• 한국식품과학회지
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• 제20권4호
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• pp.585-593
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• 1988

다수계 품종인 남풍, 밀양 23호와 일반계 품종인 화성, 진흥을 각각 현미, 백미, 겨로 구분하여 준비한 12가지 시료의 지질 성분을 비교하여 보고자 총 지질의 함량, thin layer chromatography(TLC)를 이용한 중성지질의 조성, gas chromatography(GC)를 이용한 각 지질의 지방산 조성을 살펴 보았다. 1. 다수계 2품종, 일반계 2품종을 각각 현미, 백미, 겨로 구분한 12종류의 시료에서 추출한 총 지질의 함량은 현미가 평균 2.65%, 백미가 1.09%, 겨가 20.24%였으며, 품종, 다수계, 일반계 간에 통계적으로 유의적인 차이를 나타내지 않았다. 중성지질의 함량비는 현미가 평균 83.53%, 백미가 87.72%, 겨가 91.06%로 겨의 중성지질 비율이 높았으나 통계적으로 유의적인 차이는 아니었다. 당지질은 현미가 12.39%로 가장 높았고. 백미와 겨는 같은 수준이었다. 인지질의 함량비는 겨가 가장 낮았는데 그중에서도 일반계는 다수계 보다 인지질 함량비가 높았으며, 백미에서도 같은 경향이었다. 2. 중성지질의 조성은 thin layer chromatography(TLC) 상에 7가지가 분리 되었고 그 중 6가지 종류의 중성지질을 표준품의 Rf치와 비교하여 확인하였다. 그 결과 triglyceride(TG) 함량이 현미 56.73%, 백미 52.48%, 겨가 36.42%로 가장 높았고. 다음이 free fatty acids(FFA), steryl esters(SE) 순이었다. 현미와 백미에 비해 겨의 TG함량은 매우 낮은 편이고, FFA는 32.49%로 현미의 17.63%, 백비의 24.39%에 비해 높은 편이었다. 3. 총지질의 지방산 조성은 oleic acid가 37.28%, linoleic acid가 39.08%로 함량이 비슷한 정도로 가장 높았고, 다음이 palmitic acid였다. 겨의 oleic acid 함량이 40.42%로 현미와 백미에 비해 높았고, linoleic acid는 현미와 백미에 비해 낮았다. 이러한 결과는 통계적으로 다수계, 일반계, 품종 그리고 도정에 의해 총 지질의 조성에 유의적인 차이가 없었다. 4. 중성지질의 지방산조성은 총 지질의 지방산 조성과 별 차이 없이 oleic acid와 linoleic acid 함량이 가장 높았고, 다음이 palmitic acid였다. 현미는 oleic acid와 linoleic acid 함량이 각각 37.47%, 38.40%로 거의 차이가 없었고, 백미는 linoleic acid 함량이 43.16%로 oleic acid에 비해 높았으며, 겨는 oleic acid 함량이 40.97%로 높고 linoleic acid 함량이 낮았다.

• 한국식품영양과학회지
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• 제22권3호
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• pp.307-312
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• 1993

감잎의 메탄올 추출물이 Salmonella typhimurium TA100에서 aflatoxin B$_1$(AFB$_1$), DMAB, MNNG, 그리고 4-NQO의 돌연변이 유발성을 억제시키는 효과가 있었다. 메탄올 추출물을 다시 hexane, chloroform, ethyl acetate, butanol, 그리고 수용성층으로 분획하여 각 획분의 수득율과 항돌연변이 효과를 조사하였다. Hexane, butanol, 그리고 수용성 획분의 수득율이 높았으며, 이중 hexane 획분이 AFB$_1$, DMAB, MNNG, 그리고 4-NQO에 대한 Salmonella typhimurium TA100에서 항돌연변이효과가 가장 크게 나타났다. Hexane 획분을 silica gel column과 thin layer chromatography (TLC)법으로 연속분리하여 TLC상에서 8개의 bands로 분리하였다. 그중 항돌연변이 효과가 가장 컸던 band를 hexane/ethylacetate (1 : 1, v/v)로 추출한 다음 그중에 존재하는 화합물을 GC-MS를 이용하여 분리동정하였다. 활성획분에서는 1'-oxocannabinol, 3$\beta$-acetoxy-17-methyl-5$\alpha$-18 (13-17) abeoard-rost-13-ene, 4-methoxy-2'6'-dinitro-3,5-di-t-butylbiphenyl, 8, 9-dihydro-5,6-dimethoxy-dibenz［c,h］isoquino ［2, 1, 8-1ma］carbazole-11, 16-dione 등이 분리동정되었다.

• 셀메드
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• 제11권4호
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• pp.21.1-21.9
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• 2021

Background: Unani System of Medicine (USM) has its origin to Greece. To ensure and develop the quality, authenticity of Unani drugs, standardization on modern analytical parameter is essential requirement for drugs. Objectives: The aimed of the present study was to develop a standard profile of "Qurṣ-e-Mafasil" by systematic study through authenticated ingredients, pharmacognostic identification followed by physicochemical, TLC, HPTLC fingerprinting analysis as per standard protocol. Material and Methods: In this study three batches of "Qurṣ-e-Mafasil" QM were prepared by standard method as per UPI had been followed by organoleptic properties of formulation such as appearance, color, odor, taste. Powder Microscopy and physicochemical studies were carried out such as Uniformity of weight, Friability, Disintegration time, hardness, LOD, ash vales and extractive values in like aqueous, alcohol & hexane. Further qualitative tests such as Thin-Layer Chromatography (TLC), and High-Performance Thin Layer Chromatography (HPTLC) studies were also carried out to develop fingerprint pattern of the alcoholic solvent extract of QM. Phytochemical screening was carried out in different solvent extracts such as alcoholic, aqueous and chloroform extracts to detect the presence phytoconstituents in the formulation QM. Heavy metals, Microbial Load Contamination and pesticidal residues were also determined. Results: Qurṣ-e-Mafasil showed tablet-like appearance, light brown colour, mild pungent odour and acrid taste. Uniformity of weight (mg), friability (rpm), and hardness (kg/cm) and disintegration time was ranged between (500 to 503), (0.0340 to 0.038), (8.40 to 8.67) and (4-5 minutes) respectively for the three batches. Loss in weight on drying at 105℃ was ranged between (8.3425 to 8.7346). Extracted values were calculated in distilled water ranged between (30.9091 to 31.4358), hexane (1.1419 to 1.4281), and alcohol (3.3352 to 3.3962). The ash values recorded were ranged between (3.7336 to 3.8378), and acid insoluble ash (0.5859 to 0.6112).

• Biomolecules & Therapeutics
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• 제1권1호
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• pp.58-64
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• 1993

DNA addicts induced by putative chemical related to carcinogenesis were detected and determined by $^{32}$P-Postlabelling assay after exposure of 4 compounds comprising two auto dyes (amaranth, new coccine) and two flavonoid compounds (rutin, quercetin) to ICR mouse. DNA was isolated from mouse liver and digested enzymatically to deoxyribonucleoside 3'-monophosphate. The postincubation of DNA digests with nuclease Pl before $^{32}$P-labelling enhanced the technique's sensitivity. Nuclease Pl cleaves deoxyribonucleoside 3'-mono-phosphates of normal nucleotides to deoxyrihonucleosides which do not serve as substrates for polynucleotide kinase, while most of addicts were found to be totally or partially resistant to the 3'-dephosphorylating action of nuclease Pl. The adducted deoxyribonucleoside 3'-monophosphate was converted to 5'-$^{32}$P-labelled deoxynucleoside 3',5'-bisphosphate by T4 polynucleotide kinase. The nucleotides were separated by anion-exchange thin layer chromatography(TLC) on polyethyleneimine cellulose by 4-dimensional or 2-dimensional TLC then detected by autoradiography. The results show that DNA addicts were detected in liver DNA of ICR mouse after administration of amaranth and quercetin by 2-dimensional and/or 4-dimensional TLC.

• 한국환경농학회지
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• 제11권2호
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• pp.125-132
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• 1992

토양 및 수용액조건에서와 자외선조사시의 bifenthrin의 주 분해대사산물을 확인하고 토양중 에서의 용탈을 조사한 결과는 다음과 같다. 토양 및 수용액조건에서와 자외선조사시 bifenthrin의 일차분해산물은 2-methylbiphenyl-3-ylmethanol로 HPLC, UV, Mass 및 NMR로 확인되었으며 bifenthrin의 주 분해경로는 ester결합의 가수분해 작용으로 나타났다. 자외선 조사시 bifenthrin은 첨가농도 10,100ppm에서 24시간만에 거의 분해 소실되었으며 1,000ppm일 때는 약 80%정도 분해되었다. Soil TLC 및 column상에서 bifenthrin은 거의 용탈되지 않고 표토에 존재하였다.

• 약학회지
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• 제38권1호
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• pp.12-19
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• 1994

Capsaicin(8-methyl-N-vanillyl-6-nonenamide) is the principal pungent component of Capsicum fruits. This work is directed to the capsaicin-hydrolyzing enzyme playing a key role in the rate limiting and critical step of capsaicin metabolism. In order to get precise information on the enzyme's subcellular location, rat liver homogenate was divided into six subcellular fractions by differential centrifugation technique: crude nuclear pellet, PNS(post nuclear supernatant) fraction, lysosomal pellet, cytosol, Tris wash fraction, micrisomes. Capsaicin-hydrolysing enzyme activity was analysed by high performance liquid chromatography(HPLC). This enzyme was found at the highest specific activity in the microsomal fraction and co-distributed with marker enzymes of the endoplasmic reticulum, NADPH-cytochrome c reductase and nucleoside diphosphatase. This is compatible with the result of ninhydrin color reaction of vanillylamine, primary metabolite of capsaicin hydrolysis, on thin layer chromatography(TLC). This enzyme is most active at pH $8.0{\sim}9.0$. Definite subcellular location of this enzyme will make it easy to proceed with further study.

• International Journal of Industrial Entomology and Biomaterials
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• 제16권2호
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• pp.57-59
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• 2008

While searching for pancreatic lipase inhibitors, the active compound was found in a methanol extract of Apis mellifera venome. The active compound was isolated by Diaion HP-20 column chromatography, thin layer chromatography and HPLC. The active compound is stable to the extreme pH and heat. There is no loss of activity both in acidic and alkaline solution in the pH range of 2 to 11 by heating for 15 minutes at $90^{\circ}C$. The rf value of the compound was 0.51 at TLC with butanol : methanol: water (4:1:2) solvent system. The molecular weight of the compound was determined to be 293 by EI-MS.

• Journal of Microbiology and Biotechnology
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• 제17권6호
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• pp.919-927
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• 2007

Antagonistic fluorescent pseudomonads isolated from rhizospheric soil of rice were characterized by 16S rRNA amplicon and fatty acid methyl ester (FAME) analyses. Antagonistic isolates were grown in the fermentation media, and production of antibiotics was confirmed by thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC). Production of fungal cell-wall-degrading enzymes such as protease, cellulase, pectinase, and chitinase was determined. Dendrogram based on the major and differentiating fatty acids resulted into 5 clusters, viz., cluster I (P. pseudoalcaligenes group), cluster II (P. plecoglossicida group), cluster III (P. fluorescens group), cluster IV (P. aeruginosa group), and cluster V (P. putida group). Characteristic presence of high relative proportions of cyclopropane (17:0 CYCLO w7c) was observed in antagonistic bacteria. Data revealed biodiversity among antagonistic fluorescent pseudomonads associated with the rice rhizosphere. Results presented in this study will help to identify the antagonistic isolates and to determine their mechanisms that mediate antagonism against fungal pathogens of rice.

• 한국철도학회:학술대회논문집
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• 한국철도학회 2007년도 추계학술대회 논문집
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• pp.1843-1845
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• 2007

As the preservation law of soil environment has reinforced, several soil remediation projects have been performing for railroad sites. One of the main sources of soil contamination is the leakage of diesel from locomotives or underground storage tank. Also, the lubricant used to maintain turnouts causes railroad soil contamination. The purpose of this study was to develop the analysis and the remediation method for lubricant-contaminated soil. The lubricant in the contaminated soil was analyzed qualitatively and quantitatively by TLC (Thin Layer Chromatography) and GC (Gas Chromatography), respectively. The organic pollutants were removed from the soil using microorganisms degrading lubricant. Hereafter it will be necessary to apply this bioremediation method in the railroad field.

• 한국한의학연구원논문집
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• 제2권1호
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• pp.496-505
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• 1996

In order to improve the qualities of boiling extract the availability of standard compounds was investigated in extract of Scutellariae Radix. The standard compounds used baicalin(1), baicalein(2), and wogonin(3). The availabilities were analyzed by thin layer chromatography (TLC) and high performance liquid chromatography(HPLC) on $C_18$ column. The extract of RS-4(W/V=10g/100m1) showed the highest availabilities as 7.95% of baicalin(1), 1.04% of baicatein(2), and 0.31% of wogonin(3).