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European Congress of Chemical Engineering - 6
Copenhagen 16-21 September 2007

Abstract 2419 - Protein-based drugs encapsulation in biodegradable microparticles by co-axial electrospray

Protein-based drugs encapsulation in biodegradable microparticles by co-axial electrospray

Multi-scale and/or multi-disciplinary approach to process-product innovation

Controlled Release of the Active Ingredient: Mechanisms, Devices & Analysis (T3-2P)

Asc. Prof Chi-Hwa Wang
National University of Singapore
Chemical and Biomolecular Engineering
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4
Singapore 117576
Singapore

Mr Jingwei Xie
National University of Singapore
Chemical and Biomolecular Engineering
National University of Singapore
4 Engineering Drive 4
Singapore 117576
Singapore

Mrs Lai Yeng Lee
National University of Singapore
Chemical and Biomolecular Engineering
National University of Singapore
4 Engineering Drive 4
Singapore 117576
Singapore

Keywords: co-axial, electrospray, encapsulation, drug delivery.

A co-axial electrospray process was developed to encapsulate protein-based drugs in biodegradable polymeric microparticles eliminating the key problem faced by other conventional methods of protein encapsulation – the primary emulsion being a major cause for protein denaturation and aggregation. Bovine serum albumin (BSA) and lysozyme were chosen as model protein drugs for this study. Scanning electron microscopy observation of the morphology of particles showed spherical microparticles of several microns could be achieved. The in vitro release profiles measured using Micro BCA assay suggested that sustained release of proteins could be attained for more than 30 days. The results of circular dichroism suggest that the secondary structure of released BSA can be retained. The bioactivity of released lysozyme was found to be more than 90%. Therefore, co-axial electrospray could be a very promising approach to encapsulate biomacromolecules such as proteins, enzymes, DNA plasmids or living cells inside microparticles for the controlled release drug delivery applications.

Presented Tuesday 18, 13:30 to 15:00, in session Controlled Release of the Active Ingredient: Mechanisms, Devices & Analysis (T3-2P).

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