Synthesis and characterization of alginate/poly-L-ornithine/alginate microcapsules for local immunosuppression
Autor: | Andy Leung, Matt Trau, Gwen Lawrie, Lars K. Nielsen |
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Rok vydání: | 2008 |
Předmět: |
Streptavidin
Materials science Alginates Surface Properties Chemistry Pharmaceutical Pharmaceutical Science Capsules Bioengineering chemistry.chemical_compound Drug Delivery Systems Colloid and Surface Chemistry Glucuronic Acid Fluorescence microscope Humans Biotinylation Physical and Theoretical Chemistry Microparticle Carbodiimide Microscopy Confocal Tumor Necrosis Factor-alpha Hexuronic Acids Organic Chemistry Ornithine Cross-Linking Reagents Membrane Microscopy Fluorescence chemistry Biochemistry Drug Design Biophysics Surface modification Peptides Azo Compounds Immunosuppressive Agents |
Zdroj: | Journal of Microencapsulation. 25:387-398 |
ISSN: | 1464-5246 0265-2048 |
DOI: | 10.1080/02652040802008857 |
Popis: | Alginate/poly-L-ornithine/alginate (APA) coherent microencapsulation, which provides an immunoselective and highly biocompatible membrane, creates a viable option for cellular or tissue transplantation. This study explored the potential of incorporating immunosuppressive drugs onto the capsule surface to provide local immunosuppression in addition to immunoisolation. A thorough investigation has been conducted to optimize and characterize alginate biotinylation via carbodiimide chemistry by a 4'-hydroxyazobenzene-2-carboxylic acid (HABA) based assay and by ATR-FTIR, H-NMR and XPS. To minimize the formation of by-product, a theoretical 40% activation of the carboxylic group on the alginate was employed to manufacture an optimal modification of approximately 10% biotinylated alginate. Confocal fluorescence microscopy was used to assess the conjugation of streptavidin and assembly of antibodies on the microcapsules. Local immunosuppressive capacity was assimilated on the APA microcapsules by binding of anti-tumour necrosis factor-alpha (TNF-alpha) antibodies via streptavidin-biotin conjugation, shown from the clear reduction of TNF-alpha in in-vitro medium. |
Databáze: | OpenAIRE |
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