Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Cosmetic – antiperspirant – dentifrice
Reexamination Certificate
2000-10-18
2002-06-11
Prats, Francisco (Department: 1651)
Drug, bio-affecting and body treating compositions
Preparations characterized by special physical form
Cosmetic, antiperspirant, dentifrice
C424S769000, C424S755000, C514S844000
Reexamination Certificate
active
06403111
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a method for preparing a clear, aqueous solution containing as much as 5-10% of phytosphingosine by use of water, and using no alcohols or other organic solvents.
More particularly, the present invention relates to a method for preparing an aqueous phytosphingosine solution by heating a solution of 5-10 weight % of a phytosphingosine powder in distilled water at 60-90° C. with stirring, solubilizing the phytosphingosine with the pH being neutralized with lactic acid, and adding 0.1-1 wt % of a willow bark extract containing 10 weight % or more of salicylic acid or its analogues such as salicylin to give a clear phase of the aqueous phytosphingosine solution.
2. Description of the Prior Art
Phytosphingosine, a kind of sphingolipid serving as an important component of cell membranes, is a physiologically active material with a variety of biological functions, including being an important structural constituent of cell membranes and an important signal transmitter in a signal transduction system (Okasaki et al., 1989; Kim et al., 1991).
Recent research has revealed that sphingolipids play a critical role in cellular functions, including the growth, proliferation, differentiation and apoptosis of cells, through a signal transduction process known as the “sphinogmyelin cycle” (Hannun, 1994, 1996; Hannun and Obeid, 1995) in which many other factors such as TNF-&agr;, IL-1, &ggr;-IFN and FAS ligands are involved.
Sphingolipids are responsible for maintaining moisture balance of skin and regenerating stratum corneum as well as functioning as a primary defense against external attack from microbes. In addition, sphingolipids are now used in cancer research, as they are known to be involved in the inactivation and activation of protein kinase C, the regulation of EGF receptors, the induction of Ca
2+
ion mobilization, and the regulation of the NF-&kgr;B gene expression. Disclosing that most skin diseases, including atopic dermatitis, from which over 3-4% of the world population is suffering, are at least partially attributed to a decrease in the content of various sphingolipids in the stratum corneum, recent research reports strongly suggest that the use of sphingolipids is highly feasible as active ingredients of next generation curing agents for skin diseases, substituting for antibiotics and steroid hormones which serve as anti-inflammatory agents.
Ceramides III and VI, which have phytosphingosine as their sphingolipid long-chain base, have been used as important cosmeceuticals in a broad spectrum of cosmetic and pharmaceutical industries for recent years. For instance, ceramides (e.g., N-acylated sphingosine and N-acylated phytosphingosine), which constitute higher than 40 weight % of the total lipids in stratum corneum, are being used worldwide in various products from cosmetic compositions for skin care to hair tonics. Phytosphingosine itself is used as a functional material for moisturizing compositions and anti-aging compositions in the cosmetic industry. The applications of phytosphingosine are sharply increasing because it is better in skin recovery properties and anti-bacterial and anti-inflammatory activity than are ceramides. In the pharmaceutical industry, for example, the use of phytosphingosine in the treatment of atopic dermatitis, acne, psoriasis, itching and wound recovery is under study. Therefore, it is expected that phytosphingosine would be used as a core material of functional cosmeceuticals applicable in, for example, anti-aging agents, moisturizing agents, damaged skin-recovery agents, and applicable for the healing of, for example, atopic dermatitis, acne, psoriasis and itching, and wounds.
Until recently, sphingolipids had usually been obtained from animals. However, the cosmetic industry is reluctant to use sphingolipids from animals for fear of contamination with Mad Cow Disease. Their chemical synthesis suffers from many disadvantages. For example, the chemical synthesis is prohibitively expensive. Further, in many cases, the stereochemical structures of the compounds synthesized are different from those of the sphingolipids occurring naturally in the body. It is also difficult to chemically synthesize pure stereochemical structures of sphingolipids. In recent, there have been developed processes for preparing phytosphingosine through the fermentation of the yeast Pichia cifferi. Since the phytosphingosine prepared from the yeast fermentation was also found to be stereo-chemically the same as that existing in the human body, it is being used in many industries in sharply increasing quantities. The phytosphingosine which can be prepared from the yeast fermentation, however, finds difficulty in its application to cosmetics and pharmaceuticals owing to its low solubility. Phytosphingosine is not soluble in water at all and shows a solubility of 1 wt % even in isocetyl alcohol, a widely used cosmetic solvent. Thus, phytosphingosine is difficult to use at an amount large enough to exert its efficacy when being used as a cosmetic material. Moreover, it cannot be used in a transparent liquid product, such as a skin lotion, at all.
At present, phytosphingosine is being used at an amount of 0.1-0.3 weight % in cosmetic products, but these concentrations are too low to obtain desired effects. The expression of functions of phytosphingosine requires at least 0.5 weight % and preferably 1-2 weight % of the active compound in cosmetic products. Therefore, there remains a need for developing a process of solubilizing phytosphingosine at a higher concentration in order for phytosphingosine to be applied for use in cosmetics and pharmaceuticals.
SUMMARY OF THE INVENTION
Leading to the present invention, the intensive and thorough research on the effective application of phytosphingosine for use in cosmetics and pharmaceuticals, repeated by the present inventors aiming to solve the above problems encountered in prior arts, resulted in the finding that a mixture of water and lactic acid can solubilize a large quantity of phytosphingosine with the aid of a willow bark extract, and no recrystallization occurs in the resulting phytosphingosine solution.
Therefore, it is an object of the present invention to provide a method for preparing a clear aqueous solution with a high content of phytosphingosine.
It is another object of the present invention to provide use of the aqueous phytosphingosine solution in cosmetics.
In accordance with the present invention, there is provided a method for preparing an aqueous phytosphingosine solution, comprising the steps of: heating a solution of a predetermined concentration of a Phytosphingosine powder in distilled water at 60-90° C. with stirring; neutralizing, in pH, the solution with lactic acid to solubilize the Phytosphingosine with stirring; and adding a willow bark extract to prevent the recrystallization of the solution.
The aqueous phytosphingosine solution prepared according to the present invention is able to care troubled skin with inhibitory activity against bacteria and inflammation. In addition, when being applied for cosmetics, the aqueous phytosphingosine solution allows them to contain as much as 1-2 weight % of phytosphingosine by virtue of its high content of phytosphingosine. Thus, the present Phytosphingosine solution provides a significant improvement in applications over conventional solutions that require additional dissolution of phytosphingosine in solvents. Further, the phytosphingosine solution of the present invention is greatly improved in compatibility with cosmetic components so that it can be readily applied for aqueous cosmetics such as skin lotions, essence lotions, aqueous pack products, body essence compositions, etc., for which phytosphingosine has not yet been applied thus far.
Accordingly, the phytosphingosine solution of the present invention gives a great contribution to the functional improvement of aqueous cosmetics. An aqueous phase of phytosphingosine is applied for conventional cosmetic cream products
Jeong Jee Hean
Kim Jin Wook
Park Chang Seo
Coe Susan D.
Doosan Corporation
Ladas & Parry
Prats Francisco
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