Cargando…
Gelatin-based Hydrogel Degradation and Tissue Interaction in vivo: Insights from Multimodal Preclinical Imaging in Immunocompetent Nude Mice
Hydrogels based on gelatin have evolved as promising multifunctional biomaterials. Gelatin is crosslinked with lysine diisocyanate ethyl ester (LDI) and the molar ratio of gelatin and LDI in the starting material mixture determines elastic properties of the resulting hydrogel. In order to investigat...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039684/ https://www.ncbi.nlm.nih.gov/pubmed/27698944 http://dx.doi.org/10.7150/thno.16614 |
_version_ | 1782456111107932160 |
---|---|
author | Tondera, Christoph Hauser, Sandra Krüger-Genge, Anne Jung, Friedrich Neffe, Axel T. Lendlein, Andreas Klopfleisch, Robert Steinbach, Jörg Neuber, Christin Pietzsch, Jens |
author_facet | Tondera, Christoph Hauser, Sandra Krüger-Genge, Anne Jung, Friedrich Neffe, Axel T. Lendlein, Andreas Klopfleisch, Robert Steinbach, Jörg Neuber, Christin Pietzsch, Jens |
author_sort | Tondera, Christoph |
collection | PubMed |
description | Hydrogels based on gelatin have evolved as promising multifunctional biomaterials. Gelatin is crosslinked with lysine diisocyanate ethyl ester (LDI) and the molar ratio of gelatin and LDI in the starting material mixture determines elastic properties of the resulting hydrogel. In order to investigate the clinical potential of these biopolymers, hydrogels with different ratios of gelatin and diisocyanate (3-fold (G10_LNCO3) and 8-fold (G10_LNCO8) molar excess of isocyanate groups) were subcutaneously implanted in mice (uni- or bilateral implantation). Degradation and biomaterial-tissue-interaction were investigated in vivo (MRI, optical imaging, PET) and ex vivo (autoradiography, histology, serum analysis). Multimodal imaging revealed that the number of covalent net points correlates well with degradation time, which allows for targeted modification of hydrogels based on properties of the tissue to be replaced. Importantly, the degradation time was also dependent on the number of implants per animal. Despite local mechanisms of tissue remodeling no adverse tissue responses could be observed neither locally nor systemically. Finally, this preclinical investigation in immunocompetent mice clearly demonstrated a complete restoration of the original healthy tissue. |
format | Online Article Text |
id | pubmed-5039684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-50396842016-10-03 Gelatin-based Hydrogel Degradation and Tissue Interaction in vivo: Insights from Multimodal Preclinical Imaging in Immunocompetent Nude Mice Tondera, Christoph Hauser, Sandra Krüger-Genge, Anne Jung, Friedrich Neffe, Axel T. Lendlein, Andreas Klopfleisch, Robert Steinbach, Jörg Neuber, Christin Pietzsch, Jens Theranostics Research Paper Hydrogels based on gelatin have evolved as promising multifunctional biomaterials. Gelatin is crosslinked with lysine diisocyanate ethyl ester (LDI) and the molar ratio of gelatin and LDI in the starting material mixture determines elastic properties of the resulting hydrogel. In order to investigate the clinical potential of these biopolymers, hydrogels with different ratios of gelatin and diisocyanate (3-fold (G10_LNCO3) and 8-fold (G10_LNCO8) molar excess of isocyanate groups) were subcutaneously implanted in mice (uni- or bilateral implantation). Degradation and biomaterial-tissue-interaction were investigated in vivo (MRI, optical imaging, PET) and ex vivo (autoradiography, histology, serum analysis). Multimodal imaging revealed that the number of covalent net points correlates well with degradation time, which allows for targeted modification of hydrogels based on properties of the tissue to be replaced. Importantly, the degradation time was also dependent on the number of implants per animal. Despite local mechanisms of tissue remodeling no adverse tissue responses could be observed neither locally nor systemically. Finally, this preclinical investigation in immunocompetent mice clearly demonstrated a complete restoration of the original healthy tissue. Ivyspring International Publisher 2016-09-12 /pmc/articles/PMC5039684/ /pubmed/27698944 http://dx.doi.org/10.7150/thno.16614 Text en © Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions. |
spellingShingle | Research Paper Tondera, Christoph Hauser, Sandra Krüger-Genge, Anne Jung, Friedrich Neffe, Axel T. Lendlein, Andreas Klopfleisch, Robert Steinbach, Jörg Neuber, Christin Pietzsch, Jens Gelatin-based Hydrogel Degradation and Tissue Interaction in vivo: Insights from Multimodal Preclinical Imaging in Immunocompetent Nude Mice |
title | Gelatin-based Hydrogel Degradation and Tissue Interaction in vivo: Insights from Multimodal Preclinical Imaging in Immunocompetent Nude Mice |
title_full | Gelatin-based Hydrogel Degradation and Tissue Interaction in vivo: Insights from Multimodal Preclinical Imaging in Immunocompetent Nude Mice |
title_fullStr | Gelatin-based Hydrogel Degradation and Tissue Interaction in vivo: Insights from Multimodal Preclinical Imaging in Immunocompetent Nude Mice |
title_full_unstemmed | Gelatin-based Hydrogel Degradation and Tissue Interaction in vivo: Insights from Multimodal Preclinical Imaging in Immunocompetent Nude Mice |
title_short | Gelatin-based Hydrogel Degradation and Tissue Interaction in vivo: Insights from Multimodal Preclinical Imaging in Immunocompetent Nude Mice |
title_sort | gelatin-based hydrogel degradation and tissue interaction in vivo: insights from multimodal preclinical imaging in immunocompetent nude mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039684/ https://www.ncbi.nlm.nih.gov/pubmed/27698944 http://dx.doi.org/10.7150/thno.16614 |
work_keys_str_mv | AT tonderachristoph gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT hausersandra gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT krugergengeanne gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT jungfriedrich gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT neffeaxelt gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT lendleinandreas gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT klopfleischrobert gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT steinbachjorg gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT neuberchristin gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice AT pietzschjens gelatinbasedhydrogeldegradationandtissueinteractioninvivoinsightsfrommultimodalpreclinicalimaginginimmunocompetentnudemice |