Bile Is a Selective Elevator for Mucosal Mechanics and Transport

Mucus mechanically protects the intestinal epithelium and impacts the absorption of drugs, with a largely unknown role for bile. We explored the impacts of bile on mucosal biomechanics and drug transport within mucus. Bile diffused with square-root-of-time kinetics and interplayed with mucus, leadin...

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Veröffentlicht in:Molecular pharmaceutics Jg. 20; H. 12; S. 6151
Hauptverfasser: Hanio, Simon, Möllmert, Stephanie, Möckel, Conrad, Choudhury, Susobhan, Höpfel, Andreas I, Zorn, Theresa, Endres, Sebastian, Schlauersbach, Jonas, Scheller, Lena, Keßler, Christoph, Scherf-Clavel, Oliver, Bellstedt, Peter, Schubert, Ulrich S, Pöppler, Ann-Christin, Heinze, Katrin G, Guck, Jochen, Meinel, Lorenz
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 04.12.2023
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ISSN:1543-8392, 1543-8392
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Abstract Mucus mechanically protects the intestinal epithelium and impacts the absorption of drugs, with a largely unknown role for bile. We explored the impacts of bile on mucosal biomechanics and drug transport within mucus. Bile diffused with square-root-of-time kinetics and interplayed with mucus, leading to transient stiffening captured in Brillouin images and a concentration-dependent change from subdiffusive to Brownian-like diffusion kinetics within the mucus demonstrated by differential dynamic microscopy. Bile-interacting drugs, Fluphenazine and Perphenazine, diffused faster through mucus in the presence of bile, while Metoprolol, a drug with no bile interaction, displayed consistent diffusion. Our findings were corroborated by rat studies, where co-dosing of a bile acid sequestrant substantially reduced the bioavailability of Perphenazine but not Metoprolol. We clustered over 50 drugs based on their interactions with bile and mucin. Drugs that interacted with bile also interacted with mucin but not vice versa. This study detailed the dynamics of mucus biomechanics under bile exposure and linked the ability of a drug to interact with bile to its abbility to interact with mucus.
AbstractList Mucus mechanically protects the intestinal epithelium and impacts the absorption of drugs, with a largely unknown role for bile. We explored the impacts of bile on mucosal biomechanics and drug transport within mucus. Bile diffused with square-root-of-time kinetics and interplayed with mucus, leading to transient stiffening captured in Brillouin images and a concentration-dependent change from subdiffusive to Brownian-like diffusion kinetics within the mucus demonstrated by differential dynamic microscopy. Bile-interacting drugs, Fluphenazine and Perphenazine, diffused faster through mucus in the presence of bile, while Metoprolol, a drug with no bile interaction, displayed consistent diffusion. Our findings were corroborated by rat studies, where co-dosing of a bile acid sequestrant substantially reduced the bioavailability of Perphenazine but not Metoprolol. We clustered over 50 drugs based on their interactions with bile and mucin. Drugs that interacted with bile also interacted with mucin but not vice versa. This study detailed the dynamics of mucus biomechanics under bile exposure and linked the ability of a drug to interact with bile to its abbility to interact with mucus.Mucus mechanically protects the intestinal epithelium and impacts the absorption of drugs, with a largely unknown role for bile. We explored the impacts of bile on mucosal biomechanics and drug transport within mucus. Bile diffused with square-root-of-time kinetics and interplayed with mucus, leading to transient stiffening captured in Brillouin images and a concentration-dependent change from subdiffusive to Brownian-like diffusion kinetics within the mucus demonstrated by differential dynamic microscopy. Bile-interacting drugs, Fluphenazine and Perphenazine, diffused faster through mucus in the presence of bile, while Metoprolol, a drug with no bile interaction, displayed consistent diffusion. Our findings were corroborated by rat studies, where co-dosing of a bile acid sequestrant substantially reduced the bioavailability of Perphenazine but not Metoprolol. We clustered over 50 drugs based on their interactions with bile and mucin. Drugs that interacted with bile also interacted with mucin but not vice versa. This study detailed the dynamics of mucus biomechanics under bile exposure and linked the ability of a drug to interact with bile to its abbility to interact with mucus.
Mucus mechanically protects the intestinal epithelium and impacts the absorption of drugs, with a largely unknown role for bile. We explored the impacts of bile on mucosal biomechanics and drug transport within mucus. Bile diffused with square-root-of-time kinetics and interplayed with mucus, leading to transient stiffening captured in Brillouin images and a concentration-dependent change from subdiffusive to Brownian-like diffusion kinetics within the mucus demonstrated by differential dynamic microscopy. Bile-interacting drugs, Fluphenazine and Perphenazine, diffused faster through mucus in the presence of bile, while Metoprolol, a drug with no bile interaction, displayed consistent diffusion. Our findings were corroborated by rat studies, where co-dosing of a bile acid sequestrant substantially reduced the bioavailability of Perphenazine but not Metoprolol. We clustered over 50 drugs based on their interactions with bile and mucin. Drugs that interacted with bile also interacted with mucin but not vice versa. This study detailed the dynamics of mucus biomechanics under bile exposure and linked the ability of a drug to interact with bile to its abbility to interact with mucus.
Author Möckel, Conrad
Zorn, Theresa
Höpfel, Andreas I
Meinel, Lorenz
Guck, Jochen
Scherf-Clavel, Oliver
Schlauersbach, Jonas
Heinze, Katrin G
Keßler, Christoph
Endres, Sebastian
Choudhury, Susobhan
Schubert, Ulrich S
Bellstedt, Peter
Hanio, Simon
Scheller, Lena
Möllmert, Stephanie
Pöppler, Ann-Christin
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  organization: Institute of Organic Chemistry, University of Würzburg, Am Hubland, 97074 Wuerzburg, Germany
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  givenname: Sebastian
  surname: Endres
  fullname: Endres, Sebastian
  organization: Institute of Organic Chemistry, University of Würzburg, Am Hubland, 97074 Wuerzburg, Germany
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  givenname: Jochen
  surname: Guck
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Keywords NMR
diffusion
predictive algorithm
bioavailability
FCS
Brillouin microscopy
differential dynamic microscopy
drug
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Snippet Mucus mechanically protects the intestinal epithelium and impacts the absorption of drugs, with a largely unknown role for bile. We explored the impacts of...
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SubjectTerms Animals
Bile
Elevators and Escalators
Mucins
Mucus
Perphenazine
Rats
Title Bile Is a Selective Elevator for Mucosal Mechanics and Transport
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