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Temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma

The past decades have witnessed great progress in nanoparticle‐based cancer‐targeting drug delivery systems, but their therapeutic potentials is yet to be fully exploited. In this research, temozolomide (TMZ) and chloroquine (CQ) were loaded into the mesoporous silica nanoparticles (MSNs), the surfa...

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Detalles Bibliográficos
Autores principales: Zhang, Peng, Cao, Fang, Zhang, Jiqin, Tan, Ying, Yao, Shengtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412909/
https://www.ncbi.nlm.nih.gov/pubmed/37576252
http://dx.doi.org/10.1016/j.heliyon.2023.e18490
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author Zhang, Peng
Cao, Fang
Zhang, Jiqin
Tan, Ying
Yao, Shengtao
author_facet Zhang, Peng
Cao, Fang
Zhang, Jiqin
Tan, Ying
Yao, Shengtao
author_sort Zhang, Peng
collection PubMed
description The past decades have witnessed great progress in nanoparticle‐based cancer‐targeting drug delivery systems, but their therapeutic potentials is yet to be fully exploited. In this research, temozolomide (TMZ) and chloroquine (CQ) were loaded into the mesoporous silica nanoparticles (MSNs), the surface was coated with polydopamine (PDA), and the complex was coupled with arginine-glycine-aspartic (RGD) to successfully prepare TMZ/CQ@MSN-RGD. RGD-MSNs accumulated more in the cell and tumor models than in unmodified MSNs in the in vitro and in vivo experiments and can directly induce apoptosis and autophagy in tumor cells. In addition, TMZ/CQ@MSN-RGD therapy enhanced the apoptosis effect of the RGD-MSNs in glioma. Therefore, the combination of autophagy inhibitor with chemotherapy drugs in nanocarriers may promote therapeutic efficacy in treating glioma.
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spelling pubmed-104129092023-08-11 Temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma Zhang, Peng Cao, Fang Zhang, Jiqin Tan, Ying Yao, Shengtao Heliyon Research Article The past decades have witnessed great progress in nanoparticle‐based cancer‐targeting drug delivery systems, but their therapeutic potentials is yet to be fully exploited. In this research, temozolomide (TMZ) and chloroquine (CQ) were loaded into the mesoporous silica nanoparticles (MSNs), the surface was coated with polydopamine (PDA), and the complex was coupled with arginine-glycine-aspartic (RGD) to successfully prepare TMZ/CQ@MSN-RGD. RGD-MSNs accumulated more in the cell and tumor models than in unmodified MSNs in the in vitro and in vivo experiments and can directly induce apoptosis and autophagy in tumor cells. In addition, TMZ/CQ@MSN-RGD therapy enhanced the apoptosis effect of the RGD-MSNs in glioma. Therefore, the combination of autophagy inhibitor with chemotherapy drugs in nanocarriers may promote therapeutic efficacy in treating glioma. Elsevier 2023-07-20 /pmc/articles/PMC10412909/ /pubmed/37576252 http://dx.doi.org/10.1016/j.heliyon.2023.e18490 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Zhang, Peng
Cao, Fang
Zhang, Jiqin
Tan, Ying
Yao, Shengtao
Temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma
title Temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma
title_full Temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma
title_fullStr Temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma
title_full_unstemmed Temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma
title_short Temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma
title_sort temozolomide and chloroquine co-loaded mesoporous silica nanoparticles are effective against glioma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412909/
https://www.ncbi.nlm.nih.gov/pubmed/37576252
http://dx.doi.org/10.1016/j.heliyon.2023.e18490
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