Ward C, McNally A J, Rusyniak D, Salamone S J
Department of Toxicology, Roche Diagnostic Systems, Inc., Branchburg, NJ.
J Forensic Sci. 1994 Nov;39(6):1486-96.
A radioimmunoassay that exhibits a nearly equivalent response to D-amphetamine and D-methamphetamine in urine over the assay range of 0 to 1000 ng/mL while displaying low cross-reactivity to L-amphetamine and L-methamphetamine (4.6% and 2.4%, respectively) has been developed. In addition, methylenedioxy-amphetamine (MDA) and methylenedioxymethamphetamine (MDMA) were detectable in the assay with cross-reactivity levels of > 100% and 77% respectively. Little cross-reactivity was observed with the commonly encountered over-the-counter (OTC) drugs and this cross-reactivity was further reduced by the addition of sodium periodate into the reaction mixture to oxidize the beta-hydroxylamines. The double (second) antibody assay uses 125I-radiolabeled derivatives of both D-amphetamine and D-methamphetamine as tracers in combination with two highly specific sheep antisera directed against D-amphetamine and D-methamphetamine. The assay exhibits a dose-response of approximately 90,000 dpm from 0 to 1000 ng/mL of D-amphetamine or D-methamphetamine with a minimum detectable dose for either drug of approximately 25 ng/mL. With a cut-off level of 500 ng/mL, the assay gave a positive result for 100% of the 111 clinical samples containing GC/MS confirmed (at or above the NIDA GC/MS cut-off values) levels of amphetamine and/or methamphetamine. Eighty-eight samples that screened negative in a clinical laboratory were all negative in the assay. Nineteen samples which were incorrectly identified as positive by other commercially available amphetamine assays were negative in this RIA.
已开发出一种放射免疫分析法,在0至1000 ng/mL的检测范围内,该方法对尿液中的D-苯丙胺和D-甲基苯丙胺表现出几乎相同的反应,而对L-苯丙胺和L-甲基苯丙胺的交叉反应性较低(分别为4.6%和2.4%)。此外,该检测方法可检测到亚甲二氧基苯丙胺(MDA)和亚甲二氧基甲基苯丙胺(MDMA),其交叉反应水平分别>100%和77%。与常见的非处方药几乎没有交叉反应,通过向反应混合物中加入高碘酸钠氧化β-羟胺,这种交叉反应进一步降低。双(第二)抗体分析法使用D-苯丙胺和D-甲基苯丙胺的125I放射性标记衍生物作为示踪剂,结合两种针对D-苯丙胺和D-甲基苯丙胺的高度特异性羊抗血清。该检测方法在0至1000 ng/mL的D-苯丙胺或D-甲基苯丙胺范围内表现出约90,000 dpm的剂量反应,两种药物的最低检测剂量约为25 ng/mL。以500 ng/mL的临界值,该检测方法对111份含有气相色谱/质谱法(GC/MS)确认(达到或高于美国国立药物滥用研究所GC/MS临界值)苯丙胺和/或甲基苯丙胺水平的临床样本的检测结果均为阳性。在临床实验室筛查为阴性的88份样本在该检测中均为阴性。在其他市售苯丙胺检测方法中被错误鉴定为阳性的19份样本在该放射免疫分析中为阴性。