Abstract

Improvements of the oral bioavailability of lipophilic drugs can be obtained using lipidic formulations such as the self-emulsifying drug delivery systems. The high shear wet granulation (HSWG), using microemulsions as binder, is a viable process to produce self-emulsifying granules. However only few information are present in the literature on the effect of process variables on the properties of the granules obtained with these binders. Consequently, this article compares the effects of some relevant experimental variables (impeller speed and massing time) on the final technological and pharmaceutical properties of the granules produced using simple water, or alternatively, a microemulsion as binder and containing simvastatin (SV) as model drug. The effects of the variables were determined by evaluating the granule median diameter, their particle size distribution, roundness, disintegration time and dissolution rate of SV. Results clearly demonstrated that the microemulsion-based process was less sensitive to operating conditions than the water-based process. With microemulsion the nucleation process and growth regimes were more difficult to control, resulting in products with broader PSDs. At the same operating conditions microemulsion-based granules were more brittle but rounder and showed smaller median diameter compared to water-based granules. The dissolution rate of simvastatin was not significantly affected by the operating conditions.

Highlights

  • In order to improve the oral bioavailability of lipophilic drugs, in recent years much attention has been focused on lipidic formulations, with particular emphasis on self-emulsifying drug delivery systems (SEDDS)

  • Franceschinis and coworker (Franceschinis et al, 2005; Franceschinis et al 2011) have already demonstrated that it is possible to produce solid-SEDDS by high shear granulation using a microemulsion as granulating liquid, few information is found in the literature on the link between this type of granulating liquid, the operating variables and the final granule properties

  • In order to evaluate their effect on the drug release, simvastatin an hydroxymethylglutarylcoenzyme A (HMG-CoA) reductase inhibitors having a water solubility of 0.0010 mg/ml was selected as model drug

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Summary

Introduction

In order to improve the oral bioavailability of lipophilic drugs, in recent years much attention has been focused on lipidic formulations, with particular emphasis on self-emulsifying drug delivery systems (SEDDS). SEDDS are mixtures of drug, oils, surfactants and/or co-solvents which form fine oil-in-water emulsions upon dilution with aqueous medium or in vivo administration. The digestive motility of the stomach and intestine provide the agitation necessary for the self-emulsification process (Hauss, 2007; Gursoy and Benita, 2004). The small oil droplets produced by self-emulsification provide a large interfacial area for pancreatic lipase and promote rapid release of the drug. The key step for SEDDS formulation is to find a suitable oil-surfactant mixture that can dissolve the drug within the required therapeutic concentrations. Liquid SEDDS can be used to fill either soft or hard gelatine capsules (Porter et al, 2008; Costantinides, 1995)

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