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Separation and Performance lest of Wnitening Agent in Rhodiola Sachalinensis  

최두영 (초정밀생물분리기술연구센터, 인하대학교)
안소영 (초정밀생물분리기술연구센터, 인하대학)
이승기 (초정밀생물분리기술연구센터, 인하대학)
한정선 (초정밀생물분리기술연구센터, 인하대학)
김은철 (초정밀생물분리기술연구센터, 인하대학)
이향복 (초정밀생물분리기술연구센터, 인하대학)
신정현 (인하대병원 피부)
김은기 (초정밀생물분리기술연구센터, 인하대학)
노경호 (초정밀생물분리기술연구센터, 인하대학교)
Publication Information
KSBB Journal / v.19, no.3, 2004 , pp. 169-173 More about this Journal
Abstract
The Rhodiola Sachalinensis 5 g were mixed and extracted with methanol 150 $m\ell$ at the room temperature for 12 h. The effluents were collected and grouped into the two. Un this experimental condition, the mobile phase composition were linearly changed as follows; water/methanol : 90/10 - 30/70 (vol. %, for 5 min), 30/70 - 10/90 (vol. %, for 15 min) and an analytical column (3.9 ${\times}$ 25 em, 15 $\mu\textrm{m}$ particle size, and 300 ${\AA}$ pore size) was utilized. The performance of the extracted Rhodiola Sachalinensis as a whitening agent was not favorable, so it classifies the Rhodiola Sachalinensis extractions with two fractions and collects each fraction for whitening agent assay. For the in-vivo melanin production ratio assay that used melanin-a cell in 10 ppm concentration, it was 58.6%, the first fraction of the effluents collected between 1.0 and 4.0 min, while it was 60% between 10.4 and 17.6 min for the second fraction, which were more efficient than that of arbutin, 45.6%.
Keywords
Rhodiola Sachalinensis; HPLC; melan-a; melanin production ratio; tyrosinase inhibitory activity;
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