Application and Research Center for Testing and Analysis, Ege University, Bornova, İzmir, Turkey.
Department of Chemistry, Faculty of Science, Ege University, Bornova, İzmir, Turkey.
J Sep Sci. 2019 Jun;42(12):2115-2122. doi: 10.1002/jssc.201900158. Epub 2019 May 2.
A sensitive and selective method based on the determination of haloperidol with the usage of magnetite-molecularly imprinted polymer and high-resolution liquid chromatography has been developed. This novel method is rapid as the detection procedure for haloperidol can be completed within a total time of 1 h. The same imprinted polymer can be used for the determination of haloperidol at least 20 times. The proposed method has been succesfully applied to synthetic urine and serum samples and the recoveries of the spiked samples were in the range of 94.7-100.7%. The limit of detection and limit of quantification of the method were 2.25 and 7.50 μg/L, respectively. Linearity of the calibration graph was observed within the range of 10-250 μg/L. By combining the high capacity, high selectivity, and reusability of the magnetic adsorbent with the dynamic calibration range, high sensitivity and high resolution of liquid chromatography with quadrupole time-of-flight mass spectrometry, the proposed method is an ideal method for the determination and preconcentration of trace levels of haloperidol. A magnetite-molecularly imprinted polymer has been used for the first time as a selective adsorbent for the determination of haloperidol.
建立了一种基于磁性分子印迹聚合物和高分辨液相色谱法测定氟哌啶醇的灵敏、选择性方法。该新方法快速,氟哌啶醇的检测过程可在 1 小时内完成。同一印迹聚合物至少可用于 20 次氟哌啶醇的测定。该方法已成功应用于合成尿样和血清样品,加标样品的回收率在 94.7-100.7%范围内。该方法的检出限和定量限分别为 2.25 和 7.50μg/L。校准曲线的线性范围为 10-250μg/L。通过将磁性吸附剂的高容量、高选择性和可重复使用性与液相色谱-四极杆飞行时间质谱的动态校准范围、高灵敏度和高分辨率相结合,该方法是测定和预浓缩痕量氟哌啶醇的理想方法。首次将磁性分子印迹聚合物用作测定氟哌啶醇的选择性吸附剂。