Imaging of Liposomes by Transmission Electron Microscopy
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 t...
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Published in | Methods in molecular biology (Clifton, N.J.) Vol. 1682; p. 73 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
United States
2018
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Abstract | 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. |
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AbstractList | 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. |
Author | Baxa, Ulrich |
Author_xml | – sequence: 1 givenname: Ulrich surname: Baxa fullname: Baxa, Ulrich email: Ulrich.Baxa@nih.gov organization: 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. Ulrich.Baxa@nih.gov |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29039095$$D View this record in MEDLINE/PubMed |
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Keywords | Negative staining Lipids Emulsions Transmission electron microscopy Liposomes Cryo-electron microscopy |
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SubjectTerms | Cryoelectron Microscopy - methods Freezing Liposomes - ultrastructure Microscopy, Electron, Transmission - methods Negative Staining - methods |
Title | Imaging of Liposomes by Transmission Electron Microscopy |
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