원문정보
Anti-inflammatory and Skin Whitening Activity of Chaetomorpha torta Extract
초록
영어
This study evaluated the antioxidant activity of the extract from Chaetomorpha torta, and measured its anti-inflammatory and whitening activities. First, the antioxidant activity was evaluated, and the EC50 was found to be 4.68 ± 0.68 mg/mL in the DPPH radical scavenging assay, and 8.99 ± 2.70 mg/mL in the ABTS radical scavenging assay. Total phenolic contents and total flavonoid contents were found to be 9.65 ± 0.64 mg gallic acid/g and 2.93 ± 0.06 mg quercetin/g. Subsequently, a cell experiment using B16F10 was conducted to investigate the whitening activity. In the whitening activity assay, there was no cytotoxicity in the range of 12.5-100 μg/mL, and a melanin synthesis inhibition effect of 32.5 ± 3.3% was observed at 100 μg/mL. To investigate the anti-inflammatory activity, a cell experiment using Raw 264.7 was performed. In the anti-inflammatory activity assay, there was no cytotoxicity in the range of 12.5-100 μg/mL, and 80.3 ± 1.6% inhibition of NO production was observed decreasing proportionally to the extract treatment concentration.
한국어
본 연구는 녹조류인 Chaetomorpha torta 추출물의 항산화능을 평가하고, 이를 바탕으로 항염 활성 측정 과 미백 활성 측정을 진행하였다. 먼저 항산화능의 측정을 진행하여 DPPH 라디칼 소거능 측정에서 EC50은 4.68±0.68 mg/mL로 나타났으며, ABTS 라디칼 소거능 측정에서 EC50은 8.99±2.70 mg/mL로 나타났다. Total phenolic contents와 total flavonoid contents는 각각 9.65±0.64 mg gallic acid/g, 2.93±0.06 mg quercetin/g으 로 나타났다. 그 후 미백 활성을 알아보기 위해 B16F10을 이용한 세포실험을 진행하였다. 미백 활성 측정에서 세 포 독성은 12.5-100 μg/mL의 구간에서 세포독성을 나타내지 않았으며, 100 μg/mL에서 32.5±3.3%의 멜라닌 생성 억제효과를 나타내었다. 항염 활성을 알아보기 위해서 Raw 264.7을 이용한 세포실험을 진행하였다. 항염 활성 측 정에서 세포 독성은 12.5-100 μg/mL의 구간에서 세포독성을 나타내지 않았으며, 100 μg/mL에서 80.3±1.6%의 NO 생성 억제효과를 나타내었다.
목차
Abstract
Ⅰ. 서론
Ⅱ. 실험방법
2.1 Chaetomorpha torta 추출물 제조
2.2 DPPH assay
2.3 ABTS assay
2.4 Total phenolic contents assay
2.5 Total flavonoid contents assay
2.6 MTT assay
2.7 Melanin assay
2.8 NO assay
Ⅲ. 결과 및 고찰
3.1 DPPH scarvenging activity
3.2 ABTS scarvenging activity
3.3 TPC & TFC of C. torta extract
3.4 Cytotoxicity evaluation by MTT assay
3.5 Anti melanin activity
3.6 Anti inflammation activity
Ⅳ. 결론
REFERENCES
