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Original Research Article | OPEN ACCESS

Characterization of Diclofenac Liposomes Formulated with Palm Oil Fractions

Bahareh Sabeti1, Mohamed Ibrahim bin Noordine1, Hamid Akbari Javar1,2 , Ehsan Taghizadeh Davoudi1, Ali Kadivar1

1Department of Pharmacy, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia; 2Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

For correspondence:-  Hamid Javar   Email: akbarijo@tums.ac.ir   Tel:+989121303177

Received: 5 September 2012        Accepted: 23 December 2013        Published: 20 February 2014

Citation: Sabeti B, Noordine MI, Javar HA, Davoudi ET, Kadivar A. Characterization of Diclofenac Liposomes Formulated with Palm Oil Fractions. Trop J Pharm Res 2014; 13(2):185-190 doi: 10.4314/tjpr.v13i2.3

© 2014 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To characterize diclofenac sodium (DS) liposomes prepared using palm oil fractions.
Methods: Reverse-phase evaporation method was used to prepare liposomes containing 10, 20, 30 , 40  or 50% palm oil fractions. The effect of palm oil content on liposome formation, surface morphology, shape, size and zeta potential of the liposomes were studied using scanning electron microscopy (SEM) transmission electron microscopy (TEM) and particle analyzer. Drug loading, entrapment efficiency and in vitro drug release were measured in phosphate-buffered saline (PBS, pH 7.4) by UV spectrophotometry.
Results TEM and SEM images showed formation of liposomes for all formulations, However, increase in the proportion of palm oil in the formulations significantly reduced particle size and increased zeta potential. The effect on drug loading and drug release varied with palm oil fraction. The best release pattern with appropriate entrapment efficiency and stability was obtained with liposomes containing 33 % palm oil fraction. Introduction of 46 and 56 % of palm oil fractions yielded zeta potential of -42.8 and -50.7 mV, respectively, compared with -31.2 mV for the formulation without palm oil.
Conclusion: The results demonstrate the potentials of palm oil fractions in the preparation of suitable DS liposomes with good bioavailability.

Keywords: Liposome, Drug delivery, Palm oil, Diclofenac

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