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Nanoemulsions as novel oral carriers of stiripentol: insights into the protective effect and absorption enhancement

Authors Lu R, Liu S, Wang Q, Li X

Received 28 April 2015

Accepted for publication 15 June 2015

Published 31 July 2015 Volume 2015:10(1) Pages 4937—4946


Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Zhaogang Yang

Peer reviewer comments 5

Editor who approved publication: Dr Lei Yang

Rong Lu,1 Shan Liu,1 Qilin Wang,1 Xia Li1,2

1School of Ocean, Shandong University, Weihai, 2School of Pharmaceutical Sciences, Shandong University, Jinan, People’s Republic of China

Abstract: Oral administration remains a significant challenge in regards to drugs with serious solubility and stability issues. This article aimed to investigate the suitability of nanoemulsions as oral carriers of stiripentol (STP), an acid-labile drug, for enhancement of stability and bioavailability. STP-loaded nanoemulsions (STP-NEs) were prepared by using a solvent-diffusion/ultrasonication technique. STP-NEs were characterized in a variety of ways such as by particle size, entrapment efficiency, in vitro drug release, and transmission electron microscopy. A bioavailability study was performed in rats after oral administration of either STP-NEs, or commercial formulation (Diacomit®). The resultant nanoemulsions were 146.6 nm in particle size with an entrapment efficiency of 99.47%. It was demonstrated that nanoemulsions significantly improved the biochemical stability and bioavailability of STP. The bioavailability of STP-NEs was up to 206.2% relative to Diacomit®. Nanoemulsions fabricated from poly(ethylene glycol) monooleate/medium-chain triglycerides exhibited excellent performance in drug stabilization and absorption enhancement. The results suggest that STP-NEs are a promising means to solve the problems associated with stability and solubility of STP.

Keywords: stiripentol, nanoemulsions, stability, intestinal permeability, bioavailability

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