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AU2003203452A8 - Topical composition - Google Patents

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Publication number
AU2003203452A8
AU2003203452A8 AU2003203452A AU2003203452A AU2003203452A8 AU 2003203452 A8 AU2003203452 A8 AU 2003203452A8 AU 2003203452 A AU2003203452 A AU 2003203452A AU 2003203452 A AU2003203452 A AU 2003203452A AU 2003203452 A8 AU2003203452 A8 AU 2003203452A8
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AU
Australia
Prior art keywords
topical composition
composition according
emollient
microbial
topical
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.)
Abandoned
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AU2003203452A
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AU2003203452A1 (en
Inventor
Michael Lindsay Grayson
Suzanne Wendy Kirsa
Alan Douglas Shilson
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Austin Health
Original Assignee
Austin Health
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Filing date
Publication date
Application filed by Austin Health filed Critical Austin Health
Priority to AU2003203452A priority Critical patent/AU2003203452A1/en
Assigned to AUSTIN HEALTH reassignment AUSTIN HEALTH Amend patent request/document other than specification (104) Assignors: AUSTIN AND REPATRIATION MEDICAL CENTRE
Publication of AU2003203452A1 publication Critical patent/AU2003203452A1/en
Priority to AU2006235798A priority patent/AU2006235798B2/en
Publication of AU2003203452A8 publication Critical patent/AU2003203452A8/en
Abandoned legal-status Critical Current

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  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Cosmetics (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

AUSTRALIA Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Applicant: AUSTIN & REPATRIATION MEDICAL CENTRE Invention Title: TOPICAL COMPOSITION The following statement is a full description of this invention, including the best method of performing it known to
US:
-2 FIELD OF THE INVENTION The present invention relates to topical compositions, which may be used as an antiseptic and/or 5 disinfectant. BACKGROUND OF THE INVENTION Control of nosocomial infection and exposure to 10 infectious disease is of paramount concern to doctors, nurses, and clinicians that work in hospitals, clinics and surgical and medical centres. One of the most effective methods for controlling infection is regimented hand disinfection before and after each patient contact and 15 before invasive procedures. Hand disinfection is generally accomplished using anti-microbial soaps with water. These soaps are usually formulated to include either povidone-iodine or 20 chlorhexidine gluconate as the active anti-microbial agent. In addition, these formulated soaps may contain surfactants and possibly low levels of humectants such as glycerin. 25 Hand disinfection is also accomplished using hand wash replacements. These are used instead of the soap and water scrub. Hand wash replacements ideally achieve bacterial kill equal to or better than a traditional soap and water scrub and in a shorter period of time. 30 Additionally, they maintain or improve the skin's natural barrier to microbial and chemical contamination while providing acceptable tactile properties. Examples of hand wash replacements include hydroalcoholic gels, which H:\Shona1\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 -3 generally include high levels of either ethanol or isopropanol as the disinfecting agent and also include a thickener and/or surfactant and optionally include a humectant (e.g. glycerin). 5 SUMMARY OF THE INVENTION The present invention provides a topical composition comprising: 10 at least one C 1 to C 4 alcohol; at least one anti-microbial; and at least one emollient. The C 1 to C 4 alcohols may include straight or 15 branched chain alcohols. Preferably, the alcohols are selected from ethanol, n-propanol and isopropanol. Preferably, the alcohol is isopropanol. The alcohol concentration is preferably about 20 60% v/v to about 90% v/v, more preferably about 65% v/v to about 75% v/v, most preferably about 70% v/v of the total concentration of the topical composition. The anti-microbial may be selected from 25 chlorhexidine and its salts. A preferred anti-microbial is chlorhexidine gluconate. The anti-microbial is preferably present in an amount of about 3 g/L to about 10 g/L, more preferably 30 about 4 g/L to about 7 g/L, most preferably about 5 g/L of the topical composition. The emollient may be selected from general H.\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 -4 emollients, occlusive emollients and humectants. Preferably, the emollient is a humectant. More preferably, the emollient is selected from humectants such 5 as glycerol, propylene glycol, dipropylene glycol, polypropylene glycol, polyethylene glycol, sorbitol, pantothenol and gluconic acid salts. Most preferably, the emollient is polyethylene glycol. 10 The concentration of the emollient in the topical composition is preferably about 1.0% to about 2.0%, more preferably about 1.5%'to about 1.8%, most preferably about 1.5%. 15 The present invention also provides a method of reducing and/or preventing the transmission of a microorganism by applying an effective amount of a topical composition as defined above to any part of the body excluding mucous membranes. 20 The topical composition as defined above may therefore be used to reduce and/or prevent the transmission of a microorganism. 25 The topical composition may also be used in the manufacture of a disinfectant and/or antiseptic to reduce and/or prevent the transmission of a microorganism. The microorganism is preferably a multi 30 resistant organism such as, for example, methicillian resistant staphylococcus aureus. The topical composition may be applied before H:\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 -5 and after routine or specialised health-care delivery or preparatory to invasive procedures. An effective amount of the topical composition 5 is preferably about 1 ml to about 3 ml. The present invention further provides a method of preparing a topical composition as defined above comprising the step of mixing at least one C 1 to C 4 10 alcohol, at least one anti-microbial, and at least one emollient, with stirring, until complete homogenisation is achieved. DETAILED DESCRIPTION OF THE INVENTION 15 The present invention provides a topical composition comprising at least one C 1 to C 4 alcohol, at least one anti-microbial, and at least one emollient. 20 Alcohols Alcohol is an effective vehicle for a disinfectant. It provides a broad spectrum bactericidal effect and is fast drying. 25 The C 1 to C 4 alcohols in the topical composition of the present invention may include straight or branched chain alcohols. Suitable alkanols include ethanol, n propanol and isopropanol. 30 While the topical composition of the present invention may comprise only one alcohol, a combination of alcohols may be used. H:\Shona1\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 -6 Isopropanol is a good disinfectant with a pleasant odour and, compared to other alcohols, it has a less cutaneous drying effect of the skin. Therefore, 5 isopropanol is a preferred alcohol for the topical composition of the present invention. The alcohol concentration of the topical composition should provide the greatest possible bacterial 10 kill effect. Therefore, the alcohol concentration is preferably about 60% v/v to about 90% v/v, more preferably about 65% v/v to about 75% v/v, most preferably about 70% v/v of the total concentration of the topical composition. 15 Anti-microbials The term "anti-microbials" is used herein in its broadest sense and refers to any agent that can treat any infection caused by a microorganism and includes viral and 20 bacterial infections. Examples of such infectious microorganisms may be found in a number of well known texts such as 'Medical Microbiology' (Greenwood, D., Slack, R., Peutherer, J., Churchill Livingstone Press, 2002); 'Mims' Pathogenesis of Infectious Disease' (Mims, 25 C., Nash, A., Stephen, J., Academic Press, 2000); '"Fields" Virology. (Fields, B.N., Knipe, D.M., Howley, P.M., Lippincott Williams and Wilkins, 2001). Chlorhexidine and its salts are is an anti 30 microbial effective against a wide-range of Gram-positive and Gram-negative bacteria. While chlorhexidine may be used as an anti H.\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 -7 microbial in the topical composition of the present invention, a salt of chlorhexidine is preferred due to its solubility properties. Preferred salts of chlorhexidine include chlorhexidine gluconate, chlorhexidine acetate and 5 chlorhexidine hydrochloride. The most preferred anti microbial for the topical composition of the present invention is chlorhexidine gluconate because it has excellent instantaneous bacterial effect that persists after use. 10 The amount of anti-microbial present in the topical composition should provide a balance between the desired antibacterial effect and unwanted adverse effects. 15 The anti-microbial is preferably present in an amount of about 3 g/L to about 10 g/L, more preferably about 4 g/L to about 7 g/L, most preferably about 5 g/L of the topical composition. 20 While a single anti-microbial may be used in the topical composition of the present invention, additional anti-microbials may be added to enhance the anti-microbial action of the topical composition. This may be particularly desirable in critical uses such as 25 preparatory to invasive procedures. Emollients Emollients are typically added to topical 30 compositions because they act to increase the moisture content of the stratum corneum. Emollients are generally separated into two H:\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 -8 broad classes based on their function. The first class of emollients function by forming an occlusive barrier to prevent water evaporation from the stratum corneum. The second class of emollients penetrate into the stratum 5 corneum and physically bind water to prevent evaporation. The first class of emollients is subdivided into compounds that are waxes at room temperature and compounds that are liquid oils. The second class of emollients includes those that are water-soluble and are often referred to as 10 humectants. The emollient may be selected from the following non-limiting list of general emollients, occlusive emollients and humectants. 15 Examples of general emollients includes short chain alkyl or aryl esters (Ci-C 6 ) of long straight or branched chain alkyl or alkenyl alcohols or acids (Cs-C 32 ) and their polyethoxylated derivatives; short chain alkyl 20 or aryl esters (Ci-C 6 ) or C 4
C
12 diacids or diols optionally substituted in available positions by -OH; alkyl or aryl
C
1
-C
10 esters of glycerol, pentaerythritol, ethylene glycol, propylene glycol, as well as polyethoxylated derivatives of these and polyethylene glycol; C1 2
-C
22 alkyl 25 esters or ethers of polypropylene glycol; C 12
-C
2 2 alkyl esters or ethers of polypropylene glycol/polyethylene glycol copolymer; and polyether polysiloxane copolymers. Examples of occulsive emollients include cyclic 30 and linear dimethicones, polydialkysiloxanes, polyaryl/alkylsiloxanes, long chain (Cs-C 36 ) alkyl and alkenyl esters of long straight or branched chain alkyl or alkenyl alcohols or acids; long chain (C8-C 36 ) alkyl and H.\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 -9 alkenyl amides of long straight or branched chain alkanes and alkenes such as squalene, squalane and mineral oil; jojoba oil polysiloxane polyalkylene copolymers, dialkoxy dimethyl polysiloxanes, short chain alkyl or aryl esters 5 (Cl-C) of C 12
-C
2 2 diacids or diols optionally substituted in available positions by -OH, such as diisostearyl dimer dilinoleate; lanolin and lanolin derivatives, and beeswax and its derivatives. 10 Examples of humectant type emollients include glycerol, propylene glycol, dipropylene glycol, polypropylene glycol, polyethylene glycol, sorbitol, pantothenol, gluconic acid salts and the like. 15 Humectant type emollients are preferred for the topical composition of the present invention. The most preferred humectant is polyethylene glycol. Polyethylene glycol is pleasant to use, readily available and economical. 20 The concentration of the emollient in the topical composition is preferably about 1.0% to about 2.0%, more preferably about 1.5% to about 1.8%, most preferably about 1.5%. 25 The inventors have determined that having a 1.5% concentration of polyethylene glycol in the topical composition of the present invention provides adequate moisturising while not causing irritation and/or allergic 30 reactions. There are also no unwanted abnormal feelings after application such as sliminess or stickiness. Hs\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 10 Additional ingredients The topical composition may optionally comprise ingredients such as water, oils, salts, fragrances, 5 perfumes, colorants, stabilisers, emulsifiers, propellants, additives, preservatives or preserving agents, anti-oxidants, surfactants, thickeners and other excipients normally used in topical compositions. If additional ingredients are included in the topical 10 composition, ingredients that are known to cause skin irritation and/or sensitisation reactions should be avoided. Formulations 15 The topical composition may be formulated into the form of an aerosol, balm, cream, emolument, foam, gel, liniment, lotion, ointment, salve, solution, spray, suspension, unguent or the like. 20 Application The present invention is a topical composition, which is useful as a broad-spectrum antiseptic and/or 25 disinfectant for use in many environments including hospitals and clinics, veterinarian, industrial, food industry, livestock and home environments. The topical composition may be used, for example, as a skin disinfectant. 30 The topical compositions of the present invention are highly efficacious in preventing the transmission of microorganisms within hospitals. H:\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 11 The term "microorganism" includes any microscopic organism or taxonomically related macroscopic organism within the categories algae, bacteria, fungi, 5 protozoa, viruses and subviral agents or the like. The microorganism is preferably a multi-resistant organism such as, for example, methicillian-resistant staphylococcus aureus. 10 In addition, preferred topical compositions of this invention maintain moisture after both single and multiple applications without allergic reaction or unwanted side effects such as abnormal feelings of sliminess or stickiness. 15 Topical compositions of the present invention are suitable for frequent and repeated usage during routine and specialised health-care delivery in environments such as hospital or clinic. In hospitals and 20 clinics, these topical compositions may be used before and after each patient contact or preparatory to invasive procedures. If topical compositions of the present invention 25 are formulated into a hand lotion, only a small amount, about 1 ml to about 3 ml, of the hand lotion would be needed to be effective disinfectant and/or antiseptic. Topical compositions of the present invention 30 have advantages over known topical compositions in that they may be applied frequently with minimal adverse effects, dry rapidly, provide both instantaneous and prolonged anti-microbial activity, and have a low toxicity Hs\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 12 profile. The term "topical composition" as used herein generally refers to a composition that is applied S externally to any part of the body excluding mucous membranes such as the eyes, mouth, and so on. The topical composition may, therefore, be applied directly to any part of the body excluding mucous membranes such as the eyes, mouth, and so on. However, topical compositions of 10 the present invention may also be incorporated into sponges, swabs, pads and/oriwipes, which are then used to apply the topical solution to any part of the body excluding mucous membranes such as the eyes, mouth, and so on. The topical compositions may also be incorporated into 15 cosmetic products. Stability The topical composition of the invention 20 conserves its activity for, at least, two years from its production. However, it is preferable to use it at least within 12 months of being prepared. Even so, incorporating appropriate preserving agents can extend the period to sustain activity. 25 In this specificat ion, except where the context requires otherwise, the words "comprise", "comprises", and "comprising" mean "include", "includes", and "including", respectively, i.e. when the invention is described or 30 defined as comprising specified features, various embodiments of the same invention may also include additional features. H;\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 13 EXAMPLES The invention will now be further described with reference to the following Examples. These Examples are 5 not intended to limit the invention in any way. The topical composition of the present invention may be prepared by a variety of techniques. 10 One method of preparing the topical composition of the present invention involves mixing the components of the topical composition, in suitable quantities, with stirring, until complete homogenisation is achieved. 15 The following examples are topical compositions of the present invention that were prepared according to the above method. Example 1 20 isopropyl alcohol 70% v/v chlorhexidine gluconate 5 g/L polyethylene glycol 1.5% concen. water balance 25 The topical composition of Example 1 was formulated into the form of a lotion, in particular a hand lotion. 30 The hand lotion was shown to be an effective disinfectant and/or antiseptic. It was also gentle on the skin, dried rapidly and provided both instantaneous and prolonged anti-microbial activity. The hand lotion showed H:\Shona1\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 14 no unwanted side effects such as abnormal feelings of sliminess or stickiness. The hand lotion of Example 1 was also trialed as 5 a disinfectant hand lotion in an intervention/study ward of the Austin & Repatriation Medical Centre, Victoria, Australia. The trial was conducted over a period of ten or 10 so months. The staff of the intervention/study ward were instructed to use about 1 ml to about 3 ml of the disinfectant hand lotion before and after each patient 15 contact. The results of the trial showed that there was an approximately 21% to 25% reduction in clinical infections with methicillian-resistant staphylococcus 20 aureus ("MRSA"). Since the disinfectant hand lotion was easy to use, there was also a 25% to 100% improvement in hand hygiene compliance. Hand hygiene compliance refers to the 25 rates of hand washing, which in the present case would refer to the rates of use of the topical composition as a disinfectant hand lotion. Furthermore, there were no allergic reactions 30 identified through repeated use of the hand lotion during the trial. Accordingly, this trial showed that the topical H:\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 15 composition of the present invention would be very effective as a disinfectant hand lotion in hospitals, clinics, surgical and medical centres and the like. 5 Example 2 isopropyl alcohol 70% v/v chlorhexidine gluconate 5 g/L polyethylene glycol 2.0% concen. 10 water balance The topical composition of Example 2 was formulated into the form of a lotion, in particular a hand lotion. 15 The hand lotion was shown to be an effective disinfectant and/or antiseptic. It was also gentle on the skin, dried rapidly and provided both instantaneous and prolonged anti-microbial activity. 20 The hand lotion was found, however, to have a slight unwanted after effect. Specifically, after repeated use of the hand lotion, there was a feeling of stickiness. 25 It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments 30 are, therefore, to be considered in all respects as illustrative and not restrictive. H.\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03

Claims (45)

1. A topical composition comprising: at least one C 1 to C 4 alcohol; 5 at least one anti-microbial; and at least one emollient.
2. A topical composition according to claim 1, wherein the C 1 to C 4 alcohol is a straight or branched 10 chain alcohol.
3. A topical composition according to claim 1 or claim 2, wherein the alcohol is selected from ethanol, n propanol, isopropanol or a combination thereof. 15
4. A topical composition according to any one of the preceding claims, wherein the alcohol is isopropanol.
5. A topical composition according to any one of 20 the preceding claims, wherein the alcohol concentration is about 60% v/v to about 90% v/v of the total concentration of the topical composition.
6. A topical composition according to any one of 25 the preceding claims, wherein the alcohol concentration is about 65% v/v to about 75% v/v of the total concentration of the topical composition.
7. A topical composition according to any one of 30 the preceding claims, wherein the alcohol concentration of the topical composition is about 70% v/v of the total concentration of the topical composition. H,\Shona1\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 17
8. A topical composition according to any one of the preceding claims, wherein the anti-microbial is selected from chlorhexidine and its salts. 5
9. A topical composition according to any one of the preceding claims, wherein the anti-microbial is selected from chlorhexidine gluconate, chlorhexidine acetate and chlorhexidine hydrochloride.
10 10. A topical composition according to any one of the preceding claims, wherein the anti-microbial is chlorhexidine gluconate.
11. A topical composition according to any one of 15 the preceding claims, wherein additional anti-microbials are added to the topical composition to enhance its anti microbial action.
12. A topical composition according to any one of 20 the preceding claims, wherein the anti-microbial is present in an amount of about 3 g/L to about 10 g/L of the topical composition.
13. A topical composition according to any one of 25 the preceding claims, wherein the anti-microbial is present in an amount of about 4 g/L to about 7 g/L of the topical composition.
14. A topical composition according to any one of 30 the preceding claims, wherein the anti-microbial is present in an amount of about 5 g/L of the topical composition. H:\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 18
15. A topical composition according to any one of the preceding claims, wherein the emollient is selected from general emollients, occlusive emollients and humectants. 5
16. A topical composition according to any one of the preceding claims, wherein the emollient is a general emollient selected from short chain alkyl or aryl esters (Ci-C 6 ) of long straight or branched chain alkyl or alkenyl 10 alcohols or acids (CS-C 32 ) and their polyethoxylated derivatives; short chain alkyl or aryl esters (Ci-C) or C 4 -C 2 diacids or diols optionally substituted in available positions by -OH; alkyl or aryl Ci-Cio esters of glycerol, pentaerythritol, ethylene glycol, propylene glycol, as 15 well as polyethoxylated derivatives of these and polyethylene glycol; C 1 2 -C 2 2 alkyl esters or ethers of polypropylene glycol; C 12 -C 22 alkyl esters or ethers of polypropylene glycol/polyethylene glycol copolymer; and polyether polysiloxane copolymers. 20
17. A topical composition according to any one of the preceding claims, wherein the emollient is an occlusive emollient selected from cyclic and linear dimethicones, polydialkysiloxanes, 25 polyaryl/alkylsiloxanes, long chain (C8-C 3 6 ) alkyl and alkenyl esters of long straight or branched chain alkyl or alkenyl alcohols or acids; long chain (Cs-C 36 ) alkyl and alkenyl aides of long straight or branched chain alkanes and alkenes such as squalene, squalane and mineral oil; 30 jojoba oil polysiloxane polyalkylene copolymers, dialkoxy dimethyl polysiloxanes, short chain alkyl or aryl esters (Cl-C 6 ) of C 12 -C 22 diacids or diols optionally substituted in available positions by -OH, such as diisostearyl dimer H:\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 19 dilinoleate; lanolin and lanolin derivatives, and beeswax and its derivatives.
18. A topical composition according to any one of 5 the preceding claims, wherein the emollient is a humectant selected from glycerol, propylene glycol, dipropylene glycol, polypropylene glycol, polyethylene glycol, sorbitol, pantothenol and gluconic acid salts. 10
19. A topical composition according to any one of the preceding claims, wherein the emollient is polyethylene glycol.
20. A topical composition according to any one of 15 the preceding claims, wherein the concentration of the emollient in the topical composition is about 1.0% to about 2.0%.
21. A topical composition according to any one of 20 the preceding claims, wherein the concentration of the emollient in the topical composition is about 1.5% to about 1.8%.
22. A topical composition according to any one of 25 the preceding claims, wherein the concentration of the emollient in the topical composition is about 1.5%.
23. A topical composition according to any one of the preceding claims, wherein further comprises water, 30 oils, salts, fragrances, perfumes, colorants, stabilisers, emulsifiers, propellants, additives, preservatives or preserving agents, anti-oxidants, surfactants, thickeners and other excipients normally used in topical H.\Shona1\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 20 compositions.
24. A topical composition according to any one of the preceding claims, wherein the topical composition is 5 formulated into the form of an aerosol, balm, cream, emolument, foam, gel, liniment, lotion, ointment, salve, solution, spray, suspension, unguent or the like.
25. A topical composition according to any one of 10 the preceding claims, wherein the topical composition is incorporated into sponges, swabs, pads and/or wipes.
26. A topical composition according to any one of the preceding claims, wherein the topical composition is 15 incorporated into cosmetic products.
27. A topical composition according to any one of the preceding claims, wherein the topical composition is used on any part of the body excluding mucous membranes. 20
28. A method of reducing and/or preventing the transmission of a microorganism by applying an effective amount of a topical composition as defined in any one of claims 1 to 27 to any part of the body excluding mucous 25 membranes.
29. The method according to claim 28, wherein the microorganism is a multi-resistant organism.
30 30. The method according to claim 29, wherein the multi-resistant organism is methicillian-resistant staphylococcus aureus. H \Shona1\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 21
31. The method according to any one of claims 28 to 30, wherein the topical composition is applied before and after routine or specialised health-care delivery or preparatory to invasive procedures. 5
32. The method according to any one of claims 28 to 31, wherein an effective amount is about 1 ml to about 3 ml. 10
33. Use of a topical composition as defined in any one of claims 1 to 27 to reduce and/or prevent the transmission of a microorganism.
34. The use according to claim 33, wherein the 15 microorganism is a multi-resistant organism.
35. The use according to claim 34, wherein the multi-resistant organism is methicillian-resistant staphylococcus aureus. 20
36. The use according to any one of claims 33 to 35, wherein the topical composition is used before and after routine or specialised health-care delivery or preparatory to invasive procedures. 25
37. The use according to any one of claims 33 to 36, wherein about 1 ml to about 3 ml of the topical composition is used. 30
38. Use of a topical composition as defined in any one of claims 1 to 27 in the manufacture of a disinfectant and/or antiseptic to reduce and/or prevent the transmission of a microorganism. H.\Shonal\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03 - 22
39. The use according to claim 38, wherein the microorganism is a multi-resistant organism.
40. The use according to claim 39, wherein the 5 multi-resistant organism is methicillian-resistant staphylococcus aureus.
41. A disinfectant and/or antiseptic comprising a topical composition as defined in any one of claims 1 to 10 27.
42. A method of preparing a topical composition as defined in any one of claims 1 to 27 comprising the step of mixing at least one C 1 to C 4 alcohol, at least one anti 15 microbial, and at least one emollient, with stirring, until complete homogenisation is achieved.
43. A topical composition substantially as herein described with reference to any one of the Examples. 20
44. A disinfectant hand lotion comprising a topical composition substantially as herein described with reference to any one of the Examples. 25
45. A method of preparing a topical composition substantially as herein described with reference to any one of the Examples. Dated this 28 day of March 2003 30 AUSTIN REPATRIATION MEDICAL CENTRE By their Patent Attorneys GRIFFITH HACK Fellows Institute of Patent and Trade Mark Attorneys of Australia H\Shona\Keep\Speci\P49134 TOPICAL COMPOSITION 28/03/03
AU2003203452A 2003-03-28 2003-03-28 Topical composition Abandoned AU2003203452A1 (en)

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CN105147829B (en) * 2015-08-28 2019-05-10 爱品尚客(北京)电子商务有限公司 A kind of maca externally applied spray

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