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Drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time

Long-circulating drug carriers are highly desirable in drug delivery system. However, nonspecific protein adsorption leaves a great challenge in drug delivery of intravenous administration and significantly affects both the pharmacokinetic profiles of the carrier and drugs, resulting in negatively a...

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Detalles Bibliográficos
Autores principales: Liu, Ruiyuan, Li, Yan, Zhang, Zhenzhong, Zhang, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669018/
https://www.ncbi.nlm.nih.gov/pubmed/26813147
http://dx.doi.org/10.1093/rb/rbv003
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author Liu, Ruiyuan
Li, Yan
Zhang, Zhenzhong
Zhang, Xin
author_facet Liu, Ruiyuan
Li, Yan
Zhang, Zhenzhong
Zhang, Xin
author_sort Liu, Ruiyuan
collection PubMed
description Long-circulating drug carriers are highly desirable in drug delivery system. However, nonspecific protein adsorption leaves a great challenge in drug delivery of intravenous administration and significantly affects both the pharmacokinetic profiles of the carrier and drugs, resulting in negatively affect of therapeutic efficiency. Therefore, it is important to make surface modification of drug carriers by protein-resistant materials to prolong the blood circulation time and increase the targeted accumulation of therapeutic agents. In this review, we highlight the possible mechanism of protein resistance and recent progress of the alternative protein-resistant materials and their drug carriers, such as poly(ethylene glycol), oligo(ethylene glycol), zwitterionic materials, and red blood cells adhesion.
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spelling pubmed-46690182016-01-26 Drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time Liu, Ruiyuan Li, Yan Zhang, Zhenzhong Zhang, Xin Regen Biomater Reviews Long-circulating drug carriers are highly desirable in drug delivery system. However, nonspecific protein adsorption leaves a great challenge in drug delivery of intravenous administration and significantly affects both the pharmacokinetic profiles of the carrier and drugs, resulting in negatively affect of therapeutic efficiency. Therefore, it is important to make surface modification of drug carriers by protein-resistant materials to prolong the blood circulation time and increase the targeted accumulation of therapeutic agents. In this review, we highlight the possible mechanism of protein resistance and recent progress of the alternative protein-resistant materials and their drug carriers, such as poly(ethylene glycol), oligo(ethylene glycol), zwitterionic materials, and red blood cells adhesion. Oxford University Press 2015-06 2015-05-21 /pmc/articles/PMC4669018/ /pubmed/26813147 http://dx.doi.org/10.1093/rb/rbv003 Text en © The Author(s) 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Liu, Ruiyuan
Li, Yan
Zhang, Zhenzhong
Zhang, Xin
Drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time
title Drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time
title_full Drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time
title_fullStr Drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time
title_full_unstemmed Drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time
title_short Drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time
title_sort drug carriers based on highly protein-resistant materials for prolonged in vivo circulation time
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669018/
https://www.ncbi.nlm.nih.gov/pubmed/26813147
http://dx.doi.org/10.1093/rb/rbv003
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