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Flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates

Biological and bioinspired polymer microparticles have broad biomedical and industrial applications, including drug delivery, tissue engineering, surface modification, environmental remediation, imaging, and sensing. Full realization of the potential of biopolymer microparticles will require methods...

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Detalles Bibliográficos
Autores principales: Marvin, Laura, Paiva, Wynter, Gill, Nicole, Morales, Marissa A., Halpern, Jeffrey Mark, Vesenka, James, Balog, Eva Rose M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508725/
https://www.ncbi.nlm.nih.gov/pubmed/31071134
http://dx.doi.org/10.1371/journal.pone.0216406
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author Marvin, Laura
Paiva, Wynter
Gill, Nicole
Morales, Marissa A.
Halpern, Jeffrey Mark
Vesenka, James
Balog, Eva Rose M.
author_facet Marvin, Laura
Paiva, Wynter
Gill, Nicole
Morales, Marissa A.
Halpern, Jeffrey Mark
Vesenka, James
Balog, Eva Rose M.
author_sort Marvin, Laura
collection PubMed
description Biological and bioinspired polymer microparticles have broad biomedical and industrial applications, including drug delivery, tissue engineering, surface modification, environmental remediation, imaging, and sensing. Full realization of the potential of biopolymer microparticles will require methods for rigorous characterization of particle sizes, morphologies, and dynamics, so that researchers may correlate particle characteristics with synthesis methods and desired functions. Toward this end, we evaluated biopolymer microparticles using flow imaging microscopy. This technology is widely used in the biopharmaceutical industry but is not yet well-known among the materials community. Our polymer, a genetically engineered elastin-like polypeptide (ELP), self-assembles into micron-scale coacervates. We performed flow imaging of ELP coacervates using two different instruments, one with a lower size limit of approximately 2 microns, the other with a lower size limit of approximately 300 nanometers. We validated flow imaging results by comparison with dynamic light scattering and atomic force microscopy analyses. We explored the effects of various solvent conditions on ELP coacervate size, morphology, and behavior, such as the dispersion of single particles versus aggregates. We found that flow imaging is a superior tool for rapid and thorough particle analysis of ELP coacervates in solution. We anticipate that researchers studying many types of microscale protein or polymer assemblies will be interested in flow imaging as a tool for quantitative, solution-based characterization.
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spelling pubmed-65087252019-05-23 Flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates Marvin, Laura Paiva, Wynter Gill, Nicole Morales, Marissa A. Halpern, Jeffrey Mark Vesenka, James Balog, Eva Rose M. PLoS One Research Article Biological and bioinspired polymer microparticles have broad biomedical and industrial applications, including drug delivery, tissue engineering, surface modification, environmental remediation, imaging, and sensing. Full realization of the potential of biopolymer microparticles will require methods for rigorous characterization of particle sizes, morphologies, and dynamics, so that researchers may correlate particle characteristics with synthesis methods and desired functions. Toward this end, we evaluated biopolymer microparticles using flow imaging microscopy. This technology is widely used in the biopharmaceutical industry but is not yet well-known among the materials community. Our polymer, a genetically engineered elastin-like polypeptide (ELP), self-assembles into micron-scale coacervates. We performed flow imaging of ELP coacervates using two different instruments, one with a lower size limit of approximately 2 microns, the other with a lower size limit of approximately 300 nanometers. We validated flow imaging results by comparison with dynamic light scattering and atomic force microscopy analyses. We explored the effects of various solvent conditions on ELP coacervate size, morphology, and behavior, such as the dispersion of single particles versus aggregates. We found that flow imaging is a superior tool for rapid and thorough particle analysis of ELP coacervates in solution. We anticipate that researchers studying many types of microscale protein or polymer assemblies will be interested in flow imaging as a tool for quantitative, solution-based characterization. Public Library of Science 2019-05-09 /pmc/articles/PMC6508725/ /pubmed/31071134 http://dx.doi.org/10.1371/journal.pone.0216406 Text en © 2019 Marvin et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Marvin, Laura
Paiva, Wynter
Gill, Nicole
Morales, Marissa A.
Halpern, Jeffrey Mark
Vesenka, James
Balog, Eva Rose M.
Flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates
title Flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates
title_full Flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates
title_fullStr Flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates
title_full_unstemmed Flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates
title_short Flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates
title_sort flow imaging microscopy as a novel tool for high-throughput evaluation of elastin-like polymer coacervates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508725/
https://www.ncbi.nlm.nih.gov/pubmed/31071134
http://dx.doi.org/10.1371/journal.pone.0216406
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