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一次性电聚合分子印迹电化学传感器用于测定人血清样本中的乳腺癌标志物 CA 15-3。

Disposable electropolymerized molecularly imprinted electrochemical sensor for determination of breast cancer biomarker CA 15-3 in human serum samples.

机构信息

Departamento de Ciências Naturais, Universidade Federal de São João del-Rei, UFSJ, São João del-Rei, MG, CEP, 36307-352, Brazil.

Departamento de Ciências Naturais, Universidade Federal de São João del-Rei, UFSJ, São João del-Rei, MG, CEP, 36307-352, Brazil.

出版信息

Talanta. 2023 Jan 15;252:123819. doi: 10.1016/j.talanta.2022.123819. Epub 2022 Aug 10.

DOI:10.1016/j.talanta.2022.123819
PMID:35973345
Abstract

Initially, a printed electrode was fabricated in a paper substrate using carbon nanotube ink, graphite pencil and silver nanoparticle ink. For that the electrode was modified with gold nanoparticles and a molecularly imprintedpolymer (MIP) using CA 15-3 as target molecule. The Atomic Force Microscopy (AFM) images exhibited the change in the morphology after each electrode modification. The roughness increasedafter the electropolymerization, and decreased after the extraction procedure. Next, slightly increased again associated to the interaction of CA 15-3 and the imprinted sites. Finally, the Fourier Transform Infrared Spectroscopy (FTIR) results suggested the extraction/rebinding of CA 15-3 in the MIP sensor and also indicated that the NIP sample do not have specific cavities for the CA 15-3. In short, under optimized conditions, the CNE/AuNP is incubated with CA 15-3 (40 U mL) for 2 h at 4 °C. Then the electropolymerization was carried out in the potential range of -0.2 to 1.0 V during 20 cycles at scan rate of 50 mV s using a solution containing 15 mM of oPD. After electropolymerization, the sensor was washed with oxalic acid solution for 2 h, leading to the formation of imprinted cavities. The rebinding process was subsequently constructed for 1 h at 4 °C using CA 15-3 solution. The reproducibility and interference studies showed that the sensor can be reproducible and specific for CA 15-3. Then the sensor was applied in determination of CA 15-3 in samples of serum and saliva. The use in serum presented good recovery, but the application in saliva was not satisfactory. Therefore, the sensor CNE/AuNP/MIP could be used in the determination of CA 15-3 in serum samples.

摘要

最初,在纸基板上使用碳纳米管墨水、石墨铅笔和银纳米粒子墨水制造了印刷电极。为此,使用金纳米粒子和作为靶分子的 CA 15-3 对电极进行了修饰。原子力显微镜(AFM)图像显示了每次电极修饰后的形态变化。电聚合后粗糙度增加,提取后粗糙度降低。接下来,与 CA 15-3 和印迹部位的相互作用略有增加。最后,傅里叶变换红外光谱(FTIR)结果表明,CA 15-3 在 MIP 传感器中的提取/再结合,也表明 NIP 样品没有针对 CA 15-3 的特定腔。简而言之,在优化条件下,将 CNE/AuNP 与 CA 15-3(40 U mL)在 4°C 下孵育 2 小时。然后,在 50 mV s 的扫描速率下,在 -0.2 至 1.0 V 的电位范围内进行 20 个循环的电聚合,使用含有 15 mM oPD 的溶液。电聚合后,用草酸溶液洗涤传感器 2 小时,形成印迹腔。随后在 4°C 下使用 CA 15-3 溶液构建 1 小时的再结合过程。重现性和干扰研究表明,该传感器可用于 CA 15-3 的重现性和特异性。然后,该传感器用于血清和唾液样本中 CA 15-3 的测定。在血清中的应用具有良好的回收率,但在唾液中的应用并不令人满意。因此,传感器 CNE/AuNP/MIP 可用于血清样本中 CA 15-3 的测定。

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