AU2006246966B2

AU2006246966B2 - Method and composition for use in preparation of a patient for surgery

Info

Publication number: AU2006246966B2
Application number: AU2006246966A
Authority: AU
Inventors: Steven Kritzler
Original assignee: Novapharm Research Australia Pty Ltd
Current assignee: Novapharm Research Australia Pty Ltd
Priority date: 2005-05-16
Filing date: 2006-04-28
Publication date: 2012-01-19
Anticipated expiration: 2026-04-28
Also published as: AU2006246966A1

Abstract

Composition for application to skin comprising a biocide or combination of biocides (such as chlorhexidine, halogenated phenols, quaternary ammonium compounds; povidone-iodine; zinc pyridinethione; alcohols etc)and at least one transcutaneous vehicle (for example alkyl methyl sulfoxides, alkyl pyrrolidones, glycols, glycol ethers and glycol esters) effective to convey the biocide to a sub epidermal "resident" micro-organism. Also a method for preparing a patient for surgery comprising the step of treating an area of the patient's skin at, and in the surrounding the vicinity of, the site of an intended surgical incision with a composition effective to kill more than 93% of both "transient" and "resident" micro-organisms.

Description

WO 2006/122345 PCT/AU2006/000553 1 TITLE: METHOD AND COMPOSITION FOR USE IN PREPARATION OF A PATIENT FOR SURGERY FIELD OF THE INVENTION 5 The present invention is concerned with an improved method for preparing a patient for surgery. More particularly, the present invention is concerned with reducing the risk (in comparison with methods currently employed) of a patient contracting an infection as a result of undergoing a surgical procedure. The present invention is also concerned with compositions suitable for use in the method. 10 Although the method will be herein described with reference to preparation of human patients for surgery it will be understood that the method is equally applicable to other animals. BACKGROUND OF THE INVENTION 15 It is usual when preparing a patient for surgery to treat an area surrounding the intended site of an incision by applying a biocide such as iodine or chlorhexidine to the skin surface. This is usually applied immediately preoperatively. After treatment, the area is covered with a sterile sheet or drape leaving an opening through which the surgeon can make an incision and perform an operation. The purpose of this 20 procedure is to kill any colonies of micro-organism which exist on the patient's skin and which may access the surgical site giving rise to infection of the surgical wound. Although this procedure is largely effective in reducing the occurrence of post operative infection, a high proportion of cases in which infection does occur are attributed to autologous infection. Such infection if it does occur may have serious, or 25 even fatal, consequences. It is the practice in some hospitals as an added precaution to ask patients to wash themselves, or at least the areas intended for surgery, with an antiseptic soap once a day for one or two days prior to surgery. This wash is usually done under the shower and is thought to reduce the bacterial load on the patient's skin, and to remove 30 micro-organisms from a wider area of skin than is practical in the operating theatre prior an operation.

WO 2006/122345 PCT/AU2006/000553 2 The above treatments have in common that they are only effective against "transient" micro-organisms. "Transient" micro-organisms are those that exist on the surface of skin. The efficacy of such treatments against transient micro-organisms is discussed by Paulson, D. S. (American Journal of Infection Control (1993), 21, 205 5 209) in respect of 4% chlorhexidine gluconate shower baths and Byrne, D. J. et al (J. Hospital Infection (1990), 15, 183-187) in respect of 4% chlorhexidine detergent. Garibaldi, R.A. (J. Hospital Infection (1988), 11, Sup B 5-9) showed that 4% chlorhexidine gluconate was more effective than povidone iodine or triclocarban medicated soap for treating skin surface colonization. Nevertheless the frequency of 10 intra-operative wound cultures was at best 4% , i.e. surface cultures were found on 4 patients in 100 intra-operatively. Any discussion of the prior art throughout the specification should in no way be considered as an admission that such prior art is widely known or forms part of common general knowledge in the field.. 15 The present inventor has observed that while a patient's skin is treated pre operatively with a biocide effective against "transient" micro-organism populations, surgeons are obliged to "scrub up" and this "surgical scrubbing" involves intensive scrubbing treatment with biocides and surfactants extending over several minutes under running water according to complex set down protocols. These scrubbing 20 protocols are intended not only to remove "transient" organisms from the surface of the surgeon's hands, but also to kill "resident" micro-organisms which may reside within pores of the skin. The epidermis which is the outer layer of skin consists of five stratum, of which the stratum corneum is the outermost. Some micro-organisms may reside sub corneum, particularly but not only in sweat glands, hair follicles, and 25 subcutaneous glands. Such "resident" micro-organisms are difficult to kill even with scrubbing and studies have shown that their removal is only partially accomplished by surgical scrubbing. It would be impracticable to scrub patients under running water to the same extent prior to surgery and doing so would only be partially effective The commonly used preoperative compositions result in approximately a 30 reduction of 2 log in "transient" micro-organisms on dry areas of skin, a reduction of 3 log on moist areas of skin (when measured in-vivo on hands and wrists using the "glove juice method" and when measured on fingertips using the "European method"), and have substantially no effect on the population of "resident" micro-organisms in the WO 2006/122345 PCT/AU2006/000553 3 skin. The occurrence of "resident" micro-organisms varies greatly from one person to another and variations of up to ten fold in resident micro-organism counts can be found in a representative sample of a population. Since the normal preoperative treatment is relatively effective against "transient" micro-organisms, this implies that "resident" 5 micro-organisms may play a role in autologous infection. Neilsen et al. (J.Clinical Pat., (1975), 28, 793-797) examined the effect of 0.5% chlorhexidine in 62% ethyl alcohol on both superficial "transient" and "resident" flora. They concluded that a two step process including a pre-treatment with a detergent was essential for treating "resident" flora. Of fourteen volunteers examined, 10 sub-corneum aerobic micro-organisms were found in each prior to treatment and remained in at least one case subsequent to the preferred treatment - i.e. a failure rate of 7%. The authors could only conclude that the treatment must be said "to eliminate to a high degree" the patients skin as a source of anaerobic and aerobic operation wound bacteria. Regretfully the intervening 30 years have shown even that conclusion 15 to be unrealistically optimistic and the problem remains. PCT/US98/06779 describes a method for preoperative skin preparation involving iodine and ethyl alcohol in a gel. Although the specification notes that micro-organisms may be "transient' or "resident', it contains no data or claim as to efficacy in respect of "resident" micro-organisms. Although primarily directed to an 20 iodine based composition, the method disclosed (page 26) involves application of the gel to the surgical site immediately preoperatively with scrubbing for about 30 seconds. Both the composition and method differ from that herein disclosed. It is also critically important to note that in the cited examples the primary biocides are chlorhexidine or iodine and with those biocides little, if any, subcutaneous 25 penetration is possible because of the strong interactions between these biocidal actives and all body proteins. In the case of chlorhexidine these interactions cause the biocide to become attached (substantive) to the protein and in the case of iodine cause it to be deactivated by the protein. Therefore any subcutaneous action is dependant upon the ethanol contained therein. 30 This penetrating ethanol is quickly dissipated within the body and therefore there is no residual biocidal activity sub corneum beyond a few minutes.

-4 Recolonisation of these areas begins immediately after alcohol dissipation. Most surgical procedures take between 15 minutes and six hours. Because of the currently perceived risk of post operative infection (including autologous infection) surgeons today routinely prescribe preoperative antibiotics as a 5 prophylactic measure. This practice risks increasing the resistance of micro-organisms to antibiotics and is a major medical and social concern. It is an object of the present invention to overcome or ameliorate at least one of the disadvantages of the prior art. It is an object of preferred embodiments of the invention to provide improved methods of preparing a patient for surgery and compositions for use 10 in that method which in highly preferred embodiments are more effective at reducing post operative infection than one or more prior art methods. BRIEF STATEMENT OF INVENTION The present inventor has found that a preparation including one or more biocides and a transcutaneous vehicle effective to carry the biocide as a solution across the 15 dermal barrier is effective to kill the "resident" micro-organisms especially when applied repeatedly several times a day over several days preceding an operation. Desirably the composition is applied as a gel or cream and spread over a relevant area of skin. The composition may be self applied by the patient on instruction by the surgeon and will usually be left in place until a subsequent application. 20 According to a first aspect the invention provides a composition for application to skin comprising: at least one biocide; at least one transcutaneous vehicle effective to convey the biocide to a subcutaneous resident micro-organism; and 25 wherein the at least one transcutaneous vehicle is selected from the group consisting of alkyl methyl sulfoxides, alkyl pyrrolidones, glycols, glycol ethers and glycol esters. The "resident" micro-organisms may be sub epidermal.

-5 "Transcutaneous" in respect of the vehicle means that the vehicle penetrates at least to the subcutis and desirable through the subcutis. Skin is the largest human organ and consists of three functional layers: epidermis, dermis, and subcutis. Skin is designed to protect the organism from water loss and mechanical, chemical, microbial, and physical 5 penetration and is specially structured to achieve these tasks. Those skilled in the art will recognise that while ethanol and similar alkyl alcohols have some ability to penetrate into the corneum, they are not transcutaneous and do not penetrate to the subcutis. Transcutaneous vehicles have been developed for transporting systemic drugs across the skin barrier, but have not previously been used to transport biocides into skin. 10 Combinations of biocides are preferred for use in the invention and an especially preferred combination is triclosan with phenoxyethanol. Care needs to be taken that in the concentrations used the biocides have no adverse systemic effect. According to a second aspect the invention provides a method for preparing a patient for surgery comprising the step of treating an area of the patient's skin at, and in 15 the surrounding the vicinity of, the site of an intended surgical incision with a composition according to the first aspect effective to kill more than 93% of both transient and subcutaneous resident micro-organisms and wherein said step is repeated at least twice, during the 24 hours preceding an operation. Preferred embodiments employ a composition according to the first aspect and 20 leave virtually no survving "resident" or "transient" micro-organisms. The term "comprising" is herein used in an inclusive sense that is to say in the sense of "including" or "containing". The term is not intended in an exclusive sense ("consisting of' or "composed of'). In preferred embodiments the composition contains at least one, and preferably a 25 combination of biocides and these are formulated so as to be able to access subcutaneous "resident" micro-organisms. In preferred embodiments of the invention the method is used in conjunction with prior art methods of preparation including showering with antibacterial soap and skin prepping on the operating table. It is not intended that the method be used as a substitute for skin prepping.

- 5a According to a third aspect, the invention provides a method according to the first aspect, wherein said step is repeated at least once, during the 24 hours preceding an operation. According to a fourth aspect, the invention provides use of a composition 5 according to the first aspect for treating the area of the patient's skin at, and in the surrounding vicinity of, the site of an intended surgical incision to kill more than 93% of both "transient" and "resident" micro-organisms. According to a fifth aspect, the invention provides a method for preparing a patient for surgery comprising the step of treating an area of the patient's skin at, and in 10 the surrounding the vicinity of, the site of an intended surgical incision with a composition effective to kill more than 93% of both "transient" and subcutaneous "resident" micro-organisms; wherein the composition comprises at least one biocide and at least one transcutaneous vehicle effective to convey the biocide to a "resident" micro organism; and wherein the at least one transcutaneous vehicle is selected from the group 15 consisting of alkyl methyl sulfoxides, alkyl pyrrolidones, glycols, glycol ethers and glycol esters. Suitable biocides for use in compositions according to the invention include, without limitation, chlorhexidine and its salts; dichlorophene, other chlorophenol derivatives such as p-chloro-m-xylenol, chlorophene and o-phenylphenol, 2,4,4 20 trichloro-2-hydroxy-diphenylether (triclosan); octenidindihydrochloride (CH 3

-(CH

2

)

7 WO 2006/122345 PCT/AU2006/000553 6

-NHON-(CH

2 ) 10 -NO-NH(CH 2)7 -CH 2 or any other salt thereof, quaternary ammonium compounds, povidone-iodine, and zinc pyridinethione, and phenoxy ethanol Suitable salts of chlorhexidine include the gluconate, isethionate, formate, 5 acetate, glutamate, succinamate, monodiglycolate, dimethanesulfonate, lactate, diisobutyrate or the glucoheptonate salts. Other suitable biocides include selected alcohols such as ethyl, methyl, isopropyl and phenyl alcohol. Preferably the antimicrobial agent has a water solubility of at least 0.001% w/v 10 at ambient temperature. When the antimicrobial agent is chlorhexidine digluconate it is used in an amount preferably not exceeding 4.5% w/v. When the antimicrobial agent is 2,4,4 trichloro-2-hydroxydiphenylether (triclosan) it is used in an amount preferably not exceeding 3% w/v. Preferably two or more biocides are used in combination. Biocides 15 such as iodine compounds and chlorhexidine compounds react with protein and are not suitable for dermal penetration since they would be deactivated by skin protein, but are effective against "transient" micro-organisms. Combinations of triclosan with phenoxy ethanol have been found to be unexpectedly effective for use in the invention and exhibit a desirable synergy. 20 Compositions according to the invention may be formulated into a liquid, lotion, cream, gel, or other topical vehicle, or may be formulated as a spray. The composition can be aqueous or alcoholic utilising ethanol, n-propanol or isopropanol. In addition to one or more biocides, the formulation includes at least one vehicle in which a biocide is soluble and which is effective to transport the biocide 25 transdermally. The vehicle is selected from the group consisting of suitable alkyl sulfoxides, alkyl pyrrolidones, glycols, glycol ethers and suitable esters. Examples of such vehicles include, without limitation, dimethyl sulfoxide as an example of a suitable alkyl sulfoxide; N-methyl-2- pyrrolidone as an example of a suitable alkyl pyrrolidone; propylene glycol as an example of a suitable glycol, isopropylmyristate as 30 an example of a suitable ester and diethylene glycol monoethyl ether as an example of a suitable glycol ether. The use of sulfoxides may require medical prescription in some jurisdictions.

WO 2006/122345 PCT/AU2006/000553 7 PREFERRED EMBODIMENTS OF THE INVENTION Preferred embodiments of the invention will now be described by way of example only. 5 Example 1: A gel suitable for use in a method according to the invention. Ethanol: 70.00% w/w Water 10.39% Hydroxypropyl cellulose 0.60% Phenoxy ethanol 2.00% Triclosan 1.00% Dimethylsulfoxide 10.00% Propylene Glycol 5.00% Isopropylmyristate 1.00% Dyestuff 0.01% In example 1 the ethanol serves as a biocide for transient organisms, as a skin penetrant, a solvent, and as a drying aid. Water acts as a solvent, and activator of ethanol as biocide. Hydroxypropyl cellulose acts as a gelling agent. Phenoxy ethanol acts as a preservative and as a secondary biocide for transient and subcutaneous micro 10 organisms. Triclosan acts as the primary biocide for killing transient and subcutaneous micro-organisms. Dimethylsulfoxide is the transcutaneous vehicle. Propylene Glycol also acts as a transcutaneous vehicle. Isopropylmyristate also acts as a transcutaneous vehicle and skin emollient. Dyestuff is added as an indicator that the required area of skin has been appropriately treated. 15 An example of a suitable method according to the invention involves a patient being instructed by the patient's surgeon to spread the gel of Example 1 over an area of the skin covering at least a margin of about 5cm around the site of intended incision in all directions at a rate of from about 0.03 to 0.1 g / sq. cm. of skin surface. The gel should be rubbed into the skin twice per day at 8 hr intervals for three days prior to the WO 2006/122345 PCT/AU2006/000553 8 date of the operation and once applied should be left in place and desirably should not be washed off. Example 2: An embodiment of a cream according to the invention and suitable for use in a method according to the invention has the following composition. The 5 main function of each component is indicated in the table. Commercial Chemical name Contents Function name (%w/w) BPO Benzoyl peroxide 5.00% Actives Irgasan DP300 Triclosan 1.00% Actives N - Methyl Transdermal Pharmasolv pyrrolidone 10.00% enhancer Disodium Ethylene Diamine Tetra Chelating agent, EDTA 2Na Acetic Acid 3.00% stabiliser Glycerol Glycerol 2.00% Moisturiser Carbomer(Acrylic Carbopol 940 copolymer) 0.90% Viscosity modifier Pentane - DB Benzyl benzoate 3.00% Skin emollient DPG Dipropylene glycol 3.00% Moisturiser Sodium Lauroyl Crodasinic LS30 Sarcosinate(30%) 2.00% Emulsifier Stearyl alcohol (and) Polyethyleneglycol 1000 cetyl/stearyl Promulgen - G ether 2.00% Emollient/emulsifier PVP K-15 Polyvinylpyrrolidone 0.10% Skin feel enhancer Active - secondary Phenoxyethanol Phenoxyethanol 2.00% biocide TEA 99% Triethanolamine 0.19% pH modifier Solvent/ Ethanol 100% Ethyl alcohol 10.00% formulation aid P-water Water 55.80% Solvent Dyestuff 0.01% Treatment marker TOTAL 100.00% WO 2006/122345 PCT/AU2006/000553 9 In use a patient is instructed by the patient's surgeon to spread the cream of Example 2 over an area of the skin covering at least a margin of about 5cm around the site of intended incision in all directions at a rate of from about 0.03 to 0.1 g / sq. cm. of skin surface. The cream should be rubbed into the skin at least twice per day 5 (preferably at 8 hr intervals) for three days prior to the date of the operation and, once applied, should be left in place. Example 3: A second embodiment of a cream according to the invention and suitable for use in a method according to the invention has the following composition. The main function of each component is indicated. 10 Commercial Chemical name Contents Function name (%w/w) BPO Benzoyl peroxide 5.00% Actives Irgasan DP300 Triclosan 1.00% Actives Diethylene Glycol Transdermal Trancutol P Monoethyl Ether 10.00% enhancer Disodium Ethylene Diamine Tetra Chelating agent, EDTA 2Na Acetic Acid 3.00% stabiliser Glycerol Glycerol 2.00% Moisturiser Carbomer(Acrylic Carbopol 940 copolymer) 0.90% Viscosity modifier Pentane - DB Benzyl benzoate 3.00% Skin emollient DPG Dipropylene glycol 3.00% Moisturiser Sodium Lauroyl Crodasinic LS3 0 Sarcosinate(30%) 2.00% Emulsifier Emollient/ Promulgen - G Stearyl alcohol (and) 2.00% emulsifier Polyethyleneglycol 1000 cetyl/stearyl ether PVP K-15 Polyvinylpyrrolidone 0.10% Skin feel enhancer Active - secondary Phenoxyethanol Phenoxyethanol 2.00% biocide TEA 99% Triethanolamine 0.19% pH modifier Solvent/ Ethanol 100% Ethyl alcohol 10.00% formulation aid P-water Water 55.80% Solvent __ Dyestuff 0.01% Treatment marker TOTAL 100.00% .

WO 2006/122345 PCT/AU2006/000553 10 The cream of example 3 is applied in a similar manner as described above with reference to example 1 or 2. Example 4: A third embodiment of a cream according to the invention and suitable for use in a method according to the invention has the following composition. 5 The main function of each component is indicated in the following table. Commercial Chemical name Contents Function name (%w/w) BPO Benzoyl peroxide 5.00% Actives Irgasan DP300 Triclosan 1.00% Actives N - Methyl Transdermal Pharmasolv pyrrolidone 5.00% enhancer Diethylene Glycol Transdermal Trancutol P Monoethyl Ether 5.00% enhancer Disodium Ethylene Diamine Tetra Chelating agent, EDTA 2Na Acetic Acid 3.00% stabiliser Glycerol Glycerol 2.00% Moisturiser Carbomer(Acrylic Carbopol 940 copolymer) 0.90% Viscosity modifier Pentane - DB Benzyl benzoate 3.00% Skin emollient DPG Dipropylene glycol 3.00% Moisturiser Sodium Lauroyl Crodasinic LS30 Sarcosinate(30%) 2.00% Emulsifier Stearyl alcohol (and) Polyethyleneglycol 1000 cetyl/stearyl Emollient/ Promulgen - G ether 2.00% emulsifier PVP K-15 Polyvinylpyrrolidone 0.10% Skin feel enhancer Active - secondary Phenoxyethanol Phenoxyethanol 2.00% biocide TEA 99% Triethanol amine 0.19% pH modifier Solvent/ Ethanol 100% Ethyl alcohol 10.00% formulation aid P-water Water 55.80% Solvent Dyestuff 0.01% Treatment marker TOTAL 100.00% WO 2006/122345 PCT/AU2006/000553 11 The cream of example 4 is applied in a similar manner as described above with reference to examples 1, 2 or 3. In each of the previous examples it is preferable for the patient in addition to the treatments described to shower or conduct a whole body wash using a disinfecting 5 soap on the day of, and prior to, the operation Example 5: Relative efficacy. The transcutaneous penetration and comparative release of active ingredient were compared using a horizontal glass Franz-type diffusion cells such as are described in R. Danids, (Skin Care Forum, Issue 37, August 2004, Cognis) ; S. Jung, 10 (The University of California Irvine Undergraduate Research Journal, p. 25-26, Vol V, 2002, University of California Irvine); Guideline for Industry Non-sterile Semisolid Dosage Forms(SUPAC-SS CMC7), May 1997, U.S. Department of Health and Human Services FDA CDER. A standard cellophane dialysis membrane of MW cut off 6 8000 was used for the diffusion studies. The Franz cell receiving solution was 15 composed of 50% v/v methanol/ water. Cellophane membranes were mounted horizontally in the Franz cells. 0.5 g of sample were used for each test. The cell receptor was continuously stirred magnetically and maintained at 35 +/-2 C. At the designated time 150microlitre aliquots were sampled from the receiving vessel of the Franz cells. 20 microliters were injected into HLPC. The residue was returned to the 20 Franz -cell and the cells topped up with additional receiving solution. 0.5 g samples of compositions according to examples 2, 3 and 4 were compared over periods of 2, 4 and 7 hours with a prior art composition comprising 5% chlorhexidine in 62% ethyl alcohol. The active ingredient was increased from 0.5% to 5% for the purposes of comparison with examples 2-4. Each test was in duplicate. 25 HLPC analysis was performed using a C18 column, mobile phase 75% methanol, flow rate 1.5 mL/min. detector -UV 270nm. The mean result of duplicate tests is tabulated below. Column A shows the composition example number, column B shows the time in hours. Column C, D, and E give the results for the actives in the respective formulations, both in mg and as a % of the sample quantity tested. 30 WO 2006/122345 PCT/AU2006/000553 12 A B C D E Example time phenoxyethanol triclosan chlorhexidine no. (hrs) mg % mg % mg % 2 2 0.6865 13.73 0.0119 0.24 4 1.0745 21.49 0.0246 0.49 7 1.4970 29.94 0.038 0.76 3 2 0.6495 12.99 0.0103 0.21 4 1.0150 20.3 0.0201 0.40 7 1.4080 28.16 0.0331 0.66 4 2 0.3355 6.71 0.0131 0.26 4 0.9960 19.92 0.0241 0.48 7 1.3645 27.29 0.0388 0.78 5 2 0.0026 0.052 4 0.0027 0.054 7 0.0039 0.078 It can be seen that phenoxy ethanol penetrates at a very much faster rate than either of the other biocides and to a much greater extent. After 2 hours more than 13 % has penetrated compared with 0.24% of triclosan and even less of chlorhexidine. The 5 difference is more substantial after 7 hrs. The penetration of biocides was much greater than for the prior art. Example 6: Synergism between triclosan and phenoxy ethanol An aqueous handwash formulation was prepared with three differing actives. Formula 1 contained triclosan 1% alone, formula 2 phenoxyethanol 2% alone, formula 10 3 triclosan 1% in combination with phenoxyethanol 2%. The three formulations were tested against an inoculum of Pseudomonas aeruginosa against which triclosan alone is known to be relatively ineffective. The results were as follows: Initial conc. Reduction Reduction ATTC at 30 secs at 60 secs Formulation Active ingredients 15442 contact contact formula 1 Triclosan 1% 1.2 x log 7 9.2 x log 2 3.0 log 3 formula 2 Phenoxyethanol 2% 6.8 x log 6 1.2 log 2 3.0 log 3 formula 3 Triclosan 1% & 1.2 log 7 1.2 log 7 Phenoxyethanol 2% (total kill) (total kill) WO 2006/122345 PCT/AU2006/000553 13 This data demonstrates a synergistic interaction between triclosan and phenoxy ethanol. This is particularly advantageous in the present case since the data in example 5 shows that phenoxyethanol penetrates at about 40 times the rate that triclosan alone or chlorhexidine alone would penetrate. In view of this data it is predictable that no 5 subdermal micro-organisms would survive treatment over 2 hours, although repetitive treatment and treatment over longer periods would clearly be preferable. Example 7: Cream employing CHG/phenoxyethanol as actives In this case the CHG is effective only against transient micro-organisms and the cream relies upon phenoxyethanol against resident micro-organisms. 10 Commercial Chemical name Contents Function name (%w/w) CHG 1.00% Actives N - Methyl Transdermal Pharmasolv pyrrolidone 10.00% enhancer Disodium Ethylene Diamine Tetra Chelating agent, EDTA 2Na Acetic Acid 3.00% stabiliser Glycerol Glycerol 2.00% Moisturiser Carbomer(Acrylic Carbopol 940 copolymer) 0.90% Viscosity modifier Pentane - DB Benzyl benzoate 3.00% Skin emollient DPG Dipropylene glycol 3.00% Moisturiser Sodium Lauroyl Crodasinic LS30 Sarcosinate(30%) 2.00% Emulsifier Stearyl alcohol (and) Polyethyleneglycol 1000 cetyl/stearyl Emollient/ Promulgen - G ether 2.00% emulsifier PVP K-15 Polyvinylpyrrolidone 0.10% Skin feel enhancer Active - secondary Phenoxyethanol Phenoxyethanol 2.00% biocide TEA 99% Triethanol amine 0.19% pH modifier Solvent/ Ethanol 100% Ethyl alcohol 10.00% formulation aid P-water Water 55.80% Solvent Dyestuff 0.01% Treatment marker TOTAL 100.00% WO 2006/122345 PCT/AU2006/000553 14 Example 8 Cream employing povidone iodine/phenoxyethanol as actives Commercial Chemical name Contents Function name (%w/w) Povidone -iodine 6.00% Actives N - Methyl Transdermal Pharmasolv pyrrolidone 10.00% enhancer Disodium Ethylene Diamine Tetra Chelating agent, EDTA 2Na Acetic Acid 3.00% stabiliser Glycerol Glycerol 2.00% Moisturiser Carbomer(Acrylic Carbopol 940 copolymer) 0.90% Viscosity modifier Pentane - DB Benzyl benzoate 3.00% Skin emollient DPG Dipropylene glycol 3.00% Moisturiser Sodium Lauroyl Crodasinic LS30 Sarcosinate(30%) 2.00% Emulsifier Stearyl alcohol (and) Polyethyleneglycol 1000 cetyl/stearyl Emollient/ Promulgen - G ether 2.00% emulsifier PVP K-15 Polyvinylpyrrolidone 0.10% Skin feel enhancer Active - secondary Phenoxyethanol Phenoxyethanol 2.00% biocide TEA 99% Triethanol amine 0.19% pH modifier Solvent/ Ethanol 100% Ethyl alcohol 10.00% formulation aid P-water Water 50.81% Solvent TOTAL 100.00% In this case the povidone iodine is effective only against transient micro 5 organisms and the cream relies upon phenoxyethanol against resident micro organisms. The combination of triclosan with phenoxyethanol is preferred because the triclosan is persistently effective against transient micro-organisms (high residual activity) and also is persistent when transported sub cutaneously where it acts synergistically with the phenoxyethanol against resident micro-organisms. 10 The amount of gel applied will of course vary according to the formulation and the total area to be treated. Likewise, the frequency of application and the number of days prior the operation on which it should be applied as well as the exact area of application will vary with the formulation, skin type etc. and will need to be determined for each formulation in accordance with the invention by the surgeon in WO 2006/122345 PCT/AU2006/000553 15 accordance with "best practice" guidelines. The detennination of such protocols is a matter of routine testing upon large samples of patients. Although developed for the preparation of patients for surgery with the intention of preventing or reducing the incidence of post operative infection, it will be 5 apparent to those skilled in the art from the teaching hereof that compositions according to the invention have application for treating acne and other sub dermal or sub cutaneous infections. Although the method is herein described with reference to preparation of human patients for surgery it will be understood that the method is equally applicable 10 to other animals. It will also be apparent to those skilled in the art from the teaching hereof that the invention may be performed in other ways and using different formulations without departing from the inventive concept herein disclosed. 15

Claims

2. A composition according to claim I wherein the at least one vehicle includes an 10 alkyl pyrrolidone, a glycol or a combination thereof
3. A composition according to claim 1 wherein the at least one vehicle includes dimethylsulfoxide.
4. A composition according to any one of the preceding claims wherein the at least one biocide is a combination of biocides selected from the group consisting of 15 chlorhexidine and its salts; halogenated phenols and salts thereof; quaternary ammonium compounds; povidone-iodine; zinc pyridinethione; and alcohols.
5. A composition according to claim 4 wherein the halogenated phenol is selected from the group consisting of dichlorophene, p-chloro-m-xylenol, chlorophene and o phenylphenol, 2,4,4-trichloro-2-hydroxy-diphenylether (triclosan); 20 andoctenidindihydrochloride (CH 3 -(CH 2 ) 7 -NHON-(CH 2 )lo-NO-NH(CH 2 ) 7 -CH 2 and a salt of any of the foregoing.
6. A composition according to any one of the preceding claims wherein the at least one biocide includes triclosan.
7. A composition according to any one of the preceding claims wherein the at least 25 one biocide includes phenoxyethanol.
8. A composition according to any one of the preceding claims wherein the at least one biocide includes phenoxyethanol in combination with triclosan. - 17
9. A composition according to claim 4 wherein the at least one biocide includes chlorhexidine and salts of chlorhexidine selected from the group consisting of gluconate, isethionate, formate, acetate, glutamate, succinamate, monodiglyco late, dimethanesulfonate, lactate, diisobutyrate and glucoheptonate salts.
10. A composition according to claim 9 including phenoxyethanol.
11. A composition according to any one of the preceding claims further including one or more component serving as a transdermal enhancer, chelating agent, stabiliser, skin emollient, moisturiser, or feel enhancer of the like.
12. A method for preparing a patient for surgery comprising the step of treating an area of the patient's skin at, and in the surrounding the vicinity of, the site of an intended surgical incision with a composition according to any one of claims 1 to I I effective to kill more than 93% of both transient and subcutaneous resident micro-organisms and wherein said step is repeated at least twice, during the 24 hours preceding an operation.
13. A method according to claim 12 comprising the step of treating an area of the patient's skin at, and in the surrounding the vicinity of, the site of an intended surgical incision with a composition according to any one of claims 1 to 11.
14. A method according to claim 12 or claim 13 wherein said step is repeated at least four times during the 48 hours preceding an operation.
15. A method according to claim 12 wherein said step is repeated at least six times, during the 72 hours preceding an operation.
16. A method according to any one of claims 12 to 15 wherein the step or steps are conducted in combination with washing or showering using a biocidal soap or detergent.
17. Use of a composition according to any one of claims I to I I for treating the area of the patient's skin at, and in the surrounding vicinity of, the site of an intended surgical incision to kill more than 93% of both "transient" and subcutaneous "resident" micro organisms.
18. A method for preparing a patient for surgery comprising the step of treating an area of the patient's skin at, and in the surrounding the vicinity of, the site of an intended -18 surgical incision with a composition effective to kill more than 93% of both "transient" and subcutaneous "resident" micro-organisms; wherein the composition comprises at least one biocide and at least one transcutaneous vehicle effective to convey the biocide to a "resident" micro-organism; and wherein the at least one transcutaneous vehicle is 5 selected from the group consisting of alkyl methyl sulfoxides, alkyl pyrrolidones, glycols, glycol ethers and glycol esters.
19. A composition; a method; use of a composition substantially as herein described with reference to any one the examples but excluding any comparative examples.