• 한국환경보건학회지
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• 제36권1호
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• pp.27-32
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• 2010

The indoor environmental condition was assessed in houses with allergy (asthma and atopy) patients by use of a fungal detector. The fungal index was calculated from the growth rate of the sensor fungi in a fungal detector encapsulating the spores, Alternaria alternata S-78, Eurotium herbariorum J-183 and Aspergillus penicillioides K-712. Fungal indices were higher in asthma patient's houses than in control houses and Eurotium herbariorum showed the highest growth response among the sensor fungi. Dust mites allergen, Der f1, was also significantly high in allergy patient's houses where fungal indices above 10 were detected. A correlation was observed between the fungal indices and dust mite allergen proliferations in examined houses. Therefore, the fungal index can be a useful tool as an indirect indication for detecting chronic dampness that brings both contaminations by fungi and dust mite.

• 설비공학논문집
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• 제24권12호
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• pp.852-857
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• 2012

Recently, the indoor air pollution by microbes such as fungi and mites have become a concern as important research topic on indoor air quality. Fungal growth is significantly affected by humidity. In this study, we examined the influence of relative humidity on the surface of building materials and the water content of building materials on the fungal growth rate by measuring the mycelium length of fungi in the fungal detector placed on the surface of building materials. As a result, even if the relative humidity on the surface of building materials is identical, the more water content of building materials is, the more fungi grow faster. It was suggested that fungal growth rate depends on not only the relative humidity on the surface of building materials but also the water content of building materials.

• 한국식품과학회지
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• 제17권4호
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• pp.295-303
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• 1985

고속액체 크로마토 그라피에 CN컬럼과 분리용매로 핵산-테트라 하이드로퓨란-아이소프로필알콜-물을 사용하고 형광 검출기의 검출관에 리클로솔브로 채워 아플라톡신 $B_1$, $B_2$, $G_1$, $G_2$를 분리 정량하었다. 이 조건에서 아플라톡신 $B_1$의 최저 검출한계는 0.2ng이었다. 대량생산 대두발효 식품과 메주에서 아플라톡신함량을 조시하였고, 대두 발효식품에서 사용되는 균주의 아폴라톡신 생성능을 알아보았다. TLC에서는 아플라톡신 유사물질이 검출되었지만 HPLC에서 아플라톡신이 아닌 것으로 나타났다. 시험한 균주의 아폴라톡신의 생성능은 없었다.

• Journal of Pharmaceutical Investigation
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• 제30권2호
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• pp.133-138
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• 2000

Terbinafine is an orally active antifungal agent as it inhibits the fungal enzyme squalene epoxidase, which is important in the early biosynthetic pathway of ergosterol. This leads to abnormal development of the fungal cell membrane. Bioequivalence of two terbinafine tablets, $Lamisil^{TM}$ (Novartis Korea Ltd.) and $Terbina^{TM}$ (Korean Drug Co., Ltd.), was evaluated according to the guidelines of Korea Food and Drug Administration (KFDA). Sixteen normal male volunteers, $23.56{\pm}1.75$ years old and $65.60{\pm}8.54\;kg$ of body weight, were divided into two groups and a randomized $2{\times}2$ cross-over study was employed. After one tablet containing 125 mg of terbinafine was orally administered, blood was taken at predetermined time intervals and the serum concentrations of terbinafine were determined using an HPLC method with UV detector. The pharmacokinetic parameters $(AUC_t,\;C_{max}\;and\;T_{max})$ were calculated and ANOVA test was utilized for the statistical analysis of parameters. The results showed that the differences in $AUC_t,\;C_{max}\;and\;T_{max}$ between two tablets based on $Lamisil^{TM}$, tablet were -2.53%, -2.98% and 8.13%, respectively. The powers $(1-{\beta})$ for $AUC_t,\;C_{max}\;and\;T_{max}$ were 85.21%, 98.21% and 93.11%, respectively. Minimum detectable differences $({\Delta})$ at ${\alpha}=0.1\;and\;1-{\beta}=0.8$ were all less than 20%. The 90% confidence intervals were all within ${\pm}20%$. All the parameters above met the criteria of KFDA for bioequivalence, indicating that $Terbina^{TM}$ tablet is bioequivalent to $Lamisil^{TM}$ tablet.

• 한국약용작물학회지
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• 제18권5호
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• pp.338-344
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• 2010

Our paper shows the results of 302 samples of herb medicines about fungal contamination at Yakyeang markets in Seoul. The sample medicines were treated VICAM pretreatment and analysed by post column derivatisation procedure(PHRED-HPLC) with a fluorescence detector. Aflatoxin B1 was founded from 50.3% of samples, aflatoxin B2 was 39.7%, aflatoxin G1 was 21.2% and aflatoxin G2 was 23.5%. The detected ranges of aflatoxin B1, B2, G1 and G2 were from 0.1 to $57.2\;{\mu}g/kg$, 0.1 to $42.6\;{\mu}g/kg$, 0.1 to $23.5\;{\mu}g/kg$ and 0.1 to $9.5\;{\mu}g/kg$ respectively. Among total samples, 26 samples contained aflatoxin B1 violated the regulation (less than 10 ug/kg) for aflatoxin B1 of KFDA. From the result, we could presumed that more than a half of samples were contaminated by aflatoxins. Therefore, it seems to be necessary that the new safety giudeline will be established aflatoxin B2, G1 and G2 from herb medicines as aflatoxin B1.

• 한국임상약학회지
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• 제10권2호
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• pp.62-67
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• 2000

Terbinafine has a primary fungicidal action mediated by squalene epoxidase inhibition. Treated fungi accumulate squalene while becoming deficient in ergosterol, an essential component of fungal cell membranes. Bioequivalence of two terbinafine tablets, $Lamisil^{TM}$ (Novartis Korea Ltd., Seoul, Korea) and $Mycosil^{TM}$ (Daewon Pharmaceutical Co., Ltd., Seoul, Korea), was evaluated according to the guidelines of Korea Food and Drug Administration (KFDA). Sixteen normal male volunteers ($20\sim29$ years old) were randomly divided into two groups and a randomized $2\times2$ cross-over study was employed. After oral administration of $Mycosil^{TM}\;or\;Lamisil^{TM}$ (125 mg terbinafine), blood samples were taken at predetermined time intervals and the serum terbinafine concentrations were determined using an HPLC method with UV/VIS detector. The pharmacokinetic parameters $(AUC_t,\;C_{max}\;and\;T_{max})$ were calculated and ANOVA was utilized for the statistical analysis. The results showed that the differences in $AUC_t,\;C_{max}\;and\;T_{max}$ between two tablets based on the $Lamisil^{TM}$ tablet were $-2.24\%,\;-7.68\%\;and\;2.92\%$, respectively. The powers %(1-\beta)\;for\;AVC_t,\;C_{max}\;and\;T_{max}\;were\;87.11\%,\;95.36\%\;and\;99.99\%$, respectively. Minimum detectable differences $(\Delta)\;and\;90\%$ confidence intervals were all less than $\pm20\%$. All these parameters met the criteria of KFDA for bioequivalence, indicating that $Mycosil^{TM}$ tablet is bioequivalent to $Lamisil^{TM}$ tablet.

• 농약과학회지
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• 제19권4호
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• pp.354-360
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• 2015

본 연구는 소면적 재배작물인 산마늘을 대상으로 tebuconazole 및 fludioxonil의 잔류특성을 조사하여 잔류허용기준(MRL) 및 안전사용기준 설정을 위한 자료로 활용하고자 수행하였다. Tebuconazole 20% 액상수화제 및 fludioxonil 20% 액상수화제 농약을 기준량과 배량의 농도로 토양관주처리한 후, 15, 30, 45일차에 시료를 채취하여 분석하였다. 두 약제 모두 dichloromethane을 이용하여 분배하였으며, SPE-Silica cartridge와 SPE-$NH_2$ cartridge를 사용하여 정제한 후, GC/NPD를 이용하여 분석하였다. Tebuconazole과 fludioxonil의 회수율은 각각 108.8~119.5%, 91.3~104.8%였으며, 이 때의 분석검출한계는 모두 $0.01mg\;kg^{-1}$이었다. 산마늘 중 tebuconazole의 잔류량은 <$0.01{\sim}0.12mg\;kg^{-1}$이었으며, fludioxonil의 경우 $0.01{\sim}0.09mg\;kg^{-1}$이었다. 두 약제의 잔류량으로부터 산출한 ADI 대비 식이섭취율(% ADI)은 각각 17.44%, 25.75%로 산마늘 중 tebuconazole 및 fludioxonil에 대한 ADI 대비 식이섭취율(% ADI)은 80%를 초과하지 않으며, 식이를 통한 두 약제의 노출 위험도는 안전한 수준인 것으로 판단된다. 이에 따라 tebuconazole 20% 액상수화제 및 fludioxonil 20% 액상수화제는 산마늘의 병해를 방제하는데 활용할 수 있으며, 잔류농약 문제를 효율적으로 관리할 수 있을 것이라 판단된다.

• Biomolecules & Therapeutics
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• 제11권1호
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• pp.65-71
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• 2003

Terbinafine is a synthetic allylamine that is available in an oral formulation and is used at a dosage of 250mg/day. It is used as an active antifungal agent and inhibits the fungal enzyme squalene epoxidase, which leads to the accumulation of the sterol squalene, which is toxic to the organism. The purpose of the present study was to evaluate the bioequivalence of two terbinafine tablets, Lamisil (Novartis Korea Ltd.) and Terbinex (C-TRI Ltd.), according to the guidelines of Korea Food and Drug Administration (KFDA). Eighteen normal male volunteers, 26.00$\pm$2.57 year in age and 70.51$\pm$9.36 kg in body weight, were divided into two groups and a randomized 2${\times}$2 cross-over study was employed. After one tablet containing 125 mg of terbinafine was orally administered, blood was taken at predetermined time intervals and the concentrations of terbinafine in plasma were determined using HPLC with UV detector. Pharmacokinetic parameters such as AUC, $C_{max}$ and $T_{max}$ were calculated and ANOVA test was utilized for the statistical analysis of the parameters. The results showed that the differences in AUC, $C_{max}$ and $T_{max}$ between two tablets were －4.191％, 5.223％ and －25.720％, respectively when calculated against the Lamisil, tablet. The powers (1-$\beta$) for AUC, $C_{max}$ and $T_{max}$ were 81％, 87％ and below 60％, respectively. Minimum detectable differences(.il) at alpha=O.1 and 1-/3=0.8 were less than 20％ (e.g., 19.72％ and 17.77％ for AUC and $C_{max}$, respectively). But minimum detectable differences($\Delta$) at alpha=0.1 and 1-$\beta$=0.8 for $T_{max}$ were more than 20％ (e.g., 26.25％). The 90％ confidence intervals were within $\pm$20％ (e.g., －17.440∼9.06 and －6.713∼17.160 for AUC and $C_{max}$ respectively). But 90％ confidence intervals for $T_{max}$ were not within $\pm$20％ (e.g., －43.346∼8.083). Another ANOVA test was conducted for logarithmically transformed AUC and $C_{max}$. These results showed that there are no significant differences in AUC and $C_{max}$ between the two formulations: The differences between the formulations in these log transformed parameters were all for less than 20％ (e.g., －4.19％ and 5.22％ for AUC and $C_{max}$, respectively). The 90％ confidence intervals for the log transformed data were not the acceptance range of log 0.8 to log 1.25 in AUC but the acceptance range of log 0.8 to log 1.25 in $C_{max}$ (e.g., log 1.13∼log 1.50 and log 0.94-log 1.22 for AUC and $C_{max}$ respectively). The major parameters, AUC and $C_{max}$ met the criteria of KFDA for bioequivalence although $T_{max}$ did not meet the criteria of KFDA (1998 year) for bioequivalence, indicating that Onfran tablet is bioequivalent to Zofran tablet. But in another ANOVA test AUC did not meet the criteria of KFDA (2002) for bioequivalence but $C_{max}$ met the criteria of KFDA (2002 year) for bioequivalence.or bioequivalence.equivalence.equivalence.equivalence.

• 한국식품과학회지
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• 제35권5호
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• pp.764-768
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• 2003

본 연구는 생물학적, 비생물학적인 스트레스에 대한 방어물질중의 한가지인 trans-resveratrol를 포도와 포도가공품(포도주, 포도쥬스)으로부터 분석하는 방법을 확립하였다. trans-Resveratrol 기기분석 조건은 다음과 같다. 분석 column은 Nucleosil 100-5 C18을 사용하였으며 이동상은 acetonitrile: water(40:60, v/v)로서 UV검출기(306 nm)를 이용하여 0.3 mL/min의 유속으로 측정하였다. 분석한 결과, 재현성과 반복성의 CV%는 10%이하였으며, 회수율은 $90{\sim}110%$이었다. 또한, 포도, 포도주 그리고 포도쥬스의 최소검출한계는 14.5 ng/g, 3.62 ng/mL 그리고 4.02 ng/mL이고, 최소정량한계는 14.8 ng/g, 3.69 ng/mL 그리고 4.10 ng/mL이었다. 표준물질인 trans-resveratrol 농도가 $0.048{\sim}2.4\;{\mu}g/mL$일때 $R^2$ 값은 0.999이었다. 32품종의 포도, 9종류의 포도주 그리고 9종류의 포도쥬스 내의 trans-resveratrol 함량은 각각 $0.76{\sim}207.14\;{\mu}g/100\;g$, $5.41{\sim}275.66\;{\mu}g/L$ 그리고 $63.25{\sim}751.55\;{\mu}g/L$로 분석되었다.

• 한국잠사곤충학회지
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• 제47권2호
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• pp.51-55
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• 2005

레스베라트롤(Resveratrol)은 UV 조사, 금속이온 혹은 Botrytis cinerea나 Plasmopara viticola에 의한 감염 등 생물학적, 비생물학적 스트레스에 대해 자신을 방어하기 위하여 만드는 항독성 물질(stilbene phytoalexin)로서 인체내에서 지질대사 제어, 혈소판 응집 억제 및 암 예방 등 다양한 효능을 가지는 것으로 알려져 있는 생리활성물질이다. 본 연구는 우리나라에 유전자원으로 보존 중인 뽕 나무의 결실 오디를 계통별로 채취하여 레스베라트를 함량을 분석함으로써, 레스베라트롤의 새로운 공급원으로서 오디 생산용 뽕 품종의 육종 효율을 높이는 동시에 오디의 기능성 및 이용성을 증대시키고자 하였다. 그 결과를 요약하면 다음과 같다. 1. 공시계통의 평균함량은 $777.3{\pm}585.94ppm$으로 계통간 변이가 매우 심하였다. '만생백피노상 II'는 3450.6 ppm으로 가장 높은 함량을 나타낸 반면, '사방소 I', '심설', '국부' 및 '야상오디'에서는 검출되지 않았다. 2. 과실적 특성인자인 수량, 단과중 및 당도 값을 동시에 만족시켜 오디 생산용 우량 계통으로 선발된 8계통의 레스베라트롤 함량은 각각 '절곡조생(충북)' 777.8 ppm, '팔청시평' 1475.9ppm, '강선' 864.0 ppm, '수원노상' 639.7 ppm, '죽천조생' 1458.5 ppm, '수성뽕' 31.1 ppm, '당상7호' 771.1 ppm, '장소상' 133.p ppm이었다. 3. 우리나라 최초의 오디생산용 뽕품종으로 등록된 '대성뽕' 오디의 레스베라트롤 함량은 1236.7 ppm으로 매우 높았다. 따라서 와인 등의 가공제품 개발시 이 품종의 오디를 선택한다면 기능성 및 이용성에서 유리할 것으로 판단된다. 4. 이상에서 오디는 C3G, 루틴, 지방산, 아미노산 등 여러 가지 생리활성물질 뿐 만 아니라 레스베라트롤 함량도 매우 높음을 알 수 있었다. 그러나 계통간 변이가 심하므로 품종선택시 '만생백피노상', '죽천조생', '팔청시평', '대성뽕' 등 고함유 계통을 선택하여 이용성을 높이도록 해야 할 것이다.