• 분석과학
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• 제35권2호
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• pp.82-91
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• 2022

Grayanotoxin-contaminated honey exhibits toxicity. In this study, a reliable and sensitive liquid-chromatography-tandem-mass-spectrometric method (LC-MS/MS) was developed and validated for the quantitation of grayanotoxin I and grayanotoxin III in honey. The grayanotoxins were extracted from honey via solid phase extraction and separated on a biphenyl column with a mobile phase consisting of 0.5 % acetic acid in water and methanol. Mass spectrometric detection was performed in the multiple-reaction monitoring mode with positive electrospray ionization. The calibration curve covered the range 0.25 to 100 ㎍/g. The intra- and inter-day deviations were less than 10.6 %, and the accuracy was between 94.3 and 114.0 %. The validated method was successfully applied to the determination of grayanotoxins in mad honey from Nepal. The concentrations of grayanotoxin I and grayanotoxin III in 33 out of 60 mad honey samples were 0.75 - 64.86 ㎍/g and 0.25 - 63.99 ㎍/g, respectively. The method established herein would help in preventing and confirming grayanotoxin poisoning.

• Bulletin of the Korean Chemical Society
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• 제27권9호
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• pp.1315-1322
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• 2006

The following study describes the gas chromatography-mass spectrometry (GC-MS) based screening and confirmation analysis of urinary androgenic steroids. Four commercially available solid-phase extraction (SPE) cartridges, Serdolit PAD-1, Sep-pak $C_{18}$, amino-propyl, and Oasis HLB, and three different extractive organic solvents, diethyl ether, methyl tert-butyl ether (MTBE), and n-pentane, were tested for sample preparation. Overall, Oasis HLB combined with MTBE extraction provided the highest recoveries in 39 of 46 total androgenic steroids examined and it showed a good extraction yield (>82.1%) for polar steroids, such as metabolites of fluoxymesterone, oxandrolone, and stanozolol, which gave a poor recovery in both n-pentane (9.2-64.3%) and diethyl ether (22.2-73.6%) extractions. All SPE sorbents tested showed potential, because they were efficient in extraction for most or selective steroids. When applied to positive urine samples based on the results obtained, the present method allowed selective and sensitive analysis for detection of urinary androgenic steroids. The experiments showed that the high-resolution MS method is clearly more efficient than the low-resolution MS technique for the detection of many urinary steroids. However, comprehensive sample clean-up procedures also might be needed especially in confirmation analysis to increase detectability.

• 한국물환경학회지
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• 제21권6호
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• pp.549-563
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• 2005

The study was carried out to develop and standardize the analytical method of 1,4-dioxane in water. The National Institute of Environmental Research in Korea has monitored for 1,4-dioxane in water since 1998 and it has been detected in environmental water occasionally. But the environmental pollution and analytical method in water is not well known over the world. The trace analytical method at low-${\mu}/L$ level is prerequisite in order to evaluate the residue of 1,4-dioxane in water. Evaluation of the method was demonstrated by comparing and analyzing with liquid-liquid extraction, solid-phase extraction and purge & trap technique. As a result of experiment by standard solutions and raw samples, the precision and accuracy for three methods were obtained within error rate of about 10%. Therefore, three methods were standardized as official monitoring method in Korea. Also, a convenient and simple liquid-liquid extraction method for the analysis of 1,4-dioxane in water was developed by combined with gas chromatography/mass spectrometry and applied to the water samples in Korea

• 분석과학
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• 제7권4호
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• pp.441-453
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• 1994

수질에서 유해물질을 농축하는 방법으로 액체 추출법과 고체상 추출법을 GC/MS를 검출기로 사용하여 비교하였다. 비휘발성 유해물질 중 11종의 산과 44종의 염기/중성 화합물들을 reagent water에 첨가하여 분석한 결과, 액체추출법은 54종의 화합물에 대해 91%의 평균회수율과 4.6%의 평균상대표준편차를 나타내었으며, 고체상 추출법은 52종의 화합물에 대해 63%의 평균회수율과 8.9%의 평균상대표준편차를 보였다. 두 방법의 검출한계는 $1{\sim}5{\mu}g/l$였다.

• 센서학회지
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• 제23권4호
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• pp.217-223
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• 2014

Nerve agents are major chemical warfare agents with the "G series" and "V series" being the most widely known because of their lethal effect. Although not conspicuously used in major wars, the potential detrimental impact on modern society had been revealed from the sarin terror attack on Tokyo subway, which affected thousands of people. In this mini-review, major nerve agents of the "G series" and "V series" have been described along with various types of their detection methods. The physical properties and hydrolysis mechanisms of the major nerve agents are discussed since these are important factors to be considered in choosing detection methods, and specifying the procedures for sample preparations in order to enhance detection precision. Various types of extraction methods, including liquid-phase, solid-phase, gas-phase and solid-phase microextraction (SPME), are described. Recent development in the use of gas sensors for detecting nerve agents is also summarized.

• 한국식품과학회지
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• 제42권3호
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• pp.257-262
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• 2010

Patulin은 곰팡이의 이차 대사산물로 주로 썩은 사과의 병반에서 발견된다. 사과주스 중에 포함된 patulin에 대한 실험법은 LLE법을 이용한 방법이 대부분이다. 이를 대체하기 위해 SPE 법을 통한 사과주스 중 patulin 분석법을 본 연구에서 시행하였다. 시료인 사과주스를 다공성 중합체인 고체상 카트리지에 주입한 후 1% sodium bicarbonate 용액 5 mL와 1% acetic acid 5 mL를 차례로 흘려 방해물질 등을 제거해준 다음 정제가 끝난 카트리지를 상온에서 1시간 정도 방치한 후 ethyl acetate/ethyl ether 5 mL를 이용해 추출하였다. 추출된 용액을 질소 농축기를 이용해 완전 농축한 후 1% acetic acid 용액 0.5 mL를 넣고 혼합 후 syringe filter로 여과하여 amber vial에 보관하여 분석에 사용하였다. HPLC 분석에 사용된 이동상은 THF 8 mL를 1 L 정용 플라스크에 넣고 물로 채워 사용하였다. HPLC 분석조건은 이동상을 0.7 mL/min 유속으로 흘려 276 nm에서 흡광도를 측정하였고, 샘플주입은 $20\;{\mu}g/L$로 하였다. LOD는 30 ng/mL 수준이었다. 실험 결과 SPE 법은 기존의 식품공전시험법(LLE)보다 분석시간이 1/3로 줄어들었고, 적은 양의 용매만으로 추출 및 정제가 가능하였으며 실험과정이 간단하여 공전의 방식보다 손쉽게 분석할 수 있었다. 특히, strata-X를 통한 SPE 추출방법은 재연성과 회수율 또한 우수해 저 농도 분석에도 적합하였다. 이와 같이 기존 분석법에 비해 신속하고 간소하며 정확한 정량분석 및 우수한 회수율과 신뢰도를 얻을 수 있어 다량의 분석을 요하는 연구기관 및 단체에 매우 효율적일 것으로 사료된다.

• 농약과학회지
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• 제4권1호
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• pp.26-31
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• 2000

콩나물중 잔류농약의 효율적인 분석법을 확립하기 위하여 carbendazim과 thiabendazole을 0.1, 0.3, 0.5 mg/kg 씩 첨가하여 농약성분의 추출방법을 비교하였고, 잔류성을 평가하기 위하여 thiophanate-methyl 1.0, 2.0 g/L 용액에 수침시킨 콩으로 콩나물을 재배하면서 매일 잔류량을 조사하였으며, 또한 시중에 유통되는 콩나물중 benzimidazole계 농약의 잔류실태 조사를 실시하였다. 추출방법에 따라 carbendazim의 회수율은 LLE $69.25{\sim}79.16%$, SPE $79.99{\sim}90.42%$, MSPD $92.40{\sim}98.48%$이었으며, thiabendazole의 회수율은 LLE $64.86{\sim}83.26%$, SPE $79.12{\sim}94.04%$, MSPD $65.44{\sim}73.92%$로 고체상 추출방법이 우수하였다. 또 재배기간별 carbendazim 잔류량은 콩나물 출하적기인 재배 5일 째 $0.10{\sim}0.25$ mg/kg이었으며, 출하적기를 넘긴 7일째에도 농약이 잔류되었다. 유통 콩나물 448건을 검사한 결과 6건에서 carbendazim이 검출되었고 검출량은 3건에서 0.1 mg/kg 미만이었으나 3건에서는 0.1 mg/kg을 초과하여 최대 0.37 mg/kg까지 검출되었다.

• 한국어병학회지
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• 제12권1호
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• pp.24-31
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• 1999

어류의 edwardsiellosis를 진단하기 위한 solid phase ELISA법에 대한 최적화 분석을 실시하였다. 부분 정제한 E. tarda Edk-2에 대한 토끼 항혈청을 sodium bicarbonate 완충용액에 $50{\mu}g/ml$ 농도로 희석하여 overnight 반응시켜 주었을 때 polystyrene bead 표면의 항체 immobilization이 최적화되었다. $50{\mu}g/ml$의 biotin 표지화 항체와 1:2000으로 희석된 extravidin-peroxidase를 차례로 처리하였을 때 최적의 반응을 나타내었으며 이렇게 최적화시킨 정성적 solid phase ELISA법은 EDTA 추출법으로 조제된 항원에 대해서는 $1{\times}10^5$ cells/ml, 열 추출법으로 조제된 항원에 대해서는 $1{\times}10^5$ cells/ml의 검출한계를 나타내었다. E. tarda Edk-2에 대한 토끼 항혈청을 이용한 본 연구의 solid phase ELISA법은 우리나라 양어장의 넙치 병어로부터 분리한 여러 한국형 E. tarda 균주와도 높은 교차반응을 나타내었다. 이러한 것은 본 기법을 다른 지역에서 분리한 여러 strain의 E. tarda에 대한 진단을 위하여 본 실험의 항혈청을 사용하여 가능하다는 것을 보여 주었다.

• 한국물환경학회지
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• 제22권5호
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• pp.879-886
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• 2006

The analytical methods of polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans (PCDD/Fs) for water sample with extremely low concentration was developed to extract large volume and to improve fast chromatography for clean up. Semi-automated solid phase extraction (SPE) system and column coupling chromatography using elution pump was optimized and applied to each processes of treatment plant. Results of disk type SPE indicated that this system was applicable below 40 L of aqueous sample with a flow rate of 0.08 ~ 0.2 L/min. Average recoveries of SPE using labeled sampling spike of $^{37}Cl$-2,3,7,8-TCDD was 97%. Column coupling method resulted in reduced clean up time, solvent volume, increased average recoveries with constant elution rate. The combined methods were applied to the monitoring of drinking water treatment plant. Limits of detection (LOD) of each process were calculated. For example, LOD of raw and treated water ranged 0.094~0.968 pg/L and 0.028~0.364 pg/L, respectively. Combined methods of extraction and cleanup techniques provided fast analysis of PCDD/Fs with high accuracy and low LODs for water samples.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2019년도 춘계학술논문요약집
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• pp.291-292
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• 2019