Preparation of Solid Self-Emulsifying Drug Delivery System of Manidipine Hydrochloride

Article Preview

Abstract:

The ability of self-emulsifying drug delivery system (SEDDS), which is a mixture of oils, surfactants and co-surfactants, to improve dissolution rate of a poorly water-soluble drug, manidipine hydrochloride (MDP), was evaluated in this study. Liquid form of SEDDS containing caprylic/capric glyceride, polyoxyl 35 castor oil, and diethylene glycol monoethyl ether at a weight ratio of 1:1:8 was converted to solid SEDDS by adsorption on to different solid carriers, i.e., Aerosil® 200 and Sylysia® 320. The results demonstrated that the solid carrier of at least 50% (w/w) was required to adsorb liquid SEDDS containing MDP. The results from powder X-ray diffraction, differential scanning colorimetry and scanning electron microscopy showed that MDP in solid SEDDS formulations was in amorphous form while a crystalline form was observed only in MDP raw material and its physical mixture. The in vitro dissolution of MDP from solid SEDDS using Sylysia® 320 was higher than that using Aerosil® 200 as a solid carrier. In summary, the solid SEDDS could be used as a carrier to improve the dissolution of MDP, a poorly water-soluble drug.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

143-146

Citation:

Online since:

August 2013

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] K. Csabai, M. Vikmon, J. Szejtli, E. Redenti, G. Poli, P. Ventura, Complexation of manidipine with cyclodextrins and their derivatives, J. Incl. Phenom. Macro. 31 (1998) 167-178.

DOI: 10.1023/a:1007959417684

Google Scholar

[2] N. Patel, D.M. Dalrymple, A.T.M. Serajuddin, Development of solid SEDDS, III: application of Acconon® C-50 and Gelucire® 50/13 as both solidifying and emulsifying agents for medium chain triglycerides, J. Excipients Food Chem. 3 (2012) 83-92.

Google Scholar

[3] A.A. Kale, V.B. Patravale, Design and evaluation of self-emulsifying drug delivery system (SEDDS) of nimodipine, AAPS PharmSciTech. 9 (2008) 191-196.

DOI: 10.1208/s12249-008-9037-9

Google Scholar

[4] D.R. Rao, R.N. Kankan and M.G. Ghagare, U.S. Patent 20120232091 A1. (2012).

Google Scholar

[5] M. Milović, J. Djuriš, L. Djekić, D. Vasiljević, S. Ibrić, Characterization and evaluation of solid self-microemulsifying drug delivery systems with porous carrier as systems for improved carbamazepine release, Int. J. Pharm. 436 (2012) 58-65.

DOI: 10.1016/j.ijpharm.2012.06.032

Google Scholar