oral composition
A composition and oral cavity technology, which can be used in oral care, drug combination, cosmetic preparations, etc., can solve the problem of no bactericidal effect, etc., and achieve the effect of excellent cell damage inhibition effect.
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[0051] Hereinafter, the present invention will be described in more detail by way of Examples, Comparative Examples, and Prescription Examples, but the present invention is not limited to the following Examples. In addition, in the following examples, % represents mass % unless otherwise specified.
[0052] [Example, comparative example]
[0053] A sample solution having the composition shown in Table 1 was prepared by a normal method, and the cell damage inhibitory effect and the oral bacteria sterilizing effect were evaluated by the method shown in the following experimental example. The results are recorded together in the table.
experiment example 1
[0054] Cell damage inhibitory effect test
[0055] Commercially available gingival fibroblast Gin-1 (manufactured by DS Pharmaceutical Biomedical Co., Ltd.) was incubated in Dullbecco's Modified Eagle's Medium (D-MEM) containing 10% fetal bovine serum (FBS) at 37°C, 5% CO 2 pre-cultured under conditions. Prepare 400 μL to make 5 × 10 4 Gin-1 cells / ml were seeded in 48-well plates and further cultured for 24 hours. After removing the culture medium, 400 μL of the sample solutions shown in the table (diluted 20 times with D-MEM containing 10% FBS) were added, respectively, and treated with drugs for 48 hours.
[0056] After the treatment was completed, 1 mM hydrogen peroxide aqueous solution (assumed to be active oxygen) was added for 60 minutes. After the treatment, the sample solution was removed, and 400 μL of a solution containing 1 mM hydrogen peroxide (D-MEM containing 10% FBS) was added, and treated for 60 minutes. After the solution was removed, 200 μL of a cell vi...
experiment example 2
[0064] Bactericidal effect test on bacteria in the oral cavity
[0065] Todd-Hewitt broth (Becton Dickinson, Japan) supplemented with hemin (manufactured by Wako Pure Chemical Industries, Ltd., 500 μg / mL) and menadione (manufactured by Wako Pure Chemical Industries, Ltd., 100 μg / mL) was added with physiological saline. Porphyromonas gingivalis strain ATCC33277 pre-cultured in the 9 cells / mL of bacterial suspension. Mix the bacterial solution with the sample solution shown in the table at a ratio of 1:1 (volume ratio), and let stand for 3 minutes. Then, perform four dilutions with physiological saline, each dilution is 10 times, and smear on the blood agar plate medium with a spiral inoculator. As a control, a mixture of physiological saline and bacterial solution mixed at 1:1 (volume ratio) was used instead of the drug.
[0066] The blood plate medium was cultured at 37° C. under anaerobic conditions (95 vol % nitrogen, 5 vol % carbon dioxide) for 5 days, and the number of...
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