In vivo anti-apoptosis activity of novel berberine-loaded chitosan nanoparticles effectively ameliorates osteoarthritis

被引:88
|
作者
Zhou, Yan [1 ]
Liu, Shi-qing [1 ]
Peng, Hao [1 ]
Yu, Ling [1 ]
He, Bin [1 ]
Zhao, Qi [1 ]
机构
[1] Wuhan Univ, Renmin Hosp, Cent Lab, Dept Orthoped, Wuhan 430060, Peoples R China
关键词
Chitosan; Berberine; Nanoparticles; Osteoarthritis; Drug release; INTRAARTICULAR DELIVERY; DIABETIC-RATS; CHONDROCYTES; CARTILAGE; INHIBITION; EXPRESSION; MICE; NANOMATERIALS; AUTOPHAGY; CASPASE-3;
D O I
10.1016/j.intimp.2015.05.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Berberine chloride (BBR) is an isoquinoline alkaloid that possesses promising protective efficacies against osteoarthritis (OA). Nevertheless, the therapeutic agent of this substance in OA is limited by its poor aqueous solubility, low bioavailability and short biological half-life. In this study, chitosan (CS)-based nanoparticles were prepared for the sustained release of BBR. Novel BBR-loaded chitosan nanoparticles (CNs) were successfully synthesized by the ionic cross-linking method. BBR-loaded CNs were spherical and homogeneous in shape. Moreover, they exhibited good stability and had ideal releasing profile in vitro. After intra-articular injection of BBR-loaded CNs, the level of BBR in rat plasma decreased and the retention time in synovial fluid increased compared with free BBR solution. In vivo evaluation of BBR-loaded CNs further showed higher anti-apoptosis activity in the treatment of OA compared with BBR solution at equivalent concentration. This result was evidenced by the changes of gross morphology and histological analyses in rat articular cartilage, TUNEL assay, quantitative real-time polymerase chain reaction, Western blot, and immunohistochemical analyses of caspase-3, Bcl-2 and Bax expressions. Given these results, BBR-loaded CNs are potential therapeutic agents for OA (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:34 / 43
页数:10
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