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Impact of biopolymers chemical heterogeneity on drug release from | 17530
Journal of Chemical Engineering & Process Technology

Journal of Chemical Engineering & Process Technology
Open Access

ISSN: 2157-7048

+44-20-4587-4809

Impact of biopolymers chemical heterogeneity on drug release from matrix formulations - An experimental study combined with simulations of the drug release


International Conference on Chemical Engineering

September 12-14, 2016 Phoenix, USA

Anette Larsson

Chalmers University of Technology, Sweden

Scientific Tracks Abstracts: J Chem Eng Process Technol

Abstract :

A common way to control the release of drugs is to mix the drug with hydrophilic polymers and compact the mixture to tablets. The water ingresses in the hydrophilic matrix tablets leads to a slow gradual dissolution of the polymer and the dry polymer in the core of the tablet protects the active substance from being dissolved and released. A preferred biopolymer for such formulations is hydroxypropyl methyl cellulose, HPMC, which is available in many pharmaceutical approved grades. The HPMC�?´s molecular weight (SEC/RI/MALLS), degree of substitution (NMR) and substitution pattern (enzymatic degradation) along the cellulose backbone were characterized and by combining these data with release experiments, magnetic resonance imaging of HPMC tablets and computer simulations, we were able to show that the interactions between HPMC and water depend strongly on HPMC�?´s substitution pattern and this gave that: 1) The drug and polymer release rates were different with 20 and 100 h to completely eroded tablets for homogeneous and heterogeneous HPMC batches, respectively; 2) The formulations with the heterogeneous HPMC batch swelled almost a factor of two more compared to formulation of the more homogenous HPMC batch; and 3) The distribution of water in the swollen matrix tablets was more flat for water concentration of 60 w/w% water and above for the heterogeneous batch than for the homogenous batch. Based on this one can conclude that the substitution pattern for biopolymers like HPMC, as well as the molecular weight and degree of substitution, have large influences on the functionality of the polymers.

Biography :

Anette Larsson has completed her PhD from Chalmers University of Technology in the year 1995. She has worked for seven years as an Associate Principal Scientist at AstraZeneca. Since 2003, she is leading a Pharmaceutical Technology group. Since 2012, she is the Director of SuMo BIOMATERIALS, an industry academy research consortium with six industrial partners and one institute. She has published more than 60 papers in reputed journals and has been serving as an evaluator regularly for PhD grades and academic promotion committees.

Email: anette.larsson@chalmers.se

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