WO1990007325A1 - A pessary containing antibacterial drugs - Google Patents

A pessary containing antibacterial drugs Download PDF

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Publication number
WO1990007325A1
WO1990007325A1 PCT/GB1989/001546 GB8901546W WO9007325A1 WO 1990007325 A1 WO1990007325 A1 WO 1990007325A1 GB 8901546 W GB8901546 W GB 8901546W WO 9007325 A1 WO9007325 A1 WO 9007325A1
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WO
WIPO (PCT)
Prior art keywords
pessary
surfactant
metronidazole
drugs
miconazole
Prior art date
Application number
PCT/GB1989/001546
Other languages
French (fr)
Inventor
Oswald Morton
Original Assignee
Edko Trading And Representation Company Limited
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from GB888830405A external-priority patent/GB8830405D0/en
Application filed by Edko Trading And Representation Company Limited filed Critical Edko Trading And Representation Company Limited
Publication of WO1990007325A1 publication Critical patent/WO1990007325A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0034Urogenital system, e.g. vagina, uterus, cervix, penis, scrotum, urethra, bladder; Personal lubricants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles

Definitions

  • This invention relates to improvements in pessaries, and in particular to a pessary having one or more active ingredients together with a surfactant to improve the clinical effectiveness of these ingredients.
  • a pessary it is desirable for a pessary to be able to treat all the common forms of vaginitis, which are most often caused by infection with Candida albicans, trichomonas vaginalis or gardnerella sp, either singly or mixed.
  • Commonly derivatives of imidazole and nitroimidazole are used to treat such conditions, examples of such drugs being miconazole, clotrimazole and metronidazole, but despite the good activity of these compounds none has so far individually achieved the broad spectrum of activity required to combat all the common types of infection.
  • Other types of drugs used in such infections include nitrofurfuryl derivatives and various antibiotics.
  • one aspect of the invention provides a pessary for human administration comprising an effective amount of one or more drugs active against trichomonas vaginalis, a pessary base and a surfactant.
  • the preferred an itrichomonal drug is metronidazole.
  • a surfactant according to the invention allows the active antitrichomonal drug fully to penetrate between the apposed layers of vaginal epithelium which occur in the rugose surface of the vagina so reaching the.trichomonas sp. which otherwise would be protected by such apposition from contact with the active ingredients of conventional pessary formulations.
  • the relapse rate when treatment ceases can therefore be expected to be lower than when metronidazole is administered intravaginally in a conventional pessary formulation.
  • fungicidally active derivative of nitroimdazole such as butoconazole or, more preferably, miconazole, is advantageously used as the drug active against Candida albicans.
  • metronidazole is used as the antitrichomonal drug, it will also be effective against gardnerella sp.
  • a broad spectrum antibiotic such as pivampicillin may advantageously also be included.
  • an antiinflammatory drug such as hydrocortisone. Lactic acid may also advantageously be included as a further active ingredient.
  • the pessaries of the present invention may also advantageously include chlorophyll as a deodorant.
  • chlorophyll as a deodorant. We have found that although some staining of clothes by the green coloration of the chlorophyll may take place, the surfactant in the composition ensures that this such stains are readily removed.
  • the quantity of metronidazole is conveniently from 250 to 750 mg per pessary, more preferably from 400 to 600 mg and suitably about 500 mg.
  • the pessary may conveniently contain from 50 to 150 mg of miconazole, more preferably from 80 to 120 mg.
  • the miconazole may be in the form of the free base or as a salt, for instance the nitrate - a suitable quantity of miconazole nitrate per pessary is then about 100 mg.
  • the active components are preferably incorporated in the size range 5 to 200 microns but are preferably at the low end of this range, for example 10 to 50 microns, e.g. about 20 microns.
  • the pessary base may be of any conventional material for vaginal administration such as glycerol/ gelatin,glyco-gelatin, macrogols (polyethylene glycols), natural, synthetic or semisynthetic hard fats, and fractionated palm kernel oil.
  • a particularly preferred material is a hard fat such as cocoa butter (theobroma oil) , for instance the range of cocoa butter-based products sold under the trade name Witepsol by Dynamit Nobel, Slough, England.
  • the surfactant may be a cationic, non-ionic, anionic or amphoteric surfactant although non-ionic surfactants are preferred.
  • Anionic surfactants include salts of long chain alkyl sulphonate esters such as sodium lauryl sulphate, sodium cetostearyl sulphate and sodium tetradecyl sulphate; salts of long chain carboxylic acids such as stearates.
  • Cationic surfactants include quaternary ammonium or pyridinium compounds such as benzalkonium chloride (a mixture of benzyl alkyl dimethyl chlorides, the alkyl chain ranging from C g to ⁇ g ) , tetradecyltri- methyl ammonium bromide and cetylpyridi ium chloride.
  • Amphoteric surfactants include lauryl 1-carboxy glycine and lecithins such as soya lecithin.
  • Non-ionic surfactants include glycol and glycerol esters such as glyceryl monostearate; macrogol esters and ethers such as cetomacrogol; sorbitan and annitan esters such as sorbitan tristearate; and polyoxye h lene derivatives of such sorbitan esters, for instance polyoxyethylene (20) sorbitan mono-oleate.
  • the level of surfactant required in the pessary formulation will be readily determined by those skilled in the art and will depend on the specific surfactant and the nature of the pessary base; conveniently it is in the range 0.1 to 10 percent by weight, preferably 1 to 5 percent.
  • a cetomacrogol surfactant in conjunction with a cocoa-butter base such as Witepsol.
  • the surfactant is suitably present in the range 1 to 5 per cent by weight, for instance about 40mg in an overall pessary weight of 2540mg (including active ingredients) .
  • the pessaries may be manufactured by conventional methods, for instance by admixture of the active ingredients and surfactant in the molten pessary base and pouring the resulting mixture into chilled moulds.
  • the two active ingredients and the surfactant are mixed into the molten pessary base and the resulting mixture is poured into pre-cooled moulds.
  • the , moulds are passed through a cooling tunnel at - 10 C f the pessaries are removed from the moulds and packaged.
  • composition of pessary Polyethylene glycol 4000 Polyethylene glycol 1000 Polyethylene glycol 400 MONATERIC 951A metronidazole miconazole nitrate
  • the pessary is prepared according to the method of Example 1.
  • the MONATERIC 951A may be replaced by MONAQUAT PT-C, PT-L, PT-S or Phospholipid EFA.

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  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Reproductive Health (AREA)
  • Urology & Nephrology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Disclosed are pessaries for human administration comprising an effective amount of one or more drugs active against trichomonas vaginalis, a pessary base and a surfactant. The active ingredients are advantageously metronidazole and miconazole in combination.

Description

A pessary containing antibacterial drugs.
This invention relates to improvements in pessaries, and in particular to a pessary having one or more active ingredients together with a surfactant to improve the clinical effectiveness of these ingredients.
It is desirable for a pessary to be able to treat all the common forms of vaginitis, which are most often caused by infection with Candida albicans, trichomonas vaginalis or gardnerella sp, either singly or mixed. Commonly derivatives of imidazole and nitroimidazole are used to treat such conditions, examples of such drugs being miconazole, clotrimazole and metronidazole, but despite the good activity of these compounds none has so far individually achieved the broad spectrum of activity required to combat all the common types of infection. Other types of drugs used in such infections include nitrofurfuryl derivatives and various antibiotics.
While such drugs have been formulated as pessaries and vaginal tablets, it has been found for metronidazole that the relapse rate with trichomonal infections (i.e. the rate of reappearance of infection after cessation of the medicament) is higher when administered in this way than when administration is by the oral route. Consequently the oral route is now the preferred route for administration of metronidazole, and pessaries containing this compound have been virtually discontinued. This results in mixed vaginal infections being treated by both the oral and vaginal routes, with consequent inconven¬ ience to the patient.
We have now developed an improved pessary formulation which combats the problem of higher relapse rate when antitrichomonal drugs such as metronidazole are administered as a pessary thus enabling the use of the intravaginal route in combating trichomonal infections and hence the possibility of a single route of application of therapy against all three of the principal infective agents in vaginitis.
Thus one aspect of the invention provides a pessary for human administration comprising an effective amount of one or more drugs active against trichomonas vaginalis, a pessary base and a surfactant.
The preferred an itrichomonal drug is metronidazole.
The use of a surfactant according to the invention allows the active antitrichomonal drug fully to penetrate between the apposed layers of vaginal epithelium which occur in the rugose surface of the vagina so reaching the.trichomonas sp. which otherwise would be protected by such apposition from contact with the active ingredients of conventional pessary formulations. The relapse rate when treatment ceases can therefore be expected to be lower than when metronidazole is administered intravaginally in a conventional pessary formulation.
In order to produce a broad spectrum of activity against vaginal infections, it is desirable to include one or more drugs active against Candida albicans and/or gardnerella sp. A fungicidally active derivative of nitroimdazole such as butoconazole or, more preferably, miconazole, is advantageously used as the drug active against Candida albicans. Where metronidazole is used as the antitrichomonal drug, it will also be effective against gardnerella sp. However, a broad spectrum antibiotic such as pivampicillin may advantageously also be included. In order to counter the inflammation and itching associated with vaginitis, it may be beneficial to include an antiinflammatory drug such as hydrocortisone. Lactic acid may also advantageously be included as a further active ingredient. The pessaries of the present invention may also advantageously include chlorophyll as a deodorant. We have found that although some staining of clothes by the green coloration of the chlorophyll may take place, the surfactant in the composition ensures that this such stains are readily removed.
The quantity of metronidazole is conveniently from 250 to 750 mg per pessary, more preferably from 400 to 600 mg and suitably about 500 mg.
The pessary may conveniently contain from 50 to 150 mg of miconazole, more preferably from 80 to 120 mg. The miconazole may be in the form of the free base or as a salt, for instance the nitrate - a suitable quantity of miconazole nitrate per pessary is then about 100 mg.
The active components are preferably incorporated in the size range 5 to 200 microns but are preferably at the low end of this range, for example 10 to 50 microns, e.g. about 20 microns.
The pessary base may be of any conventional material for vaginal administration such as glycerol/ gelatin,glyco-gelatin, macrogols (polyethylene glycols), natural, synthetic or semisynthetic hard fats, and fractionated palm kernel oil. A particularly preferred material is a hard fat such as cocoa butter (theobroma oil) , for instance the range of cocoa butter-based products sold under the trade name Witepsol by Dynamit Nobel, Slough, England.
The surfactant may be a cationic, non-ionic, anionic or amphoteric surfactant although non-ionic surfactants are preferred. Anionic surfactants include salts of long chain alkyl sulphonate esters such as sodium lauryl sulphate, sodium cetostearyl sulphate and sodium tetradecyl sulphate; salts of long chain carboxylic acids such as stearates.
. Cationic surfactants include quaternary ammonium or pyridinium compounds such as benzalkonium chloride (a mixture of benzyl alkyl dimethyl chlorides, the alkyl chain ranging from Cg to ιg) , tetradecyltri- methyl ammonium bromide and cetylpyridi ium chloride.
Amphoteric surfactants include lauryl 1-carboxy glycine and lecithins such as soya lecithin.
Non-ionic surfactants include glycol and glycerol esters such as glyceryl monostearate; macrogol esters and ethers such as cetomacrogol; sorbitan and annitan esters such as sorbitan tristearate; and polyoxye h lene derivatives of such sorbitan esters, for instance polyoxyethylene (20) sorbitan mono-oleate.
The level of surfactant required in the pessary formulation will be readily determined by those skilled in the art and will depend on the specific surfactant and the nature of the pessary base; conveniently it is in the range 0.1 to 10 percent by weight, preferably 1 to 5 percent.
It is especially preferred to use a cetomacrogol surfactant in conjunction with a cocoa-butter base such as Witepsol. In such a formulation the surfactant is suitably present in the range 1 to 5 per cent by weight, for instance about 40mg in an overall pessary weight of 2540mg (including active ingredients) .
The pessaries may be manufactured by conventional methods, for instance by admixture of the active ingredients and surfactant in the molten pessary base and pouring the resulting mixture into chilled moulds.
The invention is illustrated by the following Examples.MONATERIC and MONAQUAT surfactants are available from Mona Industries Ltd, Paterson, New Jersey, U.S.A. Example 1
(1) Composition of pessary =
Metronidazole 500.Omg
Miconazole nitrate 100.Omg
Witepsol w35 1940.4mg
Cetomacrogol 39.6mg
2000 mg per pessary
(2) Method of manufacture
The two active ingredients and the surfactant are mixed into the molten pessary base and the resulting mixture is poured into pre-cooled moulds. The , moulds are passed through a cooling tunnel at - 10 Cf the pessaries are removed from the moulds and packaged.
Example 2
(1) Composition of pessary = Polyethylene glycol 4000 Polyethylene glycol 1000 Polyethylene glycol 400 MONATERIC 951A metronidazole miconazole nitrate
Figure imgf000007_0001
The pessary is prepared according to the method of Example 1. The MONATERIC 951A may be replaced by MONAQUAT PT-C, PT-L, PT-S or Phospholipid EFA.

Claims

CLAIMS :
1. A pessary for human administration comprising an effective amount of one or more drugs active agains trichomonas vaginalis, a pessary base and a surfactant.
2. A pessary as claimed in claim 1 in which metronidazole is used as the drug active against trichomonas vaginalis.
3. A pessary as claimed in claim 1 or claim
2 which further comprises one or more drugs active against Candida albicans and/or gardnerella sp,
4. A pessary as claimed in claim 1 comprising effective amounts of metronidazole and miconazole.
5. A pessary as claimed in any of the preceding claims also comprising one or more antiinflammatory drugs.
6. A pessary as claimed in any of the previous claims containing 250 to 750 mg of metronidazole.
7. A pessary as claimed in any of the preceding claims containing 50 to 150 mg of miconazole.
8. A pessary as claimed in any of the preceding claims in which the pessary base is cocoa butter.
9. A pessary as claimed in any of the preceding claims in which the surfactant is an anionic, cationic, amphoteric or non-ionic surfactant.
10. A pessary as claimed in claim 9 in which the surfactant is a macrogol ester or ether.
11. A pessary as claimed in claim 10 in which the surfactant is cetomacrogol.
12. A pessary as claimed in any of the previous claims in which the concentration of the surfactant in the pessary composition is 0.1 to 10 percent.
PCT/GB1989/001546 1988-12-30 1989-12-29 A pessary containing antibacterial drugs WO1990007325A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB888830405A GB8830405D0 (en) 1988-12-30 1988-12-30 Pharmaceutical formulation
GB8830405.0 1988-12-30
US36134289A 1989-06-05 1989-06-05

Publications (1)

Publication Number Publication Date
WO1990007325A1 true WO1990007325A1 (en) 1990-07-12

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ID=26294788

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB1989/001546 WO1990007325A1 (en) 1988-12-30 1989-12-29 A pessary containing antibacterial drugs

Country Status (1)

Country Link
WO (1) WO1990007325A1 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994008594A1 (en) * 1992-10-15 1994-04-28 Smithkline Beecham Plc Pharmaceutical composition containing an antimicrobial agent and an antibiotic
WO1995007071A1 (en) * 1993-09-08 1995-03-16 Edko Trading And Representation Company Limited Multi-phase compositions for an initial and delayed release of a medicament
FR2777783A1 (en) * 1998-04-24 1999-10-29 Innothera Lab Sa Pharmaceutical composition for treatment of infectious vulvovaginitis and vaginosis
WO2001054691A1 (en) * 2000-01-26 2001-08-02 Nicox, S.A. Nitrate salts of antimicrobial agents
EP1301150A1 (en) * 2000-07-11 2003-04-16 UMD, Inc. Device and method for intravaginal or transvaginal treatment of fungal, bacterial, viral or parasitic infections
US20150164837A1 (en) * 2012-03-19 2015-06-18 Dr. August Wolff Gmbh & Co. Kg Arzneimittel Use of amphoteric surfactants for the prevention and treatment of pathogenic vaginal biofilms in vaginal infections

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0103995A2 (en) * 1982-08-24 1984-03-28 Cilag Ag Medicated suppository
DE3800256A1 (en) * 1987-01-08 1988-07-21 Squibb & Sons Inc BIOADHAESIVE SUPPOSITORIES
US4765978A (en) * 1986-12-16 1988-08-23 Schering Corporation Novel vaginal suppository

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0103995A2 (en) * 1982-08-24 1984-03-28 Cilag Ag Medicated suppository
US4765978A (en) * 1986-12-16 1988-08-23 Schering Corporation Novel vaginal suppository
DE3800256A1 (en) * 1987-01-08 1988-07-21 Squibb & Sons Inc BIOADHAESIVE SUPPOSITORIES

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994008594A1 (en) * 1992-10-15 1994-04-28 Smithkline Beecham Plc Pharmaceutical composition containing an antimicrobial agent and an antibiotic
WO1995007071A1 (en) * 1993-09-08 1995-03-16 Edko Trading And Representation Company Limited Multi-phase compositions for an initial and delayed release of a medicament
US5985319A (en) * 1993-09-08 1999-11-16 Edko Trading And Representation Company Limited Multi-phase compositions for an initial and delayed release of a vaginal medicament
FR2777783A1 (en) * 1998-04-24 1999-10-29 Innothera Lab Sa Pharmaceutical composition for treatment of infectious vulvovaginitis and vaginosis
WO1999055333A1 (en) * 1998-04-24 1999-11-04 Laboratoire Innothera (Societe Anonyme) Pharmaceutical imidazole combination for locally treating vulvovaginitis and vaginosis
WO2001054691A1 (en) * 2000-01-26 2001-08-02 Nicox, S.A. Nitrate salts of antimicrobial agents
EP1301150A1 (en) * 2000-07-11 2003-04-16 UMD, Inc. Device and method for intravaginal or transvaginal treatment of fungal, bacterial, viral or parasitic infections
EP1301150A4 (en) * 2000-07-11 2004-08-11 Umd Inc Device and method for intravaginal or transvaginal treatment of fungal, bacterial, viral or parasitic infections
US20150164837A1 (en) * 2012-03-19 2015-06-18 Dr. August Wolff Gmbh & Co. Kg Arzneimittel Use of amphoteric surfactants for the prevention and treatment of pathogenic vaginal biofilms in vaginal infections

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