首页> 外文期刊>International Journal of Pharmaceutics >Chitosan-g-poly(N-isopropylacrylamide) based nanogels for tumor extracellular targeting.
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Chitosan-g-poly(N-isopropylacrylamide) based nanogels for tumor extracellular targeting.

机译:基于壳聚糖-g-聚(N-异丙基丙烯酰胺)的纳米凝胶用于肿瘤细胞外靶向。

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摘要

The principle objective of this research was to develop and characterize pH-responsive and biocompatible nanogels as a tumor-targeting drug delivery system. The nanogels were self-assembled from chitosan-based copolymers, chitosan-graft-poly(N-isopropylacrylamide) (CS-g-PNIPAm). The copolymers were synthesized via free radical copolymerization and characterized for their chemical structure by FT-IR and (1)H NMR. These copolymers could be efficiently loaded with oridonin (ORI) and the characteristics of ORI-loaded nanogels were evaluated. Drug release researches indicated that the ORI-loaded nanogels displayed pH-dependent release behaviors. Based on MTT assay and cellular morphological analysis, the anti-tumor activity of ORI-loaded nanogels was higher at pH 6.5 than at pH 7.4. In conclusion, the obtained nanogels appeared to be of great promise in tumor extracellular pH targeting for ORI.
机译:这项研究的主要目的是开发和表征pH响应和生物相容性纳米凝胶作为靶向肿瘤的药物传递系统。纳米凝胶是由壳聚糖基共聚物,壳聚糖接枝聚(N-异丙基丙烯酰胺)(CS-g-PNIPAm)自组装而成。通过自由基共聚合成共聚物,并通过FT-IR和(1)H NMR对其化学结构进行表征。这些共聚物可以有效地负载oridonin(ORI),并评估了ORI负载的纳米凝胶的特性。药物释放研究表明,加载ORI的纳米凝胶具有pH依赖性的释放行为。基于MTT分析和细胞形态分析,在pH 6.5时,负载ORI的纳米凝胶的抗肿瘤活性高于在pH 7.4时。总之,所获得的纳米凝胶在靶向ORI的肿瘤细胞外pH中似乎具有很大的希望。

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