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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...

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Detalles Bibliográficos
Autores principales: Chen, Jun, Zhou, Beth, Li, Qi, Ouyang, Jun, Kong, Jiming, Zhong, Wen, Xing, Malcolm MQ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
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.
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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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