Regulating Interactions Between Targeted Nanocarriers and Mononuclear Phagocyte System via an Esomeprazole-Based Preconditioning Strategy

Zakia Belhadj,1 Bing He,1 Jijun Fu,2 Hua Zhang,1 Xueqing Wang,1 Wenbing Dai,1 Qiang Zhang1 1Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, Peo...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Belhadj Z, He B, Fu J, Zhang H, Wang X, Dai W, Zhang Q
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2020
Materias:
Acceso en línea:https://doaj.org/article/19714c8882864d97a16ad25139fd9f14
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:19714c8882864d97a16ad25139fd9f14
record_format dspace
spelling oai:doaj.org-article:19714c8882864d97a16ad25139fd9f142021-12-02T03:36:23ZRegulating Interactions Between Targeted Nanocarriers and Mononuclear Phagocyte System via an Esomeprazole-Based Preconditioning Strategy1178-2013https://doaj.org/article/19714c8882864d97a16ad25139fd9f142020-08-01T00:00:00Zhttps://www.dovepress.com/regulating-interactions-between-targeted-nanocarriers-and-mononuclear--peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Zakia Belhadj,1 Bing He,1 Jijun Fu,2 Hua Zhang,1 Xueqing Wang,1 Wenbing Dai,1 Qiang Zhang1 1Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, People’s Republic of China; 2School of Pharmaceutical Sciences, Guangzhou Medical University, Guangzhou, 511436, People’s Republic of ChinaCorrespondence: Qiang Zhang; Wenbing Dai Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery SystemsState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xueyuan Road, Haidian District, Beijing 100191, People’s Republic of ChinaTel +86-10-82802791; Tel +86-10-82802791Email zqdodo@bjmu.edu.cn; daiwb@bjmu.edu.cnPurpose: The mononuclear phagocyte system (MPS) presents a formidable obstacle that hampers the delivery of various nanopreparations to tumors. Therefore, there is an urgent need to improve the off-MPS targeting ability of nanomedicines. In the present study, we present a novel preconditioning strategy to substantially increase the circulation times and tumor targeting of nanoparticles by regulating nanocarrier-MPS interactions.Methods: In vitro, the effect of different vacuolar H+-ATPase inhibitors on macrophage uptake of targeted or nontargeted lipid vesicles was evaluated. Specifically, the clinically approved proton-pump inhibitor esomeprazole (ESO) was selected as a preconditioning agent. Then, we further investigated the blocking effect of ESO on the macrophage endocytosis of nanocarriers. In vivo, ESO was first intravenously administered into A549-tumor-bearing nude mice, and 24 h later, the c(RGDm7)-modified vesicles co-loaded with doxorubicin and gefitinib were intravenously injected.Results: In vitro, ESO was found to reduce the interactions between macrophages and c(RGDm7)-modified vesicles by interfering with the latter’s lysosomal trafficking. Studies conducted in vivo confirmed that ESO pretreatment greatly decreased the liver and spleen distribution of the targeted vesicles, enhanced their tumor accumulation, and improved the therapeutic outcome of the drug-loaded nanomedicines.Conclusion: Our findings indicate that ESO can regulate the nanoparticle-MPS interaction, which provides a feasible option for enhancing the off-MPS targeting of nanomedicines.Keywords: mononuclear phagocyte system, preconditioning strategy, esomeprazole, V-ATPase inhibitors, targeted lipid vesiclesBelhadj ZHe BFu JZhang HWang XDai WZhang QDove Medical Pressarticlemononuclear phagocyte systempreconditioning strategyesomeprazolev-atpase inhibitorstargeted lipid vesiclesMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 15, Pp 6385-6399 (2020)
institution DOAJ
collection DOAJ
language EN
topic mononuclear phagocyte system
preconditioning strategy
esomeprazole
v-atpase inhibitors
targeted lipid vesicles
Medicine (General)
R5-920
spellingShingle mononuclear phagocyte system
preconditioning strategy
esomeprazole
v-atpase inhibitors
targeted lipid vesicles
Medicine (General)
R5-920
Belhadj Z
He B
Fu J
Zhang H
Wang X
Dai W
Zhang Q
Regulating Interactions Between Targeted Nanocarriers and Mononuclear Phagocyte System via an Esomeprazole-Based Preconditioning Strategy
description Zakia Belhadj,1 Bing He,1 Jijun Fu,2 Hua Zhang,1 Xueqing Wang,1 Wenbing Dai,1 Qiang Zhang1 1Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, People’s Republic of China; 2School of Pharmaceutical Sciences, Guangzhou Medical University, Guangzhou, 511436, People’s Republic of ChinaCorrespondence: Qiang Zhang; Wenbing Dai Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery SystemsState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xueyuan Road, Haidian District, Beijing 100191, People’s Republic of ChinaTel +86-10-82802791; Tel +86-10-82802791Email zqdodo@bjmu.edu.cn; daiwb@bjmu.edu.cnPurpose: The mononuclear phagocyte system (MPS) presents a formidable obstacle that hampers the delivery of various nanopreparations to tumors. Therefore, there is an urgent need to improve the off-MPS targeting ability of nanomedicines. In the present study, we present a novel preconditioning strategy to substantially increase the circulation times and tumor targeting of nanoparticles by regulating nanocarrier-MPS interactions.Methods: In vitro, the effect of different vacuolar H+-ATPase inhibitors on macrophage uptake of targeted or nontargeted lipid vesicles was evaluated. Specifically, the clinically approved proton-pump inhibitor esomeprazole (ESO) was selected as a preconditioning agent. Then, we further investigated the blocking effect of ESO on the macrophage endocytosis of nanocarriers. In vivo, ESO was first intravenously administered into A549-tumor-bearing nude mice, and 24 h later, the c(RGDm7)-modified vesicles co-loaded with doxorubicin and gefitinib were intravenously injected.Results: In vitro, ESO was found to reduce the interactions between macrophages and c(RGDm7)-modified vesicles by interfering with the latter’s lysosomal trafficking. Studies conducted in vivo confirmed that ESO pretreatment greatly decreased the liver and spleen distribution of the targeted vesicles, enhanced their tumor accumulation, and improved the therapeutic outcome of the drug-loaded nanomedicines.Conclusion: Our findings indicate that ESO can regulate the nanoparticle-MPS interaction, which provides a feasible option for enhancing the off-MPS targeting of nanomedicines.Keywords: mononuclear phagocyte system, preconditioning strategy, esomeprazole, V-ATPase inhibitors, targeted lipid vesicles
format article
author Belhadj Z
He B
Fu J
Zhang H
Wang X
Dai W
Zhang Q
author_facet Belhadj Z
He B
Fu J
Zhang H
Wang X
Dai W
Zhang Q
author_sort Belhadj Z
title Regulating Interactions Between Targeted Nanocarriers and Mononuclear Phagocyte System via an Esomeprazole-Based Preconditioning Strategy
title_short Regulating Interactions Between Targeted Nanocarriers and Mononuclear Phagocyte System via an Esomeprazole-Based Preconditioning Strategy
title_full Regulating Interactions Between Targeted Nanocarriers and Mononuclear Phagocyte System via an Esomeprazole-Based Preconditioning Strategy
title_fullStr Regulating Interactions Between Targeted Nanocarriers and Mononuclear Phagocyte System via an Esomeprazole-Based Preconditioning Strategy
title_full_unstemmed Regulating Interactions Between Targeted Nanocarriers and Mononuclear Phagocyte System via an Esomeprazole-Based Preconditioning Strategy
title_sort regulating interactions between targeted nanocarriers and mononuclear phagocyte system via an esomeprazole-based preconditioning strategy
publisher Dove Medical Press
publishDate 2020
url https://doaj.org/article/19714c8882864d97a16ad25139fd9f14
work_keys_str_mv AT belhadjz regulatinginteractionsbetweentargetednanocarriersandmononuclearphagocytesystemviaanesomeprazolebasedpreconditioningstrategy
AT heb regulatinginteractionsbetweentargetednanocarriersandmononuclearphagocytesystemviaanesomeprazolebasedpreconditioningstrategy
AT fuj regulatinginteractionsbetweentargetednanocarriersandmononuclearphagocytesystemviaanesomeprazolebasedpreconditioningstrategy
AT zhangh regulatinginteractionsbetweentargetednanocarriersandmononuclearphagocytesystemviaanesomeprazolebasedpreconditioningstrategy
AT wangx regulatinginteractionsbetweentargetednanocarriersandmononuclearphagocytesystemviaanesomeprazolebasedpreconditioningstrategy
AT daiw regulatinginteractionsbetweentargetednanocarriersandmononuclearphagocytesystemviaanesomeprazolebasedpreconditioningstrategy
AT zhangq regulatinginteractionsbetweentargetednanocarriersandmononuclearphagocytesystemviaanesomeprazolebasedpreconditioningstrategy
_version_ 1718401653473804288