期刊
CLINICA CHIMICA ACTA
卷 538, 期 -, 页码 221-230出版社
ELSEVIER
DOI: 10.1016/j.cca.2022.11.025
关键词
HPLC-DMS; MS; DMSPE; In situ derivatization; Classic androgens; 11-Oxygenated androgens; PCOS
A fast and sensitive HPLC-DMS/MS/MS method was developed for the simultaneous determination of seven androgens and 17-hydroxyprogesterone. Dispersive magnetic solid phase extraction (DMSPE) using Fe3O4@GO nanoparticles and in situ derivatization with Girard's Reagent P were employed. The method showed good precision, accuracy, and extraction recoveries, and was successfully applied to clinical sample analysis.
Background and aims: Androgens play important roles in polycystic ovarian syndrome (PCOS). However, measures of androgens based on mass spectrometry (MS) remain complex due to endogenous inferences of isomers or compounds with similar structures. Lack of sensitivity can also affect the accurate quantification of androgens, especially for very low level of 11-oxygenated androgens. Materials and methods: We developed a fast and sensitive high-performance liquid chromatography-differential mobility spectrometry tandem mass spectrometry (HPLC-DMS/MS/MS) method for the simultaneous determination of seven androgens and 17-hydroxyprogesterone. Dispersive magnetic solid phase extraction (DMSPE) was conducted with core-shell structured nanoparticles of magnetic graphene oxide (Fe3O4@GO). In situ derivatization was performed using Girard's Reagent P. Results: Linear ranges of the eight analytes were set in terms of clinical use. Intra- and inter-run precisions were < 16.7 % and 12.9 % for all the analytes and relative error was - 14.7-13.3 % and - 9.3-11.0 %, respectively. Extraction recoveries were 54.0-92.7 % for different analytes. The method was validated and was applied to assay 432 clinical samples. Conclusion: The developed method is green, fast, sensitive and accurate for the determination of endogenous androgens. It can be readily implemented in medical laboratories to provide superior analytical performance over the traditional electrochemiluminescence immunoassay method.
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