posted on 2020-07-29, 20:15authored byJessica
A. Kretzmann, Cameron W. Evans, Lei Feng, Nicholas B. Lawler, Marck Norret, Michael J. Higgins, K. Swaminathan Iyer
Successful
intracellular delivery of therapeutics requires interactions
at several liquid–solid interfaces, including cell surface,
endosomal membranes, anddepending on the therapeuticthe
nuclear membrane. Understanding the dynamics of polymer kinetics at
the liquid–solid interface is fundamental for the design of
polymers for such biomedical delivery applications. However, the effect
of polymer architecture and charge density on polymer kinetics is
not readily investigated using routine techniques, and the role of
such parameters in the context of gene delivery remains unknown. We
adopted a synthetic strategy which enabled the systematic manipulation
of charge density, flexibility, and molecular weight using a dendronized
linear polymeric architecture. High-speed atomic force microscopy
(HS-AFM) was used as a label-free method to directly observe the polymers’
dynamic properties, such as velocity, displacement, and diffusion,
in physiologically relevant conditions. Importantly, we found that
the physical parameters measured by HS-AFM relate to the transfection
potential of the individual polymers and may be a valuable tool in
screening structural polymer variants.