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    Preparation and In Vitro Release of Drug-Loaded Microparticlesfor Oral Delivery Using Wholegrain Sorghum Kafirin Protein

    226918_160258_Lau_et_al_2015_IntJPolySci.pdf (2.018Mb)
    Access Status
    Open access
    Authors
    Lau, E.
    Johnson, Stuart
    Stanley, R.
    Mikkelsen, D.
    Fang, Zhongxiang
    Halley, P.
    Steadman, K.
    Date
    2015
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Lau, E. and Johnson, S. and Stanley, R. and Mikkelsen, D. and Fang, Z. and Halley, P. and Steadman, K. 2015. Preparation and In Vitro Release of Drug-Loaded Microparticlesfor Oral Delivery Using Wholegrain Sorghum Kafirin Protein. International Journal of Polymer Science. 2015: Article ID 343647.
    Source Title
    International Journal of Polymer Science
    DOI
    10.1155/2015/343647
    ISSN
    1687-9422
    School
    School of Public Health
    Remarks

    This open access article is distributed under the Creative Commons license http://creativecommons.org/licenses/by/3.0/

    URI
    http://hdl.handle.net/20.500.11937/40510
    Collection
    • Curtin Research Publications
    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 vitro protein 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 in in vitro conditions 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.

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    • Formulation and Characterization of Drug-Loaded Microparticles Using Distillers Dried Grain Kafirin
      Lau, E.; Johnson, Stuart; Stanley, R.; Mereddy, R.; Mikkelsen, D.; Halley, P.; Steadman, K. (2015)
      Kafirin, a protein extracted from sorghum grain, has been formulated into microparticles and proposed for use as a delivery system owing to the resistance of kafirin to upper gastrointestinal digestion. However, extracting ...
    • Optimizing prednisolone loading into distiller’s dried grain kafirin microparticles, and in vitro release for oral delivery
      Lau, E.; Johnson, Stuart; Williams, B.; Mikkelsen, D.; McCourt, E.; Stanley, R.; Mereddy, R.; Halley, P.; Steadman, K. (2017)
      Kafirin microparticles have potential as colon-targeted delivery systems because of their ability to protect encapsulated material from digestive processes of the upper gastrointestinal tract (GIT). The aim was to optimize ...
    • Encapsulation of hydrocortisone and mesalazine in zein microparticles
      Lau, E.; Giddings, S.; Mohammed, S.; Dubois, Paul; Johnson, Stuart; Stanley, R.; Halley, P.; Steadman, K. (2013)
      Zein was investigated for use as an oral-drug delivery system by loading prednisolone into zein microparticles using coacervation. To investigate the adaptability of this method to other drugs, zein microparticles were ...
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