GB2338651A

GB2338651A - Liquid polymer composition

Info

Publication number: GB2338651A
Application number: GB9813827A
Authority: GB
Inventors: David Rawdon; John Dorothy
Original assignee: Trevor P Woollard
Current assignee: Trevor P Woollard
Priority date: 1998-06-27
Filing date: 1998-06-27
Publication date: 1999-12-29
Also published as: AU4378999A; WO2000000024A1; GB2338651A8; GB9813827D0

Abstract

A liquid polymer composition comprises polydimethylsiloxane and a solvent for an active agent such as a bactericide or fungicide. It can be applied to continuous surfaces such as glass without damaging the surface.

Description

2338651 1 LIQUID POLYMER FILM COMPOSITIONS The present invention relates

to a liquid polymer film composition which contains one or more bactericidal, fungicidal, algicidal, yeasticidal or moldicidal agents, its application to substantially continuous surfaces such as glass, its incorporation into a wide range of other materials such as coatings, cleaning materials, building materials and to articles treated with the composition.

A great deal of time and effort in a wide range of technical research areas is devoted to overcoming the problems of infection and cross infection in medical, industrial, commercial, domestic and marine environments.

Many compositions are known which contain bactericidal, fungicidal, algicidal, yeasticidal and moldicidal agents. However, such compositions are often toxic to humans or animals or are difficult to use because of their toxicity when wet. Many of these products are unsuitable for mixing with other materials as they either affect the properties of the other material or their own properties are affected.

Furthermore, products such as disinfectants of the type often used in food preparation areas are only effective when wet and can damage substantially continuous surfaces such as glass by staining or etching the surface.

It is one object of the present invention to provide a liquid polymer film composition which contains one or more bactericidal, fungicidal, algicidal, yeasticidal or moldicidal agents and which can be applied to substantially continuous surfaces such as glass without damaging the 30 surface.

2 A further object of the present invention is to provide a liquid polymer film composition as set out in the immediately preceding paragraph which can be incorporated into other materials such as coatings, surfaces, or cleaning agents to give those materials sterilizing properties.

A still further object of the present invention is to provide a liquid polymer film composition as set out in the two immediately preceding paragraphs which is an effective sterilizer when dry and imparts sterilizing properties to an object to which it is applied for many months.

In a first aspect the present invention provides a composition consisting essentially of a polymer composition capable of adhering to a substantially continuous surface.

In a second aspect the present invention provides a composition consisting essentially of a polymer composition capable of incorporation into a material.

The polymer composition preferably comprises a mixture of isopropanol butyl acetate, sulphuric acid and polydimethylsiloxane.

Preferably there is 87 - 91% isoproponal which preferably acts as a carrier, 1 - 6% of butyl acetate which preferably acts as a drying agent, 1.5 - 3% sulphuric acid which preferably acts as a scavenger and 3 - 6% polydirnethylsiloxane (all percentages are by volume).

Preferably the composition includes at least one anti-bacterial agent and most preferably the composition includes two anti-bacterial agents, which may be the same or different.

3 The anti-bacterial agents suitable for use in the present invention may include amphoteric compounds, iodophores, phenolic compounds, quaternary ammonium compounds, hypochlor,ites and nitrogen based 5 heterocyclic antibacterial compounds.

Examples of amphoteric compounds include long chain N-alkyl derivatives of amino acids such as glycine, alanine and beta-amino butyric acid, particular examples being dodecyl beta-alanine, dodecyl beta-aminobutyric acid, dodecylamino-di {aminoethylamino} glycine and N- (3 -dodecyl amino) propyIglycine.

The term iodophores as used herein refers to complexes of iodine or triodide with a carrier, such as a neutral polymer. The carrier typically is one which increases the solubility of iodine in water, provides a sustained release of the iodine and reduces the equilibrium concentrations of free iodine. Examples of polymeric carriers from which iodophore compositions can be made include polyvinylpyrolidone, polyether glycols such as polyethylene glycols, polyvinyl alcohols, polyacrylates, polyamides, polyalkylenes and polysaccharides. A preferred iodophore is povidone iodine, in which the carrier is polyvinylpyrrolidone.

Examples of quaternary ammonium compounds include compounds of the general formula R1 R 2 N+ R 3 R 4 X- wherein or one or two of the R groups are alkyl chains optionally substituted by an aryl group, or optionally interrupted by an aryl group or a heteroatom such as oxygen, and the other R groups are the same or different and are Cl - C4 alkyl groups and in particular methyl groups. Examples of classes of quaternary ammonium compounds within this general formula include benzalkonium halides, aryl ring substituted benzalkonium halides such as ethyl- 1 4 substituted benzalkonium halides (e.g. Barquat 4250 available from Lonza), and twin chain quaternary ammonium compounds such as dialkyldimethyl ammonium compounds wherein the two non-methyl alkyl groups are selected from medium and long chain alkyl groups such as octyl groups and dodecyl groups. Examples of quaternary ammonium compounds in which an alkyl group R contains an oxygen heteroatom include domiphen bromide, benzalkonium. chloride and methylbenzalkonium chloride.

Other examples of quaternary ammonium compounds include alkylpyridinium compounds such as cetylpyridinium chloride and bridged cyclic amino compounds such as the hexaminium compounds, e.g: N-(3-chlorallyl) hexaminium chloride.

Examples of phenolic compounds include methyl, halo-and aryl substituted phenolic compounds such as 2-phenylphenol, 2-benzyl-4-chlorophenol, 2eyclopentyl-4-chlorophenol, 4-t-amylphenol, 44-butylphenol, 4-chloro-2pentylphenol, 6-chloro-2-pentylphenol, p-chloro-meta-xylenol, 2,4,4 trichloro-2 -hydroxydiphenol, thymol {2-i-propyl-3-methylphenol}, chlorothymol, 3-methyl-4-chlorophenol, 2,6, -dichloro-4-n- alkyl phenol s, 2,4-dichloro-meta-xylenol, 2,4,5-trichlorophenol and 2-benzyl-4-chlorophenol.

Examples of hypochlorites include alkali-metal and alkaline earth metal hypochlorites such as lithium hypochlorites, sodium hypochlorites, potassium hypochlorites, calcium hypochlorites, and chlorinated trisodium phosphate and their various hydrates. Other chlorine-containing or chlorine releasing agents include chlorine dioxide and its precursors, as well as 4-sulpho-dichloramido-benzoicacid {halazonel, 1,3-dichloro-5-5- 1 dimethylhydantoin {halane}, derivatives.

and various chloroisocyanuric acid Examples of nitrogen-containing anti -bacterial.. agents include pyridine derivatives such as 4-pyridine carboxylic acid hydrazide, sodium 2-pyridinethiol -1-oxide (Sodium Ornadine TM) bis- (2-pyridylthio) zinc 1, 1 -dioxide (zinc Omadine), triazoles and imidazoles such as 2-(4- thiazolyl) benzimidazole (Metasol T K-100}; 12-benzisothiazoline-3-one (ProxcelTM) 2-n-octyI-4-isothiazolin-3-one (Kathen TM), 2-brorno-2-nitro-1-3propanediol), (Bromonopo,TM), 3-trifluornethyl-4, 4'-dichlorocarbanilide Orgasan Tm) quinacrine hydrochloride (Atabrine TM), ciprofloxacin and nalidixic acid and its various derivatives.

The anti-bacterial agent or combination of anti-bacterial agents selected will depend on the polymer composition and on the intended use of the end product.

Preferably the anti-bacterial agent is contained in a non-volatile carrier. The non-volatile carrier may be a glycol, an ester derivative of a glycol or an ether derivative of a glycol. In particular, alkylene glycols and polyalkylene glycols such as diethylene glycol, hexylene glycol, propylene glycol and polyethylene glycol are used. The most preferred glycol carrier is diethylene glycol (DEG).

Alternatively, the carrier may be an alcohol having a high number of carbon atoms, preferably at least six carbon atoms, more preferably at least eight carbon atoms and most preferably at least ten carbon atoms.

Preferably the composition further includes - at least one surfactant. 30 Preferably the surfactant includes an amphoteric, an ionic and a non-ionic 6 surfactant. An example of such a surfactant is PERSIL' washing up liquid manufactured by Lever Brothers.

The compound is preferably diluted with water to provide a final product.

The polymer composition acts as a key to introduce the anti-bacterial agents to the substantially continuous surface, to adhere them thereto to protect that surface and also to incorporate the anti-bacterial agents into other materials and especially to allow incorporation of the composition into oil or water based products.

In a third aspect the present invention provides materials incorporating the composition of the present invention.

Such materials may include coatings such as paints and varnishes, which may be oil based or water soluble. The composition may be incorporated into settable or curable compositions such as fillers, grouts, adhesives, mastics, putties and other materials which form a solid matrix over a period of time. Such compositions are prone to the growth of mold and fungus, particularly in damp environments such as bathrooms and kitchens.

The composition of the present invention may include a co-solvent or a codiluent which evaporates readily. The co-solvent or co-diluent may be aqueous or non-aqueous, depending upon the nature of the material with which it is to be mixed.

The composition can also be incorporated into plastics materials which can then be used to manufacture food processing implements, work 7 surfaces, packaging materials, containers, floor and wall cladding materials, bathroom and kitchen furniture.

When the composition is incorporat 1 ed into materials inclusing those detailed above the surfactant aids mixing of the material and the composition.

A fourth aspect of the present invention provides a substantially continuous surface coated with the composition of the present invention.

The surface is preferably glass, which may then be used in a variety of places such as hospitals, where sterility is of great importance.

The surface may alternatively be a metal, for example, door touch plates, 15 door and window furniture, metal kitchen furniture, especially that used in restaurants.

The surface may alternatively be a plastics material, for example, toilet seats, bathroom furniture, work surfaces and kitchen implements. The surface may alternatively be a glazed ceramic surface such as floor and wall tiles.

The composition may be used in the components of ventilation and air conditioning systems, for example, the conduits, panels, grills and filters may incorporate or be coated with the composition of the present invention.

The polymer composition of the present invention adheres to substantially continuous surfaces without damaging them and as a result forms a coating layer on the surface which contains anti-bacterial agents, so that any bacteria present on or subsequently contacting the surface are eliminated.

The surfactant in this case acts to help the composition to spread over a substantially continuous surface and imparts cleaning and detergent properties to the composition.

The polymer composition works even when it is dry. This is believed to be because even when the surface appears to be dry a low concentration of the anti-bacterial compound is still present as a solution in the nonvolatile carrier.

The materials into which the composition of the present invention are incorporated may include other agents such as bactericidal agents, biocidal agents, algicidal agents, fungicidal agents and moldicidal agents as well as other standard additives for the material in question.

The composition and articles of the present invention have anti-bacterial effect against a wide range of gram-positive and gram-negative bacteria, such as: Bacillus cereus, Bacillus subtilis, Brevibacterium ammoniagenes, Brucella abortus, Klebsiella pneumonia, Lactobacillus casei, Proteus vulgaris, Listeria monocytogenes, Pseudomonas aeruginosa, Salmonella gallinarum, Salmonella typhosa, Staphylococcus aureus, Streptococcus faecalis, Flavobacterium species, Bacillus species, Escherichia species, Aeromonas species, Anchromobacter species and Alcaligenes species. The compositions and articles of the present invention also have activity against fungi such as: Cephalosporium species, Cladosporium species, Fusarium species, Paecilomyces species, Penicillium species, Streptomyces species, Trichophytoninterdigitale, Chaetorariumglobesom, Aspergillus niger, and Ceniphora puteana, yeasts such as Monilia C> 9 albicans and Saccharomyces cerevisiae, and algae such as ChloreIla pyrenoidosa and Anabaena cylindrica.

In a fifth aspect the present invention provides a method of imparting sterilizing properties to a substantially continuous surface by applying thereto a composition consisting essentially of a polymer film composition including at least one and preferably two anti-bacterial agents incorporated in a non-volatile carrier.

In a sixth aspect the present invention provides a method of imparting sterilizing properties to materials by incorporating therein a composition consisting essentially of a liquid polymer film composition including at least one and preferably two, anti-bacterial agents incorporated in a non-volatile carrier.

The composition preferably includes a surfactant, especially when the composit ion is incorporated into materials.

The composition may further include a preservative, and a co-solvent which readily evaporates off.

The present invention will be illustrated, merely by way of example, as follows:

Composition of the present invention (named 42AP) 1) Polymer composition (all percentages are by volume) Isopropanol 87 - 91% Butyl acetate 1 - 6% Sulphuric acid 1.5 - 3% Polydimethylsiloxane 3 - 6% 2) Surf actant composition Anionic surfactant 15 - 30% Non-ionic surfactant 1 - 5% Amphoteric surfactant 1 - 5% Ethanol 1 - 5% Preservative 1 - 5% 3) First anti-bacterial agent composition 5-chloro-2-methyl-4-isothiazolin-3-1 -ones 2-methyl-4-isothiazolin-3-ones; and 85% Diethylene glycol 4) Second anti-bacterial agent composition Alkyldimethyl-benzylammonium chloride; and 50% Diethylene glycol An example of the polymer film composition containing anti-bacterial agents is made by the following steps:- a) Prepare the first and second anti-bacterial compositions and mix 25 them together in a 1: 1 ratio by volume; b) Mix water with the anti-bacterial composition mixture in a 2:1 ratio by volume of water to anti-bacterial mixture.

11 c) Add 10OmI of the dilute anti-bacterial agent mixture to 20OmI of the surfactant composition; d) Add 10OmI of the polymer composition to the surfactant and anti5 bacterial agent mixture; e) Add 60OmI of water to the mixture and mix well to give the polymer film composition of the present invention incorporating antibacterial agents.

This product can now be used on substantially continuous surfaces to impart an anti-bacterial film or it can be incorporated into a variety of other materials as hereinbefore described. If the product is to be incorporated into oil based materials it will be used in its concentrated form (i.e. step e) will be omitte4.

Examples of the Anti-bacterial Nature of the Composition of the Present Invention Example 1

Two panes of glass were treated, i.e. coated with the active liquid polymer composition, which was allowed to dry. The coated glass panes were then placed in sealed bags. A further untreated {control} pane of glass was also placed in a sealed bags. The panes of glass were then stored for three weeks before being submitted for microbiological testing by P.H.L.S. Poole Hospital, Poole Dorset. The micro-organism used in this test was Methicillin Resistant Staphylococcus aureus. {M.R.S.AJ.

12 Method A broth culture of a wild strain of methicillin-resistant staphylococcus aureaus (MRSA) was grown in peptone saline diluent for 20 24 hours.

Serial decimal dilutions were then prepared in peptone saline diluent and a surface drop (Miles and Misra) count performed on blood agar. Plates were incubated at 300C for 18 hours, colonies counted and counts estimated for each dilution.

Two dilutions (1 and 3) were used for inoculation. Dilution 1 contained 14,000 organisms per 20 pl and dilution 3 contained 140 organisms per 20pl. Volumes of 20 M1 of each dilution were applied to each of the three plates and left in contact for a range of times from 0 seconds to 6 hours.

After the designated time the liquid from each inoculation was aspirated and pipetted onto the surface of a blood agar plate. If the inoculum had dried, 20 ul of sterile distilled water was applied, carefully mixed and then aspirated. The aspirate was spread over the aga r surface using a sterile spreader. Plates were incubated at 3TC for 18 hours and then colonies counted.

Results Counts obtained are shown in the tables. Plate 1 showed a reduction in count over 5 minutes with no recovery after 10 minutes. For the heavier inoculum of 14,000 organisms, this represents a four log reduction within 10 minutes and a 97.98% reduction within 5 minutes. Plate 2 showed a 3.5 log or 99.95% reduction within 1 minute and a four log reduction (100%) within 2 minutes.

13 It will be noted that there was a slight reduction on the control plate with time; this was most likely due to the effect of drying, as all inocula had dried out after 1-1.5 hours.

Conclusion The treatment used for plate 2 resulted in 100% reduction of an inoculum of 14,000 MRSA organisms within 2 minutes and 99.95% reduction within 1 minute.

The treatment used for plate 1 resulted in 100% reduction of an inoculum of 14,000 MRSA organisms within 10 minutes and 97.98% reduction within 5 minutes.

14 Cont^ct time Plate 1 P-late:2 Control linoculum 14000 14 0 0 0 14000 0 min uncountable uncountable uncountable 1 min uncountable 7 uncountable 2 min 2000 approx 0 uncountable MIn 283 0 uncountable min 0 0 uncountable Tnin 0 0 uncountable 1 hour 0 0 2000 5000 2 hour 0 0 281 3 hour 0 0 248 4 hour 0- 0 195-- hour 0 0 128 Time Plate 1 Plate 2 'Control IrLoculum 140 140 140 0 Min 112 72 108 1 min 54 26 106 2 Inin 28 0 99 -nin 12 0 127 min 0 0 90 3 0 min 0 0 35 1 hour 0 18 2 hour 0 0 1 3 hour 0 0 1 4 hour 0 0 1 hour 0 0 0 6 hour 0 0 J_ 0 Example 2

Approximately 50 mI of clear colourless liquid.,(42AP) was submitted for microbiological testing by P.H.L.S Poole Hospital, Poole, Dorset in a clear plastic screwtop bottle. The concentration was said to be 15 mI liquid polymer diluted to 50 ml.

Method A 1 mI volume of the liquid was inoculated with 20 pi of an undiluted 7 overnight broth of MRSA; this inoculum was estimated to contain 10 8 organisms. Using a fresh sterile pipette tip each time, a 20 pI volume was immediately withdrawn and another 20 ul volume withdrawn after 1, 2, 5, 10, 30 and 60 minutes. This volume was spread over the surface of a blood agar plate which was then incubated at 300C for 20 hours. After incubation plates were examined for the presence of colonies.

Results No colonies of MRSA were recovered on any plate.

Conclusion

An inoculum of approximately 107 organisms was killed within 10 seconds 25 when added to 1 mI of 'D' stage 1 surface preparation (where D is 42AP).

Example 3

A detergent/cleaner called Envirociene was obtained from H. Marcel Guest Ltd., Manchester, in a concentrated form.30rnl. of the 16 concentrate was diluted 15:1 with water and mixed by conventional methods. 30rnl. of 42AP concentrate was then added to the diluted detergent/cleaner. Aftermixing, the product (a clear mobile liquid) was then submitted for microbiological testing by.. Microbac Analytica Ltd 5 Consett Co. Durham.

Example 4

A detergent/c leaner called Deep-Clean was obtained from MGM Ltd Southampton in a concentrated form. 30mi. of concentrate was diluted 15-1 with water and mixed by conventional methods. 30mi. of 42AP concentrate was then added to the diluted detergent/cleaner. After mixing, the product (a light pink coloured mobile liquid) was then submitted for microbiological testing by Microbac Analytica Ltd Consett Co. Durham.

Example 5

A detergent/cleaner called XIGNIx was obtained from NIGM Ltd Southampton in a concentrated form. 30rnl. of concentrate was diluted 15-1 with water and mixed by conventional methods. 30rnl. of 42AP concentrate was then added to the diluted detergent/cleaner. Af ter mixing, the product (a light straw coloured mobile liquid) was then submitted for microbiological testing by Microbac Analytica Ltd Consett Co. Durham.

The principle of the test requires that the product under test, diluted in hard water, shall demonstrate at least a 10 -5 reduction in viable count when tested under simulated clean conditions (0.3 g/1.bovine albumin) and dirty 30 conditions (3 gIl bovine albumin).

17 While the original procedure determines that the test should be undertaken at 2TC, concern has been expressed that the temperature does not adequately reflect the temperatures experienced. during application of the 5 product.

In most food processing companies, the environment is controlled in such a way as to discourage the growth of pathogenic micro-organisms and working temperatures are usually well below the WC specified in the suspension test methodology. As most chemical/biochemical reactions occur more rapidly at higher temperatures, it has been suggested that biocides which work effectively at WC may display reduced efficacy at lower temperatures.

Initial testing on a number of products has indicated that the biocidal activity is adversely affected at lTC.

The following tests were undertaken to determine the efficiency at WC.

Test Samples:

The three samples comprised Environclene FS Active Polymer D, DeepClene FA Active Polymer D and MGMX FS Active Polymer D which are subsequently diluted with potable water to provide a 1% working concentration. Prior to testing, all samples were stored at room temeprature, in dark conditions. The samples were tested on 9th January 1,097.

(Active polymer D is 42AP).

Sample and storage details are summarised in Table 1.

18 Methodology:

The method used to assess the bactericidal activity of the samples is detailed in Appendix 1 of the Bacterial Activity.. Suspension Test specified by European Standard (Final Draft) Pr EN 1276: November 1995.

The test conditions were as described in Appendix 1, Section 5,5,2,2 (Dilution neutralisation method) with the following modifications:(i) Temperature: 10 The tests were undertaken at 10'C only. The temperature was controlled throughout the test prodcedure at 100C 10C using a temperature controlled coolant waterbath. (ii) Bacterial strains: Only one organisms, Pseudomonas aeruginosa, was used for the 15 purpose of this test. The neutraliser selected from Annex B of the appended method comprised 30 g/1 Polysorbate 80 and 3 g/1 Lecithin. The experimental conditions are summarised in Table 2.

Verification of Methodology: Several control procedures were undertaken to ensure that the materials used did not affect the validity of the f inal result. (Appendix 1, section 5.6.2.) Results: The results of the tests are shown in Table 3. All of the formulations, when exposed to the test organism, Pseudomonas aeruginosa, for five minutes at 100C, reduced the viable count by, greater than 10 5 as specified in the method. In all cases total kill was achieved.

19 Conclusions: According to the test procedure, Enviroclene FS Active Polymer D, Deepclene FS Active Polymer D and MGMX FS Active Polymer D, possess the required bacterial activity specified by the Suspension Test at 100C.

BACTERIAL ACTIVITY SUSPENSION TEST TABLE 1 - SAMPLE AND STORAGE DETAILS Identification of the samples:

Name of Products:

Manufacturer Date of Delivery:

Storage Conditions:

Product Diluent Recommended by the Manufacturer for use:

Active Substance(s) and their Concentrations:

Enviroclene FS Active Polymer D Deep-clene FS Active Polymer D MGMX FS Active Polymer D Research Holdings Ltd.

18/11/96 Room Temperature and Darkness Potable Water

Neat BACTERIAL ACTIVITY SUSPENSION TEST TABLE 2 - TEST METHOD AND EXPERIMENTAL CONDITIONS Test Method and its Validation:

Method:

Neutraliser:

Product Diluent Used During the Test:

Product Test Concentration:

Contact Time:

Test Temperature:

Interfering Substance: (Clean Conditions) Interfering Substance: (Dirty Conditions) Dilution Neutralisation:

g/1 Polysorbate,80.3 g/1 Lecithin Sterile Hard Water 300 mg/Kg CaCO, As received min 10 seconds 100C 10C 0.3 g/1 of Bovine Albumin 3.0 g/1 of Bovine Albumin Stability of the Mixture:

(interfering substance and Precipitate absent throughout product diluted in hard water) the test Temperature of Incubators:

Bacterial Strain Used:

370C 1C Pseudomonas aeroginosa NCTC 10332 BACTERIAL ACTIVITY SUSPENSION TEST TABLE 3 - TEST RESULTS Enviro-clene FS Active Polymer D Initial Concentration 8 x 108 of Microorganism (cfu/ml) Deep-clene FS MGM FA Active Active Polymer Polymer D 8 X 10, 8X 101 Experimental ex 106 8X 101 8X 101 Concentration (cfu/ml) Pass Level <80 <80 <80 (cfu/(ml) Actual Count at 37cC Clean Conditions 0 0 0 (Average of Duplicate Plates) Actual Count 370C Dirty Conditions 0 0 0 (Average of Duplicate Plates) Pass/Fail Pass Pass Pass

Claims

1. A liquid polymer composition comprising polydimethylsiloxane and a solvent for an active agent.

2. A liquid polymer composition as claimed in claim 1 comprising a surface adhesion promoter to assist the adherence of the composition to a substantially continuous surface.

3. A liquid polymer composition as claimed in claim 2 wherein the surface adhesion promoter is a strong acid.

4. A liquid polymer composition as claimed in claim 2 or 3 wherein the surface adhesion promoter is sulphuric acid, phosphoric acid, sulphamic acid, hydrochloric acid, nitric acid, hydrofluoric acid or chromic acid or a mixture thereof.

5. A liquid polymer composition as claimed in claim 2, 3 or 4 wherein the surface adhesion promoter is sulphuric acid.

6. A liquid polymer composition as claimed in any preceding claim wherein the solvent is butyl acetate or isopropanol or a mixture thereof.

7. A liquid polymer composition as claimed in any preceding cl-aim comprising isopropanol, butyl acetate, sulphuric acid and polydimethylsiloxane.

8. A liquid polymer composition as claimed in any preceding claim comprising (percentages by volume): 88-97% of a solvent for an active agent, 3-6% polydimethylsiloxane and optionally 1.5-3% of a surface adhesion promoter.

9. A liquid polymer composition as claimed in any preceding claim comprising (percentages by volume):

isopropanol 87-91% butyl acetate 1-6% sulphuric acid 1.5-3% polydimethylsiloxane 3-6%.

10. A liquid polymer composition as claimed in any preceding claim comprising at least one of the active agents selected from the group consisting of a biocidal, anti-microbial, germicidal, bactericidal, fungicidal, yeasticidal, moldicidal, algicidal or virucidal agent.

11. A liquid polymer composition as claimed in any preceding claim comprising at least one anti-microbial agent.

12. A liquid polymer composition as claimed in any preceding claim comprising at least two anti-microbial agents.

13. A liquid polymer composition as claimed in any of claims 10 to 12 wherein the or each anti-microbial agent is effective against grampositive and gram negative bacteria.

14. A liquid polymer composition as claimed in any of claims 10 to 13 comprising an ani-microbial agent selected from the groups consisting of amphoteric compounds, iodophores, phenolic compounds, quaternary ammonium compounds, hypochlorites and nitrogen based heterocyclic compounds.

15. A liquid polymer composition as claimed in any of claims 10 to 14 wherein the or each active agent is contained in a non-volatile carrier.

16. A liquid polymer composition as claimed in claim 15 wherein the carrier is a glycol or an alcohol having a high number of carbon atoms.

17. A liquid polymer composition as claimed in claim 15 or 16 wherein the carrier is diethylene or monopropylene glycol.

18. A liquid polymer composition as claimed in any preceding claim comprising a surfactant or detergent.

19. A liquid polymer composition as claimed in any preceding claim comprising an aqueous or non-aqueous co-solvent or codiluent which evaporates rapidly.

20. A liquid polymer composition as claimed in any of claims 10 to 19 which is active when dry.

21. A liquid polymer composition as claimed in any preceding claim incorporated into a functional material.

22. A liquid polymer composition as claimed in claim 21 wherein the functional material is a coating material, a cleaning material or a building material.

23. A liquid polymer composition as claimed in claim 21 or 22 wherein the functional material is paint or a powder coating.

24. A substantially continuous surface coated with a composition as claimed in any of claims 1 to 23.

25. A substantially continuous surface as claimed in claim 24 which is a glass, metal, plastic, composite or ceramic surface.

26. A substantially continuous surface as claimed in claim 24 or 25 which is a glass surface.

-26

27. A building component comprising a substantially continuous surface as claimed in any of claims 24 to 26.

28. A method for substantially sterilizing a substantially continuous surface comprising: applying to said surface a composition as claimed in any of claims 10 to 23.

29. A method for substantially sterilizing a functional material comprising: incorporating in said functional material a composition as claimed in any of claims 10 to 23.

30. A composition, substantially continuous surface, building component or method as hereinbefore described with reference to the accompanying Examples.