Caravati E Martin, Juenke Joetta M, Crouch Barbara I, Anderson Kathleen T
Utah Poison Control Center, Salt Lake City, UT 84108-1208, USA.
Ann Pharmacother. 2005 Sep;39(9):1446-9. doi: 10.1345/aph.1G107. Epub 2005 Jul 26.
Toxicology screens obtained on patients who have overdosed on drugs frequently include tricyclic antidepressants (TCAs) as part of the evaluation. Quetiapine is an antipsychotic agent with structural similarity to the TCAs.
To determine whether quetiapine may cross-react with plasma TCA immunoassays in vitro using commonly available autoanalyzers.
Quetiapine stock solution was added to 9 separate samples of pooled drug-free human plasma to produce concentrations ranging from 1 to 640 ng/mL that were verified by gas chromatography. No quetiapine metabolites were present. Each spiked plasma sample was tested in a blinded fashion using the Abbott Tricyclic Antidepressant TDx Assay on the TDxFLx autoanalyzer in 2 separate laboratories, the Syva Emit tox Serum Tricyclic Antidepressant Assay on the AU400 autoanalyzer and the S TAD Serum Tricyclic Antidepressant Screen on the ACA-Star 300 autoanalyzer. The TDx assay is quantitative, while Emit and S TAD are qualitative screening assays with a threshold of 300 ng/mL for TCA positivity. The outcome of interest was a positive TCA result.
The quantitative assay showed concentration-related TCA cross-reactivity beginning at quetiapine concentrations of 5 ng/mL. The 640-ng/mL spiked sample produced TCA results of 379 and 385 ng/mL in labs 1 and 2, respectively. The qualitative assays were screened as TCA positive at quetiapine concentrations of 160 and 320 ng/mL for the S TAD and Emit assays, respectively.
Quetiapine cross-reacts with quantitative and qualitative plasma TCA immunoassays in a concentration-dependent fashion. Therapeutic use or overdose of quetiapine may result in a false-positive TCA immunoassay result.
对药物过量患者进行的毒理学筛查通常将三环类抗抑郁药(TCA)作为评估的一部分。喹硫平是一种抗精神病药物,其结构与三环类抗抑郁药相似。
使用常用的自动分析仪在体外确定喹硫平是否可能与血浆三环类抗抑郁药免疫测定发生交叉反应。
将喹硫平储备液添加到9份单独的不含药物的混合人血浆样本中,使其浓度范围为1至640 ng/mL,通过气相色谱法进行验证。不存在喹硫平代谢物。每个加标血浆样本在两个独立实验室中使用雅培三环类抗抑郁药TDx测定法在TDxFLx自动分析仪上、使用Syva Emit tox血清三环类抗抑郁药测定法在AU400自动分析仪上以及使用S TAD血清三环类抗抑郁药筛查法在ACA-Star 300自动分析仪上进行盲法检测。TDx测定法是定量的,而Emit和S TAD是定性筛查测定法,三环类抗抑郁药阳性阈值为300 ng/mL。感兴趣的结果是三环类抗抑郁药检测呈阳性。
定量测定显示,从喹硫平浓度为5 ng/mL开始出现与浓度相关的三环类抗抑郁药交叉反应。加标浓度为640 ng/mL的样本在实验室1和实验室2中分别产生的三环类抗抑郁药检测结果为379 ng/mL和385 ng/mL。对于S TAD和Emit测定法,定性测定在喹硫平浓度分别为160 ng/mL和320 ng/mL时被筛查为三环类抗抑郁药阳性。
喹硫平与血浆三环类抗抑郁药定量和定性免疫测定以浓度依赖方式发生交叉反应。喹硫平的治疗使用或过量可能导致三环类抗抑郁药免疫测定结果出现假阳性。