• 대한약침학회지
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• 제21권2호
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• pp.48-60
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• 2018

Objective: The aim of this study is to optimize the extraction of beneficial substance from Cudrania tricuspidata leaves grown at Jirisan Mountain in South Korea by three different solvents depending on extraction time and at different temperature. Methods: The total phenolic contents were determined by the method reported by $S{\acute{a}}nchez$-Moreno et al. The total flavonoid contents were analyzed by Slinkard and Singleton. The DPPH radical scavenging activity was determined according to the method reported by Blois Results: The extraction yield for each solvent is 9.05-14.1%, 2.17-5.67%, and 2.3-3.9% for D.W., ethanol, and hexane, respectively. The overall results were maximized for the extract obtained with D.W. for 5 min at $100^{\circ}C$. The average phenol contents were 77.11, 45.64, and 0.343 mg/g at $100^{\circ}C$ in water, $78^{\circ}C$ in ethanol, and $68^{\circ}C$ in hexane, respectively. The flavonoid contents were the highest in the materials extracted with D.W., and were increased with increasing temperature, regardless of the extraction solvents, whether water (green), polar organic ethanol, or nonpolar organic hexane. In the ethanol extract, the flavonoid contents are increased gradually from 5.66 mg/g to 7.73 mg/g. The total flavonoid contents were proportional to the concentrations of the water extracts, ranging from 4.14 mg/g to 48.89 mg/g. The antioxidative activities of the water-extracted compounds are generally increased with increasing temperature from 42.5% to 85.5%. Those of the hexane extracts are increased slowly from 3.79% to 8.8%, while those of ethanol extracts are increased from 29.8% to 47.4%. Conclusion: The extraction yields were dependent upon solvents for extraction as well as extraction time and the temperature. The optimal extraction time was 5 min and the extraction yields were increased with increasing temperature excepted hexane. Of the three tested extraction solvents, the greenest solvent of water shows excellent results, suggesting that water is among the most effective solvents for natural sample extractions for general medicinal, pharmaceutical, and food applications.

• 한국식품저장유통학회지
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• 제14권1호
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• pp.67-72
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• 2007

탐라오가피를 기능성 식품소재로 활용하기 위하여 물과 주정의 비율을 달리하여 추출시간에 따른 유용성분의 경시적 변화를 검토하였다. 물 및 주정농도를 각각 $30{\sim}95%$로 조절한 다음 0.5 cm 이하로 세절한 줄기를 300 g/7.5 L의 비율로 첨가하여 9시간 동안 $100^{\circ}C$를 유지하는 항온수조에서 환류냉각 추출하였다. 추출 중에 pH의 변화는 대체로 주정농도가 높을수록 높아지는 경향을 보였고, 추출 후 3시간까지 pH가 낮아졌으며 $pH\;4.0{\sim}6.5$ 범위였다. 색도 a 값은 추출용매에 따라 차이가 있었으나, 추출 $2{\sim}3$시간까지에 변화가 컸다. 색도 b 값은 주정농도가 낮을수록, 추출시간이 경과함에 따라 증가하는 경향이었다. 가용성고형물은 추출 직후부터 $2{\sim}3$시간 안에 급증하였으며, 물 및 주정농도가 낮을수록 많이 추출되었다. 주정농도 $30%{\sim}70%$인 경우 줄기에서 $0.27{\sim}0.47%(w/v)$로 가용성고형물 함량이 높았다. 추출액에 함유된 주요 유리당은 sucrose, fructose, glucose였다. Eleutherosides 성분은 주정농도가 높을수록 추출 직후부터 3시간까지 급속히 증가하였으며, 주정 원액보다 물 및 주정을 혼합하여 추출하였을 때가 함량이 높았다. 물 및 주정용액으로 $3{\sim}5$ 시간 추출하였을 때, 원료의 약 97% 추출되었다. 추출잔사를 분석한 결과에서 acanthoic acid의 추출은 물만으로는 추출이 어려웠으며 주정농도 40% 이상 유지할 필요가 있었다. 따라서 탐라오가피의 기능성분의 추출에서는 주정농도 $40{\sim}70%$로 $3{\sim}5$시간 동안 환류 추출하는 것이었다.

• 한국식품저장유통학회지
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• 제30권5호
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• pp.857-867
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• 2023

본 연구에서는 홍삼과 흑삼의 기능성 성분 추출 극대화를 위해 추출 용액의 ethanol 농도와 추출 온도를 고려하여 추출 수율, 산성다당체 및 ginsenosides의 함량 변화를 반응표면분석법을 통해 모니터링해 보고 적정 추출조건을 찾아보았다. 홍삼 및 흑삼의 가용성 고형분 함량에 대한 모델식의 R²는 각각 0.9679(p<0.01), 0.8545(p<0.1)였다. 홍삼가용성 고형분의 최적 추출조건은 ethanol 농도 1.52%에서 67.27℃로 추출 시 그 함량이 5.29%였으며, 흑삼 가용성 고형분의 최적 추출조건은 ethanol 농도 3.12%에서 66.13℃로 추출 시 그 함량이 6.11%였다. 홍삼 및 흑삼의 산성다당체 함량에 대한 모델식의 R²는 각각 0.9251(p<0.05), 0.88379(p<0.1)였다. 홍삼의 산성다당체 최적 추출조건은 ethanol 농도 4.03%에서 69.61℃로 추출 시 그 함량이 1.86 mg/mL였다. 흑삼의 산성다당체 최적 추출조건은 ethanol 용액 농도 24.67%에서 71.14℃로 추출 시 그 함량이 1.80 mg/mL였다. 홍삼의 ginsenoside Rg₁ 및 Rb₁ 함량에 대한 모델식의 R²는 각각 0.8941(p<0.05), 0.8718(p<0.1)이었다. 홍삼의 ginsenosides 최적 추출조건은 ethanol 농도 79.92%에서 70.62℃로 추출 시 ginsenoside Rg₁ 함량이 0.22 mg/mL였으며, ethanol 농도 79.94%에서 69.46℃에서 ginsenoside Rb₁ 함량이 0.36 mg/mL였다. 흑삼의 ginsenosides 최적 추출조건은 ethanol 농도 75.11%에서 65.21℃로 추출할 경우 ginsenoside Rb₁ 함량이 0.28 mg/mL였으며, ethanol 농도 75.70%에서 65.49℃에서 ginsenoside Rg₃ 함량이 0.31 mg/mL였다. 홍삼 및 흑삼의 산성다당체 수율과 ginsenoside 수율을 모두 만족하는 최적추출조건은 ethanol 농도 35-50%의 범위 내에서 70℃였다.

• 식품보건융합연구
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• 제5권5호
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• pp.11-25
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• 2019

Extraction of oil from Moringa oleifera seed using Response Surface Methodology (RSM) was investigated. Effects of three factors namely: sample mass, particle size and extraction time on the response, Moringa oleifera a volume extracted, were determined. The Box-Behnken design of RSM was employed which resulted in 15 experimental runs. Extraction was carried out in a 250 ml Soxhlet extractor with Hexane and Ethanol as solvent. The Moringa oleifera seed powder was packed inside a muslin cloth placed in a thimble of the Soxhlet extractor. The extraction was carried out at 60℃ using thermostatic heating mantle. The solvent in the extracted oil was evaporated and the resulting oil further dried to constant weight in the oven. This study demonstrates that Moringa oleifera oil can be extracted from its seed using ethanol and acetone as extraction solvent. The optimum process variables for both solvent (ethanol and acetone) was determined at sample weight of 40 g, particle size of 325 ㎛ and extraction time of 8 hours. It can be deduced that using acetone as solvent produces a higher yield of oil at the same optimum variable conditions compared to when ethanol was used.

• 한국환경과학회지
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• 제20권10호
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• pp.1265-1272
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• 2011

In this study, the extraction characteristics of soluble solid from Rumex crispus(Curled dock) was studied from the investigation of the effects of experimental conditions on extraction rate; extraction ratio, composition of extractants, extraction time and pH of extractant, etc. The proximate composition of Rumex crispus was 2.58% crude lipid, 5.59% crude protein, 7.39% crude ash, 6.13% moisture and 78.31% carbohydrate, respectively. Turbidity of extract by distilled water was higher and increased with extraction time and extraction temperature, where as the turbidity didn't increase by ethanol and methanol in 20 folds of extraction ratio. Turbidity was inversely proportional to the extraction ratio for the three extractants at 25$^{\circ}C$ and 1 hour extraction. But turbidity of extract was highest by composition of 50% methanol-water extractant than any other compositions of extractants. Eighteen and fifteen free aminoacids were detected in extracts with distilled water, methanol and ethanol extractant, respectively, and it's contents were order of glutamic acid>proline>aminobutyric acid>alanine. The extraction rate of soluble solid from Rumex crispus was order of distilled water>methanol>ethanol within experimental extraction ratio. In extraction with distilled water, the contents of soluble solid was inversely proportional to the pH of extractant.

• Journal of Ginseng Research
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• 제44권1호
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• pp.44-49
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• 2020

Background: Salting-out extraction (SOE) had been developed as a special branch of aqueous two-phase system recently. So far as we know, few reports involved in extracting ginsenosides with SOE because of the lower recovery caused by the unique solubility and surface activity of ginsenosides. A new SOE method for rapid pretreatment of ginsenosides from the enzymatic hydrolysates of Panax quinquefolium was established in this article. Methods: The SOE system comprising ethanol and sodium carbonate was selected to extract ginsenosides from the enzymatic hydrolysates of Panax quinquefolium, and HPLC was applied to analyze the ginsenosides. Results: The optimized extraction conditions were as follows: the aqueous two-phase extraction system comprising ethanol, sodium carbonate, ethanol concentration of 41.51%, and the mass percent of sodium carbonate of 7.9% in the extraction system under the experimental condition. Extraction time had minor influence on extraction efficiency of ginsenosides. The results also showed that the extraction efficiencies of three ginsenosides were all more than 90.0% only in a single step. Conclusion: The proposed method had been successfully applied to determine ginsenosides in enzymatic hydrolysate and demonstrated as a powerful technique for separating and purifying ginsenosides in complex samples.

• 한국식품영양과학회지
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• 제29권5호
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• pp.943-947
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• 2000

The purpose of this study was to investigate the extraction method of phenolic compounds from Rubus coreanum and antioxidative activity. antioxidative activities of Rubus coreanum were tested with ability of donating hydrogen to DPPH, and HPLC, fluorometry which measure the amount of MDA after reacting linoleic acid with $H_2O$$_2$, and LDL with $H_2O$$_2$ and FeCl$_2$. The most suitable extraction conditions of the phenolic compounds from Rubus coreanum was 3 times with 60% ethanol, and the yield of extract containing 35% moisture was 15.28%. In extraction efficacy of phenolic compounds, 60% ethanol was superior to water as extraction solvent, and extraction efficacy with 60% ethanol did not differ from disolving by water after evaporation of 60% ethanol extract. 60% ethanol extract of Rubus coreanum had an ability of hydrogen donating to DPPH, MDA determination showed the antioxidative effect with inhibition ratio of 77.91% on linoleic acid oxidation by addition of Rubus coreanum extract with the concentration of 1.500 ppm. and about 65.74% of LDL oxidation was inhibited by addition of 1,000 ppm.

• 한국식품영양학회지
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• 제34권2호
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• pp.137-145
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• 2021

This study was conducted in order to investigate the antioxidant and antimicrobial activity of Solanum nigrum L. fruit powder after undergoing different extraction solvent processes. The total phenolic content of Solanum nigrum L. fruit powder measured a 14.66 GAE mg/g after undergoing ethanol extraction, and the total flavonoid content measured at 201.23 mg CE/g when undergoing ethanol extraction. The ABTS radical scavenging activity was 160.38~209.53 TEAC umol/g, and the DPPH radical scavenging activity was 53.99~90.76 TEAC umol/g, which indicated a higher level of antioxidant power in the ethanol extract as opposed to in the water extract. The FRAP (ferric reducing antioxidant power) of Solanum nigrum L. fruit powder was 115.58~194.58 TEAC umol/g, and B. subtilis KCTC 2189 showed greater antimicrobial activity in the ethanol extract (concentration 200 ug/uL) as opposed to the water extract. Solanum nigrum L. fruit powder revealed differences in antioxidant and antimicrobial activity between the different extraction solvents. In particular, ethanol extract had higher antioxidant and antibacterial activity, meaning it is more favorable for usage as a functional food material.

• 한방안이비인후피부과학회지
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• 제23권2호
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• pp.69-80
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• 2010

Objective : The purpose of this study was to compare anti-Inflammation and anti-oxidation of Jeondo-San(JDS) extracted with two kinds of solvents, ethanol and water. Methods : Two kinds of JDS extractions were prepared 20, 50, $100\;{\mu}g/mg$. The Cytotoxicity was measured by MTT assay in Raw 264.7 cell. The anti-inflammation effects were measured by inhibitory efficacy on $PGE_2$, NO, TNF-$\alpha$, COX-2 and iNOS in Raw 264.7 cell. The anti-oxidation effects were measured by ROS inhibitory efficacy, intracellular GSH synthesis and DPPH Radical scavenging in HaCaT cell. Results : 1. All of JDS extraction groups had no cytotoxicity in Raw 264.7 cell. 2. All of JDS extraction groups showed significantly inhibitory effect on production of $PGE_2$. Inhibitory efficacy increased in accodance with concentration. 3. All of JDS extraction groups showed significantly inhibitory effect on production of NO. Inhibitory efficacy increased in accodance with concentration. 4. All of JDS extraction groups did not show significantly inhibitory effect on production of TNF-$\alpha$. 5. $100\;{\mu}g/ml$ JDS extracted with ethanol and $50\;{\mu}g/ml$, $100\;{\mu}g/ml$ JDS extracted with water showed inhibitory effect on iNOS expression. 6. All of JDS extraction groups showed significantly inhibitory effect on production of ROS. Inhibitory efficacy increased in accodance with concentration. Ethanol extractions were better than water extractions. 7. $100\;{\mu}g/ml$ JDS extracted with ethanol only produced GSH of $32{\pm}5.2%$. 8. All of JDS extraction groups showed significantly scavenging effect of DPPH radicals. Inhibitory efficacy increased in accodance with concentration. Ethanol extractions were better than water extractions. Conclusion : Two kinds of JDS extractions have not cytotoxicity and inhibit production of NO. JDS extracted with water was effective in anti-inflammation, JDS extracted with ethanol was effective in anti-oxidation.

• 한국한의학연구원논문집
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• 제18권3호
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• pp.147-154
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• 2012

Objectives : This study was performed to find best extraction solvent for application of Ulmi cortex to food or herbal medicine as an antioxidant only using water, ethanol and their mixtures. Methods : The Ulmi cortex extracts were prepared using water and 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% and 100% (v/v) ethanol, and were evaluated yields, total polyphenol contents, DPPH and ABTS radical scavenging activities, lipid peroxidation activities, and catechin and epicatechin contents. Results : Among the Ulmi cortex extracts, the yield was highest in water extract (8.9%) and lowest in ethanol extract (3.8%). The yield of 30% ethanol extract (8.5%) also was very high to similar with water extract. The total polyphenol content was highest in the 30% ethanol extract ($253.6{\mu}g/mg$ extract) and lowest in water extract ($109.0{\mu}g/mg$ extract). The DPPH radical scavenging activity was highest in ethanol extract (IC50, $8.53{\mu}g/ml$), ABTS radical scavenging activity was highest in 60% ethanol extract (IC50, $3.08{\mu}g/ml$), and the inhibition of lipid peroxidation was highest in 70% ethanol extract (IC50, $7.96{\mu}g/ml$). As ethanol content of extraction solvent increased from 0% to 30%, the antioxidant activities were remarkably increased whereas from 30% to 100%, the antioxidant activities were increased or decreased a little. Conclusions : The findings of the present study suggest that 30% ethanol is best solvent for extraction of Ulmi cortex, considering yield, polyphenol content, and antioxidant activities with extraction cost.