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使用微型硅胶整体柱从尿液中提取氯胺酮,然后用液相色谱串联质谱法(LC-MS/MS)定量。

Extraction of ketamine from urine using a miniature silica monolithic cartridge followed by quantification with liquid chromatography tandem mass spectrometry (LC-MS/MS).

机构信息

Department of Pharmacy, National University of Singapore, Singapore.

出版信息

J Sep Sci. 2011 May;34(9):1041-6. doi: 10.1002/jssc.201000922. Epub 2011 Mar 4.

DOI:10.1002/jssc.201000922
PMID:21374813
Abstract

The high surface area monolith with reactive hydroxyl group on its surface enables it to function as a miniature solid-phase extraction (SPE) cartridge in size of 1 cm in diameter and 0.5 cm in length. The prepared silica monolith was characterized by Brunauer-Emmett-Teller method, scanning electron microscopy, X-ray diffraction and Fourier transform infrared (FTIR) spectroscopy. Ketamine was selected as model analyte to validate the extraction efficiency of the prepared cartridge. The extracted ketamine from urine sample was quantitated by liquid chromatography tandem mass spectrometry (LC-MS/MS) using positive electrospray ionization. The limit of detection and quantification for ketamine was found to be 0.5 and 1.6 ng/mL, respectively. The analysis exhibited linearity in the range of 10-500 ng/mL with coefficient of correlation >0.99. The recovery was found to be in the range of 89-107% with relative standard deviation (RSD) less than 10%. The prepared cartridge was found robust in extracting ketamine efficiently and repeatedly without any significant deterioration in its performance. Moreover, the batch-to-batch variations in the performance of the prepared cartridges in terms of % ion suppression of the extracts and recoveries of samples were small, suggesting the consistency in the properties of the monolith.

摘要

这种具有反应性羟基的高表面积整体式材料,其尺寸为 1 厘米直径和 0.5 厘米长,可作为微型固相萃取 (SPE) 小柱使用。通过比表面积、孔径分布、扫描电子显微镜、X 射线衍射和傅里叶变换红外(FTIR)光谱对制备的硅胶整体式材料进行了表征。选择氯胺酮作为模型分析物来验证制备的小柱的萃取效率。通过正电喷雾电离的液相色谱串联质谱 (LC-MS/MS) 对尿样中的氯胺酮进行定量。氯胺酮的检测限和定量限分别为 0.5 和 1.6ng/mL。分析表明,氯胺酮在 10-500ng/mL 范围内具有良好的线性关系,相关系数>0.99。回收率在 89-107%之间,相对标准偏差 (RSD) 小于 10%。制备的小柱在高效、重复提取氯胺酮方面表现出良好的稳定性,且性能无明显下降。此外,制备的小柱在萃取物的离子抑制百分比和样品回收率方面的批次间性能变化较小,表明整体式材料的性能具有一致性。

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