• 제목/요약/키워드: Solid Phase Microextraction-GC/MS

검색결과 104건 처리시간 0.022초

털진달래(Rhododendon mucronulatum Turcz. var. ciliatum Nakai) 정유의 성분분석과 독성평가 (Composition and Cytotoxicity of Essential Oil from Korean rhododendron (Rhododendon mucronulatum Turcz. var. ciliatum Nakai))

  • 박유화;김성문
    • Applied Biological Chemistry
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    • 제51권3호
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    • pp.233-237
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    • 2008
  • 우리나라의 자생식물인 털진달래(Rhododendon mucronulatum Turcz. var. ciliatum Nakai)지상부위로부터 정유를 얻고, 휘발성분을 headspace(HS)와 solid-phase microextraction(SPME)법으로 흡착시킨 다음 GC-MS로 분석하였다. 털진달래 정유에는 탄화수소 15종, 알코올 3종, 아세테이트 1종 등 총 19종의 화학성분이 함유되어 있었으며, 다함량 성분은 2-${\beta}$-pinene(16.1%), camphene(11.9%), ${\delta}$-3-carene(11.4%), d,l-limonene(9.5%), and ${\gamma}$-terpinene(9.5%)이었다. SPME법으로 흡착된 시료에는 탄화수소 13종, 알코올 1종, 질소화합물 1종 등 총 17종의 휘발성 화학물질이 함유되어 있었고, 이들 중 다함량 성분은 camphene(19.6%), 2-${\beta}$-pinene(18.0%), ${\delta}$-3-carene(17.4%), timethyl hydrazine(9.7%), ${\gamma}$-terpinene(8.5%), and d,l-limonene(5.5%)이었다. 그리고 HS법으로 흡착된 시료에는 탄화수소 11종, 알코올 1종, 질소화합물 1종 등 총 13종의 휘발성 화학물질이 함유되어 있었으며, 이들 중 다함량 성분은 camphene(25.8%), ${\delta}$-3-carene(24.8%), 2-${\beta}$-pinene(20.2%), d,l-limonene(5.4%), tricyclene(5.1%), trimethyl hydrazine(4.6%)이었다. 털진달래 정유의 향취는 coniferous, balsamic, woody하였으며, HaCaT 각질형성세포에 대한 $IC_{50}$ 값은 0.030 ${\mu}g/mg$이었다.

Evaluation of Volatile Compounds Isolated from Pork Loin (Longissimus dorsi) as Affected by Fiber Type of Solid-phase Microextraction (SPME), Preheating and Storage Time

  • Park, Sung-Yong;Yoon, Young-Mo;Schilling, M. Wes;Chin, Koo-Bok
    • 한국축산식품학회지
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    • 제29권5호
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    • pp.579-589
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    • 2009
  • This study was conducted to investigate the effects of heating, fiber type used in solid-phase microextraction (SPME, two phase vs three phase) and storage time on the volatile compounds of porcine M. longissimus dorsi (LD). Volatile compounds were measured using a gas chromatography and mass spectrometry (GC/MS) with a quadrupole mass analyzer. Among the volatile compounds identified, aldehydes (49.33%), alcohols (24.63%) and ketones (9.85%) were higher in pre-heated loins ($100^{\circ}C$/30 min), whereas, alcohols (34.33%), hydrocarbons (22.84%) and ketones (16.88%) were higher in non-heated loins. Heating of loins induced the formation of various volatile compounds such as aldehydes (hexanal) and alcohols. The total contents of hydrocarbons, alcohols, and carboxylic acids were higher in two phase fibers, whereas those of esters tended to be higher in three-phase fibers (p<0.05). Most volatile compounds increased (p<0.05) with increased storage time. Thus, the analysis of volatile compounds were affected by the fiber type, while heating and refrigerated storage of pork M. longissimus dorsi increased the volatile compounds derived from lipid oxidation and amino acid catabolism, respectively.

Analysis of Agrochemical Residues in Tobacco Using Solid Phase Microextraction-Gas Chromatography with Different Mass Spectrometric Techniques

  • Lee, Jeong-Min;Jang, Gi-Chul;Kim, Hyo-Keun;Hwang, Geon-Joong
    • 한국연초학회지
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    • 제30권2호
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    • pp.117-124
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    • 2008
  • A solid phase microextraction (SPME) method in combination with gas chromatography/mass spectrometric techniques was used for the extraction and quantification of 12 selected agrochemical residues in tobacco. The parameters such as the type of SPME fiber, adsorption/desorption time and the extraction temperature affecting the precision and accuracy of the SPME method were investigated and optimized. Among three types of fibers investigated, polyacrylate (PA), polydimethylsiloxane (PDMS) and polydimethylsiloxane-divinylbenzene (PDMS-DVB), PDMS fiber was selected for the extractions of the agrochemicals. The SPME device was automated and on-line coupled to a gas chromatograph with a mass spectrometer. Mass spectrometry (MS) was used and two different instruments, a quadrupole MS and triple quadrupole MS-MS mode, were compared. The performances of the two GC-MS instruments were comparable in terms of linearity (in the range of 0.01$\sim$0.5 $\mu$g/mL) and sensitivity (limits of detection were in the low ng/mL range). The triple quadrupole MS-MS instrument gave better precision than that of quadrupole MS system, but generally the relative standard deviations for replicates were acceptable for both instruments (< 15%). The LODs was fully satisfied the requirements of the CORESTA GRL. Recoveries of 12 selected agrochemicals in tobacco yielded more than 80% and reproducibility was found to be better than 10% RSD so that SPME procedure could be applied to the quantitative analysis of agrochemical residues in tobacco.

Effect of Stewing Time on the Small Molecular Metabolites, Free Fatty Acids, and Volatile Flavor Compounds in Chicken Broth

  • Rong Jia;Yucai Yang;Guozhou Liao;Yuan Yang;Dahai Gu;Guiying Wang
    • 한국축산식품학회지
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    • 제44권3호
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    • pp.651-661
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    • 2024
  • Chicken broth has a taste of umami, and the stewing time has an important effect on the quality of chicken broth, but there are fewer studies on the control of the stewing time. Based on this, the study was conducted to analyze the effects of different stewing times on the sensory, small molecular metabolites, free fatty acids, and volatile flavor compounds contents in chicken broths by liquid chromatography-quadrupole/time-of-flight mass spectrometry, gas chromatography-mass spectrometry, headspace solid-phase microextraction, and gas chromatography-mass spectrometry. Eighty-nine small molecular metabolites, 15 free fatty acids, and 86 volatile flavor compounds were detected. Palmitic and stearic acids were the more abundant fatty acids, and aldehydes were the main volatile flavor compounds. The study found that chicken broth had the best sensory evaluation, the highest content of taste components, and the richest content of volatile flavor components when the stewing time was 2.5 h. This study investigated the effect of stewing time on the quality of chicken broth to provide scientific and theoretical guidance for developing and utilizing local chicken.

HS-SPME-GC/MS를 이용한 해수 내 유류계 방향족탄화수소 분석법 (Determination of Petroleum Aromatic Hydrocarbons in Seawater Using Headspace Solid-Phase Microextraction Coupled to Gas Chromatography/Mass Spectrometry)

  • 안준건;심원준;하성용;임운혁
    • 한국해양환경ㆍ에너지학회지
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    • 제17권1호
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    • pp.27-35
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    • 2014
  • 해수 내 유류계 방향족탄화수소인 BTEX(benzene, toluene, ethylbenzene, xylene)와 다환방향족탄화수소(polycyclic aromatic hydrocarbons: PAHs)를 동시에 분석할 수 있는 기술 개발을 위해 GC/MS에서 고체상미량추출법(solid phase microextraction: SPME)을 이용하여 최적의 분석기법을 정립하였다. SPME 기법은 전통의 분석 방법과 비교할 때 조작이 간단하고, 파이버를 재사용할 수 있고, 휴대하기 쉽고, 시료의 운반이나 저장하는 동안 오염을 최소화 할 수 있는 장점이 있다. 최적의 SPME 조건을 정립하기 위해 여러 변수 즉, SPME 수착제, 흡착 시간, 흡착 온도, 교반 속도, GC 탈착 시간들을 확인하였다. 다양한 SPME 수착제($100{\mu}m$ PDMS, $75{\mu}m$ CAR/PDMS, $65{\mu}m$ PDMS/DVB)를 이용하여 BTEX와 PAHs(분자량 78부터 202까지)를 동시에 분석한 결과 $65{\mu}m$ PDMS/DVB를 최적의 수착제로 선정하였다. 최적의 수착제로 $65{\mu}m$ PDMS/DVB 선정한 다음 순차적으로 다른 변수들을 확인하였다. 그 결과 BTEX와 PAHs 동시 분석하기 위한 최적의 SPMD 조건은 흡착시간 60분, 흡착온도 $50^{\circ}C$, 교반속도 750 rpm, GC 탈착시간 3분으로 결정되었다. 최적화한 HS-SPME-GC/MS 분석법을 이용하여 인공오염해수 내 유류계 방향족탄화수소 분석 결과 이전 연구 방법과 유사하였다. HP-SPME-GC/MS 분석법은 기존에 유기용매를 사용한 방법이 가졌던 단점과 제한점을 보완할 수 있으며, 해수 내 유류에 의한 BTEX 및 PAHs 분석에 효율적으로 적용할 수 있다.

전자코와 GC/MS를 이용한 포도 품종별 저장 조건에 따른 휘발성 향기 성분 연구 (Identification of Volatile Compounds of 4 Grape Species by Storage Conditions)

  • 이윤정;이기택
    • 한국식품영양과학회지
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    • 제36권7호
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    • pp.874-880
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    • 2007
  • 품종에 따른 포도를 이용하여 3일 동안 $4^{\circ}C$와 실온에 각각 저장함에 따라 변화하는 전체적인 향의 패턴을 전자코를 통하여 분석하였고 SPME-GC/MS 분석 결과를 통하여 휘발성분을 분리 동정하였다. 대표적인 포도의 주요 휘발 성분은 alcohols, esters, acids, terpenes 등으로 GC/MS 분석 결과 butanoic acid/ethyl ester와 1-hexanol, hexanoic acid/ethyl ester, phenylethyl alcohol 등이 주요 성분으로 동정되었다. 캠벨은 다른 품종에 비해 다양한 휘발 성분이 동정되었고 레드글로브와 머루 품종에서는 1-hexanol, 2-decene, 8-methyl-(z)/1-dodecanol 등을 제외한 나머지 휘발 성분은 거의 나타나지 않았다. 또한 전자코를 이용하여 휘발성 향기성분 패턴 분석결과 $4^{\circ}C$와 실온 저장한 시료의 제 1주성분 값의 기여율은 각각 99.30, 99.36%로 품종에 따라 구분이 가능하였다. $4^{\circ}C$ 저장 시 저장 기간에 따른 제 1주성분 값의 변화 범위는 실온에서 저장한 것에 비해 적었음을 확인할 수 있었다.

녹차와 후발효차의 유리형 및 결합형 향기성분에 대한 연구 (Studies on the Free and Bound Aroma Compounds in Green and Fermented Teas)

  • 이혜진;박승국
    • 한국식품과학회지
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    • 제43권4호
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    • pp.407-412
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    • 2011
  • 본 연구에서는 녹차와 녹차에 미생물을 접종하여 발효시킨 후 발효차의 유리형 및 결합형 향기성분을 headspace-solid phase microextraction(HS-SPME)-GC/GC-MS를 이용하여 분석하였다. 녹차가 미생물학적 발효과정을 거치는 중에 녹차에 존재하는 aldehyde류와 ketone류는 감소하였고 linalool과 geraniol은 증가하였다. 녹차와 후발효차 잎에 추가적으로 효소를 처리하여 분석한 결과 녹차에서는 (Z)-3-hexen-1-ol>benzaldehyde>3-hexenyl acetate>geraniol순으로 향기성분이 증가되었고, 후발효차에서는 (Z)-3-hexen-1-ol>benzaldehyde>geraniol>3-hexenyl acetate>1-hexanol 순으로 증가하였으며, 녹차보다는 후발효차에서 효소에 의해 증가되는 향기성분이 많았다. 효소양을 달리하여 처리하였을 때 녹차와 후발효차 모두 효소의 양이 증가함에 따라 휘발성 향기성분이 증가하는 양상을 보였다. 본 실험을 통하여 효소처리를 통해 녹차와 후발효차의 향기를 증가시킴으로써 녹차와 후발효차의 향기 품질을 향상시킬 수 있는 가능성을 확인할 수 있었다.

Development of Analysis Condition and Detection of Volatile Compounds from Cooked Hanwoo Beef by SPME-GC/MS Analysis

  • Ba, Hoa Van;Oliveros, Maria Cynthia;Ryu, Kyeong-Seon;Hwang, In-Ho
    • 한국축산식품학회지
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    • 제30권1호
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    • pp.73-86
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    • 2010
  • The current study was designed to optimize solid phase microextraction (SPME)-GC-MS conditions for extraction and analysis of volatile components for Hanwoo beef and to establish a tentative database of flavor components. Samples were taken from Hanwoo longissimus muscle (30 mon old steer, $1^+B$ carcass grade) at 24 h postmortem. Results indicated that the optimum adsorption time for $75{\mu}m$ CAR/PDMS fiber was 60 min at $60^{\circ}C$. Thermal cleaning at $250^{\circ}C$ for 60 min was the best practice for decontamination of the fiber. A short analysis program with a sharp oven temperature ramp resulted in a better resolution and higher number of measurable volatile components. With these conditions, 96 volatile compounds were identified with little variation including 22 aldehydes, 8 ketones, 31 hydrocarbons, 12 alcohols, 8 nitrogen- and sulfurcontaining compounds, 5 pyrazines and 10 furans. A noticeable observation was the high number of hydrocarbons, aldehydes, ketones, alcohols and 2-alkylfurans which were generated from lipid decomposition especially the oxidation and degradation of unsaturated and saturate fatty acids. This implies that these compounds can be candidates for flavor specification of highly marbled beef such as Hanwoo flavor.

Elicitation of Innate Immunity by a Bacterial Volatile 2-Nonanone at Levels below Detection Limit in Tomato Rhizosphere

  • Riu, Myoungjoo;Kim, Man Su;Choi, Soo-Keun;Oh, Sang-Keun;Ryu, Choong-Min
    • Molecules and Cells
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    • 제45권7호
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    • pp.502-511
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    • 2022
  • Bacterial volatile compounds (BVCs) exert beneficial effects on plant protection both directly and indirectly. Although BVCs have been detected in vitro, their detection in situ remains challenging. The purpose of this study was to investigate the possibility of BVCs detection under in situ condition and estimate the potentials of in situ BVC to plants at below detection limit. We developed a method for detecting BVCs released by the soil bacteria Bacillus velezensis strain GB03 and Streptomyces griseus strain S4-7 in situ using solid-phase microextraction coupled with gas chromatography-mass spectrometry (SPME-GC-MS). Additionally, we evaluated the BVC detection limit in the rhizosphere and induction of systemic immune response in tomato plants grown in the greenhouse. Two signature BVCs, 2-nonanone and caryolan-1-ol, of GB03 and S4-7 respectively were successfully detected using the soil-vial system. However, these BVCs could not be detected in the rhizosphere pretreated with strains GB03 and S4-7. The detection limit of 2-nonanone in the tomato rhizosphere was 1 µM. Unexpectedly, drench application of 2-nonanone at 10 nM concentration, which is below its detection limit, protected tomato seedlings against Pseudomonas syringae pv. tomato. Our finding highlights that BVCs, including 2-nonanone, released by a soil bacterium are functional even when present at a concentration below the detection limit of SPME-GC-MS.

Handspace Solid Phase Microextraction 방법에 의한 HANs 분석에 관한 연구 (Analysis of Haloacetonitriles in Drinking Water Using Headspace-SPME Technique with GC-MS)

  • 조덕희
    • 상하수도학회지
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    • 제18권5호
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    • pp.628-637
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    • 2004
  • In many drinking water treatment plants, chlorination process is one of the main techniques used for the disinfection of water. This disinfecting treatment leads to the formation of disinfection by-products (DBPs) such as haloacetonitriles (HANs), trihalomethanes (THMs), haloacetic acids (HAAs). In this study, headspace-solid phase microextraction (HS- SPME) technique was applied for the analysis of HANs in drinking water. The effects of experimental parameters such as selection of SPME fiber, the addition of salts, magnetic stirring, extraction temperature, extraction time and desorption time on the analysis were investigated. Analytical parameters such as linearity, repeatability and detection limits were also evaluated. The $50/30{\mu}m$-divinylbenzene/carboxen/polydimethylsiloxane fiber, extraction time of 30 minutes, extraction temperature of $20^{\circ}C$ and desorption time of 1 minute at $260^{\circ}C$ were the optimal experimental conditions for the analysis of HANs. The correlation coefficients ($r^2$) for HANs was 0.9979~0.9991, respectively. The relative standard deviations (%RSD) for HANs was 2.3~7.6%, respectively. Detection limits (LDs) for HANs was $0.01{\sim}0.5{\mu}g/L$, respectively.