• 제목/요약/키워드: SPME(solid-phase microextraction)

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Solid-Phase Microextraction(SPME)을 이용한 둥굴레차의 증자 여부에 따른 향기성분 특성 비교 (Comparison of Flavor Compounds in Steamed- and Nonsteamed-Roasted Polygonatum odoratum Roots by Solid-Phase Microextraction)

  • 박난영;서지형;김영회;권중호
    • 한국식품과학회지
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    • 제32권3호
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    • pp.507-512
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    • 2000
  • 고품질 둥굴레차의 제조를 위한 기반연구로서 solid-phase microextraction(SPME)을 이용한 headspace 방법에 의해 볶음 전 중자(steaming) 여부에 따른 둥굴레차의 향기성분 특성을 비교하였다. SPME fiber에 대한 향기성분의 흡착조건은 $60^{\circ}C$에서 30분이 적합하였고, 무중자 및 중자(120분)된 시료를 $130^{\circ}C$에서 15분간 볶음 처리하여 분석 GC chromatogram에서는 40여 종의 peak가 분리되었고, 전반적인 pattern은 유사하였으나 서로 상이한 peak특성이 관찰되었다. 분리된 성분들을 GC-MS와 retention time 비교에 의해 25종을 동정하였으며, 무중자 볶음처리 둥굴레는 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyran-4-one, 2,5-di-methyl-4-hydroxy-3(2H)-furanone, 2-acetyl-1-pyrroline 등의 pyrazine류 함량이 중자 후 볶음 둥굴레보다 높게 나타나 둥굴레의 고유한 향과 맛에 큰 영향을 미칠 것으로 추정되었다. 특히 중자 후 볶음 처리한 둥굴레의 경우에는 acetic acid(8.17%)와 hexanoic acid(5.43%)의 함량이 무중자 시료(2.40%와 2.00%)보다 높게 나타났다.

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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.

Volatile Metabolic Markers for Monitoring Pectobacterium carotovorum subsp. carotovorum Using Headspace Solid-Phase Microextraction Coupled with Gas Chromatography-Mass Spectrometry

  • Yang, Ji-Su;Lee, Hae-Won;Song, Hyeyeon;Ha, Ji-Hyoung
    • Journal of Microbiology and Biotechnology
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    • 제31권1호
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    • pp.70-78
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    • 2021
  • Identifying the extracellular metabolites of microorganisms in fresh vegetables is industrially useful for assessing the quality of processed foods. Pectobacterium carotovorum subsp. carotovorum (PCC) is a plant pathogenic bacterium that causes soft rot disease in cabbages. This microbial species in plant tissues can emit specific volatile molecules with odors that are characteristic of the host cell tissues and PCC species. In this study, we used headspace solid-phase microextraction followed by gas chromatography coupled with mass spectrometry (HS-SPME-GC-MS) to identify volatile compounds (VCs) in PCC-inoculated cabbage at different storage temperatures. HS-SPME-GC-MS allowed for recognition of extracellular metabolites in PCC-infected cabbages by identifying specific volatile metabolic markers. We identified 4-ethyl-5-methylthiazole and 3-butenyl isothiocyanate as markers of fresh cabbages, whereas 2,3-butanediol and ethyl acetate were identified as markers of soft rot in PCC-infected cabbages. These analytical results demonstrate a suitable approach for establishing non-destructive plant pathogen-diagnosis techniques as alternatives to standard methods, within the framework of developing rapid and efficient analytical techniques for monitoring plant-borne bacterial pathogens. Moreover, our techniques could have promising applications in managing the freshness and quality control of cabbages.

Volatile Compounds for Discrimination between Beef, Pork, and Their Admixture Using Solid-Phase-Microextraction-Gas Chromatography-Mass Spectrometry (SPME-GC-MS) and Chemometrics Analysis

  • Zubayed Ahamed;Jin-Kyu Seo;Jeong-Uk Eom;Han-Sul Yang
    • 한국축산식품학회지
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    • 제44권4호
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    • pp.934-950
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    • 2024
  • This study addresses the prevalent issue of meat species authentication and adulteration through a chemometrics-based approach, crucial for upholding public health and ensuring a fair marketplace. Volatile compounds were extracted and analyzed using headspace-solid-phase-microextraction-gas chromatography-mass spectrometry. Adulterated meat samples were effectively identified through principal component analysis (PCA) and partial least square-discriminant analysis (PLS-DA). Through variable importance in projection scores and a Random Forest test, 11 key compounds, including nonanal, octanal, hexadecanal, benzaldehyde, 1-octanol, hexanoic acid, heptanoic acid, octanoic acid, and 2-acetylpyrrole for beef, and hexanal and 1-octen-3-ol for pork, were robustly identified as biomarkers. These compounds exhibited a discernible trend in adulterated samples based on adulteration ratios, evident in a heatmap. Notably, lipid degradation compounds strongly influenced meat discrimination. PCA and PLS-DA yielded significant sample separation, with the first two components capturing 80% and 72.1% of total variance, respectively. This technique could be a reliable method for detecting meat adulteration in cooked meat.

Comparative Analyses of the Flavors from Hallabong (Citrus sphaerocarpa) with Lemon, Orange and Grapefruit by SPTE and HS-SPME Combined with GC-MS

  • Yoo, Zoo-Won;Kim, Nam-Sun;Lee, Dong-Sun
    • Bulletin of the Korean Chemical Society
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    • 제25권2호
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    • pp.271-279
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    • 2004
  • The aroma component of Hallabong peel has been characterized by GC-MS with two different extraction techniques: solid-phase trapping solvent extraction (SPTE) and headspace solid-phase microextraction (HSSPME). Aroma components emitted from Hallabong peel were compared with those of other citrus varieties: lemon, orange and grapefruit by SPTE and GC-MS. d-Limonene (96.98%) in Hallabong was the main component, and relatively higher peaks of cis- ${\beta}$-ocimene, valencene and -farnesene were observed. Other volatile aromas, such as sabinene, isothujol and ${\delta}$-elemene were observed as small peaks. Also, principal components analysis was employed to distinguish citrus aromas based on their chromatographic data. For HSSPME, the fiber efficiency was evaluated by comparing the partition coefficient ($K_{gs}$Kgs) between the HS gaseous phase and HS-SPME fiber coating, and the relative concentration factors (CF) of the five characteristic compounds of the four citrus varieties. 50/30 ${\mu}$m DVB/CAR/PDMS fiber was verified as the best choice among the four fibers evaluated for all the samples.

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.

물중의 잔류농약 분석을 위한 SPME의 최적조건 선정에 관한 연구 (Preparation of Optimal Condition for Residual Pesticides Analysis by Solid-Phase Microextraction in Water)

  • 장미라;정효준;이홍근
    • 한국물환경학회지
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    • 제18권4호
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    • pp.421-433
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    • 2002
  • This study was conducted to develope a simple, rapid and solvent-free solid-phase microextraction(SPME) procedure for extracting three organochlorine, one triazine and nine organophosphorus pesticides from water. The optimal conditions of SPME for analyses of organochlorine pesticides were obtained at $250^{\circ}C$ of desorption temperature, 45 minutes of equilibrium time, pH 6 and NaCl 0% addition using $100{\mu}m$ polydimethylsiloxane fiber and those of triazine and organophosphorus pesticides were obtained at $270^{\circ}C$ of desorption temperature, 60 minutes of equilibrium time, pH 6 and NaCl 0% addition using $100{\mu}m$ polydimethylsiloxane fiber. This method showed good lineality for organochlorine pesticides between 0.0001 and $10{\mu}g/L$ with regression coefficients ranging 0.9986~0.9992 and for triazine and organophosphorus pesticides between 0.01 and $10{\mu}g/L$ with regression coefficients ranging 0.9867~0.9998.

Headspace Solid Phase Microextraction-Gas Chromatography/Mass Spectrometry를 이용한 비타민드링크 제품 중 Benzene의 미량분석 (Determination of the presence of benzene in vitamin drinks using headspace - solid phase microextraction and gas chromatography - mass spectrometry)

  • 김종훈;이경민
    • 분석과학
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    • 제20권3호
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    • pp.237-245
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    • 2007
  • 현재 시중에서 판매되고 있는 비타민드링크 제품 중 20개사 31개 제품의 벤젠 함량을 headspace-solid phase microextraction(HS-SPME)법을 이용하여 GC/MS-SIM으로 분석을 하였다. SPME fiber는 $100{\mu}m$ PDMS를 사용하였다. 또한 정량방법은 표준물첨가법을 사용하였으며 40 mL vial에 용액 25 mL를 취하고 그 안에 자석젓개를 넣어 1200 rpm에서 교반시키고 4분 동안 흡착시킨 후 1분 동안 GC에서 탈착시켜 표준검량곡선을 작성하였다. 이 때 검량곡선의 상관계수 값은 0.999이상을 나타내었다. 검출한계는 시료를 분석할 때마다 산출하였는데 평균값이 0.56 ng/mL(${\pm}0.43$)이었으며 회귀식이 존재하는 농도의 범위는 0~40 ng/mL였다. 그 결과 시료 중 벤젠의 함유량은 nd~47.35 ng/mL의 농도의 범위였다. 전체 시료 중 15개의 제품에서 벤젠이 검출되었으며 그 중 5개의 제품에서는 벤젠의 함량이 먹는 물 수질기준인 10 ng/mL를 넘는 각각 16.99 ng/mL, 35.14 ng/mL, 16.03 ng/mL, 47.35 ng/mL, 14.28 ng/mL가 검출되었다.

HS-SPME 방식에 기초한 물 중 VOC 성분의 분석기법에 대한 연구: 3가지 실험 조건의 변화와 분석감도의 관계 (Determination of VOC in aqueous samples by the combination of headspace (HS) and solid-phase microextraction (SPME))

  • 박신영;김기현;양혜순;하주영;이기한;안지원
    • 분석과학
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    • 제21권2호
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    • pp.93-101
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    • 2008
  • SPME 분석기법은 헤드스페이스(Headspace: HS) 방식으로 기체상태의 흡착을 유도하거나, 액상시료에 직접 접촉하는 방식으로 분석대상 물질을 추출할 수 있다. 본 연구에서는 CAR/PDMS fiber를 이용하여, 액상시료의 VOC 분석을 시도하였다. 3 가지 변수 (흡착온도, 흡착시간, 교반여부)의 강약을 동시에 감안한 8가지 조합조건에서 분석효율을 조사하였다. (1) 용출온도: 30 대비 $50^{\circ}C$. (2) SPME fiber 시료노출시간: 10과 30 min. (3) 교반적용 여부: 무 교반 대비 1200 rpm. 8가지의 조합형 분석조건에서 HS-SPME 방식을 적용하여분석한 결과, S50-30 (stirring speed: 1200 rpm, exposure temp: 50oC, exposure time: 30 min)에서 가장 분석효율이 높게 나타났다. 가장 좋은 감도를 보인 S50-30방식의 분석 회수율을 GC에 직접주입하는 방식을 임의의 기준으로 평가하였을 때, 성분에 따라 상대 회수율이 45.5~68.5%로 나타났다. 본 연구의 결과, 3가지 변수 중에서 교반여부는 검량 특성을 결정짓는 가장 중요한 인자로 나타났다.

대기중의 악취성 황화물분석을 위한 SPME 분석법 (Analysis of Odorous Sulfur compounds in Air by Solid Phase Microextraction)

  • 허귀석;김대원;윤영경;정용순
    • 한국대기환경학회:학술대회논문집
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    • 한국대기환경학회 2000년도 추계학술대회 논문집
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    • pp.343-344
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    • 2000
  • 대기중의 황화합물 분석은 현행 우리나라 악취공정시험법에 고시되어 있으나 복잡한 농축장치를 필요로하고 조작법이 복잡하고 시간이 많이 소요된다. 특히 황화합물은 주요 악취물질로서 대기오염을 일으키고 있으며, 극미량에서(ppb) 악취를 발생시키는 악취물질임에도 불구하고 분석방법 및 정확도에 많은 문제점을 갖고 있다. 본 연구에서는 황화물 시료농축이 간단하며, 직접 주입, 분석할 수 있는 SPME(Solid-phase microextraction)을 이용하여 황화물을 신속하게 분석할 수 있는 분석법을 개발하고 저 하였다. 분석방법에 대한 분석재현성, 분석한계를 조사하였으며, 이 분석방법이 대기중 황화물분석 방법으로 활용될 수 있도록 분석법을 확립하고자 하였다. (중략)

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