참비름(Amaranthus mangostanus ) 추출물의 미백 및 주름 개선 효과
Skin Whitening and Anti-wrinkle Effects of Chambirum (Amaranthus mangostanus)
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목적: 나물로만 사용되는 참비름(Amaranthus mangostanus) 추출물을 대상으로 화장품 소재적 특성을 조사하기 위하여 항산화 효과, 미백 활성 및 주름개선 효능을 진행하였다. 방법: 항산화 활성으로는 DPPH와 SOD-like activity, 미백활성으로는 tyrosinase 저해 활성과 melanin 함량을 조사하였고, 주름개선 효능으로는 elastase 저해 활성과 type 1 pro-collagen을 측정하였다. B16F10 mouse melanoma cells과 CCD986sk human dermal fibroblast cells을 대상으로 세포 생존력을 측정하였다. 결과: DPPH 방법으로조사한 항산화 활성은 시료의 농도 500 μg/mL의 농도에서 AME (49%), AMW (56%)의 radical 소거 활성을 나타내었고, SOD-like activity를 측정한 결과, 시료의 농도는 동일하게 500 μg/mL에서 AME (67%), AMW (57%)의 활성을 나타내었다. 미백활성으로는L-tyrosine을 기질로 사용한 tyrosinase 저해 활성은 AME (25.9%), AMW (23.4%)로 나타내었고 L-DOPA의 경우 AME (17.8%), AMW (18.5%)의 높은 미백효과를 확인 할 수 있었다. B16F10 mouse melanoma cell line을 대상으로 melanin양을 측정한 결과, AME (25.5%), AMW (27.8%)의 melanin 감소율을 나타내었다. 주름개선 효능으로는, 시료의 농도, 500 μg/mL에서 elastase 저해활성은 AME (19.7%), AMW (17.2%)로 조사되었고, type I procollagen의 collagen 양은 미미한 것으로 나타내었다. B16F10 mouse melanoma cells에 대한 세포 독성은 시료의 농도 100 μg/mL에서 AME (76%), AMW (86%)의 세포 생존율을 나타내었고, CCD- 986sk fibroblast cells에 대한 세포독성 결과는 시료의 농도 100 μg/mL에서 AME (94.5%), AMW (83.6%)의 생존율을 확인할 수 있었다. 결론: 참비름 추출물은 항산화 및 미백 활성에 탁월한 효능을 보여주었고, 천연물 유래의 화장품 소재로서의 가능성과 항노화산업의 잠재적인 소재로서의 가치를 확인할 수 있었다.
Abstract
To investigate the cosmetic effects of a chambirum (Amaranthus mangostamus ) extract on the skincare by measuring the extract’s antioxidant, antiwrinkle, and whitening. Methods: To confirm the antioxidant effect of chambirum, DPPH radical scavenging activity and SOD-like activity was determined. To confirm whitening effect of chambirum, tyrosinase inhibitory activity and melanin content were investigated. To confirm anti-wrinkle effect of chambirum, the elastase inhibition effect and type I procollagen production was assayed. B16F10 mouse melanoma cells and CCD986sk human dermal fibroblast cells were used to assay cell viability. Results: The DPPH radical scavenging activity of AME and AMW was 49% and 56%, respectively, at 500 μg/mL. The SOD-like activity of AME and AMW was 67% and 57%, respectively, compared with that of the standard sample L-ascorbic acid at 38% at 1 mM. AME showed 25.9% (L-tyrosine) and 17.8% (L-DOPA), and AMW showed 23.4% (L-tyrosine) and 18.5% (L-DOPA) of tyrosinase inhibition assay. In addition, the intracellular melanin production in B16F10 mouse melanoma cells was decreased by AME and AMW by 25.5% and 27.8%, respectively. Additionally, the elastase inhibition assay results demonstrated inhibition by AME (19.7%) and AMW (17.2%) at 500 μg/mL and the amount of type I procollagen was shown to be insignificant. Furthermore, B16F10 mouse melanoma cells were 76% and 86% showed a viability 76% and 86% when treated with 100 μg/mL AME and AMW, respectively. CCD-986sk fibroblast cells showed a viability 94.5% and 83.6% when we treated with 100 μg/mL AME and AMW, respectively. Conclusion: These results suggest that the chambirum (Amaranthus mangostamus) extract has excellent antioxidants, anti-wrinkle, and whitening effects. Therefore, it may have a significant industrial value as a functional material for cosmetic or anti-aging related bioproducts.
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