Paradis Chantal, Dufresne Christelle, Bolon Magali, Boulieu Roselyne
Département de Pharmacie Clinique, de Pharmacocinétique et d'Evaluation du Médicament, Institut des Sciences Pharmaceutiques et Biologiques, Université Claude Bernard Lyon 1, Lyon, France.
Ther Drug Monit. 2002 Dec;24(6):768-74. doi: 10.1097/00007691-200212000-00014.
A solid-phase microextraction (SPME) method has been developed for the quantitative analysis of sufentanil from human plasma by gas chromatography-mass spectrometry (GC-MS). The immersion SPME sampling technique was optimized for the extraction of sufentanil from plasma. The influence of the pH and the ionic strength of the sample on the extraction of the analytes by the SPME fiber were investigated. Sufentanil and fentanyl (internal standard) were extracted from plasma with a 65-microm polydimethylsiloxane-divinylbenzene (PDMS-DVB) fiber for 30 minutes using salting out agents in basic conditions. The calibration curve was linear over a concentration range of 6-50 ng/mL. Intraday and interday relative standard deviations were 3.6% and 10.6%, respectively. The limit of quantification was 6 ng/mL for a plasma volume of 1 mL. With regard to selectivity, simplicity, and low cost, the SPME method described should be useful for a rapid extraction of sufentanil from human plasma.
已开发出一种固相微萃取(SPME)方法,用于通过气相色谱 - 质谱联用(GC - MS)对人血浆中的舒芬太尼进行定量分析。对浸入式SPME采样技术进行了优化,以从血浆中提取舒芬太尼。研究了样品的pH值和离子强度对SPME纤维萃取分析物的影响。在碱性条件下,使用盐析剂,用65微米的聚二甲基硅氧烷 - 二乙烯基苯(PDMS - DVB)纤维从血浆中提取舒芬太尼和芬太尼(内标)30分钟。校准曲线在6 - 50 ng/mL的浓度范围内呈线性。日内和日间相对标准偏差分别为3.6%和10.6%。对于1 mL血浆体积,定量限为6 ng/mL。就选择性、简便性和低成本而言,所述的SPME方法对于从人血浆中快速提取舒芬太尼应该是有用的。