PMID- 27709890 OWN - NLM STAT- MEDLINE DCOM- 20181106 LR - 20181106 IS - 1944-8252 (Electronic) IS - 1944-8244 (Linking) VI - 8 IP - 43 DP - 2016 Nov 2 TI - A Biodegradable Polycationic Paint that Kills Bacteria in Vitro and in Vivo. PG - 29298-29309 AB - Bacterial colonization and subsequent formation of biofilms onto surfaces of medical devices and implants is a major source of nosocomial infections. Most antibacterial coatings to combat infections are either metal-based or nondegradable-polymer-based and hence limited by their nondegradability and unpredictable toxicity. Moreover, to combat infections effectively, the coatings are required to display simultaneous antibacterial and antibiofilm activity. Herein we report biocompatible and biodegradable coatings based on organo-soluble quaternary chitin polymers which were immobilized noncovalently onto surfaces as bactericidal paint. The polycationic paint was found to be active against both drug-sensitive and -resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Enterococcus faecium (VRE), and beta-lactam-resistant Klebsiella pneumoniae. The cationic polymers were shown to interact with the negatively charged bacterial cell membrane and disrupt the membrane integrity, thereby causing leakage of intracellular constituents and cell death upon contact. Importantly, surfaces coated with the polymers inhibited formation of biofilms against both Gram-positive S. aureus and Gram-negative E. coli, two of the most clinically important bacteria that form biofilms. Surfaces coated with the polymers displayed negligible toxicity against human erythrocytes and embryo kidney cells. Notably, the polymers were shown to be susceptible toward lysozyme. Furthermore, subcutaneous implantation of polymer discs in rats led to 15-20% degradation in 4 weeks thereby displaying their biodegradability. In a murine model of subcutaneous infection, polymer-coated medical-grade catheter reduced MRSA burden by 3.7 log compared to that of noncoated catheter. Furthermore, no biofilm development was observed on the coated catheters under in vivo conditions. The polycationic materials thus developed herein represent a novel class of safe and effective coating agents for the prevention of device-associated infections. FAU - Hoque, Jiaul AU - Hoque J AD - Chemical Biology and Medicinal Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research , Jakkur, Bengaluru 560064, India. FAU - Akkapeddi, Padma AU - Akkapeddi P AD - Chemical Biology and Medicinal Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research , Jakkur, Bengaluru 560064, India. FAU - Ghosh, Chandradhish AU - Ghosh C AD - Chemical Biology and Medicinal Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research , Jakkur, Bengaluru 560064, India. FAU - Uppu, Divakara S S M AU - Uppu DS AD - Chemical Biology and Medicinal Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research , Jakkur, Bengaluru 560064, India. FAU - Haldar, Jayanta AU - Haldar J AD - Chemical Biology and Medicinal Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research , Jakkur, Bengaluru 560064, India. LA - eng PT - Journal Article DEP - 20161020 PL - United States TA - ACS Appl Mater Interfaces JT - ACS applied materials & interfaces JID - 101504991 RN - 0 (Anti-Bacterial Agents) SB - IM MH - Animals MH - Anti-Bacterial Agents MH - Biofilms MH - Escherichia coli MH - Humans MH - Mice MH - Microbial Sensitivity Tests MH - *Paint MH - Rats MH - Staphylococcus aureus OTO - NOTNLM OT - anti-infective biomaterials OT - biodegradable bactericidal paint OT - biofilm inhibition OT - drug-resistant bacteria OT - organo-soluble quaternary chitin derivatives EDAT- 2016/11/03 06:00 MHDA- 2018/11/07 06:00 CRDT- 2016/10/07 06:00 PHST- 2016/11/03 06:00 [pubmed] PHST- 2018/11/07 06:00 [medline] PHST- 2016/10/07 06:00 [entrez] AID - 10.1021/acsami.6b09804 [doi] PST - ppublish SO - ACS Appl Mater Interfaces. 2016 Nov 2;8(43):29298-29309. doi: 10.1021/acsami.6b09804. Epub 2016 Oct 20.