Couchman Lewis, Fisher Danielle S, Subramaniam Krithika, Handley Simon A, Boughtflower Robert J, Benton Christopher M, Flanagan Robert J
Viapath Analytics, Toxicology Unit, Department of Clinical Biochemistry, King's College Hospital NHS Foundation Trust, London, UK.
Pharmaceutical Sciences Clinical Academic Group, King's College London, London, UK.
Drug Test Anal. 2018 Feb;10(2):323-329. doi: 10.1002/dta.2223. Epub 2017 Jul 19.
A novel approach to high-throughput, targeted liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis has been developed. A single chromatographic system can be used for the analysis of a range of 20 drugs and metabolites with a total analysis time of 36 s (one 96-well plate of prepared samples per hour). To demonstrate the applicability of this approach to quantitative analysis, a method has been validated for the therapeutic drug monitoring of clozapine and norclozapine following automated extraction from human plasma. Chromatographic retention times were 11.4 and 12.4 s for norclozapine and clozapine, respectively (for both analytes the chromatographic peak width was less than 1 s). Comparison with a conventional LC-MS/MS method (5 min analysis time) showed excellent agreement. This new approach offers analysis times more akin to flow-injection analysis, but is likely to be more widely applicable because of chromatographic resolution from residual matrix components and isobaric interferences.
一种用于高通量、靶向液相色谱-串联质谱(LC-MS/MS)分析的新方法已经开发出来。一个单一的色谱系统可用于分析一系列20种药物和代谢物,总分析时间为36秒(每小时分析一板96孔制备好的样品)。为了证明该方法在定量分析中的适用性,已验证了一种从人血浆中自动提取后用于氯氮平和去甲氯氮平治疗药物监测的方法。去甲氯氮平和氯氮平的色谱保留时间分别为11.4秒和12.4秒(两种分析物的色谱峰宽均小于1秒)。与传统的LC-MS/MS方法(分析时间为5分钟)比较显示出极佳的一致性。这种新方法提供的分析时间更类似于流动注射分析,但由于与残留基质成分和等压干扰的色谱分辨率,可能具有更广泛的适用性。