• 분석과학
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• 제25권3호
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• pp.178-189
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• 2012

생식독성 및 내분비계 장애물질로 분류되는 프탈레이트가 근자에 유럽 신화학물질관리제도(REACH)의 허가대상 고위험성 물질(SVHC) 목록 및 유럽의 전기전자제품에 함유된 유해물질 규제인 RoHS II의 최우선 고려 물질 등으로 규제가 강화되면서 IEC TC 111에서 분석법 표준화가 진행되고 있으며 KS 개정도 이루어지고 있다. 본 고에서는 프탈레이트 분석법의 KS 개정 및 한국 NC에서 제안하여 진행되고 있는 IEC 62321에 프탈레이트 분석법을 추가함에 있어 기술적 자료로 사용될 수 있도록 현존하는 국가별 표준의 용매 추출 전처리를 비교 및 검증해 보았다. PVC (polyvinyl chloride)에서의 DEHP (diethylhexyl phthalate)의 추출 효율은 메탄올, 톨루엔, 디클로로메테인. 헥세인 순으로 46.9%에서 95.3%까지 증가하였다. DBP (dibutyl phthalate), BBP (butylbenzyl phthalate) 및 DEHP의 속슬렛을 사용한 추출 시간은 6시간이 최적임이 입증되었고, PVC, nitro cellulose, ABS (acrylonitrile butadiene styrene), and EPDM (ethylene propylene diene monomer) rubber 등의 매트리스로부터의 추출 효율도 90%~99%로 측정되었다. 용매추출에 이은 GC-MS 분석법의 검출한계는 용액 및 고분자 샘플에서 각각 0.08 ~0.3 ${\mu}g/mL$ 및 8~30 mg/kg으로 산출되었다. 공산품에서 프탈레이트를 분석하는 국가표준에서 용매 추출 전처리를 사용하는 EN 14372, ASTM D 7083, 일본 후생노동성 시험법(MHLW 0906-4) 및 KS M 1991을 비교한 결과 4개 국가별 표준 모두 98%~99%의 추출효율을 가짐이 검증되었다. 또한, 국내에서 유통되는 어린이 장난감, 전기 코드, 매니큐어의 공산품 3종에서 프탈레이트 함유 여부를 분석한 결과 DBP 및 DEHP가 22~1,910 mg/kg 범위로 검출되었다.

• Mass Spectrometry Letters
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• 제13권4호
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• pp.146-151
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• 2022

Rotigotine (RTG) is a non-ergot dopamine agonist used to manage the early stage of Parkinson's disease (PD) as transdermal patch. However, the poor medication compliance of PD patients and skin issues related with repeated applications of RTG patches lead to the search for alternative formulations and it also requires appropriate analytical methods for their in vivo evaluation. Thus, here, a sensitive, efficient, and cost-effective method to determine RTG in rat plasma using liquid-liquid extraction (LLE) and multiple reaction monitoring was developed. The use of 20 µL of rat plasma for sample treatment, 8-OH-DPAT as the internal standard, and methyl tert-butyl ether as the LLE solvent in the present method gives it advantages over previous methods for the analysis of RTG in biological samples. The good analytical performance of the developed method was confirmed in specificity, linearity (the coefficient of determination ≥0.999 within 0.1-100 ng/mL), sensitivity (the lower limit of quantitation at 0.1 ng/mL), accuracy (81.00-115.05%), precision (≤10.75%), and recovery (81.00-104.48%) by following the FDA guidelines. Finally, the applicability test of the validated method to the in vivo evaluation of a RTG formulation showed that the present method is the only method which can be accurately applied to that longer than 24 hours, critical for the development of formulations with reduced dosing frequencies. Therefore, the present method could contribute to the development of new RTG formulations helpful to people suffering from PD.

• 분석과학
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• 제29권5호
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• pp.219-224
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• 2016

A sensitive method to detect trace anions in hydrofluoric acid (HF) by solid-phase extraction (SPE) clean-up and ion chromatography (IC) was described. Fluoride in HF solution was eliminated with solid-phase extraction, and residual fluoride, acetate, chloride, bromide, nitrate, phosphate and sulfate were consecutively separated with IC. The SPE parameters (selection of adsorbent, sample volume and pH, elution solvent and its volume) were optimized and selected. The removal effect of fluoride in HF solution was the best on Oasis WAX column, and the optimum conditions (1.0 mL of 25 % HF solution and 50 mM ammonium acetate 5 mL as elution solvent) were established by the variation of parameters. Under the established condition, the method detection limits of chloride, bromide, nitrate, phosphate, and sulfate were 0.04~0.30 µg/L in 25 % HF solutions (w/w) and the relative standard deviation was less than 5 % at concentrations of 20.0 and 40.0 µg/L. The concentrations of anions in a 25 % HF had detectable levels of 4.2 to 47.5 µg/L. The method was sensitive, reproducible and simple enough to permit the reliable routine analysis of anions in HF solution used in the process of producing semiconductors.

• 한국지하수토양환경학회지:지하수토양환경
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• 제17권4호
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• pp.63-72
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• 2012

The main objective of this study is to assess the compatibility between Korean ministry of environment (KME) standard and ISO (KS I ISO) standard for the determination of BTEX and TPH content in soil. We carried out comparison analysis for both methods using CRM and matrix spiked samples. In case of GC-MS analysis for BTEX, we got statistically (significance level: 0.05) the same results from KME standard (ES 07600.1) and ISO standard (KS I ISO 15009). However, it showed statistically (significance level: 0.05) different results when TPH was analyzed by KME standard (ES 07552.1) and ISO standard (KS I ISO 16703). To clarify the reason why both methods produced different results for TPH content, we also did some additional experiments in terms of differences in extraction, clean-up and target hydrocarbon range. Extraction with polar and non-polar compounds mixed solvent (acetone+n-heptane) of KS I ISO 16703 showed higher extraction efficiency than with only non polar solvent (dichloromethane) extraction of ES 07552.1 by about 9%. While column type clean-up of KS I ISO 16703 showed the reduction in TPH content between before and after clean-up, batch type of clean-up of ES 07552.1 did not show any changes in TPH content through clean-up process. The target hydrocarbon range of ES 07552.1 and KS I ISO 16703 is $C_8{\sim}C_{40}$ and $C_{10}{\sim}C_{40}$, respectively. From this point of view, kerosene and JP-8 contaminated soil showed higher RPD (relative producibility deviation) values between results by both method than that of lubricant or diesel contaminated soil. The higher content of hydrocarbon ($C_8{\sim}C_{10}$) in kerosene and JP-8 played an important role in increasing RPD values in addition to the effects caused by different solvents and clean-up method. Consequently, it was concluded that both methods (ES 07552.1 and KS I ISO 16703) were not compatible.

• 약학회지
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• 제35권1호
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• pp.15-21
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• 1991

Quaternary amines which are widely used as medicines are nitrogen compounds. Metanil yellow(MY) and benzalkonium chloride(BKC) were mixed and added to 10ml of the buffer solution and then the solution was shaken for 5 minutes. The maximum absorption wavelength of the reaction product was 402 nm. Dichloromethane was the best extracting solvent among the several organic solvents and the most suitable pH range was 2~8. When the BKC-MY calibration curve was made in the best experimental condition, the Lambert-Beer's law was obeyed in the range of BKC concentration of 2$\times$$10^{-6}$~9$\times$$10^{-6}$M by UV spectrophotometer. This method was possible to determine quaternary ammonium salts in the pharmaceutical preparation.

• Archives of Pharmacal Research
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• 제13권2호
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• pp.174-179
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• 1990

Second derivative (D2) spectrometry using ion-pair extraction technique was development for the determination of total glycyrrhetic acid (GA) in Glycyrrhizae Radix, Glycyr-rhizin (G) obtained from Glycyrrhizae Radix was hydrolyzed into GA in 2 N-HCI and methanol (1:1) and extracted from aqueous phase in the form of an ion-pair complex with tetrapentylammonium bromide (TPA) as a counter ion. Maximum D2 amplitude (Z value) was obtained when 1000-fold or greater molar ratio of TPA was used at pH 11. Reaction an effective extraction solvent of the ion-pair complex. The linearity of standard curve of ion-pair GA was obtained in the range of 4.120 $\mu$g/ml as GA. Assayed contents of GA in dry powder by D2 UV spectrometry and HPLC method were 5.31 $\pm$ 0.04% and 5.20 $\pm$ 0.008%, respectively.

• 대한화학회지
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• 제8권3호
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• pp.103-108
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• 1964

Ac$^{227}$을 溶媒抽出法에 依하여 그의 崩壞系列元素로부터 分離하는 迅束한 方法을 考察해 보았다. HDEHP 및 TBPO로 二段階抽出過程을 거침으로서 追跡子用으로 充分한 純度를 가진 Ac$^{227}$을 얻을 수 있으며 이들 過程中에 일어날 Ac$^{227}$의 損失程度도 推定해 보았다. Ac$^{227}$으로부터 Th$^{227}$의 milking도 兼하여 實驗하였다.

• 한국산업보건학회지
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• 제19권2호
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• pp.96-101
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• 2009

The purpose of this study was to conduct the field validation of alternative method(ETM method) by using non-carcinogenic, and less toxic solvents than NIOSH (National Institute for Occupational Safety and Health) analytical method 5524 for measuring the airborne metalworking fluids in workplaces. We carried out the field validation test by using the exposure chamber, guaranteeing the air sampling homogeneously in a machining environment. The ETM mixed solvent presented the complete solubility of MWFs used in test field. Based on the field test data, the bias of the ETM method from reference method, NIOSH analytical method 5524, was from -7.0% to 5.1%. The overall uncertainty of the ETM nethod was 21.6%, which satisfied the NIOSH criteria for the sampling and analytical criteria.

• 한국식품과학회지
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• 제14권2호
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• pp.174-178
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• 1982

대두유의 탈취 증류분으로 부터 토코폐롤과 스테롤을 분리해내기 위하여 분자 증류법, 용매추출법, 화학처리법 등을 이용하였으며 최종 산물로 토코폐롤 농축물과 스테롤 결정을 얻었다. 용매추출법의 경우, 얻어진 토코폐롤의 순도와 회수율은 각각 21.2%와 28.3%였으며 스테롤의 순도와 회수율은 각각 69.2%와 2.6%였다. 화학처리법의 경우, 토코폐롤의 순도와 회수율은 11.8%와 76.4%였으며 스테롤의 순도와 회수율은 85.1%와 34.3%였다. 한편 분자증류법의 경우 토코폐롤의 순도와 회수율은 45%와 68%였으며 스테롤의 순도와 회수율은 각각 49.3% 57%로 나타났다. 또한 얻어진 토코폐롤 농축물을 HPLC로 비교하였다. 이 연구의 결과로 분자증류법이 실험한 다른 방법보다 더 효과적임을 알았다.

• 한국식품위생안전성학회:학술대회논문집
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• 한국식품위생안전성학회 2001년도 The Asia-Pacific Conference on Reproductive Biology and Environmental Sciences
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• pp.171-174
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• 2001

Solid phase micro-extraction (SPME), a solvent-free, rapid and inexpensive method for the extraction of organic compounds from aqueous sample matrices, was evaluated for determination of the 120 pesticides in vegetables such as crown daisy, perilla leaf, leafy lettuce and to mato. The analysis conditions were chosen for the SPME method: 15 min of immersion of the PDMS fiber in 10 ml of the solution with stirring at 1,000 rpm. The recovery tests were carried out in triplicate. The range of recoveries was 0-142% for organochlorine pesticides and $4.9\sim200\%$ for organophosphorus pesticides. The recoveries were very low in the pesticide groups with low solubility in water. The recoveries became lower in proportion to the interference materials in vegetables. The recovery in tomato was relatively higher than that in perilla Ie af and crown daisy. The recovery values obtained by SPE and SPME were compared. In leaf y lettuce, recovery obtained by SPE method ranged from $58.1\%\;to\;136.1\%$ and recovery by SPME ranged from $9.6\%\;to\;176.3\%$ In organophosphorus pesticides. The recovery in SPME method was satisfactory with $136\%$ for ethoprophos, $119\%$ for methidathion and $113\%$ for diazinon. Meanwhile, recovery of EPN, phenthoate and 2,4-DDT revealed relatively low value of $38\%,\;41\%\;and\;3.4\%,$ respectively. However, most of pesticides applied to SPME method sho wed constant recovery and precision. From these results, it can be concluded that solid phase micro-extraction might be an appropriate method for the screening test of pesticides in vegetables.