Yıldız Technical University, Faculty of Art and Science, Department of Chemistry, 34,210, Davutpasa, Esenler, İstanbul, Türkiye.
Yıldız Technical University, Faculty of Art and Science, Department of Chemistry, 34,210, Davutpasa, Esenler, İstanbul, Türkiye; Turkish Academy of Sciences (TÜBA), Vedat Dalokay Street, No: 112, 06670, Çankaya, 06690, Ankara, Türkiye.
J Pharmacol Toxicol Methods. 2023 Jan-Feb;119:107207. doi: 10.1016/j.vascn.2022.107207. Epub 2022 Aug 4.
In this study, an analytical method with high accuracy and precision was developed for the determination of methamphetamine in human urine and serum samples by gas chromatography-mass spectrometry (GC-MS). A simultaneous derivatization and spray assisted droplet formation-liquid phase microextraction (SADF-LPME) method was proposed to derivatize and preconcentrate target analyte. Quadruple isotope dilution (ID) was used to provide high accuracy and precision for methamphetamine determination in the samples. After the optimization studies for the derivatization and microextraction parameters, limit of detection (LOD) and limit of quantitation (LOQ) for the developed SADF-LPME method were found to be 48.0 and 159.9 μg/kg, respectively. Recovery studies were implemented to verify the applicability and accuracy of the developed method for human urine and serum samples. The SADF-LPME method gave low percent recovery results (30.5-61.0%) for the spiked urine and serum samples showing that it failed to minimize or eliminate matrix effects for the analyte. Hence, methamphetamine acetamide-d3 was synthesized and purified in our research laboratory to be used as methamphetamine isotopic analogue in the ID method. When the SADF-LPME method was combined with ID, the percent recovery values for urine and serum samples were calculated as 99.7-100.0% and 99.4-100.2%, respectively. These results demonstrated the applicability and accuracy of the proposed method for urine and serum samples.
在这项研究中,开发了一种通过气相色谱-质谱联用(GC-MS)测定人尿和血清样品中甲胺的分析方法,具有高精度和高精确度。提出了一种同时衍生化和喷雾辅助液滴形成-液相微萃取(SADF-LPME)方法来衍生和预浓缩目标分析物。四重同位素稀释(ID)用于为样品中甲胺的测定提供高精度和高精确度。在对衍生化和微萃取参数进行优化研究后,发现所开发的 SADF-LPME 方法的检测限(LOD)和定量限(LOQ)分别为 48.0 和 159.9μg/kg。进行了回收率研究,以验证所开发的方法用于人尿和血清样品的适用性和准确性。SADF-LPME 方法对尿液和血清样品中加标的回收率较低(30.5-61.0%),表明它未能最小化或消除分析物的基质效应。因此,在我们的研究实验室中合成并纯化了甲胺乙酰胺-d3,用作 ID 方法中甲胺的同位素类似物。当将 SADF-LPME 方法与 ID 结合使用时,尿液和血清样品的回收率值分别计算为 99.7-100.0%和 99.4-100.2%。这些结果证明了所提出的方法对尿液和血清样品的适用性和准确性。