Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10
Main Author: | |
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Publication Date: | 2011 |
Other Authors: | , , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://hdl.handle.net/1822/16783 |
Summary: | Interleukin-10 (IL-10) is an anti-inflammatory cytokine, which active form is a non-covalent homodimer. Given the potential of IL-10 for application in various medical conditions, it is essential to develop systems for its effective delivery. In previous work, it has been shown that a dextrin nanogel effectively incorporated and stabilized rIL10, enabling its release over time. In this work, the delivery system based on dextrin nanogels was further analyzed. The biocompatibility of the nanogel was comprehensively analyzed, through cytotoxicity (lactate dehydrogenase release, MTS, Live and Dead) and genotoxicity (comet) assays. The release profile of rIL-10 and its biological activity were evaluated in vivo, using C57BL/6 mice. Although able to maintain a stable concentration of IL-10 for at least 4 hours in mice serum, the amount of protein released was rather low. Despite this, the amount of rIL-10 released from the complex was biologically active inhibiting TNF-α production, in vivo, by LPSchallenged mice. In spite of the significant stabilization achieved using the nanogel, rIL-10 still denatures rather quickly. An additional effort is thus necessary to develop an effective delivery system for this cytokine, able to release active protein over longer periods of time. Nevertheless, the good biocompatibility, the protein stabilization effect and the ability to perform as a carrier with controlled release suggest that self-assembled dextrin nanogels may be useful protein delivery systems. |
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Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10Protein delivery systemDextrin nanogelBiocompatibilityInterleukin-10Anti-inflammatory agentScience & TechnologyInterleukin-10 (IL-10) is an anti-inflammatory cytokine, which active form is a non-covalent homodimer. Given the potential of IL-10 for application in various medical conditions, it is essential to develop systems for its effective delivery. In previous work, it has been shown that a dextrin nanogel effectively incorporated and stabilized rIL10, enabling its release over time. In this work, the delivery system based on dextrin nanogels was further analyzed. The biocompatibility of the nanogel was comprehensively analyzed, through cytotoxicity (lactate dehydrogenase release, MTS, Live and Dead) and genotoxicity (comet) assays. The release profile of rIL-10 and its biological activity were evaluated in vivo, using C57BL/6 mice. Although able to maintain a stable concentration of IL-10 for at least 4 hours in mice serum, the amount of protein released was rather low. Despite this, the amount of rIL-10 released from the complex was biologically active inhibiting TNF-α production, in vivo, by LPSchallenged mice. In spite of the significant stabilization achieved using the nanogel, rIL-10 still denatures rather quickly. An additional effort is thus necessary to develop an effective delivery system for this cytokine, able to release active protein over longer periods of time. Nevertheless, the good biocompatibility, the protein stabilization effect and the ability to perform as a carrier with controlled release suggest that self-assembled dextrin nanogels may be useful protein delivery systems.Contract grant sponsor: Fundacao para a Ciencia e Tecnologia (FCT), PortugalContract grant number: SFRH/BD/27359/2006Contract grant sponsor: FCTContract grant number: PTDC/BIO/67160/2006; SUDOE-FEDERIMMUNONETSOE1/P1/E014John Wiley and SonsUniversidade do MinhoCarvalho, VeraCastanheira, PedroMadureira, PedroFerreira, Sílvia A.Costa, Carlos M.Faro, CarlosTeixeira, João P.Vilanova, ManuelGama, F. M.20112011-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/16783engCarvalho, V., Castanheira, P., Madureira, P., Ferreira, S. A., Costa, C., Teixeira, J. P., … Gama, M. (2011, March 22). Self‐assembled dextrin nanogel as protein carrier: Controlled release and biological activity of IL‐10. Biotechnology and Bioengineering. Wiley. http://doi.org/10.1002/bit.231250006-35921097-029010.1002/bit.2312521391205https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/bit.23125info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-11-30T01:17:36Zoai:repositorium.sdum.uminho.pt:1822/16783Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T15:42:17.789613Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10 |
title |
Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10 |
spellingShingle |
Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10 Carvalho, Vera Protein delivery system Dextrin nanogel Biocompatibility Interleukin-10 Anti-inflammatory agent Science & Technology |
title_short |
Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10 |
title_full |
Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10 |
title_fullStr |
Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10 |
title_full_unstemmed |
Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10 |
title_sort |
Self-assembled dextrin nanogel as protein carrier: controlled release and biological activity of IL-10 |
author |
Carvalho, Vera |
author_facet |
Carvalho, Vera Castanheira, Pedro Madureira, Pedro Ferreira, Sílvia A. Costa, Carlos M. Faro, Carlos Teixeira, João P. Vilanova, Manuel Gama, F. M. |
author_role |
author |
author2 |
Castanheira, Pedro Madureira, Pedro Ferreira, Sílvia A. Costa, Carlos M. Faro, Carlos Teixeira, João P. Vilanova, Manuel Gama, F. M. |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Carvalho, Vera Castanheira, Pedro Madureira, Pedro Ferreira, Sílvia A. Costa, Carlos M. Faro, Carlos Teixeira, João P. Vilanova, Manuel Gama, F. M. |
dc.subject.por.fl_str_mv |
Protein delivery system Dextrin nanogel Biocompatibility Interleukin-10 Anti-inflammatory agent Science & Technology |
topic |
Protein delivery system Dextrin nanogel Biocompatibility Interleukin-10 Anti-inflammatory agent Science & Technology |
description |
Interleukin-10 (IL-10) is an anti-inflammatory cytokine, which active form is a non-covalent homodimer. Given the potential of IL-10 for application in various medical conditions, it is essential to develop systems for its effective delivery. In previous work, it has been shown that a dextrin nanogel effectively incorporated and stabilized rIL10, enabling its release over time. In this work, the delivery system based on dextrin nanogels was further analyzed. The biocompatibility of the nanogel was comprehensively analyzed, through cytotoxicity (lactate dehydrogenase release, MTS, Live and Dead) and genotoxicity (comet) assays. The release profile of rIL-10 and its biological activity were evaluated in vivo, using C57BL/6 mice. Although able to maintain a stable concentration of IL-10 for at least 4 hours in mice serum, the amount of protein released was rather low. Despite this, the amount of rIL-10 released from the complex was biologically active inhibiting TNF-α production, in vivo, by LPSchallenged mice. In spite of the significant stabilization achieved using the nanogel, rIL-10 still denatures rather quickly. An additional effort is thus necessary to develop an effective delivery system for this cytokine, able to release active protein over longer periods of time. Nevertheless, the good biocompatibility, the protein stabilization effect and the ability to perform as a carrier with controlled release suggest that self-assembled dextrin nanogels may be useful protein delivery systems. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011 2011-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/1822/16783 |
url |
https://hdl.handle.net/1822/16783 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Carvalho, V., Castanheira, P., Madureira, P., Ferreira, S. A., Costa, C., Teixeira, J. P., … Gama, M. (2011, March 22). Self‐assembled dextrin nanogel as protein carrier: Controlled release and biological activity of IL‐10. Biotechnology and Bioengineering. Wiley. http://doi.org/10.1002/bit.23125 0006-3592 1097-0290 10.1002/bit.23125 21391205 https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/bit.23125 |
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info:eu-repo/semantics/openAccess |
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openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
John Wiley and Sons |
publisher.none.fl_str_mv |
John Wiley and Sons |
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