Functionalizable hydrogel microparticles of tunable size and stiffness for soft-tissue filler applications

Particle size, stiffness and surface functionality are important in determining the injection site, safety and efficacy of injectable soft-tissue fillers. Methods to produce soft injectable biomaterials with controlled particle characteristics are therefore desirable. Here we report a method based o...

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Main Authors: Chan, Ka Man Carmen, Li, Randolph H, Chapman, Joseph W, Trac, Eric M, Kobler, James B, Zeitels, Steven M, Langer, Robert, Karajanagi, Sandeep S
Other Authors: Massachusetts Institute of Technology. Department of Chemical Engineering
Format: Article
Language:English
Published: Elsevier BV 2021
Online Access:https://hdl.handle.net/1721.1/134463
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author Chan, Ka Man Carmen
Li, Randolph H
Chapman, Joseph W
Trac, Eric M
Kobler, James B
Zeitels, Steven M
Langer, Robert
Karajanagi, Sandeep S
author2 Massachusetts Institute of Technology. Department of Chemical Engineering
author_facet Massachusetts Institute of Technology. Department of Chemical Engineering
Chan, Ka Man Carmen
Li, Randolph H
Chapman, Joseph W
Trac, Eric M
Kobler, James B
Zeitels, Steven M
Langer, Robert
Karajanagi, Sandeep S
author_sort Chan, Ka Man Carmen
collection MIT
description Particle size, stiffness and surface functionality are important in determining the injection site, safety and efficacy of injectable soft-tissue fillers. Methods to produce soft injectable biomaterials with controlled particle characteristics are therefore desirable. Here we report a method based on suspension photopolymerization and semi-interpenetrating network (semi-IPN) to synthesize soft, functionalizable, spherical hydrogel microparticles (MP) of independently tunable size and stiffness. MP were prepared using acrylated forms of polyethylene glycol (PEG), gelatin and hyaluronic acid. Semi-IPN MP of PEG-diacrylate and PEG were used to study the effect of process parameters on particle characteristics. The process parameters were systematically varied to produce MP with size ranging from 115 to 515 μm and stiffness ranging from 190 to 1600 Pa. In vitro studies showed that the MP thus prepared were cytocompatible. The ratio and identity of the polymers used to make the semi-IPN MP were varied to control their stiffness and to introduce amine groups for potential functionalization. Slow-release polymeric particles loaded with Rhodamine or dexamethasone were incorporated in the MP as a proof-of-principle of drug incorporation and release from the MP. This work has implications in preparing injectable biomaterials of natural or synthetic polymers for applications as soft-tissue fillers. © 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
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spelling mit-1721.1/1344632023-09-06T20:11:57Z Functionalizable hydrogel microparticles of tunable size and stiffness for soft-tissue filler applications Chan, Ka Man Carmen Li, Randolph H Chapman, Joseph W Trac, Eric M Kobler, James B Zeitels, Steven M Langer, Robert Karajanagi, Sandeep S Massachusetts Institute of Technology. Department of Chemical Engineering Particle size, stiffness and surface functionality are important in determining the injection site, safety and efficacy of injectable soft-tissue fillers. Methods to produce soft injectable biomaterials with controlled particle characteristics are therefore desirable. Here we report a method based on suspension photopolymerization and semi-interpenetrating network (semi-IPN) to synthesize soft, functionalizable, spherical hydrogel microparticles (MP) of independently tunable size and stiffness. MP were prepared using acrylated forms of polyethylene glycol (PEG), gelatin and hyaluronic acid. Semi-IPN MP of PEG-diacrylate and PEG were used to study the effect of process parameters on particle characteristics. The process parameters were systematically varied to produce MP with size ranging from 115 to 515 μm and stiffness ranging from 190 to 1600 Pa. In vitro studies showed that the MP thus prepared were cytocompatible. The ratio and identity of the polymers used to make the semi-IPN MP were varied to control their stiffness and to introduce amine groups for potential functionalization. Slow-release polymeric particles loaded with Rhodamine or dexamethasone were incorporated in the MP as a proof-of-principle of drug incorporation and release from the MP. This work has implications in preparing injectable biomaterials of natural or synthetic polymers for applications as soft-tissue fillers. © 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved. 2021-10-27T20:05:07Z 2021-10-27T20:05:07Z 2014 2019-09-05T16:21:49Z Article http://purl.org/eprint/type/JournalArticle https://hdl.handle.net/1721.1/134463 Chan, K. M., et al. "Functionalizable Hydrogel Microparticles of Tunable Size and Stiffness for Soft-Tissue Filler Applications." Acta Biomater (2014). en 10.1016/J.ACTBIO.2014.02.021 Acta Biomaterialia Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Elsevier BV PMC
spellingShingle Chan, Ka Man Carmen
Li, Randolph H
Chapman, Joseph W
Trac, Eric M
Kobler, James B
Zeitels, Steven M
Langer, Robert
Karajanagi, Sandeep S
Functionalizable hydrogel microparticles of tunable size and stiffness for soft-tissue filler applications
title Functionalizable hydrogel microparticles of tunable size and stiffness for soft-tissue filler applications
title_full Functionalizable hydrogel microparticles of tunable size and stiffness for soft-tissue filler applications
title_fullStr Functionalizable hydrogel microparticles of tunable size and stiffness for soft-tissue filler applications
title_full_unstemmed Functionalizable hydrogel microparticles of tunable size and stiffness for soft-tissue filler applications
title_short Functionalizable hydrogel microparticles of tunable size and stiffness for soft-tissue filler applications
title_sort functionalizable hydrogel microparticles of tunable size and stiffness for soft tissue filler applications
url https://hdl.handle.net/1721.1/134463
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