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Nanoscale infrared absorption imaging permits non-destructive intracellular photosensitizer localization for subcellular uptake analysis

机译:纳米级红外吸收成像可实现非破坏性细胞内光敏剂定位,用于亚细胞吸收分析

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The most immediate biological and medical advantages of therapeutic agent localization on the nanoscale arise from the increased understanding of targeted delivery, selectivity and intracellular distribution that are gained by imaging at the resolution scale of individual nanovectors and therapeutic agents themselves. This paper reports on the use of a nanoscale resolution chemical imaging method, infrared (IR) nanospectral absorption imaging, used to map the subcellular localization of a photoactive therapeutic agent - toluidine blue-conjugated gold nanoparticles (TBO) within nanoscale subsections of single colon adenocarcinoma cells. By comparison of photosensitizer distribution with diffraction limited optical imaging, the benefits of IR nanospectral localization are highlighted and the spatial and spectral accuracy of the non-destructive IR imaging method is confirmed. IR spectral ratio imaging is presented as a means to map intracellular nanoparticle density at sub 50 nm lateral resolution with IR nanospectroscopy enabling distinction of nanoparticle seeded cells from a control group with 95% confidence. In this way we illustrate that IR absorption nanoimaging combined with IR point source data does not only yield intracellular drug detection on the order of nanometres, but also permits extension of the AFM-IR technique from subcellular analysis up to studies of cell numbers that are statistically significant.
机译:纳米级治疗剂定位的最直接的生物学和医学优势来自对靶向递送,选择性和细胞内分布的日益了解,这是通过在单个纳米载体和治疗剂本身的分辨率范围内进行成像获得的。本文报道了纳米分辨率化学成像方法,红外(IR)纳米光谱吸收成像的使用,该方法用于在单结肠腺癌的纳米级区域内绘制光活性治疗剂-甲苯胺蓝共轭金纳米颗粒(TBO)的亚细胞定位图细胞。通过将光敏剂分布与衍射受限的光学成像进行比较,突出了红外纳米光谱定位的优势,并确认了非破坏性红外成像方法的空间和光谱准确性。红外光谱比成像是作为一种手段来绘制细胞内纳米颗粒密度的横向分辨率低于50 nm的红外纳米光谱仪,能够以95%的置信度区分纳米颗粒接种的细胞与对照组。通过这种方式,我们说明了红外吸收纳米成像与红外点源数据相结合,不仅可以产生纳米级的细胞内药物检测,而且还允许将AFM-IR技术从亚细胞分析扩展到统计上的细胞数量研究重大。

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