dc.creator | Dasgupta, Indrani | |
dc.creator | Tanifum, Eric A. | |
dc.creator | Srivastava, Mayank | |
dc.creator | Phatak, Sharangdhar S. | |
dc.creator | Cavasotto, Claudio Norberto | |
dc.creator | Analoui, Mostafa | |
dc.creator | Annapragada, Ananth | |
dc.date.accessioned | 2019-01-29T21:00:08Z | |
dc.date.accessioned | 2022-10-15T00:13:00Z | |
dc.date.available | 2019-01-29T21:00:08Z | |
dc.date.available | 2022-10-15T00:13:00Z | |
dc.date.created | 2019-01-29T21:00:08Z | |
dc.date.issued | 2012-01 | |
dc.identifier | Dasgupta, Indrani; Tanifum, Eric A.; Srivastava, Mayank; Phatak, Sharangdhar S.; Cavasotto, Claudio Norberto; et al.; Non inflammatory boronate based glucose-responsive insulin delivery systems; Public Library of Science; Plos One; 7; 1; 1-2012; 1-11; e29585 | |
dc.identifier | http://hdl.handle.net/11336/68938 | |
dc.identifier | 1932-6203 | |
dc.identifier | CONICET Digital | |
dc.identifier | CONICET | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4323408 | |
dc.description.abstract | Boronic acids, known to bind diols, were screened to identify non-inflammatory cross-linkers for the preparation of glucose sensitive and insulin releasing agglomerates of liposomes (Agglomerated Vesicle Technology-AVT). This was done in order to select a suitable replacement for the previously used cross-linker, ConcanavalinA (ConA), a lectin known to have both toxic and inflammatory effects in vivo. Lead-compounds were selected from screens that involved testing for inflammatory potential, cytotoxicity and glucose-binding. These were then conjugated to insulin-encapsulating nanoparticles and agglomerated via sugar-boronate ester linkages to form AVTs. In vitro, the particles demonstrated triggered release of insulin upon exposure to physiologically relevant concentrations of glucose (10 mmoles/L-40 mmoles/L). The agglomerates were also shown to be responsive to multiple spikes in glucose levels over several hours, releasing insulin at a rate defined by the concentration of the glucose trigger. | |
dc.language | eng | |
dc.publisher | Public Library of Science | |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1371/journal.pone.0029585 | |
dc.relation | info:eu-repo/semantics/altIdentifier/url/https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0029585 | |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Drug delivery | |
dc.subject | Insulin delivery systems | |
dc.subject | Inflamation | |
dc.subject | Boronates | |
dc.title | Non inflammatory boronate based glucose-responsive insulin delivery systems | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:ar-repo/semantics/artículo | |
dc.type | info:eu-repo/semantics/publishedVersion | |