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Ag NC and Ag NP/PorC Film-Based Surface-Enhanced Raman Spectroscopy-Type Immunoassay for Ultrasensitive Prostate-Specific Antigen Detection
[Image: see text] Surface-enhanced Raman scattering (SERS) is a spectral detection technology with high sensitivity and detectivity and can be used to detect the fingerprint information of the molecules with ultralow concentration. Herein, a kind of immunostructure constructed by Ag nanoparticle/por...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233843/ https://www.ncbi.nlm.nih.gov/pubmed/37273592 http://dx.doi.org/10.1021/acsomega.3c00230 |
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author | Wu, Kerong Lai, Kui Chen, Junfeng Yao, Jie Zeng, Shuwen Jiang, Tao Si, Hongjie Gu, Chenjie Jiang, Junhui |
author_facet | Wu, Kerong Lai, Kui Chen, Junfeng Yao, Jie Zeng, Shuwen Jiang, Tao Si, Hongjie Gu, Chenjie Jiang, Junhui |
author_sort | Wu, Kerong |
collection | PubMed |
description | [Image: see text] Surface-enhanced Raman scattering (SERS) is a spectral detection technology with high sensitivity and detectivity and can be used to detect the fingerprint information of the molecules with ultralow concentration. Herein, a kind of immunostructure constructed by Ag nanoparticle/porous carbon (Ag NP/PorC) films as the immunosubstrate and Ag NCs as the immunoprobes was presented for ultralow level prostate-specific antigen (PSA) detection. Experimentally, the Ag NP/PorC film was first prepared with a facile method by carbonizing the gelatin–AgNO(3) film in air, and Ag NCs were synthesized by the hydrothermal method. Then, the Ag NP/PorC film was modified by PSA antibodies as the substrate, while Ag NCs were decorated by R6G and PSA antibodies for probes. The sandwiched SERS detection embodiment was constructed by the immunoreaction between the PSA and PSA antibody predecorated on the substrate and probes. Our results show that the proposed SERS-type immunoassay is highly sensitive and selective to a wide range of PSA concentrations from 10(–5) to 10(–12) g/mL. Thereafter, it was also implemented to detect the PSA level in human serum, and the results successfully reproduce the PSA levels as those measured by the chemiluminescence method with a recovery rate above 90%. All in all, this SERS-type immunoassay provides a promising method for the early diagnosis of prostate cancer. |
format | Online Article Text |
id | pubmed-10233843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102338432023-06-02 Ag NC and Ag NP/PorC Film-Based Surface-Enhanced Raman Spectroscopy-Type Immunoassay for Ultrasensitive Prostate-Specific Antigen Detection Wu, Kerong Lai, Kui Chen, Junfeng Yao, Jie Zeng, Shuwen Jiang, Tao Si, Hongjie Gu, Chenjie Jiang, Junhui ACS Omega [Image: see text] Surface-enhanced Raman scattering (SERS) is a spectral detection technology with high sensitivity and detectivity and can be used to detect the fingerprint information of the molecules with ultralow concentration. Herein, a kind of immunostructure constructed by Ag nanoparticle/porous carbon (Ag NP/PorC) films as the immunosubstrate and Ag NCs as the immunoprobes was presented for ultralow level prostate-specific antigen (PSA) detection. Experimentally, the Ag NP/PorC film was first prepared with a facile method by carbonizing the gelatin–AgNO(3) film in air, and Ag NCs were synthesized by the hydrothermal method. Then, the Ag NP/PorC film was modified by PSA antibodies as the substrate, while Ag NCs were decorated by R6G and PSA antibodies for probes. The sandwiched SERS detection embodiment was constructed by the immunoreaction between the PSA and PSA antibody predecorated on the substrate and probes. Our results show that the proposed SERS-type immunoassay is highly sensitive and selective to a wide range of PSA concentrations from 10(–5) to 10(–12) g/mL. Thereafter, it was also implemented to detect the PSA level in human serum, and the results successfully reproduce the PSA levels as those measured by the chemiluminescence method with a recovery rate above 90%. All in all, this SERS-type immunoassay provides a promising method for the early diagnosis of prostate cancer. American Chemical Society 2023-05-15 /pmc/articles/PMC10233843/ /pubmed/37273592 http://dx.doi.org/10.1021/acsomega.3c00230 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Wu, Kerong Lai, Kui Chen, Junfeng Yao, Jie Zeng, Shuwen Jiang, Tao Si, Hongjie Gu, Chenjie Jiang, Junhui Ag NC and Ag NP/PorC Film-Based Surface-Enhanced Raman Spectroscopy-Type Immunoassay for Ultrasensitive Prostate-Specific Antigen Detection |
title | Ag NC and Ag NP/PorC
Film-Based Surface-Enhanced Raman
Spectroscopy-Type Immunoassay for Ultrasensitive Prostate-Specific
Antigen Detection |
title_full | Ag NC and Ag NP/PorC
Film-Based Surface-Enhanced Raman
Spectroscopy-Type Immunoassay for Ultrasensitive Prostate-Specific
Antigen Detection |
title_fullStr | Ag NC and Ag NP/PorC
Film-Based Surface-Enhanced Raman
Spectroscopy-Type Immunoassay for Ultrasensitive Prostate-Specific
Antigen Detection |
title_full_unstemmed | Ag NC and Ag NP/PorC
Film-Based Surface-Enhanced Raman
Spectroscopy-Type Immunoassay for Ultrasensitive Prostate-Specific
Antigen Detection |
title_short | Ag NC and Ag NP/PorC
Film-Based Surface-Enhanced Raman
Spectroscopy-Type Immunoassay for Ultrasensitive Prostate-Specific
Antigen Detection |
title_sort | ag nc and ag np/porc
film-based surface-enhanced raman
spectroscopy-type immunoassay for ultrasensitive prostate-specific
antigen detection |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233843/ https://www.ncbi.nlm.nih.gov/pubmed/37273592 http://dx.doi.org/10.1021/acsomega.3c00230 |
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