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Sensitivity Limits for in vivo ELISA Measurements of Molecular Biomarker Concentrations
The extremely high sensitivity that has been suggested for magnetic particle imaging has its roots in the unique signal produced by the nanoparticles at the frequencies of the harmonics of the drive field. That sensitivity should be translatable to other methods that utilize magnetic nanoparticle pr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302994/ https://www.ncbi.nlm.nih.gov/pubmed/34307836 http://dx.doi.org/10.18416/ijmpi.2017.1706003 |
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author | Weaver, John B. Shi, Yinpeng Ness, Dylan B. Khurshid, Hafsa Samia, Anna Cristina S. |
author_facet | Weaver, John B. Shi, Yinpeng Ness, Dylan B. Khurshid, Hafsa Samia, Anna Cristina S. |
author_sort | Weaver, John B. |
collection | PubMed |
description | The extremely high sensitivity that has been suggested for magnetic particle imaging has its roots in the unique signal produced by the nanoparticles at the frequencies of the harmonics of the drive field. That sensitivity should be translatable to other methods that utilize magnetic nanoparticle probes, specifically towards magnetic nanoparticle spectroscopy that is used to measure molecular biomarker concentrations for an “in vivo ELISA” assay approach. In this paper, we translate the predicted sensitivity of magnetic particle imaging into a projected sensitivity limit for in vivo ELISA. The simplifying assumptions adopted are: 1) the limiting noise in the detection system is equivalent to the minimum detectable mass of nanoparticles; 2) the nanoparticle’s signal arising from Brownian relaxation is completely eliminated by the molecular binding event, which can be accomplished by binding the nanoparticle to something so massive that it can no longer physically rotate and is large enough that Neel relaxation is minimal. Given these assumptions, the equation for the minimum concentration of molecular biomarker we should be able to detect is obtained and the in vivo sensitivity is estimated to be in the attomolar to zeptomolar range. Spectrometer design and nonspecific binding are the technical limitations that need to be overcome to achieve the theoretical limit presented. |
format | Online Article Text |
id | pubmed-8302994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-83029942021-07-24 Sensitivity Limits for in vivo ELISA Measurements of Molecular Biomarker Concentrations Weaver, John B. Shi, Yinpeng Ness, Dylan B. Khurshid, Hafsa Samia, Anna Cristina S. Int J Magn Part Imaging Article The extremely high sensitivity that has been suggested for magnetic particle imaging has its roots in the unique signal produced by the nanoparticles at the frequencies of the harmonics of the drive field. That sensitivity should be translatable to other methods that utilize magnetic nanoparticle probes, specifically towards magnetic nanoparticle spectroscopy that is used to measure molecular biomarker concentrations for an “in vivo ELISA” assay approach. In this paper, we translate the predicted sensitivity of magnetic particle imaging into a projected sensitivity limit for in vivo ELISA. The simplifying assumptions adopted are: 1) the limiting noise in the detection system is equivalent to the minimum detectable mass of nanoparticles; 2) the nanoparticle’s signal arising from Brownian relaxation is completely eliminated by the molecular binding event, which can be accomplished by binding the nanoparticle to something so massive that it can no longer physically rotate and is large enough that Neel relaxation is minimal. Given these assumptions, the equation for the minimum concentration of molecular biomarker we should be able to detect is obtained and the in vivo sensitivity is estimated to be in the attomolar to zeptomolar range. Spectrometer design and nonspecific binding are the technical limitations that need to be overcome to achieve the theoretical limit presented. 2017-06-22 2017 /pmc/articles/PMC8302994/ /pubmed/34307836 http://dx.doi.org/10.18416/ijmpi.2017.1706003 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Weaver, John B. Shi, Yinpeng Ness, Dylan B. Khurshid, Hafsa Samia, Anna Cristina S. Sensitivity Limits for in vivo ELISA Measurements of Molecular Biomarker Concentrations |
title | Sensitivity Limits for in vivo ELISA Measurements of Molecular Biomarker Concentrations |
title_full | Sensitivity Limits for in vivo ELISA Measurements of Molecular Biomarker Concentrations |
title_fullStr | Sensitivity Limits for in vivo ELISA Measurements of Molecular Biomarker Concentrations |
title_full_unstemmed | Sensitivity Limits for in vivo ELISA Measurements of Molecular Biomarker Concentrations |
title_short | Sensitivity Limits for in vivo ELISA Measurements of Molecular Biomarker Concentrations |
title_sort | sensitivity limits for in vivo elisa measurements of molecular biomarker concentrations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302994/ https://www.ncbi.nlm.nih.gov/pubmed/34307836 http://dx.doi.org/10.18416/ijmpi.2017.1706003 |
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