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采用稀释进样液相色谱-质谱联用分析法同时定量尿液中的78种药物和代谢物。

Simultaneous Quantitation of 78 Drugs and Metabolites in Urine with a Dilute-And-Shoot LC-MS-MS Assay.

作者信息

Cao Zheng, Kaleta Erin, Wang Ping

机构信息

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX 77030, USA.

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX 77030, USA

出版信息

J Anal Toxicol. 2015 Jun;39(5):335-46. doi: 10.1093/jat/bkv024. Epub 2015 Apr 1.

Abstract

A novel LC-MS-MS assay that simultaneously detects and quantitates 78 drugs and metabolites was developed and validated for chronic pain management. Urine specimen was diluted and mixed with internal standards (ISs) before injected into LC-MS-MS. Seventy-two analytes were detected with positive electrospray ionization mode and the remaining six analytes with negative mode. Two separate gradient elution chromatographic programs were established with the same mobile phases on the same bi-phenyl HPLC column. The assay was linear for all analytes with linear regression coefficient ranging 0.994-1.000. The intra-assay precision was between 1.7 and 8.8% and inter-assay precision between 1.9 and 12.2%, with bias <20% for all but six analytes. All analytes in urine specimens were stable for 7 days at 4°C, and no significant matrix effect or carryover was observed. A suboptimal recovery rate (60.0-156.8%) was observed for six analytes, potentially due to the lack of available deuterated ISs, requiring comparison to a chemically different IS. Method comparison using patient and proficiency testing samples demonstrated that this assay was sensitive and accurate. The assay improves on currently existing assays by including glucuronide conjugates, allowing direct detection of metabolites that might otherwise be missed by existing methods.

摘要

开发并验证了一种用于慢性疼痛管理的新型液相色谱-串联质谱(LC-MS-MS)检测方法,该方法可同时检测和定量78种药物及代谢物。尿液标本在注入LC-MS-MS之前,先进行稀释并与内标(ISs)混合。采用正电喷雾电离模式检测72种分析物,其余6种分析物采用负电喷雾电离模式检测。在同一联苯高效液相色谱柱上,使用相同的流动相建立了两个单独的梯度洗脱色谱程序。所有分析物的检测方法呈线性,线性回归系数范围为0.994 - 1.000。批内精密度在1.7%至8.8%之间,批间精密度在1.9%至12.2%之间,除6种分析物外,其余所有分析物的偏差均<20%。尿液标本中的所有分析物在4°C下可稳定保存7天,未观察到明显的基质效应或残留。6种分析物的回收率不理想(60.0 - 156.8%),可能是由于缺乏可用的氘代内标,需要与化学性质不同的内标进行比较。使用患者样本和能力验证样本进行的方法比较表明,该检测方法灵敏且准确。该检测方法在现有检测方法的基础上有所改进,纳入了葡萄糖醛酸结合物,能够直接检测现有方法可能遗漏的代谢物。

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