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Targeted Release of Probiotics from Enteric Microparticulated Formulations

The development of advanced probiotic delivery systems, which preserve bacteria from degradation of the gastrointestinal tract and achieve a targeted release mediated by pH-independent swelling, is of great interest to improve the efficient delivery of probiotic bacteria to the target tissue. Gram-p...

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Autores principales: Yus, Cristina, Gracia, Ruben, Larrea, Ane, Andreu, Vanesa, Irusta, Silvia, Sebastian, Victor, Mendoza, Gracia, Arruebo, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835770/
https://www.ncbi.nlm.nih.gov/pubmed/31614915
http://dx.doi.org/10.3390/polym11101668
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author Yus, Cristina
Gracia, Ruben
Larrea, Ane
Andreu, Vanesa
Irusta, Silvia
Sebastian, Victor
Mendoza, Gracia
Arruebo, Manuel
author_facet Yus, Cristina
Gracia, Ruben
Larrea, Ane
Andreu, Vanesa
Irusta, Silvia
Sebastian, Victor
Mendoza, Gracia
Arruebo, Manuel
author_sort Yus, Cristina
collection PubMed
description The development of advanced probiotic delivery systems, which preserve bacteria from degradation of the gastrointestinal tract and achieve a targeted release mediated by pH-independent swelling, is of great interest to improve the efficient delivery of probiotic bacteria to the target tissue. Gram-positive and Gram-negative bacteria models (Lactobacillus acidophilus (Moro) Hansen and Mocquot (ATCC® 4356™) and Escherichia coli S17, respectively) have been successfully encapsulated for the first time in pH-independent microparticulate polymethacrylates (i.e., Eudraguard biotic) used for the targeted delivery of nutraceuticals to the colon. These bacteria have also been encapsulated within the mucoadhesive polymethacrylate Eudragit RS 100 widely used as targeted release formulation for active pharmaceutical ingredients. The enteric microparticles remained unaltered under simulated gastric conditions and released the contained viable microbial cargo under simulated intestinal conditions. Buoyancies of 90.2% and 57.3% for Eudragit and Eudraguard microparticles, respectively, and long-term stability (5 months) for the encapsulated microorganisms were found. Cytotoxicity of the microparticles formulated with both polymers was evaluated (0.5–20 mg/mL) on Caco-2 cells, showing high cytocompatibility. These results underline the suitability of the synthesized materials for the successful delivery of probiotic formulations to the target organ, highlighting for the first time the potential use of Eudraguard biotic as an effective enteric coating for the targeted delivery of probiotics.
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spelling pubmed-68357702019-11-25 Targeted Release of Probiotics from Enteric Microparticulated Formulations Yus, Cristina Gracia, Ruben Larrea, Ane Andreu, Vanesa Irusta, Silvia Sebastian, Victor Mendoza, Gracia Arruebo, Manuel Polymers (Basel) Article The development of advanced probiotic delivery systems, which preserve bacteria from degradation of the gastrointestinal tract and achieve a targeted release mediated by pH-independent swelling, is of great interest to improve the efficient delivery of probiotic bacteria to the target tissue. Gram-positive and Gram-negative bacteria models (Lactobacillus acidophilus (Moro) Hansen and Mocquot (ATCC® 4356™) and Escherichia coli S17, respectively) have been successfully encapsulated for the first time in pH-independent microparticulate polymethacrylates (i.e., Eudraguard biotic) used for the targeted delivery of nutraceuticals to the colon. These bacteria have also been encapsulated within the mucoadhesive polymethacrylate Eudragit RS 100 widely used as targeted release formulation for active pharmaceutical ingredients. The enteric microparticles remained unaltered under simulated gastric conditions and released the contained viable microbial cargo under simulated intestinal conditions. Buoyancies of 90.2% and 57.3% for Eudragit and Eudraguard microparticles, respectively, and long-term stability (5 months) for the encapsulated microorganisms were found. Cytotoxicity of the microparticles formulated with both polymers was evaluated (0.5–20 mg/mL) on Caco-2 cells, showing high cytocompatibility. These results underline the suitability of the synthesized materials for the successful delivery of probiotic formulations to the target organ, highlighting for the first time the potential use of Eudraguard biotic as an effective enteric coating for the targeted delivery of probiotics. MDPI 2019-10-13 /pmc/articles/PMC6835770/ /pubmed/31614915 http://dx.doi.org/10.3390/polym11101668 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yus, Cristina
Gracia, Ruben
Larrea, Ane
Andreu, Vanesa
Irusta, Silvia
Sebastian, Victor
Mendoza, Gracia
Arruebo, Manuel
Targeted Release of Probiotics from Enteric Microparticulated Formulations
title Targeted Release of Probiotics from Enteric Microparticulated Formulations
title_full Targeted Release of Probiotics from Enteric Microparticulated Formulations
title_fullStr Targeted Release of Probiotics from Enteric Microparticulated Formulations
title_full_unstemmed Targeted Release of Probiotics from Enteric Microparticulated Formulations
title_short Targeted Release of Probiotics from Enteric Microparticulated Formulations
title_sort targeted release of probiotics from enteric microparticulated formulations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835770/
https://www.ncbi.nlm.nih.gov/pubmed/31614915
http://dx.doi.org/10.3390/polym11101668
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