| Literature DB >> 34562656 |
Haiting Xu1, Ruifeng Luo1, Lingling Dong1, Xiulan Pu1, Qiyan Chen1, Naijing Ye1, Shanshan Qi1, Xiaoqin Han1, Wenbiao Nie1, Chaomei Fu1, Yichen Hu2, Jinming Zhang3, Fei Gao4.
Abstract
An oral nanoparticle (NPs) encapsulated in chitosan/alginate hydrogel (CA-Gel) with dual-sensitive in pH and reactive oxygen species (ROS) was developed to load curcumin (CUR) based on the intracellular-specific characteristics of macrophages. Chondroitin sulfate (CS) wrapped PBAE-SA-PAPE with intracellular pH/ROS dual-sensitive characteristics and CUR via a simple nanoprecipitation method to form NPs (CS-CUR-NPs), and mixed CA-Gel to acquire the final preparation (CS-CUR-NPs-Gel). CS-CUR-NPs displayed an ideal average particle size (179.19±5.61nm) and high encapsulating efficiency (94.74±1.15%). CS showed a good targeting ability on macrophages and the CA-Gel contribution in protecting NPs from being destroyed in the upper gastrointestinal tract. As expected, CS-CUR-NPs-Gel could significantly alleviate inflammation in DSS-induced UC mice via TLR4-MAPK/NF-κB pathway. This study is the first to attempt to design a novel pH/ROS dual-stimulated release strategy in helping intracellular CUR delivery and anticipated for efficient anti-UC therapy.Entities:
Keywords: Curcumin; Macrophage-targeted drug delivery; Oral administration; Ulcerative colitis; pH/ROS sensitive
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Year: 2021 PMID: 34562656 DOI: 10.1016/j.nano.2021.102461
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307