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 >Rapid determination of tramadol in human plasma by headspace solid-phase microextraction and capillary gas chromatography-mass spectrometry.
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Rapid determination of tramadol in human plasma by headspace solid-phase microextraction and capillary gas chromatography-mass spectrometry.

机译:顶空固相微萃取和毛细管气相色谱-质谱法快速测定人血浆中的曲马多。

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摘要

A simple, rapid and sensitive method for determination of tramadol in plasma samples was developed using headspace solid-phase microextraction (HS-SPME) and gas chromatography with mass spectrometry (GC-MS). The optimum conditions for the SPME procedure were: headspace extraction on a 65-microm polydimethylsiloxane/divinylbenzene (PDMS/DVB) fiber; 0.5 mL of plasma modified with 0.5 mL of sodium hydroxide (0.1 M); extraction temperature of 100 degrees C, with stirring at 2000 rpm for 30 min. The calibration curve showed linearity in the range of 1-400 ng mL(-1) with regression coefficient corresponding to 0.9986 and coefficient of the variation of the points of the calibration curve lower than 10%. The detection limit for tramadol in plasma was 0.2 ng mL(-1). The proposed method was successfully applied to determination of tramadol in human plasma samples from 10 healthy volunteers after a single oral administration.
机译:建立了一种使用顶空固相微萃取(HS-SPME)和气相色谱-质谱联用(GC-MS)测定血浆样品中曲马多的简单,快速,灵敏的方法。 SPME程序的最佳条件是:在65微米的聚二甲基硅氧烷/二乙烯基苯(PDMS / DVB)纤维上进行顶空萃取;用0.5 mL氢氧化钠(0.1 M)改性的0.5 mL血浆;萃取温度为100摄氏度,在2000 rpm下搅拌30分钟。校准曲线在1-400 ng mL(-1)范围内显示线性,回归系数对应为0.9986,校准曲线的点变化系数低于10%。血浆中曲马多的检出限为0.2 ng mL(-1)。所建议的方法已成功地用于测定单次口服给药后来自10名健康志愿者的人血浆样品中的曲马多。

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