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Magnetic dipole interaction of endogenous magnetic nanoparticles with magnetoliposomes for targeted drug delivery

机译:内源性磁性纳米粒子与磁脂质体的磁偶极相互作用,用于靶向药物递送

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摘要

Dynamics of magnetoliposomes binding to the tumor cells and the efficiency of their recognition for targeted drug delivery is largely determined by physical interaction. In this paper we assess the strength of magnetic dipole interaction that occurs between endogenous magnetic nanoparticles in tumor cells and exogenous magnetic nanoparticles as a component of magnetoliposomes, and compare it with the forces of specific binding of the antigen-antibody complex. To assess the strength of magnetic dipole interaction the model of chains of identical particles was used, and an order of magnitude, 10-9 N, was obtained. Thus, the indicated force has an order of magnitude close to the forces of specific binding, and even more. The force of magnetic dipole interaction between a magnetically marked dosage form and tumor cells is virtually the additional specific binding force - "passive targeting" for targeted drug delivery in consequence of the fact that tumor cells tend to contain the number of biogenic nanoparticles of magnetite (Fe3O4) by an order of magnitude greater than normal.
机译:磁脂质体与肿瘤细胞结合的动力学及其对靶向药物递送的识别效率在很大程度上取决于物理相互作用。在本文中,我们评估了肿瘤细胞中内源性磁性纳米颗粒与作为脂质体组分的外源性磁性纳米颗粒之间发生的磁偶极相互作用的强度,并将其与抗原-抗体复合物的特异性结合力进行了比较。为了评估磁偶极子相互作用的强度,使用了相同颗粒的链模型,得到的量级为10-9N。因此,指示的力的数量级接近于特异性结合力,甚至更大。磁性标记剂型与肿瘤细胞之间的磁偶极相互作用力实际上是额外的特异性结合力-靶向药物递送的“被动靶向”,原因是肿瘤细胞倾向于包含磁铁矿的生物纳米颗粒( Fe3O4)比正常值大一个数量级。

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