FORM - 2
THE PATENTS ACT, 1970
(39 of 1970)
&
The Patents Rules, 2006
PROVISIONAL SPECIFICATION
(See Section 10 and Rule 13)


A TOPICAL COMPOSITION
HINDUSTAN UNILEVER LIMITED, a company incorporated under
the Indian Companies Act, 1913 and having its registered office
at 165/166, Backbay Reclamation, Mumbai -400 020, Maharashtra, India
The following specification describes the invention

TECHNICAL FIELD
The invention relates to a topical composition and a method for reducing or preventing occurrence of acne on the skin.
BACKGROUND AND PRIOR ART
Acne, also known as Acne vulgaris, is a common skin condition that affects nearly ail adolescents and adults at some times in their lives. It has a complex etiology, involving abnormal keratinization, excess sebum production, androgen function, bacterial growth, and immune hypersensitivity. Although one or more of the above processes is correlated with acne, the one triggering factor and the exact sequence of events leading to the formation of acne lesions is not been fully understood. Other factors which have been linked to acne are presence of free radicals with subsequent oxidative stress leading to cellular damage. It has been observed that acne usually occurs in areas rich in sebaceous glands like the face, neck and back. A bacteria Propionibacterium acnes (P. acnes) has also been implicated in occurrence of acne.
The earliest acne lesion is known as the microcomedone. These evolve into comedones which may either be open ("blackhead") or closed ("whitehead"). The various stages of acne have been classified as comedones, papules, pustules, and cysts.
Acne has been treated in many ways. Most treatments take several weeks to months before a noticeable change is seen. Benzoyl peroxide which has an antibacterial effect has been used for mild cases of comedones and is also believed to prevent formation of other comedones. Tretinoin which is a derivative of Vitamin A has been used in the treatment of whiteheads and blackheads and is believed to convert closed comedones into open comedones. Isotretinoin has been used to treat severe cystic acne. Azelaic acid has been used to treat acne
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and is believed to act by inhibiting growth of P. Acnes and by decreasing the
ductal hypercornification. In very severe cases of acne antibiotics like
tetracycline, erythromycin and clindamycin have been used Antibiotics are believed to work by several mechanisms, the most important being the decrease in the number of bacteria in and around the follicie They are also thought to reduce the irritating chemicals produced by the white blood cells in the sebum, thereby reducing the inflammatory response.
Most of the treatments, involve use of synthetic chemicals Many people do not prefer use of synthetic chemicals since they are believed to be harsh on the human body. Some people believe that synthetic Chemicals cause side effects. Hence, more and more people prefer use of materials which are "natural" e.g. actives based on herbal origin jain a and Basal E in the article inhabition of Propionibacterium acnes- induced mediators of inflammation by Indian herb", in the Journal Phytomedicine, 2003, 10:34-38 have indicated that herbs like Rubia Cordifolia, Curcuma longa, Hemidesmus indicus and Azadirachta indica have the capacity to suppress P. Acnes induced inflammatory mediators.
The present inventors have also been working towards providing such "natural" solutions to solving the problem of acne. They tried a large number of combinations of herbal extracts and found that two specific combinations of herbs interact synergistically to help solve the problem of acne
Use of some of these herbs for skin benefit are descried below.
WO2001005417 claims a process for treating skin having acne or furuncle comprising applying a composition containing an exract of Momordica charantia L over an area of skin having acne or furuncle.
JP2002212050 claims a cosmetic exhibiting beauty Promoting effects, promoting metabolism of the skin without damaging the skin, Smoothing the skin and also
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providing prevention of acne, skin chapping and skin aging when directly applied to the skin as an external preparation. The cosmetic is prepared by formulating an extract or a squeezed liquid from fruit of balsam pear (family Cucurbitaceae; scientific name is Momordica charantia) to a base of the cosmetic for the skin or the hair.
US20070014749 relates to the preparation and use of compositions for the treatment of skin disorders itchy and/or infected skin such as impetigo, acne (on face, forehead scalp and on the back of the body) and fungal infection of skin and nails. The skin composition comprises freeze dried water extracts of Cassia tora, Melia azadirachta, and Centratherum anthetminticum.
JP10279428A claims a stable, highly safe, cosmetic having skin whitening effect by including (A) 0.01-20.0 wt.% of a water-soluble extract from Sesamum Indicum L. and (B) as necessary, an aqueous ingredient, powder, surfactant, lubricant, moisturizer, alcohol(s), pH adjustor, antiseptic, color, antioxidant, ultraviolet light absorber, thickening agent, perfume, skin-beautifying ingredient, etc. The ingredient A is obtained by removing, as necessary, lipid components from the roots, leaves, stems, buds, flowers, germinated matter or seeds of Sesamum Indicum L or dried product(s) and/or ground product(s) thereof by use of a water-insoluble organic solvent followed by conducting an extraction with water or a hydrous and/or anhydrous lower alcohol.
Thus, although each of the herbs have been used in skin preparation, none of the above cited prior art disclose or suggest a synergistic combination of the herb extracts found by the present inventors to give benefits in acne treatment.
It is thus an object of the present invention to provide for a combination of herbal extracts that interact synergistically to provide a cosmetic composition for prevention, reduction or treatment of acne.
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SUMMARY OF THE INVENTION
The present invention provides for a topical composition comprising
(i) an extract of a first active which is Azhadirachta indica; and
(ii) an extract of a second active selected from Momordica charantia or Sesamum
indicum.
DETAILED DESCRIPTION OF THE INVENTION
The present invention provides for a topical composition comprising a mixture of extracts of two herbal actives. The first active is the herb Azhadirachta indica. The second active is a herb selected from either Momordica charantia or Sesamum indicum. It is particularly preferred that the extract is a water extract.
Azadirachta indica also known as Melia azadirachta is a large evergreen tree which can grow up to a height of 18 meters and can have a girth of up to 2.4 meters. It grows in the wild throughout India and in similar tropical climatic countries. It is also cultivated widely in India. The tree is deeply associated with Indian culture and is known as Neem, Nim, Nimba, Nimb, Veppa, Bevinamara, Limba, Vembu etc. in different languages of India. Outside India, the tree is known as Indian Lilac, Margosa or Neem Tree. The extract of neem for use in the present invention is preferably from the leaves of the neem tree. Leaves of neem have been used in the traditional Indian medicinal system known as Ayurveda for treatment of various disorders. It has been reported to be used in treating various skin disorders, and for preventing wound infections. Decoction of the leaves is added to bath water to get rid of skin problems. Poultice of the leaves is also used in inflammation associated with wounds. The leaves are also used as an insect repellent. Neem leaves are used internally as an anthelmintic agent.
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Neem leaves are reported to contain various physiologically active compounds like stigmasterol, nimbocinone, nimbocinolide, isonimbocinolide, nimocinol, isonimocinolide and isoazadirolide. The fresh green leaves yield compounds like meldenindiol, vilasinin, azadirachtanin, margosinolide, isomargosinolide, and desacetyldihydronimbic acid.
Extract of first active i.e. extract of Azadirachta indica is preferably present in 0.01 to 2% by weight of the composition.
The second active is a herb selected from Momordica charantia or Sesamum indicum.
Momordica charantia commonly known as kareia in India is a cucurbitaceous climber cultivated throughout the tropical climate across the globe. The herb is also called bitter melon, bitter gourd, balsampear, kaippavalli, pavakka in different languages. The unripe fruit is a popular bitter vegetable. It is also used in traditional Indian medicine mostly for the management of diabetes.
Ayurveda, the traditional Indian form of medicine, uses Karela fruit as laxative, anti-pyretic and as an appetizer. It is used in Ayurveda to improve liver functions and to purify the blood. Fruits are eaten as food and used in treatment of arthritis, gout, liver and spleen enlargement.
A number of novel and biologically active phytochemicals have been identified from karela fruits including charantin, momordicin, momordin, momordicosides, and polypeptides. However, those, which are attributed with therapeutic activity include polypeptide-p, charantin and Momordin. Some other compound like vicine has also been reported to posses some hypoglycemic activity.
As per the present invention, the fruit of the karela plant is preferably used for preparing the extract.
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Sesamum indicum is also known as Sesamum orientale. The common name is sesame. It is an erect, branched plant that grows to a height of about 60-180 cm. It is an annual plant. It is cultivated throughout the plains of India and also in the hills up to an altitude of about 1200 meter. It is also grown in other countries having climatic conditions like the tropical plains of India mostly as a source of oil seed, ft is also used as a spice for seasonings. Sesame is known as Tila, Tilt, Til, or Gingelli in different regions of India. There are many varieties of sesame grown in India. The varieties are based on the colour of the seed coat which ranges from white to black. There are many intermediate varieties as well. However, the black and white Sesame are two varities largely cultivated in India. Of these two varities, the white sesame is more preferred for use in the present invention.
The extract of the second active is preferably present in 0.01 to 2% by weight of the composition.
The composition of the invention preferably comprises a cosmetically acceptable vehicle. The cosmetically acceptable vehicle is suitably chosen to provide the skin care composition in any one of the well known cosmetic formats. Such formats may be leave-on topical compositions or wash-off products. Well known leave-on formats include cream, gel, lotion, ointment, powder, mousse or spray. More preferred formats are the oil-in-water emulsions like cream or lotion, most preferred being cream. Among the creams, the vanishing cream base is most preferred. By a vanishing cream base is meant a base which has 5 to 25% C12-C2o fatty acids and 0.1-10% fatty acid soap by weight of the topical composition. Vanishing cream base gives a highly appreciated matty feel to the skin. Although C12 to C2o fatty acids are especially preferred for the present invention, more preferred are C14 to C18 fatty acids. The most preferred fatty acid is stearic acid. The fatty acid is more preferably present in 5 to 20%) by weight of the composition. Soaps in the vanishing cream base include alkali metal salt of fatty acids, like sodium or potassium salts, most preferred being potassium stearate.
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The soap in the vanishing cream base is generally present in an amount in the range of 0.1 to 10%, more preferably 0.1 to 3% by weignt of tne Composition. Generally, the vanishing cream base in cosmetic impositions is prepared by taking a desired amount of total fatty matter and mixing with potassium hydroxide in desired amounts. The soap is usually formed insitut during the mixing.
The other preferred cosmetically acceptable vehicle is a detergent composition. The detergent composition preferably comprises 5 to 85% salt of fatty acid or 2 to 20% synthetic surfactant or mixture thereof.
The topical composition may comprise an optional ingredient like skin lightening agent. The skin lightening agent is preferably chosen from one or more of a Vitamin R3 compound or its derivatives e.g niacin dicotonic acid niacinamide other well known skin lightening agents e.g. aloe extract, ammonium lactate, arbutin, azelaic acid, kojic acid, butyl hydroxy tcuene citrate esters, 2, 5 dihydroxybenzoic acid and its derivatives, ellagic acid fennel extract, gluconic acid, glycolic acid, green tea extract, hydroquinone 4 hydroxyanisole and its derivatives, 4-hydroxy benzoic acid derivatives, kcjjic acid acid, lemon extract, linoleic acid, magnesium ascorbyl phosphate 2 4 resorcinol derivatives, 3,5 resorcinol derivatives, salicylic acid, and vitamins like vitamin B6, vitamin B12, vitamin C, vitamin A, a dicarboxylic acid, extracts from p|ants viz. rubia and symplocos, hydroxycarboxylic acid like lactic acid and their salts e.g. sodium lactate, and mixtures thereof. Skin lightening agent when used, is preferably present in an amount in the range of 0.1 to 10%, rmore preferably 0.2 to 5% by weight of the composition.
Another optional ingredient in the topical composition is a uv sunscreen. The UV sunscreen may be inorganic or organic. Suitable organic sunscreen agents include, 2-hydroxy-4-methoxybenzophenone, octldimethyl- p-aminobenzoic acid, 2,2-dihydroxy-4- methoxybenzophenone, 2- ethylhexyl-2-cyano-3,3-diphenylacrylate, 2-ethylhexylsalicylate, 2-ethylhexyl_p_djmethyl_amino_benzoate

2-ethylhexyl-p-methoxycinnamate, butylmethoxydibenzoylmethane, 2-hydroxy-4-methoxybenzophenone, octyldimethyl-p-aminobenzoic acid and mixtures thereof. Most suitable organic sunscreen are 2-ethylhexyl-p-methoxycinnamate or butylmethoxydibenzoylmethane. The composition preferably comprises from about 0.1% to about 10%, more preferably from about 0.1% to about 5%, sunscreen agent by weight of the composition.
Inorganic UV sunscreens are called sunblocks. Preferred sunblocks include zinc oxide, iron oxide, silica, such as fumed silica, and titanium dioxide. Most suitable sunblocks are zinc oxide or titanium dioxide. The sun block is preferably incorporated in 0.1 to 5% by weight of the composition.
The composition according to the invention may also comprise other diluents. The diluents act as a dispersant or carrier for other materials present in the composition, so as to facilitate their distribution when the composition is applied to the skin.
Diluents other than water can include liquid or solid emollients, solvents, humectants, thickeners and powders.
The cosmetically acceptable vehicle is preferably present from 10 to 99.9%, preferably from 50 to 99% by weight of the composition, and can, in the absence of other cosmetic adjuncts, form the balance of the composition.
The compositions of the present invention can comprise a wide range of other optional ingredients. Examples of such optional ingredients include antioxidants, binders, biological additives, buffering agents, colorants, thickeners, polymers, astringents, fragrance, humectants, opacifying agents, conditioners, exfoliating agents, pH adjusters, preservatives, natural extracts, essential oils, skin sensates, skin soothing agents, and skin healing agents.
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According to another aspect of the present invention there is provided a method of preventing or reducing the occurrence of or treating acne comprising the step of applying to the skin a composition of the present invention.
According to yet another aspect of the present invention there is provided use of a composition comprising an extract of a first active which is Azhadirachta indica; and an extract of a second active selected from Momordica charantia or Sesamum indicum for preventing or reducing the occurrence of or treating acne.
The invention is now further described by way of the following non-limiting examples.
Examples
The efficacy of the extract of the actives for treating/ prevention of acne was
tested using an assay that measured the expression of involucrin mRNA. In acne
there is an abnormality in proliferation and differentiation. Involucrin marker has
been used for the screening studies. The procedure used was as follows:
Cell Culture
HaCaT human keratinocytes obtained from Dr Fusenig, Germany. The cells were
cultured in Dulbecco's modified eagle's media (Sigma Chemical Co., USA)
supplemented with 10 U/ml penicillin G, 0.1 mg/ml streptomycin sulfate, 10 mM
HEPES buffer and 10% heat inactivated fetal calf serum (Gibco, USA) at 37°C in a
humidified incubator with 5% C02 atmosphere.
Reagents
All the chemical reagents were procured from Sigma Chemical Co., USA. Retinoic
acid, 13-cis retinoic acid and testosterone stocks were prepared in dimethyl
sulfoxide (DMSO).
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Preparation of extract of actives
1 gm of each of the powdered actives was soaked in 60 ml of water overnight The next day the sample was boiled till the volume was reduced to 10 ml (final concentration equivalent to 1 gm / 10 ml) for a total for 4 hrs. This extract was filtered and cooled and used for the in vitro assays at a final concentration of 0.01%.

RT-PCR
5X105 keratinocytes were plated in a 35 mm plate and incubated at 37°C in 5% CO2 for 24 hrs. Actives were added the next day and cells were harvested 18-24 hrs later. Total cellular RNA was then extracted from these cells using TRI reagent (Sigma Chemical Co., USA) as recommended by the supplier. cDNA synthesis was carried out using oligo (dT)18 primer. Semi-quantitative RT-PCR was then carried out using specific, forward and reverse primers as listed below. The PCR was carried out in Perkin Elmer Gene Amp PCR system 2400 for 30 cycles in all cases. The PCR products were analysed on 1-2% agarose gels and detected by ethidium bromide staining. The DNA gel picture was captured and the intensities of the PCR amplified DNA fragments were analysed using PhotoCap image analysis software (Vilber Lourmat, France).
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The following primers were used for PCR amplification:

Primer Sequence Product size Annealing temperature
Beta actin
Forward Reverse 5' - GTG GGC CGC TCT AGG CAC CAA - 3' 5' - CCA AAG TAG ACC TGC CCG GAC TC -3' 300 bp 60°C
Involucrin
Forward Reverse 5' -CTC CTC AAG ACT GTT CCT CC- 3' 5' -GCA GTC ATG TGC 1 1 1 TCC TCT TOG¬S' 143 bp 64°C
The involucrin expression as a percentage of control was calculated using the
following procedure:
(Control - Active)x 100/ Control
The data on the various samples of Extracts of actives are summarized in Table - 1. The total concentration of the active was 0.01% in the assay. The control sample was water.
Table -1

Example Active Involucrin expression as a percentage of control
1 Control 100
2 Azhadirachta indica 94.2
3 Momordica charantia 80.7
4 Sesamum indicum 119.3
5 Azhadirachta indica + Momordica charantia 49.1
6 Azhadirachta indica + Sesamum indicum 24.5
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Amphotericin-B were used as standards. End points were determined after 48 hours visually and by using spectrophotometer wherever necessary. The activity parameters are enumerated in Table 1 which shows that some of the compounds exhibited significant
antifungal activity.

Formula 1
Table 1: MIC obtained by broth macro-dilution method

Sr no Compound no Structure 1 Activity against organisms MIC in µg/ml

C. albicans ATCC
24433 A. niger ATCC 16404 F.
proliferatum ATCC 10052
1 Fluconazole 1 128 >128
2 Amphotericin B 0.25 1 2
3 la n=l,X=S,Rl=H, R2=R3=F 0.25 >64 >64
4 lb n=l,X=S,RI=7-Cl, R2=R3-F 1 >16 >16
5 lc n=l,X=S,Rl=7-Br, R2=R3=F 1 >16 >16
6 Id n=l,X=S,Rl=7-OMe, R2=R3=F 4 >32 >32
7 le n=l,X=S,Rl=7-Me, R2=R3=F 2 >32 >32
8 If n=I,X=S,RI=7-Cl, R2=F, R3=H 2 >16 >16
9 lg n=l,X=S, Rl=7-OMe, R2=Br, R3=H 2 >16 >16
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