Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/995
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dc.contributor.authorGupta, Sarika-
dc.contributor.authorChattopadhyay, Tandrika-
dc.contributor.authorSingh, Mahendra Pal-
dc.contributor.authorSurolia, Avadhesha-
dc.date.accessioned2017-10-24T08:26:23Z-
dc.date.available2017-10-24T08:26:23Z-
dc.date.issued2010-07-
dc.identifier.urihttp://hdl.handle.net/123456789/995-
dc.description.abstractDiabetes is a chronic disease requiring continuous medical supervision and patient education to prevent acute secondary complications. In this study, we have harnessed the inherent property of insulin to aggregate into an oligomeric intermediate on the pathway to amyloid formation, to generate a form that exhibits controlled and sustained release for extended periods. Administration of a single dose of the insulin oligomer, defined here as the supramolecular insulin assembly II (SIA-II), to experimental animals rendered diabetic by streptozotocin or alloxan, released the hormone capable of maintaining physiologic glucose levels for >120 days for bovine and >140 days for recombinant human insulin without fasting hypoglycemia. Moreover, the novel SIA-II described here not only improved the glycemic control, but also reduced the extent of secondary diabetic complications.en_US
dc.publisherPNAS Online, HighWire Pressen_US
dc.titleSupramolecular insulin assembly II for a sustained treatment of type 1 diabetes mellitusen_US
dc.keywordprotein folding, hyperglycemia, normoglycemia, insulin-like growth factor-1en_US
dc.journalProceedings of the National Academy of Sciences of the United States of Americaen_US
dc.volumeno107en_US
dc.issueno30en_US
dc.pages13246-13251en_US
Appears in Collections:Molecular Sciences, Publications

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