Intra-articular drug delivery: The challenge to extend drug residence time within the joint

被引:109
|
作者
Edwards, Scott H. R. [1 ]
机构
[1] Charles Sturt Univ, Sch Anim & Vet Sci, Wagga Wagga, NSW 2678, Australia
来源
VETERINARY JOURNAL | 2011年 / 190卷 / 01期
关键词
Intra-articular; Drug delivery; Osteoarthritis; Non-steroidal anti-inflammatory drug NSAID; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; INTRA-ARTICULAR INJECTION; STANDARD-BRED RACEHORSES; RHEUMATOID-ARTHRITIS; SYNOVIAL-FLUID; METHYLPREDNISOLONE ACETATE; TRIAMCINOLONE ACETONIDE; SODIUM HYALURONATE; POLYSULFATED GLYCOSAMINOGLYCAN; KNEE OSTEOARTHRITIS;
D O I
10.1016/j.tvjl.2010.09.019
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The rationale behind developing sustained release microsphere formulations of non-steroidal anti-inflammatory drugs (NSAIDs) administered via the intra-articular (IA) route is to minimise the systemic bioavailability and attendant side-effects associated with oral drug administration. Overall dose is reduced whilst therapeutic benefit within the joint is maintained. The potential benefits of IA therapy for osteoarthritis (OA) are not achieved using currently available medications and delivery vehicles due to the rapid clearance of therapeutic substances from the synovial space. There is a need for sustained release delivery systems if the potential of IA drug administration is to be realised. Rationally designed microspheres taken up by synovial macrophages offer a strategy to sustain drug delivery within the joint, and to deliver NSAIDs directly to pivotal inflammatory cells. The efficacy of microsphere candidates may be evaluated in large animal models of OA. The principles of IA microsphere drug delivery may also be applicable to other classes of drugs. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:15 / 21
页数:7
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