a.Institute of Biomedical Engineering and Health Sciences, Changzhou University, Changzhou 213164, China
b.Department of Chemical and Biomolecular Engineering, National University of Singapore, 117585, Singapore
zhouchao@cczu.edu.cn
收稿:2020-07-28,
修回:2020-9-16,
录用:2020-10-5,
网络首发:2020-10-26,
纸质出版:2021-01-01
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Zhou, C.; Zhou, J. T.; Sheng, C. J.; Pranantyo, D.; Pan, Y.; Huang, X. J. Robust and self-healable antibiofilm multilayer coatings. Chinese J. Polym. Sci. 2021, 39, 425–440
Chao Zhou, Jun-Tao Zhou, Cheng-Ju Sheng, et al. Robust and Self-healable Antibiofilm Multilayer Coatings[J]. Chinese Journal of Polymer Science, 2021, 39(4): 425-440.
Zhou, C.; Zhou, J. T.; Sheng, C. J.; Pranantyo, D.; Pan, Y.; Huang, X. J. Robust and self-healable antibiofilm multilayer coatings. Chinese J. Polym. Sci. 2021, 39, 425–440 DOI: 10.1007/s10118-021-2513-3.
Chao Zhou, Jun-Tao Zhou, Cheng-Ju Sheng, et al. Robust and Self-healable Antibiofilm Multilayer Coatings[J]. Chinese Journal of Polymer Science, 2021, 39(4): 425-440. DOI: 10.1007/s10118-021-2513-3.
The infection induced by implantation of biomedical materials may result from the biofilm formation after bacteria attachment. Hence
the antibiofilm surface coating represents a novel technique to improve the antibacterial activity of biomedical materials. The traditional antibiofilm surface coatings exhibited some disadvantages and provided a limited service life. In this work
we used polyethyleneimine grafted 3-maleimidopropionic acid (PEIM) and poly(acrylic acid) grafted 2-furfurylamine (PAAF) to achieve robust and self-healable crosslinked multilayer coatings
employing Layer-by-Layer (LbL) self-assembly technique and Diels-Alder reaction. Then
thiol-terminated poly((3-acrylamidopropyl) trimethylammonium chloride) (PAMPTMA-SH) was grafted onto the crosslinked multilayer coating by thiol-ene click reaction to form a novel multilayer coating (PEIM/PAAF)
10
-PAMPTMA. We found that this coating showed robust and self-healable activity
and significantly inhibited the bacterial growth and biofilm formation after infection with
Escherichia coli
(
E. coli
) and
Staphylococcus aureus
(
S. aureus
) by
in vitro
and
in vivo
assays for 120 h. In addition
the multilayer coating did not induce significant hemolysis or affect the cell viability of red blood cells.
In vivo
studies also showed that (PEIM/PAAF)
10
-PAMPTMA coating efficiently blocked the infiltration of inflammatory cells and gene expression in the mouse skin challenged with
E. coli
or
S. aureus
. Taken together
these results showed that the prepared multilayer coating exhibited strong antibiofilm activity and provided a new strategy for the application of highly efficient antibiofilm surface coating of biomedical materials.
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