Shaunak, Sunil, Thomas, Sharyn, Gianasi, Elisabetta, Godwin, Antony, Jones, Emma, Teo, Ian, Mireskandari, Kamiar, Luthert, Philip, Duncan, Ruth, Patterson, Steve, Khaw, Peng and Brocchini, Steve 2004. Polyvalent dendrimer glucosamine conjugates prevent scar tissue formation. Nature Biotechnology 22 (8) , pp. 977-984. 10.1038/nbt995 |
Abstract
Dendrimers are hyperbranched macromolecules that can be chemically synthesized to have precise structural characteristics. We used anionic, polyamidoamine, generation 3.5 dendrimers to make novel water-soluble conjugates of D(+)-glucosamine and D(+)-glucosamine 6-sulfate with immuno-modulatory and antiangiogenic properties respectively. Dendrimer glucosamine inhibited Toll-like receptor 4–mediated lipopolysaccharide induced synthesis of pro-inflammatory chemokines (MIP-1alpha, MIP-1beta, IL-8) and cytokines (TNF-alpha, IL-1beta, IL-6) from human dendritic cells and macrophages but allowed upregulation of the costimulatory molecules CD25, CD80, CD83 and CD86. Dendrimer glucosamine 6-sulfate blocked fibroblast growth factor-2 mediated endothelial cell proliferation and neoangiogenesis in human Matrigel and placental angiogenesis assays. When dendrimer glucosamine and dendrimer glucosamine 6-sulfate were used together in a validated and clinically relevant rabbit model of scar tissue formation after glaucoma filtration surgery, they increased the long-term success of the surgery from 30% to 80% (P = 0.029). We conclude that synthetically engineered macromolecules such as the dendrimers described here can be tailored to have defined immuno-modulatory and antiangiogenic properties, and they can be used synergistically to prevent scar tissue formation.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Schools > Pharmacy |
ISSN: | 10870156 |
Last Modified: | 23 Mar 2017 02:33 |
URI: | https://orca.cardiff.ac.uk/id/eprint/909 |
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