Formulation and optimization of lyophilized nanosuspension tablets to improve the physicochemical properties and provide immediate release of silymarin

A1 Journal article (refereed)


Internal Authors/Editors


Publication Details

List of Authors: Ibrahim AH, Rosqvist E, Smått J-H, Ibrahim HM, Ismael HR, Afouna MI, Samy AM, Rosenholm JM
Publisher: Elsevier
Publication year: 2019
Journal: International Journal of Pharmaceutics
Volume number: 563
Start page: 217
End page: 227
ISSN: 0378-5173


Abstract

Silymarin (SLM) is a hepatoprotective herbal drug characterized by low aqueous solubility and, consequently, low oral bioavailability. The objective of this study was to enhance the physiochemical properties of SLM, through preparation and optimization of lyophilized nanosuspension tablets (LNTs). LNTs were prepared by sonoprecipitation technique followed by a freeze-drying process using both polyvinyl alcohol (PVA) as stabilizer and binder, and mannitol as cryoprotectant and disintegrating agent. 32 full factorial design (FFD) was applied to study the effect of independent variables at different concentrations of both PVA (X1) and mannitol (X2) on the dependent variables that included mean particle size (Y1), disintegration time (Y2), friability % (Y3) and time required to release 90% of the drug (Y4). Several physicochemical evaluations were implemented on the optimized formula; for instance differential scanning calorimetry, X-ray diffractometry, Fourier transform infrared spectroscopy, scanning electron microscopy and transmission electron microscopy. These analyses demonstrated that the drug was in an amorphous state, stable in nanosize range and displayed no chemical interaction with the polymer. Moreover, the optimized formula had highly porous structure, rapid disintegration, friability with less than 1% and noticeable improvement in saturation solubility and dissolution rate.


Last updated on 2020-31-03 at 04:00