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Non Inflammatory Boronate Based Glucose-Responsive Insulin Delivery Systems
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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260138/ https://www.ncbi.nlm.nih.gov/pubmed/22272238 http://dx.doi.org/10.1371/journal.pone.0029585 |
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author | Dasgupta, Indrani Tanifum, Eric A. Srivastava, Mayank Phatak, Sharangdhar S. Cavasotto, Claudio N. Analoui, Mostafa Annapragada, Ananth |
author_facet | Dasgupta, Indrani Tanifum, Eric A. Srivastava, Mayank Phatak, Sharangdhar S. Cavasotto, Claudio N. Analoui, Mostafa Annapragada, Ananth |
author_sort | Dasgupta, Indrani |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3260138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32601382012-01-23 Non Inflammatory Boronate Based Glucose-Responsive Insulin Delivery Systems Dasgupta, Indrani Tanifum, Eric A. Srivastava, Mayank Phatak, Sharangdhar S. Cavasotto, Claudio N. Analoui, Mostafa Annapragada, Ananth PLoS One Research Article 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. Public Library of Science 2012-01-17 /pmc/articles/PMC3260138/ /pubmed/22272238 http://dx.doi.org/10.1371/journal.pone.0029585 Text en Dasgupta et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Dasgupta, Indrani Tanifum, Eric A. Srivastava, Mayank Phatak, Sharangdhar S. Cavasotto, Claudio N. Analoui, Mostafa Annapragada, Ananth Non Inflammatory Boronate Based Glucose-Responsive Insulin Delivery Systems |
title | Non Inflammatory Boronate Based Glucose-Responsive Insulin Delivery Systems |
title_full | Non Inflammatory Boronate Based Glucose-Responsive Insulin Delivery Systems |
title_fullStr | Non Inflammatory Boronate Based Glucose-Responsive Insulin Delivery Systems |
title_full_unstemmed | Non Inflammatory Boronate Based Glucose-Responsive Insulin Delivery Systems |
title_short | Non Inflammatory Boronate Based Glucose-Responsive Insulin Delivery Systems |
title_sort | non inflammatory boronate based glucose-responsive insulin delivery systems |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260138/ https://www.ncbi.nlm.nih.gov/pubmed/22272238 http://dx.doi.org/10.1371/journal.pone.0029585 |
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