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首页> 外文期刊>RSC Advances >Chemical and pharmaceutical evaluation of the relationship between triazole linkers and pore size on cyclodextrin–calixarene nanosponges used as carriers for natural drugs
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Chemical and pharmaceutical evaluation of the relationship between triazole linkers and pore size on cyclodextrin–calixarene nanosponges used as carriers for natural drugs

机译:Cyclodextrin-Calixarene anonys用作天然药物载体的环糊蛋白 - 钙葡萄烯型隆起之间关系的化学和药物评价

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摘要

Mixed cyclodextrin–calixarene nanosponges were used to prepare some composites with the well known polyphenolic bioactive compounds quercetin and silibinin. The composites were characterized by means of different techniques (UV-vis, FT-IR, microcalorimetry, thermogravimetry), in order to assess their loading and thermal stability. The kinetics of release of the bioactive molecules into aqueous solution were studied at two different pH values (1.0, 6.4), which mimic typical physiological conditions. Finally the possible antiproliferative effects in vitro were assayed towards three triple negative breast cancer cell lines (SUM 149, SUM 159 and MDA-MB-23). Our results point out the role assumed by the triazole linkers, present in the nanosponge network, in affecting both the adsorption abilities of the materials towards the bioactive molecules, and the antiproliferative activity of the composites. This work puts forward an efficient strategy to prepare nanosponge based nanocarriers with three different cavities that could encapsulate two or more drug molecules with different physico-chemical properties.
机译:混合环糊精 - 钙喹纳酮用于制备一些复合材料,其中具有众所周知的多酚生物活性化合物槲皮素和硅蛋白。通过不同的技术(UV-Vis,FT-IR,微量微集体,热重量测定)的方式表征复合材料,以评估它们的负载和热稳定性。在两种不同的pH值(1.0,6.4)中研究生物活性分子释放到水溶液中的动力学,其模仿典型的生理条件。最后,在体外可能的抗增殖效应朝向三个阴性乳腺癌细胞系(和149,和159和MDA-MB-23)测定。我们的结果指出了在纳米分子网络中存在的三唑连接物假定的作用,从而影响材料朝向生物活性分子的吸附能力以及复合材料的抗增殖活性。这项工作提出了一种有效的策略,以制备基于纳米骨的纳米载体,其具有三种不同的腔,其可以包封具有不同的物理化学性质的两种或更多种药物分子。

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