López P, Bermejo A M, Tabernero M J, Fernández P, Alvarez I
Institute of Legal Medicine, Forensic Toxicology Service, Faculty of Medicine, San Francisco, s/n, 15782 Santiago de Compostela, Spain.
J Appl Toxicol. 2007 Sep-Oct;27(5):464-71. doi: 10.1002/jat.1227.
The analysis of meconium specimens is a relatively accurate method for the detection of fetal exposure to drugs. The purpose of this study was to develop and validate a method for meconium sample preparation for a gas chromatography-mass spectrometry (GC-MS) confirmation of meconium extracts for cocaine, benzoylecgonine, codeine, morphine and 6-monoacetylmorphine. The analytes were initially extracted from the matrix by methanol. Subsequently a solid-phase extraction with Waters Oasis HLB cartridges was applied. Analytes were determined in GC-MS single monitoring mode. The method was validated in the range 40-2000 ng g(-1) using 0.5 g of meconium per assay. The detector response was linear over the studied range, and limits of quantitation and detection were found to be acceptable. Intra- and inter-batch coefficients of variation oscillated between 2.54% and 20.5%, and mean relative errors were in the range 0.79%-19.9%. The recoveries were higher than 42.1% in all cases. Finally the method was applied to analysis of meconium in newborns to assess fetal exposure to cocaine and opiates.
胎粪样本分析是检测胎儿药物暴露情况的一种相对准确的方法。本研究的目的是开发并验证一种用于胎粪样本制备的方法,以通过气相色谱 - 质谱联用仪(GC-MS)确认胎粪提取物中的可卡因、苯甲酰爱康宁、可待因、吗啡和6-单乙酰吗啡。分析物最初通过甲醇从基质中提取。随后使用沃特世Oasis HLB固相萃取柱进行固相萃取。采用GC-MS单离子监测模式测定分析物。该方法在40 - 2000 ng g(-1)范围内进行验证,每次测定使用0.5 g胎粪。在所研究的范围内,检测器响应呈线性,定量限和检测限均可接受。批内和批间变异系数在2.54%至20.5%之间波动,平均相对误差在0.79% - 19.9%范围内。所有情况下回收率均高于42.1%。最后,该方法应用于新生儿胎粪分析,以评估胎儿对可卡因和阿片类药物的暴露情况。