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Precise Fabrication of Porous Microspheres by Iso-Density Emulsion Combined with Microfluidics

Polymer porous microspheres with large specific surface areas and good fluidity have promising important applications in the biomedical field. However, controllable fabrication of porous microspheres with precise size, morphology, and pore structure is still a challenge, and phase separation caused...

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Detalles Bibliográficos
Autores principales: Shi, Yuxiao, Zhang, Xin, Mu, Ketao, Wang, Yifan, Jiang, Ting, Jiang, Shangtong, Zhang, Shengmin, Du, Yingying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269203/
https://www.ncbi.nlm.nih.gov/pubmed/35808731
http://dx.doi.org/10.3390/polym14132687
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author Shi, Yuxiao
Zhang, Xin
Mu, Ketao
Wang, Yifan
Jiang, Ting
Jiang, Shangtong
Zhang, Shengmin
Du, Yingying
author_facet Shi, Yuxiao
Zhang, Xin
Mu, Ketao
Wang, Yifan
Jiang, Ting
Jiang, Shangtong
Zhang, Shengmin
Du, Yingying
author_sort Shi, Yuxiao
collection PubMed
description Polymer porous microspheres with large specific surface areas and good fluidity have promising important applications in the biomedical field. However, controllable fabrication of porous microspheres with precise size, morphology, and pore structure is still a challenge, and phase separation caused by the instability of the emulsion is the main factor affecting the precise preparation of porous microspheres. Herein, a method combining the iso-density emulsion (IDE) template and microfluidics was proposed to realize the controllable preparation of polymer porous microspheres. The IDE exhibited excellent stability with minimal phase separation within 4 h, thus showing potential advantages in the large-scale preparation of porous microspheres. With the IDE template combined microfluidics technique and the use of a customized amphoteric copolymer, PEG-b-polycaprolactone, polycaprolactone (PCL) porous microspheres with porosity higher than 90% were successfully prepared. Afterwards, the main factors, including polymer concentration, water–oil ratio and homogenization time were investigated to regulate the pore structure of microspheres, and microspheres with different pore sizes (1–30 μm) were obtained. PCL porous microspheres exhibited comparable cell viability relative to the control group and good potential as cell microcarriers after surface modification with polydopamine. The modified PCL porous microspheres implanted subcutaneously in rats underwent rapid in vivo degradation and tissue ingrowth. Overall, this study demonstrated an efficient strategy for the precise preparation of porous microspheres and investigated the potential of the as-prepared PCL porous microspheres as cell microcarriers and micro-scaffolds.
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spelling pubmed-92692032022-07-09 Precise Fabrication of Porous Microspheres by Iso-Density Emulsion Combined with Microfluidics Shi, Yuxiao Zhang, Xin Mu, Ketao Wang, Yifan Jiang, Ting Jiang, Shangtong Zhang, Shengmin Du, Yingying Polymers (Basel) Article Polymer porous microspheres with large specific surface areas and good fluidity have promising important applications in the biomedical field. However, controllable fabrication of porous microspheres with precise size, morphology, and pore structure is still a challenge, and phase separation caused by the instability of the emulsion is the main factor affecting the precise preparation of porous microspheres. Herein, a method combining the iso-density emulsion (IDE) template and microfluidics was proposed to realize the controllable preparation of polymer porous microspheres. The IDE exhibited excellent stability with minimal phase separation within 4 h, thus showing potential advantages in the large-scale preparation of porous microspheres. With the IDE template combined microfluidics technique and the use of a customized amphoteric copolymer, PEG-b-polycaprolactone, polycaprolactone (PCL) porous microspheres with porosity higher than 90% were successfully prepared. Afterwards, the main factors, including polymer concentration, water–oil ratio and homogenization time were investigated to regulate the pore structure of microspheres, and microspheres with different pore sizes (1–30 μm) were obtained. PCL porous microspheres exhibited comparable cell viability relative to the control group and good potential as cell microcarriers after surface modification with polydopamine. The modified PCL porous microspheres implanted subcutaneously in rats underwent rapid in vivo degradation and tissue ingrowth. Overall, this study demonstrated an efficient strategy for the precise preparation of porous microspheres and investigated the potential of the as-prepared PCL porous microspheres as cell microcarriers and micro-scaffolds. MDPI 2022-06-30 /pmc/articles/PMC9269203/ /pubmed/35808731 http://dx.doi.org/10.3390/polym14132687 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shi, Yuxiao
Zhang, Xin
Mu, Ketao
Wang, Yifan
Jiang, Ting
Jiang, Shangtong
Zhang, Shengmin
Du, Yingying
Precise Fabrication of Porous Microspheres by Iso-Density Emulsion Combined with Microfluidics
title Precise Fabrication of Porous Microspheres by Iso-Density Emulsion Combined with Microfluidics
title_full Precise Fabrication of Porous Microspheres by Iso-Density Emulsion Combined with Microfluidics
title_fullStr Precise Fabrication of Porous Microspheres by Iso-Density Emulsion Combined with Microfluidics
title_full_unstemmed Precise Fabrication of Porous Microspheres by Iso-Density Emulsion Combined with Microfluidics
title_short Precise Fabrication of Porous Microspheres by Iso-Density Emulsion Combined with Microfluidics
title_sort precise fabrication of porous microspheres by iso-density emulsion combined with microfluidics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269203/
https://www.ncbi.nlm.nih.gov/pubmed/35808731
http://dx.doi.org/10.3390/polym14132687
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