Determination of tuberculosis biomarker CFP-10 in serum by ultra-performance liquid chromatography-tandem mass spectrometry

被引:0
作者
Fang, Mei [1 ]
Xu, Wenfang [2 ]
Wang, Jiaojiao [1 ]
Wu, Xiaodan [1 ]
Jin, Faxiang [2 ]
Li, Shimin [1 ,3 ]
机构
[1] Analysis Center of Agrobiology and Environment Sciences of Zhejiang University Laboratory, Hangzhou,310058, China
[2] Department of Clinical Laboratory, Affiliated Hospital of Shaoxing University, Shaoxing,312000, China
[3] Zeta Precision (Hangzhou) Biotechnology Co, Hangzhou,310051, China
关键词
Biomarkers - Blood - High performance liquid chromatography - High pressure liquid chromatography;
D O I
10.13595/j.cnki.issn1000-0720.2023122204
中图分类号
学科分类号
摘要
An ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed to determine the tuberculosis (TB) biomarker CFP-10 in human serum. After protein precipitation and trypsin digestion, solid-phase extraction (SPE) was used to enrich the specific peptide produced during enzymatic digestion of culture filtrate protein 10( CFP-10). The separation of the target analyte was performed on a Luna Omega PS-C18 column. The specific CFP-10 peptide was quantified under positive electrospray ion electrospray ionization (ESI+) and multiple reaction monitoring (MRM) mode. The results showed that the calibration curve was linear in the range of 3.0‒100 ng/mL for CFP-10, with the correlation coefficient of r2=0.9906. The limit of detection (LOD) and limit of quantification (LOQ) for CFP-10 were 1.0 and 3.0 ng/mL, respectively. The spiked recoveries ranged from 89.8% to 108.1%, with the intra-day and inter-day relative standard deviations (RSDs) both lower than 10%. Serum CFP-10 levels in TB and non-TB control cases were compared, and the results showed that serum CFP-10 was significantly lower in TB control than in non-TB cases. The proposed method is suitable for the rapid determination of CFP-10 in clinical human serum samples. © 2025, Youke Publishing Co.,Ltd. All rights reserved.
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页码:539 / 543
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