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Single-Multiplex Detection of Organ Injury Biomarkers using SPRi based Nano-Immunosensor
The clinical assessment of multiple organ dysfunctions at early stages is recognized to be an important factor in prompting definitive treatment decisions that prevent irreversible organ damage. In this article, we propose a real-time, label-free, and multiplex nanoenhanced SPRi platform to quantita...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087088/ https://www.ncbi.nlm.nih.gov/pubmed/27796342 http://dx.doi.org/10.1038/srep36348 |
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author | Zeidan, Effat Li, Siqi Zhou, Zhiguo Miller, Jennifer Sandros, Marinella G. |
author_facet | Zeidan, Effat Li, Siqi Zhou, Zhiguo Miller, Jennifer Sandros, Marinella G. |
author_sort | Zeidan, Effat |
collection | PubMed |
description | The clinical assessment of multiple organ dysfunctions at early stages is recognized to be an important factor in prompting definitive treatment decisions that prevent irreversible organ damage. In this article, we propose a real-time, label-free, and multiplex nanoenhanced SPRi platform to quantitatively assess two biomarkers, kidney injury molecule (KIM-1) and high mobility group box-1 (HMGB-1) simultaneously in buffer. Our work involves three major contributions in the design of the immunosensor: (1) we applied site-specific immobilization of antibodies to the solid surface that avoids loss of biological activity caused by covalent attachment; (2) we constructed a well-blocked sensor surface that exhibits minimal non-specific adsorption for singleplex measurements of each biomarker in buffer; and (3) we adopted a sandwich assay that implements functionalized quantum dots (NanoEnhancers) as signal amplifiers to achieve a sensitivity level of 5 pg/mL for KIM-1 and HMGB-1 in buffer. We foresee great potential and success in extending this multiplex and ultra-sensitive platform to assess a variety of other emerging clinical biomarkers at low concentrations and in complex matrices. |
format | Online Article Text |
id | pubmed-5087088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50870882016-11-04 Single-Multiplex Detection of Organ Injury Biomarkers using SPRi based Nano-Immunosensor Zeidan, Effat Li, Siqi Zhou, Zhiguo Miller, Jennifer Sandros, Marinella G. Sci Rep Article The clinical assessment of multiple organ dysfunctions at early stages is recognized to be an important factor in prompting definitive treatment decisions that prevent irreversible organ damage. In this article, we propose a real-time, label-free, and multiplex nanoenhanced SPRi platform to quantitatively assess two biomarkers, kidney injury molecule (KIM-1) and high mobility group box-1 (HMGB-1) simultaneously in buffer. Our work involves three major contributions in the design of the immunosensor: (1) we applied site-specific immobilization of antibodies to the solid surface that avoids loss of biological activity caused by covalent attachment; (2) we constructed a well-blocked sensor surface that exhibits minimal non-specific adsorption for singleplex measurements of each biomarker in buffer; and (3) we adopted a sandwich assay that implements functionalized quantum dots (NanoEnhancers) as signal amplifiers to achieve a sensitivity level of 5 pg/mL for KIM-1 and HMGB-1 in buffer. We foresee great potential and success in extending this multiplex and ultra-sensitive platform to assess a variety of other emerging clinical biomarkers at low concentrations and in complex matrices. Nature Publishing Group 2016-10-31 /pmc/articles/PMC5087088/ /pubmed/27796342 http://dx.doi.org/10.1038/srep36348 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zeidan, Effat Li, Siqi Zhou, Zhiguo Miller, Jennifer Sandros, Marinella G. Single-Multiplex Detection of Organ Injury Biomarkers using SPRi based Nano-Immunosensor |
title | Single-Multiplex Detection of Organ Injury Biomarkers using SPRi based Nano-Immunosensor |
title_full | Single-Multiplex Detection of Organ Injury Biomarkers using SPRi based Nano-Immunosensor |
title_fullStr | Single-Multiplex Detection of Organ Injury Biomarkers using SPRi based Nano-Immunosensor |
title_full_unstemmed | Single-Multiplex Detection of Organ Injury Biomarkers using SPRi based Nano-Immunosensor |
title_short | Single-Multiplex Detection of Organ Injury Biomarkers using SPRi based Nano-Immunosensor |
title_sort | single-multiplex detection of organ injury biomarkers using spri based nano-immunosensor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087088/ https://www.ncbi.nlm.nih.gov/pubmed/27796342 http://dx.doi.org/10.1038/srep36348 |
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