Magnetic molecularly imprinted polymer based - micro-solid phase extraction of cocaine and metabolites in plasma followed by high performance liquid chromatography - tandem mass spectrometry

被引:18
|
作者
Sanchez-Gonzalez, Juan [1 ]
Barreiro-Grille, Tania [1 ]
Cabarcos, Pamela [2 ]
Jesus Tabernero, Maria [2 ]
Bermejo-Barrera, Pilar [1 ]
Moreda-Pineiro, Antonio [1 ]
机构
[1] Univ Santiago de Compostela, Fac Chem, Dept Analyt Chem Nutr & Bromatol, Ave Ciencias S-N, Santiago De Compostela 15782, Spain
[2] Univ Santiago de Compostela, Fac Med, Dept Pathol Anat & Forens Sci, Rua San Francisco S-N, Santiago De Compostela 15782, Spain
关键词
Magnetic molecularly imprinted polymer; Plasma; Cocaine; HPLC-MS/MS; ENVIRONMENTAL WATER SAMPLES; SELECTIVE EXTRACTION; BOVINE HEMOGLOBIN; AQUEOUS-SOLUTION; RHODAMINE-B; NANOPARTICLES; RECOGNITION; URINE; MICROEXTRACTION; ANTIBIOTICS;
D O I
10.1016/j.microc.2016.03.014
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel adsorbent, magnetic molecularly imprinted polymer (MMIP) based on magnetite nanoparticles surface covered with an MIP selective for cocaine (COC), was synthesised and used in batch micro-solid phase extraction (mu-SPE) for isolation of COC and metabolites (benzoylecgonine, BZE; cocaethylene, CE; and ecgonine methyl ester, EME) from plasma samples. High performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was used for performing analysis. Parameters such as sample pH, magnetic stirring speed, extraction temperature and time (loading stage), composition and volume of the eluting solution, and desorption time, were optimised. Under the most favourable conditions, the highest extraction yields were obtained by using 0.1 to 1.0 mL of plasma (pH adjusted at 8.5) plus 50 mg of MMIP, and magnetic stirring (20 degrees C, 100 rpm) for 4 min. Elution was performed with 2 mL of a dichloromethane/2-propanol/ammonium hydroxide (75:20:5) mixture under ultrasound irradiation (325 W, 35 kHz) for 5 min. The limits of detection were between 0.013 and 036 ng L-1, and the limits of quantification were from 0.043 to 1.2 ng L-1. The relative standard deviations of intra- and inter-day tests (three concentration levels tested) ranged from 1 to 9% and from 2 to 10%, respectively. Analytical recoveries were in the range of 91-102% when spiking drug-free plasma samples at three concentration levels. Accurate results were also obtained after analysing a BTMF 1/11-B control material. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:206 / 212
页数:7
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