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Multi-scale imaging of anticancer platinum(iv) compounds in murine tumor and kidney

机译:鼠肿瘤和肾脏中抗癌铂(iv)化合物的多尺度成像

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摘要

Nano-scale secondary ion mass spectrometry (NanoSIMS) enables trace element and isotope analyses with high spatial resolution. This unique capability has recently been exploited in several studies analyzing the subcellular distribution of Au and Pt anticancer compounds. However, these studies were restricted to cell culture systems. To explore the applicability to the in vivo setting, we developed a combined imaging approach consisting of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), NanoSIMS and transmission electron microscopy (TEM) suitable for multi-scale detection of the platinum distribution in tissues. Applying this approach to kidney and tumor samples upon administration of selected platinum(iv) anticancer prodrugs revealed uneven platinum distributions on both the organ and subcellular scales. Spatial platinum accumulation patterns were quantitatively assessed by LA-ICP-MS in histologically heterogeneous organs (e.g., higher platinum accumulation in kidney cortex than in medulla) and used to select regions of interest for subcellular-scale imaging with NanoSIMS. These analyses revealed cytoplasmic sulfur-rich organelles accumulating platinum in both kidney and malignant cells. Those in the tumor were subsequently identified as organelles of lysosomal origin, demonstrating the potential of the combinatorial approach for investigating therapeutically relevant drug concentrations on a submicrometer scale.
机译:纳米级二次离子质谱(NanoSIMS)使痕量元素和同位素分析具有很高的空间分辨率。最近,在分析Au和Pt抗癌化合物的亚细胞分布的多项研究中已经利用了这种独特的功能。但是,这些研究仅限于细胞培养系统。为了探索在体内环境中的适用性,我们开发了一种组合成像方法,该方法由激光烧蚀电感耦合等离子体质谱法(LA-ICP-MS),NanoSIMS和透射电子显微镜(TEM)组成,适用于多尺度检测铂在组织中的分布。施用选定的铂(iv)抗癌前药后,将该方法应用于肾脏和肿瘤样品,发现铂在器官和亚细胞尺度上均分布不均。通过LA-ICP-MS在组织学上异质的器官中定量评估了空间铂积累模式(例如,肾皮质中的铂积累高于髓质中的铂积累),并用于选择感兴趣的区域用于NanoSIMS进行亚细胞规模成像。这些分析揭示了细胞质富硫细胞器在肾脏和恶性细胞中都积累了铂。肿瘤中的那些随后被鉴定为溶酶体来源的细胞器,证明了组合方法研究亚微米级治疗相关药物浓度的潜力。

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