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Sarcosine Prostate Cancer Biomarker Detection by Controlling Oxygen in NiO Membrane on Vertical Silicon Nanowires in Electrolyte-Insulator-Nanowire Structure. | LitMetric

Sarcosine Prostate Cancer Biomarker Detection by Controlling Oxygen in NiO Membrane on Vertical Silicon Nanowires in Electrolyte-Insulator-Nanowire Structure.

Anal Chem

Thin Film Nano Technology Laboratory, Department of Electronic Engineering, Chang Gung University, 259 Wen-Hwa First Road, Kwei-Shan, Tao-Yuan, 33302, Taiwan.

Published: June 2020

Sarcosine prostate cancer biomarker with the low concentration of 1 pM has been detected by controlling oxygen from 1 to 15 sccm in a NiO membrane on chemically etched vertical Si nanowires (SiNWs) in an electrolyte-insulator-nanowire (EIN) structure. The vertical Si nanowires with approximately 17 μm length and polycrystalline NiO membrane are observed by both field-emission scanning electron microscope (FE-SEM) and high-resolution transmission electron microscope (HRTEM) images, respectively. The optimized NiO membrane with oxygen content of 4 sccm on planar SiO/Si substrate shows good pH sensitivity of approximately 50 mV/pH, low hysteresis of 3.4 mV, and low drift rate of 2.4 mV/h as compared to other oxygen content membranes of 1, 10, and 15 sccm. Further, uric acid with the concentration of 0.1 μM is detected directly by using the optimized NiO membrane. In addition, repeatable HO sensing with the low concentration of 10 pM as well as prostate cancer biomarker is detected, which is owing to the reduction-oxidation phenomena of the NiO membranes. The sensing mechanism is owing to the Ni/Ni oxidation states of the NiO membrane, which is confirmed by X-ray photoelectron spectroscopy. The optimized NiO membrane on vertical Si nanowire in the EIN structure shows a good drift rate of 3.84 mV/h and sarcosine detection with improvement of approximately 1000 times as compared to the planar Si in an electrolyte-insulator-semiconductor (EIS) structure. This sensor paves a way to detect early-stage diagnosis of prostate cancer rapidly in the near future.

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Source
http://dx.doi.org/10.1021/acs.analchem.9b04745DOI Listing

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