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GB2046093A - Benzocaine Aerosol Compositions - Google Patents

Benzocaine Aerosol Compositions Download PDF

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Publication number
GB2046093A
GB2046093A GB8007867A GB8007867A GB2046093A GB 2046093 A GB2046093 A GB 2046093A GB 8007867 A GB8007867 A GB 8007867A GB 8007867 A GB8007867 A GB 8007867A GB 2046093 A GB2046093 A GB 2046093A
Authority
GB
United Kingdom
Prior art keywords
benzocaine
composition
propellant
polyethylene glycol
solvent
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.)
Granted
Application number
GB8007867A
Other versions
GB2046093B (en
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.)
Wyeth LLC
Original Assignee
American Home Products Corp
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
Application filed by American Home Products Corp filed Critical American Home Products Corp
Publication of GB2046093A publication Critical patent/GB2046093A/en
Application granted granted Critical
Publication of GB2046093B publication Critical patent/GB2046093B/en
Expired legal-status Critical Current

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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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/235Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
    • A61K31/24Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group having an amino or nitro group
    • A61K31/245Amino benzoic acid types, e.g. procaine, novocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/12Aerosols; Foams

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Emergency Medicine (AREA)
  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Liquid anaesthetic compositions comprising mixtures of a propellant and a water washable base of benzocain in a solvent have as propellant, difluoroethane and at least one of n-butane, isobutane and n- propane. The solvent is at least one of polyoxyethylene sorbitan trioleate and polyethylene glycol mono and dilaurate. The compositions are single phase and are resistant to low temperatures.

Description

SPECIFICATION Anaesthetic Compositions This invention relates to liquid anaesthetic compositions in aerosol containers. More specifically, this invention relates to liquid compositions of the anaesthetic benzocaine which form single phase mixtures in combination with solvent and hydrocarbon propellants, and which are single phase after exposure to low temperatures and with high concentrations of benzocaine.
Benzocaine, the ethyl ester of p-aminobenzoic acid, is a well known local anaesthetic which has been topically administered in the form of ointments, lotions, sprays, gels and as an impregnant in first aid pads. In order to enhance or prolong benzocaine's anaesthetic activity, various efforts have been made to increase the concentration of benzocaine in various solvents or to more effectively maintain the anaesthetic at its site of administration. Increasing the concentration of benzocaine, however, had to be balanced against the increasing probability of benzocaine precipitation, particularly at colder temperatures, thereby limiting their field of use.The goal of formulating highly concentrated benzocaine compositions characterized by cold temperature resistance is even greater in aerosol anaesthetic compositions wherein even small amounts of precipitate can clog valves and orifices, and wherein-sufficient pressure must be maintained to both completely deliver all the benzocaine solution within the container and evenly distribute the benzocaine solution with desirable spray characteristics.
Many solvents have been disclosed for benzocaine. For example, U.S. Patent 2,187,597 discloses anaesthetic formulations containing up to five percent of the anaesthetic agent in a mixture of benzyl alcohol and ethyl chloride. Other formulations containing up to 10% benzocaine in mixtures with a procaine salt, water, water miscible poly-hydroxy aliphatic alcohols and their ethers have been disclosed in U.S. Patent 2,382,546. U.S. Patent 2,457,188 discloses benzocaine solutions containing at least 10% benzocaine at 200C utilizing solvents selected from certain polyoxyalkylene glycols, aliphatic ethers of dihydric alcohols, aromatic ethers of aliphatic dihydric alcohols, carboxylic acid esters of aliphatic dihydric alcohols, and carboxylic acid esters of aromatic and aliphatic ethers of aliphatic dihydric alcohols. In U.S.Patent 2,682,182, benzocaine solutions containing up to 16% benzocaine at OOC were disclosed in a mixture employing a major amount of propylene glycol and a polyoxyethylene (8-25) hexitan monolaurate.
Anaesthetic aerosol preparations containing at least 10% benzocaine in diesters of C8-C12 carboxylic acids and polyethylene glycols having a molecular weight of approximately 300-600, and a propellant system made from mixture of chlorofluorohydrocarbons have been disclosed in U.S. Patent 3,322,634. These aerosol formulations, however, are no longer acceptable because of certain atmospheric effects associated with chlorofluorohydrocarbons.
Benzocaine has also been employed in formulations containing certain other therapeutic irlgredients, for example, as disclosed in U.S. Patent 3,808,319 wherein the solvent is volatile alcohol such as ethyl alcohol or isopropyl alcohol. Solvents of this type, however, are generally counterproductive to desirable anaesthetic properties because of their stinging nature to sensitive or wounded skin and the like. Compositions containing up to 1 5% benzocaine are further disclosed in U.S.
Patent 4,052,513 in the form of oil in water emulsions.
This invention provides a liquid anaesthetic composition in an aerosol container comprising a single phase mixture of a propellant and a water washable base comprising benzocaine in a solvent wherein (a) the weight percent of the benzocaine in the solvent is from 0.5% up to its maximum solubility in the solvent; (b) the solvent is selected from at least one of polyoxyethylene sorbitan trioleate having an average of about 20 units of ethylene oxide in the polyoxyethylene chain, polyethylene glycol dilaurate, wherein the polyethylene glycol has an average molecular weight of about 400 and polyethylene glycol monolaurate; and (c) the propellant is selected from difluoroethane and at least one of n-butane, isobutane and npropane; with the proviso that the composition is a single phase mixture after exposure to temperatures of about -2O0C when the benzocaine comprises about 20% of said base.
The liquid anaesthetic compositions in aerosol containers of the present invention comprise a single phase mixture of a water washable base of benzocaine in a solvent and a propellant. The weight percent of benzocaine in the water washable base is from about 0.5% up to its maximum solubility in the solvent. For most effective anaesthetic properties, the benzocaine comprises at least 10% by weight of the base and preferred compositions contain about 20% by weight of benzocaine.
Solvents useful in this invention may be at least one of polyoxyethylene sorbitan trioleate having an average of about 20 units of ethylene oxide in the polyoxyethylene chain, polyethylene glycol monolaurate wherein the polyethylene glycol has an average molecular weight of about 200 to about 600 (e.g. about 400) and polyethylene glycol dilaurate wherein the polyethylene glycol has an average molecular weight of about 400. Although wider ranges of one solvent to another are acceptable, the solvent is preferably selected from two of the herein listed class of solvents in a ratio of 40:60 to each other, and most desirably in a ratio of 50:50.
The propellant system comprises difluoroethane and at least one of n-butane, isobutane and npropane. In the preferred system which utilizes n-butane, the difluoroethane comprises about 3570% by weight of the propellant system. In the most preferred embodiments each of the propellants in a two propellant system comprise- about 50% of the total propellant Preferably, the water washable base of benzocaine in solvent and the propellant each comprise about 45% to about 55% by weight of the liquid anaesthetic composition, and in preferred embodiments, about 50%.
The compositions of this invention are further defined by the provision that the compositions form a single phase mixture following exposure to temperatures of about -2O0C, when the benzocaine comprises about 20% of said water washable base. Illustratively, when the benzocaine content of the base is other than about 20% the above mentioned single phase characteristics of the compositions may be determined by adjusting the benzocaine content of the base to about 20%. In preferred embodiments, the composition is a single phase mixture (clear liquid solution) when at about 200 C.
Compositions having the preferred single phase characteristics at -2O0C employ polyethylene glycol monolaurate, or mixtures of polyoxyethylene sorbitan trioleate with the polyethyleneglycol mono- or dilaurate as the solvent.
In formulating the composition of this invention, other ingredients such as anti-pruritic agents, anti-infectives, anti-fungal agents and anti-bacterial agents may be typically incorporated.
The following composition is an illustration of a preferred embodiment of this invention: Water Washable Base Benzocaine 200.0 g Menthol 5.0 g Methylparaben 10.0 g Polyoxyethylene 20 Sorbitan Trioleate 392.5 g Polyethyleneglcyol 400 Monolaurate 392.5 g The composition of the invention may be prepared by charging the solvent into a suitable container equipped with a stirrer, adding the benzocaine and/or other active ingredients and mixing until dissolution. The solution may be then fiitered through a suitable screen and loaded into an aerosol container along with the propellants in a conventional manner.
A suitable container for the composition of this invention is a can having a "2P" rating as specified by the United States Department of Transportation. Among the valve systems which have been employed satisfactorily in any position are those similar to Seaquist NS-36 or NS-34 (Seaquist Valve Co., Cary, Ill.) or those similar to ARC-KN-37 (Ethyl Products Co., North Riverside, Ill.).
The invention is further illustrated by the following Examples 1 to 6, 10 to 16,21 to 25,27 to 34, 36 and 38 to 41. The compositions of these Examples form a single phase mixture at room temperature and/or at -200C after exposure at -200C. The other Examples below are included for reference.
Examples The following bulk concentrates were prepared for further evaluation: Bulk Concentrates 11 Ill Benzocaine 20% 20% 20% Menthol 0.5% 0.5% 0.5% Methylparaben 1.0% 1.0% 1.0% Polyoxyethylene 20 Sorbitan Trioleate 78.5% PEG 400 Monolaurate - 78.5% PEG 400 Dilaurate - - 78.5% Pressure Example Bulk Concentrates Propellants psig Physical Stability No. I II III difluoroethane n-butane @; 70 F RT -20 C (for 1 day) 1. 25% 25% - 25% 25% 57 OK* OK 2. 22.5% 22.5% - 27.5% 27.5% 71** OK OK 3. 27.5% 27.5% - 22.5% 22.5% 71** OK OK 4. 25% - 25% 25% 25% 57 OK OK 5. 22.5% - 22.5% 27.5% 27.5% - OK OK 6. 27.5% - 27.5% 22.5% 22.5% - OK OK 7. - 25% 25% 25% 25% 45 OK Wt. ppt.
wt. pp @; RT 8. - 22.5% 22.5% 27.5% 27.5% - OK Wt. ppt.
wt. ppt @ RT 9. - 27.5% 27.5% 22.5% 22.5% - OK Wt. ppt.
wt. ppt. @ RT 10. - 50% - 35% 15% - OK OK 11. - 50% - 30% 20% 57 OK Wt. ppt.
OK @ RT 12. - 50% - 25% 25% 56 OK Wt. ppt.
OK @ RT 13. - 50% - 20% 30% 51 OK Wt. ppt.
OK @ RT 14. - - 50% 35% 15% - OK Wt. ppt.
OK @ RT 15. - - 50% 30% 20% - OK Wt. ppt.
OK @ RT 16. - - 50% 25% 25% - OK Wt. ppt.
OK @ RT 17. - - 50% 20% 30% - OK Wt. ppt.
wt. ppt. @ RT 18. - - 50% 15% 35% 43 OK Wt. ppt.
wt. ppt. @ RT 19. - - 50% 10% 40% 39 OK Wt. ppt.
wt. ppt. @ RT 20. - - 50% 5% 45% 31 OK Wt. ppt.
wt. ppt. @ RT 21. 25% 25% - 35% 15% 63 OK OK 22. 10% 40% - 30% 20% 60 OK OK 23. 25% 25% - 30% 20% 58 OK OK 24. 25% 25% - 25% 25% 57 OK OK 25. 25% 25% - 20% 30% 52 OK OK 26. 25% 25% - 15% 35% - Separation 27. 25% 25% - 18% 32% - OK OK 28. 25% - 25% 35% 15% - OK Ppt.
OK @ RT Pressure Example Bulk Concentrates Propellants psig Physical Stability No. I II III difluoroethane n-butane @; 70 F RT -20 C (for 1 day) 29. 10% - 40% 30% 20% - OK Ppt.
OK @ RT 30. 25% - 25% 30% 20% 60 OK OK 31. 25% - 25% 25% 25% 57 OK OK 32. 25% - 25% 20% 30% 50 OK Wt. ppt.
OK @ RT 33. - 25% 25% 35% 15% - OK Wt. ppt.
OK @ RT 34. - 25% 25% 30% 20% - OK Wt. ppt.
OK @ RT 35. - 25% 25% 25% 25% 45 OK Wt. ppt.
wt. ppt. @ RT 36. - 25% 25% 20% 30% 50 OK Wt. ppt.
OK @ RT 37. - 25% 25% 15% 35% 45 OK Wt. ppt.
wt. ppt. @ RT 38. 25% 25% - 25% 25% 57 OK OK 39. 20% 30% - 25% 25% 79** OK OK 40. 30% 20% - 25% 25% 78** OK OK 41. 25% - 25% 25% 25% 57 OK OK 42. 20% - 30% 25% 25% - OK Ppt.
ppt. @ RT 43. 30% - 20% 25% 25% - OK Ppt.
ppt. @ RT 44. - 25% 25% 25% 25% 45 OK Wt. ppt.
wt. ppt. @ RT 45. - 20% 30% 25% 25% - OK Ppt.
ppt. @ RT 46. - 30% 20% 25% 25% - OK ppt. @ RT *One phase system, clear solution **Measured at RT ppt.=precipitate wt. ppt.=white precipitate

Claims (11)

Claims
1. A liquid anaesthetic composition in an aerosol container comprising a single phase mixture of a propellant and a water washable base comprising benzocaine in a solvent wherein.
(a) the weight percent of the benzocaine in the solvent is from 0.5% up to its maximum solubility in the solvent; (b) the solvent is selected from at least one of polyoxyethylene sorbitan trioleate having an average of about 20 units of ethylene oxide in the polyoxyethylene chain, polyethylene glycol dilaurate wherein the polyethylene glycol has an average molecular weight of about 400 and polyethylene glycol monolaurate; and (c) the propellant is selected from difluoroethane and at least one of n-butane, isobutane and npropane; with the proviso that the composition is a single phase mixture after exposure to temperatures of about -200C when the benzocaine comprises about 20% of said base.
2. A composition as claimed in Claim 1 when the propellant comprises about 35% to about 70% by weight of difluoroethane.
3. A composition as claimed in Claim 1 or 2 wherein the propellant comprises about 50% by weight of difluoroethane and about 50% by weight of n-butane, isobutane or n-propane.
4. A composition as claimed in any one of Claims 1 to 3 wherein the solvent comprises polyoxyethylene sorbitan trioleate having an average of about 20 units of ethylene oxide in the polyoxyethylene chain and one of polyethylene glycol monolaurate and polyethylene glycol dilaurate wherein the polyethylene glycol has an average molecular weight of about 400.
5. A composition as claimed in any one of Claims 1 to 4 wherein the benzocaine comprises at least 10% by weight of the base.
6. A composition as claimed in any one of Claims 1 to 5 wherein the benzocaine comprises about 20% by weight of the base.
7. A composition as claimed in any one of Claims 1 to 6 wherein the base and propellant each comprise about 45% to about 55% of the composition.
8. A composition as claimed in any one of Claims 1 to 7 which comprises at least 10% benzocaine in the base the solvent comprises polyoxyethylene sorbitan trioleate having an average of about 20 units of ethylene oxide in the polyoxyethylene chain and polyethylene glycol monolaurate wherein the polyethylene glycol has an average molecular weight of about 400; and the propellant comprises difluoroethane and n-butane.
9. A composition as claimed in any one of Claims 1 to 8 wherein the polyoxyethylene sorbitan trioleate comprises about 40% to about 60% of the solvent; the difluoroethane comprises about 35% to about 70% of the propellant; and the propellant comprises about 45% to about 55% of the composition.
10. A liquid anaesthetic composition in an aerosol container comprising a single phase mixture of a propellant and a water washable base comprising benzocaine in a solvent, wherein the base comprises by weight about 20% benzocaine, about 40% polyoxyethylene sorbitan trioleate having an average of about 20 units of ethylene, oxide in the polyoxyethylene claim and about 40% polyethylene glycol monolaurate, the polyethylene glycol having an average molecular weight of about 400; the propellant comprises about 50:50 by weight mixture of difluoroethane and n-butane; and wherein each of the base and propellant comprise about 50% of the composition.
11. A liquid anaesthetic composition substantially as hereinbefore described with reference to any one of Examples 1 to6, lOto 16,21 to25,27to34,36 and38to4l.
GB8007867A 1979-03-08 1980-03-07 Benzocaine aerosol compositions Expired GB2046093B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US1853579A 1979-03-08 1979-03-08

Publications (2)

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GB2046093A true GB2046093A (en) 1980-11-12
GB2046093B GB2046093B (en) 1983-04-20

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KR (1) KR830001642A (en)
CA (1) CA1136547A (en)
CY (1) CY1310A (en)
GB (1) GB2046093B (en)
HK (1) HK85085A (en)
KE (1) KE3558A (en)
MY (1) MY8600371A (en)
SG (1) SG66285G (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0372777A2 (en) * 1988-12-06 1990-06-13 Riker Laboratories, Inc. Medicinal aerosol formulations
WO1992000061A1 (en) * 1990-06-29 1992-01-09 Fisons Plc Pressurised aerosol compositions
WO1992014466A1 (en) * 1991-02-16 1992-09-03 Smithkline Beecham Plc Pharmaceutical antitussive compositions
US5225183A (en) * 1988-12-06 1993-07-06 Riker Laboratories, Inc. Medicinal aerosol formulations
US5439670A (en) * 1989-11-28 1995-08-08 Riker Laboratories, Inc. Medicinal aerosol formulations
US5766573A (en) * 1988-12-06 1998-06-16 Riker Laboratories, Inc. Medicinal aerosol formulations
US5891420A (en) * 1997-04-21 1999-04-06 Aeropharm Technology Limited Environmentally safe triancinolone acetonide aerosol formulations for oral inhalation
US5891419A (en) * 1997-04-21 1999-04-06 Aeropharm Technology Limited Environmentally safe flunisolide aerosol formulations for oral inhalation
CN1050285C (en) * 1991-09-25 2000-03-15 菲索斯有限公司 Pressurised Aerosol compositions
US6129905A (en) * 1997-04-21 2000-10-10 Aeropharm Technology, Inc. Aerosol formulations containing a sugar as a dispersant
US6458338B1 (en) 1998-09-22 2002-10-01 Aeropharm Technology Incorporated Amino acid stabilized medicinal aerosol formulations
US7160538B2 (en) 1990-02-03 2007-01-09 Boehringer Ingelheim Kg Suspension aerosol formulations of pharmaceutical products

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0372777A2 (en) * 1988-12-06 1990-06-13 Riker Laboratories, Inc. Medicinal aerosol formulations
US5681545A (en) * 1988-12-06 1997-10-28 Riker Laboratories, Inc. Medicinal aerosol formulations
EP0995434A3 (en) * 1988-12-06 2003-11-26 Riker Laboratories, Inc. Medicinal aerosol formulations
EP0499344A3 (en) * 1988-12-06 1992-09-02 Riker Laboratories, Inc. Medicinal aerosol formulations
US6352684B1 (en) 1988-12-06 2002-03-05 Riker Laboratories Inc. CRC-free medicinal aerosol formulations of 1,1,1,2-tetrafluoroethane (134A) with polar adjuvant
US5225183A (en) * 1988-12-06 1993-07-06 Riker Laboratories, Inc. Medicinal aerosol formulations
EP0372777A3 (en) * 1988-12-06 1990-11-22 Riker Laboratories, Inc. Medicinal aerosol formulations
US5605674A (en) * 1988-12-06 1997-02-25 Riker Laboratories, Inc. Medicinal aerosol formulations
EP0995434A2 (en) * 1988-12-06 2000-04-26 Riker Laboratories, Inc. Medicinal aerosol formulations
US5674473A (en) * 1988-12-06 1997-10-07 Riker Laboratories, Inc. Medicinal aerosol formulations
EP0653204A3 (en) * 1988-12-06 1995-11-15 Riker Laboratories Inc Medicinal aerosol formulations.
US5683677A (en) * 1988-12-06 1997-11-04 Riker Laboratories, Inc. Medicinal aerosol formulations
US5695743A (en) * 1988-12-06 1997-12-09 Riker Laboratories, Inc. Medicinal aerosol formulations
US5720940A (en) * 1988-12-06 1998-02-24 Riker Laboratories, Inc. Medicinal aerosol formulations
US5766573A (en) * 1988-12-06 1998-06-16 Riker Laboratories, Inc. Medicinal aerosol formulations
US5439670A (en) * 1989-11-28 1995-08-08 Riker Laboratories, Inc. Medicinal aerosol formulations
US7160538B2 (en) 1990-02-03 2007-01-09 Boehringer Ingelheim Kg Suspension aerosol formulations of pharmaceutical products
US5846521A (en) * 1990-06-29 1998-12-08 Fisons Plc Pressurized solvent-free drug aerosol compositions containing hydrofluorocarbon propellants
WO1992000061A1 (en) * 1990-06-29 1992-01-09 Fisons Plc Pressurised aerosol compositions
WO1992014466A1 (en) * 1991-02-16 1992-09-03 Smithkline Beecham Plc Pharmaceutical antitussive compositions
CN1050285C (en) * 1991-09-25 2000-03-15 菲索斯有限公司 Pressurised Aerosol compositions
US5891420A (en) * 1997-04-21 1999-04-06 Aeropharm Technology Limited Environmentally safe triancinolone acetonide aerosol formulations for oral inhalation
US5891419A (en) * 1997-04-21 1999-04-06 Aeropharm Technology Limited Environmentally safe flunisolide aerosol formulations for oral inhalation
US6129905A (en) * 1997-04-21 2000-10-10 Aeropharm Technology, Inc. Aerosol formulations containing a sugar as a dispersant
US6458338B1 (en) 1998-09-22 2002-10-01 Aeropharm Technology Incorporated Amino acid stabilized medicinal aerosol formulations

Also Published As

Publication number Publication date
HK85085A (en) 1985-11-08
KR830001642A (en) 1983-05-18
SG66285G (en) 1986-06-13
MY8600371A (en) 1986-12-31
GB2046093B (en) 1983-04-20
CA1136547A (en) 1982-11-30
KE3558A (en) 1985-10-04
CY1310A (en) 1986-03-28

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Effective date: 20000306