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Single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles
The behavior of nanoparticles in biological systems is determined by their dimensions, size distribution, shape, surface chemistry, density, drug loading and stability; the characterization of these parameters in realistic conditions and the possibility to follow their evolution in vitro and in vivo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678328/ https://www.ncbi.nlm.nih.gov/pubmed/26667064 http://dx.doi.org/10.1038/srep18228 |
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author | Potenza, M. A. C. Sanvito, T. Argentiere, S. Cella, C. Paroli, B. Lenardi, C. Milani, P. |
author_facet | Potenza, M. A. C. Sanvito, T. Argentiere, S. Cella, C. Paroli, B. Lenardi, C. Milani, P. |
author_sort | Potenza, M. A. C. |
collection | PubMed |
description | The behavior of nanoparticles in biological systems is determined by their dimensions, size distribution, shape, surface chemistry, density, drug loading and stability; the characterization of these parameters in realistic conditions and the possibility to follow their evolution in vitro and in vivo are, in most of the cases, far from the capabilities of the standard characterization technologies. Optical techniques such as dynamic light scattering (DLS) are, in principle, well suited for in line characterization of nanoparticle, however their fail in characterizing the evolution of nanoparticle in solution where change in particle dimension and density is present. Here we present an in-line optical technique based on single particle extinction and scattering (SPES) overcoming the limitations typical of DLS and allowing for the efficient characterization of nanoparticle polydispersity, index of refraction and degradation dynamics in solution. Using SPES, we characterized the evolution of PLGA nanoparticles with different structures and drug payloads in solution and we compared the results with DLS. Our results suggest that SPES could be used as a process analytical technology for pharmaceutical nanoparticle production. |
format | Online Article Text |
id | pubmed-4678328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46783282015-12-17 Single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles Potenza, M. A. C. Sanvito, T. Argentiere, S. Cella, C. Paroli, B. Lenardi, C. Milani, P. Sci Rep Article The behavior of nanoparticles in biological systems is determined by their dimensions, size distribution, shape, surface chemistry, density, drug loading and stability; the characterization of these parameters in realistic conditions and the possibility to follow their evolution in vitro and in vivo are, in most of the cases, far from the capabilities of the standard characterization technologies. Optical techniques such as dynamic light scattering (DLS) are, in principle, well suited for in line characterization of nanoparticle, however their fail in characterizing the evolution of nanoparticle in solution where change in particle dimension and density is present. Here we present an in-line optical technique based on single particle extinction and scattering (SPES) overcoming the limitations typical of DLS and allowing for the efficient characterization of nanoparticle polydispersity, index of refraction and degradation dynamics in solution. Using SPES, we characterized the evolution of PLGA nanoparticles with different structures and drug payloads in solution and we compared the results with DLS. Our results suggest that SPES could be used as a process analytical technology for pharmaceutical nanoparticle production. Nature Publishing Group 2015-12-15 /pmc/articles/PMC4678328/ /pubmed/26667064 http://dx.doi.org/10.1038/srep18228 Text en Copyright © 2015, Macmillan Publishers Limited 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 Potenza, M. A. C. Sanvito, T. Argentiere, S. Cella, C. Paroli, B. Lenardi, C. Milani, P. Single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles |
title | Single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles |
title_full | Single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles |
title_fullStr | Single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles |
title_full_unstemmed | Single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles |
title_short | Single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles |
title_sort | single particle optical extinction and scattering allows real time quantitative characterization of drug payload and degradation of polymeric nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678328/ https://www.ncbi.nlm.nih.gov/pubmed/26667064 http://dx.doi.org/10.1038/srep18228 |
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