Recyclable SERS-Based Immunoassay Guided by Photocatalytic Performance of Fe<sub>3</sub>O<sub>4</sub>@TiO<sub>2</sub>@Au Nanocomposites

A novel recyclable surface-enhanced Raman scattering (SERS)-based immunoassay was demonstrated and exhibited extremely high sensitivity toward prostate specific antigen (PSA). The immunoassay, which possessed a sandwich structure, was constructed of multifunctional Fe<sub>3</sub>O<sub...

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Bibliographic Details
Main Authors: Yuanyuan Du, Hongmei Liu, Yiran Tian, Chenjie Gu, Ziqi Zhao, Shuwen Zeng, Tao Jiang
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:Biosensors
Subjects:
Online Access:https://www.mdpi.com/2079-6374/10/3/25
Description
Summary:A novel recyclable surface-enhanced Raman scattering (SERS)-based immunoassay was demonstrated and exhibited extremely high sensitivity toward prostate specific antigen (PSA). The immunoassay, which possessed a sandwich structure, was constructed of multifunctional Fe<sub>3</sub>O<sub>4</sub>@TiO<sub>2</sub>@Au nanocomposites as immune probe and Ag-coated sandpaper as immune substrate. First, by adjusting the density of outside Au seeds on Fe<sub>3</sub>O<sub>4</sub>@TiO<sub>2</sub> core-shell nanoparticles (NPs), the structure-dependent SERS and photocatalytic performance of the samples was explored by monitoring and degradating 4-mercaptobenzonic acid (4MBA). Afterwards, the SERS enhancement capability of Ag-coated sandpaper with different meshes was investigated, and a limit of detection (LOD), as low as 0.014 mM, was achieved by utilizing the substrate. Subsequently, the recyclable feasibility of PSA detection was approved by zeta potential measurement, absorption spectra, and SEM images and, particularly, more than 80% of SERS intensity still existed after even six cycles of immunoassay. The ultralow LOD of the recyclable immunoassay was finally calculated to be 1.871 pg/mL. Therefore, the recyclable SERS-based immunoassay exhibits good application prospects for diagnosis of cancer in clinical measurements.
ISSN:2079-6374