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Electrospun Polyhydroxybutyrate/Poly(ε-caprolactone)/Sol–Gel-Derived Silica Hybrid Scaffolds with Drug Releasing Function for Bone Tissue Engineering Applications
[Image: see text] Electrospun hybrid scaffolds are an effective platform to deliver drugs site specifically for the prevention and treatment of diseases in addition to promote tissue regeneration because of the flexibility to load drugs therein. In the present study, electrospun hybrid scaffolds con...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108537/ https://www.ncbi.nlm.nih.gov/pubmed/29624366 http://dx.doi.org/10.1021/acsami.8b02656 |
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author | Ding, Yaping Li, Wei Correia, Alexandra Yang, Yuyun Zheng, Kai Liu, Dongfei Schubert, Dirk W. Boccaccini, Aldo R. Santos, Hélder A. Roether, Judith A. |
author_facet | Ding, Yaping Li, Wei Correia, Alexandra Yang, Yuyun Zheng, Kai Liu, Dongfei Schubert, Dirk W. Boccaccini, Aldo R. Santos, Hélder A. Roether, Judith A. |
author_sort | Ding, Yaping |
collection | PubMed |
description | [Image: see text] Electrospun hybrid scaffolds are an effective platform to deliver drugs site specifically for the prevention and treatment of diseases in addition to promote tissue regeneration because of the flexibility to load drugs therein. In the present study, electrospun hybrid scaffolds containing antibiotics were developed to support cellular activities and eliminate potential postoperative inflammation and infection. As a model drug, levofloxacin (LFX) was successfully incorporated into pure polyhydroxybutyrate/poly(ε-caprolactone) (PHB/PCL) scaffolds and PHB/PCL/sol–gel-derived silica (SGS) scaffolds. The influence of LFX on the morphology, mechanical performance, chemical structure, drug release profile, and antibacterial effect of the scaffolds was thoroughly and comparatively investigated. MG-63 osteoblast-like cell cultivation on both scaffolds certified that LFX inclusion did not impair the biocompatibility. In addition to the favorable cellular proliferation and differentiation, scaffolds containing both LFX and SGS displayed highly increased mineralization content. Therefore, the present multifunctional hybrid scaffolds are promising in tissue engineering applications. |
format | Online Article Text |
id | pubmed-6108537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-61085372018-08-27 Electrospun Polyhydroxybutyrate/Poly(ε-caprolactone)/Sol–Gel-Derived Silica Hybrid Scaffolds with Drug Releasing Function for Bone Tissue Engineering Applications Ding, Yaping Li, Wei Correia, Alexandra Yang, Yuyun Zheng, Kai Liu, Dongfei Schubert, Dirk W. Boccaccini, Aldo R. Santos, Hélder A. Roether, Judith A. ACS Appl Mater Interfaces [Image: see text] Electrospun hybrid scaffolds are an effective platform to deliver drugs site specifically for the prevention and treatment of diseases in addition to promote tissue regeneration because of the flexibility to load drugs therein. In the present study, electrospun hybrid scaffolds containing antibiotics were developed to support cellular activities and eliminate potential postoperative inflammation and infection. As a model drug, levofloxacin (LFX) was successfully incorporated into pure polyhydroxybutyrate/poly(ε-caprolactone) (PHB/PCL) scaffolds and PHB/PCL/sol–gel-derived silica (SGS) scaffolds. The influence of LFX on the morphology, mechanical performance, chemical structure, drug release profile, and antibacterial effect of the scaffolds was thoroughly and comparatively investigated. MG-63 osteoblast-like cell cultivation on both scaffolds certified that LFX inclusion did not impair the biocompatibility. In addition to the favorable cellular proliferation and differentiation, scaffolds containing both LFX and SGS displayed highly increased mineralization content. Therefore, the present multifunctional hybrid scaffolds are promising in tissue engineering applications. American Chemical Society 2018-04-06 2018-05-02 /pmc/articles/PMC6108537/ /pubmed/29624366 http://dx.doi.org/10.1021/acsami.8b02656 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Ding, Yaping Li, Wei Correia, Alexandra Yang, Yuyun Zheng, Kai Liu, Dongfei Schubert, Dirk W. Boccaccini, Aldo R. Santos, Hélder A. Roether, Judith A. Electrospun Polyhydroxybutyrate/Poly(ε-caprolactone)/Sol–Gel-Derived Silica Hybrid Scaffolds with Drug Releasing Function for Bone Tissue Engineering Applications |
title | Electrospun
Polyhydroxybutyrate/Poly(ε-caprolactone)/Sol–Gel-Derived
Silica Hybrid Scaffolds with Drug Releasing Function for Bone Tissue
Engineering Applications |
title_full | Electrospun
Polyhydroxybutyrate/Poly(ε-caprolactone)/Sol–Gel-Derived
Silica Hybrid Scaffolds with Drug Releasing Function for Bone Tissue
Engineering Applications |
title_fullStr | Electrospun
Polyhydroxybutyrate/Poly(ε-caprolactone)/Sol–Gel-Derived
Silica Hybrid Scaffolds with Drug Releasing Function for Bone Tissue
Engineering Applications |
title_full_unstemmed | Electrospun
Polyhydroxybutyrate/Poly(ε-caprolactone)/Sol–Gel-Derived
Silica Hybrid Scaffolds with Drug Releasing Function for Bone Tissue
Engineering Applications |
title_short | Electrospun
Polyhydroxybutyrate/Poly(ε-caprolactone)/Sol–Gel-Derived
Silica Hybrid Scaffolds with Drug Releasing Function for Bone Tissue
Engineering Applications |
title_sort | electrospun
polyhydroxybutyrate/poly(ε-caprolactone)/sol–gel-derived
silica hybrid scaffolds with drug releasing function for bone tissue
engineering applications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108537/ https://www.ncbi.nlm.nih.gov/pubmed/29624366 http://dx.doi.org/10.1021/acsami.8b02656 |
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