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Design, Preparation, and Characterization of Novel Calix4arene Bioactive Carrier for Antitumor Drug Delivery

机译:新型CALIX 4抗肿瘤药物递送的校友生物活性载体的设计,制备和表征

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摘要

An amphiphilic and bioactive calix[4]arene derivative 8 (CA) is designed and successfully synthesized from tert-butyl calix[4] arene 1 by sequential inverse F-C alkylation, nitration, O-alkylation, esterification, aminolysis, reduction, and acylation reaction. The blank micelles of FA-CA and doxorubicin (DOX) loaded micelles FA-CA-DOX are prepared subsequently undergoing self-assembly and dialysis of CA and DSPE-PEG2000-FA. The drug release kinetics curve of the encapsulated-DOX micelle demonstrates a rapid release under mild conditions, indicating the good pH-responsive ability. Furthermore, the cytotoxicity of DOX-loaded micelle respect to the blank micelle against seven different human carcinoma (A549, HeLa, HepG2, HCT116, MCF-7, MDA-MB231, and SW480) cells has been also investigated. The results confirm the more significant inhibitory effect of DOX-loaded micelle than those of DOX and the blank micelles. The CDI calculations show a synergistic effect between blank micelles and DOX in inducing tumor cell death. In conclusion, FA-CA micelles reported in this work was a promising drug delivery vehicle for tumor targeting therapy.
机译:通过顺序反相Fc烷基化,硝化,O-烷基化,酯化,氨基溶解,减少和酰化反应,设计并成功地设计并成功地从叔丁基杯[4]芳烃1中设计并成功地合成了叔丁基块[4]芳烃1 。随后经受CA和DSPE-PEG2000-FA的自组装和透析制备FA-CA和多柔比蛋白(DOX)装载胶束FA-CA-DOX的空白胶束。包封-Dox胶束的药物释放动力学曲线在温和条件下显示出快速释放,表明良好的pH响应能力。此外,还研究了DOX加载的胶束的细胞毒性对七种不同人癌(A549,HELA,HEPG2,HCT116,MCF-7,MDA-MB231和SW480)细胞的坯料胶束上的坯料胶束。结果证实了DOX加载胶束的抑制作用比DOX和坯料胶束更明显。 CDI计算在诱导肿瘤细胞死亡中表现出空白胶束和DOX之间的协同效应。总之,这项工作中报告的Fa-Ca胶束是肿瘤靶向治疗的有希望的药物输送型载体。

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