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pH-responsive self-healing injectable hydrogel based on N-carboxyethyl chitosan for hepatocellular carcinoma therapy

机译:基于N-羧乙基壳聚糖的pH响应自愈式可注射水凝胶肝细胞癌治疗

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Injectable hydrogels with pH-responsiveness and self-healing ability have great potential for anti-cancer drug delivery. Herein, we developed a series of polysaccharide-based self-healing hydrogels with pH sensitivity as drug delivery vehicles for hepatocellular carcinoma therapy. The hydrogels were prepared by using N-carboxyethyl chitosan (CEC) synthesized via Michael reaction in aqueous solution and dibenzaldehyde-terminated poly(ethylene glycol) (PEGDA). Doxorubicin (Dox), as a model of water-soluble small molecule anti-cancer drug was encapsulated into the hydrogel in situ. Self-healing behavior of the hydrogels was investigated at microscopic and macroscopic levels, and the hydrogels showed rapid self-healing performance without any external stimulus owing to the dynamic covalent Schiff-base linkage between amine groups from CEC and benzaldehyde groups from PEGDA. The chemical structures, theological property, in vitro gel degradation, morphology, gelation time and in vitro Dox release behavior from the hydrogels were characterized. Injectability was verified by in vitro injection and in vivo subcutaneous injection in a rat. pH-responsive behavior was verified by in vitro Dox release from hydrogels in PBS solutions with different pH values. Furthermore, the activity of Dox released from hydrogel matrix was evaluated by employing human hepatocellular liver carcinoma (HepG2). Cytotoxicity test of the hydrogels using L929 cells confirmed their good cytocompatibility. Together, these pH-responsive self healing injectable hydrogels are excellent candidates as drug delivery vehicles for liver cancer treatment.
机译:可注射水凝胶具有pH-反应性和自我愈合能力具有很大的抗癌药物递送潜力。在此,我们开发了一系列基于多糖的自我愈合水凝胶,pH敏感性作为用于肝细胞癌治疗的药物递送载体。通过在水溶液中使用迈克尔反应合成的N-羧乙基壳聚糖(CEC)制备水凝胶,并在水溶液中合成,二苯甲醛封端的聚(乙二醇)(PEGDA)。 Doxorubicin(Dox),作为水溶性小分子抗癌药模型,原位包封在水凝胶中。在微观和宏观水平下研究了水凝胶的自我愈合行为,并且水凝胶显示出快速的自我愈合性能,而由于来自PEGDA的CEC和苯甲醛基团的胺基之间的动态共价席克基碱基,而没有任何外部刺激。特征在于,化学结构,体外凝胶降解,形态,凝胶化时间和来自水凝胶的体外凝胶释放行为的化学结构。通过体外注射和大鼠体内皮下注射验证可注射性。通过具有不同pH值的PBS溶液中的水凝胶中的体外Dox释放pH-响应行为。此外,通过使用人肝细胞癌(Hepg2)评估从水凝胶基质中释放的DOx的活性。使用L929细胞的水凝胶的细胞毒性试验证实了它们的良好细胞粘合性。这些pH-响应自愈合的注射水凝胶是肝癌治疗的药物递送载体的优异候选者。

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