Abstract
| Original language | English |
|---|---|
| Article number | 155 |
| Journal | Molecular Pharmaceutics |
| Volume | 11 |
| Issue number | 4 |
| Number of pages | 17 |
| ISSN | 1543-8384 |
| DOIs | |
| Publication status | Published - 2019 |
Keywords
- Xanthan gum
- Electrospinning
- Gallic acid
- (−)-epigallocatechin gallate
- Permeability
Cite this
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Enhanced Transepithelial Permeation of Gallic Acid and (-)-Epigallocatechin Gallate across Human Intestinal Caco-2 Cells Using Electrospun Xanthan Nanofibers. / Faralli, Adele; Shekarforoush, Elhamalsadat; Mendes, Ana Carina Loureiro; Chronakis, Ioannis S.
In: Molecular Pharmaceutics, Vol. 11, No. 4, 155, 2019.Research output: Contribution to journal › Journal article › Research › peer-review
TY - JOUR
T1 - Enhanced Transepithelial Permeation of Gallic Acid and (-)-Epigallocatechin Gallate across Human Intestinal Caco-2 Cells Using Electrospun Xanthan Nanofibers
AU - Faralli, Adele
AU - Shekarforoush, Elhamalsadat
AU - Mendes, Ana Carina Loureiro
AU - Chronakis, Ioannis S.
PY - 2019
Y1 - 2019
N2 - Electrospun xanthan polysaccharide nanofibers (X) were developed as an encapsulation and delivery system of the poorly absorbed polyphenol compounds, gallic acid (GA) and (-)-epigallocatechin gallate (EGCG). Scanning electron microscopy was used to characterize the electrospun nanofibers, and controlled release studies were performed at pH 6.5 and 7.4 in saline buffer, suggesting that the release of polyphenols from xanthan nanofibers follows a non-Fickian mechanism. Furthermore, the X-GA and X-EGCG nanofibers were incubated with Caco-2 cells, and the cell viability, transepithelial transport, and permeability properties across cell monolayers were investigated. An increase of GA and EGCG permeability was observed when the polyphenols were loaded into xanthan nanofibers, compared to the free compounds. The observed in vitro permeability enhancement of GA and EGCG was induced by the presence of the polysaccharide nanofibers, which successfully inhibited efflux transporters, as well as by tight junctions opening.
AB - Electrospun xanthan polysaccharide nanofibers (X) were developed as an encapsulation and delivery system of the poorly absorbed polyphenol compounds, gallic acid (GA) and (-)-epigallocatechin gallate (EGCG). Scanning electron microscopy was used to characterize the electrospun nanofibers, and controlled release studies were performed at pH 6.5 and 7.4 in saline buffer, suggesting that the release of polyphenols from xanthan nanofibers follows a non-Fickian mechanism. Furthermore, the X-GA and X-EGCG nanofibers were incubated with Caco-2 cells, and the cell viability, transepithelial transport, and permeability properties across cell monolayers were investigated. An increase of GA and EGCG permeability was observed when the polyphenols were loaded into xanthan nanofibers, compared to the free compounds. The observed in vitro permeability enhancement of GA and EGCG was induced by the presence of the polysaccharide nanofibers, which successfully inhibited efflux transporters, as well as by tight junctions opening.
KW - Xanthan gum
KW - Electrospinning
KW - Gallic acid
KW - (−)-epigallocatechin gallate
KW - Permeability
U2 - 10.3390/pharmaceutics11040155
DO - 10.3390/pharmaceutics11040155
M3 - Journal article
VL - 11
JO - Molecular Pharmaceutics
JF - Molecular Pharmaceutics
SN - 1543-8384
IS - 4
M1 - 155
ER -