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Daunomycin-loaded superparamagnetic iron oxide nanoparticles: Preparation, magnetic targeting, cell cytotoxicity, and protein delivery research

机译:载有陶霉素的超顺磁性氧化铁纳米粒子:制备,磁性靶向,细胞毒性和蛋白质递送研究

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摘要

The clinical use of daunomycin is restricted by dose-dependent toxicity and low specificity against cancer cells. In the present study, modified superparamagnetic iron oxide nanoparticles were employed to load daunomycin and the drug-loaded nanospheres exhibited satisfactory size and smart pH-responsive release. The cellular uptake efficiency, targeted cell accumulation, and cell cytotoxicity experimental results proved that the superparamagnetic iron oxide nanoparticle-loading process brings high drug targeting without decreasing the cytotoxicity of daunomycin. Moreover, a new concern for the evaluation of nanophase drug delivery's effects was considered, with monitoring the interactions between human serum albumin and the drug-loaded nanospheres. Results from the multispectroscopic techniques and molecular modeling calculation elucidate that the drug delivery has detectable deleterious effects on the frame conformation of protein, which may affect its physiological function.
机译:剂量依赖性毒性和对癌细胞的低特异性限制了道诺霉素的临床应用。在本研究中,改性的超顺磁性氧化铁纳米粒子被用于负载道诺霉素,并且负载药物的纳米球表现出令人满意的尺寸和智能的pH响应释放。细胞吸收效率,靶向细胞蓄积和细胞毒性实验结果证明,超顺磁性氧化铁纳米粒子负载过程在不降低道诺霉素细胞毒性的情况下具有较高的靶向性。此外,考虑到监测人血清白蛋白与载药纳米球之间的相互作用,人们对纳米级药物递送效果的评估提出了新的关注。多光谱技术和分子模型计算的结果表明,药物递送对蛋白质的构象构象具有可检测的有害作用,这可能影响其生理功能。

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