共 31 条
Cow Milk and Intestinal Epithelial Cell-Derived Extracellular Vesicles as Systems for Enhancing Oral Drug Delivery
被引:110
作者:

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Mantaj, Julia
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机构:
Kings Coll London, Fac Life Sci & Med, Sch Canc & Pharmaceut Sci, London SE1 9NH, England Kings Coll London, Fac Life Sci & Med, Sch Canc & Pharmaceut Sci, London SE1 9NH, England

Ferrari, Enrico
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Univ Lincoln, Sch Life Sci, Lincoln LN6 7TS, England Kings Coll London, Fac Life Sci & Med, Sch Canc & Pharmaceut Sci, London SE1 9NH, England

Vllasaliu, Driton
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Kings Coll London, Fac Life Sci & Med, Sch Canc & Pharmaceut Sci, London SE1 9NH, England Kings Coll London, Fac Life Sci & Med, Sch Canc & Pharmaceut Sci, London SE1 9NH, England
机构:
[1] Kings Coll London, Fac Life Sci & Med, Sch Canc & Pharmaceut Sci, London SE1 9NH, England
[2] Univ Padua, Dept Pharmaceut & Pharmacol Sci, Via 8 Febbraio 2, I-35122 Padua, Italy
[3] Univ Lincoln, Sch Life Sci, Lincoln LN6 7TS, England
基金:
英国工程与自然科学研究理事会;
关键词:
drug absorption;
exosomes;
extracellular vesicles;
intestinal permeability;
oral drug bioavailability;
EXOSOMES;
BOVINE;
TRANSPORT;
BIOAVAILABILITY;
MICRORNAS;
DIGESTION;
CURCUMIN;
D O I:
10.3390/pharmaceutics12030226
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
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.
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