Baxa Ulrich
Cancer Research Technology Program, Electron Microscopy Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, P.O. Box B, Frederick, MD, 21702, USA.
Methods Mol Biol. 2018;1682:73-88. doi: 10.1007/978-1-4939-7352-1_8.
TEM is an important method for the characterization of size and shape of nanoparticles as it can directly visualize single particles and even their inner architecture. Imaging of metal particles in the electron microscope is quite straightforward due to their high density and stable structure, but the structure of soft material nanoparticles, such as liposomes, needs to be preserved for the electron microscope. The best method to visualize liposomes close to their native structure is cryo-electron microscopy, where thin films of suspensions are plunge frozen to create vitrified ice films that can be imaged directly in the electron microscope under liquid nitrogen temperature. Although subject to artifacts, negative staining TEM can also be a useful method to image liposomes, as it is faster and simpler than cryo-EM, and requires less advanced equipment.
透射电子显微镜(TEM)是表征纳米颗粒尺寸和形状的重要方法,因为它可以直接观察单个颗粒甚至其内部结构。由于金属颗粒密度高且结构稳定,在电子显微镜中对其成像相当简单,但对于脂质体等软材料纳米颗粒,其结构需要为电子显微镜进行保留。观察接近其天然结构的脂质体的最佳方法是冷冻电子显微镜,即将悬浮液薄膜快速冷冻以形成玻璃化冰膜,该冰膜可在液氮温度下直接在电子显微镜中成像。尽管存在假象,但负染色透射电子显微镜也可以是一种用于脂质体成像的有用方法,因为它比冷冻电镜更快、更简单,并且所需设备不太先进。