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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...

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Autores principales: Dasgupta, Indrani, Tanifum, Eric A., Srivastava, Mayank, Phatak, Sharangdhar S., Cavasotto, Claudio N., Analoui, Mostafa, Annapragada, Ananth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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