首页> 外文期刊>Nanobiotechnology, IET >Polyacrylamide–punicic acid conjugate-based micelles for flutamide delivery in PC3 cells of prostate cancer: synthesis, characterisation and cytotoxicity studies
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Polyacrylamide–punicic acid conjugate-based micelles for flutamide delivery in PC3 cells of prostate cancer: synthesis, characterisation and cytotoxicity studies

机译:基于聚丙烯酰胺 - 偶酸缀合物的氟胺蛋白递送在前列腺癌的PC3细胞中:合成,表征和细胞毒性研究

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摘要

The aim of the present study was to synthesize a novel biopolymeric micelle based on punicic acid (PA) and polyacrylamide (PAM) for carrying chemotherapeutic drugs used in prostate cancer treatment. A polymer composite micelle was prepared by chemical conjugation between PAM and PA. The micelles were prepared by self-assembly via film casting followed by ultrasonication method. The successful production of PAMPA copolymeric micelles was confirmed using FTIR, 1H-NMR, and TEM. Then, flutamide was loaded in the designed nanomicelles and they were characterized. The cell cytotoxicity of the micelles was studied on PC3 cells of prostate cancer. The prepared nanomicelles showed the particle size of 88 nm, PDI of 0.246, zeta potential of -9 mV, drug loading efficiency of 94.5%, drug release of 85.6% until 10 hours in pH 7.4 and CMC of 74.13 mu g/ml. The cell viability in blank nanocarriers was about 70% in PC3 cells at concentration of 25 mu M. More significant cytotoxic effects were seen for flutamide loaded micelles at this concentration compared to the free drug. The results suggest that the PAMPA co-polymeric nanomicelles can be utilized as an effective carrier to enhance the cytotoxic effects of flutamide in prostate cancer.
机译:本研究的目的是基于基于偶酸(PA)和聚丙烯酰胺(PAM)的新型生物聚合物胶束合成用于携带用于前列腺癌治疗的化学治疗药物。通过PAM和PA之间的化学缀合来制备聚合物复合胶束。通过通过薄膜浇铸之后通过薄膜铸件自组装制备胶束。使用FTIR,1H-NMR和TEM确认潘巴共聚胶束的成功生产。然后,将氟胺纳米在设计的纳米切片中加载,其特征在于。在前列腺癌的PC3细胞上研究了胶束的细胞细胞毒性。制备的纳米钙显示出88nm,PDI的粒径为0.246,Zeta电位为-9mV,药物负载效率为94.5%,药物释放为85.6%,直至10小时在pH 7.4和CMC为74.13μg/ ml。在浓度为25μmM的PC3细胞中,在PC3细胞中,在PC 3细胞中的细胞活力为约70%。与游离药物相比,在该浓度上看到氟胺的加载胶束的更显着的细胞毒性效应。结果表明,PAMPA共聚物纳米钙可用作有效载体,以增强氟胺在前列腺癌中的细胞毒性作用。

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