Anti-androgenic agent, sebum secretion blocker, hair growth stimulant, and food or beverage
An anti-androgen and sebum secretion technology, applied in the field of sebum secretion inhibitors and hair growth agents, can solve the problems of no lactoferrin, no specific disclosure details, no anti-androgen effect, etc., to achieve high efficacy and safety excellent effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0038] Testosterone 5α-reductase inhibition test
[0039]
[0040] 1. Add 0.5 ml of 5 mM Tris-HCl buffer (pH7.2) to 0.1 ml of 3.0 mM testosterone solution (dissolved in propylene glycol).
[0041] 2. Add 0.1ml of 6.7mM NADPH solution (dissolved in 5mM Tris-HCl buffer (pH7.2)) and 0.05ml of sample solution (dissolved in 50% ethanol), preheat at 37°C, then add enzyme solution (S-9, oriental yeast (オリエンタル yeast)) 0.1ml, keep the temperature for 1 hour.
[0042] In this test, bovine-derived lactoferrin was prepared and used as lactoferrin, and Nokogiriyashi was used as a control.
[0043] 3. Then, add 3ml of dichloromethane to stop the reaction, add 0.5ml of internal standard solution (0.1mg / ml n-hexyl p-hydroxybenzoate), shake for 10 minutes, and centrifuge at 3000rmp for 10 minutes.
[0044] 4. Separate the dichloromethane layer and dry it under reduced pressure. 5 ml of methanol was added to the dried product to dissolve it to prepare a sample solution. The content of tes...
Embodiment 2
[0053] androgen receptor binding inhibition test
[0054]
[0055] 1. Use MEM medium containing 2% DCC-treated FCS to 1.0×10 4 The cell density of cells / well / 100μl seeded androgen-dependent mouse breast cancer cell SC-3 cells in 96-well microplates, at 37°C, 5% CO 2 Cultured under -95% air.
[0056] 2. After 24 hours, replace the culture medium with the addition of the test sample and 10 -8 M in DHT's HMB medium (Ham F12+MEM medium containing 0.1% BSA), cultured for 48 hours.
[0057] In this test, bovine-derived lactoferrin was prepared and used as lactoferrin, and spironolactone was used as a positive control.
[0058] 3. Next, the absorbance at 570 nm, which is the maximum absorption point of formazan blue (ブル-ボルマザン), was measured by the MTT reduction method to evaluate cell proliferation.
[0059] In order to correct the influence of attached cells, the absorbance at 650nm was also measured, and the difference between the two absorbances was used as the amount of for...
Embodiment 3
[0068] Sebocyte culture test
[0069]
[0070] 1. In this test, hamster sebocyte culture kit KB-1000 (manufactured by Kuraboo Co., Ltd.) was used for the test.
[0071] Sebocytes from normal golden hamster auricle were seeded in 24-well plates at a density of 5.0×104 cells / well. During the test, at 1×10 -6 The concentration of M was cultured in medium containing testosterone.
[0072] 2. Cultivate for several days until confluence, and then, exchange to the medium containing the test sample. The medium was exchanged with the sample medium every other day, and the culture was continued for about 2 weeks.
[0073] In this experiment, lactoferrin from bovine was prepared and used as lactoferrin, and spironolactone was used as a control.
[0074] 3. Next, the WST-8 solution was added to each well using a sebum synthesis assay kit SE-3001 (manufactured by Kuraboo Co., Ltd.), and incubated at a constant temperature of 37° C. for 30 minutes. The supernatant was measured at a w...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com