Please use this identifier to cite or link to this item: http://lib.jncasr.ac.in:8080/jspui/handle/10572/2301
Title: A Biodegradable Polycationic Paint that Kills Bacteria in Vitro and in Vivo
Authors: Hoque, Jiaul
Akkapeddi, Padma
Ghosh, Chandradhish
Uppu, Divakara S. S. M.
Haldar, Jayanta
Keywords: Materials Science
biodegradable bactericidal paint
anti-infective biomaterials
drug-resistant bacteria
biofilm inhibition
organo-soluble quaternary chitin derivatives
Broad-Spectrum Antibacterial
Eradicate Biofilms
Small Molecules
One-Step
Coatings
Resistance
Surface
Infection
Release
Films
Issue Date: 2016
Publisher: American Chemical Society
Citation: Hoque, J.; Akkapeddi, P.; Ghosh, C.; Uppu, Dssm; Haldar, J., A Biodegradable Polycationic Paint that Kills Bacteria in Vitro and in Vivo. Acs Applied Materials & Interfaces 2016, 8 (43), 29298-29309 http://dx.doi.org/10.1021/acsami.6b09804
ACS Applied Materials & Interfaces
8
43
Abstract: 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.
Description: Open Access (Accepted Manuscript)
URI: http://hdl.handle.net/10572/2301
ISSN: 1944-8244
Appears in Collections:Research Papers (Jayanta Haldar)

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