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PH-sensitive BSA-modified resveratrol micelles targeting macrophages alleviate symptoms of rheumatoid arthritis.

Authors :
Xie, Hongjun
Zhao, Jing
Wang, Shuo
Kong, Liang
Li, Xuetao
Aga, Erbu
Gong Ga, Lan Zi
Ye, Bengui
Source :
International Immunopharmacology. Jul2024, Vol. 136, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

[Display omitted] • A novel formulation can effectively target and inhibit activated macrophages. • The modification of BSA increases the targeting of BSA-Res@Ms. • BSA-Res@Ms enhance Res targeting ability and increase bioavailability. • BSA-Res@Ms have good pH sensitivity and can quickly release Res. Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease, leading to severe inflammatory infiltration and joint damage, accompanied by a decrease in pH of joint microenvironment. Macrophages play an important role in the pathogenesis of RA, with high expression of bovine serum albumin (BSA) receptors on the surface of macrophages. Resveratrol (Res) has strong anti-inflammatory effects, but its application is limited due to its poor water solubility and low bioavailability. Therefore, we constructed pH-sensitive micelles by encapsulating Res and modifying BSA on the surface of the micelles (BSA-Res@Ms), thereby greatly improving the therapeutic effect of RA. Our research results indicated that BSA-Res@Ms had a smooth and uniform appearance, small particle size, high drug encapsulation efficiency, good stability, and pH-sensitive properties. In vitro, BSA-Res@Ms increased the uptake of Res by RAW264.7 cells, reduced the levels of pro-inflammatory cytokines and cleared excess ROS produced by activated RAW264.7 cells, and inhibited the generation of osteoclasts. In vivo, BSA-Res@Ms could target inflamed joint sites, significantly alleviate joint inflammation symptoms, inhibit activated macrophages, improve synovial hyperplasia and inflammatory cell infiltration, and protect cartilage. BSA-Res@Ms provide a very promising method for the treatment of RA, which can effectively improve the inflammatory manifestations of RA. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15675769
Volume :
136
Database :
Academic Search Index
Journal :
International Immunopharmacology
Publication Type :
Academic Journal
Accession number :
177863367
Full Text :
https://doi.org/10.1016/j.intimp.2024.112324