College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000, P. R. China.
J Mater Chem B. 2021 May 26;9(20):4249-4256. doi: 10.1039/d1tb00565k.
Thrombin plays an essential role in blood coagulation and some physiological and pathological processes. The convenient, rapid, sensitive, and specific detection of thrombin is of great significance in clinical research and diagnosis. Herein, surface molecularly imprinted polymer (MIP) was modified on aptamer-functionalized Fe3O4 nanoparticles (MIP-aptamer-Fe3O4 NP) for thrombin colorimetric assay by taking advantage of the peroxidase-like activity of Fe3O4 NP. With the adsorption of thrombin into imprinted cavities, the exposed surface area of Fe3O4 NP decreased, causing a decrease in its peroxidase-like activity toward 3,3',5,5'-tetramethylbenzidine (TMB) in the presence of H2O2. On the other hand, the reductive amino acids on the thrombin surface also impeded the oxidation of TMB. Both phenomena caused the light blue color of the sensing solution. Thus, a specifically sensitive colorimetric approach for the visual detection of thrombin was proposed with a linear range and limit of detection of 108.1 pmol L-1-2.7 × 10-5 mol L-1 and 27.8 pmol L-1, respectively. Moreover, due to the double recognition elements of MIP and aptamer, the prepared MIP-aptamer-Fe3O4 NP showed higher selectivity to thrombin than that based on only one recognition element. It is worth noting that no special property (e.g. electrochemical or fluorescence activity) of the template was required in this work. Thus, more template molecules can be easily, selectively, and sensitively detected based on the proposed MIP-aptamer-mimic enzyme colorimetric sensing strategy.
凝血酶在血液凝固和一些生理及病理过程中起着至关重要的作用。方便、快速、灵敏、特异的凝血酶检测在临床研究和诊断中具有重要意义。在此,通过利用 Fe3O4 NP 的过氧化物酶样活性,将适配体功能化的 Fe3O4 纳米粒子(MIP-aptamer-Fe3O4 NP)上修饰表面分子印迹聚合物(MIP),用于凝血酶比色测定。随着凝血酶被吸附到印迹腔中,Fe3O4 NP 的暴露表面积减少,导致在 H2O2 存在下其对 3,3',5,5'-四甲基联苯胺(TMB)的过氧化物酶样活性降低。另一方面,凝血酶表面的还原氨基酸也阻碍了 TMB 的氧化。这两种现象都导致了传感溶液的浅蓝色。因此,提出了一种用于视觉检测凝血酶的特异性灵敏比色方法,其线性范围和检测限分别为 108.1 pmol L-1-2.7 × 10-5 mol L-1和 27.8 pmol L-1。此外,由于 MIP 和适配体的双重识别元件,与仅基于一种识别元件的方法相比,所制备的 MIP-aptamer-Fe3O4 NP 对凝血酶表现出更高的选择性。值得注意的是,在这项工作中不需要模板的特殊性质(例如电化学或荧光活性)。因此,基于所提出的 MIP-aptamer-模拟酶比色传感策略,可以更容易、更选择性和更灵敏地检测更多的模板分子。