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      • KCI등재

        한약재의 약용부위별 중금속 함량 및 탕 액에서의 이행률 조사

        정삼주,강성태,한창호,김수진,고숙경,김윤희,김유경,김복순,최병현 한국식품위생안전성학회 2010 한국식품위생안전성학회지 Vol.25 No.4

        The study was conducted to estimate the contents of heavy metal in commercial herbal medicines (1047 samples of 132 species) which were collected from markets in Seoul and to analyze the contents of heavy metals of herbal medicines by classifying them by parts. The samples were digested using microwave method. The contents of heavy metal (Pb, Cd, and As) and Hg were determined using Inductively coupled plasma-Mass spectrometer (ICP/MS). And the contents of Hg were obtained by Mercury analyzer. The average values of heavy metal in herbal medicines were as follows [mean (minimum-maximum), mg/kg]; Pb 0.870 (ND-69.200), As 0.148 (ND-2.965), Cd 0.092(ND-2.010), and Hg 0.007 (ND-0.137). And the average values of heavy metal by parts in herbal medicines were as follows [mean (minimum-maximum), mg/kg]; Ramulus 2.046 (0.065-4.474), Herba 1.886 (0.048-10.404), Flos 1.874(0.052-5.393), Cortex 1.377 (0.011-4.837), Radix 1.165 (0.012-70.111), Rhizoma 1.116 (0.016-5.490, Fructus 0.838(0.017-4.527), Perithecium 0.729 (0.013-4.953), Semen 0.646 (0.006-4.416). The average values of heavy metal of imported herbal medicines except Radix were higher than domestic ones. By decoction of herbal medicines exceeding the tolerances, average intake rates of Pb, As, Cd and Hg were obtained as 6.1%, 40.3%, 4.7%, and 2.2%, respectively.

      • KCI등재

        2010년 서울지역 유통 한약재의 잔류이산화황 함량 모니터링

        정삼주,이성득,김수진,조성애,김남훈,정희정,김화순,한기영 한국식품위생안전성학회 2011 한국식품위생안전성학회지 Vol.26 No.4

        This study was investigated to determine the contents of sulfur dioxide residues in medicinal herbs in Seoul Yang Nyoung Shi in 2010 (1,522 samples of 189 kinds). Samples were measured by modified Monier-Williams method. Of the total samples, 618 samples (84 kinds) were domestic, and 904 samples (158 kinds) were imported. The content of sulfur dioxide in the domestics showed the range of 0.0 to 1,298.0 mg/kg (average 12.7 mg/kg), while those in imported samples were the range of 0.0 to 3,982.2 mg/kg (average 42.4 mg/kg). The average (mg/kg) amount of sulfur dioxide by parts in medicinal herbs was as follows; Tuber 122.3, Radix 69.3, Rhizoma 37.4, Cortex 33.3, Fructus 8.8, Ramulus 4.9, Semen 4.6, Folium 3.4, Flos 2.7, Perithecium 1.4. Of the total samples (1,522), 52 samples (3.4%) were violated the KFDA regulatory guidance of sulfur dioxide. Among these 52 unsuitable samples, 16samples (7 kinds) were domestic, and 36 samples (23 kinds) were imported. Approximately 88.1% of the total samples was less than 10 mg/kg of sulfur dioxide and 6.3% of the total samples showed more than 30 mg/kg of sulfur dioxide.

      • KCI등재

        어린이용 화장품에 사용되는 보존제 및 함유량 조사

        정삼주 ( Sam Ju Jung ),황영숙 ( Young Sook Hwang ),최채만 ( Chae Man Choi ),박애숙 ( Ae Suk Park ),김수언 ( Su Un Kim ),김현정 ( Hyun Jung Kim ),김정헌 ( Jung Hun Kim ),정권 ( Kweon Jung ) 대한화장품학회 2015 대한화장품학회지 Vol.41 No.3

        본 연구에서는 시중에서 유통 중인 어린이용 화장품 총 125건(n = 125)을 대상으로 하여 파라벤 6종과 벤질알콜, 페녹시에탄올, 소르빈산, 벤조산 등 10종의 보존제에 대한 혼합 사용실태와 함량을 HPLC를 이용하여 조사하였다. 유형별 보존제 검출률은 세정제 63%, 크림류 48%, 자외선차단제 46%, 로션류 38%, 오일이 13%의 순으로 검출되어 총 125건 중 63건(50%)의 제품에서 1종류 이상의 보존제를 사용하고 있는 것으로 조사되었다. 보존제별 검출범위는 페녹시에탄올 0.01 ~ 0.91% (n = 35), 벤조산 0.01 ~ 0.48% (n = 28), 벤질알콜 0.01 ~ 0.78% (n = 9), 소르빈산 0.01 ~ 0.11% (n = 3)였으며, 파라벤류 중 메틸 파라벤과 프로필 파라벤은 0.04 ~ 0.21% (n = 8)와 0.02 ~ 0.09% (n = 8)의 검출범위를 보였고, 에틸 파라벤은 1개 제품에서 0.04%로 모두 배합한도 이내로 검출되었다. 조사결과 어린이용 화장품에서는 파라벤류 보다 페녹시에탄올과 벤조산의 사용빈도가 높았으며 검출된 파라벤류 중에서는 메틸 파라벤과 프로필 파라벤이 주로 혼합 사용되는 것으로 나타났다. This study was conducted to determine 10 preservatives (benzyl alcohol (BAl), phenoxyethanol (PE), benzoic acid (BA), sorbic acid (SA), methyl paraben (MP), ethyl paraben (EP), propyl paraben (PP), isopropyl paraben (IPP), butyl paraben (BP), isobutyl paraben (IBP)) levels in 125 cosmetics (n = 125) for children by the simultaneous analysis of HPLC. The detection ranges were as follows; 0.01 ~ 0.91% (n = 35) for PE, 0.01 ~ 0.48% (n = 28) for BA, 0.01 ~ 0.78% (n = 9) for BAl, 0.01 ~ 0.11% (n = 3) for SA, 0.04 ~ 0.21% (n = 8) for MP, 0.02 ~ 0.09% (n = 8) for PP, and 0.04% (n = 1) for EP. The order of detection rates was cleanser (63%) > cream (48%) > sunscreen (46%) > lotion (38%) > oil (13%). At least one of target preservatives was contained in 50% (63/125) of samples and the content of the detected preservatives was within maximum allowed amount established by KFDA. Phenoxyethanol and benzoic acid were used more frequently than paraoxybenzoate esters (parabens) in cosmetics for children and the detected parabens was mainly the mixture of methyl paraben and propyl paraben.

      • KCI등재

        Conventional-PCR 및 Real-time PCR을 이용한 백수오와 이엽우피소의 유전자 종감별 시험법 비교

        류회진,김애경,김성단,정삼주,장정임,이희진,이정미,유인실,정권 한국생약학회 2018 생약학회지 Vol.49 No.1

        Recently, it has been a big issue to distinguish the dried roots of Cynanchum wilfordii and C. auriculatum in health functional food market. The original plant species of Cynanchi Wilfordii Radix belong to the Asclepiadaceae family is differentially described in the national pharmacopoeia of Korea, China and Japan. Owing to the morphological similarities of the dried roots of this plant to those of C. auriculatum, which is often misidentified in Korean herbal medicine marketplace, distinguishing these two species is exceedingly difficult. The purpose of this study was to compare the conventional-PCR with the real-time PCR for detection of C. wilfordii and C. auriculatum DNA. We also tried to realize a quantitative real-time PCR assay using species-specific matK primers, which allowed us to estimate the ratio of C. willfordii and C. auriculatum using varying ratios of mixed genomic DNA template from the two species. The differentiation of intentional and unintentional mixture in this study would be applied to food safety management and can be helpful for protection of consumer’s right and cultivators.

      • KCI등재

        LC-MS/MS를 이용한 종자류 생약의 곰팡이독소 동시분석 및 위해도 평가

        최은정,박영애,최수정,정삼주,박윤선,황인숙,유인실,신기영 한국생약학회 2020 생약학회지 Vol.51 No.4

        This study analyzed mycotoxins, aflatoxin B1, B2, G1, G2, fumonisin B1, B2, ochratoxin A and zearalenone, using LC-MS/MS and conducted risk assessment on 54 samples of seeds distributed in SeoulYangnyeongsi and the management status of extramural herbal dispensary facility. The matched calibration showed a good linearity as observed in 6 concentration levels(r2>0.999) as a result of method validation applied with Arecae semen. Limits of detection(LOD) and quantification(LOQ) were in the range of 0.02-0.11 μg/kg and 0.08-0.34 μg/kg, respectively. Recoveries also estimated, ranging from 65.1-99.7% with relative standard deviation(RSD) 0.5-6.3%. As a result of the method on 54 samples, mycotoxins were detected in 16 samples. Among them, two Thujae semen showed a degree of concentration that exceeded the aflatoxin specification. In the risk assessment, the human exposure safety standard values were calculated as ADI(Acceptable Daily Intake) for aflatoxin B1, fumonisin and zearalenone. Ochratoxin A was calculated as PTWI(Provisional Tolerable Weekly Intake). The MOE(Margine of Exposure) of aflatoxin B1 was in the range of 40.36-3536.88. And no items exceeded 100% in %TDI(Tolerable Daily Intake) and %TWI(Tolerable Weekly Intake) of fumonisin, zearalenone and ochratoxin A.

      • KCI등재

        LC-MS/MS를 이용한 식·약 공용 농산물의 곰팡이독소 분석 및 위해평가

        최수정,고숙경,박영애,정삼주,최은정,김은정,황인숙,신기영,유인실,신용승 한국식품위생안전성학회 2021 한국식품위생안전성학회지 Vol.36 No.1

        2019년 1월부터 11월까지 서울약령시장에서 유통되는 식·약 공용 농산물 총 187건을 대상으로 곰팡이독소 동시 다성분 SPE 컬럼으로 정제 후 LC-MS/MS로 분석하여 곰팡이독소 8종의 동시분석법 유효성을 검증하고, 확립된 분석법으로 곰팡이독소 오염도 파악 및 위해평가를 실시하였다. LC-MS/MS를 이용한 동시분석법의 유효성 검증은 매질효과, 직선성, 검출한계, 정량한계, 정확성 및 정밀성으로 하였다. 매질 보정 검량선의 상관계수(r2)는 0.9999이상의 우수한 직선성을 보였고, 검출한계는 0.02-0.11 μg/ kg였고, 정량한계는 0.06-0.26 μg/kg였고, 회수율은 81.2- 118.7%였고, 상대표준편차는 0.33-8.90%로 우수한 재현성을 나타냈다. 확립된 분석법으로 검사한 결과 기준이 설정된 아플라톡신은 B1이 1.18-7.29 μg/kg (기준: 총 아플라톡신 15.0 μg/kg이하, B1 10.0 μg/kg이하)으로 기준 이내로 검출되었고, 아플라톡신 B2, G1 및 G2는 검출되지 않았다. 기준이 미설정된 곰팡이독소는 푸모니신(0.84-14.25 μg/ kg) 오크라톡신 A (0.76-17.42 μg/kg) 및 제랄레논(1.73- 15.96 μg/kg)이 검출되었다. 위해평가 결과 아플라톡신 B1의 1일 인체노출량은 0.00052 μg/kg b.w./day였고, 푸모니신 및 제랄레논의 일일섭취한계량 대비 각각 0.04%, 0.24% 였고, 오크라톡신 A의 주간섭취한계량 대비 4.76%로 우리나라 국민들이 식·약 공용 농산물 섭취로 인한 곰팡이 독소 위해도는 안전한 것으로 평가되었다. For this study, we surveyed concentrations of 8 mycotoxins (aflatoxin B1, B2, G1, G2, ochratoxin A, fumonisin B1, B2 and zearalenone) in agricultural products used for food and medicine by liquid chromatographytandem mass spectrometry and conducted a risk assessment. Samples were collected at the Yangnyeong Market in Seoul, Korea, between January and November 2019. Mycotoxins were extracted from these samples by adding 0.1% formic acid in 50% acetonitrile and cleaned up by using an ISOLUTE Myco cartridge. The method was validated by assessing its matrix effects, linearity, limit of detection (LOD), limit of quantification (LOQ), recovery and precision using four representative matrices. Matrix-matched standard calibration was used for quantification and the calibration curves of all analytes showed good linearity (r2>0.9999). LODs and LOQs were in the range of 0.02-0.11 μg/kg and 0.06-0.26 μg/kg, respectively. Sample recoveries were from 81.2 to 118.7% and relative standard deviations lower than 8.90%. The method developed in this study was applied to analyze a total of 187 samples, and aflatoxin B1 was detected at the range of 1.18-7.29 μg/kg (below the maximum allowable limit set by the Ministry of Food and Drug Safety, MFDS), whereas aflatoxin B2, G1 and G2 were not detected. Mycotoxins that are not regulated presently in Korea were also detected: fumonisin (0.84-14.25 μg/kg), ochratoxin A (0.76-17.42 μg/kg), and zearalenone (1.73- 15.96 μg/kg). Risk assessment was evaluated by using estimated daily intake (EDI) and specific guideline values. These results indicate that the overall exposure level of Koreans to mycotoxins due to the intake of agricultural products used for food and medicine is unlikely to be a major risk factor for their health.

      • KCI우수등재

        글리터를 포함한 네일 에나멜 제품의 유해 금속 분석

        고숙경(Suk Kyung Ko),정삼주(),박영혜(),박애숙(),김현정(),박건용(),오영희() 한국환경보건학회 2017 한국환경보건학회지 Vol.43 No.2

        Objectives: This study was performed to provide basic data for the re-establishment of standards (criteria) and analytical methods for hazardous metals in nail enamel. Methods: Ten metals (lead; Pb, arsenic; As, cadminum; Cd, antimony: Sb, cobalt; Co, nikel; Ni, copper; Cu, chromium; Cr, aluminum; Al, and mercury; Hg) were measured in 67 commercial nail enamels containing glitter and/or pearls. The content of hazardous metals (excepting Hg) was determined by using an inductively coupled plasma-optical emission spectrophotometer (ICP-OES) after microwave digestion. Mercury content was measured by a mercury analyzer without any preparation. Results: The detected ranges of the intact samples were as follows: ND - 1.756 µg/g for Pb, ND - 1.24 µg/g for As, ND for Cd, ND - 20.41 µg/g for Sb, ND - 12.36 µg/g for Co, ND - 7.908 µg/g for Ni, 0.088 - 79.27 µg/g for Cu, 0.281 - 18.54 µg/g for Cr, 13.78 - 3 563 µg/g for Al, and ND - 0.044 µg/g for Hg. After centrifugation, the detected ranges of supernatant were as follows: ND - 0.435 µg/g for Pb, ND -0.504 µg/g for As, ND for Cd, ND - 0.035 µg/g for Sb, ND - 13.17 µg/g for Co, ND - 0.232 µg/g for Ni, 0.117 - 90.07 µg/g for Cu, 0.174 - 2.787 µg/g for Cr, and 9.459 - 1 565 µg/g for Al. The results of this analysis showed that the levels of heavy metals such as Pb, As, and Sb were much higher in the intact samples than those of supernatant. Conclusion: In the present study, we found that the levels of hazardous metals were significantly different depending on the status of the presence of glitter. Based on the results, we recommend that the product consumer refrain from prolonged application of nail enamel, avoid biting or chewing the nails, and wear gloves during cooking and washing dishes.

      • KCI등재

        한약재 중 아플라톡신 분석에 관한 연구

        이성득,김연선,김남훈,정희정,정삼주,김화순,김경식,한기영 한국식품위생안전성학회 2011 한국식품위생안전성학회지 Vol.26 No.4

        The increase in the consumption of herb medicines have made their use a public health problem due to the potential fungal contamination and the risk of the presence of mycotoxins. 360 samples of herb medicines were evaluated for the aflatoxin contamination. The natural occurrence of aflatoxins in these samples were determined using immunoaffinity column clean up and high performance liquid chromatography (HPLC) with post-column derivatization. For samples analyzed, mean levels (incidence) of AFB1, AFB2, AFG1 and AFG2 in positive samples were 1.4 μg/kg (46.4%), 0.4 μg/kg (25.4%), 1.1 μg/kg (37.8%) and 0.9 μg/kg (24.3%), respectively. Recoveries of the full analytical procedure were 71.7~99.7% for AFB1, 88.1~99.2% for AFB2, 82.8~95.5% for AFG1 and 77.9~90.0%for AFG2. The excess cancer risk estimated using the cancer potency of aflatoxin B1 (7 (mg/kg/day)−1 for HBsAg− and 230 (mg/kg/day)−1 for HBsAg+) were 1.30 × 10^(−5) ~ 1.22 × 10^(−7) for hepatits B surface antigen negative (HBsAg−) and 3.31 × 10^(−4)~ 3.12 × 10^(−6) for hepatits B surface antigen positive (HBsAg+) respectively. In conclusion, although the contamination levels of samples used in the study were low, further actions are also required to undertake a program of herbal surveys in order to access mycotoxin contamination overall so that the safety of public will be protected.

      • KCI등재

        질량분석기를 이용한 약령시장 내 유통 식물성 식품원료의 곰팡이독소 분석 및 위해성 평가

        최은정,고숙경,조성애,박영애,정삼주,홍성초,조석주,정지헌,박주성 한국생약학회 2022 생약학회지 Vol.53 No.3

        This study investigated the mycotoxins (aflatoxin B1, B2, G1, G2, fumonisin B1, B2, ochratoxin A and zearalenone) contained in edible and medicinal plants in Seoul Yangnyeong market during 2020–2021. We analyzed contamination of mycotoxins using LC-MS/MS and evaluated risk assessment. The method was validated by assessing matrix effects, linearity, limit of detection (LOD), limit of quantification(LOQ) and recovery. Matrix-matched standard calibration was used for calibration curves showed good linearity (r2>0.999). The LOD, LOQ and recovery were 0.01-0.23 mg/kg, 0.04-0.71 mg/kg and 75.5-117.9% respectively. Mycotoxins were detected in 22 of 171 samples; aflatoxin B1 (6.66 mg/kg), fumonisin (7.54-64.68 mg/kg), ochratoxin A (4.21-10.56 mg/kg) and zearalenone (7.31-60.76 mg/kg). In the risk assessment, the MOE (Margine of Exposure) of aflatoxin B1 and ochratoxin A were in the range of 1.48×103-2.36×105. No items exceeded 100% in %TDI (Tolerable Daily Intake) of fumonisin (B1+B2) and zearalenone.

      • KCI등재

        식·약공용 농·임산물의 다환방향족탄화수소 오염도 조사 및 위해도 결정

        박영애,고숙경,조성애,정삼주,최은정,홍성초,조석주,정지헌,박주성 한국생약학회 2022 생약학회지 Vol.53 No.3

        Polycyclic aromatic hydrocarbons(PAHs) contents were analyzed by measuring benz(a)anthracene(BaA), chrysene(Chr), benzo(b)fluoranthene(BbF) and benzo(a)pyrene(BaP), and the related risk characterization was conducted for 113 samples out of 14 different agricultural products used for food and medicine. Detection rate of PAHs was 90.3% as a whole, and the highest one was 80.5% for BaP. The detection rate of BaP exceeding the maximum permitted concentration of Rehmanniae Radix Preparata and Rehmanniae Radix, 5.0 μg/kg was 1.8%, and the detection rates of BaA, Chr and BbF were within the range of 2.7~10.6%. The highest average concentration of BaA was 3.41 μg/kg detected from Lycii Fructus, while those of Chr, BbF, BaP and PAH4(sum of detected BaA, Chr, BbF and BaP) were 5.00, 1.79, 2.36, 12.36 μg/kg, respectively, detected from Rehmanniae Radix Preparata. As for the risk characterization on PAHs, the overall MOE(Margin of Exposure) values were measured within the range of 105~107, which is unlikely to cause direct health concerns, but the worring values of MOE were measured 6.57×104 for BaP and 6.10×104 for PAH4 from Rehmanniae Radix Preparata, which may require an improvement plan to reduce BaP contents.

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