PMID- 21851105 OWN - NLM STAT- MEDLINE DCOM- 20120125 LR - 20220408 IS - 1936-086X (Electronic) IS - 1936-0851 (Linking) VI - 5 IP - 9 DP - 2011 Sep 27 TI - Antibacterial activity of graphite, graphite oxide, graphene oxide, and reduced graphene oxide: membrane and oxidative stress. PG - 6971-80 LID - 10.1021/nn202451x [doi] AB - Health and environmental impacts of graphene-based materials need to be thoroughly evaluated before their potential applications. Graphene has strong cytotoxicity toward bacteria. To better understand its antimicrobial mechanism, we compared the antibacterial activity of four types of graphene-based materials (graphite (Gt), graphite oxide (GtO), graphene oxide (GO), and reduced graphene oxide (rGO)) toward a bacterial model-Escherichia coli. Under similar concentration and incubation conditions, GO dispersion shows the highest antibacterial activity, sequentially followed by rGO, Gt, and GtO. Scanning electron microscope (SEM) and dynamic light scattering analyses show that GO aggregates have the smallest average size among the four types of materials. SEM images display that the direct contacts with graphene nanosheets disrupt cell membrane. No superoxide anion (O(2)(*-)) induced reactive oxygen species (ROS) production is detected. However, the four types of materials can oxidize glutathione, which serves as redox state mediator in bacteria. Conductive rGO and Gt have higher oxidation capacities than insulating GO and GtO. Results suggest that antimicrobial actions are contributed by both membrane and oxidation stress. We propose that a three-step antimicrobial mechanism, previously used for carbon nanotubes, is applicable to graphene-based materials. It includes initial cell deposition on graphene-based materials, membrane stress caused by direct contact with sharp nanosheets, and the ensuing superoxide anion-independent oxidation. We envision that physicochemical properties of graphene-based materials, such as density of functional groups, size, and conductivity, can be precisely tailored to either reducing their health and environmental risks or increasing their application potentials. CI - (c) 2011 American Chemical Society FAU - Liu, Shaobin AU - Liu S AD - School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore 637459. FAU - Zeng, Tingying Helen AU - Zeng TH FAU - Hofmann, Mario AU - Hofmann M FAU - Burcombe, Ehdi AU - Burcombe E FAU - Wei, Jun AU - Wei J FAU - Jiang, Rongrong AU - Jiang R FAU - Kong, Jing AU - Kong J FAU - Chen, Yuan AU - Chen Y LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. DEP - 20110824 PL - United States TA - ACS Nano JT - ACS nano JID - 101313589 RN - 0 (Anti-Bacterial Agents) RN - 0 (Reactive Oxygen Species) RN - 7782-42-5 (Graphite) RN - GAN16C9B8O (Glutathione) SB - IM MH - Anti-Bacterial Agents/*pharmacology MH - Cell Membrane/*drug effects MH - Escherichia coli/drug effects MH - Glutathione/metabolism MH - Graphite/*pharmacology MH - Light MH - Microscopy, Electron, Scanning MH - Oxidative Stress/*drug effects MH - Reactive Oxygen Species/metabolism MH - Scattering, Radiation EDAT- 2011/08/20 06:00 MHDA- 2012/01/26 06:00 CRDT- 2011/08/20 06:00 PHST- 2011/08/20 06:00 [entrez] PHST- 2011/08/20 06:00 [pubmed] PHST- 2012/01/26 06:00 [medline] AID - 10.1021/nn202451x [doi] PST - ppublish SO - ACS Nano. 2011 Sep 27;5(9):6971-80. doi: 10.1021/nn202451x. Epub 2011 Aug 24.