• BMB Reports
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• 제29권5호
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• pp.393-397
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• 1996

Sprague-Dawley male rats (150 g) were chronically treated with 5 v/v % ethanol admixed with nutritionally complete liquid diet and fed ad libitum for 3 weeks. Controls were pair fed with the isocaloric sucrose liquid diet. One half of each group was exposed to cold stress at $4^{\circ}C$ either for 24 h (for determination of mRNA by in situ hybridization) or for 48 h (for determination of enzyme activity). Chronic ethanol treatment (ethanol) did not affect tyrosine hydroxylase (TH) mRNA level in locus coeruleus (LC) of brain and adrenal medulla (AM) compared to controls. Cold stress showed strong increase of TH mRNA level in LC and AM compared to controls. Pretreated ethanol reduced the increased TH mRNA level by cold stress in LC and AM. Ethanol did not affect TH activity in LC and adrenal glands (adrenals). Cold stress increased TH activity in LC but not in adrenals. Pretreated ethanol did not reduce the increased TH activity by cold stress in LC but this result was not shown in adrenals. It is suggested that ethanol does not affect the message level and enzyme protein level for TH in LC and AM in normal rat. It is also hypothesized that pretreated ethanol reduces the magnitude of acute cold stress response, that is induction of TH mRNA in LC and AM, and does not reduce the increased TH enzyme protein that is also acute cold stress response in LC.

• 센서학회지
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• 제33권2호
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• pp.70-77
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• 2024

In this study, a fluorescent ethanol sensor is developed to determine the ethanol concentration in the liquid phase. The sensor is developed using a complex of resazurin (RA)/resorufin (RO) and a hydrotalcite (HT) catalyst in a sol-gel matrix of methyltrimethoxysilane (MTMS) to produce a fluorescent ethanol-sensing membrane (RA/RO^*HT membrane). The operation mechanism of the RA/RO^*HT membrane is based on (i) the oxidation of ethanol to acetaldehyde and (ii) the reduction of RA to RO, through electron flows followed by EtOH ↔ HT ↔ RA/RO ↔ EtOH interactions. These possible redox reactions can lead to an increased fluorescence intensity of the RA/RO^*HT membrane as the ethanol concentration increases. The RA/RO^*HT membrane shows a linear detection range of 1-20 vol.% EtOH with limit of detection (LOD) of 0.178%. Additionally, the RA/RO^*HT membrane has high sensitivity and accuracy for determining the alcohol content in several Korean alcoholic beverages.

• 한국식품과학회지
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• 제30권1호
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• pp.22-34
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• 1998

고정화효소와 산소전극 시스템을 이용한 효소센서를 제작하여 식품 중의 당, 유기산, 알코올 성분을 동시 측정 하였다. 효소가 기질과 반응하여 소비한 산소의 변화량이 전압차이로 나타나므로 시간당 전압 감소량이 최대인 값으로부터 각 성분의 농도를 측정하였으며, 이때 1분내에 최대기울기를 구할 수 있어 신속한 측정이 가능하였다. 효소의 고정화 지지체로는 nylon cloth를 사용하였고, asymmetrical coupling 방법에 의하여 기질 작용 순으로 위치하도록 효소를 고정화하였다. 한 개의 양극과 6개의 음극으로 제작된 multiple cathode system으로 포도당, 젖산, 에탄올 성분을 동시 측정할 수 있는 효소 센서를 제작하였다. 위의 센서 제작을 위하여 mutarotase과 glucose oxidase/lactate oxidase/alcohol oxidase와 catalase가 각기 사용되었다. 이들 효소센서의 최적조건은 $pH\;7.0,\;40^{\circ}C$의 0.1 M 인산완충용액이었으며 각 효소 센서의 방해물질을 알아 보기 위하여 여러 가지 당과 각종 유기산, 알콜류에 대한 효소 감응도를 살펴 본 결과 포도당 센서에서 유기산의 영향을 제외하고는 10% 내외였다. 따라서 포도당과 유기산을 동시 측정하기 위하여 포도당/젖산의 영향을 고려한 적절한 보정관계식을 도입하여 순수한 유리당과 유기산의 값을 측정할 수 있었다. 제작된 효소센서의 검증을 위하여 분광광도법. HPLC, GC를 이용한 결과, 분석방법간에 높은 상관관계를 보여 주었다. 아울러 각 효소센서의 안정성을 살펴본 결과 알코올 센서를 제외하고는 30일 이후에도 80%이상 효소감응도가 유지되었다.

• Bulletin of the Korean Chemical Society
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• 제15권1호
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• pp.9-12
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• 1994

The gravimetric determination of scandium by di-(2-ethylhexyl)phosphate(DEHPA) as a precipitant and the mole ratio of Sc-DEHPA arecipitation obtained in ethanol medium have been investigated. Scandium can be determined by gravimetric method of precipitation of Sc-DEHPA and the mole ratio of Sc-DEHPA is found as 1 :2 in ethanol medium.

• 한국식품과학회지
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• 제28권5호
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• pp.974-980
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• 1996

멥쌀로 탁주를 제조하여 발효과정 중에 변화되는 에탄올 및 포도당의 함량을 동시에 측정할 수 있는 바이오센서를 dual cathode electrode를 이용하여 제작하였다. Alcohol oxidase와 glucose oxidase는 nylon net에 고정화시켜 anode가 한 개이고 cathode가 두 개인 dual cathode electrode에 부착하여 용존산소가 소모되는 변화량을 측정하여 간접적으로 포도당과 에탄올의 농도를 동시에 측정할 수 있도록 하였다. 이 시스템의 최적 조건은 $35^{\circ}C$에서 pH 7.5인 0.1 M 인산 완충용액이었다. 바이오센서를 이용하여 측정한 값을 분광광도법과 gas chromatography를 이용한 값과 비교해 본 결과 유사한 것으로 나타났다. Dual cathode electrode를 이용한 바이오센서로 측정할 경우 다른 분석방법과 같은 복잡한 전처리 과정없이 두 가지 성분을 동시에 측정하는 것이 가능함으로써 신속하게 측정할 수 있었으며, 탁주와 같은 발효식품의 발효 중 변화하는 두 가지 성분을 동시에 측정할 수 있었다.

• 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.

• Archives of Pharmacal Research
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• 제19권5호
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• pp.374-380
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• 1996

Sprague-Dawley male rats (150 g) were chronically treated with 5 v/v % ethanol admixed with nutritionally complete liquid diet and fed ad libitum for 3 weeks. One half of each group was exposed to cold stress at 4 ^{\circ}C either for 24 h (for determination of mRNA by in situ hybridization) or for 48 h (for determination of enzyme activity). Chronic ethanol treatment (ethanol) did not affect tyrosine hydroxylase(TH) mRNA level in locus coeruleus(LC) of brain and adrenal medulla(AM) compared to controls. Cold stress showed strong increase of TH mRNA level in LC and AM compared to controls. Pretreated ethanol reduced the increased TH mRNA level by cold stress in LC and AM. Ethanol did not affect TH activity in LC and adenal glands(adrenals). Cold stress increased TH activity in LC but not in adrenals. Pretreated ethanol did not reduce the increased TH activity by cold stress in LC but this result was not shown in adrenals. Phenylethanolamine-N-methyltransferase(PNMT) activity in $C_{1}$$C_{2}$ and adrenals increased only in ethanol treated group. THese results suggest that ethanol does not affect TH mRNA level and activity in LC and adrenals, but increases PNMT activity in $C_{1}$$C_{2}$ and adrenals in normal rat. It is also suggested that pretreated ethanol reduces the magnitude of cold stress response, that is induction of TH mRNA in LC and AM, and does not reduce the protein activation of TH that is also cold stress response in LC.

• Journal of Ginseng Research
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• 제5권1호
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• pp.24-34
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• 1981

For bioassay of the various extracts of ginseng, the growth determination method using Saccharomyces cerevisiae which was cultured with various doses of the extracts, was studied The water extract, Powder. and ethanol extract were more effective (about 45∼ 110% increase) than saponins or its fractions (about 20∼35% increase). The cold methanol residue showed a increase effect but it was not significant. The bioassay curves for the water extract, ethanol extract, the butanol extracted saponins and the cold methanol- residue were made from the experimental data. From these curves it is possible to find the relation between dose and effectiveness and the optimal doses of various ginseng extracts, and the amount of extract in a sample can be estimated The .angers of sample amount were 0.01% (100ppm) ∼0.32% (3200ppm) fo. the water extract, 0.025% (150ppm)∼0.1% (1000ppm) for the ethanol extract, and 0.008% (80ppm)∼0.016% (160ppm) for the saponins. It was impossible to determine the range for the cold methanol- residue, The acceleration effects on the cell proliferation by a only 0.0008% (8ppm) of the diol- and triol-saponin were measurable in earlier Period (24 hour treatment).

• Toxicological Research
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• 제14권4호
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• pp.557-562
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• 1998

Allyl alcohol is metabolized in the liver through two steps, first to reactive acrolein by alcohol dehydrogenase (ADH), subsequently to acrylic acid by aldehyde dehydrogenase (ALDH). Since ethanol could compete the same enzymes to be metabolized in the liver, we have determined the plasma concentrations of allyl alcohol and ethanol followed by combined treatment. Pretreatment of rats with 2g/kg ethanol followed by ip administration of 40mg/kg allyl alcohol increased the lethality significantly. Determination of in vivo blood concentrations revealed that ethanol pretreatment caused the apparent decrease in allyl alcohol clearance, whereas acetaldehyde level in blood increased significantly by allyl alcohol treatment, as determined by head space GC analysis. Treatment of 4-methylpyrazole, an inhibitor of ADH, delayed allyl alcohol elimination significantly and reduced its lethality. Collectively, these findings suggested that reduction of allyl alcohol clearance in the presence oj ethanol was mediated through ADH competitive inhibition.

• 분석과학
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• 제22권4호
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• pp.307-312
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• 2009

수용액 중의 carbaryl을 형광분광법을 이용하여 정량하기 위한 분석방법에 대하여 연구하였다. 분석의 최적 조건을 구하기 위해서 들뜸 파장, 계면활성제의 농도, 보조계면활성제인 ethanol의 농도 및 방출 파장의 방출 세기에 대한 영향을 조사하였다. Carbaryl 용액에 계면활성제인 sodium dodecyl sulfate (SDS)을 첨가하였을 때 방출세기가 조금 증가하였으며 보조계면활성제인 ethanol을 첨가하였을 때 방출 세기가 현저히 증가함을 관찰하였다. 최적 분석 조건의 들뜸 파장, 계면활성제의 농도, 보조계면활성제인 ethanol의 농도 및 방출 파장은 각각 281 nm, $1.0{\times}10^{-2}mol/L$, 20% (v/v), 349 nm 이었다. 최적 분석조건에서 carbaryl의 검정곡선의 감응범위와 검출한계($3{\sigma}$)는 각각 $5{\times}10^{-7}$에서 $1.0{\times}10^{-4}mol/L$ 및 $1.1{\times}10^{-8}mol/L$이었다. 검정곡선에서 직선성이 성립하는 농도 범위에서 상관계수(S/N=3)는 0.9996이었다.