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Engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy
Nanotechnology offers the possibility of revolutionizing cancer theranostics in the new era of precision oncology. Extracellular vesicles (EVs)-like biomimetic nanoparticles (EBPs) have recently emerged as a promising platform for targeted cancer drug delivery. Compared with conventional synthetic v...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463632/ https://www.ncbi.nlm.nih.gov/pubmed/37608298 http://dx.doi.org/10.1186/s12951-023-02064-1 |
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author | Liu, Xinyi Xiao, Chunxiu Xiao, Kai |
author_facet | Liu, Xinyi Xiao, Chunxiu Xiao, Kai |
author_sort | Liu, Xinyi |
collection | PubMed |
description | Nanotechnology offers the possibility of revolutionizing cancer theranostics in the new era of precision oncology. Extracellular vesicles (EVs)-like biomimetic nanoparticles (EBPs) have recently emerged as a promising platform for targeted cancer drug delivery. Compared with conventional synthetic vehicles, EBPs have several advantages, such as lower immunogenicity, longer circulation time, and better targeting capability. Studies on EBPs as cancer therapeutics are rapidly progressing from in vitro experiments to in vivo animal models and early-stage clinical trials. Here, we describe engineering strategies to further improve EBPs as effective anticancer drug carriers, including genetic manipulation of original cells, fusion with synthetic nanomaterials, and direct modification of EVs. These engineering approaches can improve the anticancer performance of EBPs, especially in terms of tumor targeting effectiveness, stealth property, drug loading capacity, and integration with other therapeutic modalities. Finally, the current obstacles and future perspectives of engineered EBPs as the next-generation delivery platform for anticancer drugs are discussed. |
format | Online Article Text |
id | pubmed-10463632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104636322023-08-30 Engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy Liu, Xinyi Xiao, Chunxiu Xiao, Kai J Nanobiotechnology Review Nanotechnology offers the possibility of revolutionizing cancer theranostics in the new era of precision oncology. Extracellular vesicles (EVs)-like biomimetic nanoparticles (EBPs) have recently emerged as a promising platform for targeted cancer drug delivery. Compared with conventional synthetic vehicles, EBPs have several advantages, such as lower immunogenicity, longer circulation time, and better targeting capability. Studies on EBPs as cancer therapeutics are rapidly progressing from in vitro experiments to in vivo animal models and early-stage clinical trials. Here, we describe engineering strategies to further improve EBPs as effective anticancer drug carriers, including genetic manipulation of original cells, fusion with synthetic nanomaterials, and direct modification of EVs. These engineering approaches can improve the anticancer performance of EBPs, especially in terms of tumor targeting effectiveness, stealth property, drug loading capacity, and integration with other therapeutic modalities. Finally, the current obstacles and future perspectives of engineered EBPs as the next-generation delivery platform for anticancer drugs are discussed. BioMed Central 2023-08-22 /pmc/articles/PMC10463632/ /pubmed/37608298 http://dx.doi.org/10.1186/s12951-023-02064-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Liu, Xinyi Xiao, Chunxiu Xiao, Kai Engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy |
title | Engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy |
title_full | Engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy |
title_fullStr | Engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy |
title_full_unstemmed | Engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy |
title_short | Engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy |
title_sort | engineered extracellular vesicles-like biomimetic nanoparticles as an emerging platform for targeted cancer therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463632/ https://www.ncbi.nlm.nih.gov/pubmed/37608298 http://dx.doi.org/10.1186/s12951-023-02064-1 |
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