The effects of chitosan-coated vesicles on the paracellular permeability of Caco-2 and 16HBE14o-cell lines, and their toxicity towards the same cell lines, have been compared to equivalent concentration of chitosan in solution. Chitosan-coated phospholipid vesicles and the same concentration of chit
The effect of novel surfactants and solutol® HS 15 on paclitaxel aqueous solubility and permeability across a Caco-2 monolayer
✍ Scribed by Adam W.G. Alani; Deepa A. Rao; Ron Seidel; Jian Wang; Jim Jiao; Glen S. Kwon
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 355 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
✦ Synopsis
The effect of novel surfactants on the aqueous solubility and the permeability of paclitaxel across a Caco-2 cell monolayer were examined in this work. The solubility and permeability of paclitaxel was evaluated in the presence of four soft surfactants (SS) KXN441, KXN424, KXN437, and KXN 337 and Solutol HS15. All surfactants increased the aqueous solubility of paclitaxel. Caco-2 cell membrane integrity in the presence of SS and Solutol HS15 was assessed by mannitol permeability and LDH release. All surfactants were tested at 0.5x CMC, 5x CMC and 1.5 mM concentrations. The effect of SSs on paclitaxel permeability was concentration dependent. At all concentrations tested, KXN 441 and Solutol HS 15 showed partially inhibition of drug efflux with no discernable change in mannitol permeability or cytotoxicity as observed with LDH release. At these concentrations, other SSs exhibited some partial efflux inhibition along with compromised membrane integrity and increasing mannitol permeability. In conclusion, all SSs were able to increase the aqueous solubility and permeability of paclitaxel across Caco-2 cells monolayer. However, KXN441 and Solutol HS15 were able to enhance paclitaxel permeability across Caco-2 monolayer without cytotoxicity.
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