Przejdź do zawartości
Merck

Anti-photoaging capability of antioxidant extract from Camellia japonica leaf.

Experimental dermatology (2014-09-23)
Taeko Mizutani, Hitoshi Masaki
ABSTRAKT

It is well known that the Camellia japonica leaf exhibits antioxidant activity because of its high content of polyphenolic compounds. Thus, the extract prepared from mature leaves of C. japonica (CJML) has been widely used as an anti-ageing material in foods and cosmetics. Concerning the process of growing C. japonica, it is expected that the extract from green leaves (CJGL) has superior effects compared with that from mature leaves. However, there are few reports that discuss the difference between green and mature leaves. In this study, both CJML and CJGL were extracted with 50% 1,3-butylene glycol (1,3-BG) and used for investigations. In a chemical examination, we compared both extracts in terms of scavenging activities against hydrogen peroxide (H2 O2 ) and hydroxyl radicals. CJGL exhibited higher scavenging activities against both types of ROSs compared with CJML. In addition, CJGL reduced the carbonylation of tape-stripped stratum corneum (SC) after UVB irradiation. In a biological study, the intra-cellular ROS level of HaCaT keratinocytes precultured with CJGL for 24 h was significantly lower than that of the control cells. Furthermore, cell damage induced by H2 O2 exposure was attenuated by 24 h precultivation with CJGL but not by 2 h precultivation. The results of examinations indicate that CJGL possess properties that reduce oxidative stress. In addition, the result of 2 h precultivation with CJGL suggests that CJGL might affect the status of intra-cellular antioxidants.

MATERIAŁY
Numer produktu
Marka
Opis produktu

Supelco
Hydrogen peroxide solution, 30 % (w/w), for ultratrace analysis
Supelco
5,5-Dimethyl-1-pyrroline N-oxide, for ESR-spectroscopy
Millipore
Hydrogen peroxide solution, 3%, suitable for microbiology
Sigma-Aldrich
Hydrogen peroxide solution, tested according to Ph. Eur.
Sigma-Aldrich
Methylamine solution, 33 wt. % in absolute ethanol ((denatured with 1% toluene))
Supelco
Hydrogen peroxide solution, ≥30%, for trace analysis
Sigma-Aldrich
Hydrogen peroxide solution, 34.5-36.5%
Sigma-Aldrich
Methylamine solution, 2.0 M in methanol
Sigma-Aldrich
Methylamine solution, 2.0 M in THF
Sigma-Aldrich
Methylamine solution, 40 wt. % in H2O
Sigma-Aldrich
Hydrogen peroxide solution, 30 % (w/w) in H2O, contains stabilizer
Sigma-Aldrich
Hydrogen peroxide solution, contains inhibitor, 30 wt. % in H2O, ACS reagent
Sigma-Aldrich
Hydrogen peroxide solution, contains inhibitor, 30 wt. % in H2O, meets USP testing specifications
Sigma-Aldrich
Hydrogen peroxide solution, 50 wt. % in H2O, stabilized
Sigma-Aldrich
MES solution, BioUltra, Molecular Biology, 0.5 M in H2O
Supelco
Phenol solution, certified reference material, 500 μg/mL in methanol
Supelco
Phenol solution, 5000 μg/mL in methanol, certified reference material
Sigma-Aldrich
Phenol, ≥99%
Sigma-Aldrich
Phenol, BioUltra, Molecular Biology, ≥99.5% (GC)
Sigma-Aldrich
Phenol, ACS reagent, ≥99.0%
Sigma-Aldrich
Phenol, unstabilized, ReagentPlus®, ≥99%
Sigma-Aldrich
Phenol, puriss., meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (GC)
Supelco
o-Xylene, analytical standard
Sigma-Aldrich
Fluorescein-5-thiosemicarbazide, suitable for fluorescence, ~80% (HPCE)
Sigma-Aldrich
Phenol, ≥96.0% (calc. on dry substance, T)
Sigma-Aldrich
Phenol, BioUltra, Molecular Biology, TE-saturated, ~73% (T)
Sigma-Aldrich
Phenol solution, Saturated with 0.01 M citrate buffer, pH 4.3 ± 0.2, BioReagent, Molecular Biology
Sigma-Aldrich
Phenol, BioXtra, ≥99.5% (GC)
Sigma-Aldrich
Phenol, Molecular Biology
Sigma-Aldrich
Liquified Phenol, ≥89.0%