• Bulletin of the Korean Chemical Society
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• 제30권9호
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• pp.2011-2016
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• 2009

To resolve the differentiation problem of acetone and acrolein in the analysis of carbonyls by high-performance liquid chromatography (HPLC), we investigated the optimum analytical conditions for their separation. Carbonyl compounds were collected by 2,4-dinitrophenylhydrazine (DNPH)-coated cartridges. We examined the influence of three experimental variables: temperature (25, 30, 40, 50 and 60 ${^{\circ}C}$), flow rate (1.0 and 1.2 mL/min), and relative mobile phase composition (among acetonitrile, water and tetrahydrofuran). The experimental results revealed the optimum analytical condition of a flow rate of 1.2 mL/min, temperature of 32 ${^{\circ}C}$ and mobile phase composition of acetonitrile: water: tetrahydrofuran = 34 : 52.8 : 13.2. The analysis of indoor air composition indicated that acrolein and acetone comprised 11% and 42% of all aldehydes, respectively.

• Asian-Australasian Journal of Animal Sciences
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• 제7권4호
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• pp.509-512
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• 1994

High performance liquid chromatography (HPLC) analysis was applied for determination of guanine plus cytosine (G + C) contents of DNA of Butyrivibrio fibrisolvens. By values of G + C contents, a reference strain and 20 wild strains of B. fibrisolvens were classified into at least two distinct subgroups, i.e. G + C contents of 18 strains were 38-40 mol% and those of 3 strains including the reference strain were 43-45 mol%. Clear relationships were not observed between G + C contents and biological properties of 21 strains of B. Fibrisolvens.

• 한국동물위생학회지
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• 제23권1호
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• pp.1-8
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• 2000

This study was carried out to simultaneous determination of penicillin G and chloramphenicol in livestock products by HPLC. The results obstained were as follows; 1. Penicillin G and chloramphenicol were analyzed by HPLC on symmetry $C_{18}$ column with acetonitrile-0.1 M phosphate buffer containing 0.0157 M thiosulfate (25 : 75) as mobile phase at UV 325nm and 280nm, respectively. 2. Samples were applied to a SeP-Pak $C_{18}$ cartridge, from which eluted penicillin derivatized with 2 M 1,2,4-triazole containing 0.001 M mercuric chloride. 3. The average recovery rates of penicillin G and chloramphenicol were 81.8% and 80.3%, respectively, and the detection limits were 5 ppb (5$\mu\textrm{g}$/kg: 7.9IU/kg) for penicillin G and chloramphenicol in porcine and bovine muscle.

• 한국동물위생학회지
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• 제21권3호
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• pp.261-266
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• 1998

A method for the determination of noboviocin in milk was presented by high performance liquid chromatography(HPLC). The novobiocin in the spiked sample was extracted with methanol and evaporated under vacuum. After evaporating, the residue was mixed with distilled water for 2$m\ell$, filtrates with 0.45$\mu\textrm{m}$ acrodisc was injected into HPLC. The results obtained were as follows ; 1. The calibration curve of novobiocin was showed constantly linear(r 0.999) in the range of 100~500ng/$m\ell$. 2. The mean recovery rate of novobiocin from the spiked milk sample were 88~98%. 3. The coefficients of variation were 2.6~5.8% 4. The lowest detectable limit of novobiocin was 25ppb.

• Journal of Applied Biological Chemistry
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• 제66권
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• pp.338-344
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• 2023

Curcuma longa is a plant belonging to the genus Curcuma and is distributed across various Asian regions. This plant is widely known for its rhizomes, which possess a variety of pharmacological properties. However, although the leaves and stems of this plant also contain several health-promoting secondary metabolites, very few studies have characterized these compounds. Therefore, our study sought to quantify the secondary metabolites from the leaves and stems of Curcuma longa L. (LSCL) using liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) and high-performance liquid chromatography (HPLC). Our LC-ESI-MS analyses detected twenty-one phenolic compounds in the LSCL, among which fifteen compounds were detected via HPLC analysis. Four compounds, namely vanillic acid (0.129 mg/g), p-coumaric acid (0.431 mg/g), 4-methylcatechol (0.199 mg/g), and afzelin (0.074 mg/g) were then quantified. These findings suggest that LSCL is rich in secondary metabolites and holds potential as a valuable resource for the development of functional and nutritional supplements in the future.

• Applied Biological Chemistry
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• 제36권4호
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• pp.310-314
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• 1993

HPLC를 이용하여 fructose oligomer인 fructo올리고당(GF2-GF7) 및 inulo올리고당(F2-F4)의 분리, 정량을 실시하였다. TSK-gel amide 80 column과 acetonitrile-water(65:35; v/v) 용매를 사용하여 각 표준당들을 효과적으로 분리할 수 있었으며 이들의 retention time은 분석시마다 거의 변하지않아 재현성이 있었다. 각 당의 농도에 따른 peak면적을 이용하여 표준곡선을 작성한 결과 넓은 당량의 범위에 걸쳐 결정계수가 0.9884이상의 값을 보여 본 HPLC방법에 의한 정량법이 타당한 것으로 나타났다. 또한 기울기는 비슷하나 y축 절편 값이 당마다 크게 상이하여 몇가지 표준당들을 기준으로 하여 모든 당을 일률적으로 정량하는 것은 적합하지 않으며 각 당에 대한 표준곡선을 하나씩 작성하여 정량하여야함을 알 수 있었다.

• Journal of the Korean Wood Science and Technology
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• 제36권4호
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• pp.102-108
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• 2008

현재 메인 주립대학에서는 펄프용 목재 성분 중 헤미셀룰로오스 추출 기술에 관한 연구개발이 한창 진행 중이다. 펄프의 수율 향상과 용액 회수에 필요한 유기 및 무기물 사용을 줄이고 새로운 바이오 물질 생산에 필요한 도입부 추가 공정이 연구의 핵심이다. 바이오 물질 중 경제적으로 상용 가능한 에탄올 생산(pilot-scale)에 있어 전 처리되지 않은 기질, 전 처리된 기질 및 펄핑 선 추출액의 화학적 성분분석은 아주 중요한 공정이다. HPLC (High Performance Liquid Chromatography)를 이용한 펄프목재 성분분석 결과, H-column으로 분석한 총 물질수지(total analytical mass balance)는 전 처리되지 않은 칩의 경우 100.6%, 전 처리된 목재 칩은 100.3%, 그리고 펄핑 선 추출액은 81.6%의 결과를 보였다. 한편, P-column으로 분석한 결과, 전 처리되지 않은 기질, 전 처리된 기질, 그리고 선 추출액은 각각, 97.8%, 97.4%, 그리고 80.7%로 나타났다. 총 물질수지가 100%를 넘거나 부족한 수치는 분석해석 중 발생한 약간의 오류로 보인다. 펄프-바이오리파이너리(Biorefinery) 공정을 통해 생성된 기질(substrate) 각각의 정확한 성분분석 결과는 에탄올 상용화 공정에 필요한 중요한 자료가 될 것으로 기대한다.

• 약학회지
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• 제29권1호
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• pp.50-54
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• 1985

Seven different sorbents were evaluated for their adsorptivity and desorptivity of antibiotic, chloramphenicol. Among the sorbents studied, Carbopak B was found to be the most efficient in enriching the chloramphenicol from dilute aqueous solution. Interfering components in the milk matrix could be washed off by water and petroleum ether from Carbopak B column, while the chloramphenicol was retained on the surface of Carbopak B. The method of simple and efficient purification and enrichment of chloramphenicol using Carbopak B, followed by quantitative analysis employing $C_{18}$ reversed phase high performance liquid chromatography has been applied to the determination of chloramphenicol in milk.

• 생약학회지
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• 제24권4호
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• pp.309-312
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• 1993

A new method for separation and quantitative determination of isoflavone glucosides in rhizomes of Belamcanda chinensis (Iridaceae) by high performance liquid chromatography was elaborated. A reverse-phase system with a Spheri-5 RP-18 column using MeOH:HOAc:$H_2O$(24 : 5 : 71) as a mobile phase was developed. The isoflavonoids were detected at 268 nm and the analysis was successfully carried out within 15 min.

• 한국자원식물학회지
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• 제25권5호
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• pp.640-646
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• 2012

This research was attempted to determine the composition of flavone glycosides (luteolin 7-O-glucoside, luteolin 7-O-glucuronide, linarin) in addition to luteolin simultaneously in aerial part of Youngia japonica (Compositae) by high-performance liquid chromatography. The MeOH extract was further fractionated into the three parts, $CHCl_3$ fraction, EtOAc fraction and BuOH fraction, to investigate the contents of the four flavones in the three fractions. The content of luteolin 7-O-glucuronide (10.07 mg/g) was highest in the MeOH extract among those of the flavones. These four compounds were observed to be less than 1.0 mg/g in $CHCl_3$- and EtOAc fractions but relatively high in BuOH fraction.