Tailored beads made of dissolved cellulose—investigation of their drug release properties

A1 Journal article (refereed)


Internal Authors/Editors


Publication Details

List of Authors: Emrah Yildir, Ruzica Kolakovic, Natalja Genina, Jani Trygg, Martin Gericke, Leena Hanski, Henrik Ehlers, Jukka Rantanen, Mikko Tenho, Pia Vuorela, Pedro Fardim, Niklas Sandler
Publication year: 2013
Journal: International Journal of Pharmaceutics
Journal acronym: Int J Pharm
Volume number: 456
Issue number: 2
Start page: 417
End page: 423
ISSN: 1873-3476
eISSN: 1873-3476


Abstract

In the frame of this work, we have investigated drug entrapping and release abilities of new type of porous cellulose beads (CBs) as a spherical matrix system for drug delivery. For that purpose, CBs prepared with three different methods were used as drug carriers and three compounds, anhydrous theophylline (Thp), riboflavin 5'-phosphate sodium (RSP) and lidocaine hydrochloride monohydrate (LiHCl) were used as model drug substances. The loading procedure was carried out by immersing swollen empty beads into the solutions of different concentrations of model drugs. The morphology of empty and loaded beads was examined using a field emission scanning electron microscopy (FE-SEM). Near-infrared (NIR) imaging was performed to identify the drug distributions on and within the loaded CBs. The drug amount incorporated into CBs was examined spectrophotometrically and in vitro drug release studies were performed to determine the drug release rates. The results of FE-SEM and chemical NIR imaging analyses revealed that incorporated drug were distributed on the surface and but also within the internal structure of the CBs. Physical properties of CBs and solubility of model drugs had effect on loading efficacy. Also, the drug release rates were controlled by solubility of model drugs (diffusion controlled release). In conclusion, CBs from dissolved cellulose show promise in achieving controlled drug delivery.

Last updated on 2019-19-10 at 04:30