Antioxidant activities and α-glucosidase inhibitory activities of Taraxacum officinale solvent fractions were measured. Extraction yields (relative to raw material) of 50% ethanol, hexane, ethyl acetate, butanol, and water were found to be 10.29, 2.61, 5.54, 2.15, and 0.96%, respectively. Polyphenol and flavonoid contents were high in ethyl acetate extract of Taraxacum officinale at 56.88 mg gallic acid/g and 33.27 mg gallic acid/g, respectively. DPPH, hydroxyl radical scavenging activity, and SOD-like activity measurement (IC50%) of Taraxacum officinale 50% ethanol extract, hexane, butanol, ethyl acetate, and water fractions were 22.64, 18.65, 10.29, 20.81, 20.46 mg/mL, 24.68, 10.69, respectively. It was found to be 9.66, 15.81, 13.77 mg/mL, 32.84, 17.09, 12.73, 33.63, and 33.91 mg/mL, and was high in the ethyl acetate layer. Results showed that α-glucosidase inhibitory activities of Taraxacum officinale solvent fraction were 25.75, 15.93, 35.87, 15.96, and 2.88% for 50% ethanol extract, hexane, butanol, ethyl acetate, and water fractions, respectively.

The antioxidant activity and α-glucosidase inhibitory activity of the solvent fraction fractionated from the methanol extract of Saururus chinensis Baill were examined. As a result of measuring the yields of methanol, hexane, chloroform, ethylacetate, butanol, and water fractions, the extraction yield of fraction was 18.60, 3.38, 24.03, 7.75, 8.11 and 62.57%, respectively. The total polyphenol content of the methanol extract of Saururus chinensis Baill was 13.40, 4.62, 7.39, 31.24, 25.76 and 5.64 mg GAE/g, respectively. DPPH radical scavenging activity (IC50%) results were 20.81, 5.47, 10.15, 22.63, 19.68 and 21.06 ug/mL, respectively, and hydroxyl radical scavenging activity (IC50%) results were 15.81, 2.69, 8.84, 12.80, 3.70 and 3.39 ug/mL. Hydrogen peroxide scavenging activity scavenging activity measurement (IC50%) showed 33.63, 8.88, 16.93, 32.84, 33.79, and 33.71 ug/mL in methanol, hexane, chloroform, ethyl acetate butanol, and water fractions, respectively. The α-glucosidase inhibitory activity of the solvent fraction fractionated with the methanol extract of 300 sec was measured for the α-glucosidase inhibitory activity of methanol, hexane, chloroform, ethyl acetate butanol, and water fraction, respectively, 15.85, 10.84, 15.74, 24.90, 2.58 and 35.70%.

본 연구에서는 해삼속의 폴리페놀과 플라보노이드의 생리활성물질을 추출하기 위한 용매분획의 수율을 확인하고자 연구를 시도하였다. 이미 보고된 사례에서 50%에탄올 추출 용매분획은 해삼 항산화 물질의 높은 수율 결과로 확인되었다. 해삼의 항산화물질 추출량을 결정짓는 것은 추출에 적용된 추출용 매분획의 결과로 확인되었다. 또한 ‘추출용매에 따라 해삼생리활성 항산화물질 추출함량이 크게 차이가 있다.’는 선행연구를 통해 용매분획추출에 관한 필요성의 결과를 얻었다. 50%에탄올 추출 용매분획의 해삼추 출물에 포함된 페놀물질의 높은 항산화성분 추출 결과가 증명되었다. 추출용매분획 연구사례에서 수율이 가장 저조한 아세트산에틸 용매분획은 다른 용매분획에 비해 높은 페놀함량을 수확하여 항산화효과가 확인되었다. 이에, 추출 용매분획물의 적용에 따른 수율변화를 통해 항산화추출물의 높은 수율에 미치는 영향을 확인 하였다. 따라서 본 연구를 통해 50%에탄올 용매의 최적화된 해삼생리활성물질 추출 용매분획으로 검증되었다.

The purpose of this study was to investigate the antioxidant activity and tyrosinase inhibitory activity of Codonopsis lanceolata 50% ethanol extract, and its solvent fractions (n-hexane, ethyl acetate (EA), n-butanol, water). The main components of the EA fraction were qualitatively analyzed using UPLC Q-ToF/MS. Additionally, a quantitative analysis was performed using UPLC. As a result, the total polyphenol content was 113.36 mg gallic acid/g in the EA fraction, which contained the largest amount of the C. lancolata solvent fractions. Also EA showed the highest antioxidant activity than other fractions. The IC50 of DPPH(2,2-diphenyl-1- picrylhydrazyl) radical scavenging activity was 0.03 mg/mL and the IC50 of ABTS [2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonate)] radical scavenging activity was 0.049 mg/mL. The EA fraction showed tyrosinase inhibitory activity than other fractions and especially inhibited monophenolase oxidase reaction higher than diphenolase oxidase reaction. The monophenolase oxidase inhibited 55% when the concentration of the EA fraction was 0.25 mg/mL. As a result of Q-ToF/MS analysis, it was confirmed that tangshenoside I and lobetyolin were the main components of EA fraction. Thus, these results suggest that C. lanceolata may be used as a potent source of cosmetic agents.

야생 잎새버섯 추출물을 이용하여 심혈관계 질환과 관련된 기능성 식품 개발을 위한 기초자료를 얻기 위해 준비한 물 추출물과 유기용매 분획물의 혈전용해활성과 트롬빈저해활성, acetylcholinesterase 저해활성, 항산화활성을 확인하였다. 10 mg/mL의 농도에서 물 추출물과 물 분획물은 각각 0.93 plasmin unit와 0.73 plasmin unit의 높은 혈전용해활성을 나타냈으며, 부탄올 분획물은 79.60%의 트롬빈저해활성을 나타냈다. 클로로포름 분획물은 85.88%의 높은 acetylcholinesterase 저해활성을 나타냈고, 물 추출물의 항산화 활성은 39.81%로 비교적 낮게 나타 냈다. 부분 정제된 효소를 포함하고 있는 물 분획물은 섬유소원의 Bβ chain를 모두 분해시켰지만, Aα chain은 느리게 분해시키고 γ chain 과는 반응하지 않았다. 실험 결과로부터 야생 잎새버섯 추출물은 높은 혈전용해활성과, 트롬빈저해활성, acetylcholinesterase 저해활성을 나타내 심혈관계 질환 예방을 위한 제약과 기능성식품 개발에 이용 가능할 것으로 기대된다.

This study was performed in order to analyze the fibrinolytic, thrombin inhibitory, anti-oxidative, acetylcholinesteraseinhibitory, and immuno-enhancing activities of the water extract and solvent fractions isolated from Grifola frondosa. Fibrinolyticactivity was analyzed using the fibrin plate method, and thrombin inhibitory activity was assayed using the substrate H-D-Phe-pip-arg-pna. Anti-oxidative activity was estimated using the DPPH assay, and AChE inhibitory activity was measured using thespectrophotometric method. Immuno-enhancing activity was examined using the nitric oxide (NO) production in RAW 264.7macrophage cells. Cell viability was determined using the MTS assay. Fibrinolytic activities were the highest in water extract (1.55plasmin units/mL) followed by water fraction (0.85 plasmin units/mL). The thrombin inhibitory activities of the water and ethylacetate fractions were determined to be 76.43% and 72.59%, respectively. The acetylcholinesterase inhibitory activities ofchloroform and hexane fractions exhibited values of 95.14% and 94.74%, respectively. The butanol fraction showed the highestanti-oxidative activity at 94.47%. Anti-proliferating activity against Raw 264.7 cells showed no cytotoxicity. The production of NOin Raw 264.7 cells increased up to 2-fold by adding the water fraction compared to the untreated control. These results suggestthat Grifola frondosa may serve as a useful functional food for the enhancement of immune function and the prevention andtherapy of cardiovascular diseases.

This study was designed to determine the antioxidant activity of solvent fractions of broccoli sprouts grown by controlling the growing environment at the plant factory system. Fractionation was achieved with chloroform, n-hexane, ethyl acetate, butanol, water by 70% EtOH extract of the broccoli sprouts. Each solvent fraction was put through TLC and HPLC to separate active components. Higher antioxidant activities were observed for the butanol and ethyl acetate layers. Further evaluation of each of the 5 layers (LH1 to LH5) of the butanol fraction showed that the refined LH3 extract had a high antioxidant effect. Components with similar Rf values from TLC had the same retention times and peaks in the HPLC analysis. It was also determined that the sulforaphane content was high at the chloroform and butanol layers and the sulforaphane was responsible for, the high antioxidant activity. Thus, to use for functional materials, the butanol extract/layer of broccoli sprouts is recommended as the most effective.

The purpose of this study is to determine the possibility of using Crataegi fructus as natural health food source. The research was conducted to determine the biofunctional activities of Crataegi fructus extract. Methanolic extract from Crataegi fructus was partitioned by using organic solvents, including n-hexane, ethyl acetate, n butanol, and water. Ethyl acetate soluble fraction was shown to have the strongest antioxidant activity (RC₅₀=4.39 ㎍/㎖) among the fractions. In the antimicrobial activity assays, ethyl acetate soluble fraction was effective in bacterial inhibition, against the cases of Escherichia coli and Klebsiella pneumonia, with minimum inhibitory concentrations in 125 ㎍/㎖. In the anticomplementary activity assays, water soluble fraction was the most effective exhibiting 18.4% inhibitory activity.

Twenty four fractions by solvent extraction and/or acid precipitation from fruit body and culture broth of Inonotus obliquus were prepared, and their inhibitory effect against acetylcholinesterase (AChE) was investigated. Among these fractions, acid (1 M HCl) precipitates from cell-free culture broth and fruit body exhibited the highest inhibitory effect on AChE in vitro. Acid precipitates inhibited AChE activity in a concentration-dependant manner and IC50 values of both acid precipitates were 0.53 mg/mL. The inhibition pattern was general non-competitive inhibition. The energetic parameters were also determined by dual substrate/temperature design. Both acid precipitates increased the values of Ea, ΔH, ΔG and ΔH* decreasing the value of ΔS for AChE. The results implied that the acid precipitates from I. obliquus increased the thermodynamic barrier, leading to the breakdown of ES complex and the formation of products as inhibitory mechanism.

핑크팝 보리수 열매와 잎을 기능성 식품의 재료로 활용하기 위하여 항산화 및 총 페놀성 화합물 함량을 측정한 결과는 다음과 같다. DPPH 및 ABTS radical 소거활성을 측정한 결과 분획물의 농 도가 증가함에 따라 DPPH 및 ABTS radical 소거활성이 증가하는 경향을 보였으며, 특히 잎의 부 탄올 분획물에서 가장 높은 DPPH radical 소거활성을 보였다. 또한 ABTS 라디칼 소거활성도 열매 와 잎의 여러 분획물 중 잎의 부탄올 분획물에서 가장 높은 소거활성을 보였다. 환원력과 FRAP 활 성도 분획물의 농도가 증가함에 따라 환원력과 FRAP 활성이 증가하는 경향을 보였으며, 잎의 부탄 올 분획물에서 가장 높은 환원력과 FRAP 활성을 보였다. Linoleic acid를 이용한 자동산화 억제활 성을 실험한 결과 다른 분획물에 비하여 부탄올 분획물에서 가장 높은 과산화 억제활성을 나타내었 으며, 총 페놀성 화합물은 잎과 열매의 부탄올 분획물에서 각각 106.34 및 252.46 mg/g으로 가장 높은 함량을 보였다. 핑크팝 보리수 잎 부탄올 분획물의 항산화 활성은 페놀성 화합물에 의한 것이 며, 이는 자유 라디칼에 의해 유발된 산화적 스트레스를 효과적으로 방어할 수 있을 것이다.

대두유에 율피의 용매분획별(에테르, 부탄올, 물) 추출물과 tocopherol, BHA를 각각 0.02% 첨가한 후 자동산화 및 가열 산화시 항산화효과를 비교하였다. 1. 자동산화시 과산화물가를 통한 항산화력 비교에서 45℃에서 42일간 저장한 경우 부탄올추출물 〉 에테르추출물 〉 무첨가구 〉 BHA 〉 토코페롤 순으로 항산화력이 있었고, 60℃에서 32일간 저장한 경우에도 부탄올 추출물이 강한 항산화력을 보였으며, 에테르추출물은 무첨가구와 큰 차이가 없었다. 2. 가열산화의 경우 에테르추출물이 우수한 항산화력을 나타내었다. 3. 추출물의 용매별 항산화성분의 분석결과 에테르추출물에는 ellagic acid, quercetin, morin, naringenin, flavanol로서 주요성분은 ellagic acid이었다. 이들 성분의 총량은 에테르추출물 49.09%(w/w), 부탄올추출물 76.26%(w/w)로서 부탄올 추출물에 폴리페놀성분이 다량 함유되어있어 우수한 항산화효과에 영향을 미친 것으로 판단된다. 부탄올추출물에는 ellagic acid, naringenin, gallic acid, flavanol이 있었으며, 주요성분은 naringenin, gallic acid로서 이들 성분들이 항산화 효과에 영향을 미친 것으로 사료된다.

솔잎의 향기성분을 용매분획과 수증기증류법으로 분석한 결과는 다음과 같다. 솔잎을 hexane, ethyl acetate 및 ethanol로 연속적으로 추출하였을 때, 29종의 향기성분이 분리, 확인되었고, 주요 성분은 hydrocarbon이었다. hexane 추출에 의한 솔잎의 주요 향기성분은 α-pinene, β-thujene, trans-caryophyllene, β-cubebene 순으로 높게 나타났다. 솔잎을 hexane으로 추출한 잔사에 ethyl acetate를 가하여 향기 성분을 분석하였을 경우 추출된 향기성분은 α-cubebene, 3,6,9,12,15-petaoxanonadecan-1-ol, camphene, 순으로 높았고, 솔잎을 hexane 및 ethyl cetate로 추출한 잔사에 ethanol을 가하여 분석한 경우는 β-D4-tetrahydropyran, γ-cadinene, 3-ethyl-1,4-hexadiene, α-cubebene등이 주성분이었다. 솔잎을 수증기 증류하여 향기성분을 분석한 결과 44종의 성분이 분리, 확인되었고, hydrocarbon류가 주성분이었다. β-cubebene, trans-caryophyllene, 2-hexenal, T-muurolol, δ-cadinene 순이었다. 수증기 증류법에 의한 방법으로 추출 하였을 때 용매분획 추출시 보다 더 많은 성분이 검색되었고, 용매분획에 따라 추출되는 향기성분의 함량과 조성은 차이가 있었으며, 추출방법에 따라서도 향 기성분의 조성비가 다르게 나타났다.

본 연구는 하라케케(Harakeke)로 불리는 신서란(Phormium tenax)를 화장품 및 의약품산업의 기능성 소재로서의 이용 가능 성을 확인하기 위하여 신서란 잎을 대상으로 70% 에탄올 추출물과 용매 분획물을 제조하여, 이것들의 항염증 및 항아토피의 효과를 조사하였다. LPS로 유도된 RAW 264.7 세포에서 신서란 에탄올 추출물과 용매 분획물의 항염증 효과를 조사한 결과, methylene chloride와 ethyl acetate 분획물에서 NO와 PGE2 생성 억제 활성이 가장 높게 나타났으며, 농도 의존적으로 NO와 PGE2 생성 억제 활성을 보였다. 또한, 이들 분획물에서는 iNOS 및 COX-2 발현 억제 활성을 보였다. 신서란 잎 조추출물과 용매 분획물에 의한 NO, PGE2 생성 억제 활성이 NOS 및 COX-2 발현 억제에 의한 것임을 제시한다. 더불어, hIFN-γ로 자극된 HaCaT 세포에 용매 분획물을 처리하여 MDC 및 TRAC 생성억제 효과를 조사한 바, methylene chloride 분획물은 MDC 및 TATC의 생성을 각각 65%, 52% 생성억제 시켰으며, ethyl acetate 분획물은 MDC 및 TATC의 생성을 각각 93%, 84% 억제 효과를 보였다. 이상의 결과는 신서란 잎 조추출물과 용매 분획물을 이용한 항염증 및 항아토피 효능을 갖는 유효성분 분리 및 활용화 연구에 중요한 기초자료가 될 것이며, 기능성 화장품, 의약외품 및 의약품 소재 개발에 적용 가능성이 높다고 사료 된다.

The leaves and stems of Dendropanax morbiferus were separated from organic solvents with methanol. The organic solvent fractions were fractionated with dichloromethane, ethyl acetate and butanol according to the systematic fractionation method. Oxidation in the body induces aging, and antioxidant activity has attracted the attention of many people as a preventive component to suppress negative reactions in the body. To investigate the antioxidant activity of Dendropanax morbiferus were subjected to DPPH free radical assay. In addition, acetyl cholinesterase inhibitions were performed for Alzheimer’s disease as an aging neurological disease. As a result, it was confirmed that the antioxidant effect of DPPH was generally good in the antioxidant test. The ethyl acetate fractions of Dendropanax morbiferus stems and leaves were IC50=30 ㎍/㎖. Acetyl cholinesterase inhibition experiments were carried out at a concentration of 250 ㎍/㎖. Dendropanax morbiferus stems fractions showed dichloromethane fraction of 57.68%, which significantly inhibited the activity of acetyl cholinesterase.

This study was conducted to evaluate the contents of total polyphenol and flavonoid, and the effect of antioxidant, antimicrobial activities and cytotoxicity in vitro by different solvent fractions from Orostachys japonicus. The ethylacetate fraction extract for O. japonicus contained 634.48 ㎍/g polyphenol and 205.20 ㎍/g flavonoid. The ABTS radical scavenging ability of ethylacetate fraction extract at 1 ㎎/㎖ was higher than 95% which is comparable to ascorbic acid of 97%. The APX enzymatic activity and CAT activity were 1125.89 μmol ascorbate oxidized/min/㎎ protein and 119.87 H2O2 decomposed/ min/㎎ protein, respectively. In disc agar plate diffusion assay, the extract gave rise to a larger inhibition circle with Listeria monocytogenes, Staphylococcus epidermidis, Staphylococcus aureus and Malassezia furfur strains compared with antibiotics kanamycin suggestive of high antibiotic activity. The cytotoxicity of extracts of O. japonicus was significant differences between solvent fractions. That is, the cytotoxic effect against human cancer cell was higher in ethylacetate fraction extract than other fraction extracts. These results suggest that fraction extract of O. japonicus might be very effective and economical in developing natural antioxidant and antimicrobial.

Background: In this study, we investigated the antibacterial and nitric oxide (NO) production inhibitory activities of 75% ethanol extract of Prunus sargentii branches and its fractions against acne pathogens. Methods and Results: The antibacterial activity against acne causing pathogens was determined using the disc diffusion assay. The ethyl acetate fraction showed higher activities against Propionibacterium acnes, Staphylococcus aureus and Staphylococcus epidermidis than those shown by other fractions. In the DPPH radical and NO scavenging assays, the butanol fraction showed strong DPPH radical and NO scavenging abilities. These activities were related to the total polyphenol and flavonoid contents of butanol fraction. On the other hand, the chloroform and ethyl acetate fractions exhibited the highest NO production inhibitory activity in Lipopolysaccharide (LPS)-stimulated Raw 264.7 cells compared to those exhibited by other fractions. Conclusions: The extract and its ethyl acetate fraction from the branches of P. sargentii exhibited antibacterial activity and could be used as functional materials in antimicrobial related fields. Moreover, the chloroform and ethyl acetate fractions are potential antiinflammatory agents and butanol fraction acts as an effective radical scavenger.