Reformulating cyclosporine A (CsA): More than just a life cycle management strategy

被引:51
作者
Guada, Melissa [1 ,2 ]
Beloqui, Ana [3 ]
Kumar, N. V. Ravi [4 ]
Preat, Veronique [3 ]
del Carmen Dios-Vieitez, Maria [1 ,2 ]
Blanco-Prieto, Maria J. [1 ,2 ]
机构
[1] Univ Navarra, Sch Pharm, Dept Pharm & Pharmaceut Technol, C Irunlarrea 1, E-31008 Pamplona, Spain
[2] IdiSNA, Inst Invest Sanitaria Navarra, C Irunlarrea 3, E-31008 Pamplona, Spain
[3] Catholic Univ Louvain, Louvain Drug Res Inst, Adv Drug Delivery & Biomat, B-1200 Brussels, Belgium
[4] Texas A&M Hlth Sci Ctr, Dept Pharmaceut Sci, College Stn, TX 77845 USA
关键词
Cyclosporine A; Drug delivery system; Immunosuppressant; Microparticle; Nanoparticle; SOLID LIPID NANOPARTICLES; DRUG-DELIVERY SYSTEM; ENHANCED ORAL BIOAVAILABILITY; TOPICAL OCULAR DELIVERY; IN-VITRO; PHYSICOCHEMICAL CHARACTERIZATION; POLYMERIC NANOPARTICLES; CALCINEURIN INHIBITORS; VIVO CHARACTERIZATION; PHARMACOKINETICS;
D O I
10.1016/j.jconrel.2016.01.056
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclosporine A (CsA) is a well-known immunosuppressive agent that gained considerable importance in transplant medicine in the late 1970s due to its selective and reversible inhibition of T-lymphocytes. While CsA has been widely used to prevent graft rejection in patients undergoing organ transplant it was also used to treat several systemic and local autoimmune disorders. Currently, the neuro-and cardio-protective effects of CsA (CiCloMulsion (R); NeuroSTAT (R)) are being tested in phase II and III trials respectively and NeuroSTAT (R) received orphan drug status from US FDA and Europe in 2010. The reformulation strategies focused on developing Cremophor (R) EL free formulations and address variable bioavailability and toxicity issues of CsA. This reviewis an attempt to highlight the progressmade so far and the roomavailable for further improvements to realize the maximum benefits of CsA. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:269 / 282
页数:14
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