1 %), and filtering the resultant stirred suspension. The filter cake is dried at low temperature, e.g. ca. 0°-5°C, under vacuum (e.g. below 50 mbar, preferably at 0.5 mbar). The subsequent drying can be effected at ca. 50°-90°C.
The crystals thus obtained are then formulated to granulates, preferably by wet granulation which is carried out according to standard methods.
The pharmaceutical composition is preferably prepared by compressing a granular formulation which is obtained, for example, by sieving and, if desired, by comminuting the drug, with or without the excipients, compacting with another solvent such as ethanol or water, removing the solvent or drying, with or without the addition of lubricants or glidants such as magnesium stearate or TWEEN, comminuting the granules and sieving once more.
The granules can be compressed to tablet cores in a conventional tabletting machine, for example an EKO Korsch eccentric tabletting machine, at a pressure of ca. 10 kN. Coating can be effected by applying an aqueous-ethanolic solution in which, for example, poly¬ ethylene glycol and saccharose is dissolved or dispersed.
Dragέe cores are provided with suitable coatings that may be resistant to gastric juices, there being used, inter alia, concentrated sugar solutions that may contain gum arabic, talc, polyvinylpyrrolidone or polyethylene glycol. Colorings, flavorings or pigments may be added to the syrups,tablets or dragέe coatings, for example for identification purposes, masking taste or to indicate different doses of active ingredient.
Further orally administerable pharmaceutical compositions are dry-filled capsules consis¬ ting of gelatin, and also soft sealed capsules consisting of gelatin and plasticiser, such as glycerine or sorbitol. T e dry-filled capsules may contain the active components in the form of a granulate, for example in admixture with fillers, such as lactose, binders, such as starches, and/or glidants, such as talc or magnesium stearate, and optionally stabilisers. In soft capsules, the active ingredient is preferably dissolved or suspended in suitable liquids, such as fatty oils, paraffin oil or liquid polyethylene glycols, to which stabilisers may also be added. Suitable for enteral administration are also suppositories that consist of the combination of the active ingredients and a suppository base. Suitable as suppository bases are, for example, natural or synthetic triglycerides, paraffins, polyethylene glycols or higher alkanols. It is also possible to use gelatin rectal capsules that contain a combination of the active ingredient and a base material; suitable base materials are, for example, liquid triglycerides, polyethylene glycols or paraffin hydrocarbons.
The following Examples illustrate the invention described above; they are not, however, intended to limit the scope of the invention in any way.
Example : Preparation of Tablets.
benflumetol 120 mg quinine dihydrochloride 20 mg corn starch 100 mg dextrin 40 mg
Tween®-80 0,6 mg
15 % paste of corn starch "sufficient"
Mg-stearate 3 mg
Quinine dihydrochloride crystals are passed through a 100 mesh size sieve. Benflumetol crystals are passed through a 60 mesh size sieve and mixed with the quinine solid, starch and dextrin. This mixture is passed 3 times through a 40 mesh size sieve. Tween®-80 is added to the paste of starch which is mixed with the above formulation. This mixture is granulated by way of wet-granulation, passed through a 40 mesh size sieve, dried at reduced pressure at 50-60°C. The Mg-stearate is added, and the tablets are pressed.

Claims

Claims
LA pharmaceutical composition suitable for synergistic action of the active components against malaria comprising a synergistically effective amount of a compound of the formula:
Figure imgf000013_0001
combined with a synergistically effective amount of at least one compound selected from the group (II) consisting of quinine, mefloquine, halofantrine, chloroquine, primaquine and pyronaridine or a pharmaceutically acceptable salt or derivative thereof having antimalarial efficacy.
2. A pharmaceutical composition according to claim 1 comprising a synergistically effective amount of benflumetol (I) combined with a synergistically effective amount of at least one compound selected from the group (II) consisting of quinine, mefloquine and halofantrine, or a pharmaceutically acceptable salt or derivative thereof having antimalarial efficacy.
3. A pharmaceutical composition according to claim 1 comprising a synergistically effective amount of benflumetol (I) combined with a synergistically effective amount of a pharmaceutically acceptable salt of quinine (II).
4. A process for the preparation of a pharmaceutical composition according to claim 1, which comprises combining a synergistically effective amount of benflumetol (I) with a synergistically effective amount of at least one compound selected from the group (II) consisting of quinine, mefloquine, halofantrine, chloroquine, primaquine and pyronaridine or a pharmaceutically acceptable salt or derivative thereof and formulating this combination of active components under optional addition of pharmaceuticalHy acceptable additives to a suitable dosage form.
5. A process according to claim 4 which comprises combining an effective amount of benflumetol (I) with a synergistically effective amount of a pharmaceutically acceptable salt of quinine
6. A process for the preparation of a pharmaceutical composition according to claim 4, which comprises formulating the combination of active components under the addition of solid additives to tablets.
7. Use of the combination comprising a synergistically effective amount of benflumetol (I) with a synergistically effective amount of at least one compound selected from the group (II) consisting of quinine, mefloquine, halofantrine, chloroquine, primaquine, and pyronaridine or a pharmaceutically acceptable salt or a derivative thereof for the preparation of a pharmaceutical composition.
8. A pharmaceutical composition according to claim 1 for use in therapy against malaria.
PCT/EP1993/000163 1992-02-07 1993-01-25 Antimalarial synergistic compositions containing benflumetol Ceased WO1993015727A1 (en)

Priority Applications (11)

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AU33522/93A AU668376B2 (en) 1992-02-07 1993-01-25 Antimalarial synergistic compositions containing benflumetol
RU93058291A RU2118158C1 (en) 1992-02-07 1993-01-25 Antimalarial synergistic composition containing benflumethol
HU9303152A HU220605B1 (en) 1992-02-07 1993-01-25 A method for the preparation of benflumetol-containing anti-malarial synergistic pharmaceutical compositions
FI934360A FI934360A7 (en) 1992-02-07 1993-01-25 Synergistic antimalarial compositions containing benflumetol
SG1996001151A SG45193A1 (en) 1992-02-07 1993-01-25 Antimalarial synergistic compositions containing benflumetol
EP93902246A EP0583439B1 (en) 1992-02-07 1993-01-25 Antimalarial synergistic compositions containing benflumetol
DE69323941T DE69323941T2 (en) 1992-02-07 1993-01-25 SYNERGISTIC MALARIANS CONTAINING BENFLUMETOL
PL93300806A PL172590B1 (en) 1992-02-21 1993-01-25 Synergic, benflumethol containing antipaludic agent
JP51371093A JP3560970B2 (en) 1992-02-07 1993-01-25 Antimalarial synergistic composition containing benzoflumetol
NO933271A NO304409B1 (en) 1992-02-07 1993-09-14 Synergetic antimalarial compositions containing bone flumetol
GR990401168T GR3030086T3 (en) 1992-02-07 1999-04-30 Method of preparing a radioactive rhenium complex solution.

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CZ296875B6 (en) * 2000-05-31 2006-07-12 Nicholas Piramal India Limited Combination kit used in the treatment of malaria
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CN1109546C (en) * 1998-06-17 2003-05-28 中国疾病预防控制中心寄生虫病预防控制研究所 Compound antimalarial medicine containing artemisine medicines and malaridine
JP4733918B2 (en) * 2003-10-01 2011-07-27 オリンパス株式会社 Capsule dosing system

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WO1998018462A1 (en) * 1996-10-28 1998-05-07 Pharma Mar, S.A. Antimalarial compositions containing cis-fused cyclopenteno-1,2,4-trioxane derivatives
CZ296875B6 (en) * 2000-05-31 2006-07-12 Nicholas Piramal India Limited Combination kit used in the treatment of malaria
US11738028B2 (en) 2017-04-24 2023-08-29 Novartis Ag Therapeutic regimen

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HUT66452A (en) 1994-11-28
AU3352293A (en) 1993-09-03
FI934360A7 (en) 1993-10-04
CA2105773A1 (en) 1993-08-08
NZ246606A (en) 1995-09-26
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HU220605B1 (en) 2002-03-28

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