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Budesonide-Loaded Hyaluronic Acid Nanoparticles for Targeted Delivery to the Inflamed Intestinal Mucosa in a Rodent Model of Colitis

The aim of the present study was to investigate the therapeutic potential of budesonide- (BDS-) loaded hyaluronic acid nanoparticles (HANPs) for treatment of inflammatory bowel disease (IBD) using an acute model of colitis in rats. The therapeutic efficacy of BDS-loaded HANPs in comparison with an a...

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Autores principales: Vafaei, Seyed Yaser, Abdolghaffari, Amir Hossein, Mahjub, Reza, Eslami, Seyyed Majid, Esmaeili, Motahareh, Abdollahi, Mohammad, Atyabi, Fatemeh, Dinarvand, Rassoul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532096/
https://www.ncbi.nlm.nih.gov/pubmed/36203483
http://dx.doi.org/10.1155/2022/7776092
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author Vafaei, Seyed Yaser
Abdolghaffari, Amir Hossein
Mahjub, Reza
Eslami, Seyyed Majid
Esmaeili, Motahareh
Abdollahi, Mohammad
Atyabi, Fatemeh
Dinarvand, Rassoul
author_facet Vafaei, Seyed Yaser
Abdolghaffari, Amir Hossein
Mahjub, Reza
Eslami, Seyyed Majid
Esmaeili, Motahareh
Abdollahi, Mohammad
Atyabi, Fatemeh
Dinarvand, Rassoul
author_sort Vafaei, Seyed Yaser
collection PubMed
description The aim of the present study was to investigate the therapeutic potential of budesonide- (BDS-) loaded hyaluronic acid nanoparticles (HANPs) for treatment of inflammatory bowel disease (IBD) using an acute model of colitis in rats. The therapeutic efficacy of BDS-loaded HANPs in comparison with an aqueous suspension of the drug with the same dose (30 μg/kg) was investigated 48 h following induction of colitis by intrarectal administration of acetic acid 4% in rats. Microscopic and histopathologic examinations were conducted in inflamed colonic tissue. Tissue concentration of tumor necrosis factor (TNF)-α was assessed by ELISA assay kit, while the activity of myeloperoxidase (MPO) was measured spectrophotometrically. Results from in vivo evaluations demonstrated that administrations of BDS-HANPs ameliorated the general endoscopic appearance, quite close to the healthy animals with no signs of inflammation and reduced the cellular infiltration, as well as the TNF-α level, and the MPO activity. It was found that delivery by BDS-loaded HANPSs alleviated the induced colitis significantly better than the same dose of the free drug. These data further suggest the potential of HANPs as a targeted drug delivery system to the inflamed colon mucosa.
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spelling pubmed-95320962022-10-05 Budesonide-Loaded Hyaluronic Acid Nanoparticles for Targeted Delivery to the Inflamed Intestinal Mucosa in a Rodent Model of Colitis Vafaei, Seyed Yaser Abdolghaffari, Amir Hossein Mahjub, Reza Eslami, Seyyed Majid Esmaeili, Motahareh Abdollahi, Mohammad Atyabi, Fatemeh Dinarvand, Rassoul Biomed Res Int Research Article The aim of the present study was to investigate the therapeutic potential of budesonide- (BDS-) loaded hyaluronic acid nanoparticles (HANPs) for treatment of inflammatory bowel disease (IBD) using an acute model of colitis in rats. The therapeutic efficacy of BDS-loaded HANPs in comparison with an aqueous suspension of the drug with the same dose (30 μg/kg) was investigated 48 h following induction of colitis by intrarectal administration of acetic acid 4% in rats. Microscopic and histopathologic examinations were conducted in inflamed colonic tissue. Tissue concentration of tumor necrosis factor (TNF)-α was assessed by ELISA assay kit, while the activity of myeloperoxidase (MPO) was measured spectrophotometrically. Results from in vivo evaluations demonstrated that administrations of BDS-HANPs ameliorated the general endoscopic appearance, quite close to the healthy animals with no signs of inflammation and reduced the cellular infiltration, as well as the TNF-α level, and the MPO activity. It was found that delivery by BDS-loaded HANPSs alleviated the induced colitis significantly better than the same dose of the free drug. These data further suggest the potential of HANPs as a targeted drug delivery system to the inflamed colon mucosa. Hindawi 2022-09-27 /pmc/articles/PMC9532096/ /pubmed/36203483 http://dx.doi.org/10.1155/2022/7776092 Text en Copyright © 2022 Seyed Yaser Vafaei et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vafaei, Seyed Yaser
Abdolghaffari, Amir Hossein
Mahjub, Reza
Eslami, Seyyed Majid
Esmaeili, Motahareh
Abdollahi, Mohammad
Atyabi, Fatemeh
Dinarvand, Rassoul
Budesonide-Loaded Hyaluronic Acid Nanoparticles for Targeted Delivery to the Inflamed Intestinal Mucosa in a Rodent Model of Colitis
title Budesonide-Loaded Hyaluronic Acid Nanoparticles for Targeted Delivery to the Inflamed Intestinal Mucosa in a Rodent Model of Colitis
title_full Budesonide-Loaded Hyaluronic Acid Nanoparticles for Targeted Delivery to the Inflamed Intestinal Mucosa in a Rodent Model of Colitis
title_fullStr Budesonide-Loaded Hyaluronic Acid Nanoparticles for Targeted Delivery to the Inflamed Intestinal Mucosa in a Rodent Model of Colitis
title_full_unstemmed Budesonide-Loaded Hyaluronic Acid Nanoparticles for Targeted Delivery to the Inflamed Intestinal Mucosa in a Rodent Model of Colitis
title_short Budesonide-Loaded Hyaluronic Acid Nanoparticles for Targeted Delivery to the Inflamed Intestinal Mucosa in a Rodent Model of Colitis
title_sort budesonide-loaded hyaluronic acid nanoparticles for targeted delivery to the inflamed intestinal mucosa in a rodent model of colitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532096/
https://www.ncbi.nlm.nih.gov/pubmed/36203483
http://dx.doi.org/10.1155/2022/7776092
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