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In Situ Infrared Ellipsometry for Protein Adsorption Studies on Ultrathin Smart Polymer Brushes in Aqueous Environment
Author(s) -
Annika Kroning,
Andreas Furchner,
Dennis Aulich,
Eva Bittrich,
Sebastian Rauch,
Petra Uhlmann,
KlausJochen Eichhorn,
Michael Seeber,
Igor Luzinov,
S. Michael Kilbey,
Bradley S. Lokitz,
Sergiy Minko,
Karsten Hinrichs
Publication year - 2015
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/am5075997
Subject(s) - polymer , materials science , adsorption , protein adsorption , aqueous solution , ellipsometry , chemical engineering , biosensor , bioanalysis , gelatin , in situ , nanotechnology , thin film , organic chemistry , chemistry , engineering , composite material
The protein-adsorbing and -repelling properties of various smart nanometer-thin polymer brushes containing poly(N-isopropylacrylamide) and poly(acrylic acid) with high potential for biosensing and biomedical applications are studied by in situ infrared-spectroscopic ellipsometry (IRSE). IRSE is a highly sensitive nondestructive technique that allows protein adsorption on polymer brushes to be investigated in an aqueous environment as external stimuli, such as temperature and pH, are varied. These changes are relevant to conditions for regulation of protein adsorption and desorption for biotechnology, biocatalysis, and bioanalytical applications. Here brushes are used as model surfaces for controlling protein adsorption of human serum albumin and human fibrinogen. The important finding of this work is that IRSE in the in situ experiments in protein solutions can distinguish between contributions of polymer brushes and proteins. The vibrational bands of the polymers provide insights into the hydration state of the brushes, whereas the protein-specific amide bands are related to changes of the protein secondary structure.

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