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Cow Milk and Intestinal Epithelial Cell-Derived Extracellular Vesicles as Systems for Enhancing Oral Drug Delivery
by
Mantaj, Julia
, Vllasaliu, Driton
, Carobolante, Greta
, Ferrari, Enrico
in
drug absorption
/ exosomes
/ extracellular vesicles
/ intestinal permeability
/ oral drug bioavailability
2020
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Cow Milk and Intestinal Epithelial Cell-Derived Extracellular Vesicles as Systems for Enhancing Oral Drug Delivery
by
Mantaj, Julia
, Vllasaliu, Driton
, Carobolante, Greta
, Ferrari, Enrico
in
drug absorption
/ exosomes
/ extracellular vesicles
/ intestinal permeability
/ oral drug bioavailability
2020
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Do you wish to request the book?
Cow Milk and Intestinal Epithelial Cell-Derived Extracellular Vesicles as Systems for Enhancing Oral Drug Delivery
by
Mantaj, Julia
, Vllasaliu, Driton
, Carobolante, Greta
, Ferrari, Enrico
in
drug absorption
/ exosomes
/ extracellular vesicles
/ intestinal permeability
/ oral drug bioavailability
2020
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Cow Milk and Intestinal Epithelial Cell-Derived Extracellular Vesicles as Systems for Enhancing Oral Drug Delivery
Journal Article
Cow Milk and Intestinal Epithelial Cell-Derived Extracellular Vesicles as Systems for Enhancing Oral Drug Delivery
2020
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Overview
Ingestion is the preferred way for drug administration. However, many drugs have poor oral bioavailability, warranting the use of injections. Extracellular vesicles (EVs) from cow milk have shown potential utility in improving oral drug bioavailability. However, EVs produced by intestinal epithelial cells have not been investigated for this application. We compared the capacity of cow milk EVs and intestinal epithelial cell-derived counterparts to enhance oral drug bioavailability. EVs were isolated, fluorescently labelled, and loaded with curcumin (CUR) as a model poorly absorbable drug. These were then characterised before testing in an intestinal model (Caco-2). Epithelial cell-derived EVs showed notably higher cell uptake compared to cow milk EVs. Cell uptake was significantly higher in differentiated compared to undifferentiated cells for both types of EVs. While both milk- and cell-derived EVs improved the cell uptake and intestinal permeability of CUR (confirming oral drug bioavailability enhancement potential), epithelial cell EVs demonstrated a superior effect.
Publisher
MDPI,MDPI AG
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