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Light-Scattering Detection below the Level of Single Fluorescent Molecules for High-Resolution Characterization of Functional Nanoparticles

[Image: see text] Ultrasensitive detection and characterization of single nanoparticles (<100 nm) is important in nanotechnology and life sciences. Direct measurement of the elastically scattered light from individual nanoparticles represents the simplest and the most direct method for particle d...

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Autores principales: Zhu, Shaobin, Ma, Ling, Wang, Shuo, Chen, Chaoxiang, Zhang, Wenqiang, Yang, Lingling, Hang, Wei, Nolan, John P., Wu, Lina, Yan, Xiaomei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212780/
https://www.ncbi.nlm.nih.gov/pubmed/25300001
http://dx.doi.org/10.1021/nn505162u
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author Zhu, Shaobin
Ma, Ling
Wang, Shuo
Chen, Chaoxiang
Zhang, Wenqiang
Yang, Lingling
Hang, Wei
Nolan, John P.
Wu, Lina
Yan, Xiaomei
author_facet Zhu, Shaobin
Ma, Ling
Wang, Shuo
Chen, Chaoxiang
Zhang, Wenqiang
Yang, Lingling
Hang, Wei
Nolan, John P.
Wu, Lina
Yan, Xiaomei
author_sort Zhu, Shaobin
collection PubMed
description [Image: see text] Ultrasensitive detection and characterization of single nanoparticles (<100 nm) is important in nanotechnology and life sciences. Direct measurement of the elastically scattered light from individual nanoparticles represents the simplest and the most direct method for particle detection. However, the sixth-power dependence of scattering intensity on particle size renders very small particles indistinguishable from the background. Adopting strategies for single-molecule fluorescence detection in a sheathed flow, here we report the development of high sensitivity flow cytometry (HSFCM) that achieves real-time light-scattering detection of single silica and gold nanoparticles as small as 24 and 7 nm in diameter, respectively. This unprecedented sensitivity enables high-resolution sizing of single nanoparticles directly based on their scattered intensity. With a resolution comparable to that of TEM and the ease and speed of flow cytometric analysis, HSFCM is particularly suitable for nanoparticle size distribution analysis of polydisperse/heterogeneous/mixed samples. Through concurrent fluorescence detection, simultaneous insights into the size and payload variations of engineered nanoparticles are demonstrated with two forms of clinical nanomedicine. By offering quantitative multiparameter analysis of single nanoparticles in liquid suspensions at a throughput of up to 10 000 particles per minute, HSFCM represents a major advance both in light-scattering detection technology and in nanoparticle characterization.
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spelling pubmed-42127802015-10-09 Light-Scattering Detection below the Level of Single Fluorescent Molecules for High-Resolution Characterization of Functional Nanoparticles Zhu, Shaobin Ma, Ling Wang, Shuo Chen, Chaoxiang Zhang, Wenqiang Yang, Lingling Hang, Wei Nolan, John P. Wu, Lina Yan, Xiaomei ACS Nano [Image: see text] Ultrasensitive detection and characterization of single nanoparticles (<100 nm) is important in nanotechnology and life sciences. Direct measurement of the elastically scattered light from individual nanoparticles represents the simplest and the most direct method for particle detection. However, the sixth-power dependence of scattering intensity on particle size renders very small particles indistinguishable from the background. Adopting strategies for single-molecule fluorescence detection in a sheathed flow, here we report the development of high sensitivity flow cytometry (HSFCM) that achieves real-time light-scattering detection of single silica and gold nanoparticles as small as 24 and 7 nm in diameter, respectively. This unprecedented sensitivity enables high-resolution sizing of single nanoparticles directly based on their scattered intensity. With a resolution comparable to that of TEM and the ease and speed of flow cytometric analysis, HSFCM is particularly suitable for nanoparticle size distribution analysis of polydisperse/heterogeneous/mixed samples. Through concurrent fluorescence detection, simultaneous insights into the size and payload variations of engineered nanoparticles are demonstrated with two forms of clinical nanomedicine. By offering quantitative multiparameter analysis of single nanoparticles in liquid suspensions at a throughput of up to 10 000 particles per minute, HSFCM represents a major advance both in light-scattering detection technology and in nanoparticle characterization. American Chemical Society 2014-10-09 2014-10-28 /pmc/articles/PMC4212780/ /pubmed/25300001 http://dx.doi.org/10.1021/nn505162u Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Zhu, Shaobin
Ma, Ling
Wang, Shuo
Chen, Chaoxiang
Zhang, Wenqiang
Yang, Lingling
Hang, Wei
Nolan, John P.
Wu, Lina
Yan, Xiaomei
Light-Scattering Detection below the Level of Single Fluorescent Molecules for High-Resolution Characterization of Functional Nanoparticles
title Light-Scattering Detection below the Level of Single Fluorescent Molecules for High-Resolution Characterization of Functional Nanoparticles
title_full Light-Scattering Detection below the Level of Single Fluorescent Molecules for High-Resolution Characterization of Functional Nanoparticles
title_fullStr Light-Scattering Detection below the Level of Single Fluorescent Molecules for High-Resolution Characterization of Functional Nanoparticles
title_full_unstemmed Light-Scattering Detection below the Level of Single Fluorescent Molecules for High-Resolution Characterization of Functional Nanoparticles
title_short Light-Scattering Detection below the Level of Single Fluorescent Molecules for High-Resolution Characterization of Functional Nanoparticles
title_sort light-scattering detection below the level of single fluorescent molecules for high-resolution characterization of functional nanoparticles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212780/
https://www.ncbi.nlm.nih.gov/pubmed/25300001
http://dx.doi.org/10.1021/nn505162u
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