scanning electron microscopy (SEM) were used to
assess the morphological features of the exosomes. First,
the exosomal pellet was fixed with 1% glutaraldehyde
(Sigma, USA) and then 20 μl of the fixed exosomes
were inserted on a carbon-coated grid and allowed to dry
at room temperature for 30 minutes. Then, a LEO 906
TEM (Zeiss, Germany) was used to each the samples
were washed twice with PBS for 5 minutes, and stained
with 1% uranyl acetate for 10 minutes before they were
visualized under a TEM at an accelerating voltage of 80
kV. DigitalMicrographsoftware (Gatan, Inc., Washington,
DC, USA) was used to record the TEM images that
were acquired with an Orius 200 camera (Gatan, Inc.,
Washington, DC, USA). We also assessed the particle
surface morphology by SEM. A total of 1 to 5 μl of the
dried sample was placed on a silicon chip, fixed with
2% paraformaldehyde and sputter-coated with gold-palladium, then visualised by SEM at 30 kV.