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3D Nanoporous Anodic Alumina Structures for Sustained Drug Release

机译:用于持续药物释放的3D纳米多孔阳极氧化铝结构

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摘要

The use of nanoporous anodic alumina (NAA) for the development of drug delivery systems has gained much attention in recent years. The release of drugs loaded inside NAA pores is complex and depends on the morphology of the pores. In this study, NAA, with different three-dimensional (3D) pore structures (cylindrical pores with several pore diameters, multilayered nanofunnels, and multilayered inverted funnels) were fabricated, and their respective drug delivery rates were studied and modeled using doxorubicin as a model drug. The obtained results reveal optimal modeling of all 3D pore structures, differentiating two drug release stages. Thus, an initial short-term and a sustained long-term release were successfully modeled by the Higuchi and the Korsmeyer–Peppas equations, respectively. This study demonstrates the influence of pore geometries on drug release rates, and further presents a sustained long-term drug release that exceeds 60 days without an undesired initial burst.
机译:近年来,将纳米多孔阳极氧化铝(NAA)用于药物输送系统的开发已引起了广泛关注。 NAA孔内装载的药物的释放很复杂,并且取决于孔的形态。在这项研究中,制造了具有不同三维(3D)孔结构(具有多个孔径的圆柱孔,多层纳米漏斗和多层倒漏斗)的NAA,并以阿霉素为模型研究了它们各自的药物传递速率并进行了建模。药品。获得的结果揭示了对所有3D孔结构的最佳建模,从而区分了两个药物释放阶段。因此,分别通过Higuchi和Korsmeyer-Peppas方程分别成功地模拟了初始短期释放和持续长期释放。这项研究证明了孔的几何形状对药物释放速率的影响,并进一步提出了超过60天的持续长期药物释放,而没有不希望的初始爆发。

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