Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science & Key Laboratory of Analytical Chemistry of the State Ethnic Affairs Commission, South-Central University for Nationalities, Wuhan 430074, China.
School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.
Anal Chem. 2022 Dec 27;94(51):17835-17842. doi: 10.1021/acs.analchem.2c03583. Epub 2022 Dec 12.
The low photon energy and deep penetrating ability of near-infrared (NIR) light make it an ideal light source for a photoelectrochemical (PEC) immunosensing system. Absorption wavelengths of the metal-organic frameworks (MOFs) can be regulated by adjusting the metal ions and the conjugation degree of the ligands. Herein, an ionic liquid with a large conjugated structure was synthesized and was used as a ligand to coordinate with Nd ions to prepare Nd-MOF nanorods with a band gap of 1.26 eV. The Nd-MOF rods show a good photoabsorption property from 200 to 980 nm. A PEC platform was constructed by using Nd-MOF nanorods as the photoelectroactive element. A detachable double-stranded DNA labeled with alkaline phosphatase (ALP), which is specific to VEGF165, was immobilized onto the PEC sensing interface. After blocking unspecific active sites with bovine albumin, an NIR PEC aptasensing system was developed for VEGF165 detection. After being incubated in a mixture of VEGF165, l-ascorbic acid 2-phosphate (magnesium salt hydrate) (AAP), and chloroauric acid, the aptamers for VEGF165 were detached from the PEC aptasensing interface, thus resulting in the decrease of the charge-transfer resistance and the increase of the photocurrent response. The shedding of the aptamers also makes the ALP approach the electrode surface, thus catalyzing the reduction of AAP to produce ascorbic acid (AA). Subsequently, AA reduces in situ chloroauric acid to produce AuNPs on the Nd-MOF-based sensing interface. With the excellent conductivity and localized surface plasmon resonance effect, the AuNPs can accelerate the separation of electron-hole pairs generated from Nd-MOF nanorods, thus promoting the photoelectric conversion efficiency and achieving signal amplification. Under optimized conditions, the PEC responses were linearly related to the VEGF165 concentrations in the range of 0.01-100 ng mL and exhibit a low detection limit of 3.51 pg mL (S/N = 3). VEGF165 in human serum samples was detected by the NIR PEC aptasensor. Their concentrations were found to be well consistent with that obtained from ELISA. Furthermore, the PEC aptasensor demonstrated recoveries from 96.07 to 103.8%. The relative standard deviations were within 5%, indicating good accuracy and precision. The results further verify its practicability for clinical diagnosis.
近红外(NIR)光的低光子能量和深穿透能力使其成为光电化学(PEC)免疫传感系统的理想光源。通过调整金属离子和配体的共轭度,可以调节金属有机骨架(MOFs)的吸收波长。本文合成了一种具有大共轭结构的离子液体,并将其用作配体与 Nd 离子配位,制备了带隙为 1.26 eV 的 Nd-MOF 纳米棒。Nd-MOF 纳米棒在 200 至 980nm 范围内表现出良好的光吸收性能。PEC 平台的构建是通过将 Nd-MOF 纳米棒用作光电活性元件来实现的。将标记有碱性磷酸酶(ALP)的可分离双链 DNA 固定在 PEC 传感界面上,该 DNA 特异性地针对 VEGF165。用牛血清白蛋白封闭非特异性活性位点后,开发了用于 VEGF165 检测的近红外 PEC 适体传感系统。将 VEGF165、l-抗坏血酸 2-磷酸(镁盐水合物)(AAP)和氯金酸混合孵育后,VEGF165 的适体从 PEC 适体传感界面上脱落,从而导致电荷转移电阻降低,光电流响应增加。适体的脱落也使 ALP 接近电极表面,从而催化 AAP 还原生成抗坏血酸(AA)。随后,AA 在原位还原氯金酸,在基于 Nd-MOF 的传感界面上生成 AuNPs。由于 AuNPs 具有优异的导电性和局域表面等离子体共振效应,因此可以加速从 Nd-MOF 纳米棒中产生的电子-空穴对的分离,从而提高光电转换效率并实现信号放大。在优化条件下,PEC 响应与 VEGF165 浓度在 0.01-100ng mL 范围内呈线性关系,检测限低至 3.51pg mL(S/N = 3)。用近红外 PEC 适体传感器检测人血清样品中的 VEGF165。发现它们的浓度与 ELISA 获得的浓度非常一致。此外,PEC 适体传感器的回收率在 96.07%至 103.8%之间。相对标准偏差在 5%以内,表明具有良好的准确性和精密度。这些结果进一步验证了其在临床诊断中的实用性。