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Polydopamine-Functionalized Copper Peroxide/ZIF-8 Nanoparticle-Based Fluorescence-Linked Immunosorbent Assay for the Sensitive Determination of Carcinoembryonic Antigen by Self-Supplied H(2)O(2) Generation
Copper peroxide/zeolitic imidazolate framework/polydopamine nanoparticles (CP/ZIF-8/PDA)-based fluorescence-linked immunosorbent assay (FLISA) was designed for the sensitive and high-throughput determination of carcinoembryonic antigen (CEA) by self-supplied H(2)O(2) generation. Specifically, the CE...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599728/ https://www.ncbi.nlm.nih.gov/pubmed/36290967 http://dx.doi.org/10.3390/bios12100830 |
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author | Huang, Juanjuan Yao, Yiyun Chen, Yanling Lin, Tianran Hou, Li Tang, Dianping |
author_facet | Huang, Juanjuan Yao, Yiyun Chen, Yanling Lin, Tianran Hou, Li Tang, Dianping |
author_sort | Huang, Juanjuan |
collection | PubMed |
description | Copper peroxide/zeolitic imidazolate framework/polydopamine nanoparticles (CP/ZIF-8/PDA)-based fluorescence-linked immunosorbent assay (FLISA) was designed for the sensitive and high-throughput determination of carcinoembryonic antigen (CEA) by self-supplied H(2)O(2) generation. Specifically, the CEA aptamer was modified on the surface of CP/ZIF-8/PDA to form an immunoprobe. The structures of CP and ZIF-8 could be broken under acidic conditions, and produced the Cu(2+) and H(2)O(2) due to the dissociation the CP. A subsequent Fenton-type reaction of Cu(2+) and H(2)O(2) generated hydroxyl radical (·OH). o-phenylenediamine (OPD) was oxidized by the ·OH to form 2, 3-diaminophenazine (DPA) with a significant fluorescence signal. CP/ZIF-8/PDA could be used as an efficient Fenton-type reactant to generate a large amount of ·OH to promote OPD oxidation. The sensitive detection of CEA could be realized. Under optimal conditions, the FLISA platform displayed a linear detection range from 0.01 to 20 ng mL(−1) with a detection limit of 7.6 pg mL(−1) for CEA. This strategy has great application potential for sensitive and high-throughput determination for other biomarkers in the field of biomedicine. |
format | Online Article Text |
id | pubmed-9599728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95997282022-10-27 Polydopamine-Functionalized Copper Peroxide/ZIF-8 Nanoparticle-Based Fluorescence-Linked Immunosorbent Assay for the Sensitive Determination of Carcinoembryonic Antigen by Self-Supplied H(2)O(2) Generation Huang, Juanjuan Yao, Yiyun Chen, Yanling Lin, Tianran Hou, Li Tang, Dianping Biosensors (Basel) Article Copper peroxide/zeolitic imidazolate framework/polydopamine nanoparticles (CP/ZIF-8/PDA)-based fluorescence-linked immunosorbent assay (FLISA) was designed for the sensitive and high-throughput determination of carcinoembryonic antigen (CEA) by self-supplied H(2)O(2) generation. Specifically, the CEA aptamer was modified on the surface of CP/ZIF-8/PDA to form an immunoprobe. The structures of CP and ZIF-8 could be broken under acidic conditions, and produced the Cu(2+) and H(2)O(2) due to the dissociation the CP. A subsequent Fenton-type reaction of Cu(2+) and H(2)O(2) generated hydroxyl radical (·OH). o-phenylenediamine (OPD) was oxidized by the ·OH to form 2, 3-diaminophenazine (DPA) with a significant fluorescence signal. CP/ZIF-8/PDA could be used as an efficient Fenton-type reactant to generate a large amount of ·OH to promote OPD oxidation. The sensitive detection of CEA could be realized. Under optimal conditions, the FLISA platform displayed a linear detection range from 0.01 to 20 ng mL(−1) with a detection limit of 7.6 pg mL(−1) for CEA. This strategy has great application potential for sensitive and high-throughput determination for other biomarkers in the field of biomedicine. MDPI 2022-10-06 /pmc/articles/PMC9599728/ /pubmed/36290967 http://dx.doi.org/10.3390/bios12100830 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Huang, Juanjuan Yao, Yiyun Chen, Yanling Lin, Tianran Hou, Li Tang, Dianping Polydopamine-Functionalized Copper Peroxide/ZIF-8 Nanoparticle-Based Fluorescence-Linked Immunosorbent Assay for the Sensitive Determination of Carcinoembryonic Antigen by Self-Supplied H(2)O(2) Generation |
title | Polydopamine-Functionalized Copper Peroxide/ZIF-8 Nanoparticle-Based Fluorescence-Linked Immunosorbent Assay for the Sensitive Determination of Carcinoembryonic Antigen by Self-Supplied H(2)O(2) Generation |
title_full | Polydopamine-Functionalized Copper Peroxide/ZIF-8 Nanoparticle-Based Fluorescence-Linked Immunosorbent Assay for the Sensitive Determination of Carcinoembryonic Antigen by Self-Supplied H(2)O(2) Generation |
title_fullStr | Polydopamine-Functionalized Copper Peroxide/ZIF-8 Nanoparticle-Based Fluorescence-Linked Immunosorbent Assay for the Sensitive Determination of Carcinoembryonic Antigen by Self-Supplied H(2)O(2) Generation |
title_full_unstemmed | Polydopamine-Functionalized Copper Peroxide/ZIF-8 Nanoparticle-Based Fluorescence-Linked Immunosorbent Assay for the Sensitive Determination of Carcinoembryonic Antigen by Self-Supplied H(2)O(2) Generation |
title_short | Polydopamine-Functionalized Copper Peroxide/ZIF-8 Nanoparticle-Based Fluorescence-Linked Immunosorbent Assay for the Sensitive Determination of Carcinoembryonic Antigen by Self-Supplied H(2)O(2) Generation |
title_sort | polydopamine-functionalized copper peroxide/zif-8 nanoparticle-based fluorescence-linked immunosorbent assay for the sensitive determination of carcinoembryonic antigen by self-supplied h(2)o(2) generation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599728/ https://www.ncbi.nlm.nih.gov/pubmed/36290967 http://dx.doi.org/10.3390/bios12100830 |
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