通过 UPLC-MS-MS 对在 -20°C 温度下冷冻 11 年的人体血浆中的舒芬太尼进行定量分析,发现其长期稳定性。

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL
Andreas Wehrfritz, Stefanie Schmidt, Harald Ihmsen, Jürgen Schüttler, Christian Jeleazcov
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引用次数: 0

摘要

人体血浆样本在正常实验室条件下储存数年后,其药物浓度的长期稳定性对研究目的和临床再评估以及法医毒理学都非常重要。来自一项前临床试验的 50 份人体血浆样本在-20°C 下储存 11 年后进行了重新分析。血浆样本采用固相萃取法提取。使用同位素标记的舒芬太尼-D5 作为内标。采用梯度洗脱的超高效液相色谱法(UPLC)测定舒芬太尼血浆浓度,然后采用电喷雾离子化串联质谱法进行测定。线性动态范围为 25-2500 pg/mL,检测限为 10 pg/mL,定量下限为 25 pg/mL。测定内和测定间误差不超过 6%。重新分析与首次分析之间所测得的舒芬太尼血浆浓度偏差为-63 ± 14%(平均值 ± SD)。因此,在零下 20 摄氏度冷冻 11 年的样本中,舒芬太尼在人体血浆中的浓度并不稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term stability of sufentanil quantified by UPLC-MS-MS in human plasma frozen for 11 years at -20°C.

The long-term stability of drug concentrations in human plasma samples when stored under normal laboratory conditions over several years is important for research purposes and clinical re-evaluation, but also for forensic toxicology. Fifty human plasma samples from a former clinical trial were re-analyzed after storage at -20°C for 11 years. Plasma samples were extracted using solid-phase extraction. Isotope labelled sufentanil-D5 was used as internal standard. Sufentanil plasma concentrations were determined by ultra-performance liquid chromatography (UPLC) with gradient elution, followed by tandem mass spectrometry with electrospray ionization. The linear dynamic range (LDR) was 25 - 2500 pg/mL, the limit of detection was 10 pg/mL, and the lower limit of quantification was 25 pg/mL. Intra- and inter-assay error did not exceed 6%. The deviation of the measured sufentanil plasma concentrations between the reanalysis and the first analysis was -63 ± 14% (mean ± SD). Therefore, sufentanil concentrations in human plasma were not stable in samples frozen at -20°C over 11 years.

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来源期刊
CiteScore
5.10
自引率
20.00%
发文量
92
审稿时长
6-12 weeks
期刊介绍: The Journal of Analytical Toxicology (JAT) is an international toxicology journal devoted to the timely dissemination of scientific communications concerning potentially toxic substances and drug identification, isolation, and quantitation. Since its inception in 1977, the Journal of Analytical Toxicology has striven to present state-of-the-art techniques used in toxicology labs. The peer-review process provided by the distinguished members of the Editorial Advisory Board ensures the high-quality and integrity of articles published in the Journal of Analytical Toxicology. Timely presentation of the latest toxicology developments is ensured through Technical Notes, Case Reports, and Letters to the Editor.
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