A candidate reference measurement procedure for quantification of glycocholic acid in human serum based on isotope dilution liquid chromatography-tandem mass spectrometry.

Autor: Zhang P; Reference Laboratory, Autobio Diagnostics Co., Ltd, Zhengzhou, 450016, Henan, China., Wang H; Department of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China., Liang M; Reference Laboratory, Autobio Diagnostics Co., Ltd, Zhengzhou, 450016, Henan, China., Wang Z; Reference Laboratory, Autobio Diagnostics Co., Ltd, Zhengzhou, 450016, Henan, China., Liu C; Reference Laboratory, Autobio Diagnostics Co., Ltd, Zhengzhou, 450016, Henan, China., Han Y; Reference Laboratory, Autobio Diagnostics Co., Ltd, Zhengzhou, 450016, Henan, China. hanyanlin@autobio.com.cn.
Jazyk: angličtina
Zdroj: Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2024 Sep; Vol. 416 (23), pp. 5121-5131. Date of Electronic Publication: 2024 Jul 24.
DOI: 10.1007/s00216-024-05449-9
Abstrakt: Accurate measurement of serum glycocholic acid (GCA) is crucial for evaluating the activity of chronic hepatitis. Moreover, GCA is a novel identified biomarker for hepatocellular carcinoma. Although some laboratories have used the liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to measure GCA in recent years, the problem of potential interference of GCA analogues has not been solved well yet. Neither reference measurement procedures nor reference materials for GCA have been listed in the Joint Committee for Traceability in Laboratory Medicine (JCTLM) database. For standardization of GCA, it is urgent to establish a candidate measurement procedure for GCA. In this study, a candidate reference measurement procedure for the quantification of GCA in human serum based on isotope dilution liquid chromatography-tandem mass spectrometry (ID-LC-MS/MS) by a two-step sample pretreatment of protein precipitation and MAX solid-phase extraction was developed and validated. GCA can be completely separated from its structural analogues with gradient elution in 9 min compared with short time gradients published in previous literature by Huang's group. Method validation indicated perfect quantitation precision with intra-day and inter-day values that were ≤1.30% and ≤1.80%, respectively. The method showed excellent linearity with high regression coefficients (R 2  > 0.999) over a range of 0.92 ng/g-38.38 μg/g and perfect recoveries at three spiked levels (99.87-100.43%). No interference, matrix effect, and carryover were observed. Moreover, the cRMP was successfully applied to measure GCA in serum samples and compared with two immunoassays in a clinical laboratory. As a candidate reference method, this method can promote a GCA standardization program.
(© 2024. The Author(s).)
Databáze: MEDLINE
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