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Updated: Mar 12, 2026

Direct Stochastic Optical Reconstruction Microscopy of Extracellular Vesicles in Three Dimensions
Published on: August 26, 2021
Environmental Scanning Electron Microscope Imaging of Vesicle Systems.
Yvonne Perrie1, Habib Ali2, Daniel J Kirby2
1Strathclyde Institute of Pharmacy and Biomedical Sciences, Glasgow, G4 ORE, Scotland. yvonne.perrie@strath.ac.uk.
Environmental Scanning Electron Microscopy (ESEM) allows real-time imaging of liposomes in their natural hydrated state. This technique reveals insights into liposome stability and resistance to dehydration, offering a new formulation assay.
Area of Science:
- Materials Science
- Biophysics
- Nanotechnology
Background:
- Liposome morphology is well-understood through techniques like electron microscopy.
- Existing methods often require sample dehydration or fixation, limiting observation of natural states.
- Studying liposomes in their native hydrated form is challenging.
Purpose of the Study:
- To introduce Environmental Scanning Electron Microscopy (ESEM) as a novel method for imaging liposomes and niosomes.
- To demonstrate the ability to observe liposomes in their hydrated state without extensive preparation.
- To investigate liposome behavior during hydration and dehydration processes in real-time.
Main Methods:
- Application of Environmental Scanning Electron Microscopy (ESEM) to liposomes and niosomes.
- Real-time observation of hydration dynamics (water condensation and evaporation).
- Analysis of liposome structural changes during environmental shifts.
Main Results:
- ESEM successfully imaged liposomes and niosomes in their hydrated state.
- Dynamic changes in liposome suspensions were observed as water content varied.
- Insights were gained into the resistance of liposomes to coalescence during dehydration.
Conclusions:
- ESEM provides a valuable tool for studying liposomes and niosomes in their native hydrated conditions.
- This method offers real-time insights into liposome stability and dehydration resistance.
- ESEM presents an alternative assay for evaluating liposome formulation and stability.
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