首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of fentanyl in human plasma by head-space solid-phase microextraction and gas chromatography-mass spectrometry.
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Determination of fentanyl in human plasma by head-space solid-phase microextraction and gas chromatography-mass spectrometry.

机译:顶空固相微萃取和气相色谱-质谱法测定人血浆中的芬太尼。

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摘要

A head-space solid-phase microextraction (HS-SPME) method coupled to GC-MS was developed to extract fentanyl from human plasma. The protein binding was reduced by acidification and, eventually, the sample was deproteinized with trichloroacetic acid. The parameters influencing adsorption (extraction time, temperature, pH and salt addition) and desorption (desorption time and temperature) of the analyte on the fibre were investigated and validated for method development. The developed method proved to be rapid, simple, easy and inexpensive and offers high sensitivity and reproducibility. Linear range was obtained from 0.1 ng/ml to 2 microg/ml. The limit of detection was 0.03 ng/ml while an inter-day precision of less than 5% (n=15) could be achieved. The method has been applied for the determination of fentanyl in plasma samples after application of 50 microg/h Duragesic fentanyl patch.
机译:开发了一种与GC-MS联用的顶空固相微萃取(HS-SPME)方法,可从人血浆中提取芬太尼。通过酸化作用减少了蛋白质的结合,最终用三氯乙酸对样品进行了脱蛋白处理。研究了影响分析物在纤维上的吸附(萃取时间,温度,pH和盐添加)和解吸(解吸时间和温度)的参数,并验证了方法开发的有效性。事实证明,所开发的方法快速,简单,容易且便宜,并且具有很高的灵敏度和可重复性。线性范围为0.1 ng / ml至2 microg / ml。检出限为0.03 ng / ml,而日间精度低于5%(n = 15)。该方法已应用50微克/小时的杜拉西奇芬太尼贴剂测定血浆样品中的芬太尼。

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