Determination of ecgonine and seven other cocaine metabolites in human urine and whole blood by ultra-high-pressure liquid chromatography-quadrupole time-of-flight mass spectrometry

被引:12
|
作者
Xiong, Lingjuan [1 ,2 ]
Wang, Rong [2 ]
Liang, Chen [2 ]
Cao, Fangqi [2 ]
Rao, Yulan [3 ]
Wang, Xin [2 ]
Zeng, Libo [2 ]
Ni, Chunfang [2 ]
Ye, Haiying [2 ]
Zhang, Yurong [2 ]
机构
[1] Shanghai Inst Pharmaceut Ind, State Key Lab New Drug & Pharmaceut Proc, Shanghai 200040, Peoples R China
[2] Shanghai Inst Forens Sci, Shanghai Key Lab Crime Scene Evidence, Shanghai 200083, Peoples R China
[3] Fudan Univ, Sch Basic Med Sci, Dept Forens Med, Shanghai 200032, Peoples R China
关键词
Ecgonine; Cocaine metabolites; 96-well mu Elution solid-phase extraction plate; Ultra-high-pressure liquid chromatography; Quadrupole time-of-flight mass spectrometry; METHYL-ESTER; PRODUCTS; BENZOYLECGONINE; PERFORMANCE; STABILITY; SPECTRA; SAMPLES; MS/MS; MS;
D O I
10.1007/s00216-013-7417-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ecgonine is suggested to be a promising marker of cocaine (COC) ingestion. A combined mass spectrometry (MS) and tandem MS (MS/MS) method was developed to simultaneously determine ecgonine and seven other metabolites of cocaine in human urine and whole blood with ultra-high-pressure liquid chromatography coupled with quadrupole time-of-flight mass spectrometry. The compounds were extracted from as little as 100 mu L of sample by solid-phase extraction with a 96-well mu Elution solid-phase extraction plate. The protonated molecules or fragment ions at accurate mass acquired in MS mode were used to quantify specific analytes, following by dedicated MS/MS identification. The assay was linear in the range from 5 to 50-100 ng/mL for urine samples, except for ecgonine methyl ester (10-200 ng/mL) and ecgonine (40-400 ng/mL), and was linear from 1-2 to 50 ng/mL for whole blood samples, except for ecgonine methyl ester (20-1,000 ng/mL) and ecgonine (40-2,000 ng/mL). The correlation coefficients were all greater than 0.99. The limits of detection ranged from 0.2 to 16 ng/mL, and the lower limits of quantification ranged from 1 to 40 ng/mL. The repeatability and intermediate precision were 18.1 % or less. The accuracy was in the range from 80.0 to 122.9 %, process efficiencies were in the range from 8.6 to 177.4 %, matrix effects were in the range from 28.7 to 171.0 %, and extraction recoveries were in the range from 41.0 to 114.3 %, except for ecgonine (12.8 % and 9.3 % at low and high concentrations, respectively). This method was highly sensitive in comparison with previously published methods. The validated method was successfully applied to the analysis of real samples derived from forensic cases, and the results verified that, on the basis of data from four positive samples, ecgonine is a promising marker of cocaine ingestion.
引用
收藏
页码:9805 / 9816
页数:12
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