https://scholars.lib.ntu.edu.tw/handle/123456789/508352
Title: | Development and application of a comparative fatty acid analysis method to investigate voriconazole-induced hepatotoxicity | Authors: | GUAN-YUAN CHEN Chiu H.-H. SHU-WEN LIN Tseng Y.J. Tsai S.-J. CHING-HUA KUO |
Issue Date: | 2015 | Journal Volume: | 438 | Start page/Pages: | 126-134 | Source: | Clinica Chimica Acta | Abstract: | Background: As fatty acids play an important role in biological regulation, the profiling of fatty acid expression has been used to discover various disease markers and to understand disease mechanisms. This study developed an effective and accurate comparative fatty acid analysis method using differential labeling to speed up the metabolic profiling of fatty acids. Methods: Fatty acids were derivatized with unlabeled (D0) or deuterated (D3) methanol, followed by GC-MS analysis. The comparative fatty acid analysis method was validated using a series of samples with different ratios of D0/D3-labeled fatty acid standards and with mouse liver extracts. Results: Using a lipopolysaccharide (LPS)-treated mouse model, we found that the fatty acid profiles after LPS treatment were similar between the conventional single-sample analysis approach and the proposed comparative approach, with a Pearson's correlation coefficient of approximately 0.96. We applied the comparative method to investigate voriconazole-induced hepatotoxicity and revealed the toxicity mechanism as well as the potential of using fatty acids as toxicity markers. Conclusions: In conclusion, the comparative fatty acid profiling technique was determined to be fast and accurate and allowed the discovery of potential fatty acid biomarkers in a more economical and efficient manner. ? 2014 Elsevier B.V. |
URI: | https://scholars.lib.ntu.edu.tw/handle/123456789/508352 | ISSN: | 0009-8981 | DOI: | 10.1016/j.cca.2014.08.013 | SDG/Keyword: | alanine aminotransferase; alkaline phosphatase; aspartate aminotransferase; bilirubin; gamma glutamyltransferase; linoleic acid; palmitic acid; voriconazole; behenic acid; dihomo gamma linolenic acid; Escherichia coli lipopolysaccharide; fatty acid; lignoceric acid; methanol; voriconazole; antifungal agent; biological marker; fatty acid; voriconazole; accuracy; adolescent; adult; aged; animal experiment; animal model; animal tissue; article; chemical labeling; clinical article; clinical effectiveness; comparative study; controlled study; derivatization; drug effect; drug safety; enzyme activity; fatty acid analysis; female; human; liver level; liver toxicity; male; mass fragmentography; mouse; nonhuman; priority journal; reliability; sex difference; validation study; Article; fatty acid metabolism; intermethod comparison; measurement accuracy; process development; toxic hepatitis; validation process; animal; C57BL mouse; case control study; Drug-Induced Liver Injury; metabolism; metabolomics; middle aged; procedures; very elderly; young adult; Adolescent; Adult; Aged; Aged, 80 and over; Animals; Antifungal Agents; Biological Markers; Case-Control Studies; Drug-Induced Liver Injury; Fatty Acids; Female; Gas Chromatography-Mass Spectrometry; Humans; Male; Metabolomics; Mice; Mice, Inbred C57BL; Middle Aged; Voriconazole; Young Adult [SDGs]SDG3 |
Appears in Collections: | 法醫學科所 |
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