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Simultaneous Sizing and Refractive Index Analysis of Heterogeneous Nanoparticle Suspensions

[Image: see text] Rapid and reliable characterization of heterogeneous nanoparticle suspensions is a key technology across the nanosciences. Although approaches exist for homogeneous samples, they are often unsuitable for polydisperse suspensions, as particles of different sizes and compositions can...

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Autores principales: Ortiz-Orruño, Unai, Quidant, Romain, van Hulst, Niek F., Liebel, Matz, Ortega Arroyo, Jaime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835976/
https://www.ncbi.nlm.nih.gov/pubmed/36525614
http://dx.doi.org/10.1021/acsnano.2c06883
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author Ortiz-Orruño, Unai
Quidant, Romain
van Hulst, Niek F.
Liebel, Matz
Ortega Arroyo, Jaime
author_facet Ortiz-Orruño, Unai
Quidant, Romain
van Hulst, Niek F.
Liebel, Matz
Ortega Arroyo, Jaime
author_sort Ortiz-Orruño, Unai
collection PubMed
description [Image: see text] Rapid and reliable characterization of heterogeneous nanoparticle suspensions is a key technology across the nanosciences. Although approaches exist for homogeneous samples, they are often unsuitable for polydisperse suspensions, as particles of different sizes and compositions can lead to indistinguishable signals at the detector. Here, we introduce holographic nanoparticle tracking analysis, holoNTA, as a straightforward methodology that decouples size and material refractive index contributions. HoloNTA is applicable to any heterogeneous nanoparticle sample and has the sensitivity to measure the intrinsic heterogeneity of the sample. Specifically, we combined high dynamic range k-space imaging with holographic 3D single-particle tracking. This strategy enables long-term tracking by extending the imaging volume and delivers precise and accurate estimates of both scattering amplitude and diffusion coefficient of individual nanoparticles, from which particle refractive index and hydrodynamic size are determined. We specifically demonstrate, by simulations and experiments, that irrespective of localization uncertainty and size, the sizing sensitivity is improved as our extended detection volume yields considerably longer particle trajectories than previously reported by comparable technologies. As validation, we measured both homogeneous and heterogeneous suspensions of nanoparticles in the 40–250 nm size range and further monitored protein corona formation, where we identified subtle differences between the nanoparticle–protein complexes derived from avidin, bovine serum albumin, and streptavidin. We foresee that our approach will find many applications of both fundamental and applied nature where routine quantification and sizing of nanoparticles are required.
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spelling pubmed-98359762023-01-13 Simultaneous Sizing and Refractive Index Analysis of Heterogeneous Nanoparticle Suspensions Ortiz-Orruño, Unai Quidant, Romain van Hulst, Niek F. Liebel, Matz Ortega Arroyo, Jaime ACS Nano [Image: see text] Rapid and reliable characterization of heterogeneous nanoparticle suspensions is a key technology across the nanosciences. Although approaches exist for homogeneous samples, they are often unsuitable for polydisperse suspensions, as particles of different sizes and compositions can lead to indistinguishable signals at the detector. Here, we introduce holographic nanoparticle tracking analysis, holoNTA, as a straightforward methodology that decouples size and material refractive index contributions. HoloNTA is applicable to any heterogeneous nanoparticle sample and has the sensitivity to measure the intrinsic heterogeneity of the sample. Specifically, we combined high dynamic range k-space imaging with holographic 3D single-particle tracking. This strategy enables long-term tracking by extending the imaging volume and delivers precise and accurate estimates of both scattering amplitude and diffusion coefficient of individual nanoparticles, from which particle refractive index and hydrodynamic size are determined. We specifically demonstrate, by simulations and experiments, that irrespective of localization uncertainty and size, the sizing sensitivity is improved as our extended detection volume yields considerably longer particle trajectories than previously reported by comparable technologies. As validation, we measured both homogeneous and heterogeneous suspensions of nanoparticles in the 40–250 nm size range and further monitored protein corona formation, where we identified subtle differences between the nanoparticle–protein complexes derived from avidin, bovine serum albumin, and streptavidin. We foresee that our approach will find many applications of both fundamental and applied nature where routine quantification and sizing of nanoparticles are required. American Chemical Society 2022-12-16 /pmc/articles/PMC9835976/ /pubmed/36525614 http://dx.doi.org/10.1021/acsnano.2c06883 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Ortiz-Orruño, Unai
Quidant, Romain
van Hulst, Niek F.
Liebel, Matz
Ortega Arroyo, Jaime
Simultaneous Sizing and Refractive Index Analysis of Heterogeneous Nanoparticle Suspensions
title Simultaneous Sizing and Refractive Index Analysis of Heterogeneous Nanoparticle Suspensions
title_full Simultaneous Sizing and Refractive Index Analysis of Heterogeneous Nanoparticle Suspensions
title_fullStr Simultaneous Sizing and Refractive Index Analysis of Heterogeneous Nanoparticle Suspensions
title_full_unstemmed Simultaneous Sizing and Refractive Index Analysis of Heterogeneous Nanoparticle Suspensions
title_short Simultaneous Sizing and Refractive Index Analysis of Heterogeneous Nanoparticle Suspensions
title_sort simultaneous sizing and refractive index analysis of heterogeneous nanoparticle suspensions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835976/
https://www.ncbi.nlm.nih.gov/pubmed/36525614
http://dx.doi.org/10.1021/acsnano.2c06883
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