Ultrasensitive Double-Channel Microfluidic Biosensor-Based Cathodic Photo-electrochemical Analysis via Signal Amplification of SOD-Au@PANI for Cardiac Troponin I Detection

化学 检出限 光电流 生物传感器 电子转移 电极 阴极保护 电化学 光化学 光电子学 材料科学 色谱法 生物化学 物理化学
作者
Jinhui Feng,Ning Li,Yu Du,Xiang Ren,Xueying Wang,Xuejing Liu,Hongmin Ma,Qin Wei
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:93 (42): 14196-14203 被引量:25
标识
DOI:10.1021/acs.analchem.1c02922
摘要

Interesting double-channel microfluidic chip integration with a sandwich-type cathodic photo-electrochemical (PEC) biosensor is utilized for ultrasensitive and efficient detection of cardiac troponin I (cTnI) based on a signal amplification strategy. The Pd nanoparticles loading on the I-doped bismuth oxybromide with oxygen vacancies (Pd/I:BiOBr-OVs) as a sensing platform can effectively enhance cathodic photocurrent response by improving the visible light absorption ability with I doping, facilitating the efficiency separation of photogenerated electron–hole pairs with OVs, and increasing the electron-transfer rate with Pd loading, where the photogenerated electron could be captured by dissolved O2 to boost generation of a superoxide anion radical (•O2–). To further enhance the PEC response, a novel superoxide dismutase loaded on gold@polyaniline (SOD-Au@PANI) as a signal amplification label is developed for incubating the detection antibody (dAb). It is particularly noteworthy that SOD can effectively catalyze dismutation of the •O2– to produce H2O2 and O2, and Au@PANI with a good reduction and catalytic property can catalyze the produced H2O2 into H2O and O2. Then, the produced O2 that has been dissolved or adsorbed can capture more photogenerated electrons, resulting in more electron–hole pairs to separate, so as to the cathodic photocurrent signal of this system which can be amplified more significantly. Therefore, a signal amplification cathodic PEC biosensor is prepared for sensitively detecting cTnI, in which a good linearity ranging from 0.1 pg/mL to 100 ng/mL with a low detection limit of 0.042 pg/mL is obtained. Furthermore, the proposed biosensor exhibits excellent sensitivity and high selectivity, which could be extended to detect other disease markers in biological analysis and early disease diagnosis.
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