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Mucoadhesive property and biocompatibility of methylated N-aryl chitosan derivatives

机译:甲基化的N-芳基壳聚糖衍生物的粘膜黏附特性和生物相容性

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The methylated N-aryl chitosan derivatives, methylated N-(4-N,N-dimethylaminocinnamyl) chitosan chloride (MDMCMCh) and methylated N-(4-pyridylmethyl) chitosan chloride (MPyMeCh), were synthesized by two steps, the reductive amination and the methylation. The physicochemical properties of chitosan derivatives were determined by ATR-FTIR, NMR, X-ray diffraction (XRD) and thermogravimetric (TG) techniques. The XRD analysis showed that the crystallinity and thermal stability of methylated chitosan derivatives were lower than those of chitosan. The effects of degree of quaternization (DQ), polymer structure and positive charge location on mucoadhesive property and cytotoxicity were investigated by using a mucin particle method and MTT assay compared to N,N,N-trimethylammonium chitosan chloride (TMChC). It was found that the mucoadhesive property and cytotoxicity increased with increasing DQ. At the DQ of 65%, the mucoadhesive property of the MDMCMCh was twofold lower than that of the TMChC. However, this phenomenon did not affect the mucoadhesive property when the DQ was higher than 65%. Surprisingly, the MPyMeCh showed the lowest toxicity even with the high DQ. These could be due to the resonance effect of the positive charge in the pyridine ring and the molecular weight after methylation. Finally, our result revealed that the mucoadhesive property was dependent on the DQ and polymer structure whereas the cytotoxicity was dependent on the combination of the polymer structure, positive charge location and molecular weight after methylation.
机译:甲基化的N-芳基壳聚糖衍生物,甲基化的N-(4-N,N-二甲基氨基肉桂基)壳聚糖氯化物(MDMCMCh)和甲基化的N-(4-吡啶基甲基)壳聚糖氯化物(MPyMeCh)通过还原胺化和甲基化。壳聚糖衍生物的理化性质通过ATR-FTIR,NMR,X射线衍射(XRD)和热重(TG)技术确定。 XRD分析表明,甲基化壳聚糖衍生物的结晶度和热稳定性均低于壳聚糖。与N,N,N-三甲基氯化铵壳聚糖氯化物(TMChC)相比,采用粘蛋白颗粒法和MTT法研究了季铵化度(DQ),聚合物结构和正电荷位置对粘膜粘附特性​​和细胞毒性的影响。发现粘膜粘附性质和细胞毒性随着DQ的增加而增加。在DQ为65%时,MDMCMCh的粘膜粘附特性​​比TMChC的粘膜粘附特性​​低两倍。但是,当DQ高于65%时,这种现象不会影响粘膜粘附性能。令人惊讶的是,即使高DQ,MPyMeCh的毒性也最低。这些可能是由于吡啶环中正电荷的共振效应和甲基化后的分子量引起的。最后,我们的结果表明,粘膜粘附性能取决于DQ和聚合物结构,而细胞毒性取决于聚合物结构,正电荷位置和甲基化后分子量的组合。

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