CA2847661A1

CA2847661A1 - Compositions comprising oleuropeins and flavanoids and their use

Info

Publication number: CA2847661A1
Application number: CA2847661A
Authority: CA
Inventors: Ian Ripley
Original assignee: PHYTO INNOVATIVE PRODUCTS Ltd
Current assignee: PHYTO INNOVATIVE PRODUCTS Ltd
Priority date: 2010-08-06
Filing date: 2010-08-06
Publication date: 2012-02-09
Also published as: EP2635120A1; WO2012017186A1; ZA201301608B

Abstract

Compositions are described which comprise a flavanoid, or preferably a mixture of flavanoids, and oleuropein or an acetylated derivative thereof. The use of such compositions as a pathenogenicide is also described.

Description

COMPOSITIONS COMPRISING OLEUROPEINS AND FLAVANOIDS AND THEIR USE
The present invention relates to compositions and their uses in eradicating or ameliorating unwanted infestations. More particularly the invention relates to compositions and their uses which comprise a flavanoid component and an oleuropein component. Such compositions are aptly employed to eliminate or reduce the presence of unwanted bacteria or other undesirable organisms.
A variety of flavanoids have been suggested as anti-microbial agents.
PCT/GB2007/002756 and PCT/GB2007/002758 describe particularly effective compositions containing flavanoids. However, the effectiveness of known compositions of bioflavanoids would benefit from enhancement.
The present invention is based on the finding that certain combinations of agents are particularly effective in eliminating or reducing unwanted bacteria and other undesirable organisms.
The present invention provides a pharmaceutical composition which comprises a first component being a flavanoid component and a second component being an oleuropein component.
The first component will be a one or more flavanoids of Formula (I):

0 . .
I.

OH 0 (I) x wherein wherein R1 is hydroxyl or methoxyl and R2 is hydrogen, hydroxyl or methoxyl and X is hydrogen or a saccharide.

The second component will be oleuropein or an acetylated derivative thereof. Oleuropein is (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenypethoxy]-2-oxoethy1]- 5-ethyl idene-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihyd roxy-6-(hydroxymethyl)- 2-tetrahydropyranyl]oxy]-4H-pyran-3-carboxylic acid, methyl ester.
Aptly in the first component R2 is hydrogen and R1 is in the 3- or 4-position. Alternatively, aptly in the first component R2 is 3-hydroxy and R1 is 4-methoxyl.
Suitably X in a compound of the Formula (I) is H.
Suitably X in a compound of Formula (I) is a saccharide.
Favourably X is a disaccharide.
Suitable disaccharides include combinations of two monosaccharide, suitably pyranoses, linked by a glycosidic bond, for example rhamnose and glucose, for example L-rhamnose and D-glucose.
Suitable disaccharides can have the structure:
OH OH
OH OH OH
\,,,,,,....-....................OH
R3¨C112700 R3¨C11270() HO0-......(Flay) 0 (:)---(Flav) Hozr0 it4(I) (II) OH
wherein one of R3 and R4 is H and the other OH or both are H or both are OH. Aptly R3 is H and R4 is OH so that the disaccharide is rutinose.

Favoured aglycones of flavonoids for use in this invention are the disaccharides 6-0-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranose, also known as rutinose, and 2-0-(alpha-L-rhamnopyra-nosyl)-beta-D-glucopyra-rose.
It is presently believed that the first component very suitably comprises narangin or neohesperidin or mixtures thereof. Mixtures of one or both of narangin and neohesperidin with for example, one, two or three other flavanoids of the Formula I are presently believed particularly favoured for use in this invention. Such mixtures can be obtained from extraction from bitter oranges.
Suitable compounds of Formula (I) include Neoeriocitrin, Isonaringin, Narangin, Hesperidin, Neohesperidin, Neodiosmin, Naringenin, Poncirin and Rhiofolin.
Favoured compositions for use include those which comprise either of naringin and neohespiridin or both.
Particularly aptly the invention will contain naringin and neohesperidin and other flavonoids of the Formula (I).
The mixture of flavonoids may aptly contain more than one of neohesperidin, naringin, isocriocrin, isonaringin, naringin, hesperidine, neohesperidin, neocliomin, naringenin, poncrin and rhiofolin. Such a mixture of flavonoids can be obtained from bitter oranges, see for example PCT/GB2007/002756. Suitable mixtures can include 2, 3, 4, 5, 6, 7, 8, 9 or more compounds of formula (I). Thus a mixture comprising 2, 3, 5, 6, 7, 8 or 9 of the above named flavonoids is apt, for example containing 3, or containing 4, or containing 5, or containing 6, or containing 7, or containing 8 or containing 9 of said flavonoids.
It is presently believed that mixtures of such flavonoids have advantages over the use of a single flavonoid. It is particularly advantageous that extract of bitter oranges may be employed without the need for isolating individual flavonoids if desired. The use of the composition generally comprising biomass enhances solubility of the flavanoids. Generally the flavanoids are present in mixtures with biomass by about 10% to 75%, more aptly 30% to 60%, for example 40% to 50%, preferably about 45%.
The biomass comprises pectins and other sugar derived materials.
Typically about 40% of low molecular weight pectins are present.
If it is desired to avoid biomass, other solubilising agents such as dextrins, for example cyclodextrin, may be employed if desired.
Aptly the mixture of flavonoids will comprise at least 25%, more suitably at least 40% and preferably at least 50% of narangin. More aptly the mixture will contain up to 65% of narangin.
Aptly the mixture of flavonoids will comprise at least 15%, more suitably at least 20% and preferably at least 25% of neohesperidin. More aptly the mixture will contain up to 35% of neohesperidin.
In a favoured form the mixture will contain at least 75% of neohesperidin and narangin.
It is presently believed that particularly suitably the second component is oleuropein. Aptly this is obtained from extraction from the leaf of the olive, for example olea europea. Such extracts typically contain 5% to 80% wt/wt, more aptly 10 to 70%, for example 20% wt/wt.
The other components of the extract will often contain pectins and the like.
A particular advantage of many compositions of the invention is that they may employ compounds of natural origin. Thus, for example, it is preferred to employ a first component which may be obtained from bitter oranges and a second component which may be obtained from the olive.
However synthetically or semi-synthetically obtained compounds may be employed if desired instead of the ones directly extracted from natural sources although this tends to be less favourable in view of cost.
The compositions of this invention may show synergistic anti-microbial effectiveness. Such synergistic compositions are preferred.
It is presently believed that best synergy occurs wherein the first component and the second component are present in ratios (wt/wt of flavanoids to oleuropein) of 5:1 to 1:4, more aptly 2:1 to 1:2, favourably 1:2 to 1:1 and preferably 3:2.
Such compositions may desirably contain a first component which is a mixture of flavanoids of Formula (I) wherein 50% - 100% (wt/wt) is composed of narangin and/or neohesperidin. It is presently believed that the first component may favourably contain a mixture of flavanoids containing 60% - 100% of narangin and neohesperidin, for example 65 -75% of narangin and neohesperidin.
Such compositions may preferably contain 3,4-dihydroxyphenylethanol as the second component or a mixture of compounds of formula II in which 3,4-dihydroxyphenylethanol is present by at least 50% (wt/wt), and more aptly at least 80% (wt/wt).
It has been found that compositions of this invention are particularly effective in the presence of a third component, which is one or more organic acids.
A surprisingly effective third component is salicylic acid or its pharmaceutically acceptable salt optionally together with a further organic acid or pharmaceutically acceptable salt.
It is believed favoured that the salicylic acid is present in the acid rather than its salt.

Similarly, a further organic acid if present is similarly in the form of the acid rather than its salt. Suitable further organic acids include acids of up to 8 carbon atoms which are monobasic (i.e. 1 CO2H group), di-basic or tri-basic acid which optionally contain 1, 2 or 3 hydroxyl groups. Such further organic acid may be one or more of citric acid, malic acid, latic acid, tartaric acid, fumaric acid and the like.
Such compositions can provide an approximately neutral or acid pH, when used, for example of from 3-8, more aptly 3.5-7, for example 4-5.
At present it is preferred to employ salicylic acid and citric acid in compositions.
In compositions containing a first component, a second component and a third component, the weight/weight ratio of the compound(s) of Formula (I) plus the compound(s) of Formula (II) to salicylic acid or pharmaceutically acceptable salt thereof is 2:1 to 1:7, more aptly 1:1 to 1:5, favourably 2:3 to 1:3 and preferably is 2:5.
When the third component also comprises a further organic acid (such as those named above), the weight/weight ratio of salicylic acid to further organic acid may be 2:1 to 1:5, more aptly 1:1 to 1:3, for example 3:5.
Such compositions may include a solubilising agent for the salicylic acid, for example a dextrin such as cyclodextrin.
Compositions of the invention may be adapted for application to external surfaces including external surfaces of plants or animals, or for internal administration to an animal. Often the animal is a human.
The compositions of the invention show activity against a wide range of organisms including gram positive bacteria, gram negative bacteria, fungi, virus, protazoans and insect parasites.
Particularly surprising the compositions may be employed against difficult bacteria such as methicillin resistant staphylococcus aureus (MRSA), clostridium difficile (C.diff) helicobacter pyroli (H.py), and vancomycin resistant enterobacteria. The compositions of this invention may also be used against norovirus and other pathogens whereby transmission is by contact or air.
The compositions may be administered systemically or locally if an animal is to be treated.
Suitable animals include humans and food and companion animals such as cows, pigs, horses, chickens, sheep, goats, dogs and cats. Hence the compositions may be formulated for oral administration, topical administration, injection or the like as required by the medical practitioner.
Particularly suitably such compositions are suitable for use to treat humans.
Suitable oral and topical compositions include those analogous to those described in PCT/GB2007/002756 and PCT/GB2007/002758. Injectable forms may be put up in conventional manner, for example as aqueous solutions or dispersions.
The compositions of the invention are also useful for use in conjunction with a further antibacterial agent. Thus for example, if used to treat a patient suffering from MRSA, the compositions may be used in conjunction with a 8-lactam or other antibiotic or antibacterial agent. Suitable 13-lactam antibiotics include, a penicillin such as methicillin, flucloxacillin, ampicillin, amoxicillin optionally with clavulanic acid, a cephalosporin, or a carbopenem such as imipenem or the like. The composition as a single composite form or as two or three forms, for example one of dosage form will contain the 8-lactam or other antibiotic and another composition will comprise the first and second components. Hence the 8-lactam antibiotic can be administered separately from component I and II (and if desired first and second components may also be administered separately from the further antibacterial agent). The compositions of the invention containing the first and second components adapted for oral administration and the further antibacterial agent adopted for oral administration (for orally administrable antibiotic such as amoxicillin) or for injection (for injected antibiotics such as methicillin or imipenem) may also be used together with vancomycin.
Patients suffering with infections caused by C. diff and H.py may be treated similarly. The preferred route of administration of all three agents is orally when the 13-lactam or other antibiotic is orally effective, especially for the treatment as gastric infections of H.py. However, if an antibiotic is employed that is best administered by injection that may be done in conjunction with the oral administration of the compositions of the invention.
Since the compositions of the invention are particularly effective for sterilizing surfaces, they are very suitably formulated in a composition useful for external use.
These may be in the form of solutions, gels, soaps, body wash, shampoo, dusting powders and aerially dispersible powder and liquids and the like.
Such compositions may be used to reduce the bacterial count on body surfaces, clothing and in the general environment particularly in hospitals, ambulances, nursing homes especially for the elderly or the like where it is particularly desirable to reduce the presence of bacteria such as MRSA, C. diff or the like.
Compositions suitable for washing the hands are particularly useful.
Such compositions may also be employed to wash stethoscopes.
The substantivity of the compositions (as opposed to rapid diminution of effectiveness of ethanol) is an advantage.
If external surfaces of enclosed spaces, such as ambulances, operating theatres, wards, kitchens (and even mortuaries) and so on are to be treated, it is particularly suitable to do so by "misting". In this a fine aerial dispersion of powder or microdroplets of composition are dispersed within the enclosed space. This can then offer a non-toxic alternative to the presently employed methods which often employ noxious gases.
Since the compositions of the invention have such low toxicity they may be employed on patients and their visitors and associated clothing, linen and the like by "misting". Such "misting" is of use in vehicles such as ambulances which are required to be free of pathogens but likewise free of residual odors that are typically left following the use of noxious gases.
This equally applies to other areas requiring treatment. Compositions used in this way may be in the form of a dispersible liquid, for example akin to the soap or shampoo or skin foaming compositions described hereinafter. These can also be used to what the surfaces to similar ends.
A particular use includes antibacterial soaps, detergents, lotions and the like for treating inter alia human skin and hair in order to reduce or eliminate undesired organisms.
Thus it is possible by using compositions of this invention prevented in such forms, to treat hands, the face and skin generally and the hair, both on the head and elsewhere. This can be employed to reduce bacterial count and so help to reduce the spread of methicillin resistant staphylococcus aureas, clostridium difficile and other bacteria. Similarly, the composition may be used to reduce microorganisms associated with acne, body odor or the like. A further benefit is that such compositions may be used to reduce viral transmission, for example for influenza virus, which can occur by hand contamination. Other virus that may be on the skin or membranes include HIV, herpes and the like which are also minimized by use of the compositions of the invention adapted for administration to the skin or membranes.
Parasite infestation may be treated with compositions of the invention.
Such parasites include internal parasites such as protozoa which can lead to diseases of humans such as malaria, leishumaniasis and trypanosomiasis and various diarrhoeas. Other internal parasites that may be treated include flukes. External parasites that may be treated include lice, especially head lice, and scabies and fleas. Soaps and shampoos are favoured for such external application although solutions, lotions and gels are also particularly suitable.
Fungi for treatment include those responsible for dandruff, thrush, athlete's foot and the like, for example, candida albicans. Conditions such as dandruff may be treated with soaps and shampoos but other formulation types named herein may also be used. Athlete's foot may also be treated with dusting powder. Candida albicans or other infecting agents in the vagina may be put up in the form or a pessary.
A particular use for the compositions of the invention includes mouthwashes, toothpastes and other forms suitable for use in the buccal cavity. Such forms may be formulated as indicated in the PCT
applications referred to herein before.
The compositions of the invention may also be used for the prophylaxis or treatment of dandruff or the like.
Compositions of the invention may therefore also suitably contain a pharmaceutically acceptable salt of choline such as choline chloride. This can enhance effectiveness further against organisms such as c. diff.
Formulations may be composed of conventional carriers as long as they are compatible with the first, second and optionally third component of the compositions herein.
Thus soaps, shampoos and the like may aptly contain surfactants. Many conventional surfactants may be employed but it appears certain effective formulations will employ non-ionic surfactants. Particularly effective non-ionic surfactants include alkyl polycyclosides and/or alkenyl polyglycosides (APGs) such as those containing up to 10 sugar residues coupled to a hydrocarbon chain. Oligomerisation of up to about 4 sugar residues can be desirable. Such surfactants are available under the trade name "Plantacare" for example from Henkel as "Plantacare 2000".

In some compositions minor amounts of typical anionic surfactants may be employed together with the non-ionic surfactant.
Amphoteric surfactants may also be present, for example and preferably, with the non-ionic surfactants, for example those having secondary or tertiary amino and water solubilising anionic groups, such as sulphate, phosphate, phosphonate or carboxylate groups. Such amphoteric surfactants include those available under trade names such as Miranol (of Rhone-Poulenc) and Betain, such as Dehyton from Henkel.
The compositions of the invention may optionally comprise thickening agents. Suitable thickening agents include polysaccharide thickeners such as xanthan gums, gellan gums, pectins, carageenans and the like. An apt thickening agent is xanthan gum such as Keltrol CG which is a high molecular weight polysaccharide produced by microbial fermentation.
Viscosity may also be selected by use of an amphoteric surfactant such as a cocamido-propyl betain or Tego Betain F50 as a thickening as well as surfactant agent.
The compositions of the invention may be employed for the treatment of food stuffs to reduce or eliminate unwanted pathogens or organisms leading to reduction in storage life of food stuffs. Thus vegetable, fruits and meat may be treated, for example lettuce, tomatoes, cucumbers, peppers, cereals such as wheat and maize, fruit such as apples, grapes, pears and figs, and meats such as beef, pork, lamb, bacon and the like.
Methods of treatment include washing, misting and the like.
The hand sterilization test method used in the Examples was as follows:
Experimental procedure:
1) Application of the contamination fluid.
Each of the twelve subjects was asked to wash their hands for one minute in soft soap to remove natural commensal organisms and dried thoroughly on a paper towel. The hands were then contaminated with very large numbers of bacteria well in excess of that experienced in normal everyday occurrence. The hands were immersed in the contamination fluid (containing an overnight culture of the test organism in this instance E.
coli at a concentration of approximately 108 cfu per ml) in a suitable sized container for five seconds. The hands were removed from the contamination fluid and surplus liquid allowed to drain back into the container. This time the hands were allowed to air dry for approximately three minutes holding them horizontally with fingers spread out and rotating them to and fro to avoid the formation of droplets.
2) Prevalues.
Immediately after drying, each of the twelve subjects was asked to rub their fingertips, including the thumbs for one minute on the base of a petri dish, using a separate petri dish for each hand, containing 10m1 of maximum recovery diluent (MRD) without neutraliser, in order to assess the release of test organisms before treatment of the hands. Dilutions of these sample fluids were prepared to 10-3 and 10-4. A 1m1 aliquot of each dilution for each hand was placed in a separate petri dish 10 - 15m1 of Tryptone Soy Agar sterilised and cooled to 45 C added and mixed thoroughly. Plates were allowed to set and incubated at 37 C for twenty four hours. Each plate was then examined for growth of the test organism.
3) Hygienic Handwash procedure.
Each of the twelve subjects was asked to pour 3m1 of soft soap into the cupped hands pre-moistened with tap water and wash their hands in accordance with a standard handwash procedure. This comprises five strokes backwards and forwards palm to palm, right palm over left dorsum and left palm over right dorsum, palm to palm with fingers interlaced, back of fingers to opposing palms with fingers interlocked, rotational rubbing of right thumb clasped in left palm and left thumb clasped in right palm, rotational rubbing with clasped fingers of right hand in palm of left hand and clasped fingers of left hand in right palm using as much lukewarm water as is needed to produce a lather. After sixty seconds the hands are rinsed under running tap water for fifteen seconds from distal to proximal with fingertips upright.
4) Handwash procedure with test product (P).
After first wetting the hands and arms with water approximately 3m1 of a composition of the Examples was applied and rubbed thoroughly onto these areas using the technique described above and this is then rinsed off with running water. The total washing time is limited to sixty seconds and the time for final rinse is not included in the washing time. To avoid recontamination of the sample area (i.e. the fingertips) subjects are requested to hold their hands such that the fingertips are pointing upwards. Wrists and forearms are wiped dry by another person.
Example 1 Surgical Sanitizer Water (481.5g; 96.3%) was added to a beaker and stirring commenced.
Keltrol CG-SFT (9.0g; 1.8%) was added and stirring continued until dissolved. Citrox HXT powder (2.5g; 0.5%) was added and stirring continued until dissolved. White willow bark extract (2.0g; 0.4%) was added and stirring continued until dissolved. Glycerol (5.0g; 1.0%) was added and stirring continued until dissolved.
The resulting viscous gel was de-aerated. The pH was 4-5. The viscosity 7000-10000 cp at 20 C (spindle 4/0 rpm). The pH may be adjusted with citric acid if required to bring it within the stated range.
Citrox HXT powder comprises on a wt/wt basis 7.5% HPLC 45%, citric acid 30%, willow bark extract 50% and olea Europeae extract 12.5%.
HPLC-45% contained 45% by weight of a mixed of flavanoids together with residues of extraction from bitter oranges.

The Willow Bark extract contains 90% of salicylic acid.
The Olea Europeae extract contains 20% of oleuropein.
The mixture of flavanoids in HPLC-45 comprises:
Bioflavonoid % in HPLC 45 (bioflavonoid component + biomass) Neoeriocitrin 1.1 Isonaringin 1.2 Narangin 23.4 Hesperidin 1.4 Neohesperidin 12.5 Neodiosmin 1.4 Naringenin 1.5 Poncirin 2.0 Other 0.5 (Rhio fo lin) Total 45% of HPLC 45 Example 2 Liquid Hand Soap Water (362g, 72.4%) was added to a beaker and stirring commenced.
Keltrol CG-SFT (9g, 1.8%), Plantacare 2000 (67.8g, 13.6%), Tego Betain F50 (10g, 2%), glycerol (10g, 2%) and Citrox HXT powder were sequentially added with stirring until complete dissolution occurred prior to adding subsequent ingredients.

The product was a clear viscous gel, pH 4.8 to 5 was a viscosity of about 4000 cp at 20 C (spindle 4/10 rpm).
Citrox HXT powder and Keltrol CG-SFT were as described in Example 1.
Plantacare 2000 is an aqueous solution containing 6.78g of the surfactant agent.
Tego Betain F50 is an aqueous solution containing 3.22g of the surfactant agent.
Example 3 Hand Foam Composition This was prepared by mixing as described in Example 1.
Salicylic acid 0.25%
Citric acid 0.15%
HPLC 45% 0.0375%
Olive leaf extract 0.0625%
Betafin BP20 1.0%
Glycerine 0.5%
Dermosoft GMCY 1.0%
Water 97.0%
When tested against test organism according to BS EN 13727 under dirty conditions (interfering substances bovine albumin and sheep erythrocytes), a five minute contact time at 20 C, satisfactory bactericidal activity was observed when the test organism was (i) MRSA (ATCC33591) and Clostridium difficile (NCTC 11209). When tested against spores of this C. difficile according to En 13704, satisfactory sporicidal activity was found with a 15 minute contact time at 20 C.

Example 4 Sanitizing Gel This was prepared by mixing as described in Example 1.
Keltrol CG-SFT 1.7%
HPLC 45% 0.0375%
Olive leaf extract 0.0625%
Citric acid 0.15%
Salicylic acid 0.25%
Dermosoft GMCY 1.0%
Glycerine 1.0%
Water 95.8%
When tested by the methods detailed in Example 1, the gel provided satisfactory bactericidal activity against the MRSA and satisfactory sporidical activity against the C. difficile.
Example 5 Liquid Soap Keltrol CG-SFT 1.8%
Plantacare 2000 13.56%
Tego Betain F50 9.48%
Glycerine 1.0%
HPLC 45% 0.0375%

Olive leaf extract 0.0625%
Citric acid 0.15%
Salicylic acid 0.25%
Dermosoft GMCY 1.0%
Water 72.66%
When used herein HPLC 45% means a mixture containing 45% of bioflavanoids and 55% of other matter from extraction of bitter oranges.
The bioflavanoids comprised narangin (about 52%), neohesperidin 28%, poncirin (4%), naringenin (3%), hesperidin (3%), neodiosmin (3%), isonaringin (3%), isocriocrin (2%), other minor to 100%.
Example 6 Gel Example 3 may be repeated replacing HPLC 45% with an equal weight of a 1:1 mixture of narangin and nehesperidin.
Example 7 Aerially Dispersible Form The hand foam composition of Example 3 is used in a commercial misting device to produce a mist for disinfection of surfaces.
Example 8 A commercial hand held misting device is used to direct mist at the surfaces in an ambulance and to the air space. The misting is continued until the operative is satisfied surfaces have been thoroughly treated.
The ambulance may be occupied twenty minutes after the completion of the misting.

Claims

1. A composition comprising a flavanoid component and an oleuropein component wherein:
(a) the flavanoid component is one or more flavanoids of Formula (I):
wherein R1 is hydroxyl or methoxyl and R2 is hydrogen, hydroxyl or methoxyl and X is hydrogen or a saccharide; and (b) the oleuropein component is oleuropein or an acetylated derivative thereof.

2. A composition as claimed in claim 1 wherein R1 is 4-hydroxy or methoxy group.

3. A composition as claimed in claims 1 or 2 wherein R1 is 4-hydroxy and R2 is hydrogen.

4. A composition as claimed in any of claims 1 or 2 wherein R1 is 4-methoxy and R2 is 3-hydroxy.

5. A composition as claimed in any of claims 1 to 4 wherein X is hydrogen.

6. A composition as claimed in any of claims 1 to 4 wherein X is a saccharide.

7. A composition as claimed in any of claims 1 to 4 wherein X is a disaccharide.

8. A composition as claimed in claim 7 wherein disaccharide is rutinose.

9. A composition as claimed in any of claims 1 to 8 wherein the first component comprises narangin or neohesperidine or mixtures thereof optionally with one or more other flavanoids of the Formula (I).

10. A composition as claimed in claim 9 which comprises 50 - 55% of narangin, 25 - 30% of neohesperidin and 15 - 25% of one or more other flavanoids of the Formula (I).

11. A composition as claimed in any of claims 1 to 10 wherein the hydroxyphenylethanol component comprises oleuropein or a mono- or di-acetylated derivative thereof.

12. A composition as claimed in any of claims 1 to 11 wherein the oleuropein component is oleuropein.

13. A composition as claimed in any of claims 1 to 12 wherein the flavanoid component is an extract of bitter oranges.

14. A composition as claimed in any of claims 1 to 13 wherein the oleuropein component is an extract of the olive.

15. A composition as claimed in any of claims 1 to 13 wherein the weight ratio of the flavanoid component to the oleuropein component is 5:1 to 1:4.

16. A composition as claimed in claim 15 wherein the ratio is 2:1 to 1 : 2.

17. A composition as claimed in claim 16 wherein the ratio is 1:2 to 1:1.

18. A composition as claimed in claim 17 wherein the ratio is 3:2.

19. A composition as claimed in any of claims 1 to 18 which further comprises (c) salicylic acid or pharmaceutically acceptable salt thereof.

20. A composition as claimed in claim 19 wherein the weight ratio of the flavanoid component plus the oleuropein component to salicylic acid or pharmaceutically acceptable salt thereof is 2:1 to 1:7 (i.e. (a+b):c is 2:1 to 1:7).

21. A composition as claimed in claim 20 wherein the ratio of a+b:c is 1:1 to 1:5.

22. A composition as claimed in claim 21 wherein the ratio of a+b:c is 2:3 to 1:3.

23. A composition as claimed in claim 22 wherein the ratio is 2:5.

24. A composition as claimed in any of claims 1 to 23 which comprises a further organic acid such as citric acid, malic acid, lactic acid, tartaric acid, fumaric acid or other di- or tri-basic organic acid of up to 8 carbon atoms optionally substituted by 1, 2 or 3 hydroxyl groups; of a pharmaceutically acceptable salt thereof.

25. A composition as claimed in any of claims 1 to 24 which further comprises citric acid or a pharmaceutically acceptable salt thereof.

26. A composition as claimed in claim 25 wherein the citric acid or a salt thereof is contained in a willow bark extract.

27. A composition as claimed in any of claims 23 to 26 wherein the weight ratio of the further organic acid or pharmaceutically acceptable salt thereof to salicylic acid is 2:1 to 1:5.

28. A composition as claimed in claim 27 wherein the ratio is 1:1 to 1:3.

29. A composition as claimed in claim 28 wherein the weight ratio is 3 to 5.

30. A composition as claimed in any of claims 19 to 29 wherein the salicylic acid is present together with a solubilising agent therefore.

31. A composition as claimed in claim 30 wherein the solubilising agent is a dextrin.

32. A composition as claimed in claim 31 wherein the dextrin is cyclodextrin.

33. A composition as claimed in any of claims 1 to 31 for use as a pathenogenicide.

34. A composition as claimed in any of claims 1 to 31 for use as an antibacterial agent.

35. A composition as claimed in any of claims 1 to 31 for use as an antiviral agent or an antifungal agent.

36. A composition as claimed in any of claims 1 to 31 for use as an antiparasitical agent.

37. A composition as claimed in claim 36 for use against protozoa.

38. A composition as claimed in claim 31 for the prophylaxis or treatment of an insect infestation such as an external parasite, for example head lice.

39. A composition as claimed in claim 34 for use against multiple resistant staphylococcus aureus.

40. A composition as claimed in claim 34 for use against clostridium difficile.

41. A composition as claimed in claim 34 for use against (a) helicobacter pyroli or (b) vancomycin resistant strains of enterobacter or staphylococcus or other pathogen whereby transmission is by contact or air, for example, norovirus.

42. A composition as claimed in claim 35 for use against influenza virus.

43. A composition as claimed in claim 35 for use against human immunodeficiency virus.

44. A composition as claimed in claim 33 for washing food stuffs.

45. A composition as claimed in claim 33 for sterilizing local environments, for example medical premises, hotels, ships or aircraft.

46. A composition as claimed in claim 45 wherein the local environment is a hospital ward, operating theatre, corridor or ambulance.

47. A composition as claimed in claim 33 for sterilizing clothing, exposed body parts, stethoscopes or surgical instruments.

48. A composition as claimed in any of claims 1 to 34 which further comprises an additional antibacterial agent for simultaneous or consecutive use.

49. A composition as claimed in claim 48 wherein the additional antibacterial agent is a .beta.-lactam antibiotic.

50. A composition as claimed in claim 49 wherein the .beta.-lactam antibiotic is amoxicillin.

51. A composition as claimed in claim 49 wherein the .beta.-lactam antibiotic is a carbopenem such as imipenem.

52. A composition according to any of claims 1 to 51 in the form of a pharmaceutical composition which also comprises a pharmaceutically acceptable carrier.

53. A composition according to any of claims 1 to 51 in the form of a toothpaste, mouthwash, mouth spray or mouth rinse.

54. A composition according to any of claims 1 to 51 in the form of a water based composition of pH 3 to 8.5.

55. A composition according to claim 54 wherein the pH is from 5 to 8.

56. A composition according to any of claims 1 to 53 wherein the composition is in an orally administrable unit dosage form.

57. A composition according to any of claims 1 to 53 in the form of a multidose composition from which a unit dose may be withdrawn.

58. A unit dose form as claimed in claim 56 which contains from 25 mg to 500 mg of the flavanoid component.

59. A unit dose form as claimed in claim 58 which contains from 50 mg to 1000 mg of flavanoid component.

60. A unit dose form as claimed in claim 58 which contains 100 mg to 500 mg of flavanoid component.

61. A multidose form as claimed in claim 57 in the form of a liquid from which unit doses may be withdrawn.

62. A composition according to any of claims 1 to 34 in the form of a soap or shampoo.

63. A composition according to any of claims 1 to 34 in the form of a mistable powder or liquid.

64. A composition according to any of claims 1 to 34 which comprises by weight:
(a) flavanoid component 5 - 10%;
(b) hydroxyphenylethanol component 10 - 15%;
(c) salicylic acid or pharmaceutically acceptable salt thereof 45 -55%;
(d) citric acid or a pharmaceutically acceptable salt thereof 25 -35%.

65. A composition as claimed in claim 64 in the form of a powder comprising (a) 7.5%, (b) 12.5%, (c) 50% and (d) 30%.

66. A composition as claimed in claims 64 or 65 which comprises an aqueous solution of (a), (b), (c) and (d).

67. A composition as claimed in claim 66 which further comprises a solubilising agent.

68. A composition as claimed in claim 67 wherein the solubilising agent is a dextrin.

69. A composition as claimed in claim 68 wherein the dextrin is cyclodextrin.

70. A method of pathogenicide which comprises bringing into contact with the pathogen a composition as claimed in any of claims 1 to 69.

71. A method as claimed in claim 70 wherein the method of pathogenicide is (a) a method of reducing or eliminating pathogenic bacteria, (b) a method of reducing pathogenic virus, for example, norovirus or influenza, or (c) other microbial pathogen transmissible by contact or air.

72. A method as claimed in claim 71 wherein the pathogenic bacteria is MRSA, clostridium difficile or helicobacterpyroli.

73. A method as claimed in claim 72 wherein the pathogenic bacteria reduced or eliminated is clostridium difficile and its spores.

74. A method as claimed in any of claims 70 to 73 wherein the method comprises the composition to an external surface.

75. A method as claimed in claim 74 wherein the external surface is of a human or animal subject.

76. A method as claimed in claim 74 wherein the external surface is of a food stuff, cloths, medical establishments, hospital wards, hospital corridors, hospital waiting rooms, hospital operating theatres, ambulances, hospital devices such as stethoscopes, catheters and surgical instruments, and ships and aircraft cabins.

77. A method as claimed in any of claims 70 to 76 wherein the external surface is washed with a solution of the composition.

78. A method as claimed in any of claims 70 to 76 wherein the external surface is misted with a solution of the composition.

79. A method as claimed in claim 70 wherein the pathogen is a virus, fungus or parasite.

80. A method as claimed in claim 79 wherein the virus is influenza virus or human immunodeficiency virus.

81. A method as claimed in claim 79 wherein the fungus is a yeast such as Candida albicans or is aspergillius.

82. A method as claimed in claim 79 wherein the parasite is an internal parasite such as a protozoan or fluke, for example malaria.

83. A method as claimed in claim 79 wherein the parasite is an external parasite such as an insect, for example lice, fleas or scabies.