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Bioinspired Heparin Nanosponge Prepared by Photo-crosslinking for Controlled Release of Growth Factors

Growth factors have great therapeutic potential for various disease therapy and tissue engineering applications. However, their clinical efficacy is hampered by low bioavailability, rapid degradation in vivo and non-specific biodistribution. Nanoparticle based delivery systems are being evaluated to...

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Autores principales: Choi, Won Il, Sahu, Abhishek, Vilos, Cristian, Kamaly, Nazila, Jo, Seong-Min, Lee, Jin Hyung, Tae, Giyoong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662564/
https://www.ncbi.nlm.nih.gov/pubmed/29084990
http://dx.doi.org/10.1038/s41598-017-14040-5
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author Choi, Won Il
Sahu, Abhishek
Vilos, Cristian
Kamaly, Nazila
Jo, Seong-Min
Lee, Jin Hyung
Tae, Giyoong
author_facet Choi, Won Il
Sahu, Abhishek
Vilos, Cristian
Kamaly, Nazila
Jo, Seong-Min
Lee, Jin Hyung
Tae, Giyoong
author_sort Choi, Won Il
collection PubMed
description Growth factors have great therapeutic potential for various disease therapy and tissue engineering applications. However, their clinical efficacy is hampered by low bioavailability, rapid degradation in vivo and non-specific biodistribution. Nanoparticle based delivery systems are being evaluated to overcome these limitations. Herein, we have developed a thermosensitive heparin nanosponge (Hep-NS) by a one step photopolymerization reaction between diacrylated pluronic and thiolated heparin molecules. The amount of heparin in Hep-NS was precisely controlled by varying the heparin amount in the reaction feed. Hep-NS with varying amounts of heparin showed similar size and shape properties, though surface charge decreased with an increase in the amount of heparin conjugation. The anticoagulant activity of the Hep-NS decreased by 65% compared to free heparin, however the Hep-NS retained their growth factor binding ability. Four different growth factors, bFGF, VEGF, BMP-2, and HGF were successfully encapsulated into Hep-NS. In vitro studies showed sustained release of all the growth factors for almost 60 days and the rate of release was directly dependent on the amount of heparin in Hep-NS. The released growth factors retained their bioactivity as assessed by a cell proliferation assay. This heparin nanosponge is therefore a promising nanocarrier for the loading and controlled release of growth factors.
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spelling pubmed-56625642017-11-08 Bioinspired Heparin Nanosponge Prepared by Photo-crosslinking for Controlled Release of Growth Factors Choi, Won Il Sahu, Abhishek Vilos, Cristian Kamaly, Nazila Jo, Seong-Min Lee, Jin Hyung Tae, Giyoong Sci Rep Article Growth factors have great therapeutic potential for various disease therapy and tissue engineering applications. However, their clinical efficacy is hampered by low bioavailability, rapid degradation in vivo and non-specific biodistribution. Nanoparticle based delivery systems are being evaluated to overcome these limitations. Herein, we have developed a thermosensitive heparin nanosponge (Hep-NS) by a one step photopolymerization reaction between diacrylated pluronic and thiolated heparin molecules. The amount of heparin in Hep-NS was precisely controlled by varying the heparin amount in the reaction feed. Hep-NS with varying amounts of heparin showed similar size and shape properties, though surface charge decreased with an increase in the amount of heparin conjugation. The anticoagulant activity of the Hep-NS decreased by 65% compared to free heparin, however the Hep-NS retained their growth factor binding ability. Four different growth factors, bFGF, VEGF, BMP-2, and HGF were successfully encapsulated into Hep-NS. In vitro studies showed sustained release of all the growth factors for almost 60 days and the rate of release was directly dependent on the amount of heparin in Hep-NS. The released growth factors retained their bioactivity as assessed by a cell proliferation assay. This heparin nanosponge is therefore a promising nanocarrier for the loading and controlled release of growth factors. Nature Publishing Group UK 2017-10-30 /pmc/articles/PMC5662564/ /pubmed/29084990 http://dx.doi.org/10.1038/s41598-017-14040-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Choi, Won Il
Sahu, Abhishek
Vilos, Cristian
Kamaly, Nazila
Jo, Seong-Min
Lee, Jin Hyung
Tae, Giyoong
Bioinspired Heparin Nanosponge Prepared by Photo-crosslinking for Controlled Release of Growth Factors
title Bioinspired Heparin Nanosponge Prepared by Photo-crosslinking for Controlled Release of Growth Factors
title_full Bioinspired Heparin Nanosponge Prepared by Photo-crosslinking for Controlled Release of Growth Factors
title_fullStr Bioinspired Heparin Nanosponge Prepared by Photo-crosslinking for Controlled Release of Growth Factors
title_full_unstemmed Bioinspired Heparin Nanosponge Prepared by Photo-crosslinking for Controlled Release of Growth Factors
title_short Bioinspired Heparin Nanosponge Prepared by Photo-crosslinking for Controlled Release of Growth Factors
title_sort bioinspired heparin nanosponge prepared by photo-crosslinking for controlled release of growth factors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662564/
https://www.ncbi.nlm.nih.gov/pubmed/29084990
http://dx.doi.org/10.1038/s41598-017-14040-5
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