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Size and surface charge of gold nanoparticles determine absorption across intestinal barriers and accumulation in secondary target organs after oral administration

机译:金纳米颗粒的大小和表面电荷决定了口服给药后跨肠屏障的吸收和在次级靶器官中的积累

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摘要

It is of urgent need to identify the exact physico-chemical characteristics which allow maximum uptake and accumulation in secondary target organs of nanoparticulate drug delivery systems after oral ingestion. We administered radiolabelled gold nanoparticles in different sizes (1.4-200 nm) with negative surface charge and 2.8 nm nanoparticles with opposite surface charges by intra-oesophageal instillation into healthy adult female rats. The quantitative amount of the particles in organs, tissues and excrements was measured after 24 h by gamma-spectroscopy. The highest accumulation in secondary organs was mostly found for 1.4 nm particles; the negatively charged particles were accumulated mostly more than positively charged particles. Importantly, 18 nm particles show a higher accumulation in brain and heart compared to other sized particles. No general rule accumulation can be made so far. Therefore, specialized drug delivery systems via the oral route have to be individually designed, depending on the respective target organ.
机译:迫切需要确定确切的理化特性,以允许在口服后最大程度地摄取和积累纳米颗粒药物递送系统的次要靶器官。我们通过食管内滴入健康成年雌性大鼠,施用了具有负表面电荷的不同尺寸(1.4-200 nm)的放射性标记金纳米颗粒和具有相反表面电荷的2.8 nm纳米颗粒。 24小时后通过γ光谱法测量器官,组织和排泄物中颗粒的定量数量。在次要器官中积累最多的是1.4 nm颗粒。带负电的粒子比带正电的粒子积累更多。重要的是,与其他尺寸的粒子相比,18 nm粒子在大脑和心脏中显示出更高的积累。到目前为止,尚无一般规则的积累。因此,取决于各自的靶器官,必须单独设计经由口服途径的专用药物递送系统。

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