Encapsulation of NSAIDs for inflammation management: Overview, progress, challenges and prospects

被引:93
作者
Badri, Waisudin [1 ,2 ]
Miladi, Karim [1 ]
Nazari, Qand Agha [2 ]
Greige-Gerges, Helene [3 ]
Fessi, Hatem [1 ]
Elaissari, Abdelhamid [1 ]
机构
[1] Univ Lyon, CNRS, UMR 5007, LAGEP, F-69622 Lyon, France
[2] Kabul Univ, Fac Pharm, Kabul, Afghanistan
[3] Lebanese Univ, Fac Sci, Beirut, Lebanon
关键词
Non-steroidal anti-inflammatory drugs; Encapsulation; Carriers; Liposomes; Particles; Solid lipid nanoparticles; In vivo; SOLID LIPID NANOPARTICLES; IN-VITRO CHARACTERIZATION; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; LOADED PLGA NANOPARTICLES; PARTICLE-SIZE; CARRIERS NLC; PHYSICOCHEMICAL PROPERTIES; POLYMERIC NANOPARTICLES; TRANSDERMAL DELIVERY; PROCESS PARAMETERS;
D O I
10.1016/j.ijpharm.2016.11.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Non-steroidal anti-inflammatory drugs (NSAIDs) are among the most widely prescribed drugs. Debilitating diseases such as rheumatoid arthritis and osteoarthritis are commonly managed by NSAIDs. However, NSAIDs pharmacological mechanism is often associated with the presence of gastrointestinal side effects. NSAIDs encapsulation is performed in order to overcome some of the drawbacks linked to their clinical use. To fulfill this purpose, various vectors like polymer-based nanoparticles, liposomes and solid lipid nanoparticles have been proposed. Such vehicles could have advantages but some limitations as well. This manuscript highlights current NSAIDs encapsulation approaches based on either preformed polymers or lipids. Moreover, properties of the prepared carriers and their applications are also discussed. Many factors are taken into account for selecting carrier type and encapsulation method. It was concluded that different vehicles and preparation methods have been employed for NSAIDs encapsulation. Mostly, vehicles sizes ranged within the nanoscale. Main advantages that have been confirmed by in vitro and in vivo studies include promoted stability, sustained release and bioavailability enhancement. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:757 / 773
页数:17
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