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      초고성능액체크로마토그래피-탠덤매스에 의한 혈장과 담즙 중 콜릭산의 정량 분석에 관한 연구 = Analytical Method Development of Cholic Acid in Human Plasma and Gall Bladder Bile by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry

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      https://www.riss.kr/link?id=A106513322

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      다국어 초록 (Multilingual Abstract)

      Bile acids are increasingly appreciated as bioactive molecules and important end products of cholesterol metabolism. While they have been identified as key factors in lipid emulsification and absorption due to their detergent properties. bile acids ha...

      Bile acids are increasingly appreciated as bioactive molecules and important end products of cholesterol metabolism. While they have been identified as key factors in lipid emulsification and absorption due to their detergent properties. bile acids have also been shown to act as signaling molecules and intermediates between the host and the gut microbiota. To investigate bile acid functions in humans, an advanced platform for high throughput analysis is essential. Herein, we developed the analytical method of cholic acids following simple one step protein precipitation from biological sample by UPLC-MS/MS. MRM ions was m/z=407.2 for cholic acid. The R2 of calibration curves provided 0.9995 in the calibration range of 0.005~5 μg/mL. The quantification system was validated with excellent sensitivity that allows quantitative targeted analyses of bile acids. The LOD (0.001 μg/mL), LOQ (0.005 μg/mL), recoveries (96.8~101.3%± 2.7~4.0%) on intra-day assay, and (98.4~111.0%±2.3~3.4%) on inter-day assay achieved resonable validated data for bile acids analyses. The developed method was applied for drawing plasma and bile acid profile in both normal and disease status. Our study is characterized by rapid and simple sample preparation as well as successful application to plasma and bile. These results could be usable for routine diagnostic monitoring of bile acids on human biofluids.

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      목차 (Table of Contents)

      • 서 론(Introduction) 실험방법 (Experimental Method) 결 과(Results) 고 찰(Discussion) 결 론(Conclusion) 감사의 말씀(Acknowledgment) Conflict of Interest References
      • 서 론(Introduction) 실험방법 (Experimental Method) 결 과(Results) 고 찰(Discussion) 결 론(Conclusion) 감사의 말씀(Acknowledgment) Conflict of Interest References
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      참고문헌 (Reference)

      1 방준석, "담즙산의 생체 활성 물질로서의 역할" 한국임상약학회 21 (21): 49-56, 2011

      2 노지혜, "담즙산과 대사질환" 한국임상약학회 28 (28): 273-278, 2018

      3 Nagana Gowda, G. A., "Visualization of bile homeostasis using 1H-NMR spectroscopy as a route for assessing liver cancer" 23 : 1-, 2018

      4 Van Eeckhaut A., "Validation of bioanalytical LC-MS/MS assays: Evaluation of matrix effects" 877 : 2200-, 2009

      5 Yeon, S. C., "The study on the efficiency of management plan to control nutria population" Gyeongsang National University Office of Academy and Industry Collaboration 24-, 2016

      6 Matsuoka, K., "Study on micelle formation of bile salt using nuclear magnetic resonance spectroscopy" 66 : 1129-, 2017

      7 Zollner, G., "Role of nuclear receptors in the adaptive response to bile acids and cholestasis: Pathogenetic and therapeutic considerations" 3 : 235-, 2006

      8 Scherer, M., "Rapid quantification of bile acids and their conjugates in serum by liquid chromatography-tandem mass spectrometry" 877 : 3920-3925, 2009

      9 Li, D., "Rapid analysis of 17 bile acids in human plasma by LC-MS" Restek corporation 1-8, 2018

      10 Zhu, A., "Rapid Quantitation of 15 Major Bile Acids in Human Serum by UPLCESI-MS/MS" Medpace Bioanalytical Laboratories 1-, 2015

      1 방준석, "담즙산의 생체 활성 물질로서의 역할" 한국임상약학회 21 (21): 49-56, 2011

      2 노지혜, "담즙산과 대사질환" 한국임상약학회 28 (28): 273-278, 2018

      3 Nagana Gowda, G. A., "Visualization of bile homeostasis using 1H-NMR spectroscopy as a route for assessing liver cancer" 23 : 1-, 2018

      4 Van Eeckhaut A., "Validation of bioanalytical LC-MS/MS assays: Evaluation of matrix effects" 877 : 2200-, 2009

      5 Yeon, S. C., "The study on the efficiency of management plan to control nutria population" Gyeongsang National University Office of Academy and Industry Collaboration 24-, 2016

      6 Matsuoka, K., "Study on micelle formation of bile salt using nuclear magnetic resonance spectroscopy" 66 : 1129-, 2017

      7 Zollner, G., "Role of nuclear receptors in the adaptive response to bile acids and cholestasis: Pathogenetic and therapeutic considerations" 3 : 235-, 2006

      8 Scherer, M., "Rapid quantification of bile acids and their conjugates in serum by liquid chromatography-tandem mass spectrometry" 877 : 3920-3925, 2009

      9 Li, D., "Rapid analysis of 17 bile acids in human plasma by LC-MS" Restek corporation 1-8, 2018

      10 Zhu, A., "Rapid Quantitation of 15 Major Bile Acids in Human Serum by UPLCESI-MS/MS" Medpace Bioanalytical Laboratories 1-, 2015

      11 De Aguiar Vallim, T. Q., "Pleiotropic roles of bile acids in metabolism" 17 : 657-, 2013

      12 Guo, X., "Phospholipid-based matrix effects in LCMS bioanalysis" 3 : 349-, 2011

      13 Zhang, Y., "Peroxisome proliferator-activated receptorcoactivator 1a (PGC-1a) regulates triglyceride metabolism by activation of the nuclear receptor FXR" 18 : 158-, 2004

      14 Waterhous, D. V., "Nuclear magnetic resonance spectroscopy of bile acids. Development of two-dimensional NMR methods for the elucidation of proton resonance assignments for five common hydroxylated bile acids, and their parent bile acid, 5ß-cholanoic acid" 26 : 1068-, 1985

      15 Cheng, J. B., "Molecular genetics of 3ß-hydroxy-5-C27-steroid oxidoreductase deficiency in 16 patients with loss of bile acid synthesis and liver disease" 88 : 1838-, 2003

      16 Ho, W. E., "Metabolomics reveals altered metabolic pathways in experimental asthma" 48 : 206-, 2013

      17 Comhair S. A., "Metabolomic endotype of asthma" 195 : 648-, 2015

      18 Han, J., "Metabolic profiling of bile acids in human and mouse blood by LC-MS/MS in combination with phospholipid-depletion solidphase extraction" 87 : 1127-, 2015

      19 Ulaszewska, M. M., "Isotopic dilution method for bile acid profiling reveals new sulfate glycine-conjugated dihydroxy bile acids and glucuronide bile acids in serum" 173 : 1-, 2019

      20 Zhang, L., "Impaired bile acid homeostasis in children with severe acute malnutrition" 11 : 7-, 2016

      21 Gao, T., "High performance liquid chromatography-tandem mass spectrometry for the determination of bile acids in mouse serum" 79 : 307-, 2017

      22 Hegyi, P., "Guts and gall: Bile acids in regulation of intestinal epithelial function in health and disease" 98 : 1999-, 2018

      23 Kumar, B. S., "Gas chromatography-mass spectrometry-based simultaneous quantitative analytical method for urinary oxysterols and bile acids in rats" 408 : 242-, 2011

      24 Smith, J. L., "Endogenous ursodeoxycholic acid and cholic acid in liver disease due to cystic fibrosis" 39 : 1676-, 2004

      25 Houten, S. M., "Endocrine functions of bile acids" 25 : 1419-, 2006

      26 Chen, M. L., "Emerging roles of bile acids in mucosal immunity and inflammation" 12 : 851-, 2019

      27 Peng, C., "Development and validation of a sensitive LC-MS-MS method for the simultaneous determination of multicomponent contents in artificial calculus bovis" 52 : 128-, 2014

      28 Ghaffarzadegan, T., "Determination of free and conjugated bile acids in serum of Apoe (-/-) mice fed different lingonberry fractions by UHPLC-MS" 9 : 1-, 2019

      29 Perwaiz, S., "Determination of bile acids in biological fluids by liquid chromatography-electrospray tandem mass spectrometry" 42 : 114-, 2001

      30 Shi, Y., "Definitive profiling of plasma bile acids as potential biomarker for human liver diseases using UPLCHRMS" 10 : 917-, 2017

      31 Gonzales, E., "Cholic acid for primary bile acid synthesis defects: A life-saving therapy allowing a favorable outcome in adulthood" 13 : 192-, 2018

      32 Fickert, P., "Biliary bile acids in hepatobiliary injury-What is the link?" 67 : 619-, 2017

      33 Bachmann, V., "Bile salts modulate the mucin-activated type vi secretion system of pandemic vibrio cholerae" 9 : 11-, 2015

      34 Monte, M. J., "Bile acids: Chemistry, physiology, and pathophysiology" 15 : 805-, 2009

      35 Marksteiner, J., "Bile acid quantification of 20 plasma metabolites identifies lithocholic acid as a putative biomarker in Alzheimer’s disease" 14 : 1-, 2018

      36 Chiang, J. Y. L., "Bile acid metabolism and signaling" 3 : 1192-, 2013

      37 Sugita, T., "Analysis of the serum bile acid composition for differential diagnosis in patients with liver disease" 2015 : 1-2, 2015

      38 MahmoudianDehkordi, S., "Altered bile acid profile associates with cognitive Impairment in Alzheimer’s disease-An emerging role for gut microbiome" 14 : 2018

      39 Kakiyama, G., "A simple and accurate HPLC method for fecal bile acid profile in healthy and cirrhotic subjects: Validation by GC-MS and LC-MS" 55 : 978-, 2014

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      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.2 0.2 0.22
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.23 0.18 0.403 0.02
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