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The Nano-War Against Complement Proteins
Targeted drug delivery and nanomedicine hold the potential promise of delivering drugs solely to target organs or cell types, thus decreasing off-target side effects and improving efficacy. However, nano-scale drug carriers face several barriers to this goal, with one of the most formidable being th...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432284/ https://www.ncbi.nlm.nih.gov/pubmed/34505951 http://dx.doi.org/10.1208/s12248-021-00630-9 |
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author | Wang, Zhicheng Brenner, Jacob S. |
author_facet | Wang, Zhicheng Brenner, Jacob S. |
author_sort | Wang, Zhicheng |
collection | PubMed |
description | Targeted drug delivery and nanomedicine hold the potential promise of delivering drugs solely to target organs or cell types, thus decreasing off-target side effects and improving efficacy. However, nano-scale drug carriers face several barriers to this goal, with one of the most formidable being the complement cascade. Complement proteins, especially C3, opsonize not just the microbes they evolved to contain, but also nanocarriers. This results in multiple problems, including marking the nanocarriers for clearance by leukocytes, likely fouling of the targeting moieties on nanocarriers, and release of toxins which produce deleterious local and systemic effects. Here, we review how complement achieves its blockade of nanomedicine, which nanocarrier materials properties best avoid complement, and current and future strategies to control complement to unleash nanomedicine’s potential. [Image: see text] |
format | Online Article Text |
id | pubmed-8432284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-84322842021-09-10 The Nano-War Against Complement Proteins Wang, Zhicheng Brenner, Jacob S. AAPS J Mini-Review Targeted drug delivery and nanomedicine hold the potential promise of delivering drugs solely to target organs or cell types, thus decreasing off-target side effects and improving efficacy. However, nano-scale drug carriers face several barriers to this goal, with one of the most formidable being the complement cascade. Complement proteins, especially C3, opsonize not just the microbes they evolved to contain, but also nanocarriers. This results in multiple problems, including marking the nanocarriers for clearance by leukocytes, likely fouling of the targeting moieties on nanocarriers, and release of toxins which produce deleterious local and systemic effects. Here, we review how complement achieves its blockade of nanomedicine, which nanocarrier materials properties best avoid complement, and current and future strategies to control complement to unleash nanomedicine’s potential. [Image: see text] Springer International Publishing 2021-09-10 /pmc/articles/PMC8432284/ /pubmed/34505951 http://dx.doi.org/10.1208/s12248-021-00630-9 Text en © American Association of Pharmaceutical Scientists 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Mini-Review Wang, Zhicheng Brenner, Jacob S. The Nano-War Against Complement Proteins |
title | The Nano-War Against Complement Proteins |
title_full | The Nano-War Against Complement Proteins |
title_fullStr | The Nano-War Against Complement Proteins |
title_full_unstemmed | The Nano-War Against Complement Proteins |
title_short | The Nano-War Against Complement Proteins |
title_sort | nano-war against complement proteins |
topic | Mini-Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432284/ https://www.ncbi.nlm.nih.gov/pubmed/34505951 http://dx.doi.org/10.1208/s12248-021-00630-9 |
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