Parhamifar Ladan, Moghimi S Moein
Centre for Pharmaceutical Nanotechnology and Nanotoxicology, University of Copenhagen, Copenhagen Ø, Denmark.
Methods Mol Biol. 2012;906:473-82. doi: 10.1007/978-1-61779-953-2_38.
Nanoparticulate systems are widely used for site-specific drug and gene delivery as well as for medical imaging. The mode of nanoparticle-cell interaction may have a significant effect on the pathway of nanoparticle internalization and subsequent intracellular trafficking. Total internal reflection fluorescence (TIRF) microscopy allows for real-time monitoring of nanoparticle-membrane interaction events, which can provide vital information in relation to design and surface engineering of therapeutic nanoparticles for cell-specific targeting. In contrast to other microscopy techniques, the bleaching effect by lasers in TIRF microscopy is considerably less when using fluorescent nanoparticles and it reduces photo-induced cytotoxicity during visualization of live-cell events since it only illuminates the specific area near or at the plasma membrane.
纳米颗粒系统广泛应用于特定部位的药物和基因递送以及医学成像。纳米颗粒与细胞的相互作用模式可能对纳米颗粒内化途径及随后的细胞内运输产生重大影响。全内反射荧光(TIRF)显微镜能够实时监测纳米颗粒与膜的相互作用事件,这可为用于细胞特异性靶向的治疗性纳米颗粒的设计和表面工程提供重要信息。与其他显微镜技术相比,使用荧光纳米颗粒时,TIRF显微镜中激光的漂白效应要小得多,并且由于它仅照亮质膜附近或质膜处的特定区域,因此在活细胞事件可视化过程中可降低光诱导的细胞毒性。