Department of Analytical Chemistry, Faculty of Pharmacy, Ankara University, Ankara, Turkey.
Department of Analytical Chemistry, Faculty of Pharmacy, Adıyaman University, Adıyaman, Turkey.
Mikrochim Acta. 2022 May 19;189(6):225. doi: 10.1007/s00604-022-05321-6.
A simple, selective, and accurate electrochemical chiral sensor based on molecularly imprinted polymer (MIP) has been developed for sensitive and selective detection of esomeprazole (ESOM). For this purpose, the porous MIP sensor was prepared using tetraethyl orthosilicate (TEOS) and cetyltrimethylammonium bromide (CTAB) in the presence of β-cyclodextrin (β-CD) as a chiral recognizing element on a glassy carbon electrode (GCE). The changes in the MIP-layer related to removal and rebinding of the target ESOM were performed via differential pulse voltammetry (DPV) and cyclic voltammetry (CV) by using [Fe(CN)] as the redox probe. The structures of the developed sensor surface were characterized by using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). Electrochemical impedance spectroscopy (EIS) was also utilized for a complementary electrochemical characterization. The calibration curve was obtained in the range 1.0 × 10-2.0 × 10 M with a limit of detection (LOD) of 1.9 × 10 M. The developed method has improved the accessibility of binding sites by producing the porous material via hydrolysis/condensation reaction of TEOS in presence of CTAB. The selectivity tests of the developed SiO-β-CD@MIP/GCE sensor indicated a high specificity towards ESOM compared with structurally related competitor molecules such as R-omeprazole (R-OM), R-lansoprazole, and S-lansoprazole. The developed sensor was successfully used to determine ESOM in tablets and commercial human serum samples with satisfactory recoveries (100.25 to 100.60%) and precision (RSD 0.46 to 0.66%).
一种简单、选择性好且准确的电化学手性传感器,基于分子印迹聚合物(MIP),已经被开发出来,用于灵敏和选择性检测埃索美拉唑(ESOM)。为此,在存在β-环糊精(β-CD)作为手性识别元素的情况下,使用正硅酸乙酯(TEOS)和十六烷基三甲基溴化铵(CTAB)在玻碳电极(GCE)上制备了多孔 MIP 传感器。通过差分脉冲伏安法(DPV)和循环伏安法(CV),使用[Fe(CN)]作为氧化还原探针,对 MIP 层与目标 ESOM 的去除和再结合相关的变化进行了研究。通过扫描电子显微镜(SEM)和傅里叶变换红外光谱(FTIR)对开发传感器表面的结构进行了表征。还利用电化学阻抗谱(EIS)进行了补充电化学表征。在 1.0×10-2.0×10 M 的范围内获得了校准曲线,检测限(LOD)为 1.9×10 M。通过在 CTAB 存在下水解/缩合反应生成多孔材料,该方法提高了结合位点的可及性。与结构相关的竞争分子如 R-奥美拉唑(R-OM)、R-兰索拉唑和 S-兰索拉唑相比,开发的 SiO-β-CD@MIP/GCE 传感器的选择性测试表明,它对 ESOM 具有很高的特异性。该开发的传感器成功地用于测定片剂和商业人血清样品中的 ESOM,回收率令人满意(100.25 至 100.60%),精密度(RSD 0.46 至 0.66%)高。