Composition for alleviating ultraviolet radiation-induced damage
By using a composition of free methionine and its derivatives, the problem of instability and unsafety of ultraviolet damage preventive agents in the prior art is solved, and a stable and safe ultraviolet damage reduction method is provided, suitable for daily use and treatment of ultraviolet rays Caused skin diseases and cataracts.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0061] UV damage reduction effect of methionine
[0062] method
[0063] cell culture
[0064] As the cells, commercially available human neonatal dermal fibroblasts (Cryo NHDF-Neo, Sanko Junyaku) were used. The cells according to 2×10 5Cells / mL were inoculated in a commercially available 35mm diameter Petri dish (BD FALCON 353001, Becton Dickinson, Japan), using a commercially available cell culture medium (D-MEM (1g / L glucose), Wako Pure Medicine) supplemented with 10% fetal bovine serum (hereinafter referred to as "common medium") for culture. The cells can be cultured in a medium supplemented with 1% antibiotic (15240-062, GIBCO) in the normal medium. The cells were incubated at 37°C, 5% CO 2 and cultivated under saturated water vapor conditions for about 24 hours.
[0065] Afterwards, the medium used for culturing the cells was replaced with 1×10 -3 % BSO medium 1 mL of BSO (L-buthionine-(S, R)-sulfoximine, Wako Pure Chemical Industries, Ltd.) as a biosynthesis inh...
Embodiment 2
[0086] UV damage reduction effect of serine
[0087] method
[0088] Cell culture, amino acid addition before ultraviolet irradiation, ultraviolet irradiation, amino acid addition after ultraviolet irradiation, and quantification of cell damage were performed in the same manner as in Example 1. With 7.5 or 9J / cm 2 Irradiate with ultraviolet rays (UV-A). When studying the effect of adding serine before ultraviolet irradiation (hereinafter referred to as "serine before irradiation") and adding serine after ultraviolet irradiation (hereinafter referred to as "serine after irradiation"), 0.0001 to 100 μM of L-serine (197 -00403, Wako Pure Chemicals) and D-serine (197-08823, Wako Pure Chemicals). The effect of adding serine after irradiation was evaluated by irradiating cells with 7.5 J / cm 2 After UV-A, return to normal culture medium for 21 hours, and add D-serine to the 21-hour culture medium for evaluation.
[0089] Results of adding serine before irradiation (1)
[0090] ...
Embodiment 3
[0099] UV damage reduction effect of D-cycloserine
[0100] method
[0101] Cell culture, amino acid addition before ultraviolet irradiation, ultraviolet irradiation, amino acid addition after ultraviolet irradiation, and quantification of cell damage were performed in the same manner as in Example 1. at 9J / cm 2 Irradiate with ultraviolet rays (UV-A). When examining the effect of adding D-cycloserine before ultraviolet irradiation (hereinafter referred to as "addition of D-cycloserine before irradiation"), 0.0001 to 100 μM of D-cycloserine (C6880, Sigma) was used.
[0102] Result of adding D-cycloserine before irradiation
[0103] Figure 7 shows the effect of investigating the effect of adding D-cycloserine on irradiation by UV-A9J / cm 2 Experimental results of the damage effect of ultraviolet rays on fibroblasts. The error bar of each experimental condition represents the standard deviation of the measured value of the experimental result repeated 3 to 4 times under the...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com