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Photoluminescent and multi-phonon resonance Raman scattering dual-mode immunoassays based on CdS nanoparticles for HIgG detection

A dual-mode immunoassay strategy based on CdS nanoparticles as signal probes with both of photoluminescent (PL) and multi-phonon resonance Raman scattering (MRRS) properties was developed. Simplified structural design and preparation were achieved due to the intrinsic integration of PL and MRRS dual...

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Detalles Bibliográficos
Autores principales: Li, Hongyi, Wen, Xiaokun, Ding, Yadan, Wang, Guorui, Zhu, Hancheng, Liu, Junping, Zhao, Huiying, Hong, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702599/
https://www.ncbi.nlm.nih.gov/pubmed/36435879
http://dx.doi.org/10.1007/s00604-022-05530-z
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author Li, Hongyi
Wen, Xiaokun
Ding, Yadan
Wang, Guorui
Zhu, Hancheng
Liu, Junping
Zhao, Huiying
Hong, Xia
author_facet Li, Hongyi
Wen, Xiaokun
Ding, Yadan
Wang, Guorui
Zhu, Hancheng
Liu, Junping
Zhao, Huiying
Hong, Xia
author_sort Li, Hongyi
collection PubMed
description A dual-mode immunoassay strategy based on CdS nanoparticles as signal probes with both of photoluminescent (PL) and multi-phonon resonance Raman scattering (MRRS) properties was developed. Simplified structural design and preparation were achieved due to the intrinsic integration of PL and MRRS dual signals in the single-unit CdS nanoprobes. Human immunoglobulin G (HIgG) was sensitively and specifically detected using the proposed PL-MRRS dual-mode strategy. The linear relationship between the HIgG concentration and the intensity of 707 nm PL peaks/300 cm(−1) MRRS peaks under the excitation of 488 nm laser was established. The limit of detection was 0.93 fg mL(−1) for PL and 1.10 fg mL(−1) for MRRS. In comparison with previous IgG detection methods, the proposed method exhibited prominent advantages in detection sensitivity and working range with good stability and repeatability. An internal self-calibration was realized which ensured the accuracy and reliability of detection results. Both results of specificity experiments and serum sample analysis further confirmed the feasibility of the designed immunoassay strategy in practical serological detection. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-022-05530-z.
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spelling pubmed-97025992022-11-28 Photoluminescent and multi-phonon resonance Raman scattering dual-mode immunoassays based on CdS nanoparticles for HIgG detection Li, Hongyi Wen, Xiaokun Ding, Yadan Wang, Guorui Zhu, Hancheng Liu, Junping Zhao, Huiying Hong, Xia Mikrochim Acta Original Paper A dual-mode immunoassay strategy based on CdS nanoparticles as signal probes with both of photoluminescent (PL) and multi-phonon resonance Raman scattering (MRRS) properties was developed. Simplified structural design and preparation were achieved due to the intrinsic integration of PL and MRRS dual signals in the single-unit CdS nanoprobes. Human immunoglobulin G (HIgG) was sensitively and specifically detected using the proposed PL-MRRS dual-mode strategy. The linear relationship between the HIgG concentration and the intensity of 707 nm PL peaks/300 cm(−1) MRRS peaks under the excitation of 488 nm laser was established. The limit of detection was 0.93 fg mL(−1) for PL and 1.10 fg mL(−1) for MRRS. In comparison with previous IgG detection methods, the proposed method exhibited prominent advantages in detection sensitivity and working range with good stability and repeatability. An internal self-calibration was realized which ensured the accuracy and reliability of detection results. Both results of specificity experiments and serum sample analysis further confirmed the feasibility of the designed immunoassay strategy in practical serological detection. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-022-05530-z. Springer Vienna 2022-11-26 2022 /pmc/articles/PMC9702599/ /pubmed/36435879 http://dx.doi.org/10.1007/s00604-022-05530-z Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Paper
Li, Hongyi
Wen, Xiaokun
Ding, Yadan
Wang, Guorui
Zhu, Hancheng
Liu, Junping
Zhao, Huiying
Hong, Xia
Photoluminescent and multi-phonon resonance Raman scattering dual-mode immunoassays based on CdS nanoparticles for HIgG detection
title Photoluminescent and multi-phonon resonance Raman scattering dual-mode immunoassays based on CdS nanoparticles for HIgG detection
title_full Photoluminescent and multi-phonon resonance Raman scattering dual-mode immunoassays based on CdS nanoparticles for HIgG detection
title_fullStr Photoluminescent and multi-phonon resonance Raman scattering dual-mode immunoassays based on CdS nanoparticles for HIgG detection
title_full_unstemmed Photoluminescent and multi-phonon resonance Raman scattering dual-mode immunoassays based on CdS nanoparticles for HIgG detection
title_short Photoluminescent and multi-phonon resonance Raman scattering dual-mode immunoassays based on CdS nanoparticles for HIgG detection
title_sort photoluminescent and multi-phonon resonance raman scattering dual-mode immunoassays based on cds nanoparticles for higg detection
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702599/
https://www.ncbi.nlm.nih.gov/pubmed/36435879
http://dx.doi.org/10.1007/s00604-022-05530-z
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