Antioxodative substances in Mulberry leaves were examined. Antioxidative substances in Mulberry leaves were extracted by 80% methanol agueous solution. Antioxidative activity of extract was determined by examining hydrogen donating ability on 1,1-diphenyl-2-picrylhydrazyl (DPPH) and the inhibitory effect on the formation of the peroxide from Linoleic acid in the test tube at 50℃. Antioxidative substance were, then, separated and indentified by thin layer chromatography(TLC), UV-Vis spectrum and High performance liquid chromatography(HPLC) methods. Hydrogen donating ability on DPPH and antioxidative ability on linoleic acid of the extracted antioxidative substance were higher than those of 100ppm butylated hydroxy toluene(BHT). The extracted antioxidative substances were separated by TLC using ethylacetate : chloroform : formic acid : water(8 : 1 : 1 : 1 v/v) as a solvent, and a spot at Rf=0.35 was detected. The spot was scraped from the plate, and extrated by methanol. The extract was analyzed by UV-Vis spetra and HPLC, and chlorogenic acid was identified as a antioxidative substance.

해양 미생물로부터 사람 Low Density Lipoprotein(LDL)에 대한 항산화 활성 균주를 검색 하였든 바 부산 인근연안에서 항산화 활성이 높은 Bacillus sp. RH-5를 분리 동정하였다. Bacillus sp. RH-5의 항산화 활성물질의 생산 거 배지는 1.0% glucose, 0.25% polypeptone, 0.25% yeast extract, 0.01% FeSO_4?7H_2O, 50% sea water이였다. 이때 최적 조건은 pH 7.0, 배양 온도는 30℃ 및 배양 시간은 48시간에서 항산화 활성이 가장 높았다. 사람 LDL을 1~5 μM CuSO_4 존재하에서 산화 시킨 결과 Bacillus sp. RH-5 배양액의 ethyl acetate 추출물의 500 및 1,000 ㎍/ml에서 산화가 억제되었으며 또 5 μM CuSO_4 존재하에서 산화시킨 LDL의 전기영동거리는 native LDL보다 다소 높았으나 LDL에 ethyl acetate추출물을 첨가한 경우 그 이동거리는 native LDL과 거의 비슷하였다.

The purposes of this study were to investigate the Maillard reactions of some oligosaccharides with lysine and the antioxidative effects of the ethanol extracts from their reaction mixtures on the soybean oil. The Maillard reactions were carried out of 2% oligosaccharides such as palatinose (PN), fructooligosaccharide (FO), isomaltooligosaccharide (IMO) with 2% lysine (L) for 24 hours heating at 60, 80, 100℃. The color intensity of Maillard reaction mixtures were determined by UV-VIS spectrophotometer upon reaction time and temperature. And the antioxidative effects on the soybean oil of each ethanol extract from Maillard reaction mixture of each oligosaccharide were measured by peroxide value (POV). POV's of soybean oil including reaction extracts were determined regularly every 2 days during 20 days storaged at 60±1℃. The results were obtained as follows: 1. The color intensity of the Maillard reaction mixtures were raised highly as the browning temperature and time increased. The color intensity of PN L browning mixture was the highest. The order of high color intensity at 100℃ was PN L〉FO L〉Glu L〉IMO L. 2. Comparing the antioxidative effect of Maillard reaction product (at 100℃, for 12 hours) of each oligosaccharide to that of BHT and TBHQ, the order of high antioxidative effect was TBHQ〉IMO L〉BHT〉Glu L〉PN L〉FO L. 3. From these results, it was known that PN L shown as high brown color intensity was appeared low antioxidative effect, while IMO L shown as low brown color intensity was appeared high antioxidative effect. So, it was recognized that there was no relation between brown color intensity and antioxidative effect.

This study was pcrformed to evaluate the antioxidant activity of silymarin against human low density lipoproteins(LDL) oxidation. Silymarin extracted from Silybum marianum was successively purified with solvent fractionation and followed by silica gel column chromatography. The active substances were separated by HPLC and the isolated active substances, silymarin were identified by IR, NMR, GC-MS as silymarin. Silymarin inhibited at the 5 uM Cu^(2+)-mediated oxidation of human low density lipoprotein (LDL) in a dose dependent manner. Silymarin completely inhibited LDL oxidation at 50 ug/ml concentration. These findings suggest that silymarin may protect LDL against oxidation in atherosclerotic lessions.

The yields of solvent fractions of irradiated red ginseng powder were increased in the order of petroleum ether(PE)$lt;diethyl ether(DE)$lt;ethyl acetate(EA)$lt;n-butanol (BU)$lt;aqueous fraction(AQ), and did not show any changes in fraction yields by irradiation dose levels. Inhibition activities of lipid peroxide formation were increased in the order of AQ$lt;BU $lt;PE$lt;EA$lt;DE. Inhibition activities of malonaldehyde formation were increased in the order of AQ≤BU$lt;EA$lt;PE$lt;DE. AQ fraction showed little effects on the antioxidative activity and all the activities of the samples did not changed by gamma irradiation. The reverse mutation assay using Salmonella typhunurium (TA98, TA100 and TA102) demonstrated that the nonirradiated and irradiated red ginseng powder extract did not have mutagenic activity (presence of S9 mix or not). The chromosomal aberration test in mammalian animal cell (Chinese hamster lung fibroblast, CHL) showed no significant increase in incidence of structural and numerical aberrations, comparing gamma-irradiated red ginseng powder extracts to nonirradiated red ginseng powder extract in the concentration of the sample producing cytotoxicity(presence of S9 mix or not). Therefore, gamma-irradiatied red ginseng powder (upto 10 kGy) could be safe on the genotoxic point of view.

The antioxidative effect of ethanol extract of ginger on mackerel pike(Colorabis saira) flesh was investigated by periodically measuring TBA value and perioxide value(POV) during storage. The ethanol extract of ginger was added to minced mackerel pike flesh and the fish oil by concentration(2%, 4%, 6%, 8%). Then the minced flesh was storaged at -5℃ and the fish oil was incubated at 40℃. The TBA values of minced flesh were approximately increased in inverse proportion to concentration of ginger extract. Peroxide values were attended with the same effect as TBA value in the aggregate. In addition, The relationship between TBA37℃-2hrs of the minced flesh and their lipid oxidation during storage at -5℃ for 4 weeks was observed(r=O.98). TBA37℃-2hrs can be expressed as the susceptibility to lipid oxidation of minced mackerel pike flesh during storage. In the results, the antioxidative effect of alcohol extract of ginger on mackerel pike flesh was observed.

Some seeds of the Rutaceae family, Zanthoxylum piperitum, Z. schinifolium officinalis, Poncirus trifoliata, Citrus unshin, were investigated to clarify their antioxidative components. Finely powdered samples were extracted by hexane, followed by dichioromethane and then 70% methanol in a hot bath. Its unsaponifiables containing X-and Y-tocopherol with trace amount of β-and δ-tocopherol. also showed comparatively weak activity, although the hexane fraction itself had no significant antioxidative effect on lard. Levels of total tocopherols in the samples averages 42. 24-154. 11 mg/lOOg total extractives. The dichloromethane-and 70% methanol extractives showed strong antioxidative activity, from which antioxidative substances were purified with benzene-acetone(6:5, V/V) on a silica gel column, and with a solvent mixture of acetonitrile-methanol-H2O(40:40:20, V/V/V) on a Sep-Pak C18 hydrolyzed by 5% KOH-ethanol. The recovered unsaponifiables were, then, separated on a column of high performance liquid chromatography. The unsaponifiables produced by hydrolysis of the isolates from dichloromethane extractives has epi-catechin(40.0-57.1%) and (+)-catechin〈l9.1~24.4% to total phenolic substances, on area base) as major component, accompanied by chlorogenic acid, gallic acid(?), trans-p-coumaric acid and tralls-p-ferulic acid including some unknown components, and those derived from 70% methanol extractives also comprise (+)-catechin(31.3~39.6% to total components, on area base), epi-catechin(2O.2~36.4%), trans-p-cournaric acid(8.4-15.3%) and trans-p-ferulic acid(7.7~14.1%) as predominant component with some minor coponents, but the fraction supposed to be gallic acid(?) is not present. The antioxidative activities of the phenolic components isolated in this work were in order of epi-catechin〉catechin〉chlorogenic acid〉trans-p-ferluic acid〉trans-p-coumaric acid.

탈지 가자박으로 부터 free, soluble 및 insoluble bound phenolic acids를 추출하여 식용대두유 기질에서 항산화효과률 0.02%(w/w)의 BHA, BHT의 항산화 효과와 비교하고자 각 기질과 대조구를 에서 35일간 저장하면서 매 7일 간격으로 과산화물가, TBA가를 측갱하였다. BHA, BHT와 free, soluble 및 insoluble hound phenolic acids를 첨가한 시험구와 대조구의 과산화물가는 21일의 경우 60, 30, 14, 11, 10, 100이었다. 같은 조건하에서 추출물의 TBA가는 0.150, 0.108, 0.105, 0.073, 0.078, 0.185이었다. 이것으로 보아 phenolic acids는 식용대두유 기질에서 우수한 항산화력을 나타내었다. 분리확인된 phenolic acids는 p-coumaric acid, ferulic acid, phloroglucinol, pyrogallol, vanillic acid, caffeic acid으로 확인되었다.

탈지 은행 종실 및 잎에서 유리페놀산, 에스터형 및 불용성 페놀산을 추출하여 식용 옥수수유 기질에서 항산화 효과를 비교하고자 0.02%(w/w)의 BHA, BHT와 각 추출물 (2% w/w)를 넣어 의 항온기에서 45일간 저장하면서 매 5일 간격으로 과산화물가, TBA가를 측정하여 다음과 같이 항산화 효과를 추정하였다. BHA, BHT와 은행 종실의 유리페놀산, 에스터형 및 활용성 페놀산, 잎의 유리페놀산, 에스터형 및 불용성 페놀산 추출물을 첨가한 시험구와 대조구의 45일 저장후 과산화물가는 각각 133, 52, 115, 190, 127, 95, 140, 121, 280meq/kg, oil이었다. 한편 같은 조건하에서 각 항산화성 물질의 TBA가는 0.153, 0.059, 0.175, 0.260, 0.187, 0.160, 0.1 74, 0.195 0.430이었다. G.C.로 분리 확인된 페놀산은 은행 종실 및 잎 공히 Vanillin, -Hydroxybenzoic acid, Syringic acid, Gallic acid, Protocatechuic acid가 확인되었고 은행 종실에서는 trans-Cinnamic acid, Caffeic acid가, 잎에서는 Coumaric acid, Gentisic acid, Phloroglucinol, Pyrogallol이 각각 확인되었다. 이상의 결과를 종합해 볼 때 은행 종실 및 잎의 페놀산은 식용 옥수수유 기질에서 우수한 항산화 효과가 있는 것으로 사료된다.

The extracts of Quercisemen(Quereus acutissima Carruthers seed) powder was obtained by the extraction with distilled water, water : acetonet(1:1, v/v), ethanol and ethyl ether, respectively. As a result this experiment, the antioxidative activity of each solvent extracts on linoleic acid were examined as follows: 1. Each fraction extracted by the acetone : water(1:1, v/v), water and ethanol respectively showed high antioxidative activity. 2. A fraction of the tannin extracted from the solvent, acetone, water(1:1, v/v) showed even more antioxidative activity than that of the α-tocopherol or BHT. 3. Acceleration of peroxide reaction by Fe++ and Cu++ on the linoleic acid was strongly inhibited by adding the tannin, 4. Organic acid, such as malic acid, citiric acid and tartaric acid with the tannin were showed the synergistic effect fo the antioxidation reaction.

Dried seeds of Camellia japonica and Thea sinensis were investigated to determine the nature of their antioxidative activity. Activity was measured by the induction period in the coupled oxidation of a substrate lard and extracts or isolates to be tested. 70% methanol and dichloromethane extracts were found to be antioxidative abilities. Their unsaponifiables revealed weak antioxidative activity, although hexane extracts did not show antioxidative effect on lard. Column chromatography for dlchloromethane extracts gave 4 fractions(only 2 fractions were potent). HPLC was used in isolating potent antioxidative components from the column fractions and the precolumn-passed methanol extracts. They were separated into 7 and 8 components, respectively. The column fractions obtained from both seeds comprised trans-p-coumaric acid. trans-p-ferulic acid and an unknown component with minor components such as chlorogenic acid and catechin. On the other hand, the most prominent components in the methanol extracts were an unidentified component. trans-pcoumaric acid, trans-p-ferulic acid, catechin and chlorogenic acid. The unknown compound isolated from the column fractions and methanol extracts was identified as epicatechin by 1H-and 13C-NMR. The antioxidative activities of these components were epicatechin 〉 catechin 〉 chlorogenic acid 〉 trans-p-ferulic acid 〉 trans-p-coumaric acid.

The study was observed that anti oxidation effect of each and mutual relation on BULGOGI seasoning in Fore shank and Ribs. Each antioxidation effect were appeared to higher in suger, pear juice, soya souce, clean wine, sesamed oil, green onion, toeasted sesamed powder, black pepper, garlic im seasoned immidiately. Soya souce was revealed to higher effect anti oxidation in storaged beef among 30 minuit after seasoned. In storaged sample among 9 hour after seasoned was showed to higher effect in soya souce & galic. Mutual relation of two seasoning in BULGOGI seasoning were revealed to higher effect in mixture of green onion & galic.

탈지 겨자박으로 부터 유리페놀산, 에스터형 및 불용성페놀산을 추출하여 식용대두유 기질에서 항산화 효과를 0.02%(w/w)의 BHA, BHT의 항산화 효과를 비교하였는바 다음과 같은 결과를 얻었다. 각 기질과 대조구를 에서 25일간 저장하면서 매5일간 과산화물가, TBA가를 측정하여 항산화 효과를 추정하였다. 1. BHA, BHT와 유리페놀산, 에스터형 및 불용성페놀산 추출물을 첨가한 시험구와 대조구의 25일 저장 후 과산화물가는 각각 31.9, 13.2, 16.6, 11.2, 35, 91이었다. 한편 같은 조건하에서 각 항산화성 물질의 TBA가는 0.24, 0.16, 0.19, 0.17, 0.35이었다. 이로 미루어 볼 때 페놀산 추출물들은 식용대두유 기질에서 우수한 항산화 효과를 나타내었다. 2. 겨자의 총 페놀함량은 유리페놀산 및 불용성페놀산의 추출물이 각각 13.2mg/10ml. 340.5mg/10ml, 2.1mg/10ml였다. 3. 분리 동정된 페놀산은 catechol, methylcatechol, salicylic acid, cinnamic acid, pyrogallol, p-hydroxybenzoic acid, syringic acid, caffeic acid, sinapic acid였다.

Background: To enhance the taste and physiological characteristics of Lycii fructus (Gugija) extracts, we investigated the changes in the physiological characteristics of Gugija extracts caused by adding white ginseng (WG) and red ginseng (RG) Methods and Results: Gugija extracts, including 10G10, 10GW-G8 : 2, -G6 : 4, -G4 : 6, -G2 : 8, and -G0 (mixtures made by replacing 0, 20, 40, 60, 80, and 100% of Gugija with WG), as well as 10G10, 10GR-G8 : 2, -G6 : 4, -G4 : 6, -G2 : 8, and -G0 (mixture made by replacing 0, 20, 40, 60, 80, and 100% of Gugija with RG) were extracted with water at 10 times the respective mixture's volume. The antioxidant activities of Gugija extracts were investigated by assessing their 1,1-diphenyl-2-picrydrazyl (DPPH) and 2,2’-azinobis(3ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical scavenging activity, ferric reducing antioxidant potential (FRAP) activity, nitrite scavenging activity, and angiotensin converting enzyme (ACE) inhibitory activity. As the amount of WG added increased, the DPPH, and, ABTS radical scavenging activity, and FRAP activity of the Gugija extract decreased. The half maximal inhibitory concentration (IC50) value of 10G10, 10GW-G6 : 4, 10GR-G6 : 4, and 10GR-G0 for DPPH radical scavenging activity were 25.50 ± 1.04, 52.06 ± 1.46, 16.87 ± 1.24, and 9.50 ± 0.16 ㎕/㎖, respectively. On the other hand, the physiological activity of Gugija extract increased with the addition of increasing amounts of RG. However, ACE inhibitory activity was the highest (50.25 ± 2.58%) in the Gugija 10-fold extract without any added RG. Conclusions: From the above results, we suggest that adding RG to Gugija extracts increase their antioxidant, FRAP, and nitrite scavenging activities.

Background : The Dolwoe is a native plant to Asia and a medicinal plant belonging to the family of cucurbitaceae. It is generally consumed in the form of tea. The purpose of this study was to investigate the effects of roasting treatment and the extracts of ethanol and water on antioxidant activity and to examine the possibility of raw materials for health functional food. Methods and Results : In this study, each specimen was extracted as water and ethanol by dividing it into Dolwoe leaves that were treated with roasting treatment, or hot air drying. To compare each extract, the total phenol and flavonoids content were measured, and the TEAC experimental method was conducted in which ABTS radical was indexed to trolox to measure antioxidant activity. Also, The degree of reduction of iron ions was measured using the FRAP experimental method to compare the reducing power of each extract. As a result of the experiment, the total phenol content was between 35.54 and 71.52 ㎎·GAE, the ethanol extract of roasted leaves showed more than twice the amount of phenol than the ethanol extract of dried leaves. The total flavonoids content was 5.37 to 28.91 ㎎·QE/g, with roasted leaves ethanol extracts with high total phenol content. In particular, antioxidant activity with TEAC 153.90 ± 1.72 mM·TE/g, FRAP 320.78 ± 1.44 mM·FE/g in ethanol extract of roasted leaves showed high activity in proportion to the total phenol and flavonoids content and hydroxyl radical scavenging was found to be the highest in the ethanol extract of roasted leaves. Conclusion : Total phenol and flavonoid content, antioxidant effects were highest when the Dolwoe leaves were processed for roasting treatment and extracted as ethanol. Therefore, extraction under the following conditions will have a useful effect as a health functional food.

Background : In this study, we have examined antioxidative effects and antimicrobial activity of methanol extracts of several plant resources (three varieties of Asimina triloba L., Momordica charantia L., Psidium guajava L. and Alium ampeloprasum L.) Methods and Results : The antioxidant activities were assayed by five methods based on total polyphenol and flavonoid contents, scavenging of DPPH, ABTS and reducing power analysis. Total polyphenol contents was the highest in Psidium guajava and Mango, the varieties of Asimina triloba as the contents of 95.85, 95.81 ㎎/g, respectively. Total flavonoid content was the highest in Psidium guajava (54.3 ㎎/g). DPPH free radical scavening activity of all extracts was ranged from 10.5 - 85.8%, and significantry great activities was found at Psidium guajava leaf. Methanol extracts of Psidium guajava and Asimina triloba showed showed greater ABTS scavening activities compared to others. Reducing power of all extracts was linearly proportional to the concentration. Especially, the extracts of Psidium guajava and three varieties of Asimina triloba showed greater reducing power than that of other resources. The antimicrobial activities of extracts were tested by paper disc assay and minimum inhibitory concentration test. Antimicrobial activity of Psidium guajava leaf extract was shown relatively high activity against all investigated strains. Conclusion : The results suggest that Psidium guajava leaf extract be a new functional cosmetic ingredient with antioxidant effect and antimicrobial activity.

Background: The flowering plant Hippophae rhamnoides L. has been used for many studies on fruit or leaf extracts. This study was conducted to investigate the development of a new cosmetic material from H. rhamnoides fruits and leaves that have by antioxidant, anti-inflammatory and wrinkle improvement activities. Methods and Results: The antioxidant abilities of H. rhamnoides extracts, including of a water-soluble fruit powder (FW), a fatsoluble fruit powder (FF), a supercritical extract of fruit by-product (BS), and a mixture of leaf and fruit (MIX), were investigated in vitro. A DPPH radical assay for antioxidant activity was performed for these fractions alongside assay to evaluate the total phenolic and flavonoid content (TPC and TFC). As expected, the MIX had the highest DPPH radical scavenging activity (RC50 = 10.27㎍/㎖), and the TPC and TFC also were highest in MIX (225.7 ㎎·GAE/g, and 25.18 ㎎·QE/g, respectively). Nitric oxide (NO) production in LPS-induced RAW264.7 cells was estimated and the results indicated an over 75% decrease of NO production in FF and MIX. In other assays, the highest elastase inhibitory activity was found in FW. Conclusions: These results revealed that H. rhamnoides extracts have a high potential for antioxidant, anti-inflammatory and antiwrinkle activities. H. rhamnoides products are suggested to be applied as the functional materials of cosmetic ingredients.

This study investigated the nutritional properties and biological activities of Ganoderma lucidum (GL). The round type of GL contained higher carbohydrate content, while the Nokgak type of GL contained higher crude ash, crude fat, and crude protein content. The most abundant amino acid, fatty acid, mineral, and soluble vitamin observed were valine (round type: 11.90 mg/g and Nokgak type: 17.18 mg/g), linoleic acid (round type: 47.56% and Nokgak type: 75.68%), potassium (round type: 116.50 mg/100 g and Nokgak type: 184.36 mg/100 g), and vitamin B3 (round type: 1.78 mg/100 g and Nokgak type: 1.81 mg/100 g), respectively. In addition, the β-glucan content were 34.15 g/100 g (round type) and 30.07 g/100 g (Nokgak type). The GL 70% ethanol extract at 40℃ showed higher radical scavenging as well as carbohydrate and lipid enzyme inhibition than other conditions. At 1 mg/mL of treatment with the 70% ethanol extract at 40℃ of round type GL, the DPPH, ABTS, hydroxyl radical scavenging, and α-glucosidase, α-amylase, and pancreatic lipase inhibition activities obtained were approximately 92.85, 99.74, 58.09, 89.68, 44.68, and 67.56%, respectively.