Gray Teresa, Huestis Marilyn
Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
Anal Bioanal Chem. 2007 Aug;388(7):1455-65. doi: 10.1007/s00216-007-1228-9. Epub 2007 Mar 17.
Drug use by pregnant women has been extensively associated with adverse mental, physical, and psychological outcomes in their exposed children. This manuscript reviews bioanalytical methods for in utero drug exposure monitoring for common drugs of abuse in urine, hair, oral fluid, blood, sweat, meconium, amniotic fluid, umbilical cord tissue, nails, and vernix caseosa; neonatal matrices are particularly emphasized. Advantages and limitations of testing different maternal and neonatal biological specimens including ease and invasiveness of collection, and detection time frames, sensitivities, and specificities are described, and specific references for available analytical methods included. Future research involves identifying metabolites unique to fetal drug metabolism to improve detection rates of in utero drug exposure and determining relationships between the amount, frequency, and timing of drug exposure and drug concentrations in infant biological fluids and tissues. Accurate bioanalytical procedures are vital to defining the scope of and resolving this important public health problem.
孕妇使用药物已被广泛认为与她们接触到药物的孩子出现不良心理、身体和心理后果有关。本文综述了用于监测尿液、毛发、口腔液、血液、汗液、胎粪、羊水、脐带组织、指甲和胎脂中常见滥用药物的子宫内药物暴露的生物分析方法;特别强调了新生儿样本。描述了检测不同母体和新生儿生物样本的优缺点,包括采集的难易程度和侵入性,以及检测时间范围、灵敏度和特异性,并列出了可用分析方法的具体参考文献。未来的研究包括确定胎儿药物代谢特有的代谢物,以提高子宫内药物暴露的检测率,以及确定药物暴露的量、频率和时间与婴儿生物体液和组织中药物浓度之间的关系。准确的生物分析程序对于界定和解决这一重要的公共卫生问题至关重要。