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PLLA-PEG-TCH-labeled bioactive molecule nanofibers for tissue engineering
By mimicking the native extracellular matrix, electrospun nanofibrous scaffolds (ENSs) can provide both chemical and physical cues to modulate cell adherence and differentiation and to promote tissue regeneration while retaining bioresorbable and biocompatible properties. In this study, ENSs were de...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205146/ https://www.ncbi.nlm.nih.gov/pubmed/22072887 http://dx.doi.org/10.2147/IJN.S23688 |
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author | Chen, Jun Zhou, Beth Li, Qi Ouyang, Jun Kong, Jiming Zhong, Wen Xing, Malcolm MQ |
author_facet | Chen, Jun Zhou, Beth Li, Qi Ouyang, Jun Kong, Jiming Zhong, Wen Xing, Malcolm MQ |
author_sort | Chen, Jun |
collection | PubMed |
description | By mimicking the native extracellular matrix, electrospun nanofibrous scaffolds (ENSs) can provide both chemical and physical cues to modulate cell adherence and differentiation and to promote tissue regeneration while retaining bioresorbable and biocompatible properties. In this study, ENSs were developed to deliver multiple biomolecules by loading them into the core-sheath structure and/or by conjugating them to the nanofiber surfaces. In this work, poly(L-lactide)-poly(ethylene glycol)-NH(2) and poly(L-lactide) were emulsion electrospun into nanofibers with a core-sheath structure. A model drug, tetracycline hydrochloride, was loaded within the nanofibers. Amino and carboxyl reactive groups were then activated on the fiber surfaces using saturated water vapor exposure and base hydrolysis, respectively. These reactive groups allowed the surface of the ENS to be functionalized with two other bioactive molecules, fluorescein isothiocyanate- and rhodamine-labeled bovine serum albumins, which were used as model proteins. The ENSs were shown to retain their antimicrobial capacity after two functionalization reactions, indicating that multifunctional nanofibers can potentially be developed into functional wound dressings or periodontal membranes or used in more complicated tissue systems where multiple growth factors and anti-infection precautions are critical for the successful implantation and regeneration of tissues. |
format | Online Article Text |
id | pubmed-3205146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32051462011-11-09 PLLA-PEG-TCH-labeled bioactive molecule nanofibers for tissue engineering Chen, Jun Zhou, Beth Li, Qi Ouyang, Jun Kong, Jiming Zhong, Wen Xing, Malcolm MQ Int J Nanomedicine Original Research By mimicking the native extracellular matrix, electrospun nanofibrous scaffolds (ENSs) can provide both chemical and physical cues to modulate cell adherence and differentiation and to promote tissue regeneration while retaining bioresorbable and biocompatible properties. In this study, ENSs were developed to deliver multiple biomolecules by loading them into the core-sheath structure and/or by conjugating them to the nanofiber surfaces. In this work, poly(L-lactide)-poly(ethylene glycol)-NH(2) and poly(L-lactide) were emulsion electrospun into nanofibers with a core-sheath structure. A model drug, tetracycline hydrochloride, was loaded within the nanofibers. Amino and carboxyl reactive groups were then activated on the fiber surfaces using saturated water vapor exposure and base hydrolysis, respectively. These reactive groups allowed the surface of the ENS to be functionalized with two other bioactive molecules, fluorescein isothiocyanate- and rhodamine-labeled bovine serum albumins, which were used as model proteins. The ENSs were shown to retain their antimicrobial capacity after two functionalization reactions, indicating that multifunctional nanofibers can potentially be developed into functional wound dressings or periodontal membranes or used in more complicated tissue systems where multiple growth factors and anti-infection precautions are critical for the successful implantation and regeneration of tissues. Dove Medical Press 2011 2011-10-21 /pmc/articles/PMC3205146/ /pubmed/22072887 http://dx.doi.org/10.2147/IJN.S23688 Text en © 2011 Chen et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Chen, Jun Zhou, Beth Li, Qi Ouyang, Jun Kong, Jiming Zhong, Wen Xing, Malcolm MQ PLLA-PEG-TCH-labeled bioactive molecule nanofibers for tissue engineering |
title | PLLA-PEG-TCH-labeled bioactive molecule nanofibers for tissue engineering |
title_full | PLLA-PEG-TCH-labeled bioactive molecule nanofibers for tissue engineering |
title_fullStr | PLLA-PEG-TCH-labeled bioactive molecule nanofibers for tissue engineering |
title_full_unstemmed | PLLA-PEG-TCH-labeled bioactive molecule nanofibers for tissue engineering |
title_short | PLLA-PEG-TCH-labeled bioactive molecule nanofibers for tissue engineering |
title_sort | plla-peg-tch-labeled bioactive molecule nanofibers for tissue engineering |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205146/ https://www.ncbi.nlm.nih.gov/pubmed/22072887 http://dx.doi.org/10.2147/IJN.S23688 |
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