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Article: An optimized procedure for metabonomic analysis of rat liver tissue using gas chromatography/time-of-flight mass spectrometry

TitleAn optimized procedure for metabonomic analysis of rat liver tissue using gas chromatography/time-of-flight mass spectrometry
Authors
KeywordsCarbon tetrachloride
Gas chromatography/time-of-flight mass spectrometry
Liver tissue
Metabonomics
Multivariate statistics
Issue Date2010
Citation
Journal of Pharmaceutical and Biomedical Analysis, 2010, v. 52, n. 4, p. 589-596 How to Cite?
AbstractIn this paper, we present a tissue metabonomic method with an optimized extraction procedure followed by instrumental analysis with gas chromatography/time-of-flight mass spectrometry (GC/TOFMS) and spectral data analysis with multivariate statistics. Metabolite extractions were carried out using three solvents: chloroform, methanol, and water, with design of experiment (DOE) theory and multivariate statistical analysis. A two-step metabolite extraction procedure was optimized using a mixed solvent of chloroform-methanol-water (1:2:1, v/v/v) and then followed by methanol alone. This approach was subsequently validated using standard compounds and liver tissues. Calibration curves were obtained in the range of 0.50-125.0μg/mL for standards and 0.02-0.25 g/mL acceptable for liver tissue samples. For most of the metabolites investigated, relative standard deviations (RSD) were below 10% within a day (reproducibility) and below 15% within a week (stability). Rat liver tissues of carbon tetrachloride-induced acute liver injury models (n=. 10) and healthy control rats (n=. 10) were analyzed which demonstrated the applicability of the developed procedure for the tissue metabonomic study. © 2010 Elsevier B.V.
Persistent Identifierhttp://hdl.handle.net/10722/342369
ISSN
2021 Impact Factor: 3.571
2020 SCImago Journal Rankings: 0.777
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorPan, Li-
dc.contributor.authorQiu, Yunping-
dc.contributor.authorChen, Tianlu-
dc.contributor.authorLin, Jinchao-
dc.contributor.authorChi, Yi-
dc.contributor.authorSu, Mingming-
dc.contributor.authorZhao, Aihua-
dc.contributor.authorJia, Wei-
dc.date.accessioned2024-04-17T07:03:20Z-
dc.date.available2024-04-17T07:03:20Z-
dc.date.issued2010-
dc.identifier.citationJournal of Pharmaceutical and Biomedical Analysis, 2010, v. 52, n. 4, p. 589-596-
dc.identifier.issn0731-7085-
dc.identifier.urihttp://hdl.handle.net/10722/342369-
dc.description.abstractIn this paper, we present a tissue metabonomic method with an optimized extraction procedure followed by instrumental analysis with gas chromatography/time-of-flight mass spectrometry (GC/TOFMS) and spectral data analysis with multivariate statistics. Metabolite extractions were carried out using three solvents: chloroform, methanol, and water, with design of experiment (DOE) theory and multivariate statistical analysis. A two-step metabolite extraction procedure was optimized using a mixed solvent of chloroform-methanol-water (1:2:1, v/v/v) and then followed by methanol alone. This approach was subsequently validated using standard compounds and liver tissues. Calibration curves were obtained in the range of 0.50-125.0μg/mL for standards and 0.02-0.25 g/mL acceptable for liver tissue samples. For most of the metabolites investigated, relative standard deviations (RSD) were below 10% within a day (reproducibility) and below 15% within a week (stability). Rat liver tissues of carbon tetrachloride-induced acute liver injury models (n=. 10) and healthy control rats (n=. 10) were analyzed which demonstrated the applicability of the developed procedure for the tissue metabonomic study. © 2010 Elsevier B.V.-
dc.languageeng-
dc.relation.ispartofJournal of Pharmaceutical and Biomedical Analysis-
dc.subjectCarbon tetrachloride-
dc.subjectGas chromatography/time-of-flight mass spectrometry-
dc.subjectLiver tissue-
dc.subjectMetabonomics-
dc.subjectMultivariate statistics-
dc.titleAn optimized procedure for metabonomic analysis of rat liver tissue using gas chromatography/time-of-flight mass spectrometry-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.jpba.2010.01.046-
dc.identifier.pmid20185264-
dc.identifier.scopuseid_2-s2.0-77950369068-
dc.identifier.volume52-
dc.identifier.issue4-
dc.identifier.spage589-
dc.identifier.epage596-
dc.identifier.isiWOS:000276057300021-

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