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정제봉독(PBV)과 분리정제봉독(IPBV), 봉독아민(BVA)분획시료에 대한 화장소재로서의 효능비교The Efficacy Comparison as Cosmetic Materials for Purified Bee Venom, Isolated Bee Venom, and Bee Venom Amines

Other Titles
The Efficacy Comparison as Cosmetic Materials for Purified Bee Venom, Isolated Bee Venom, and Bee Venom Amines
Authors
신연희김일광김의경김철구
Issue Date
2014
Publisher
한국미용학회
Keywords
Antioxidant; Bee venom; Cosmetic materials; MTT assay; Whitening effect
Citation
한국미용학회지, v.20, no.6, pp 967 - 975
Pages
9
Indexed
KCI
Journal Title
한국미용학회지
Volume
20
Number
6
Start Page
967
End Page
975
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/19480
ISSN
1229-4349
Abstract
The skin care efficacies for three fractions of bee venom as cosmetic raw materials were evaluated. The purified bee venom(PBV) was obtained by removing non-soluble species and bacteria through 0.2 μm syringe filter from the collected bee venom with Chung Jin Biotech’s electrical shock collector. PBV was treated to isolated bee venom(IPBV) with ultrafiltration of 10 KDa membrane and bee venom amines(BVA) with ultra filtration of 1 KDa membrane. The properties of these bee venoms were measured and evaluated by DPPH radical scavenging assay, tyrosinase inhibitory effect, elastase inhibitory effect, and MTT assay for cytotoxicity. As a result of the experiment, DPPH radical scavenging abilities were confirmed that 0.32 ±0.04 mg/mL for PBV, 0.53 ± 0.10 mg/mL for IPBV, and 0.09 ± 0.01 mg/mL for BVA as the half maximal inhibitory concentration, and tyrosinase inhibitory effect as IC50 were confirm each sample concentration of PBV, IPBV and BVA to 2.93 ± 0.01 mg/mL, 4.65± 0.012 mg/mL and 2.19± 0.01 mg/mL. The result of Elastase inhibitory effect were observed 2.09 ±0.031 mg/mL to PBV, 1.62 ±0.012 mg/mL to IPBV and none to BVA as value of IC50. It is shown that the cell viability concentration is 90% above 0.4 ±0.01 μg/mL in PBV, above 0.64±0.012 μg/mL in IPBV and 110 ± 0.01 μg/mL in BVA, respectively. There were almost same tendency between PBV and IPBV, while BVA showed better antioxidant activity and whitening effect with no citotoxicity.
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