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Comparison of the effect of different chitosan salts and N-trimethyl chitosan chloride on the permeability of intestinal epithelial cells (Caco-2)
Abstract
A partially quaternized chitosan derivative, N-trimethyl chitosan chloride (TMC) (degree of quaternization 12.28%), was synthesized and the effects of this novel polymer on the permeability of intestinal epithelial cells, using Caco-2 cell monolayers, were investigated and compared with those of chitosan hydrochloride and chitosan glutamate. Transepithelial electrical resistance (TEER) measurements at pH 6.20 revealed that all these polymers (0.25-1.5% w/v) caused an immediate and pronounced lowering in TEER values in the order chitosan hydrochloride (84% reduction after 2 h incubation) > chitosan glutamate (60% reduction) > TMC (24% reduction) at 0.25% w/v concentrations. At higher concentrations (up to 2.5% w/v), TMC was able to decrease the TEER further. Similar results were obtained in transport studies, using the hydrophilic radioactive markers, [14C]-mannitol (MW 182.2) and [14C]-polyethylene glycol 4000 (PEG-4000, MW 4000). Large increases in the permeation of these markers were found. The transport of [14C]-mannitol was increased 34-fold (chitosan hydrochloride), 25-fold (chitosan glutamate) and 11-fold (TMC) at 0.25% w/v concentrations. Further increases in the permeation of both markers were found at higher concentrations of TMC. Due to its quaternary structure, TMC is better soluble than the other chitosan salts, and its higher solubility may compensate for its lesser effectivity at similar concentrations. It is also soluble at pH 7.40, where the chitosan salts are…
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“TMC has been proven to be useful in enhancing the paracellular transport of targeted drug delivery systems through increasing the retention time of encapsulant on the mucosal surface as well as binding the protonated amino groups on the C-2 position with negatively-charged mucus and by opening the tight junctions of epithelial cells.163,164”
From Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment (2022) · cites this paper as [164]
In the citing paper
“TMC has been proven to be useful in enhancing the paracellular transport of targeted drug delivery systems through increasing the retention time of encapsulant on the mucosal surface as well as binding the protonated amino groups on the C-2 position with negatively-charged mucus and by opening the tight junctions of epithelial cells.163,164”
From Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment (2022) · cites this paper as [164]
In the citing paper
“TMC has been proven to be useful in enhancing the paracellular transport of targeted drug delivery systems through increasing the retention time of encapsulant on the mucosal surface as well as binding the protonated amino groups on the C-2 position with negatively-charged mucus and by opening the tight junctions of epithelial cells.163,164”
From Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment (2022) · cites this paper as [164]
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Research works printed but not linked: 21
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Metadata
- Authors
- Kotzé, A. F., Lueßen, H. L., de Leeuw, B. J., de Boer, (. G., Coos Verhoef, J., & Junginger, H. E.
- Venue
- Journal of Controlled Release
- Publisher
- Elsevier BV
- Published
- 1998-01
- Volume
- 51
- Issue
- 1
- Pages
- 35-46
- ISSN
- 0168-3659
- Cited by
- 226
- References
- 0
- Language
- en
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