[Fast determination of maduramicin ammonium in serum by high performance liquid chromatography-tandem mass spectrometry].

Q3 Medicine
B Zhou, B W Cheng, J Ma, F Dong, R C Liu, H L Li
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引用次数: 0

Abstract

Objective: To establish a high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method for the fast determination of maduramicin ammonium (MAD) in rat serum. Methods: In February 2024, rat serum samples were selected and directly injected after extraction and purification with methanol: acetonitrile (1: 1), separated on a C18 chromatographic column, and gradient-eluted using 0.1% formic acid aqueous solution -0.1% formic acid methanol solution as the mobile phase. Under optimized instrument conditions, electrospray positive ion multiple reaction monitoring (MRM) mode was employed for quantification using the external standard method, followed by methodological validation of the established approach. Results: The linearity of MAD in serum was good in the concentration range of 0.5-100 μg/L, and the correlation coefficient was 0.9997. The mean recoveries of MAD from spiked samples were 86.0%-109.6%, with the relative standard deviations were less than 10%. The limit of detection was 0.23 μg/L, The limit of detection was 0.75 μg/L. Conclusion: This method is high sensitive and reliable, which is suitable for the determination of MAD in in mouse serum.

高效液相色谱-串联质谱法快速测定血清中马杜拉霉素铵。
目的:建立高效液相色谱-串联质谱(HPLC-MS/MS)快速测定大鼠血清中马杜拉霉素铵(MAD)的方法。方法:于2024年2月选取大鼠血清样品,经甲醇:乙腈(1:1)萃取纯化后直接注射,用C18色谱柱分离,以0.1%甲酸水溶液-0.1%甲酸甲醇溶液为流动相梯度洗脱。在优化的仪器条件下,采用电喷雾正离子多重反应监测(MRM)模式进行外标法定量,并对所建立的方法进行方法学验证。结果:血清中MAD在0.5 ~ 100 μg/L浓度范围内线性良好,相关系数为0.9997;添加样品的平均回收率为86.0% ~ 109.6%,相对标准偏差小于10%。检出限为0.23 μg/L,检出限为0.75 μg/L。结论:该方法灵敏度高,可靠,适用于小鼠血清中MAD的测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中华劳动卫生职业病杂志
中华劳动卫生职业病杂志 Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
9764
期刊介绍:
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