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78511 Synthesis of Novel Core/Shell Polymeric Nanoparticles for Controlled Drug Release

1. Gel-Suspended SEM: nanoparticles suspended in gel matrix, bisected to reveal inner structure. 2. Fluorescent Conjugation Microscopy: visually-distinct dyes used to show polymer distribution and validated against the theoretical model predictions. 3. Modified Hydrophobic Dye Release: different mix...

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Detalles Bibliográficos
Autor principal: Hahn, Braden
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827894/
http://dx.doi.org/10.1017/cts.2021.657
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author Hahn, Braden
author_facet Hahn, Braden
author_sort Hahn, Braden
collection PubMed
description 1. Gel-Suspended SEM: nanoparticles suspended in gel matrix, bisected to reveal inner structure. 2. Fluorescent Conjugation Microscopy: visually-distinct dyes used to show polymer distribution and validated against the theoretical model predictions. 3. Modified Hydrophobic Dye Release: different mixtures of polymers with release showing if previous promising results due to core/shell structure RESULTS/ANTICIPATED RESULTS: As stated, the experiments will confirm the core/shell nanoparticle structure, validate the developed theoretical model, or provide direct evidence against any formation. This core/shell structure is key to the current design for controlling payload release rate and thus in vivo drug concentration. For the gel-suspension experiment, the interior core will be labeled with ultrasmall SPIONs and thus any layers within the particles will be distinct. While this result is qualitative, high magnification fluorescent microscope images will be analyzed using image processing software to determine core/shell formation efficiency and compared to estimated efficiencies from the model. Finally, the mixed release will clarify previous experiments’ release mechanism and either support or disprove shell influence. DISCUSSION/SIGNIFICANCE OF FINDINGS: The significance of this work is twofold: core/shell particles have been proven to provide variable control of release on the micron scale but not yet at the nanoscale, allowing for a circulating, targeted system that can finely control release. The process is also novel for producing this type of structure, at highly consistent quality and size.
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spelling pubmed-88278942022-03-04 78511 Synthesis of Novel Core/Shell Polymeric Nanoparticles for Controlled Drug Release Hahn, Braden J Clin Transl Sci Precision Medicine 1. Gel-Suspended SEM: nanoparticles suspended in gel matrix, bisected to reveal inner structure. 2. Fluorescent Conjugation Microscopy: visually-distinct dyes used to show polymer distribution and validated against the theoretical model predictions. 3. Modified Hydrophobic Dye Release: different mixtures of polymers with release showing if previous promising results due to core/shell structure RESULTS/ANTICIPATED RESULTS: As stated, the experiments will confirm the core/shell nanoparticle structure, validate the developed theoretical model, or provide direct evidence against any formation. This core/shell structure is key to the current design for controlling payload release rate and thus in vivo drug concentration. For the gel-suspension experiment, the interior core will be labeled with ultrasmall SPIONs and thus any layers within the particles will be distinct. While this result is qualitative, high magnification fluorescent microscope images will be analyzed using image processing software to determine core/shell formation efficiency and compared to estimated efficiencies from the model. Finally, the mixed release will clarify previous experiments’ release mechanism and either support or disprove shell influence. DISCUSSION/SIGNIFICANCE OF FINDINGS: The significance of this work is twofold: core/shell particles have been proven to provide variable control of release on the micron scale but not yet at the nanoscale, allowing for a circulating, targeted system that can finely control release. The process is also novel for producing this type of structure, at highly consistent quality and size. Cambridge University Press 2021-03-30 /pmc/articles/PMC8827894/ http://dx.doi.org/10.1017/cts.2021.657 Text en © The Association for Clinical and Translational Science 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Precision Medicine
Hahn, Braden
78511 Synthesis of Novel Core/Shell Polymeric Nanoparticles for Controlled Drug Release
title 78511 Synthesis of Novel Core/Shell Polymeric Nanoparticles for Controlled Drug Release
title_full 78511 Synthesis of Novel Core/Shell Polymeric Nanoparticles for Controlled Drug Release
title_fullStr 78511 Synthesis of Novel Core/Shell Polymeric Nanoparticles for Controlled Drug Release
title_full_unstemmed 78511 Synthesis of Novel Core/Shell Polymeric Nanoparticles for Controlled Drug Release
title_short 78511 Synthesis of Novel Core/Shell Polymeric Nanoparticles for Controlled Drug Release
title_sort 78511 synthesis of novel core/shell polymeric nanoparticles for controlled drug release
topic Precision Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827894/
http://dx.doi.org/10.1017/cts.2021.657
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