Corrigendum to “Activation of biologically relevant levels of reactive oxygen species by Au/g-C3N4 hybrid nanozyme for bacteria killing and wound disinfection” (Biomaterials (2017) 113 (145–157), (S0142961216305919), (10.1016/j.biomaterials.2016.10.041));Activation of biologically relevant levels of reactive oxygen species by Au/g-C3N4 hybrid nanozyme for bacteria killing and wound disinfection

Biomaterials

Volumn 113, Issue , 2017, Pages 145-157

  Wang, Zhenzhen ^a,b   Dong, Kai ^a   Liu, Zhen ^a   Zhang, Yan ^a,b   Chen, Zhaowei ^a,b   Sun, Hanjun ^a,b   Ren, Jinsong ^a   Qu, Xiaogang ^a  

^a CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Biologically relevant levels; Gold nanoparticles; Graphitic carbon nitride; Reactive oxygen species; Wound disinfection

Indexed keywords

BIOFILMS; CARBON NITRIDE; CHEMICAL ACTIVATION; DISINFECTION; FREE RADICALS; GOLD COMPOUNDS; GOLD NANOPARTICLES; NITRIDES; OXYGEN;

BACTERIAL INACTIVATION; BACTERIAL INFECTIONS; BIOLOGICALLY RELEVANT LEVELS; GRAM-POSITIVE BACTERIUM; GRAPHITIC CARBON NITRIDES; PEROXIDASE ACTIVITIES; PHYSIOLOGICAL LEVELS; REACTIVE OXYGEN SPECIES;

BACTERIA;

ANTIBIOTIC AGENT; CARBON NITRIDE GOLD NANOPARTICLE; GOLD NANOPARTICLE; GRAPHITE; HYDROGEN PEROXIDE; HYDROXYL RADICAL; NANOCOMPOSITE; PEROXIDASE; UNCLASSIFIED DRUG; VANCOMYCIN; ANTIINFECTIVE AGENT; CYANOGEN; GOLD; NITRILE; REACTIVE OXYGEN METABOLITE;

3T3 CELL LINE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BACTERIAL INFECTION; BACTERIAL VIABILITY; BACTERICIDAL ACTIVITY; BACTERIUM CULTURE; BIOCOMPATIBILITY; BIOFILM; BIOMASS; BIOSAFETY; CATALYSIS; CELL DENSITY; CONTROLLED STUDY; DECOMPOSITION; DISINFECTION; ENZYME ACTIVITY; IN VITRO STUDY; IN VIVO STUDY; LUNG INFECTION; LUNG LAVAGE; MDA MB 231 CELL LINE; METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS; MOUSE; NONHUMAN; OXIDATION; PRIORITY JOURNAL; WOUND CARE; WOUND DRESSING; ZETA POTENTIAL; ANIMAL; BACTERIUM; BAGG ALBINO MOUSE; CHEMISTRY; COMPLICATION; DRUG EFFECTS; HUMAN; INJURY; MALE; METABOLISM; MICROBIOLOGY;

ANIMALS; ANTI-BACTERIAL AGENTS; BACTERIA; BACTERIAL INFECTIONS; BIOFILMS; DISINFECTION; GOLD; GRAPHITE; HUMANS; MALE; MICE, INBRED BALB C; NITRILES; REACTIVE OXYGEN SPECIES; WOUNDS AND INJURIES;

EID: 84994259608     PISSN: 01429612     EISSN: 18785905     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2019.119754     Document Type: Erratum

References (70)

1. [1] Hook, A.L., Chang, C.Y., Yang, J., Atkinson, S., Langer, R., Anderson, D.G., et al. Discovery of novel materials with broad resistance to bacterial attachment using combinatorial polymer microarrays. Adv. Mater. 25 (2013), 2542–2547.
2. [2] Zhao, Y., Chen, Z., ChenY, Xu J., Li, J., Jiang, X., Synergy of non-antibiotic drugs and pyrimidinethiol on gold nanoparticles against superbugs. J. Am. Chem. Soc. 135 (2013), 12940–12943.
3. [3] Pham, V.T.H., Truong, V.K., Quinn, M.D.J., Notley, S.M., Guo, Y., Baulin, V.A., et al. Graphene induces formation of pores that kill spherical and rod-shaped bacteria. ACS Nano 9 (2015), 8458–8467.
4. [4] Barraud, N., Kardak, B.G., Yepuri, N.R., Howlin, R.P., Webb, J.S., Faust, S.N., et al. Cephalosporin-3'-diazeniumdiolates: targeted no-donor prodrugs for dispersing bacterial biofilms. Angew. Chem. Int. Ed. 51 (2012), 9057–9060.
5. [5] Durmus, N.G., Taylor, E.N., Kummer, K.M., Webster, T.J., Enhanced efficacy of superparamagnetic iron oxide nanoparticles against antibiotic-resistant biofilms in the presence of metabolites. Adv. Mater. 25 (2013), 5706–5713.
6. [6] Li, Y., Fukushima, K., Coady, D.J., Engler, A.C., Liu, S., Huang, Y., et al. Broad-spectrum antimicrobial and biofilm-disrupting hydrogels: stereocomplex-driven supramolecular assemblies. Angew. Chem. Int. Ed. 52 (2013), 674–678.
7. [7] Liu, R., Chen, X., Falk, S.P., Masters, K.S., Weisblum, B., Gellman, S.H., Nylon-3 polymers active against drug-resistant candida albicans biofilms. J. Am. Chem. Soc. 137 (2015), 2183–2186.
8. [8] Chen, W.Y., Chang, H.Y., Lu, J.K., Huang, Y.C., Harroun, S.G., Tseng, Y.T., et al. Self-assembly of antimicrobial peptides on gold nanodots: against multidrug-resistant bacteria and wound-healing application. Adv. Funct. Mater. 25 (2015), 7189–7199.
9. [9] Zhao, Y., Tian, Y., Cui, Y., Liu, W., Ma, W., Jiang, X., Small molecule-capped gold nanoparticles as potent antibacterial agents that target gram-negative bacteria. J. Am. Chem. Soc. 132 (2010), 12349–12356.
10. [10] Fasciani, C., Silvero, M.J., Anghel, M.A., Arguello, G.A., Becerra, M.C., Scaiano, J.C., Aspartame-stabilized gold-silver bimetallic biocompatible nanostructures with plasmonic photothermal properties, antibacterial activity and long-term stability. J. Am. Chem. Soc. 136 (2014), 17394–17397.
11. 3 nanocontainers and their antibacterial effect on tuberculosis mycobacteria. Angew. Chem. Int. Ed. 127 (2015), 12786–12791.
12. [12] Xiong, M.H., Li, Y.J., Bao, Y., Yang, X.Z., Hu, B., Wang, J., Bacteria-responsive multifunctional nanogel for targeted antibiotic delivery. Adv. Mater. 24 (2012), 6175–6180.
13. [13] Hu, W., Peng, C., Luo, W., Lv, M., Li, X., Li, D., et al. Graphene-based antibacterial paper. ACS Nano 4 (2010), 4317–4323.
14. [14] Ivanova, E.P., Hasan, J., Webb, H.K., Gervinskas, G., Juodkazis, S., Truong, V.K., et al. Bactericidal activity of black silicon. Nat. Commun. 4 (2013), 2838–2844.
15. [15] Zhao, Y., Ye, C., Liu, W., Chen, R., Jiang, X., Tuning the composite of AuPt biometallic nanoparticles for antibacterial application. Angew. Chem. Int. Ed. 53 (2014), 8127–8131.
16. [16] Richter, A.P., Brown, J.S., Bharti, B., Wang, A., Gangwal, S., Houck, K., et al. An environmentally benign antimicrobial nanoparticle based on a silver-infused lignin core. Nat. Nanotechnol 10 (2015), 817–823.
17. [17] Lucky, S.S., Soo, K.C., Zhang, Y., Nanoparticles in photodynamic therapy. Chem. Rev. 115 (2015), 1990–2042.
18. [18] Strassert, C.A., Otter, M., Albuquerque, R.Q., Höne, A., Vida, Y., Maier, B., et al. Photoactive hybrid nanomaterial for targeting, labeling, and killing antibiotic-resistant bacteria. Angew. Chem. Int. Ed. 48 (2009), 7928–7931.
19. [19] Zhu, C., Yang, Q., Liu, L., Lv, F., Li, S., Yang, G., et al. Multifunctional cationic poly(p-phenylene vinylene) polyelectrolytes for selective recognition, imaging, and killing of bacteria over mammalian cells. Adv. Mater. 23 (2011), 4805–4810.
20. [20] Su, H.L., Chou, C.C., Hung, D.J., Lin, S.H., Pao, I.C., Lin, J.H., et al. The disruption of bacterial membrane integrity through ROS generation induced by nanohybrids of silver and clay. Biomaterials 30 (2009), 5979–5987.
21. [21] Zhang, C., Zhao, K., Bu, W., Ni, D., Liu, Y., Feng, J., et al. Marriage of scintillator and semiconductor for synchronous radiotherapy and deep photodynamic therapy with diminished oxygen dependence. Angew. Chem. Int. Ed. 127 (2015), 1790–1794.
22. [22] Becker, M.H., Harris, R.N., Cutaneous bacteria of the redback salamander prevent morbidity associated with a lethal disease. PloS One 5 (2010), 10957–10962.
23. [23] Mishra, S., Imlay, J., Why do bacteria use so many enzymes to scavenge hydrogen peroxide?. Biochem. Biophys. 525 (2012), 145–160.
24. [24] Gao, L., Giglio, K.M., Nelson, J.L., Sondermann, H., Travis, A.J., Ferromagnetic nanoparticles with peroxidase-like activity enhance the cleavage of biological macromolecules for biofilm elimination. Nanoscale 6 (2014), 2588–2593.
25. [25] Dickinson, B.C., Chang, C.J., Chemistry and biology of reactive oxygen species in signaling or stress responses. Nat. Chem. Biol. 7 (2011), 504–511.
26. [26] Loo, A.E.K., Wong, Y.T., Ho, R., Wasser, M., Du, T., Ng, W.T., et al. Effects of Hydrogen peroxide on wound healing in mice in relation to oxidative damage. PloS One 7 (2012), 49215–49227.
27. [27] Natalio, F., Andre, R., Hartog, A.F., Stoll, B., Jochum, K.P., Wever, R., et al. Vanadium pentoxide nanoparticles mimic vanadium haloperoxidases and thwart biofilm formation. Nat. Nanotechnol 7 (2012), 530–535.
28. [28] Sun, H., Gao, N., Dong, K., Ren, J., Qu, X., Graphene quantum dots-band-aids used for wound disinfection. ACS Nano 8 (2014), 6202–6210.
29. 4 nanosheets for bioimaging. J. Am. Chem. Soc. 135 (2013), 18–21.
30. 4 quantum dots for two-photon fluorescence imaging of cellular nucleus. Adv. Mater. 26 (2014), 4438–4443.
31. [31] Cao, S., Low, J., Yu, J., Jaroniec, M., Polymeric photocatalysts based on graphitic carbon nitride. Adv. Mater. 27 (2015), 2150–2176.
32. 4)-based photosynthesis and environmental remediation: are we a step closer to achieving sustainability?. Chem. Rev. 116 (2016), 7159–7329.
33. [33] Pawar, R., Pyo, Y., Ahn, S., Lee, C., Photoelectrochemical properties and photodegradation of organic pollutants using hematite hybrids modified by gold nanoparticles and graphitic carbon nitride. Appl. Catal. B-Environ. 176 (2015), 654–656.
34. 4/CNTs/Au) hybrid photocatalysts for effective water splitting and degradation. RSC Adv. 5 (2015), 24281–24292.
35. [35] Jun, Y.S., Park, J., Lee, S.U., Thomas, A., Hong, W.H., Stucky, G.D., Three-dimensional macroscopic assemblies of low-dimensional carbon nitrides for enhanced hydrogen evolution. Angew. Chem. Int. Ed. 52 (2013), 11083–11087.
36. [36] Kang, Y., Yang, Y., Yin, L.C., Kang, X., Liu, G., Cheng, H.M., An amorphous carbon nitride photocatalyst with greatly extended visible-light-responsive range for photocatalytic hydrogen generation. Adv. Mater. 27 (2015), 4572–4577.
37. [37] Liang, Q., Li, Z., Yu, X., Huang, Z.H., Kang, F., Yang, Q.H., Macroscopic 3D porous graphitic carbon nitride monolith for enhanced photocatalytic hydrogen evolution. Adv. Mater. 27 (2015), 4634–4639.
38. [38] Yang, S., Gong, Y., Zhang, J., Zhan, L., Ma, L., Fang, Z., et al. Exfoliated Graphitic carbon nitride nanosheets as efficient catalysts for hydrogen evolution under visible light. Adv. Mater. 25 (2013), 2452–2456.
39. [39] Wang, X., Maeda, K., Thomas, A., Takanabe, K., Xin, G., Carlsson, J.M., et al. A metal-free polymeric photocatalyst for hydrogen production from water under visible light. Nat. Mater. 8 (2009), 76–80.
40. [40] Tian, J., Liu, Q., Asiri, A.M., Qusti, A.H., Al-Youbi, A.O., Sun, X., Ultrathin graphitic carbon nitride nanosheets: a novel peroxidase mimetic, Fe doping-mediated catalytic performance enhancement and application to rapid, highly sensitive optical detection of glucose. Nanoscale 5 (2013), 11604–11609.
41. [41] Asati, A., Santra, S., Kaittanis, C., Nath, S., Perez, J.M., Oxidase-like activity of polymer-coated cerium oxide nanoparticles. Angew. Chem. Int. Ed. 48 (2009), 2308–2312.
42. [42] Diez-Castellnou, M., Mancin, F., Scrimin, P., Efficient phosphodiester cleaving nanozymes resulting from multivalency and local medium polarity control. J. Am. Chem. Soc. 136 (2014), 1158–1161.
43. [43] Sun, H., Miao, L., Li, J., Fu, S., An, G., Si, C., et al. Self-assembly of cricoid proteins induced by “soft nanoparticles”: an approach to design multienzyme-cooperative antioxidative systems. ACS Nano 9 (2015), 5461–5469.
44. [44] Tao, Y., Lin, Y., Huang, Z., Ren, J., Qu, X., Incorporating graphene oxide and gold nanoclusters: a synergistic catalyst with surprisingly high peroxidase-like activity over a broad pH range and its application for cancer cell detection. Adv. Mater. 25 (2013), 2594–2599.
45. [45] Xue, T., Jiang, S., Qu, Y., Su, Q., Cheng, R., Dubin, S., et al. Graphene-supported hemin as a highly active biomimetic oxidation catalyst. Angew. Chem. Int. Ed. 51 (2012), 3822–3855.
46. 2 microspheres: an ideal artificial enzymatic cascade system. Chem. Commun. 49 (2013), 4643–4645.
47. [47] Ge, S., Liu, F., Liu, W., Yan, M., Song, X., Yu, J., Colorimetric assay of K-562 cells based on folic acid-conjugated porous bimetallic Pd@Au nanoparticles for point-of-care testing. Chem. Commun. 50 (2014), 475–477.
48. [48] Zheng, X., Liu, Q., Jing, C., Li, Y., Li, D., Luo, W., et al. Catalytic gold nanoparticles for nanoplasmonic detection of DNA hybridization. Angew. Chem. Int. Ed. 50 (2011), 11994–11998.
49. [49] Jv, Y., Li, B., Cao, R., Positively-charged gold nanoparticles as peroxidase mimic and their application in hydrogen peroxide and glucose detection. Chem. Commun. 46 (2010), 8017–8019.
50. [50] Zhang, Z., Berg, A., Levanon, H., Fessenden, R.W., Meisel, D., On the interactions of free radicals with gold nanoparticles. J. Am. Chem. Soc. 125 (2003), 7959–7963.
51. [51] Liu, M., Zhao, H., Chen, S., Yu, H., Quan, X., Interface engineering catalytic graphene for smart colorimetric biosensing. ACS Nano 6 (2012), 3142–3151.
52. [52] Ma, T., Tang, Y., Dai, S., Qiao, S., Proton-functionalized two-dimensional graphitic carbon nitride nanosheet: an excellent metal-/label-free biosensing platform. Small 10 (2014), 2382–2389.
53. 4 nanosheet nanohybrids used for electrochemiluminescent immunosensor. Anal. Chem. 86 (2014), 4188–4195.
54. [54] Tao, Y., Ju, E., Ren, J., Qu, X., Bifunctionalized mesoporous silica-supported gold nanoparticles: intrinsic oxidase and peroxidase catalytic activities for antibacterial applications. Adv. Mater. 27 (2015), 1097–1104.
55. [55] Liu, B., Liu, J., Accelerating peroxidase mimicking nanozymes using DNA. Nanoscale 7 (2015), 13831–13835.
56. [56] He, W., Kim, H.Y., Wamer, W.G., Melka, D., Callahan, J.H., Yin, J., Photogenerated charge carriers and reactive oxygen species in ZnO/Au hybrid nanostructures with enhanced photocatalytic and actibacterial activity. J. Am. Chem. Soc. 136 (2014), 750–757.
57. 5 nanowires with an intrinsic peroxidase-like activity. Adv. Funct. Mater. 21 (2011), 501–509.
58. [58] Tu, Y., Lv, M., Xiu, P., Huynh, T., Zhang, M., Castelli, M., et al. Destructive extraction of phospholipids from Escherichia coli membranes by graphene nanosheets. Nat. Nanotechnol 8 (2013), 594–601.
59. [59] Swartjes, J.J.T.M., Das, T., Sharifi, S., Subbiahdoss, G., Sharma, P.K., Krom, B.P., et al. A functional DNase I coating to prevent adhesion of bacteria and the formation of biofilm. Adv. Funct. Mater. 23 (2013), 2843–2849.
60. [60] Costerton, J.W., Stewart, P.S., Greenberg, E.P., Bacterial biofilms: a common cause of persistent infections. Science 284 (1999), 1318–1322.
61. [61] De Gracia Lux, C., Joshi-Barr, S., Nguyen, T., Mahmoud, E., Schopf, E., et al. Biocompatible polymeric nanoparticles degrade and release cargo in response to biologically relevant levels of hydrogen peroxide. J. Am. Chem. Soc. 134 (2012), 15758–15764.
62. [62] Balakrishnan, B., Mohanty, M., Umashankar, P.R., Jayakrishnan, A., Evaluation of an in situ forming hydrogel wound dressing based on oxidized alginate and gelatin. Biomaterials 26 (2005), 6335–6342.
63. [63] Meddahi-Pellé , A., Legrand, A., Marcellan , A., Louedec, L., Letourneur, D., Leibler, L., Organ repair, hemostasis, and in vivo bonding of medical devices by aqueous solutions of nanoparticles. Angew. Chem. Int. Ed. 53 (2014), 6369–6373.
64. [64] Okamura, Y., Kabata, K., Kinoshita, M., Miyazaki, H., Saito, A., Fujie, T., et al. Fragmentation of poly(lactic acid) nanosheets and patchwork treatment for burn wounds. Adv. Mater. 25 (2013), 545–551.
65. [65] Fan, Z.J., Liu, B., Wang, J.Q., Zhang, S.Y., Lin, Q.Q., Gong, P.W., et al. A novel wound dressing based on ag/graphene polymer hydrogel: effectively kill bacteria and accelerate wound healing. Adv. Funct. Mater. 24 (2014), 3933–3943.
66. [66] Boukerb, A.M., Rousset, A., Galanos, N., Mear, J.B., Thepaut, M., et al. Antiadhesive properties of glycoclusters against pseudomonas aeruginosa lung infection. J. Med. Chem. 57 (2014), 10275–10289.
67. [67] Huo, D., Ding, J., Cui, Y.X., Xia, L.Y., Li, H., He, J., et al. X-ray CT and pneumonia inhibition properties of gold-silver nanoparticles for targeting MRSA induced pneumonia. Biomaterials 35 (2014), 7032–7041.
68. [68] Klibanov, A.L., Maruyama, K., Torchilin, V.P., Huang, L., Amphipathic polyethyleneglycols effectively prolong the circulation time of liposomes. FBBS Lett. 268 (1990), 235–237.
69. [69] Shimizu, A., Katoh, H., Hamaoka, S., Kinoshita, M., Akiyama, K., Naito, Y., et al. Protective effects of intravenous immunoglobulin and antimicrobial agents on acute pneumonia in leukopenic mice. J. Infect. Chemother. 22 (2016), 240–247.
70. [70] Van de Bittner, G.C., Bertozzi, C.R., Chang, C.J., Strategy for dual-analyte luciferin imaging: in vivo bioluminescence detection of hydrogen peroxide and caspase activity in a murine model of acute inflammation. J. Am. Chem. Soc. 135 (2013), 1783–1795.