@article{27022b5b82ae44eca1cd4e429a9a0d44,
title = "Polyphosphazenes enable durable, hemocompatible, highly efficient antibacterial coatings",
abstract = "Biocompatible antibacterial coatings are highly desirable to prevent bacterial colonization on a wide range of medical devices from hip implants to skin grafts. Traditional polyelectrolytes are unable to directly form coatings with cationic antibiotics at neutral pH and suffer from high degrees of antibiotic release upon exposure to physiological concentrations of salt. Here, novel inorganic-organic hybrid polymer coatings based on direct layer-by-layer assembly of anionic polyphosphazenes (PPzs) of various degrees of fluorination with cationic antibiotics (polymyxin B, colistin, gentamicin, and neomycin) are reported. The coatings displayed low levels of antibiotic release upon exposure to salt and pH-triggered response of controlled doses of antibiotics. Importantly, coatings remained highly surface active against Escherichia coli and Staphylococcus aureus, even after 30 days of pre-exposure to physiological conditions (bacteria-free) or after repeated bacterial challenge. Moreover, coatings displayed low (<1\%) hemolytic activity for both rabbit and porcine blood. Coatings deposited on either hard (Si wafers) or soft (electrospun fiber matrices) materials were non-toxic towards fibroblasts (NIH/3T3) and displayed controllable fibroblast adhesion via PPz fluorination degree. Finally, coatings showed excellent antibacterial activity in ex vivo pig skin studies. Taken together, these results suggest a new avenue to form highly tunable, biocompatible polymer coatings for medical device surfaces.",
keywords = "Antibacterial, Fluoropolymers, Hemocompatible, Layer-by-layer, Polyphosphazenes, Self-defensive",
author = "Victoria Albright and Daniel Penarete-Acosta and Mary Stack and Jeremy Zheng and Alexander Marin and Hanna Hlushko and Hongjun Wang and Arul Jayaraman and Andrianov, \{Alexander K.\} and Sukhishvili, \{Svetlana A.\}",
note = "Funding Information: This work was supported by the National Science Foundation under Award DMR-1808483 (S.S.) and DMR-1808531 (A.A.) and partially by National Institute of Arthritis and Musculoskeletal and Skin Diseases, United States award number 1R01AR067859 (H.W.). V.A. acknowledges financial support from Texas A\&M University/Association of Former Students Graduate Merit Fellowship and Texas A\&M Engineering Experiment Station (TEES). M.S. was supported by the Robert Crooks Stanley Graduate Fellowship in Engineering and Science. Authors are grateful to Samantha Hernandez, Danielle Yarbrough, and Christian Frey, who participated in this work through the Aggie Research Program, for help with sample preparation and Dr. Papatya Kaner (University of Maryland) for assistance with conducting DLS experiments. Authors are grateful to Yuhao Wang (Former SIT) for conducting experiments with keratinocytes. Authors acknowledge use of the Integrated Metabolomics Analysis Core and the Materials Characterization Facility at Texas A\&M University. Authors thank Jordan Brito for preparing final samples for the ex vivo pig skin study. Funding Information: This work was supported by the National Science Foundation under Award DMR-1808483 (S.S.) and DMR-1808531 (A.A.) and partially by National Institute of Arthritis and Musculoskeletal and Skin Diseases, United States award number 1R01AR067859 (H.W.). V.A. acknowledges financial support from Texas A\&M University/Association of Former Students Graduate Merit Fellowship and Texas A\&M Engineering Experiment Station ( TEES ). M.S. was supported by the Robert Crooks Stanley Graduate Fellowship in Engineering and Science . Authors are grateful to Samantha Hernandez, Danielle Yarbrough, and Christian Frey, who participated in this work through the Aggie Research Program, for help with sample preparation and Dr. Papatya Kaner (University of Maryland) for assistance with conducting DLS experiments. Authors are grateful to Yuhao Wang (Former SIT) for conducting experiments with keratinocytes. Authors acknowledge use of the Integrated Metabolomics Analysis Core and the Materials Characterization Facility at Texas A\&M University. Authors thank Jordan Brito for preparing final samples for the ex vivo pig skin study. Publisher Copyright: {\textcopyright} 2020 Elsevier Ltd",
year = "2021",
month = jan,
doi = "10.1016/j.biomaterials.2020.120586",
language = "English",
volume = "268",
journal = "Biomaterials",
issn = "0142-9612",
publisher = "Elsevier Ltd",
}