Weissman, Jonathan S ; Maji, Samir K ; Schubert, David ; Rivier, Catherine ; Lee, Soon ; Rivier, Jean E ; Riek, Roland (2008) Amyloid as a Depot for the Formulation of Long-Acting Drugs PLoS Biology, 6 (2). e17. ISSN 1545-7885
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Official URL: http://doi.org/10.1371/journal.pbio.0060017
Related URL: http://dx.doi.org/10.1371/journal.pbio.0060017
Abstract
Amyloids are highly organized protein aggregates that are associated with both neurodegenerative diseases such as Alzheimer disease and benign functions like skin pigmentation. Amyloids self-polymerize in a nucleation-dependent manner by recruiting their soluble protein/peptide counterpart and are stable against harsh physical, chemical, and biochemical conditions. These extraordinary properties make amyloids attractive for applications in nanotechnology. Here, we suggest the use of amyloids in the formulation of long-acting drugs. It is our rationale that amyloids have the properties required of a long-acting drug because they are stable depots that guarantee a controlled release of the active peptide drug from the amyloid termini. This concept is tested with a family of short- and long-acting analogs of gonadotropin-releasing hormone (GnRH), and it is shown that amyloids thereof can act as a source for the sustained release of biologically active peptides.
Item Type: | Article |
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Source: | Copyright of this article belongs to Maji et al |
ID Code: | 126603 |
Deposited On: | 31 Oct 2022 04:25 |
Last Modified: | 31 Oct 2022 04:25 |
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