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Label-free raman spectral imaging of intracellular delivery and degradation of polymeric nanoparticle systems

机译:聚合物纳米颗粒系统细胞内递送和降解的无标记拉曼光谱成像

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摘要

Novel optical imaging methods, such as Raman microspectroscopy, have been gaining recognition in their ability to obtain noninvasively the distribution of biochemical components of a sample. Raman spectroscopy in combination with optical microscopy provides a label-free method to assess and image cellular processes, without the use of extrinsic fluorescent dyes. The submicrometer resolution of the confocal Raman instrumentation allows us to image cellular organelles on the scale of conventional microscopy. We used the technique to monitor subcellular degradation patterns of two biodegradable nanocarrier systems-poly-(ε-caprolactone) (PCL) and poly(lactic-co-glycolic acid) (PLGA). Our results suggest that both drug-delivery systems eventually are incorporated into Golgi-associated vesicles of late endosomes. These processes were monitored via the decrease of the molecule-characteristic peaks of PCL and PLGA. As the catabolic pathways proceed, shifts and variations in peak intensities and intensity ratios in the rendered Raman spectra unequivocally delineate their degradation patterns.
机译:新颖的光学成像方法(例如拉曼光谱法)已经获得了无损获取样品生化成分分布的能力的认可。拉曼光谱与光学显微镜相结合,提供了一种无需标记的方法,无需使用外部荧光染料即可评估和成像细胞过程。共焦拉曼仪器的亚微米分辨率使我们能够以常规显微镜的规模对细胞器进行成像。我们使用该技术来监测两个可生物降解的纳米载体系统-聚-(ε-己内酯)(PCL)和聚(乳酸-乙醇酸)(PLGA)的亚细胞降解模式。我们的结果表明,两种药物递送系统最终都被整合到晚期内体的高尔基体相关囊泡中。通过PCL和PLGA的分子特征峰的减少来监测这些过程。随着分解代谢途径的进行,绘制的拉曼光谱中峰强度和强度比的变化和变化明确地描绘了其降解模式。

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