聚乙烯和金包覆的磁性氧化铁纳米颗粒作为多柔比星的合适载体及其对 Mcf-7 乳腺癌细胞的影响

Fateme Sadeghi Nodoushan, F. Hakimian, B. Haghiralsadat
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引用次数: 0

摘要

前言纳米技术一直致力于为化疗药物的靶向给药提供新的解决方案,以提高癌症治疗的质量并减少化疗的副作用。本研究的目的是将抗癌药物多柔比星载入磁性氧化铁纳米颗粒,并对其对 MCF-7 细胞的作用进行物理化学评价。 研究方法本研究是一项描述性分析研究。在这项实验室研究中,首先用沉淀法合成了氧化铁纳米粒子。然后在其表面涂上聚乙烯亚胺和金。在磁性氧化铁纳米粒子中加入药物多柔比星后,从插入效率、健康细胞和癌细胞相似条件下的药物释放曲线、尺寸、ZETA电位和形态等角度测定了纳米系统的理化参数。 结果显示磁性纳米载体的直径为 90 nm,zeta 电位为 66.7 mV。在 37°C、pH=7.4 和 42°C、pH=5.4 温度条件下,48 小时后药物从纳米系统中的最大释放量分别为 48% 和 66%。扫描电镜分析表明,纳米系统呈球形,与药物之间不存在化学作用。对纳米系统性能的研究表明,与游离多柔比星相比,封装多柔比星在 MCF_7 菌株上的毒性在相似浓度下有所增加。 结论研究结果表明,磁性氧化铁纳米粒子系统具有适当的理化特性,不会改变药物的化学性质,可作为抗癌药物多柔比星的合适半靶向载体。
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Magnetic Iron Oxide Nanoparticles Coated with Polyethylene and Gold as a Suitable Carrier for Doxorubicin and its Effect on Mcf-7 Breast Cancer Cells
Introduction: Nanotechnology always seeks to provide new solutions for targeted delivery of chemotherapy drugs, in order to increase the quality of cancer treatment and reduce the side effects of chemotherapy. The aim of this study was to load the anticancer drug doxorubicin on Magnetic iron oxide nanoparticles were subjected to physico-chemical evaluation for their effect on MCF-7 cells. Methods: This research was a descriptive-analytical study. In this laboratory research, iron oxide nanoparticles were first synthesized by precipitation method. Then they were coated with polyethylene imine and gold. After loading the drug doxorubicin into the magnetic iron oxide nanoparticles, the physiochemical parameters of the nanosystem from the point of view of insertion efficiency, drug release profile under similar conditions of healthy and cancer cells, size, zeta potential and morphology were determined. Results: The magnetic nanocarriers had a diameter of 90 nm and a zeta potential of 66.7 mV. The maximum release of the drug from the nanosystem at 37°C, pH=7.4 and 42°C, pH=5.4 and after 48 hourswas 48% and 66%, respectively. The SEM analysis showed the spherical morphology and the absence of chemical interaction between the nanosystem and the drug. The investigation of the performance of the nanosystem indicated an increase in the toxicity of encapsulated doxorubicin compared to free doxorubicin at similar concentrations on the MCF_7 strain. Conclusion: The results of this research showed that the magnetic iron oxide nanoparticle system, while having appropriate physiochemical characteristics, does not change the chemical nature of the drug and can be a suitable and semi-targeted carrier for the anticancer drug doxorubicin.
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