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Patterned Liposome–Polymer Composite Coatings
Author(s) -
Zhang Yan,
Lynge Martin E.,
Nielsen Morten B.,
Schattling Philipp S.,
Han Xiaojun,
Städler Brigitte
Publication year - 2016
Publication title -
chemnanomat
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.947
H-Index - 32
ISSN - 2199-692X
DOI - 10.1002/cnma.201600022
Subject(s) - composite number , materials science , adhesion , coating , cell adhesion , adhesive , drug delivery , layer (electronics) , polymer , liposome , substrate (aquarium) , biomolecule , nanotechnology , chemical engineering , composite material , oceanography , geology , engineering
Engineered biointerfaces are crucial for many biomedical applications involving the interaction of (bio)materials with cells and tissue. Providing cues to support cell adhesion/proliferation in the form of biomolecules and/or by providing spatially controlled adhesive patches are important aspects. We demonstrate the assembly of composite films consisting of negatively charged liposomes (L n ), poly(dopamine) or cholesterol‐modified poly(methacrylic acid) (PMA c ) capping layers and (poly( l ‐lysine)/PMA c ) x terminating multilayers. We show that hepatocytes adhere to the assembled composite coatings. Their association with fluorescent lipids from the film varies depending on the capping layer and cell adhesion time. This association was suggested to be an energy‐dependent process. Further, the incorporation of paclitaxel (TX) into L n reduces the number of hepatocytes adhering to films without terminating multilayers. An exemplary composite coating is patterned, and the subsequent site‐selective adhesion of hepatocytes is shown. For the first time, composite coatings to be used for substrate‐mediated drug delivery with control over the positioning of the adhering cells are shown.