An intra-articular injectable phospholipids-based gel for the treatment of rheumatoid arthritis

被引:0
|
作者
Yuping Yang [1 ]
Shiqin Luo [1 ]
Xiong Peng [1 ]
Ting Zhao [1 ]
Qin He [1 ,2 ]
Mengying Wu [1 ]
Wei Zhang [1 ]
Tao Gong [1 ]
Zhirong Zhang [1 ]
机构
[1] Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharm
[2] Department of Pharmacy, West China Hospital Sichuan University Jintang Hospital
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
R593.22 [类风湿性关节炎];
学科分类号
1002 ; 100201 ;
摘要
Rheumatoid arthritis(RA) is a chronic inflammatory and destructive arthropathy with a high deformity rate. Despite numerous studies and clinical trials, no curative treatment is available for large weight-bearing joints. Intra-articular(IA) injections could deliver high concentrations of drug to the afflicted joint and improve the drug efficacy while reducing systemic toxicity. However, free drugs are rapidly cleared from synovial fluid and do not significantly halt the progression of joint disease. Herein, a phospholipids-based controlledrelease gel was prepared for sustained IA delivery of celastrol(CEL) and the therapeutic efficiency was evaluated in a rheumatoid arthritis rabbit model. The CEL-loaded gel(CEL-gel)contained up to 70% phospholipids yet was easy to inject. After injecting into the joint cavity,CEL-gel achieved sol to gel phase transition without special stimuli and gelling agent. In vitro release and in vivo pharmacokinetic studies evidenced the stable and sustained release action of CEL-gel. A single IA injection of CEL-gel could maintain therapeutic efficiency for about 25 d and showed much better anti-arthritic efficacy compared to repeated injections of free drug solution(CEL-sol). Furthermore, the IA injection of CEL-gel greatly reduced the systemic toxicity of CEL. With good biocompatibility and biodegradability, CEL-gel might be a promising IA drug delivery system.
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页码:122 / 133
页数:12
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