• 대한화장품학회지
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• 제42권4호
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• pp.421-432
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• 2016

본 연구에서는 화장품 신소재 개발을 위해 한의약적 포제법을 적용하여 흰점박이꽃무지 추출물을 제조하고 포제방법에 따른 항염 및 미백활성을 평가하였다. 모든 실험은 생(生), 1회 초법(炒法), 2회 초법(炒法), 3회 초법(炒法), 증법(蒸法)을 적용한 흰점박이꽃무지를 이용하였다. 각 포제법을 적용한 흰점박이꽃무지의 용매별 (80% 에탄올, 50% 에탄올, 에틸아세테이트, 헥산) 추출물에 대한 1,1-diphenyl-2-picrylhydrazyl (DPPH) 라디칼 소거 활성은 각각 85.5, 22.4, 37.0 및 19.4%의 효과를 나타내었다. 따라서 이후의 실험은 항산화 활성이 가장 큰 80% 에탄올 추출물을 이용하였다. 포제법을 적용한 흰점박이꽃무지 추출물과 포제법을 적용하지 않은 추출물 모두 농도 의존적으로 항산화능을 나타냈으며, $500{\mu}g/mL$ 농도에서 포제법을 적용한 3회 초법 및 증법은 superoxide dismutase (SOD)-like 활성이 각각 62.9 및 55.9%를 나타냈다. Lipopolysaccharide (LPS)로 염증이 유도된 RAW 264.7 세포에 포제법을 적용한 흰점박이꽃무지 추출물을 처리하였을 때, LPS를 단독으로 처리한 양성 대조군보다 포제법을 적용하지 않은 흰점박이꽃무지 추출물(38.0%), 1회 초법(41.0%), 2회 초법(69.8%), 3회 초법(70.1%), 증법(78.5%) 순으로 염증 매개물질인 $NO{\cdot}$ 생성이 유의적으로 감소하였다. 세포 내 tyrosinase 저해 활성 및 멜라닌 생합성 저해 효과를 확인한 결과, 농도 의존적으로 tyrosinase 저해 활성 및 멜라닌 생성 억제 활성을 나타내었다. 포제하지 않은 흰점박이꽃무지 추출물은 $500{\mu}g/mL$ 농도에서 ${\alpha}$-MSH만 처리한 대조군과 비교하여 멜라닌 생합성을 90.7% 감소시켰다. 이상의 결과들은 항염이나 미백활성이 있는 화장품 소재 개발에 포제법을 적용할 수 있음을 시사한다.

• Journal of Applied Biological Chemistry
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• 제61권1호
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• pp.51-57
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• 2018

영신초의 용매별 phenolic compounds는 열수 추출물과 추출 최적 농도인 50% 에탄올 추출물을 이용하여 실험을 진행하였다. 영신초 열수 추출물에 대한 항산화능을 DPPH, ABTS, PF, TBARs 실험으로 측정한 결과, $50-200{\mu}g/mL$의 농도 구간에서 각각 71.32-80.29%, 78.61-99.80%, 1.80-2.05 PF, 64.88-87.30%의 저해율을 나타냈고, 50% 에탄올 추출물에서는 각각 82.82-85.66%, 74.88-99.90%, 1.80-2.14 PF, 79.23-90.27%의 저해율을 나타냈다. 따라서, 영신초 50% 에탄올 추출물이 열수 추출물보다 항산화능이 더 우수한 것을 알 수 있었다. 영신초 열수 및 50% 에탄올 추출물의 미용식품 활성을 알아보기 위하여 tyrosinase 저해활성, elastase 및 collagenase 저해활성, hyaluronidase 저해활성을 측정하였다. Tyrosinase 저해활성은 $200{\mu}g/mL$의 농도에서 열수와 50% 에탄올 추출물은 각각 12.46, 22.10%를 나타냈다. Elastase 저해활성은 동일한 농도에서 각각 28.28, 58.36%, collagenase 저해활성은 각각 59.73, 78.90%를 나타냈으며, hyaluronidase 저해활성은 각각 35.65, 86.80%를 나타냈다. 또한 열수 추출물과 50% 에탄올 추출물 간의 생리활성의 차이는 phenolic profile의 차이에 의한 것이라 판단되었다. 이러한 결과에 따라, 영신초 열수 및 50% 에탄올 추출물은 항산화능이 높아 천연 항산화제로의 이용이 가능할 것으로 보이며, 특히 주름 개선 및 염증억제 효과가 뛰어난 것으로 나타나 기능성 식품 및 화장품 제조에 이용 가능한 천연 미용식품 소재로의 활용이 기대된다.

• 한국약용작물학회지
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• 제14권3호
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• pp.148-152
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• 2006

국내산 인삼의 부위별 quercetin, p-coumaric acid, maltol, esculetin의 함량을 측정한 결과 잎에서는 quercetin과 esculetin이 주근에서는 p-coumaric acid가 다량 함유되어 있었다. 이중잎의 EA 분획물은 melan-a 세포주에서 뛰어난 멜라닌 생성억제 활성을 보였으며, 이의 주요성분인 quercetin과 esculetin이 tyrosinase 활성억제도, melan-a 세포주에서의 멜라닌 생성억제도, UV-흡수도 측정에서 모두 우수한 활성을 나타내는 결과로 미루어 인삼의 잎은 피부미백을 목적으로 하는 기능성 소재로 이용될 수 있는 가능성을 가지는 것으로 사료된다.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 2005년도 춘계학술대회
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• pp.131-148
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• 2005

This study is peformed to investigate the effect of water extract from Vaccinium uliginosum L., on melanin production in B 16 melanoma cells, procollagen production and matrix metalloproteinase-1(MMP-1) inhibition in human fibroblast cells. One hundred grams of the Vaccinium uliginosum L. was extracted with 2000 mL of water($90^{\circ}C$, 16h, 2times). The water extracts were lyophilized and stored at $4^{\circ}C$ until used. Dry weight yields of extracts of Vaccinium uliginosum L. were $3\%$(w/w). Extracts from Vaccinium uliginosum L. showed scavenger activities on DPPH radical, superoxide anion radical, hydroxyl radical, hydrogen peroxide and singlet oxygen radical. And these substances inhibited release of cyiokines from human keratinocyte after UV B exposure. Therefore we confirmed that extracts from Vaccinium uliginosum L. had antioxidative effect. These substances inhibited purified tyrosinase activity and melanogenesis in B 16 melanoma cells treated/untreated IL-$1{\alpha}$. Moreover this extract stimulated procollagen production and inhibited MMP-1 production in human fibroblast cells treated/untreated IL-$1{\beta}$. Therefore we confirmed that extracts from Vaccinium uliginosum L. had whitening effect. And these substances decreased degree of wrinkle in hairless mouse skin that induced by UV B irradiation. Therefore we confirmed that extracts from Vaccinium uliginosum L. had anti-wrinkle effect. From the above results, it is possible that Vaccinium uliginosum L. may be developed to be an anti-melanogenesis agent and anti-wrinkle agent.

• 한국약용작물학회지
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• 제19권6호
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• pp.478-483
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• 2011

The goal of this study was to investigate the nutritional characteristics and physiological functionality of Liriope tuber for development of new bioactive compound from Liriope tuber. Crude protein and carbohydrate contents of Chenogsim were 9.25% and 77.98%, respectively and crude protein, 9.86% and carbohydrate, 79.08% were also contained in Liriope tuber No.1. Both of Liriope tubers were showed very high contents of sucrose (Cheongsim; 4.08%, Liriope tuber No.1; 4.91%), oxalic acid (0.98%, 0.86%) and glutamic acid (3.736 g/100 g, 4,196 g/100 g). Among several physiological functionalities, tyrosinase inhibitory activity were showed very high 86.4% in Cheongsim and 82.02% in Liriope tuber No.1, respectively.

• 한국약용작물학회지
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• 제22권4호
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• pp.255-261
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• 2014

Cosmetic activities of the leaves of Curcuma longa L. were compared according to different drying methods, to expand the use of the by-products of Curcuma longa L. The highest extraction yield of 29.4% was obtained from vacuum drying process (VD), whose value was very close to 29.2% from freeze drying process (FD). Relatively lower extraction yield were observed as 24.5% and 25.3% from the raw leaf (RL) as control and hot air drying process (HD). The cytotoxicity was observed lower FD and VD than RL and HD. It shows that cytotoxicity was closely related to cosmetic activities such as tyrosinase and melanin inhibition activities by showing much better cosmetic activities of the extracts from both FD and VD than those from the RL and HD. It was interesting that was differences of the cosmetic activities and cytotoxicity between FD and VD, which implies that VD method should be a more efficient process than FD method in terms of drying time and operation costs: 6 hours vs 24 hours and 3-5 times higher extraction costs in drying. It was observed that VD is more excellent dry method than others. This result could be utilized to effectively dry other soft plant biomass.

• Biomolecules & Therapeutics
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• 제21권5호
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• pp.343-348
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• 2013

We investigated the inhibitory effects of hesperidin on melanogenesis. To find melanosome transport inhibitor from natural products, we collected the structural information of natural products from Korea Food and Drug Administration (KFDA) and performed pharmacophore-based in silico screening for Rab27A and melanophilin (MLPH). Hesperidin did not inhibit melanin production in B16F10 murine melanoma cells stimulated with ${\alpha}$-melanocyte stimulating hormone (${\alpha}$-MSH), and also did not affect the catalytic activity of tyrosinase. But, hesperidin inhibited melanosome transport in melanocyte and showed skin lightening effect in pigmented reconstructed epidermis model. Therefore, we suggest that hesperidin is a useful inhibitor of melanosome transport and it might be applied to whitening agent.

• 대한화장품학회:학술대회논문집
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• 대한화장품학회 2003년도 IFSCC Conference Proceeding Book I
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• pp.733-740
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• 2003

To find a new substance with superior melanogenesis inhibitory activity, the bioactivities of alkyl-3,4-dihydroxy-5-substituted benzoate (A) and N-alkyl-3,4-dihydroxy-5-substituted benzamide (B) derivatives as substrate of tyrosinase were measured in mouse melanoma cells. And the bioactivities analyzed using comparative molecular similarity indices analysis (CoMSIA). From the CoMSIA model, when cross-validation value (q$^2$) is 0.713 at four components, the pearson correlation coefficient ($r^2$) is 0.900. Unknown compounds were predicted, using QSAR analyzed results from the CoMSIA methods. Excellent agreement was obtained between the measured and the predicted bioactivities of unknown compounds. As the results of prediction from CoMSIA, we could conclude that the bioactivities were increased from pl$_{50}$=3.18-4.80 to above 5.17 by creation of 6-methylheptyl, n-pentylphenyl and 2-hydroxypentylphenyl group etc,.,.

• Bulletin of the Korean Chemical Society
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• 제30권10호
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• pp.2345-2350
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• 2009

As part of an effort to discover bioactive natural products from marine sources, we investigated the bioactive secondary metabolites from two marine isolates of the fungi, Trichoderma viride and Rhizopus stolonifer. Three cyclopentenones, myrothenones A (1) and B (2) and trichodenone A (3), were isolated from T. viride and two cyclopentenones, 2-bromomyrothenone B (4) and botrytinone (5), were isolated from R. stolonifer. The molecular structures and absolute stereochemistries of the cyclopentenones were determined from chemical and physicochemical evidence, including quantum chemistry calculations, X-ray analysis, and the circular dichroism (CD) exciton chirality method. Myrothenone A (1) displays tyrosinase inhibitory activity, with an I$C_{50}$ value of 6.6 ${\mu}M$, and is therefore more active than the positive control, kojic acid.

• 한방안이비인후피부과학회지
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• 제17권2호
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• pp.59-71
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• 2004

Melanin pigmentation has an essential role in protecting human skin against the damaging effects of ultra violet radiation, infection, environmental factor, etc. However abnormal melanin pigmentation can directly cause a number of congenital and acquired pigmentary skin disease. This study conducted to evaluate the effects of various partition extracts of Codonopsis lanceolata on the melanogenesis in the B 16 melanoma cells. The cells were treated for 3 days with various partition extracts of Codonopsis lanceolata. While treatment with the BuOH partition extract of Codonopsis lanceolata increased significantly the tyrosinase activity and melanin content, the n-Hexane or ethyl acetate partition extract dose-dependently suppressed them compared with untreated control. But ethyl acetate partition significantly decreased the cell viability. The H2O partiton extract at various concentrations did not exhibit any significant change on the melanogenesis. These results indicate that treatment with the n-Hexane partition extract inhibits the melanogenesis in B16 melanoma cells, and raise the possibility that this extract may be effective in the abnormal melanin pigmentation as well as the whitening agent for the skin.