| Literature DB >> 27829170 |
Waisudin Badri1, Karim Miladi2, Qand Agha Nazari3, Hélène Greige-Gerges4, Hatem Fessi2, Abdelhamid Elaissari5.
Abstract
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. Copyright ÂEntities:
Keywords: Carriers; Encapsulation; In vivo; Liposomes; Non-steroidal anti-inflammatory drugs; Particles; Solid lipid nanoparticles
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Year: 2016 PMID: 27829170 DOI: 10.1016/j.ijpharm.2016.11.002
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875