Nanoparticle-assembled bioadhesive coacervate coating with prolonged gastrointestinal retention for inflammatory bowel disease therapy

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作者
Pengchao Zhao
Xianfeng Xia
Xiayi Xu
Kevin Kai Chung Leung
Aliza Rai
Yingrui Deng
Boguang Yang
Huasheng Lai
Xin Peng
Peng Shi
Honglu Zhang
Philip Wai Yan Chiu
Liming Bian
机构
[1] The Chinese University of Hong Kong,Department of Biomedical Engineering
[2] Sun Yat-sen University Cancer Center,Department of Endoscopy, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine
[3] The Chinese University of Hong Kong,Chow Yuk Ho Technology Centre for Innovative Medicine
[4] The Chinese University of Hong Kong,Department of Surgery, Institute of Digestive Disease, State Key Laboratory of Digestive Disease
[5] South China University of Technology,School of Biomedical Sciences and Engineering, Guangzhou International Campus
[6] South China University of Technology,National Engineering Research Center for Tissue Restoration and Reconstruction
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摘要
A key challenge for the effective treatment of gastrointestinal diseases including inflammatory bowel disease is to develop an orally administered drug delivery system capable of prolonged retention in the gastrointestinal tract. Herein we report a bioadhesive liquid coacervate based on hydrogen bonding-driven nanoparticle assembly. Free from electrostatic interactions, our fluid nanoparticle-assembled coacervate demonstrates significant pH- and salt-independent structural stability and forms a physically adhesive coating on a large surface area of intestinal tract with an extended residence time of more than 2 days to mediate the sustained release of preloaded water-soluble small molecule drugs in vivo. The orally administered drug-laden nanoparticle-assembled coacervate significantly mitigates the symptoms of inflammatory bowel disease, restores the diversity of gut microbiota, reduces systemic drug exposure, and improves the therapeutic efficacy in a rat acute colitis model compared with the oral administration of the same amount of drug in solution form. We suggest that the nanoparticle-assembled coacervate provides a promising drug delivery platform for management and treatment of numerous gastrointestinal diseases where controlled drug release with extended residence time is desired.
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