Preparation andIn VitroRelease of Drug-Loaded Microparticles for Oral Delivery Using Wholegrain Sorghum Kafirin Protein

Author:

Lau Esther T. L.12,Johnson Stuart K.3,Stanley Roger A.456,Mikkelsen Deirdre47,Fang Zhongxiang3,Halley Peter J.8,Steadman Kathryn J.14

Affiliation:

1. School of Pharmacy, University of Queensland, Brisbane, QLD 4072, Australia

2. School of Clinical Sciences, Queensland University of Technology, Brisbane, QLD 4000, Australia

3. Nutrition, Dietetics and Food Technology, School of Public Health, Faculty of Health Sciences, Curtin University, Perth, WA 6845, Australia

4. Centre for Nutrition and Food Sciences, Queensland Alliance for Agriculture and Food Innovation, University of Queensland, Brisbane, QLD 4072, Australia

5. Innovative Food Solutions & Technologies, Department of Agriculture, Fisheries and Forestry, Brisbane, QLD 4108, Australia

6. Centre for Food Innovation, University of Tasmania, Hobart, TAS 7001, Australia

7. ARC Centre of Excellence in Plant Cell Walls, University of Queensland, Brisbane, QLD 4072, Australia

8. Australian Institute for Bioengineering and Nanotechnology and School of Chemical Engineering, University of Queensland, Brisbane, QLD 4072, Australia

Abstract

Kafirin microparticles have been proposed as an oral nutraceutical and drug delivery system. This study investigates microparticles formed with kafirin extracted from white and raw versus cooked red sorghum grains as an oral delivery system. Targeted delivery to the colon would be beneficial for medication such as prednisolone, which is used in the management of inflammatory bowel disease. Therefore, prednisolone was loaded into microparticles of kafirin from the different sources using phase separation. Differences were observed in the protein content,in vitroprotein digestibility, and protein electrophoretic profile of the various sources of sorghum grains, kafirin extracts, and kafirin microparticles. For all of the formulations, the majority of the loaded prednisolone was not released inin vitroconditions simulating the upper gastrointestinal tract, indicating that most of the encapsulated drug could reach the target area of the lower gastrointestinal tract. This suggests that these kafirin microparticles may have potential as a colon-targeted nutraceutical and drug delivery system.

Funder

Industry Science and Research Indo-Australian Biotechnology Fund

Publisher

Hindawi Limited

Subject

Polymers and Plastics

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