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Screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro

One of the biggest challenges for oral drug absorption is the epithelial barrier of the gastrointestinal tract. The use of cell-penetrating peptides (CPPs) to modulate the epithelial barrier function is known to be an effective strategy to improve drug absorption and bioavailability. In this study w...

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Autores principales: Gelli, Hitesh P., Vazquez-Uribe, Ruben, Sommer, Morten Otto Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666501/
https://www.ncbi.nlm.nih.gov/pubmed/36408245
http://dx.doi.org/10.3389/fphar.2022.1049324
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author Gelli, Hitesh P.
Vazquez-Uribe, Ruben
Sommer, Morten Otto Alexander
author_facet Gelli, Hitesh P.
Vazquez-Uribe, Ruben
Sommer, Morten Otto Alexander
author_sort Gelli, Hitesh P.
collection PubMed
description One of the biggest challenges for oral drug absorption is the epithelial barrier of the gastrointestinal tract. The use of cell-penetrating peptides (CPPs) to modulate the epithelial barrier function is known to be an effective strategy to improve drug absorption and bioavailability. In this study we compare side-by-side, 9 most promising CPPs to study their cytotoxicity (Cytotox Red dye staining) and cell viability (AlamarBlue staining) on epithelial cells and their effects on paracellular permeability of the intestinal barrier in vitro in a differentiated Caco-2 epithelial monolayer model. The data revealed that 4 out of 9 well-studied CPPs significantly improved Caco-2 paracellular permeability without compromising on cellular health. To assess the impact of CPPs on the human microbiota we studied the antimicrobial effects of the 4 effective CPPs from our permeation studies against 10 representative strains of the gut microbiota in vitro using microbroth dilution. Our data revealed that these 4 CPPs affected the growth of almost all tested commensal strains. Interestingly, we found that two synthetic CPPs (Shuffle and Penetramax) outperformed all the other CPPs in their ability to increase intestinal paracellular permeability at 50 µM and had only a small to moderate effect on the tested gut commensal strains. Based on these data Shuffle and Penetramax represent relevant CPPs to be further characterized in vivo for safe delivery of poorly absorbed therapeutics while minimizing negative impacts on the gut microbiota.
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spelling pubmed-96665012022-11-17 Screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro Gelli, Hitesh P. Vazquez-Uribe, Ruben Sommer, Morten Otto Alexander Front Pharmacol Pharmacology One of the biggest challenges for oral drug absorption is the epithelial barrier of the gastrointestinal tract. The use of cell-penetrating peptides (CPPs) to modulate the epithelial barrier function is known to be an effective strategy to improve drug absorption and bioavailability. In this study we compare side-by-side, 9 most promising CPPs to study their cytotoxicity (Cytotox Red dye staining) and cell viability (AlamarBlue staining) on epithelial cells and their effects on paracellular permeability of the intestinal barrier in vitro in a differentiated Caco-2 epithelial monolayer model. The data revealed that 4 out of 9 well-studied CPPs significantly improved Caco-2 paracellular permeability without compromising on cellular health. To assess the impact of CPPs on the human microbiota we studied the antimicrobial effects of the 4 effective CPPs from our permeation studies against 10 representative strains of the gut microbiota in vitro using microbroth dilution. Our data revealed that these 4 CPPs affected the growth of almost all tested commensal strains. Interestingly, we found that two synthetic CPPs (Shuffle and Penetramax) outperformed all the other CPPs in their ability to increase intestinal paracellular permeability at 50 µM and had only a small to moderate effect on the tested gut commensal strains. Based on these data Shuffle and Penetramax represent relevant CPPs to be further characterized in vivo for safe delivery of poorly absorbed therapeutics while minimizing negative impacts on the gut microbiota. Frontiers Media S.A. 2022-11-02 /pmc/articles/PMC9666501/ /pubmed/36408245 http://dx.doi.org/10.3389/fphar.2022.1049324 Text en Copyright © 2022 Gelli, Vazquez-Uribe and Sommer. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Gelli, Hitesh P.
Vazquez-Uribe, Ruben
Sommer, Morten Otto Alexander
Screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro
title Screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro
title_full Screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro
title_fullStr Screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro
title_full_unstemmed Screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro
title_short Screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro
title_sort screening for effective cell-penetrating peptides with minimal impact on epithelial cells and gut commensals in vitro
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666501/
https://www.ncbi.nlm.nih.gov/pubmed/36408245
http://dx.doi.org/10.3389/fphar.2022.1049324
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