Cargando…

Fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model

Overdosage of antibiotics used to prevent bacterial infections in the human and animal gastrointestinal tract would result in disturbing of intestinal barrier, significant misbalancing effects of intestinal microflora and persuading bacterial resistance. The main objective of the present investigati...

Descripción completa

Detalles Bibliográficos
Autores principales: Wan, Xiao, Liu, Liu, Ding, Lu, Zhu, Zhiqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9255213/
https://www.ncbi.nlm.nih.gov/pubmed/35766146
http://dx.doi.org/10.1080/10717544.2022.2081381
_version_ 1784740878625013760
author Wan, Xiao
Liu, Liu
Ding, Lu
Zhu, Zhiqiang
author_facet Wan, Xiao
Liu, Liu
Ding, Lu
Zhu, Zhiqiang
author_sort Wan, Xiao
collection PubMed
description Overdosage of antibiotics used to prevent bacterial infections in the human and animal gastrointestinal tract would result in disturbing of intestinal barrier, significant misbalancing effects of intestinal microflora and persuading bacterial resistance. The main objective of the present investigation is to design and develop novel combinations of organic curcumin (Cur) and antimicrobial peptide (Amp) loaded chitosan nanoformulations (Cur/Amp@CS NPs) to improve significant effects on antibacterial action, immune response, intestine morphology, and intentional microflora. The antibacterial efficiency of the prepared nanoformulations was evaluated using Escherichia coli (E. coli) induced bacterial infections in GUT of Rat models. Further, we studied the cytocompatibility, inflammatory responses, α-diversity, intestinal morphology, and immune responses of treated nanoformulations in rat GUT models. The results indicated that Cur/Amp@CS NPs are greatly beneficial for intestinal microflora and could be a prodigious alternative of antibiotics.
format Online
Article
Text
id pubmed-9255213
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-92552132022-07-06 Fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model Wan, Xiao Liu, Liu Ding, Lu Zhu, Zhiqiang Drug Deliv Research Article Overdosage of antibiotics used to prevent bacterial infections in the human and animal gastrointestinal tract would result in disturbing of intestinal barrier, significant misbalancing effects of intestinal microflora and persuading bacterial resistance. The main objective of the present investigation is to design and develop novel combinations of organic curcumin (Cur) and antimicrobial peptide (Amp) loaded chitosan nanoformulations (Cur/Amp@CS NPs) to improve significant effects on antibacterial action, immune response, intestine morphology, and intentional microflora. The antibacterial efficiency of the prepared nanoformulations was evaluated using Escherichia coli (E. coli) induced bacterial infections in GUT of Rat models. Further, we studied the cytocompatibility, inflammatory responses, α-diversity, intestinal morphology, and immune responses of treated nanoformulations in rat GUT models. The results indicated that Cur/Amp@CS NPs are greatly beneficial for intestinal microflora and could be a prodigious alternative of antibiotics. Taylor & Francis 2022-06-29 /pmc/articles/PMC9255213/ /pubmed/35766146 http://dx.doi.org/10.1080/10717544.2022.2081381 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wan, Xiao
Liu, Liu
Ding, Lu
Zhu, Zhiqiang
Fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model
title Fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model
title_full Fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model
title_fullStr Fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model
title_full_unstemmed Fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model
title_short Fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model
title_sort fabrication of bio-engineered chitosan nanoformulations to inhibition of bacterial infection and to improve therapeutic potential of intestinal microflora, intestinal morphology, and immune response in infection induced rat model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9255213/
https://www.ncbi.nlm.nih.gov/pubmed/35766146
http://dx.doi.org/10.1080/10717544.2022.2081381
work_keys_str_mv AT wanxiao fabricationofbioengineeredchitosannanoformulationstoinhibitionofbacterialinfectionandtoimprovetherapeuticpotentialofintestinalmicrofloraintestinalmorphologyandimmuneresponseininfectioninducedratmodel
AT liuliu fabricationofbioengineeredchitosannanoformulationstoinhibitionofbacterialinfectionandtoimprovetherapeuticpotentialofintestinalmicrofloraintestinalmorphologyandimmuneresponseininfectioninducedratmodel
AT dinglu fabricationofbioengineeredchitosannanoformulationstoinhibitionofbacterialinfectionandtoimprovetherapeuticpotentialofintestinalmicrofloraintestinalmorphologyandimmuneresponseininfectioninducedratmodel
AT zhuzhiqiang fabricationofbioengineeredchitosannanoformulationstoinhibitionofbacterialinfectionandtoimprovetherapeuticpotentialofintestinalmicrofloraintestinalmorphologyandimmuneresponseininfectioninducedratmodel