Siebenhaar Markus, Küllmer Kai, Fernandes Nuno Miguel de Barros, Hüllen Volker, Hopf Carsten
Instrumental Analysis and Bioanalysis, Department of Biotechnology, Mannheim University of Applied Sciences, Paul-Wittsack-Str. 10, 68163, Mannheim, Germany.
Anal Bioanal Chem. 2015 Sep;407(23):7229-38. doi: 10.1007/s00216-015-8887-8. Epub 2015 Jul 14.
Desorption electrospray ionization (DESI) mass spectrometry is an emerging technology for direct therapeutic drug monitoring in dried blood spots (DBS). Current DBS methods require manual application of small molecules as internal standards for absolute drug quantification. With industrial standardization in mind, we superseded the manual addition of standard and built a three-layer setup for robust quantification of salicylic acid directly from DBS. We combined a dioctyl sodium sulfosuccinate weave facilitating sample spreading with a cellulose layer for addition of isotope-labeled salicylic acid as internal standard and a filter paper for analysis of the standard-containing sample by DESI-MS. Using this setup, we developed a quantification method for salicylic acid from whole blood with a validated linear curve range from 10 to 2000 mg/L, a relative standard deviation (RSD%) ≤14%, and determination coefficients of 0.997. The limit of detection (LOD) was 8 mg/L and the lower limit of quantification (LLOQ) was 10 mg/L. Recovery rates in method verification by LC-MS/MS were 97 to 101% for blinded samples. Most importantly, a study in healthy volunteers after administration of a single dose of Aspirin provides evidence to suggest that the three-layer setup may enable individual pharmacokinetic and endpoint testing following blood collection by finger pricking by patients at home. Taken together, our data suggests that DBS-based quantification of drugs by DESI-MS on pre-manufactured three-layer cartridges may be a promising approach for future near-patient therapeutic drug monitoring.
解吸电喷雾电离(DESI)质谱法是一种用于干血斑(DBS)中直接治疗药物监测的新兴技术。目前的DBS方法需要手动添加小分子作为内标进行绝对药物定量。考虑到工业标准化,我们取代了手动添加标准品的方式,构建了一个三层装置,用于直接从DBS中对水杨酸进行可靠定量。我们将促进样品铺展的磺基琥珀酸二辛酯钠织物与用于添加同位素标记水杨酸作为内标的纤维素层以及用于通过DESI-MS分析含标准品样品的滤纸相结合。使用该装置,我们开发了一种从全血中定量水杨酸的方法,其验证后的线性曲线范围为10至2000 mg/L,相对标准偏差(RSD%)≤14%,测定系数为0.997。检测限(LOD)为8 mg/L,定量下限(LLOQ)为10 mg/L。通过LC-MS/MS进行方法验证时,盲样的回收率为97%至101%。最重要的是,一项对健康志愿者单次服用阿司匹林后的研究提供了证据,表明该三层装置可能使患者在家中通过手指采血后能够进行个体药代动力学和终点测试。综上所述,我们的数据表明,在预制的三层药筒上通过DESI-MS对基于DBS的药物进行定量可能是未来床边治疗药物监测的一种有前景的方法。