Molecularly imprinted polymer for selective determination of Δ9-tetrahydrocannabinol and 11-nor-Δ9-tetrahydrocannabinol carboxylic acid using LC-MS/MS in urine and oral fluid

被引:24
作者
Lendoiro, E. [1 ]
de Castro, A. [1 ,2 ]
Fernandez-Vega, H. [1 ]
Cela-Perez, M. C. [3 ]
Lopez-Vilarino, J. M. [3 ]
Gonzalez-Rodriguez, M. V. [3 ]
Cruz, A. [1 ]
Lopez-Rivadulla, M. [1 ]
机构
[1] Univ Santiago de Compostela, Inst Ciencias Forenses, Serv Toxicol, Santiago De Compostela 15782, Spain
[2] Cienytech SL, Dept I D, Santiago De Compostela 15705, Spain
[3] Univ A Coruna, Ctr Invest Tecnol, Grp Polimeros, Ferrol 15403, Spain
关键词
Molecularly imprinted polymer; Oral fluid; Urine; THC; THC-COOH; LC-MS/MS; CHROMATOGRAPHY-MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION; LIQUID-CHROMATOGRAPHY; SIMULTANEOUS QUANTIFICATION; MONITORED ABSTINENCE; METABOLITES; SAMPLES; CANNABINOIDS;
D O I
10.1007/s00216-013-7599-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The use of molecularly imprinted polymers (MIPs) for solid phase extraction (MISPE) allows a rapid and selective extraction compared with traditional methods. Determination of Delta(9)-tetrahydrocannabinol (THC) and 11-nor-Delta(9)-tetrahydrocannabinol carboxylic acid (THC-COOH) in oral fluid (OF) and urine was performed using homemade MISPEs for sample clean-up and liquid chromatography tandem mass spectrometry (LC-MS/MS). Cylindrical MISPE shaped pills were synthesized using catechin as a mimic template. MISPEs were added to 0.5 mL OF or urine sample and sonicated 30 min for adsorption of analytes. For desorption, the MISPE was transfered to a clean tube, and sonicated for 15 min with 2 mL acetone:acetonitrile (3:1, v/v). The elution solvent was evaporated and reconstituted in mobile phase. Chromatographic separation was performed using a SunFire C18 (2.5 mu m; 2.1 x 20 mm) column, and formic acid 0.1 % and acetonitrile as mobile phase, with a total run time of 5 min. The method was fully validated including selectivity (no endogenous or exogenous interferences), linearity (1-500 ng/mL in OF, and 2.5-500 ng/mL in urine), limit of detection (0.75 and 1 ng/mL in OF and urine, respectively), imprecision (%CV < 12.3 %), accuracy (98.2-107.0 % of target), extraction recovery (15.9-53.5 %), process efficiency (10.1-46.2 %), and matrix effect (<-55 %). Analytes were stable for 72 h in the autosampler. Dilution 1:10 was assured in OF, and Quantisal (TM) matrix effect showed ion suppression (<-80.4 %). The method was applied to the analysis of 20 OF and 11 urine specimens. This is the first method for determination of THC and THC-COOH in OF using MISPE technology.
引用
收藏
页码:3589 / 3597
页数:9
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