posted on 2019-07-25, 11:34authored byXianyu Song, Chongzhi Qiao, Teng Zhao, Bo Bao, Shuangliang Zhao, Jing Xu, Honglai Liu
Membrane
wrapping pathway of injectable hydrogels (IHs) plays a
vital role in the nanocarrier effectiveness and biomedical safety.
Although considerable progress in understanding this complicated process
has been made, the mechanism behind this process has remained elusive.
Herein, with the help of large-scale dissipative particle dynamics
simulations, we explore the molecular mechanism of membrane wrapping
by systematically examining the IH architectures and hydrogel–lipid
binding strengths. To the best of our knowledge, this is the first
report on the membrane wrapping pathway on which IHs transform from
vertical capillary adhesion to lateral compressed wrapping. This transformation
results from the elastocapillary deformation of networked gels and
nanoscale confinement of the bilayer membrane, and it takes long time
for the IHs to be fully wrapped owing to the high energy barriers
and wrapping-induced shape deformation. Collapsed morphologies and
small compressed angles are identified in the IH capsules with a thick
shell or strong binding strength to lipids. In addition, the IHs binding
intensively to the membrane exhibit special nanoscale mixing and favorable
deformability during the wrapping process. Our study provides a detailed
mechanistic understanding of the influence of architecture and binding
strength on the IH membrane wrapping efficiency. This work may serve
as rational guidance for the design and fabrication of IH-based drug
carriers and tissue engineering.