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Effect of molecular weight and degree of chitosan deacetylation on the preparation and characteristics of chitosan thermosensitive hydrogel as a delivery system

机译:分子量和壳聚糖脱乙酰度对壳聚糖热敏水凝胶的制备及传递特性的影响

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摘要

A thermosensitive hydrogel has been prepared with chitosan and αβ-glycerophosphate (αβ-GP) which could be transited from solution into gel at 37 °C. The thermosensitive characteristics, appearance and structure of the hydrogel were affected by concentration, molecular weight and degree of deacetylation (DD) of chitosan. Chitosan, MW 1360kDa, DD 75.4%, solution concentration 2% was optimal for preparation of chitosan-αβ-glycerophosphate (CS-αβ-GP) thermosensitive hydrogel. The appearance of the hydrogel became more compact and regular with increasing concentration and chitosan MW. Model drugs release from CS-αβ-GP hydrogel prepared by the drug being added into chitosan solution (method I) was slower than that from hydrogel prepared by the drug being directly added into chitosan hydrogel (method II).The release rate for both adriamycin and 6-mercaptopurine from CS-αβ-GP hydrogel decreased with the increase of MW of the chitosan. The hydrophilic model adriamycin was released 60-70% over 24 h which was slower than that of the hydrophobic model 6-mercaptopurine. Therefore it was projected that the CS-αβ-GP hydrogel should be an ideal sustained release system especially for hydrophilic drugs.
机译:用壳聚糖和αβ-甘油磷酸酯(αβ-GP)制备了热敏性水凝胶,可以在37°C下从溶液转移到凝胶中。水凝胶的热敏特性,外观和结构受壳聚糖的浓度,分子量和脱乙酰度(DD)的影响。壳聚糖,分子量1360kDa,DD 75.4%,溶液浓度2%最适合制备壳聚糖-αβ-甘油磷酸(CS-αβ-GP)热敏水凝胶。随着浓度和壳聚糖分子量的增加,水凝胶的外观变得更致密和规则。药物直接加入壳聚糖溶液中制备的CS-αβ-GP水凝胶中释放的模型药物(方法I)比直接加入壳聚糖水凝胶中制备的CS-αβ-GP水凝胶中释放的模型药物(方法II)慢。 CS-αβ-GP水凝胶中的6-巯基嘌呤和6-巯基嘌呤随壳聚糖分子量的增加而降低。亲水性模型阿霉素在24小时内释放60-70%,这比疏水性模型6-巯基嘌呤的释放慢。因此,预计CS-αβ-GP水凝胶应是理想的持续释放系统,尤其是对于亲水性药物。

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