4.7 Article

Solid-phase microextraction of endogenous metabolites from intact tissue validated using a Biocrates standard reference method kit

Journal

JOURNAL OF PHARMACEUTICAL ANALYSIS
Volume 13, Issue 1, Pages 55-62

Publisher

ELSEVIER
DOI: 10.1016/j.jpha.2022.09.002

Keywords

Solid-phase microextraction; Solvent extraction; Metabolomics; Sample preparation; In vivo sampling

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Improved analytical methods using solid-phase microextraction (SPME) fibers were utilized in this study to monitor changes in endogenous compounds in homogenized and intact ovine lung tissue. The findings highlight the importance of sample preparation in tissue-based metabolomics studies and the unique ability of SPME to perform minimally invasive extractions while providing broad metabolite coverage.
Improved analytical methods for the metabolomic profiling of tissue samples are constantly needed. Currently, conventional sample preparation methods often involve tissue biopsy and/or homogenization, which disrupts the endogenous metabolome. In this study, solid-phase microextraction (SPME) fibers were used to monitor changes in endogenous compounds in homogenized and intact ovine lung tissue. Following SPME, a Biocrates AbsoluteIDQ assay was applied to make a downstream targeted metab-olomics analysis and confirm the advantages of in vivo SPME metabolomics. The AbsoluteIDQ kit enabled the targeted analysis of over 100 metabolites via solid-liquid extraction and SPME. Statistical analysis revealed significant differences between conventional liquid extractions from homogenized tissue and SPME results for both homogenized and intact tissue samples. In addition, principal component analysis revealed separated clustering among all the three sample groups, indicating changes in the metabolome due to tissue homogenization and the chosen sample preparation method. Furthermore, clear differences in free metabolites were observed when extractions were performed on the intact and homogenized tissue using identical SPME procedures. Specifically, a direct comparison showed that 47 statistically distinct metabolites were detected between the homogenized and intact lung tissue samples (P < 0.05) using mixed-mode SPME fibers. These changes were probably due to the disruptive homogenization of the tissue. This study's findings highlight both the importance of sample preparation in tissue-based metabolomics studies and SPME's unique ability to perform minimally invasive extractions without tissue biopsy or homogenization while providing broad metabolite coverage.(c) 2022 The Author(s). Published by Elsevier B.V. on behalf of Xi'an Jiaotong University. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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