Biomonitoring Research Team, Biomonitoring and Health Assessment Branch, National Institute for Occupational Safety and Health, Cincinnati, Ohio, USA.
Toxicol Mech Methods. 2010 Nov;20(9):587-93. doi: 10.3109/15376516.2010.518172. Epub 2010 Oct 13.
There are a range of applications that require the measurement of multiple drugs such as urine analysis, drug determination in water, and screening for drug contamination on surfaces. Some of the procedures used such as enzyme-linked immunosorbent assay (ELISA) are simple but can only determine one drug at a time, and others such as GC-MS or LC-MS are complex, time-consuming, and expensive. In this study, fluorescence covalent microbead immunosorbent assay (FCMIA) was investigated as a simple method for the measurement of multiple drugs simultaneously in three matrices: diluted urine, water, and on surfaces. Five different drugs of abuse or their metabolites (methamphetamine, caffeine, benzoylecgonine (a metabolite of cocaine), tetrahydrocannabinol (THC), the active ingredient in marijuana, and oxycodone) were studied over the range 0-15 ng/ml. There was no measureable cross-reactivity among the drugs at the concentrations studied. Urine dilutions from 1/50 to 1/2.5 were studied and dilutions less than 1/20 had a significant effect on the methamphetamine assay but limited effects on the benzoylecgonine and oxycodone assays and almost no effect on the THC assay. For assays performed in 1/20 urine dilution, water, and diluted surface sampling buffer, least detectable doses (LDD) were 1 ng/ml or less for the drugs. Surfaces spiked with drugs were sampled with swabs wetted with surface sampling buffer and recoveries were linear over the range 0-100 ng/100 cm(2) surface loading for all drugs. FCMIA has potential to be used for the measurement of multiple drugs in the matrices studied.
有一系列应用需要测量多种药物,如尿液分析、水中药物测定和表面药物污染筛查。一些使用的方法,如酶联免疫吸附测定(ELISA),虽然简单,但一次只能测定一种药物,而其他方法,如气相色谱-质谱(GC-MS)或液相色谱-质谱(LC-MS),则复杂、耗时且昂贵。在本研究中,荧光共价微球免疫吸附测定(FCMIA)被研究为一种简单的方法,可同时在三种基质中测量多种药物:稀释尿液、水和表面。研究了五种不同的滥用药物或其代谢物(甲基苯丙胺、咖啡因、苯甲酰古柯碱(可卡因的代谢物)、四氢大麻酚(大麻中的活性成分)和羟考酮),浓度范围为 0-15ng/ml。在所研究的浓度下,药物之间没有可测量的交叉反应。研究了从 1/50 到 1/2.5 的尿液稀释度,低于 1/20 的稀释度对甲基苯丙胺测定有显著影响,但对苯甲酰古柯碱和羟考酮测定的影响有限,对四氢大麻酚测定几乎没有影响。对于在 1/20 尿液稀释度、水和稀释表面采样缓冲液中进行的测定,药物的最低可检测剂量(LDD)为 1ng/ml 或更低。用表面采样缓冲液润湿的拭子采集表面加标药物的样品,对于所有药物,回收率在 0-100ng/100cm2 表面负载范围内呈线性。FCMIA 有可能用于研究中基质中多种药物的测量。