Laboratory of Toxicants and Drugs Analysis, Faculty of Pharmaceutical Sciences, Federal University of Alfenas-Unifal-MG, 700 Gabriel Monteiro da Silva street, 37130-000, Alfenas, MG, Brazil.
Analyst. 2011 Sep 21;136(18):3753-7. doi: 10.1039/c1an15198c. Epub 2011 Jul 21.
The association of solid phase extraction with molecularly imprinted polymers (MIP) and electrospray ionization mass spectrometry (ESI-MS) is applied to the direct extraction and quantitation of benzodiazepines in human plasma. The target analytes are sequestered by MIP and directly analyzed by ESI-MS. Due to the MIP highly selective extraction, ionic suppression during ESI is minimized; hence no separation is necessary prior to ESI-MS, which greatly increases analytical speed. Benzodiazepines (medazepam, nitrazepam, diazepam, chlordiazepoxide, clonazepam and midazolam) in human plasma were chosen as a proof-of-principle case of drug analyses by MIP-ESI-MS in a complex matrix. MIP-ESI-MS displayed good figures of merits for medazepam, nitrazepam, diazepam, chlordiazepoxide and midazolam, with analytical calibration curves ranging from 10 to 250 μg L(-1) (r > 0.98) with limit of quantification <10 μg L(-1) and acceptable within-day and between-day precision and accuracy.
固相萃取与分子印迹聚合物(MIP)和电喷雾电离质谱(ESI-MS)的联合应用于直接提取和定量人血浆中的苯并二氮杂䓬类药物。目标分析物被 MIP 螯合,并通过 ESI-MS 直接分析。由于 MIP 的高选择性萃取,ESI 过程中的离子抑制作用最小化;因此,在 ESI-MS 之前不需要进行分离,这大大提高了分析速度。选择人血浆中的苯并二氮䓬类药物(咪达唑仑、硝西泮、地西泮、氯氮䓬、氯硝西泮和咪达唑仑)作为 MIP-ESI-MS 在复杂基质中进行药物分析的原理验证案例。MIP-ESI-MS 对咪达唑仑、硝西泮、地西泮、氯氮䓬和咪达唑仑显示出良好的性能,分析校准曲线范围为 10 至 250 μg L(-1)(r > 0.98),定量限 <10 μg L(-1),日内和日间精密度和准确度可接受。