This study was conducted to verify the reliability of volatile organic compounds (VOCs) data derived from Selected Ion Flow Tube-Mass Spectrometers (SIFT-MS) measurements. In the previous study, the measurement reliability was validated using simultaneous measurements by SIFT-MS and gas chromatography-mass spectrometry (GS-MS), but in order to ensure more accuracy, and additional analysis was conducted by diluting standard gases (2 ppm) consisting of 10 types of VOCs mainly measured in industrial complexes (concentrations ranged from 0 to 500 ppb). As a result of 2 experiments, the SIFT-MS showed linearity and produced a coefficient of determination of over 0.99 for all cases. SIFT-MS has secured high measurement reliability, and it is considered to be able to efficiently manage VOCs emitted in industrial complexes.

GC-MS/MS using liquid-liquid extraction (LLE) and C18 cartridges was used to identify and quantify levels of chlorpyrifos, chlorpyrifos-methyl, cypermethrin, deltamethrin and permethrin in bulk raw milk. A calibration curve spanning 10 ng/mL to 200 ng/mL was obtained with a satisfactory correlation coefficient of 0.99. The limits of detection (LOD) and limits of quantitation (LOQ) for chlorpyrifos, chlorpyrifos-methyl, cypermethrin, deltamethrin, and permethrin in the matrix ranged from 0.06 to 1.81 ng/mL and 0.19 to 6.04 ng/mL, respectively. The recoveries of 5 pesticides from spiked samples at 37.5-125 ng/mL ranged from 86.1 to 102.1%. The measurement of uncertainty of the GC-MS/MS method for these five pesticides was developed based on the analytical process and quantification. An analysis method that is easier and faster than the method specified in the Korean food standards codes for analyzing these five pesticides in raw material milk was developed. Moreover, the analytical method for chlorpyrifos, chlorpyrifos-methyl, cypermethrin, deltamethrin, and permethrin in bulk raw milk by GC-MS/MS was established.

축산물 중 잔류허용기준이 설정되어 관리하고 있는 농약 azocyclotin, cyhexatin, fenbutatin oxide는 대표적인 유 기주석계 살비제이다. 기존 시험법은 가스크로마토그래피 를 사용하여 정량한계가 높고 분석 시 재현성이 떨어져 이에 대한 개선이 필요한 실정으로 본 연구에서는 비교적 간편하며 시간이 적게 소요되는 QuEChERS법을 활용하여 azocyclotin, cyhexatin, fenbutatin oxide의 시험법을 마련하 고자 하였다. 1% 아세트산을 함유한 아세트산에틸:아세토 니트릴(1:1) 혼합액을 이용하여 진탕 추출 후 d-SPE로 정 제하고 이를 농축 후 LC-MS/MS를 이용한 시험법을 개발 하였다. Azocyclotin, cyhexatin 및 fenbutatin oxide의 결정 계수(R2)는 0.99 이상으로 높은 직선성을 확인하였으며 정 량한계는 0.01 mg/kg으로 높은 감도를 나타내었다. 대표 축산물 5종(소, 돼지, 닭, 계란, 우유)에서 LOQ(0.01 mg/ kg), MRL(0.05 mg/kg), MRL 10배(0.5 mg/kg)의 농도에서 회수율 실험을 한 결과 평균 회수율이 76.4-115.3% 및 84.4-110.8%이었으며, 상대표준편차는 25.3% 이하로 나타 났다. 본 연구는 Codex 가이드라인(CAC/GL 40-1993, 2003) 및 ‘식품의약품안전처 식품의약품안전평가원의 식 품등 시험법 마련 표준절차에 관한 가이드라인(2016)’에 적합한 수준임을 확인하였다. 따라서 본 연구에서 확립한 시험법은 축산물 중 잔류할 수 있는 azocyclotin, cyhexatin, fenbutatin oxide의 안전관리를 위한 공정시험법으로 활용 가능할 것으로 판단된다.

We used the measurement data derived from a proton transfer reaction time-offlight mass spectrometry (PTR-ToF-MS) to ascertain the source profile of volatile organic compounds (VOCs) from 4 major industrial classifications which showed the highest emissions from a total of 26 industrial classifications of A industrial complex. Methanol (MOH) was indicated as the highest VOC in the industrial classification of fabricated metal manufacture, and it was followed by dichloromethane (DM), ethanol (EN) and acetaldehyde (AAE). In the industrial classification of printing and recording media, the emission of ethylacetate (EA) and toluene (TOL) were the highest, and were followed by acetone (ACT), ethanol (EN) and acetic acid (AA). TOL, MOH, 2-butanol (MEK) and AAE were measured at high concentrations in the classification of rubber and plastic manufacture. In the classification of sewage, wastewater and manure treatment, TOL was the highest, and it was followed by MOH, H2S, and ethylbenzene (EBZ). In future studies, the source profiles for various industrial classifications which can provide scientific evidence must be completed, and then specified mitigation plans of VOCs for each industrial classification should be established.

본 연구는 국내 유통 농산물 535건을 대상으로 잔류농 약 실태조사를 수행하였다. 서울 등 13개 지역에서 수거 한 농산물 시료를 QuEChERS법으로 추출한 후 d-SPE로 정제하여 LC-MS/MS 및 GC-MS/MS로 분석하였다. 농산 물 15품목 535건 중 14품목 288건에서 잔류농약이 검출 (53.8%)되었으며, 검출된 농산물은 사과 40건, 고추 40건, 감귤 33건, 복숭아 31건, 기타 품목 144건이었다. 이 중 잔류허용기준을 초과한 농산물은 배추 1건으로, diniconazole 이 0.18 mg/kg으로 기준치의 약 2배 검출되었다. 총 검출된 농약은 91종으로 살균제 42종, 살충제 48종, 살선충제 1종 이었으며, dinotefuran 91건, carbendazim 75건, tebuconazole 61건, pyraclostrobin 59건이 가장 빈번하게 검출되었다. 따 라서 상기의 결과를 통해 과일류 및 채소류에 대한 지속 적인 잔류실태조사가 필요할 것으로 사료된다.

This study investigated the odor emission characteristics of fertilizer manufacturing facilities. The characteristics were evaluated by measuring the odor concentration at the outlet and site boundary of the complex fertilizer and organic fertilizer manufacturing facilities. The evaluation process utilized the air dilution sensory method and PTR-ToF-MS. The complex odor dilution factor ranged from 100 to 120 times at the outlet of the compound fertilizer manufacturing facility. Specifically, the concentrations of Ammonia and Aldehydes were relatively high as designated odor substances. For the organic fertilizer facility, the dilution factor for complex odors was measured up to a maximum of 3,000. And, designated odorants such as Ammonia and Hydrogen sulfide were measured at levels up to parts per million (ppm). The odor contribution assessment of the fertilizer manufacturing facilities showed that the complex fertilizer facility exhibited similar contributions from Aldehydes and Sulfur compounds. On the other hand, the organic fertilizer facility had the highest contribution of over 62% from Sulfur compounds. As odor substances are easily changed and diffused according to weather conditions, it is difficult to obtain representative data according to the measurement time. Therefore, if continuous monitoring of odorous substances is performed using equipment that can be measured in real time without pretreatment, it becomes feasible to identify odor emission sources and regional spatio-temporal distribution. This information would then serve as a basis for analyzing odorant contamination characteristics and establishing appropriate countermeasures.

Trifludimoxazin은 triazinone 계열 제초제로 프로토포르 피리노겐-IX 산화효소(protoporphyrinogen oxidase, PPO)를 억제하며 벼와 광엽 잡초를 방제하는 데 사용된다. PPO의 결핍은 세포막의 손상을 일으켜 식물을 시들게 한다. Trifludimoxazin의 농산물 중 잔류허용기준은 미국에서 아몬 드에 대하여 0.15 mg/kg, 땅콩 등 9종에 대하여 0.01 mg/ kg으로 설정되어있으며, 모화합물을 잔류물의 정의로 설 정하여 관리하고 있다. 코덱스(CODEX), 유럽(EC) 일본 (JFCRF)에서는 잔류허용기준(MRL)과 잔류물의 정의가 설 정되어 있지 않다. 호주(APVMA)에서는 trifludimoxazin과 대사체 M850H001의 합을 잔류물의 정의로 설정하였으며, MRL은 보리와 밀에 0.01 mg/kg으로 설정되어 있다. 국내에서 신규 등록 예정임에 따라 본 연구에서는 농산물 중 trifludimoxazin의 잔류량을 분석하기 위한 공정시험법을 마련하고자 하였다. Trifludimoxazin의 물리 화학적 특성을 고려하여 아세토니트릴을 추출용매로 사용하는 Quick, easy, cheap, effective, rugged and safe (QuEChERS)법을 이용하 여 추출 및 정제조건을 확립한 후 LC-MS/MS를 분석기기 로 선정하였다. Trifludimoxazin의 결정계수(R2)는 모두 0.99 이상으로 우수하였으며 정량한계는 0.01 mg/kg으로 나타났 다. 대표 농산물 5종(현미, 감자, 대두, 감귤, 고추)에 대하여 정량한계, 정량한계 10배, 정량한계 50배 수준으로 처리하 여 회수율 실험을 한 결과 평균 회수율은(5반복) 73.5-85.3% 로 나타났으며, 상대 표준편차(RSD)는 3.8% 이하로 나타 났다. 본 연구는 국제식품규격위원회 농약 분석법 가이드 라인의 잔류농약 분석 기준 및 식품의약품안전평가원의 식 품등 시험법 마련 표준절차에 관한 가이드라인(2016)에 적 합한 수준이며, 향후 공정시험법으로 활용될 예정이다. 본 연구에서 개발한 시험법에 대해 농산물 125건을 대상으로 잔류농약 모니터링을 한 결과 trifludimoxazin의 잔류량이 확인되지 않았다.

Cordyceps militaris (C. militaris) is a unique and valuable medicinal fungus belonging to the Cordyceps species. C. militaris is the only fungus that contains cordycepin which is a biologically active compound. In previous studies, light-emitting diodes (LEDs) are known to be effective in increasing cordycepin content, but metabolic profiling of LED-stimulated C. militaris has not been confirmed. Metabolic profiling is essential to understanding the metabolic regulation of cordycepin. This study studied the physiologically active secondary metabolites of C. militaris according to the presence or absence of stimulation of LEDs through GC-MS analysis. Most of the metabolites were detected in both samples, but there was a clear difference in the detected concentration. In particular, C. militaris had a significant difference in amino acid levels when stimulated with LEDs. Our results suggested that LEDs could stimulate amino acid synthesis in C. militaris mycelium to increase the cordycepin content.

본 연구에서는 DWI 적용 시 X축 거리에 따른 신호 손실과 인공물 발생 여부를 SS-EPI 기법과 비교 분석하여, MS-EPI 기법의 특성을 제시하고 임상 적용 관련 기초자료를 제시하고자 하였다. 3.0T 자기공명영상장치와 팬텀을 사용 하여 자기장 중심축과 좌우 끝 지점 ±3cm, 3번씩 움직여 표준 영상인 T2 강조영상과 SS-EPI DWI, MS-EPI DWI(RESOLVE) 축상면 영상을 획득하였다. 각 동일 부위에서의 SS-EPI DWI, MS-EPI DWI 영상을 T2 강조영상과 감산하여 신호 손실 직경을 측정하여 정량적 분석을 하였다. 정성적 평가는 나이퀴스트 허상과 기하학적 왜곡과 신호 손실, 인공물 발생 여부를 방사선사 3명이 비교평가 하였다. 두 기법 모두 오프 센터(off-center)로 이동할수록 신호 손실구간 또는 기하학적 왜곡이 나타나는데, 특히 MS-EPI 기법에서는 좌우 신호 손실 현상이 매우 증가해 –25, +25 cm 구간에서 는 약 50% 길이가 감소하였다. MS-EPI 기법은 근골격계 질환에서 기존에 매우 높은 영상 유용성을 인정받고 있다. 그러 나 k-공간을 분할 하여 채우는 MS-EPI 기법은 오프 센터의 낮은 공간 주파수 획득 시 위상변동 보정이 안 되어 신호 손실구간이 나타나며, 이에 관한 연구는 전혀 없는 실정이다. 이에 따라 본 연구는 기존의 선행 연구에서의 보여주지 못한 임상적 적용 시 MS-EPI 기법의 문제점을 파악하면서 이러한 정보를 공유하고 추가적인 연구에 토대가 될 수 있는 기초를 마련했다는 점에 의의가 있다.

The annual number of odor complaints increased about 10 times over 14 years from 4,302 in 2005 to 40,854 in 2019, in Korea. Especially, livestock facilities account for more than 50% of the odor complaints and the swine farms account for the most odor complaints among livestock. It is therefore necessary to manage swine farms as the major odor emission source. In this study, a real-time odor monitoring system equipped with PTR-TOF-MS (proton transfer reaction time-of-flight mass spectrometric) was used to measure the odorous substances in two swine farms. Odorous substances emitted from outlets were sampled and measured at the two types of swine farms. In addition, the boundary spots were designated as measurement points. As a result, the rankings of the odorous substances in order, from highest to lowest, were ammonia, acetaldehyde, methyl mercaptan, fatty acids, etc. and the level of odor intensity was 0.8-4.4 at the outlet of the swine farms. The concentration at the boundary decreased between 1/100 ~ 1/10000 compared to the concentration emitted from outlets. Base on the results of evaluating odor activity values, Skatole and p-Cresol were estimated as major odor substances in swine farms.

This study aims to establish a modified analytical method with sensitivity and reliability for streptomycin (STP) and dihydrostreptomycin (DHS) of residues level in pig tissues, plasma and urine by LC-MS/MS on the basis of previous studies. The mass parameters of quantitative and qualitative ions for STP and DHS were optimized using multiple reaction monitoring in positive mode. The separation of compounds was conducted using BEH Amide column according to material’s characteristics. The analytes in plasma were extracted with only organic solvents. In muscle and kidney, KH2PO4 buffer solution containing 2% CCl3COOH and EDTA-Na was used as extraction solvent. The WCX cartridege was selected as SPE cartridge in considering high recoveries for STP and DHS. The analytes in urine were extracted by organic solvents with acid and addition of EDTA. The limits of detection (LODs) in STP and DHS ranged 0.45~3.66 μg/kg and 0.22~0.78 μg/kg, respectively. The limits of quantification (LOQs) were 1.35~11.10 μg/kg in STP and 0.66~2.36 μg/kg in DHS. The recoveries (%) were 94.29~104.5% in STP and 92.32~108.45% in DHS except for plasma with lower values (61.45/68.5%, respectively). In the precision evaluation, the coefficient of variation (CV, %) of STP showed <10.50% on intra-day and <18.04% on inter-day. The CV (%) of DHS showed <8.42% on intra-day, whereas <17.98% on inter-day. The modified method is reliable for continuous residual monitoring in pig to ensure food safety for consumer’s health. In addition, this method could be used in study relation to residue depletion and pharmacokinetics of veterinary drug.

The research aims to develop a rapid and easy analytical method for methoprene using liquid chromatography- tandem mass spectrometry (LC-MS/MS). A simple, highly sensitive, and specific analytical method for the determination of methoprene in livestock products (beef, pork, chicken, milk, eggs, and fat) was developed. Methoprene was effectively extracted with 1% acetic acid in acetonitrile and acetone (1:1), followed by the addition of anhydrous magnesium sulfate (MgSO4) and anhydrous sodium acetate. Subsequently, the lipids in the livestock sample were extracted by freezing them at -20oC. The extracts were cleaned using MgSO4, primary secondary amine (PSA), and octadecyl (C18), which were then centrifuged to separate the supernatant. Nitrogen gas was used to evaporate the supernatant, which was then dissolved in methanol. The matrix-matched calibration curves were constructed using 8 levels (1, 2.5, 5, 10, 25, 50, 100, 150 ng/mL) and the coefficient of determination (R2) was above 0.9964. Average recoveries spiked at three levels (0.01, 0.1, and 0.5 mg/kg), and ranged from 79.5-105.1%, with relative standard deviations (RSDs) smaller than 14.2%, as required by the Codex guideline (CODEX CAC/GL 40). This study could be useful for residue safety management in livestock products.

The official analytical method for the analysis of harmful heavy metals in Meju, distributed in Korea, employs a strong acid to decompose the organic components. This analysis is time consuming and harmful to the users and/or the environment. This study aimed to develop a new pre-treatment technology using laser ablation, to rapidly analyze harmful heavy metals without using strong acids. The results obtained from this method were validated by the National Institute of Food and Drug Safety Evaluation guideline (NIFDS, 2016). Moreover, a comparison of the two methods showed that the analytical time for 55 Meju samples was shortened by 96% or more in the new method. The results showed no significant difference in the recovery ranging from 90–120%. The proposed method proved suitable for detecting harmful heavy metals in Meju.