Methylated N-(4-N,N-Dimethylaminobenzyl) Chitosan, a Novel Chitosan Derivative, Enhances Paracellular Permeability Across Intestinal Epithelial Cells (Caco-2) (original) (raw)
Related papers
AAPS PharmSciTech, 2010
The aim of this study was to investigate the effects of a type of hydrophobic moiety, extent of N-substitution (ES), and degree of quaternization (DQ) of chitosan (CS) on the transepithelial electrical resistance and permeability of Caco-2 cells monolayer, using fluorescein isothiocyanate dextran 4,400 (FD-4) as the model compound for paracellular tight junction transport. CS was substituted with hydrophobic moiety, an aliphatic aldehyde (n-octyl) or aromatic aldehyde (benzyl), for the improved hydrophobic interaction with cell membrane, and they were quaternized with Quat-188 to render CS soluble. The factors affecting the epithelial permeability have been evaluated in the intestinal cell monolayers, Caco-2 cells. Cytotoxicity was evaluated by using the trypan blue and MTT viability assay. The results revealed that at pH 7.4 CSQ appeared to increase cell permeability in dose-dependent manner, and this effect was relatively reversible at the lower doses of 0.05-1.25 mM. The higher DQ and ES caused the higher permeability of FD-4. Cytotoxicity of CSQ was concentration, %DQ, and %ES dependent. Substitution with hydrophobic moiety caused decreasing in permeability of FD-4 and cytotoxicity by benzyl group had more effect than octyl group. These studies demonstrated that these novel modified chitosan derivatives had potential for using as absorption enhancers.
Carbohydrate Polymers, 2011
The aim of this study was to investigate three kinds of methylated chitosan containing different aromatic moieties; methylated N-(4-N,N-dimethylaminobenzyl) chitosan (TM-Bz-CS), methylated N-(4-N,N-dimethylaminocinnamyl) chitosan (TM-CM-CS) and methylated N-(4-pyridylmethyl) chitosan (TM-Py-CS), on the paracellular permeability of Caco-2 cell monolayers and their toxicity towards the cell lines. The factors affecting epithelial permeability were evaluated in intestinal cell monolayers of Caco-2 cells using the transepithelial electrical resistance (TEER) and permeability of Caco-2 cell monolayers, with fluorescein isothiocyanate dextran 4400 (FD-4) as a model compound for paracellular tight junction transport. The results revealed that methylated chitosan containing different aromatic moieties showed the different absorption enhancing ability. The rank of enhancing paracellular permeability was TM 65 CM 50 CS > TM 56 Bz 42 CS > TM 65 CS > TM 53 Py 40 CS. The cytotoxicity of these modified chitosans on Caco-2 cells was also studied by MTT assay where the TM 53 Py 40 CS exhibited less toxicity than other derivatives. These studies demonstrated that the chemical structure and the positive charge location play an important role for absorption enhancement and cytotoxicity.
Drug Delivery, 2010
The effect of methylated N-(4-N,N-dimethylaminocinnamyl) chitosan (TM-CM-CS) was investigated on paracellular permeability and its toxicity towards Caco-2 cells. Fluorescein isothiocyanate dextran 4,400 (FD-4) was used as the model compound for paracellular transport. The factors, i.e. the degree of quaternization (DQ) and the extent of N-substitution (ES) of the derivatives, were studied for the effect on transepithelial electrical resistance (TEER) and permeability. The results revealed that at pH 7.4, TM-CM-CS appeared to increase cell permeability in a dose-dependent manner, and the effect was relatively reversible at lower doses of 0.05-0.5 mM. The difference of the DQ and the ES of TM-CM-CS slightly affected the decrease of TEER values and the FD-4 permeability. The cytotoxicity of TM-CM-CS was concentration-dependent and did not cause an acute cytotoxic effect as analyzed by the MTT assay. These studies demonstrated that this novel modified chitosan has the potential to be used as an intestinal absorption enhancer of therapeutic macromolecules.
Induction of permeability and apoptosis in colon cancer cell line with chitosan
Journal of Food and Drug Analysis, 2020
The effect of chitosan on tight junctions (TJs) permeability on Caco-2 cell monolayer intestinal model was investigated. We have also investigated the effects of low molecular weight water-soluble chitosan (LMWC) on apoptosis in HT-29 cell. The changes in barrier properties of Caco-2 cell monolayers, including transepithelial electrical resistance (TEER) and permeability to lucifer yellow, were assessed in response to chitosan treatment. High molecular weight chitosan (HMWC) was found to cause up to 50% dose-dependent reduction in TEER of Caco-2 cell monolayer without damage to the cell membrane under lower concentration. The effect of HMWC on TJs was confirmed by increased permeability of lucifer yellow when cells were treated with 0.00-0.000% HMWC for 20 min compared to control cells. Results showed that HMWC did not affect the F-actin of cytoskeleton. LMWC was proven to be an antitumor compound as shown by inducing apoptosis as a function of DNA fragmentation. These results suggest that HMWC is an useful drug delivery agent in paracellular pathway and LMWC has potential value in colon cancer therapy.
Journal of Pharmaceutical Sciences and Pharmacology, 2014
N,N,N-Trimethylated chitosan has been extensively used as an absorption enhancer for macromolecules and as a mucosal vaccine carrier. Both of these properties are molecular weight (MW) and degree of quaternization (DQ) dependent. The aim of the present study was to evaluate the impact of some synthesized trimethylated chitosan with various MW and DQ on biological systems in terms of biocompatibility and providing guidelines for the rational design of chitosan derivatives for effective and safe drug delivery. For this purpose, cytotoxicity in HT29 cell line was monitored using the MTT assay and the release of the cytosolic enzyme lactate dehydrogenase (LDH). Microscopic observation was carried out as indicators for blood cell compatibility. Furthermore, haemolysis was quantified spectrophotometrically for evaluation of haematotoxicity. Two polymer doses were used for sub acute toxicity study in BALBc mice. After oral administration, animals were monitored over 28 days and necropised. Signs of toxicity were evaluated via mortality and histopathology of liver, kidney and spleen. The magnitude of the cytotoxic effects all chitosan derivatives were found to be concentration dependent. Higher concentration of trimethylated chitosan with 22% DQ and native chitosan did not cause significant abnormalities among experimental group of mice, whereas, trimethylated chitosan with higher DQ as 50% and 61% may lead to concentration dependent cytotoxicity, hematotoxicity and increased renal and hepatotoxicity. All assays yielded comparable results and concluded cationic charge density of the chitosan derivatives seems as key parameters for the interaction with the cell membranes and consequently the cell damage. These results indicate that structure-toxicity relationship is necessary to optimize the degree of modification of chitosan for the development of biocompatible and biodegradable derivatives.
Novel transmucosal absorption enhancers obtained by aminoalkylation of chitosan
European Journal of Pharmaceutical Sciences, 2006
Quaternary chitosan derivative NMR analysis Transmucosal absorption enhancer Buccal absorption enhancer Transcellular transport enhancer Paracellular transport enhancer a b s t r a c t Literature data suggest that quaternized chitosans have a transmucosal drug absorption enhancing property depending on their MW, quaternization degree and other structural features. With the purpose of preparing novel effective promoters, a chitosan (Ch) from crab shell (ChC; viscometric MW, 800 kDa; deacetylation: 90%, IR; 84%, NMR) and one from shrimp shell (ChS; viscometric MW, 590 kDa; deacetylation: 90%, IR; 82%, NMR) were reacted with 2-diethylaminoethyl chloride (DEAE-Cl) and novel derivatives containing different percentages of pendant quaternary ammonium groups were obtained. NMR analysis, based on HSQC, COSY, TOCSY and ROESY maps, indicated that three partially substituted N,O-[N,N-diethylaminomethyl(diethyldimethylene ammonium) n ]methyl chitosans, coded N + -ChS-2 (degree of substitution, DS = 40%; n = 1.6), N + -ChS-4 (DS = 132%; n = 2.5), and N + -ChC-4 (DS = 85%; n = 1.7) resulted from the reaction, depending on whether the DEAE-Cl/Ch repeating unit molar ratio, was 2:1 or 4:1. The effects of the derivatives on the permeability of rhodamine 123 (Rh-123), hydrophobic, marker of the transcellular absorption route, and of fluorescein sodium (NaFlu), polar, marker of the paracellular route, across excised porcine
Journal of Controlled Release, 2000
N-Trimethyl chitosan chloride (TMC) is a permanently quaternized chitosan derivative with improved aqueous solubility compared to native chitosan. TMC is able to open the tight junctions of intestinal epithelia at physiological pH values, where chitosan is insoluble and therefore ineffective. TMCs with degrees of substitution of 40 and 60% were synthesized according to a novel synthesis procedure and their effect on the permeability of the tight junctions of the intestinal Caco-2 monolayers was studied, measuring the transepithelial electrical resistance and the transport of a mainly paracellularly transported 14 compound, [ C]-mannitol. Toxicity studies using nucleic stains were done to establish the transport as a cause of opening of the tight junctions and not of possible cytotoxicity. TMC60 showed higher transport enhancement ratios than TMC40 in all concentrations tested (0.05-1.0%, w / v). Both derivatives did not affect the viability of the Caco-2 cell monolayers. These results suggest that high charge density is necessary for TMC to substantially improve the paracellular permeability of intestinal epithelia. It is expected that TMC40 and TMC60 will enhance the intestinal permeation of hydrophilic macromolecular drugs such as peptides and proteins.
Diethyl methyl chitosan as an intestinal paracellular enhancer: ex vivo and in vivo studies
International journal of pharmaceutics, 2005
Chitosan exhibits favorable biological properties such as no toxicity, biocompatibility and biodegradability; therefore, it has attracted great attention in both pharmaceutical and biomedical fields. Chitosan exhibits poor solubility at pH values above 6 that prevents enhancing effects at the sites of absorption of drugs. In the present work, N-diethyl methyl chitosan (DEMC) was prepared and the enhancing effect of this polymer was investigated. Ex vivo studies have shown a significant increase in absorption of brilliant blue in the presence of diethyl methyl chitosan in comparison with chitosan. DEMC with positive charges is able to interact with tight junctions of colon epithelial cells and hence increases permeability of brilliant blue across the tight junctions. In vivo investigations have exhibited the absorption enhancer effects of DEMC on the colon absorption of insulin in normal and diabetic rats. The insulin absorption from the rat's colon was evaluated by its hypoglyce...
Journal of Pharmacy and Pharmacology, 2008
In recent years, researchers have been working extensively on various novel properties of polymers to develop increased efficiency of drug delivery and improve bioavailability of various drug molecules, especially macromolecules. Chitosan, a naturally occurring polysaccharide, because of its protonated/polymeric nature, provides effective and safe absorption of peptide and protein drugs. Its transmucosal absorption is, however, limited to acidic media because of its strong intermolecular hydrogen bonds. A new partially quaternized chitosan derivative, N-trimethyl chitosan chloride (TMC), has been synthesized with improved solubility, safety and effectiveness as an absorption enhancer at neutral pH and in aqueous environment. It enhances the absorption, especially of peptide drugs, by reversible opening of tight junctions in between epithelial cells, thereby facilitating the paracellular diffusion of peptide drugs. This derivative thus opens new perspectives as a biomaterial for various pharmaceutical applications/drug delivery systems. This review deals with the potential use of the quaternized chitosan derivative as a permeation enhancer for the mucosal delivery of macromolecular drugs along with its other biomedical applications.