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Detecting ordered small molecule drug aggregates in live macrophages: a multi-parameter microscope image data acquisition and analysis strategy

机译:检测活巨噬细胞中有序的小分子药物聚集体:多参数显微镜图像数据采集和分析策略

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摘要

Following prolonged administration, certain orally bioavailable but poorly soluble small molecule drugs are prone to precipitate out and form crystal-like drug inclusions (CLDIs) within the cells of living organisms. In this research, we present a quantitative multi-parameter imaging platform for measuring the fluorescence and polarization diattenuation signals of cells harboring intracellular CLDIs. To validate the imaging system, the FDA-approved drug clofazimine (CFZ) was used as a model compound. Our results demonstrated that a quantitative multi-parameter microscopy image analysis platform can be used to study drug sequestering macrophages, and to detect the formation of ordered molecular aggregates formed by poorly soluble small molecule drugs in animals.
机译:长时间给药后,某些口服生物利用度但难溶的小分子药物易于在活生物体细胞内沉淀并形成晶体状药物夹杂物(CLDI)。在这项研究中,我们提出了一个定量的多参数成像平台,用于测量细胞内CLDI的细胞的荧光和偏振衰减信号。为了验证成像系统,将FDA批准的药物clofazimine(CFZ)用作模型化合物。我们的结果表明,定量多参数显微镜图像分析平台可用于研究螯合巨噬细胞,以及检测由难溶性小分子药物在动物体内形成的有序分子聚集体的形成。

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