Faradaic electrochemical impedimetric analysis on MoS2/Au-NPs decorated surface for C-reactive protein detection

材料科学 电化学 纳米技术 化学 电极 物理化学
作者
N. Dalila R,M. K. Md Arshad,Subash C. B. Gopinath,Conlathan Ibau,M. Nuzaihan M.N.,M. F. M. Fathil,Umi Zulaikha Mohd Azmi,Periasamy Anbu
出处
期刊:Journal of The Taiwan Institute of Chemical Engineers [Elsevier BV]
卷期号:138: 104450-104450 被引量:19
标识
DOI:10.1016/j.jtice.2022.104450
摘要

• Faradaic impedimetric for detecting C-RP by Au-interdigitated microelectrode. • Enhanced by AuNP-decorated molybdenum disulfide nanosheet via chemical linkers. • Modified surfaces were evidenced by high-resolution images (SEM, AFM). • 5 µm microelectrode gap size detected C-RP as low as 1 fg/ml and LOD 0.01 fg/ml. • Sensing system is suitable for cellular milieu with serum containing samples. A label-free Faradaic electrochemical impedimetric was developed for a highly sensitive detection of C-reactive protein using a gold interdigitated microelectrode bio-sensing platform enhanced by a gold nanoparticle-decorated molybdenum disulfide (Au-NPs/MoS 2 ) nanosheet via selected chemical linking processes. C-reactive protein (C-RP), a crystalline protein, generates by the liver and hikes when there is inflammation throughout the patients’ body. The concentrations of C-RP plasma levels tend to increase rapidly when the patient facing major injury which will lead to cardiovascular disease (CVD). The 5 µm microelectrode and gap size g-IDE with the nanostructured materials was demonstrated to increase the impedimetric detection response in Faradaic-mode electrochemical impedance spectroscopy high performance detection environment. The high surface area-to-volume ratio of the modified Au-NPs/MoS 2 nanocomposite increased the probes loading onto the transducer and enhanced the impedimetric detection response of the C-RP target post-binding due to an amplified net change in the charge transfer resistance. The developed immunoassay revealed a linear detection of C-RP biomarker in a logarithmic-scale from as low as 1 fg/mL up to 1 µg/mL, and a limit of detection of 0.01 fg/mL. The sensor shows great potential as an early warning risk for cardiovascular disease at a threshold concentration value of C-RP at 1 µg/mL. The biosensor demonstrates an excellent discrimination against other competing proteins in serum, exhibiting the highest predilection to C-RP spiked human serum target. The sensor's reproducibility is reported within an acceptable range of relative standard deviation of 1–4% for n = 3.

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