Biomedical Engineering Reference
In-Depth Information
Fig. 6.7
Lipid bilayer formation in the presence of particles larger than the lipid bilayer thickness.
AFM images (
left
) of lipid bilayer formation over a surface with 5-20nm silica nanoparticles (a-d):
a
substrate with particles and no lipid,
b
a surface partially covered by lipid bilayer (shown in
silver
color
),
c
a lipid bilayer formed on the substrate,
d
an image of the lipid bilayer after “subtraction”
of the particles and the substrate. AFM images (
right
) of lipid bilayer formation over the surface
with mixed 5-140nm silica particles (e-h):
e
the substrate with particles and no lipid,
f
partial
coverage of the surface by a lipid bilayer,
g
a lipid bilayer formed on the substrate, and
h
an image
of the lipid bilayer after “subtraction” of the particles and the substrate. Schematics in the center
illustrate how the lipid bilayer forms a pore around particles smaller than 22nm (
i
) and how it may
envelop the larger particles (
j
). The structure of the bilayer area encircled in
j
is speculative because
it cannot be resolved or assumed from AFM experiments. This figure with its description has been
taken with the publisher's permission from [
22
]
time, the nanoparticles may use that time-dependent opening to travel to the cellular
interior. Based on this hypothesis we aim to develop a novel nanotechnology-based
drug delivery method. A detailed explanation is presented below.
6.4.1 Membrane Transport of Nanoparticles Through
Lipid-Lined Ion Pores
Chemotherapy drugs are found to induce lipid-lined toroidal pores in lipid mem-
peptides such as magainin, melittin, colicin, etc., also induce toroidal pores (see
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