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Atomic Force Microscopy Images Label-Free Drug Encapsulated Nanoparticles In Vivo and Detects Difference in Tissue Mechanical Properties of Treated and Untreated: A Tip for Nanotoxicology

机译:原子力显微镜图像体内无标签药物包裹的纳米颗粒并检测处理过的和未处理的组织力学性能的差异:纳米毒理学的技巧

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摘要

Overcoming the intractable challenge of imaging of label-free, drug encapsulated nanoparticles in tissues in vivo would directly address associated regulatory concerns over 'nanotoxicology'. Here we demonstrate the utility of Atomic Force Microscopy (AFM) for visualising label-free, drug encapsulated polyester particles of ∼280 nm distributed within tissues following their intravenous or peroral administration to rodents. A surprising phenomenon, in which the tissues' mechanical stiffness was directly measured (also by AFM) and related to the number of embedded nanoparticles, was utilised to generate quantitative data sets for nanoparticles localisation. By coupling the normal determination of a drug's pharmacokinetics/pharmacodynamics with post-sacrifice measurement of nanoparticle localisation and number, we present for the first time an experimental design in which a single in vivo study relates the PK/PD of a nanomedicine to its toxicokinetics.
机译:克服体内组织中无标签,药物包裹的纳米颗粒成像的棘手挑战,将直接解决有关“纳米毒理学”的相关监管问题。在这里,我们展示了原子力显微镜(AFM)的实用性,可用于可视化无标记,约280 nm的药物包裹的聚酯包封的聚酯颗粒,这些颗粒在静脉内或经口给予啮齿动物后分布在组织内。令人惊讶的现象被用来生成定量数据集以进行纳米粒子定位,在这种现象中,直接测量了组织的机械刚度(也通过AFM),并且与嵌入的纳米粒子的数量有关。通过将药物的药代动力学/药效学的正常测定与牺牲后的纳米颗粒定位和数量测量相结合,我们首次提出了一项实验设计,其中一项体内研究将纳米药物的PK / PD与它的毒代动力学联系起来。

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