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Bioadhesive Tannic-Acid-Functionalized Zein Coating Achieves Engineered Colonic Delivery of IBD Therapeutics via Reservoir Microdevices

The biggest challenge in oral delivery of anti-inflammatory drugs such as 5-aminosalicylic acid (5-ASA) is to (i) prevent rapid absorption in the small intestine and (ii) achieve localized release at the site of inflammation in the lower gut, i.e., the colon. Here, we present an advanced biopolymeri...

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Autores principales: Kamguyan, Khorshid, Kjeldsen, Rolf Bech, Moghaddam, Saeed Zajforoushan, Nielsen, Melanie Randahl, Thormann, Esben, Zór, Kinga, Nielsen, Line Hagner, Boisen, Anja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699562/
https://www.ncbi.nlm.nih.gov/pubmed/36432727
http://dx.doi.org/10.3390/pharmaceutics14112536
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author Kamguyan, Khorshid
Kjeldsen, Rolf Bech
Moghaddam, Saeed Zajforoushan
Nielsen, Melanie Randahl
Thormann, Esben
Zór, Kinga
Nielsen, Line Hagner
Boisen, Anja
author_facet Kamguyan, Khorshid
Kjeldsen, Rolf Bech
Moghaddam, Saeed Zajforoushan
Nielsen, Melanie Randahl
Thormann, Esben
Zór, Kinga
Nielsen, Line Hagner
Boisen, Anja
author_sort Kamguyan, Khorshid
collection PubMed
description The biggest challenge in oral delivery of anti-inflammatory drugs such as 5-aminosalicylic acid (5-ASA) is to (i) prevent rapid absorption in the small intestine and (ii) achieve localized release at the site of inflammation in the lower gut, i.e., the colon. Here, we present an advanced biopolymeric coating comprising of tannic-acid-functionalized zein protein to provide a sustained, colon-targeted release profile for 5-ASA and enhance the mucoadhesion of the dosage form via a mussel-inspired mechanism. To enable localized delivery and provide high local concentration, 5-ASA is loaded into the microfabricated drug carriers (microcontainers) and sealed with the developed coating. The functionality and drug release profile of the coating are characterized and optimized in vitro, showing great tunability, scalability, and stability toward proteases. Further, ex vivo experiments demonstrate that the tannic acid functionalization can significantly enhance the mucoadhesion of the coating, which is followed up by in vivo investigations on the intestinal retention, and pharmacokinetic evaluation of the 5-ASA delivery system. Results indicate that the developed coating can provide prolonged colonic delivery of 5-ASA. Therefore, the here-developed biodegradable coating can be an eco-friendly substitute to the state-of-the-art commercial counterparts for targeted delivery of 5-ASA and other small molecule drugs.
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spelling pubmed-96995622022-11-26 Bioadhesive Tannic-Acid-Functionalized Zein Coating Achieves Engineered Colonic Delivery of IBD Therapeutics via Reservoir Microdevices Kamguyan, Khorshid Kjeldsen, Rolf Bech Moghaddam, Saeed Zajforoushan Nielsen, Melanie Randahl Thormann, Esben Zór, Kinga Nielsen, Line Hagner Boisen, Anja Pharmaceutics Article The biggest challenge in oral delivery of anti-inflammatory drugs such as 5-aminosalicylic acid (5-ASA) is to (i) prevent rapid absorption in the small intestine and (ii) achieve localized release at the site of inflammation in the lower gut, i.e., the colon. Here, we present an advanced biopolymeric coating comprising of tannic-acid-functionalized zein protein to provide a sustained, colon-targeted release profile for 5-ASA and enhance the mucoadhesion of the dosage form via a mussel-inspired mechanism. To enable localized delivery and provide high local concentration, 5-ASA is loaded into the microfabricated drug carriers (microcontainers) and sealed with the developed coating. The functionality and drug release profile of the coating are characterized and optimized in vitro, showing great tunability, scalability, and stability toward proteases. Further, ex vivo experiments demonstrate that the tannic acid functionalization can significantly enhance the mucoadhesion of the coating, which is followed up by in vivo investigations on the intestinal retention, and pharmacokinetic evaluation of the 5-ASA delivery system. Results indicate that the developed coating can provide prolonged colonic delivery of 5-ASA. Therefore, the here-developed biodegradable coating can be an eco-friendly substitute to the state-of-the-art commercial counterparts for targeted delivery of 5-ASA and other small molecule drugs. MDPI 2022-11-21 /pmc/articles/PMC9699562/ /pubmed/36432727 http://dx.doi.org/10.3390/pharmaceutics14112536 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kamguyan, Khorshid
Kjeldsen, Rolf Bech
Moghaddam, Saeed Zajforoushan
Nielsen, Melanie Randahl
Thormann, Esben
Zór, Kinga
Nielsen, Line Hagner
Boisen, Anja
Bioadhesive Tannic-Acid-Functionalized Zein Coating Achieves Engineered Colonic Delivery of IBD Therapeutics via Reservoir Microdevices
title Bioadhesive Tannic-Acid-Functionalized Zein Coating Achieves Engineered Colonic Delivery of IBD Therapeutics via Reservoir Microdevices
title_full Bioadhesive Tannic-Acid-Functionalized Zein Coating Achieves Engineered Colonic Delivery of IBD Therapeutics via Reservoir Microdevices
title_fullStr Bioadhesive Tannic-Acid-Functionalized Zein Coating Achieves Engineered Colonic Delivery of IBD Therapeutics via Reservoir Microdevices
title_full_unstemmed Bioadhesive Tannic-Acid-Functionalized Zein Coating Achieves Engineered Colonic Delivery of IBD Therapeutics via Reservoir Microdevices
title_short Bioadhesive Tannic-Acid-Functionalized Zein Coating Achieves Engineered Colonic Delivery of IBD Therapeutics via Reservoir Microdevices
title_sort bioadhesive tannic-acid-functionalized zein coating achieves engineered colonic delivery of ibd therapeutics via reservoir microdevices
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699562/
https://www.ncbi.nlm.nih.gov/pubmed/36432727
http://dx.doi.org/10.3390/pharmaceutics14112536
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