The Potential of Liposomal Drug Delivery for the Treatment of Inflammatory Arthritis

被引:57
作者
Vanniasinghe, Anne S. [1 ]
Bender, Veronika
Manolios, Nicholas [1 ]
机构
[1] Univ Sydney, Westmead Hosp, Dept Rheumatol, Westmead, NSW 2145, Australia
关键词
liposomes; rheumatoid arthritis; drug delivery; targeted delivery; STERICALLY STABILIZED LIPOSOMES; LONG-CIRCULATING LIPOSOMES; COLLAGEN-INDUCED ARTHRITIS; ANTIGEN-INDUCED ARTHRITIS; CELL-PENETRATING PEPTIDE; RHEUMATOID-ARTHRITIS; INTRACELLULAR DELIVERY; PROTEIN TRANSDUCTION; SUPEROXIDE-DISMUTASE; IN-VITRO;
D O I
10.1016/j.semarthrit.2008.08.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To review the use of liposomes as a delivery agent in inflammatory arthritis. Methods: The literature on liposomes and liposomal drug delivery for the treatment of inflammatory arthritis was reviewed. A PubMed search of articles in the English-language journals from 1965 to 2007 was performed. The index words used were as follows: "rheumatoid arthritis," "liposomes," and "targeted delivery." Papers identified were reviewed, abstracted, and summarized. Results: Liposomes have the capacity to be used as delivery and targeting agents for the administration of antirheumatic drugs at lower doses with reduced toxicity. In other areas of medicine, the pace of progress has been rapid. In the case of infectious diseases and cancer, liposomal drug delivery has progressed and developed into commercially viable therapeutic options for the treatment of fungal infections (amphotericin B), or metastatic breast cancer and Kaposi sarcoma (doxorubicin, daunorubicin), respectively. In arthritis, the efficacy of prednisolone-loaded long-circulating liposomes is currently being evaluated in a phase II clinical trial. Liposome's application to arthritis is still in its infancy but appears promising as new patents are filed. With improvements in liposomal formulation and targeted synovial delivery, liposomes offer increased therapeutic activity and improvement in the risk benefit ratio. Conclusion: Recent research into synovial targets and improved liposomal formulations continues to improve our capacity to use liposomes for targeted delivery. With time, this approach has the potential to improve drug delivery and reduce systemic complications. (C) 2009 Elsevier Inc. All rights reserved. Semin Arthritis Rheum 39:182-196
引用
收藏
页码:182 / 196
页数:15
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