Unitat de Recerca Infància i Entorn (URIE), Institut Municipal d'Investigació Mèdica-Hospital del Mar, Barcelona, Spain.
Forensic Sci Int. 2010 Mar 20;196(1-3):38-42. doi: 10.1016/j.forsciint.2009.12.044. Epub 2010 Jan 6.
We describe the development and validation of a method for the quantification of drugs of abuse, using gas chromatography-mass spectrometry (GC/MS), in human placenta. Concentration ranges covered were 5-500 ng/g for amphetamine, methamphetamine, MDMA, methadone, cocaine, benzoylecgonine, cocaethylene, morphine, 11-nor-9-carboxy-delta-9-tetrahydrocannabinol, nicotine, and cotinine. Intra-assay and inter-assay imprecisions were less than 15.7% for lower quality control samples and less than 14.9% for medium and high quality control samples. Recovery range was 36.2-83.7%. Placenta samples were kept at -80 degrees C until analysis; analytes were stable after three freeze-thaw cycles (samples stored at -20 degrees C). This accurate and precise assay has sufficient sensitivity and specificity for the analysis of specimens collected from women who voluntarily terminated their pregnancy at 12th week of gestation. The method has proven to be robust and accurate for the quantification of the principal recreational drugs of abuse in this period of the prenatal life. This is the first report that highlights the presence of drugs of abuse during the first trimester of gestation.
我们描述了一种使用气相色谱-质谱联用(GC/MS)定量人胎盘内滥用药物的方法的开发和验证。涵盖的浓度范围为:安非他命、甲基苯丙胺、摇头丸、美沙酮、可卡因、苯甲酰古柯碱、可卡乙碱、吗啡、11-去甲-9-羧酸-Δ9-四氢大麻酚、尼古丁和可替宁的 5-500ng/g。对于较低质量控制样本,日内和日间精密度小于 15.7%,对于中、高质量控制样本,小于 14.9%。回收率范围为 36.2-83.7%。胎盘样本在-80°C 下保存直至分析;在三个冻融循环后(样本储存在-20°C),分析物稳定。该方法具有足够的灵敏度和特异性,可用于分析自愿终止妊娠 12 周的女性的样本。该方法已被证明在该产前阶段对主要娱乐性滥用药物的定量分析中具有稳健性和准确性。这是第一个强调在妊娠早期存在滥用药物的报告。