Cargando…

Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy

Acute lung injury (ALI) is a disease associated with suffering and high lethality, but to date without any effective pharmacological management in the clinic. In the pathological mechanisms of ALI, a strong inflammatory response plays an important role. Herein, based on macrophage ‘homing’ into infl...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Caihong, Zheng, Jinpeng, Ding, Yaning, Meng, Yuanyuan, Tan, Fangyun, Gong, Wei, Chu, Xiaoyang, Kong, Xiaolong, Gao, Chunsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654408/
https://www.ncbi.nlm.nih.gov/pubmed/34866533
http://dx.doi.org/10.1080/10717544.2021.2009936
_version_ 1784611854511767552
author Lu, Caihong
Zheng, Jinpeng
Ding, Yaning
Meng, Yuanyuan
Tan, Fangyun
Gong, Wei
Chu, Xiaoyang
Kong, Xiaolong
Gao, Chunsheng
author_facet Lu, Caihong
Zheng, Jinpeng
Ding, Yaning
Meng, Yuanyuan
Tan, Fangyun
Gong, Wei
Chu, Xiaoyang
Kong, Xiaolong
Gao, Chunsheng
author_sort Lu, Caihong
collection PubMed
description Acute lung injury (ALI) is a disease associated with suffering and high lethality, but to date without any effective pharmacological management in the clinic. In the pathological mechanisms of ALI, a strong inflammatory response plays an important role. Herein, based on macrophage ‘homing’ into inflammation sites and cell membrane coating nanotechnology, we developed a biomimetic anti-inflammation nanosystem (MM-CEP/NLCs) for the treatment of ALI. MM-CEP/NLCs were made with nanostructured lipid carriers (NLCs) coated with natural macrophage membranes (MMs) to achieve effective accumulation of cepharanthine (CEP) in lung inflammation to achieve the effect of treating ALI. With the advantage of suitable physicochemical properties of NLCs and unique biological functions of the macrophage membrane, MM-CEP/NLCs were stabilized and enabled sustained drug release, providing improved biocompatibility and long-term circulation. In vivo, the macrophage membranes enabled NLCs to be targeted and accumulated in the inflammation sites. Further, MM-CEP/NLCs significantly attenuated the severity of ALI, including lung water content, histopathology, bronchioalveolar lavage cellularity, protein concentration, and inflammation cytokines. Our results provide a bionic strategy via the biological properties of macrophages, which may have greater value and application prospects in the treatment of inflammation.
format Online
Article
Text
id pubmed-8654408
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-86544082021-12-09 Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy Lu, Caihong Zheng, Jinpeng Ding, Yaning Meng, Yuanyuan Tan, Fangyun Gong, Wei Chu, Xiaoyang Kong, Xiaolong Gao, Chunsheng Drug Deliv Research Article Acute lung injury (ALI) is a disease associated with suffering and high lethality, but to date without any effective pharmacological management in the clinic. In the pathological mechanisms of ALI, a strong inflammatory response plays an important role. Herein, based on macrophage ‘homing’ into inflammation sites and cell membrane coating nanotechnology, we developed a biomimetic anti-inflammation nanosystem (MM-CEP/NLCs) for the treatment of ALI. MM-CEP/NLCs were made with nanostructured lipid carriers (NLCs) coated with natural macrophage membranes (MMs) to achieve effective accumulation of cepharanthine (CEP) in lung inflammation to achieve the effect of treating ALI. With the advantage of suitable physicochemical properties of NLCs and unique biological functions of the macrophage membrane, MM-CEP/NLCs were stabilized and enabled sustained drug release, providing improved biocompatibility and long-term circulation. In vivo, the macrophage membranes enabled NLCs to be targeted and accumulated in the inflammation sites. Further, MM-CEP/NLCs significantly attenuated the severity of ALI, including lung water content, histopathology, bronchioalveolar lavage cellularity, protein concentration, and inflammation cytokines. Our results provide a bionic strategy via the biological properties of macrophages, which may have greater value and application prospects in the treatment of inflammation. Taylor & Francis 2021-12-06 /pmc/articles/PMC8654408/ /pubmed/34866533 http://dx.doi.org/10.1080/10717544.2021.2009936 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lu, Caihong
Zheng, Jinpeng
Ding, Yaning
Meng, Yuanyuan
Tan, Fangyun
Gong, Wei
Chu, Xiaoyang
Kong, Xiaolong
Gao, Chunsheng
Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy
title Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy
title_full Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy
title_fullStr Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy
title_full_unstemmed Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy
title_short Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy
title_sort cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654408/
https://www.ncbi.nlm.nih.gov/pubmed/34866533
http://dx.doi.org/10.1080/10717544.2021.2009936
work_keys_str_mv AT lucaihong cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy
AT zhengjinpeng cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy
AT dingyaning cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy
AT mengyuanyuan cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy
AT tanfangyun cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy
AT gongwei cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy
AT chuxiaoyang cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy
AT kongxiaolong cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy
AT gaochunsheng cepharanthineloadednanoparticlescoatedwithmacrophagemembranesforlunginflammationtherapy