Antisebum and antioxidant composion
A composition and anti-sebum technology, applied in skin care preparations, cosmetics, plant raw materials, etc., can solve the problem of no disclosed antioxidant activity, no disclosed preparation method, use and activity of alcohol fraction or low molecular weight fraction, no disclosure Disclosure of issues such as anti-sebum activity of guggal to reduce the appearance of wrinkles and aging skin, improve radiance, and improve oil control
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Embodiment 1
[0064]This example illustrates the procedure for the fractionation of gugulipid into fractions of increased polarity (procedure A) and for the preparation of a low molecular weight fraction of gugulipid (procedure B). Procedure A Materials: Gugulipid (Lot No. 42941, Lipo Chemicals Inc. Paterson NJ) medium pressure column (5 cm internal diameter X 62 cm long) silica (Gel, Merck), Aldrich, Cat no. 22, 719-6, Grade9385, 230, 400, mesh 60A. Thin Layer Chromatography Plate, LHP-kk 20 x 10cc Lot # 004966, Cat # 4805-711 Whatman. Hexane, HPLC Grade (Fisher) Ethyl Ethanol, HPLC Grade (Fisher) Methanol, HPLC Grade (Fisher) Chloroform, HPLC Grade (Fisher) Phosphoric Acid (Fisher) Copper Sulfate CuSO 4 (Fisher) petroleum ether (Fisher) 24 beakers (400ml) scintillation tube capillary (5μl) 2 measuring cylinders (2000ml) 1 developing dish 1 oven (Napco type 420) 1 heating / stirring plate 2 round bottom flasks ( 500ml) rotary evaporator water (Milli-Q water) method:
[0065] 1. Weigh 5.06...
Embodiment 2
[0112] This example reports the in vitro analysis of the sebum suppressing effect of gugulipid and its various fractions.
[0113] In vitro test of fat formation by sebocytes
[0114] Human sebaceous glands were isolated from the nose of a male (60 years old) and cultured using the soak tissue culture technique (Bajor et al, J. Invest Dermatol. 102:1994, p. 564). These sebocytes aggregate the intracellular lipid droplets characteristic of mature human sebum.
[0115] Add the harvested and passaged sebocytes to each well of a 48-well tissue culture dish and incubate in 7.5% CO 2 and cultured at 37°C for 10 days. On the day of the experiment, the growth medium was removed and the sebocytes were washed three times with phosphate-buffered saline (PBS). 0.5 ml of fresh PBS was added to each well at various concentrations shown in Table 1, and 10 μl of the reagent to be tested was added. Three wells use the same sample. Control samples consisted of phosphate-buffe...
Embodiment 4
[0129] This example reports chemical tests and in vitro analyzes of the antioxidant activity of gugulipid and its various fractions. Chemical test:
[0130] The chemical assay measures the antioxidant activity of the various test compounds indicated in Table 3 (all tested at 0.08% except for the low molecular weight fractions which were tested at 1.67% and 0.17%). Solubilize 2,2'-azino-bis-(3-ethylbenzothiazoline sulfonate) (6.1 μmol / l) and intermyoglobin ( metmyoglobin) (610 μmol / l). The test substances are then added and the absorbance at 734 nm is measured before and after addition of the substrate, hydrogen peroxide (250 μmol / l). The initial absorbance was subtracted from the absorbance containing the matrix. This prevents absorbance differences caused by the test compound itself. Absorbance changes over time, so multiple times were examined for absorbance. Results are expressed as percent oxidation relative to a control sample (100% oxidation) containing all test com...
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