Department of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Avenue, Houston, TX 77030, United States.
School of Biological and Health Systems Engineering, Virginia G. Piper Biodesign Center for Personalized Diagnostics, The Biodesign Institute, Arizona State University, 727 E. Tyler St. B 130-B, Tempe, AZ 85287, United States.
Anal Chem. 2016 Dec 20;88(24):12001-12005. doi: 10.1021/acs.analchem.6b03661. Epub 2016 Nov 28.
Nanoparticles have become a powerful tool for cell imaging and biomolecule, cell and protein interaction studies, but are difficult to rapidly and accurately measure in most assays. Dark-field microscope (DFM) image analysis approaches used to quantify nanoparticles require high-magnification near-field (HN) images that are labor intensive due to a requirement for manual image selection and focal adjustments needed when identifying and capturing new regions of interest. Low-magnification far-field (LF) DFM imagery is technically simpler to perform but cannot be used as an alternate to HN-DFM quantification, since it is highly sensitive to surface artifacts and debris that can easily mask nanoparticle signal. We now describe a new noise reduction approach that markedly reduces LF-DFM image artifacts to allow sensitive and accurate nanoparticle signal quantification from LF-DFM images. We have used this approach to develop a "Dark Scatter Master" (DSM) algorithm for the popular NIH image analysis program ImageJ, which can be readily adapted for use with automated high-throughput assay analyses. This method demonstrated robust performance quantifying nanoparticles in different assay formats, including a novel method that quantified extracellular vesicles in patient blood sample to detect pancreatic cancer cases. Based on these results, we believe our LF-DFM quantification method can markedly decrease the analysis time of most nanoparticle-based assays to impact both basic research and clinical analyses.
纳米粒子已成为细胞成像和生物分子、细胞和蛋白质相互作用研究的有力工具,但在大多数检测中很难快速准确地测量。用于量化纳米粒子的暗场显微镜 (DFM) 图像分析方法需要高倍近场 (HN) 图像,由于需要手动选择图像和调整焦点以识别和捕获新的感兴趣区域,因此这项工作非常耗时。低倍远场 (LF) DFM 成像是一种技术上更简单的操作方法,但不能替代 HN-DFM 定量,因为它对表面伪影和碎片非常敏感,这些伪影和碎片很容易掩盖纳米粒子的信号。我们现在描述了一种新的降噪方法,该方法可显著减少 LF-DFM 图像伪影,从而可以从 LF-DFM 图像中对纳米粒子信号进行灵敏、准确的定量。我们已经使用这种方法为流行的 NIH 图像分析程序 ImageJ 开发了一种“暗散射主”(DSM) 算法,该算法可以很容易地适应自动化高通量检测分析。该方法在不同检测方案中对纳米粒子的表现出了稳健的定量性能,包括一种在患者血液样本中定量检测细胞外囊泡以检测胰腺癌病例的新方法。基于这些结果,我们相信我们的 LF-DFM 定量方法可以显著减少大多数基于纳米粒子的检测的分析时间,从而对基础研究和临床分析产生影响。