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Biomimetic Boron Nitride Nanoparticles for Targeted Drug Delivery and Enhanced Antitumor Activity

Boron nitride nanomaterials are being increasingly recognized as vehicles for cancer drug delivery that increase drug loading and control drug release because of their excellent physicochemical properties and biocompatibility. However, these nanoparticles are often cleared rapidly by the immune syst...

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Autores principales: Li, Hui, Qiao, Wei, Shen, Yizhe, Xu, Huashan, Fan, Yuan, Liu, Yuxiang, Lan, Yadi, Gong, Yan, Chen, Fuxue, Feng, Shini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145272/
https://www.ncbi.nlm.nih.gov/pubmed/37111754
http://dx.doi.org/10.3390/pharmaceutics15041269
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author Li, Hui
Qiao, Wei
Shen, Yizhe
Xu, Huashan
Fan, Yuan
Liu, Yuxiang
Lan, Yadi
Gong, Yan
Chen, Fuxue
Feng, Shini
author_facet Li, Hui
Qiao, Wei
Shen, Yizhe
Xu, Huashan
Fan, Yuan
Liu, Yuxiang
Lan, Yadi
Gong, Yan
Chen, Fuxue
Feng, Shini
author_sort Li, Hui
collection PubMed
description Boron nitride nanomaterials are being increasingly recognized as vehicles for cancer drug delivery that increase drug loading and control drug release because of their excellent physicochemical properties and biocompatibility. However, these nanoparticles are often cleared rapidly by the immune system and have poor tumor targeting effects. As a result, biomimetic nanotechnology has emerged to address these challenges in recent times. Cell-derived biomimetic carriers have the characteristics of good biocompatibility, long circulation time, and strong targeting ability. Here, we report a biomimetic nanoplatform (CM@BN/DOX) prepared by encapsulating boron nitride nanoparticles (BN) and doxorubicin (DOX) together using cancer cell membrane (CCM) for targeted drug delivery and tumor therapy. The CM@BN/DOX nanoparticles (NPs) were able to target cancer cells of the same type on its own initiative through homologous targeting of cancer cell membranes. This led to a remarkable increase in cellular uptake. In vitro simulation of an acidic tumor microenvironment could effectively promote drug release from CM@BN/DOX. Furthermore, the CM@BN/DOX complex exhibited an excellent inhibitory effect against homotypic cancer cells. These findings suggest that CM@BN/DOX are promising in targeted drug delivery and potentially personalized therapy against their homologous tumor.
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spelling pubmed-101452722023-04-29 Biomimetic Boron Nitride Nanoparticles for Targeted Drug Delivery and Enhanced Antitumor Activity Li, Hui Qiao, Wei Shen, Yizhe Xu, Huashan Fan, Yuan Liu, Yuxiang Lan, Yadi Gong, Yan Chen, Fuxue Feng, Shini Pharmaceutics Article Boron nitride nanomaterials are being increasingly recognized as vehicles for cancer drug delivery that increase drug loading and control drug release because of their excellent physicochemical properties and biocompatibility. However, these nanoparticles are often cleared rapidly by the immune system and have poor tumor targeting effects. As a result, biomimetic nanotechnology has emerged to address these challenges in recent times. Cell-derived biomimetic carriers have the characteristics of good biocompatibility, long circulation time, and strong targeting ability. Here, we report a biomimetic nanoplatform (CM@BN/DOX) prepared by encapsulating boron nitride nanoparticles (BN) and doxorubicin (DOX) together using cancer cell membrane (CCM) for targeted drug delivery and tumor therapy. The CM@BN/DOX nanoparticles (NPs) were able to target cancer cells of the same type on its own initiative through homologous targeting of cancer cell membranes. This led to a remarkable increase in cellular uptake. In vitro simulation of an acidic tumor microenvironment could effectively promote drug release from CM@BN/DOX. Furthermore, the CM@BN/DOX complex exhibited an excellent inhibitory effect against homotypic cancer cells. These findings suggest that CM@BN/DOX are promising in targeted drug delivery and potentially personalized therapy against their homologous tumor. MDPI 2023-04-18 /pmc/articles/PMC10145272/ /pubmed/37111754 http://dx.doi.org/10.3390/pharmaceutics15041269 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Hui
Qiao, Wei
Shen, Yizhe
Xu, Huashan
Fan, Yuan
Liu, Yuxiang
Lan, Yadi
Gong, Yan
Chen, Fuxue
Feng, Shini
Biomimetic Boron Nitride Nanoparticles for Targeted Drug Delivery and Enhanced Antitumor Activity
title Biomimetic Boron Nitride Nanoparticles for Targeted Drug Delivery and Enhanced Antitumor Activity
title_full Biomimetic Boron Nitride Nanoparticles for Targeted Drug Delivery and Enhanced Antitumor Activity
title_fullStr Biomimetic Boron Nitride Nanoparticles for Targeted Drug Delivery and Enhanced Antitumor Activity
title_full_unstemmed Biomimetic Boron Nitride Nanoparticles for Targeted Drug Delivery and Enhanced Antitumor Activity
title_short Biomimetic Boron Nitride Nanoparticles for Targeted Drug Delivery and Enhanced Antitumor Activity
title_sort biomimetic boron nitride nanoparticles for targeted drug delivery and enhanced antitumor activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145272/
https://www.ncbi.nlm.nih.gov/pubmed/37111754
http://dx.doi.org/10.3390/pharmaceutics15041269
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