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pH-sensitive carbon quantum dots-doxorubicin nanoparticles for tumor cellular targeted drug delivery

机译:pH敏感碳量子点 - 多柔比星纳米粒子用于肿瘤细胞靶向药物递送

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摘要

A kind of pH-responsive carbon quantum dots-doxorubicin nanoparticles drug delivery platform (D-Biotin/DOX-loaded mPEG-OAL/N-CQDs) was designed and synthesized. The system consists of fluorescent carbon dots as cross-linkers, and D-Biotin worked as targeting groups, which made the system have a pH correspondence, doxorubicin hydrochloride (DOX) as the target drug, oxidized sodium alginate (OAL) as carrier materials. Ultraviolet (UV)-Vis spectrum showed that the drug-loading rate of DOX is 10.5%, and the drug release in vitro suggested that the system had a pH response and tumor cellular targeted, the drug release rate is 65.6% at the value of pH is 5.0, which is much higher than that at the value of pH is 7.4. The cytotoxicity test and laser confocal fluorescence imaging showed that the synthesized drug delivery system has high cytotoxicity to cancer cells, and the drug-loaded nanoparticles could enter the cells through endocytosis.
机译:设计并合成了一种类型的pH-响应碳量子点-Oxorubicin纳米粒子药物递送平台(D-Biotin / Dox-OAL / N-CQDS)。 该系统由荧光碳点作为交联剂组成,并且D-生物素作为靶向基团,使该系统具有pH对应,盐酸盐素(DOX)作为靶药物,氧化藻酸钠(OAL)作为载体材料。 紫外线(UV)-VIS谱表明,DOX的药物负载率为10.5%,体外药物释放表明该系统具有pH反应和肿瘤细胞靶向,药物释放率为65.6% pH为5.0,远高于pH值为7.4。 细胞毒性试验和激光共焦荧光成像表明,合成的药物递送系统对癌细胞具有高细胞毒性,药物负载纳米颗粒可以通过内吞作用进入细胞。

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