Recent advances in metal-organic framework-based materials for anti-staphylococcus aureus infection

Mei Yang; Jin Zhang; Yinhao Wei; Jie Zhang; Chuanmin Tao

doi:10.1007/s12274-022-4302-x

1

Mermel, L. A.; Cartony, J. M.; Covington, P.; Maxey, G.; Morse, D. Methicillin-resistant Staphylococcus aureus colonization at different body sites: A prospective, quantitative analysis. J. Clin. Microbiol. 2011, 49, 1119–1121.

DOI Google Scholar

2

Blicharz, L.; Michalak, M.; Szymanek-Majchrzak, K.; Młynarczyk, G.; Skowroński, K.; Rudnicka, L.; Samochocki, Z. The propensity to form biofilm in vitro by Staphylococcus aureus strains isolated from the anterior nares of patients with atopic dermatitis: Clinical associations. Dermatology 2021, 237, 528–534.

DOI Google Scholar

3

Von Eiff, C.; Becker, K.; Machka, K.; Stammer, H.; Peters, G. Nasal carriage as a source of Staphylococcus aureus bacteremia. N. Engl. J. Med. 2001, 344, 11–16.

DOI Google Scholar

4

Sollid, J. U. E.; Furberg, A. S.; Hanssen, A. M.; Johannessen, M. Staphylococcus aureus: Determinants of human carriage. Infect. Genet. Evol. 2014, 21, 531–541.

DOI Google Scholar

5

Tong, S. Y. C.; Davis, J. S.; Eichenberger, E.; Holland, T. L.; Fowler, V. G. Jr. Staphylococcus aureus infections: Epidemiology, pathophysiology, clinical manifestations, and management. Clin. Microbiol. Rev. 2015, 28, 603–661.

DOI Google Scholar

6

Laupland, K. B. Incidence of bloodstream infection: A review of population-based studies. Clin. Microbiol. Infect. 2013, 19, 492–500.

DOI Google Scholar

7

Sampedro, G. R.; DeDent, A. C.; Becker, R. E. N.; Berube, B. J.; Gebhardt, M. J.; Cao, H. Y.; Bubeck Wardenburg, J. Targeting Staphylococcus aureus α-toxin as a novel approach to reduce severity of recurrent skin and soft-tissue infections. J. Infect. Dis. 2014, 210, 1012–1018.

DOI Google Scholar

8

Laxminarayan, R.; Duse, A.; Wattal, C.; Zaidi, A. K. M.; Wertheim, H. F. L.; Sumpradit, N.; Vlieghe, E.; Hara, G. L.; Gould, I. M.; Goossens, H. et al. Antibiotic resistance—The need for global solutions. Lancet Infect. Dis. 2013, 13, 1057–1098.

DOI Google Scholar

9

Blair, J. M. A.; Webber, M. A.; Baylay, A. J.; Ogbolu, D. O.; Piddock, L. J. V. Molecular mechanisms of antibiotic resistance. Nat. Rev. Microbiol. 2015, 13, 42–51.

DOI Google Scholar

10

Li, R.; Chen, T. T.; Pan, X. L. Metal-organic-framework-based materials for antimicrobial applications. ACS Nano 2021, 15, 3808–3848.

DOI Google Scholar

11

Pettinari, C.; Pettinari, R.; Di Nicola, C.; Tombesi, A.; Scuri, S.; Marchetti, F. Antimicrobial MOFs. Coord. Chem. Rev. 2021, 446, 214121.

DOI Google Scholar

12

Nong, W. Q.; Wu, J.; Ghiladi, R. A.; Guan, Y. G. The structural appeal of metal-organic frameworks in antimicrobial applications. Coord. Chem. Rev. 2021, 442, 214007.

DOI Google Scholar

13

Gorai, T.; Schmitt, W.; Gunnlaugsson, T. Highlights of the development and application of luminescent lanthanide based coordination polymers, MOFs and functional nanomaterials. Dalton Trans. 2021, 50, 770–784.

DOI Google Scholar

14

Sun, T. T.; Xu, L. B.; Wang, D. S.; Li, Y. D. Metal organic frameworks derived single atom catalysts for electrocatalytic energy conversion. Nano Res. 2019, 12, 2067–2080.

DOI Google Scholar

15

Giliopoulos, D.; Zamboulis, A.; Giannakoudakis, D.; Bikiaris, D.; Triantafyllidis, K. Polymer/metal organic framework (MOF) nanocomposites for biomedical applications. Molecules 2020, 25, 185.

DOI Google Scholar

16

Liu, Y. W.; Zhou, L. Y.; Dong, Y.; Wang, R.; Pan, Y.; Zhuang, S. Z.; Liu, D.; Liu, J. Q. Recent developments on MOF-based platforms for antibacterial therapy. RSC Med. Chem. 2021, 12, 915–928.

DOI Google Scholar

17

Omidi, M. ; Firoozeh, F. ; Saffari, M. ; Sedaghat, H. ; Zibaei, M. ; Khaledi, A. Ability of biofilm production and molecular analysis of spa and ica genes among clinical isolates of methicillin-resistant Staphylococcus aureus. BMC Res. Notes 2020, 13, 19.https://doi.org/10.1186/s13104-020-4885-9

DOI

18

Williams, R. E. O. Healthy carriage of Staphylococcus aureus: Its prevalence and importance. Bacteriol. Rev. 1963, 27, 56–71.

DOI Google Scholar

19

Wertheim, H. F. L.; Melles, D. C.; Vos, M. C.; van Leeuwen, W.; van Belkum, A.; Verbrugh, H. A.; Nouwen, J. L. The role of nasal carriage in Staphylococcus aureus infections. Lancet Infect. Dis. 2005, 5, 751–762.

DOI Google Scholar

20

Boyle-Vavra, S.; Daum, R. S. Community-acquired methicillinresistant Staphylococcus aureus: The role of Panton-Valentine leukocidin. Lab. Invest. 2007, 87, 3–9.

DOI Google Scholar

21

Lowy, F. D. Staphylococcus aureus infections. N. Engl. J. Med. 1998, 339, 520–532.

DOI Google Scholar

22

Archer, G. L. Staphylococcus aureus: A well-armed pathogen. Clin. Infect. Dis. 1998, 26, 1179–1181.

DOI Google Scholar

23

Boyce, J. M.; Pittet, D. Guideline for hand hygiene in health-care settings. Recommendations of the healthcare infection control practices advisory committee and the HICPAC/SHEA/APIC/IDSA hand hygiene task force. Society for healthcare epidemiology of America/Association for professionals in infection control/infectious diseases society of America. MMWR Recomm. Rep. 2002, 51, 1–45.

DOI Google Scholar

24

Sherertz, R. J.; Reagan, D. R.; Hampton, K. D.; Robertson, K. L.; Streed, S. A.; Hoen, H. M.; Thomas, R.; Gwaltney, J. M. Jr. A cloud adult: The Staphylococcus aureus–virus interaction revisited. Ann. Intern. Med. 1996, 124, 539–547.

DOI Google Scholar

25

Zimmerli, W.; Sendi, P. Pathogenesis of implant-associated infection: The role of the host. Semin. Immunopathol. 2011, 33, 295–306.

DOI Google Scholar

26

Foster, T. J. Immune evasion by staphylococci. Nat. Rev. Microbiol. 2005, 3, 948–958.

DOI Google Scholar

27

Gladstone, G. P. Van Heyningen, W. E. Staphylococcal leucocidins. Br. J. Exp. Pathol. 1957, 38, 123–137.

Google Scholar

28

Grumann, D.; Nübel, U.; Bröker, B. M. Staphylococcus aureus toxins—Their functions and genetics. Infect. Genet. Evol. 2014, 21, 583–592.

DOI Google Scholar

29

Ma, T. M. ; VanEpps, J. S. ; Solomon, M. J. Structure, mechanics, and instability of fibrin clot infected with Staphylococcus epidermidis. Biophys. J. 2017, 113, 2100–2109.https://doi.org/10.1016/j.bpj.2017.09.001

DOI

30

Prestinaci, F.; Pezzotti, P.; Pantosti, A. Antimicrobial resistance: A global multifaceted phenomenon. Pathog. Glob. Health 2015, 109, 309–318.

DOI Google Scholar

31

Manna, D. K.; Mandal, A. K.; Sen, I. K.; Maji, P. K.; Chakraborti, S.; Chakraborty, R.; Islam, S. S. Antibacterial and DNA degradation potential of silver nanoparticles synthesized via green route. Int. J. Biol. Macromol. 2015, 80, 455–459.

DOI Google Scholar

32

Alabi, A. S.; Frielinghaus, L.; Kaba, H.; Kösters, K.; Huson, M. A. M.; Kahl, B. C.; Peters, G.; Grobusch, M. P.; Issifou, S.; Kremsner, P. G. et al. Retrospective analysis of antimicrobial resistance and bacterial spectrum of infection in Gabon, Central Africa. BMC Infect. Dis. 2013, 13, 455.

DOI Google Scholar

33

Klein, E. Y.; Sun, L.; Smith, D. L.; Laxminarayan, R. The changing epidemiology of methicillin-resistant Staphylococcus aureus in the United States: A national observational study. Am. J. Epidemiol. 2013, 177, 666–674.

DOI Google Scholar

34

Santajit, S.; Indrawattana, N. Mechanisms of antimicrobial resistance in ESKAPE pathogens. BioMed Res. Int. 2016, 2016, 2475067.

DOI Google Scholar

35

Ansari, S.; Nepal, H. P.; Gautam, R.; Shrestha, S.; Chhetri, M. R.; Chapagain, M. L. Staphylococcus Aureus: Methicillin resistance and small colony variants from pyogenic infections of skin, soft tissue and bone. J. Nepal Health Res. Counc. 2015, 13, 126–132.

Google Scholar

36

Lakhundi, S.; Zhang, K. Y. Methicillin-resistant Staphylococcus aureus: Molecular characterization, evolution, and epidemiology. Clin. Microbiol. Rev. 2018, 31, e00020–18.

DOI Google Scholar

37

Ansari, S.; Jha, R. K.; Mishra, S. K.; Tiwari, B. R.; Asaad, A. M. Recent advances in Staphylococcus aureus infection: Focus on vaccine development. Infect. Drug Resist. 2019, 12, 1243–1255.

DOI Google Scholar

38

Johnson, N. B.; Hayes, L. D.; Brown, K.; Hoo, E. C.; Ethier, K. A. CDC national health report: Leading causes of morbidity and mortality and associated behavioral risk and protective factors United States, 2005–2013. MMWR Suppl. 2014, 63, 3–27.

Google Scholar

39

Jean, S. S.; Hsueh, P. R. High burden of antimicrobial resistance in Asia. Int. J. Antimicrob. Agents 2011, 37, 291–295.

DOI Google Scholar

40

Wolk, D. M.; Struelens, M. J.; Pancholi, P.; Davis, T.; Della-Latta, P.; Fuller, D.; Picton, E.; Dickenson, R.; Denis, O.; Johnson, D. et al. Rapid detection of Staphylococcus aureus and methicillinresistant S. aureus (MRSA) in wound specimens and blood cultures: Multicenter preclinical evaluation of the Cepheid Xpert MRSA/SA skin and soft tissue and blood culture assays. J. Clin. Microbiol. 2009, 47, 823–826.

DOI Google Scholar

41

Hurley, J. C. Risk of death from methicillin-resistant Staphylococcus aureus bacteraemia: A meta-analysis. Med. J. Aust. 2002, 176, 188.

DOI Google Scholar

42

Fortuin-de Smidt, M. C.; Singh-Moodley, A.; Badat, R.; Quan, V.; Kularatne, R.; Nana, T.; Lekalakala, R.; Govender, N. P.; Perovic, O. Staphylococcus aureus bacteraemia in Gauteng academic hospitals, South Africa. Int. J. Infect. Dis. 2015, 30, 41–48.

DOI Google Scholar

43

Zou, L. L.; Wang, J.; Gao, Y.; Ren, X. Y.; Rottenberg, M. E.; Lu, J.; Holmgren, A. Synergistic antibacterial activity of silver with antibiotics correlating with the upregulation of the ROS production. Sci. Rep. 2018, 8, 11131.

DOI Google Scholar

44

Mohammed, Y. H. E.; Manukumar, H. M.; Rakesh, K. P.; Karthik, C. S.; Mallu, P.; Qin, H. L. Vision for medicine: Staphylococcus aureus biofilm war and unlocking key’s for anti-biofilm drug development. Microb. Pathog. 2018, 123, 339–347.

DOI Google Scholar

45

Yougbare, S.; Chang, T. K.; Tan, S. H.; Kuo, J. C.; Hsu, P. H.; Su, C. Y.; Kuo, T. R. Antimicrobial gold nanoclusters: Recent developments and future perspectives. Int. J. Mol. Sci. 2019, 20, 2924.

DOI Google Scholar

46

Fletcher, S. Understanding the contribution of environmental factors in the spread of antimicrobial resistance. Environ. Health Prev. Med. 2015, 20, 243–252.

DOI Google Scholar

47

Andersson, D. I.; Hughes, D. Kubicek-Sutherland, J. Z. Mechanisms and consequences of bacterial resistance to antimicrobial peptides. Drug Resist. Updates 2016, 26, 43–57.

DOI Google Scholar

48

Archer, N. K.; Mazaitis, M. J.; Costerton, J. W.; Leid, J. G.; Powers, M. E.; Shirtliff, M. E. Staphylococcus aureus biofilms: Properties, regulation, and roles in human disease. Virulence 2011, 2, 445–459.

DOI Google Scholar

49

Yaghi, O. M.; O'Keeffe, M.; Ockwig, N. W.; Chae, H. K.; Eddaoudi, M.; Kim, J. Reticular synthesis and the design of new materials. Nature 2003, 423, 705–714.

DOI Google Scholar

50

Lee, J. Y.; Farha, O. K.; Roberts, J.; Scheidt, K. A.; Nguyen, S. B. T.; Hupp, J. T. Metal-organic framework materials as catalysts. Chem. Soc. Rev. 2009, 38, 1450–1459.

DOI Google Scholar

51

Xue, Y. P.; Zhao, G. C.; Yang, R. Y.; Chu, F.; Chen, J.; Wang, L.; Huang, X. B. 2D metal-organic framework-based materials for electrocatalytic, photocatalytic and thermocatalytic applications. Nanoscale 2021, 13, 3911–3936.

DOI Google Scholar

52

Shen, M. F.; Forghani, F.; Kong, X. Q.; Liu, D. D.; Ye, X. Q.; Chen, S. G.; Ding, T. Antibacterial applications of metal-organic frameworks and their composites. Compr. Rev. Food Sci. Food Saf. 2020, 19, 1397–1419.

DOI Google Scholar

53

Usman, K. A. S.; Maina, J. W.; Seyedin, S.; Conato, M. T.; Payawan, L. M.; Dumée, L. F.; Razal, J. M. Downsizing metalorganic frameworks by bottom-up and top-down methods. NPG Asia Mater. 2020, 12, 58.

DOI Google Scholar

54

Zhang, Y. M.; Zhang, X.; Song, J.; Jin, L. M.; Wang, X. T.; Quan, C. S. Ag/H-ZIF-8 nanocomposite as an effective antibacterial agent against pathogenic bacteria. Nanomaterials 2019, 9, 1579.

DOI Google Scholar

55

Tippayawat, P.; Phromviyo, N.; Boueroy, P.; Chompoosor, A. Green synthesis of silver nanoparticles in aloe vera plant extract prepared by a hydrothermal method and their synergistic antibacterial activity. PeerJ 2016, 4, e2589.

DOI Google Scholar

56

Wang, H.; Synatschke, C. V.; Raup, A.; Jérôme, V.; Freitag, R.; Agarwal, S. Oligomeric dual functional antibacterial polycaprolactone. Polym. Chem. 2014, 5, 2453–2460.

DOI Google Scholar

57

Carović-Stanko, K. ; Orlić, S. ; Politeo, O. ; Strikić, F. ; Kolak, I. ; Milos, M. ; Satovic, Z. Composition and antibacterial activities of essential oils of sevenOcimum taxa. Food Chem. 2010, 119, 196–201.https://doi.org/10.1016/j.foodchem.2009.06.010

DOI

58

Mao, C. Y.; Xiang, Y. M.; Liu, X. M.; Cui, Z. D.; Yang, X. J.; Li, Z. Y.; Zhu, S. L.; Zheng, Y. F.; Yeung, K. W. K.; Wu, S. L. Repeatable photodynamic therapy with triggered signaling pathways of fibroblast cell proliferation and differentiation to promote bacteria-accompanied wound healing. ACS Nano 2018, 12, 1747–1759.

DOI Google Scholar

59

Liu, Z. W.; Tan, L.; Liu, X. M.; Liang, Y. Q.; Zheng, Y. F.; Yeung, K. W. K.; Cui, Z. D.; Zhu, S. L.; Li, Z. Y.; Wu, S. L. Zn2+-assisted photothermal therapy for rapid bacteria-killing using biodegradable humic acid encapsulated MOFs. Colloids Surf. B Biointerfaces 2020, 188, 110781.

DOI Google Scholar

60

Pang, X.; Xiao, Q. C.; Cheng, Y.; Ren, E.; Lian, L. L.; Zhang, Y.; Gao, H. Y.; Wang, X. Y.; Leung, W.; Chen, X. Y. et al. Bacteria responsive nanoliposomes as smart sonotheranostics for multidrug resistant bacterial infections. ACS Nano 2019, 13, 2427–2438.

DOI Google Scholar

61

Zhang, L.; Liu, Z. W.; Deng, Q. Q.; Sang, Y. J.; Dong, K.; Ren, J. S.; Qu, X. G. Nature-inspired construction of MOF@COF nanozyme with active sites in tailored microenvironment and pseudopodia-like surface for enhanced bacterial inhibition. Angew. Chem. Int. Ed. 2021, 60, 3469–3474.

DOI Google Scholar

62

Li, T.; Qiu, H. Q.; Liu, N.; Li, J. W.; Bao, Y. H.; Tong, W. J. Construction of self-activated cascade metal-organic framework/enzyme hybrid nanoreactors as antibacterial agents. Colloids Surf. B Biointerfaces 2020, 191, 111001.

DOI Google Scholar

63

Lin, S.; Liu, X. M.; Tan, L.; Cui, Z. D.; Yang, X. J.; Yeung, K. W. K.; Pan, H. B.; Wu, S. L. Porous iron-carboxylate metal-organic framework: A novel bioplatform with sustained antibacterial efficacy and nontoxicity. ACS Appl. Mater. Interfaces 2017, 9, 19248–19257.

DOI Google Scholar

64

Fan, X.; Yang, F.; Huang, J. B.; Yang, Y.; Nie, C. X.; Zhao, W. F.; Ma, L.; Cheng, C.; Zhao, C. S.; Haag, R. Metal-organic-framework derived 2D carbon nanosheets for localized multiple bacterial eradication and augmented anti-infective therapy. Nano Lett. 2019, 19, 5885–5896.

DOI Google Scholar

65

Luo, Y.; Li, J.; Liu, X. M.; Tan, L.; Cui, Z. D.; Feng, X. B.; Yang, X. J.; Liang, Y. Q.; Li, Z. Y.; Zhu, S. L. et al. Dual metal-organic framework heterointerface. ACS Cent. Sci. 2019, 5, 1591–1601.

DOI Google Scholar

66

Ge, C. C.; Wu, R. F.; Chong, Y.; Fang, G.; Jiang, X. M.; Pan, Y.; Chen, C. Y.; Yin, J. J. Synthesis of Pt hollow nano dendrites with enhanced peroxidase-like activity against bacterial infections: Implication for wound healing. Adv. Funct. Mater. 2018, 28, 1801484.

DOI Google Scholar

67

Zirak Hassan Kiadeh, S.; Ghaee, A.; Farokhi, M.; Nourmohammadi, J.; Bahi, A.; Ko, F. K. Electrospun pectin/modified copper-based metal-organic framework (MOF) nanofibers as a drug delivery system. Int. J. Biol. Macromol. 2021, 173, 351–365.

DOI Google Scholar

68

Xiang, Y. M.; Mao, C. Y.; Liu, X. M.; Cui, Z. D.; Jing, D. D.; Yang, X. J.; Liang, Y. Q.; Li, Z. Y.; Zhu, S. L.; Zheng, Y. F. et al. Rapid and superior bacteria killing of carbon quantum dots/ZnO decorated injectable folic acid-conjugated PDA hydrogel through dual-light triggered ROS and membrane permeability. Small 2019, 15, 1900322.

DOI Google Scholar

69

Geveke, D. J.; Gurtler, J.; Zrang, H. Q. Inactivation of Lactobacillus plantarum in apple cider, using radio frequency electric fields. J. Food. Prot. 2009, 72, 656–661.

DOI Google Scholar

70

Donlan, R. M.; Costerton, J. W. Biofilms: Survival mechanisms of clinically relevant microorganisms. Clin. Microbiol. Rev. 2002, 15, 167–193.

DOI Google Scholar

71

Liu, Z. W.; Wang, F. M.; Ren, J. S.; Qu, X. G. A series of MOF/Cebased nanozymes with dual enzyme-like activity disrupting biofilms and hindering recolonization of bacteria. Biomaterials 2019, 208, 21–31.

DOI Google Scholar

72

Haas, K. L.; Franz, K. J. Application of metal coordination chemistry to explore and manipulate cell biology. Chem. Rev. 2009, 109, 4921–4960.

DOI Google Scholar

73

Ma, Z.; Jacobsen, F. E.; Giedroc, D. P. Coordination chemistry of bacterial metal transport and sensing. Chem. Rev. 2009, 109, 4644–4681.

DOI Google Scholar

74

Pearson, R. G. Hard and soft acids and bases—The evolution of a chemical concept. Coord. Chem. Rev. 1990, 100, 403–425.

DOI Google Scholar

75

Nies, D. H. Efflux-mediated heavy metal resistance in prokaryotes. FEMS Microbiol. Rev. 2003, 27, 313–339.

DOI Google Scholar

76

Harrison, J. J.; Ceri, H.; Turner, R. J. Multimetal resistance and tolerance in microbial biofilms. Nat. Rev. Microbiol. 2007, 5, 928–938.

DOI Google Scholar

77

Howarth, A. J.; Liu, Y. Y.; Li, P.; Li, Z. Y.; Wang, T. C.; Hupp, J. T.; Farha, O. K. Chemical, thermal and mechanical stabilities of metal-organic frameworks. Nat. Rev. Mater. 2016, 1, 15018.

DOI Google Scholar

78

Feng, M. B.; Zhang, P.; Zhou, H. C.; Sharma, V. K. Water-stable metal-organic frameworks for aqueous removal of heavy metals and radionuclides: A review. Chemosphere 2018, 209, 783–800.

DOI Google Scholar

79

Gordon, O.; Slenters, T. V.; Brunetto, P. S.; Villaruz, A. E.; Sturdevant, D. E.; Otto, M.; Landmann, R.; Fromm, K. M. Silver coordination polymers for prevention of implant infection: Thiol interaction, impact on respiratory chain enzymes, and hydroxyl radical induction. Antimicrob. Agents Chemother. 2010, 54, 4208–4218.

DOI Google Scholar

80

Lemire, J. A.; Harrison, J. J.; Turner, R. J. Antimicrobial activity of metals: Mechanisms, molecular targets and applications. Nat. Rev. Microbiol. 2013, 11, 371–384.

DOI Google Scholar

81

Medina, E. ; Pieper, D. H. Tackling threats and future problems of multidrug-resistant bacteria. In How to Overcome the Antibiotic Crisis: Facts, Challenges, Technologies and Future Perspectives, Cham, 2016, pp 3–33.https://doi.org/10.1007/82_2016_492

DOI

82

Singh, S. B.; Barrett, J. F. Empirical antibacterial drug discovery foundation in natural products. Biochem. Pharmacol. 2006, 71, 1006–1015.

DOI Google Scholar

83

Fasnacht, M.; Polacek, N. Oxidative stress in bacteria and the central dogma of molecular biology. Front. Mol. Biosci. 2021, 8, 671037.

DOI Google Scholar

84

West, J. D.; Marnett, L. J. Endogenous reactive intermediates as modulators of cell signaling and cell death. Chem. Res. Toxicol. 2006, 19, 173–194.

DOI Google Scholar

85

Van Acker, H.; Coenye, T. The role of reactive oxygen species in antibiotic-mediated killing of bacteria. Trends Microbiol. 2017, 25, 456–466.

DOI Google Scholar

86

Kiley, P. J.; Beinert, H. The role of Fe-S proteins in sensing and regulation in bacteria. Curr. Opin. Microbiol. 2003, 6, 181–185.

DOI Google Scholar

87

Soltani, S.; Akhbari, K. Cu-BTC metal-organic framework as a biocompatible nanoporous carrier for chlorhexidine antibacterial agent. J. Biol. Inorg. Chem 2022, 27, 81–81.

DOI Google Scholar

88

Yu, P. L.; Han, Y. J.; Han, D. L.; Liu, X. M.; Liang, Y. Q.; Li, Z. Y.; Zhu, S. L.; Wu, S. L. In-situ sulfuration of Cu-based metalorganic framework for rapid near-infrared light sterilization. J. Hazard. Mater. 2020, 390.

DOI Google Scholar

89

Ren, X. Y.; Yang, C. Y.; Zhang, L.; Li, S. H.; Shi, S.; Wang, R.; Zhang, X.; Yue, T. L.; Sun, J.; Wang, J. L. Copper metal-organic frameworks loaded on chitosan film for the efficient inhibition of bacteria and local infection therapy. Nanoscale 2019, 11, 11830–11838.

DOI Google Scholar

90

Wang, H. T.; Ao, D.; Lu, M. C.; Chang, N. Alteration of the morphology of polyvinylidene fluoride membrane by incorporating MOF-199 nanomaterials for improving water permeation with antifouling and antibacterial property. J. Chin. Chem. Soc. 2020, 67, 1807–1817.

DOI Google Scholar

91

Singbumrung, K.; Motina, K.; Pisitsak, P.; Chitichotpanya, P.; Wongkasemjit, S.; Inprasit, T. Preparation of Cu-BTC/PVA fibers with antibacterial applications. Fibers Polym. 2018, 19, 1373–1378.

DOI Google Scholar

92

Wang, S. Y.; Yan, F.; Ren, P.; Li, Y.; Wu, Q.; Fang, X. D.; Chen, F. F.; Wang, C. Incorporation of metal-organic frameworks into electrospun chitosan/poly (vinyl alcohol) nanofibrous membrane with enhanced antibacterial activity for wound dressing application. Int. J. Biol. Macromol. 2020, 158, 9–17.

DOI Google Scholar

93

Tang, S. L. ; Zhang, L. L. ; Mao, X. Y. ; Shao, Y. L. ; Cao, M. G. ; Zhang, L. ; Liang, X. M. Pullulan-based nanocomposite films with enhanced hydrophobicity and antibacterial performances. Polym. Bull. , in press,https://doi.org/ 10.1007/s00289-021-03996-0.

94

Gizer, S. G.; Sahiner, N. The effect of sulphur on the antibacterial properties of succinic acid-Cu(II) and mercaptosuccinic acid-Cu(II) MOFs. Inorg. Chim. Acta 2021, 528, 120611.

DOI Google Scholar

95

Han, D. L.; Han, Y. J.; Li, J.; Liu, X. M.; Yeung, K. W. K.; Zheng, Y. F.; Cui, Z. D.; Yang, X. J.; Liang, Y. Q.; Li, Z. Y. et al. Enhanced photocatalytic activity and photothermal effects of Cu doped metal-organic frameworks for rapid treatment of bacteria infected wounds. Appl. Catal. B-Environ. 2020, 261, 118248.

DOI Google Scholar

96

Liu, X. P.; Yan, Z. Q.; Zhang, Y.; Liu, Z. W.; Sun, Y. H.; Ren, J. S.; Qu, X. G. Two-dimensional metal-organic framework/enzyme hybrid nanocatalyst as a benign and self-activated cascade reagent for in vivo wound healing. ACS Nano 2019, 13, 5222–5230.

DOI Google Scholar

97

Allahbakhsh, A.; Jarrahi, Z.; Farzi, G.; Shavandi, A. Three dimensional nanoporous Cu-BTC/graphene oxide nanocomposites with engineered antibacterial properties synthesized via a one-pot solvosonication process. Mater. Chem. Phys. 2022, 277, 125502.

DOI Google Scholar

98

Wang, Z. Y. ; Guo, W. ; Zhang, K. ; Ye, Y. M. ; Wang, Y. M. ; Sui, D. ; Zhao, N. N. ; Xu, F. J. Two-dimensional copper metal-organic frameworks as antibacterial agents for biofilm treatment. Sci. ChinaTechnol. Sci. , in press,DOI: 10.1007/s11431-021-1963-3.https://doi.org/10.1007/s11431-021-1963-3

DOI

99

Gwon, K.; Kim, Y.; Cho, H.; Lee, S.; Yang, S. H.; Kim, S. J.; Lee, D. N. Robust copper metal-organic framework-embedded polysiloxanes for biomedical applications: Its antibacterial effects on MRSA and in vitro cytotoxicity. Nanomaterials 2021, 11, 719.

DOI Google Scholar

100

Azizabadi, O.; Akbarzadeh, F.; Danshina, S.; Chauhan, N. P. S. Sargazi, G. An efficient ultrasonic assisted reverse micelle synthesis route for Fe3O4@Cu-MOF/core–shell nanostructures and its antibacterial activities. J. Solid State Chem. 2021, 294, 121897.

DOI Google Scholar

101

Can, M.; Demirci, S.; Sunol, A. K.; Sahiner, N. An amino acid, Lglutamic acid-based metal-organic frameworks and their antibacterial, blood compatibility, biocompatibility, and sensor properties. Microporous Mesoporous Mater. 2020, 309, 110533.

DOI Google Scholar

102

Liu, Z.; Ye, J. W.; Rauf, A.; Zhang, S. Q.; Wang, G. Y.; Shi, S. Q.; Ning, G. L. A flexible fibrous membrane based on copper(II) metalorganic framework/poly(lactic acid) composites with superior antibacterial performance. Biomater. Sci. 2021, 9, 3851–3859.

DOI Google Scholar

103

Bhardwaj, N.; Pandey, S. K.; Mehta, J.; Bhardwaj, S. K.; Kim, K. H.; Deep, A. Bioactive nano-metal-organic frameworks as antimicrobials against Gram-positive and Gram-negative bacteria. Toxicol. Res. 2018, 7, 931–941.

DOI Google Scholar

104

Restrepo, J.; Serroukh, Z.; Santiago-Morales, J.; Aguado, S.; Gómez-Sal, P.; Mosquera, M. E. G.; Rosal, R. An antibacterial ZnMOF with hydrazinebenzoate linkers. Eur. J. Inorg. Chem. 2017, 2017, 574–580.

DOI Google Scholar

105

Tamames-Tabar, C.; Imbuluzqueta, E.; Guillou, N.; Serre, C.; Miller, S. R.; Elkaïm, E.; Horcajada, P.; Blanco-Prieto, M. J. A Zn azelate MOF: Combining antibacterial effect. Crystengcomm 2015, 17, 456–462.

DOI Google Scholar

106

Yang, Y.; Wu, X. Z.; He, C.; Huang, J. B.; Yin, S. Q.; Zhou, M.; Ma, L.; Zhao, W. F.; Qiu, L.; Cheng, C. et al. Metal-organic framework/Ag-based hybrid nanoagents for rapid and synergistic bacterial eradication. ACS Appl. Mater. Interfaces 2020, 12, 13698–13708.

DOI Google Scholar

107

Ahmed, S. A.; Bagchi, D.; Katouah, H. A.; Hasan, M. N.; Altass, H. M.; Pal, S. K. Enhanced water stability and photoresponsivity in metal-organic Framework (MOF): A potential tool to combat drug resistant bacteria. Sci. Rep. 2019, 9, 19372.

DOI Google Scholar

108

Ahmad, N.; Samavati, A.; Nordin, N. A. H. M.; Jaafar, J.; Ismail, A. F.; Malek, N. A. N. N. Enhanced performance and antibacterial properties of amine-functionalized ZIF-8-decorated GO for ultrafiltration membrane. Sep. Purif. Technol. 2020, 239, 116554.

DOI Google Scholar

109

Sacourbaravi, R.; Ansari-Asl, Z.; Kooti, M.; Nobakht, V.; Darabpour, E. Fabrication of Ag NPs/Zn-MOF nanocomposites and their application as antibacterial agents. J. Inorg. Organomet. Polym. Mater. 2020, 30, 4615–4621.

DOI Google Scholar

110

Balasamy, R. J.; Ravinayagam, V.; Alomari, M.; Ansari, M. A.; Almofty, S. A.; Rehman, S.; Dafalla, H.; Marimuthu, P. R.; Akhtar, S.; Al Hamad, M. Cisplatin delivery, anticancer and antibacterial properties of Fe/SBA-16/ZIF-8 nanocomposite. RSC Adv. 2019, 9, 42395–42408.

DOI Google Scholar

111

Chen, X. Y.; Ji, P. A microporous Zn(II)-MOF for solvent-free cyanosilylation and treatment effect against bacterial infection on burn patients via inhibiting the Staphylococcus aureus biofilm formation. J. Inorg. Organomet. Polym. Mater. 2021, 31, 492–499.

DOI Google Scholar

112

Nakhaei, M.; Akhbari, K.; Kalati, M.; Phuruangrat, A. Antibacterial activity of three zinc-terephthalate MOFs and its relation to their structural features. Inorg. Chim. Acta 2021, 522.

DOI Google Scholar

113

Hao, Q. Q.; Cheng, L.; Dong, Z. Two Zn(II)-organic frameworks: Catalytic knoevenagel condensation and treatment activity on spine surgery incision infection via inhibiting Staphylococcus aureus biofilms formation. J. Exp. Nanosci. 2021, 16, 31–42.

DOI Google Scholar

114

Dutta, B.; Pal, K.; Jana, K.; Sinha, C.; Mir, M. H. Fabrication of a Zn(II)-based 2D pillar bilayer metal-organic framework for antimicrobial activity. Chemistryselect 2019, 4, 9947–9951.

DOI Google Scholar

115

Hu, Y. C.; Yang, H.; Wang, R. H.; Duan, M. L. Fabricating Ag@MOF-5 nanoplates by the template of MOF-5 and evaluating its antibacterial activity. Colloids Surf. A:Physicochem. Eng. Aspects 2021, 626, 127093.

DOI Google Scholar

116

Xie, B. P.; Chai, J. W.; Fan, C.; Ouyang, J. H.; Duan, W. J.; Sun, B.; Chen, J.; Yuan, L. X.; Xu, X. Q.; Chen, J. X. Water-stable silver based metal-organic frameworks of quaternized carboxylates and their antimicrobial activity. ACS Appl. Bio Mater. 2020, 3, 8525–8531.

DOI Google Scholar

117

Huang, X. J.; Yu, S. J.; Lin, W. X.; Yao, X.; Zhang, M. Y.; He, Q.; Fu, F. Y.; Zhu, H. L.; Chen, J. J. A metal-organic framework MIL- 53(Fe) containing sliver ions with antibacterial property. J. Solid State Chem. 2021, 302, 122442.

DOI Google Scholar

118

Arenas-Vivo, A.; Amariei, G.; Aguado, S.; Rosal, R.; Horcajada, P. An Ag-loaded photoactive nano-metal organic framework as a promising biofilm treatment. Acta Biomater. 2019, 97, 490–500.

DOI Google Scholar

119

Zhang, M.; Wang, G. H.; Wang, D.; Zheng, Y. Q.; Li, Y. X.; Meng, W. Q.; Zhang, X.; Du, F. F.; Lee, S. Ag@MOF-loaded chitosan nanoparticle and polyvinyl alcohol/sodium alginate/chitosan bilayer dressing for wound healing applications. Int. J. Biol. Macromol. 2021, 175, 481–494.

DOI Google Scholar

120

Huang, R. ; Cai, G. Q. ; Li, J. ; Li, X. S. ; Liu, H. T. ; Shang, X. L. ; Zhou, J. D. ; Nie, X. M. ; Gui, R. Platelet membrane-camouflaged silver metal-organic framework drug system against infections caused by methicillin-resistant Staphylococcus aureus. J. Nanobiotechnol. 2021, 19, 229.https://doi.org/10.1186/s12951-021-00978-2

DOI

121

Hajibabaei, M.; Zendehdel, R.; Panjali, Z. Imidazole-functionalized Ag/MOFs as promising scaffolds for proper antibacterial activity and toxicity reduction of Ag nanoparticles. J. Inorg. Organomet. P 2020, 30, 4622–4626.

DOI Google Scholar

122

Lu, X. Y.; Ye, J. W.; Zhang, D. K.; Xie, R. X.; Bogale, R. F.; Sun, Y.; Zhao, L. M.; Zhao, Q.; Ning, G. L. Silver carboxylate metalorganic frameworks with highly antibacterial activity and biocompatibility. J. Inorg. Biochem. 2014, 138, 114–121.

DOI Google Scholar

123

Jaros, S. W.; da Silva, M. F. C. G.; Florek, M.; Oliveira, M. C.; Smoleński, P.; Pombeiro, A. J. L. Kirillov, A. M. Aliphatic dicarboxylate directed assembly of silver(I) 1, 3, 5-triaza-7-phosphaadamantane coordination networks: Topological versatility and antimicrobial activity. Cryst. Growth Des. 2014, 14, 5408–5417.

DOI Google Scholar

124

Zirehpour, A.; Rahimpour, A.; Shamsabadi, A. A.; Sharifian, G. M.; Soroush, M. Mitigation of thin-film composite membrane biofouling via immobilizing nano-sized biocidal reservoirs in the membrane active layer. Environ. Sci. Technol. 2017, 51, 5511–5522.

DOI Google Scholar

125

Seyedpour, S. F.; Firouzjaei, M. D.; Rahimpour, A.; Zolghadr, E.; Shamsabadi, A. A.; Das, P.; Afkhami, F. A.; Sadrzadeh, M.; Tiraferri, A.; Elliott, M. Toward sustainable tackling of biofouling implications and improved performance of TFC FO membranes modified by Ag-MOF nanorods. ACS Appl. Mater. Interfaces 2020, 12, 38285–38298.

DOI Google Scholar

126

Fan, X.; Yang, F.; Nie, C. X.; Yang, Y.; Ji, H. F.; He, C.; Cheng, C.; Zhao, C. S. Mussel-inspired synthesis of NIR-responsive and biocompatible Ag-graphene 2D nanoagents for versatile bacterial disinfections. ACS Appl. Mater. Interfaces 2018, 10, 296–307.

DOI Google Scholar

127

Yang, Y.; Ma, L.; Cheng, C.; Deng, Y. Y.; Huang, J. B.; Fan, X.; Nie, C. X.; Zhao, W. F.; Zhao, C. S. Nonchemotherapic and robust dual-responsive nanoagents with on-demand bacterial trapping, ablation, and release for efficient wound disinfection. Adv. Funct. Mater. 2018, 28, 1705708.

DOI Google Scholar

128

D'Agostino, A.; Taglietti, A.; Desando, R.; Bini, M.; Patrini, M.; Dacarro, G.; Cucca, L.; Pallavicini, P.; Grisoli, P. Bulk surfaces coated with triangular silver nanoplates: Antibacterial action based on silver release and photo-thermal effect. Nanomaterials 2017, 7, 7.

DOI Google Scholar

129

Zhang, C.; Hu, D. F.; Xu, J. W.; Ma, M. Q.; Xing, H. B.; Yao, K.; Ji, J.; Xu, Z. K. Polyphenol-assisted exfoliation of transition metal dichalcogenides into nanosheets as photothermal nanocarriers for enhanced antibiofilm activity. ACS Nano 2018, 12, 12347–12356.

DOI Google Scholar

130

Li, Y. T.; Jin, J.; Wang, D. W.; Lv, J. W.; Hou, K.; Liu, Y. L.; Chen, C. Y.; Tang, Z. Y. Coordination-responsive drug release inside gold nanorod@metal-organic framework core–shell nanostructures for near-infrared-induced synergistic chemophotothermal therapy. Nano Res. 2018, 11, 3294–3305.

DOI Google Scholar

131

Leighton, T. G.; Pickworth, M. J. W.; Walton, A. J.; Dendy, P. P. Studies of the cavitational effects of clinical ultrasound by sonoluminescence: 1. Correlation of sonoluminescence with the standing wave pattern in an acoustic field produced by a therapeutic unit. Phys. Med. Biol. 1988, 33, 1239–1248.

DOI Google Scholar

132

Pan, X. T.; Wang, H. Y.; Wang, S. H.; Sun, X.; Wang, L. J.; Wang, W. W.; Shen, H. Y.; Liu, H. Y. Sonodynamic therapy (SDT): A novel strategy for cancer nanotheranostics. Sci. China Life Sci. 2018, 61, 415–426.

DOI Google Scholar

133

Pan, X. T.; Bai, L. X.; Wang, H.; Wu, Q. Y.; Wang, H. Y.; Liu, S.; Xu, B. L.; Shi, X. H.; Liu, H. Y. Metal-organic-framework-derived carbon nanostructure augmented sonodynamic cancer therapy. Adv. Mater. 2018, 30, 1800180.

DOI Google Scholar

134

Karimi Alavijeh, R.; Beheshti, S.; Akhbari, K.; Morsali, A. Investigation of reasons for metal-organic framework’s antibacterial activities. Polyhedron 2018, 156, 257–278.

DOI Google Scholar

135

Huxford, R. C.; Della Rocca, J.; Lin, W. B. Metal-organic frameworks as potential drug carriers. Curr. Opin. Chem. Biol. 2010, 14, 262–268.

DOI Google Scholar

136

Yang, Q. H.; Xu, Q.; Jiang, H. L. Metal-organic frameworks meet metal nanoparticles: Synergistic effect for enhanced catalysis. Chem. Soc. Rev. 2017, 46, 4774–4808.

DOI Google Scholar

137

Liang, S.; Wu, X. L.; Xiong, J.; Zong, M. H.; Lou, W. Y. Metalorganic frameworks as novel matrices for efficient enzyme immobilization: An update review. Coord. Chem. Rev. 2020, 406, 213149.

DOI Google Scholar

138

McGuire, C. V.; Forgan, R. S. The surface chemistry of metalorganic frameworks. Chem. Commun. 2015, 51, 5199–5217.

DOI Google Scholar

139

Kitagawa, S.; Furukawa, S. Porous coordination polymers having guest accessible functional organic sites. Acta Cryst. 2008, A64, C104.

DOI Google Scholar

140

Miller, S. R.; Heurtaux, D.; Baati, T.; Horcajada, P.; Grenèche, J. M.; Serre, C. Biodegradable therapeutic MOFs for the delivery of bioactive molecules. Chem. Commun. 2010, 46, 4526–4528.

DOI Google Scholar

141

Xing, L.; Cao, Y. Y.; Che, S. A. Synthesis of core–shell coordination polymernanoparticles (CPNs) for pH-responsive controlled drug release. Chem. Commun. 2012, 48, 5995–5997.

DOI Google Scholar

142

Lashkari, E.; Wang, H.; Liu, L. S.; Li, J.; Yam, K. Innovative application of metal-organic frameworks for encapsulation and controlled release of allyl isothiocyanate. Food Chem. 2017, 221, 926–935.

DOI Google Scholar

143

Kornblatt, A. P.; Nicoletti, V. G.; Travaglia, A. The neglected role of copper ions in wound healing. J. Inorg. Biochem. 2016, 161, 1–8.

DOI Google Scholar

144

Mallick, S.; Sharma, S.; Banerjee, M.; Ghosh, S. S.; Chattopadhyay, A.; Paul, A. Iodine-stabilized Cu nanoparticle chitosan composite for antibacterial applications. ACS Appl. Mater. Interfaces 2012, 4, 1313–1323.

DOI Google Scholar

145

Chen, S.; Tang, F.; Tang, L. Z.; Li, L. D. Synthesis of Cu nanoparticle hydrogel with self-healing and photothermal properties. ACS Appl. Mater. Interfaces 2017, 9, 20895–20903.

DOI Google Scholar

146

Shams, S. ; Ahmad, W. ; Memon, A. H. ; Shams, S. ; Wei, Y. ; Yuan, Q. P. ; Liang, H. Cu/H3BTC MOF as a potential antibacterial therapeutic agent against Staphylococcus aureus and Escherichia coli. New J. Chem. 2020, 44, 17671–17678.https://doi.org/10.1039/D0NJ04120C

DOI

147

Chui, S. S. Y. ; Lo, S. M. F. ; Charmant, J. P. H. ; Orpen, A. G. ; Williams, I. D. A chemically functionalizable nanoporous material [Cu3(TMA)2(H2O)3]n. Science 1999, 283, 1148–1150.https://doi.org/10.1126/science.283.5405.1148

DOI

148

Abbasi, A. R.; Akhbari, K.; Morsali, A. Dense coating of surface mounted CuBTC metal-organic framework nanostructures on silk fibers, prepared by layer-by-layer method under ultrasound irradiation with antibacterial activity. Ultrason. Sonochem. 2012, 19, 846–852.

DOI Google Scholar

149

Zhang, S. Q.; Ye, J. W.; Sun, Y.; Kang, J.; Liu, J. H.; Wang, Y.; Li, Y. C.; Zhang, L. H.; Ning, G. L. Electrospun fibrous mat based on silver(I) metal-organic frameworks-polylactic acid for bacterial killing and antibiotic-free wound dressing. Chem. Eng. J. 2020, 390, 124523.

DOI Google Scholar

150

da Silv Pinto, M.; Sierra-Avila, C. A.; Hinestroza, J. P. In situ synthesis of a Cu-BTC metal-organic framework (MOF 199) onto cellulosic fibrous substrates: Cotton. Cellulose 2012, 19, 1771–1779.

DOI Google Scholar

151

Emam, H. E.; Darwesh, O. M.; Abdelhameed, R. M. In-growth metal organic framework/synthetic hybrids as antimicrobial fabrics and its toxicity. Colloids Surf. B Biointerfaces 2018, 165, 219–228.

DOI Google Scholar

152

Kohsari, I.; Shariatinia, Z.; Pourmortazavi, S. M. Antibacterial electrospun chitosan-polyethylene oxide nanocomposite mats containing ZIF-8 nanoparticles. Int. J. Biol. Macromol. 2016, 91, 778–788.

DOI Google Scholar

153

Mohanta, G. C.; Pandey, S. K.; Maurya, I. K.; Sahota, T. S.; Mondal, S. K.; Deep, A. Synergistic antimicrobial activity in ampicillin loaded core–shell ZnO@ZIF-8 Particles. ChemistrySelect 2019, 4, 12002–12009.

DOI Google Scholar

154

Tao, B. L.; Zhao, W. K.; Lin, C. C.; Yuan, Z.; He, Y.; Lu, L.; Chen, M. W.; Ding, Y.; Yang, Y. L.; Xia, Z. Z. L. et al. Surface modification of titanium implants by ZIF-8@Levo/LBL coating for inhibition of bacterial-associated infection and enhancement of in vivo osseointegration. Chem. Eng. J. 2020, 390, 124621.

DOI Google Scholar

155

Fan, X.; Yang, F.; Nie, C. X.; Ma, L.; Cheng, C.; Haag, R. Biocatalytic nanomaterials: A new pathway for bacterial disinfection. Adv. Mater. 2021, 33, 2100637.

DOI Google Scholar

156

Rubin, H. N.; Neufeld, B. H.; Reynolds, M. M. Surface-anchored metal-organic framework-cotton material for tunable antibacterial copper delivery. ACS Appl. Mater. Interfaces 2018, 10, 15189–15199.

DOI Google Scholar

157

Peng, C.; Kuai, Z. Y.; Zeng, T. Q.; Yu, Y.; Li, Z. F.; Zuo, J. T.; Chen, S.; Pan, S. J.; Li, L. WO3 nanorods/MXene composite as high performance electrode for supercapacitors. J. Alloys Compd. 2019, 810, 151928.

DOI Google Scholar

158

Abednejad, A.; Ghaee, A.; Nourmohammadi, J.; Mehrizi, A. A. Hyaluronic acid/carboxylated zeolitic imidazolate framework film with improved mechanical and antibacterial properties. Carbohydr. Polym. 2019, 222, 115033.

DOI Google Scholar

159

Liang, K.; Ricco, R.; Doherty, C. M.; Styles, M. J.; Bell, S.; Kirby, N.; Mudie, S.; Haylock, D.; Hill, A. J.; Doonan, C. J. et al. Biomimetic mineralization of metal-organic frameworks as protective coatings for biomacromolecules. Nat. Commun. 2015, 6, 7240.

DOI Google Scholar

160

Li, S. X.; Wang, K. K.; Shi, Y. J.; Cui, Y. N.; Chen, B. L.; He, B.; Dai, W. B.; Zhang, H.; Wang, X. Q.; Zhong, C. L. et al. Novel biological functions of ZIF-NP as a delivery vehicle: High pulmonary accumulation, favorable biocompatibility, and improved therapeutic outcome. Adv. Funct. Mater. 2016, 26, 2715–2727.

DOI Google Scholar

161

Huang, X. C.; Lin, Y. Y.; Zhang, J. P.; Chen, X. M. Ligand directed strategy for zeolite-type metal-organic frameworks: Zinc(II) imidazolates with unusual zeolitic topologies. Angew. Chem. , Int. Ed. 2006, 45, 1557–1559.

DOI Google Scholar

162

Esfahanian, M.; Ghasemzadeh, M. A.; Razavian, S. M. H. Synthesis, identification and application of the novel metal-organic framework Fe3O4@PAA@ZIF-8 for the drug delivery of ciprofloxacin and investigation of antibacterial activity. Artif. Cells Nanomed. Biotechnol. 2019, 47, 2024–2030.

DOI Google Scholar

163

Bradshaw, D.; Garai, A.; Huo, J. Metal-organic framework growth at functional interfaces: Thin films and composites for diverse applications. Chem. Soc. Rev. 2012, 41, 2344–2381.

DOI Google Scholar

164

Tejero, R.; Anitua, E.; Orive, G. Toward the biomimetic implant surface: Biopolymers on titanium-based implants for bone regeneration. Prog. Polym. Sci. 2014, 39, 1406–1447.

DOI Google Scholar

165

Tan, L.; Li, J.; Liu, X. M.; Cui, Z. D.; Yang, X. J.; Zhu, S. L.; Li, Z. Y.; Yuan, X. B.; Zheng, Y. F.; Yeung, K. W. K. et al. Rapid biofilm eradication on bone implants using red phosphorus and nearinfrared light. Adv. Mater. 2018, 30, 1801808.

DOI Google Scholar

166

Shen, X. K.; Zhang, Y. Y.; Ma, P. P.; Sutrisno, L.; Luo, Z.; Hu, Y.; Yu, Y. L.; Tao, B. L.; Li, C. Q.; Cai, K. Y. Fabrication of magnesium/zinc-metal organic framework on titanium implants to inhibit bacterial infection and promote bone regeneration. Biomaterials 2019, 212, 1–16.

DOI Google Scholar

167

Joubani, M. N.; Zanjanchi, M. A.; Sohrabnezhad, S. A novel Ag/Ag3PO4-IRMOF-1 nanocomposite for antibacterial application in the dark and under visible light irradiation. Appl. Organomet. Chem. 2020, 34, e5575.

DOI Google Scholar

168

Tao, B. L.; Lin, C. C.; He, Y.; Yuan, Z.; Chen, M. W.; Xu, K.; Li, K.; Guo, A.; Cai, K. Y.; Chen, L. X. Osteoimmunomodulation mediating improved osteointegration by OGP-loaded cobalt-metal organic framework on titanium implants with antibacterial property. Chem. Eng. J. 2021, 423, 130176.

DOI Google Scholar

169

Kim, Y. K.; Han, S. W.; Min, D. H. Graphene oxide sheath on Ag nanoparticle/graphene hybrid films as an antioxidative coating and enhancer of surface-enhanced Raman scattering. ACS Appl. Mater. Interfaces 2012, 4, 6545–6551.

DOI Google Scholar

170

Khanna, P. K.; Singh, N.; Kulkarni, D.; Deshmukh, S.; Charan, S.; Adhyapak, P. V. Water based simple synthesis of re-dispersible silver nano-particles. Mater. Lett. 2007, 61, 3366–3370.

DOI Google Scholar

171

Chen, S. Y.; Lu, J.; You, T. H.; Sun, D. P. Metal-organic frameworks for improving wound healing. Coord. Chem. Rev. 2021, 439, 213929.

DOI Google Scholar

172

Mao, D.; Hu, F.; Kenry; Ji, S. L.; Wu, W. B.; Ding, D.; Kong, D. L.; Liu, B. Metal-organic-framework-assisted in vivo bacterial metabolic labeling and precise antibacterial therapy. Adv. Mater. 2018, 30, 1706831.

DOI Google Scholar

173

Blissett, A. R.; Deng, B.; Wei, P.; Walsh, K. J.; Ollander, B.; Sifford, J.; Sauerbeck, A. D.; McComb, D. W.; McTigue, D. M.; Agarwal, G. Sub-cellular in-situ characterization of Ferritin(iron) in a rodent model of spinal cord injury. Sci. Rep. 2018, 8, 3567.

DOI Google Scholar

174

Jambovane, S. R.; Nune, S. K.; Kelly, R. T.; McGrail, B. P.; Wang, Z. M.; Nandasiri, M. I.; Katipamula, S.; Trader, C.; Schaef, H. T. Continuous, one-pot synthesis and post-synthetic modification of nanoMOFs using droplet nanoreactors. Sci. Rep. 2016, 6, 36657.

DOI Google Scholar

175

Wang, D. D.; Zhou, J. J.; Chen, R. H.; Shi, R. H.; Xia, G. L.; Zhou, S.; Liu, Z. B.; Zhang, N. Q.; Wang, H. B.; Guo, Z. et al. Magnetically guided delivery of DHA and Fe ions for enhanced cancer therapy based on pH-responsive degradation of DHA-loaded Fe3O4@C@MIL-100(Fe) nanoparticles. Biomaterials 2016, 107, 88–101.

DOI Google Scholar

176

Khatoon, Z.; McTiernan, C. D.; Suuronen, E. J.; Mah, T. F.; Alarcon, E. I. Bacterial biofilm formation on implantable devices and approaches to its treatment and prevention. Heliyon 2018, 4, e01067.

DOI Google Scholar

177

Easun, T. L.; Moreau, F.; Yan, Y.; Yang, S. H.; Schröder, M. Structural and dynamic studies of substrate binding in porous metalorganic frameworks. Chem. Soc. Rev. 2017, 46, 239–274.

DOI Google Scholar

178

Motoyama, S.; Makiura, R.; Sakata, O.; Kitagawa, H. Highly crystalline nanofilm by layering of porphyrin metal-organic framework sheets. J. Am. Chem. Soc. 2011, 133, 5640–5643.

DOI Google Scholar

179

Cui, C. L.; Liu, Y. Y.; Xu, H. B.; Li, S. Z.; Zhang, W. N.; Cui, P.; Huo, F. W. Self-assembled metal-organic frameworks crystals for chemical vapor sensing. Small 2014, 10, 3672–3676.

DOI Google Scholar

180

Mazloom-Jalali, A.; Shariatinia, Z.; Tamai, I. A.; Pakzad, S. R.; Malakootikhah, J. Fabrication of chitosan-polyethylene glycol nanocomposite films containing ZIF-8 nanoparticles for application as wound dressing materials. Int. J. Biol. Macromol. 2020, 153, 421–432.

DOI Google Scholar

181

Duan, C.; Meng, J. R.; Wang, X. Q.; Meng, X.; Sun, X. L.; Xu, Y. J.; Zhao, W.; Ni, Y. H. Synthesis of novel cellulose-based antibacterial composites of Ag nanoparticles@metal-organic frameworks@carboxymethylated fibers. Carbohydr. Polym. 2018, 193, 82–88.

DOI Google Scholar

182

Liu, J. Y.; Sonshine, D. A.; Shervani, S.; Hurt, R. H. Controlled release of biologically active silver from nanosilver surfaces. ACS Nano 2010, 4, 6903–6913.

DOI Google Scholar

183

Liu, Z. G.; Wang, Y. L.; Zu, Y. G.; Fu, Y. J.; Li, N.; Guo, N.; Liu, R. S.; Zhang, Y. M. Synthesis of polyethylenimine (PEI) functionalized silver nanoparticles by a hydrothermal method and their antibacterial activity study. Mater. Sci. Eng. C 2014, 42, 31–37.

DOI Google Scholar

184

Kim, J. S.; Kuk, E.; Yu, K. N.; Kim, J. H.; Park, S. J.; Lee, H. J.; Kim, S. H.; Park, Y. K.; Park, Y. H.; Hwang, C. Y. et al. Antimicrobial effects of silver nanoparticles. Nanomed. :Nanotechnol. , Biol. Med. 2007, 3, 95–101.

DOI Google Scholar

185

Huang, Y.; Zhao, M. T.; Han, S. K.; Lai, Z. C.; Yang, J.; Tan, C. L.; Ma, Q. L.; Lu, Q. P.; Chen, J. Z.; Zhang, X. et al. Growth of Au nanoparticles on 2D metalloporphyrinic metal-organic framework nanosheets used as biomimetic catalysts for cascade reactions. Adv. Mater. 2017, 29, 1700102.

DOI Google Scholar

186

Feng, G. N.; Huang, X. T.; Jiang, X. L.; Deng, T. W.; Li, Q. X.; Li, J. X.; Wu, Q. N.; Li, S. P.; Sun, X. Q.; Huang, Y. G. et al. The antibacterial effects of supermolecular nano-carriers by combination of silver and photodynamic therapy. Front. Chem. 2021, 9, 666408.

DOI Google Scholar

187

Gunawan, C.; Teoh, W. Y.; Marquis, C. P.; Amal, R. Cytotoxic origin of copper(II) oxide nanoparticles: Comparative studies with micron-sized particles, leachate, and metal salts. ACS Nano 2011, 5, 7214–7225.

DOI Google Scholar

188

Fang, F. C. Perspectives series: Host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity. J. Clin. Invest. 1997, 99, 2818–2825.

DOI Google Scholar

189

Wheatley, P. S.; Butler, A. R.; Crane, M. S.; Fox, S.; Xiao, B.; Rossi, A. G.; Megson, I. L.; Morris, R. E. NO-releasing zeolites and their antithrombotic properties. J. Am. Chem. Soc. 2006, 128, 502–509.

DOI Google Scholar

190

Fox, S.; Wilkinson, T. S.; Wheatley, P. S.; Xiao, B.; Morris, R. E.; Sutherland, A.; Simpson, A. J.; Barlow, P. G.; Butler, A. R.; Megson, I. L. et al. NO-loaded Zn2+-exchanged zeolite materials: A potential bifunctional anti-bacterial strategy. Acta Biomater. 2010, 6, 1515–1521.

DOI Google Scholar

191

Pinto, M. L.; Rocha, J.; Gomes, J. R. B.; Pires, J. Slow release of NO by microporous titanosilicate ETS-4. J. Am. Chem. Soc. 2011, 133, 6396–6402.

DOI Google Scholar

192

Cattaneo, D.; Warrender, S. J.; Duncan, M. J.; Kelsall, C. J.; Doherty, M. K.; Whitfield, P. D.; Megson, I. L.; Morris, R. E. Tuning the nitric oxide release from CPO-27 MOFs. RSC Adv. 2016, 6, 14059–14067.

DOI Google Scholar

193

Taylor-Edinbyrd, K.; Li, T. P.; Kumar, R. Effect of chemical structure of S-nitrosothiols on nitric oxide release mediated by the copper sites of a metal organic framework based environment. Phys. Chem. Chem. Phys. 2017, 19, 11947–11959.

DOI Google Scholar

194

Duncan, M. J.; Wheatley, P. S.; Coghill, E. M.; Vornholt, S. M.; Warrender, S. J.; Megson, I. L.; Morris, R. E. Antibacterial efficacy from NO-releasing MOF-polymer films. Mater. Adv. 2020, 1, 2509–2519.

DOI Google Scholar

195

Luan, X. K.; Wang, H. Z.; Xiang, Z. H.; Ma, Z. F.; Zhao, J. R.; Feng, Y.; Shi, Q.; Yin, J. H. Biomimicking dual-responsive extracellular matrix restoring extracellular balance through the Na/K-ATPase pathway. ACS Appl. Mater. Interfaces 2019, 11, 21258–21267.

DOI Google Scholar

196

Vatansever, F.; de Melo, W. C. M. A.; Avci, P.; Vecchio, D.; Sadasivam, M.; Gupta, A.; Chandran, R.; Karimi, M.; Parizotto, N. A.; Yin, R. et al. Antimicrobial strategies centered around reactive oxygen species-bactericidal antibiotics, photodynamic therapy, and beyond. FEMS Microbiol. Rev. 2013, 37, 955–989.

DOI Google Scholar

197

Tao, Y.; Ju, E. G.; Ren, J. S.; Qu, X. G. Bifunctionalized mesoporous silica-supported gold nanoparticles: Intrinsic oxidase and peroxidase catalytic activities for antibacterial applications. Adv. Mater. 2015, 27, 1097–1104.

DOI Google Scholar

198

Jiao, L.; Wang, Y.; Jiang, H. L.; Xu, Q. Metal-organic frameworks as platforms for catalytic applications. Adv. Mater. 2018, 30, 1703663.

DOI Google Scholar

199

Nath, I.; Chakraborty, J.; Verpoort, F. Metal organic frameworks mimicking natural enzymes: A structural and functional analogy. Chem. Soc. Rev. 2016, 45, 4127–4170.

DOI Google Scholar

200

Sun, H. J.; Gao, N.; Dong, K.; Ren, J. S.; Qu, X. G. Graphene quantum dots-band-aids used for wound disinfection. ACS Nano 2014, 8, 6202–6210.

DOI Google Scholar

201

Gao, L. Z.; 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 2014, 6, 2588–2593.

DOI Google Scholar

202

Natalio, F.; André, R.; Hartog, A. F.; Stoll, B.; Jochum, K. P.; Wever, R.; Tremel, W. Vanadium pentoxide nanoparticles mimic vanadium haloperoxidases and thwart biofilm formation. Nat. Nanotechnol. 2012, 7, 530–535.

DOI Google Scholar

203

Gao, L. Z.; Zhuang, J.; Nie, L.; Zhang, J. B.; Zhang, Y.; Gu, N.; Wang, T. H.; Feng, J.; Yang, D. L.; Perrett, S. et al. Intrinsic peroxidase-like activity of ferromagnetic nanoparticles. Nat. Nanotechnol. 2007, 2, 577–583.

DOI Google Scholar

204

Wei, H.; Wang, E. K. Nanomaterials with enzyme-like characteristics (nanozymes): Next-generation artificial enzymes. Chem. Soc. Rev. 2013, 42, 6060–6093.

DOI Google Scholar

205

Zhang, J. Y.; Chen, Y. P.; Miller, K. P.; Ganewatta, M. S.; Bam, M.; Yan, Y.; Nagarkatti, M.; Decho, A. W.; Tang, C. B. Antimicrobial metallopolymers and their bioconjugates with conventional antibiotics against multidrug-resistant bacteria. J. Am. Chem. Soc. 2014, 136, 4873–4876.

DOI Google Scholar

206

Wang, D. D.; Jana, D.; Zhao, Y. L. Metal-organic framework derived nanozymes in biomedicine. Acc. Chem. Res. 2020, 53, 1389–1400.

DOI Google Scholar

207

Ali, A.; Ovais, M.; Zhou, H. G.; Rui, Y. K.; Chen, C. Y. Tailoring metal-organic frameworks-based nanozymes for bacterial theranostics. Biomaterials 2021, 275, 120951.

DOI Google Scholar

208

Hu, W. C.; Younis, M. R.; Zhou, Y.; Wang, C.; Xia, X. H. In situ fabrication of ultrasmall gold nanoparticles/2D MOFs hybrid as nanozyme for antibacterial therapy. Small 2020, 16, 2000553.

DOI Google Scholar

209

Zhang, P.; Sun, D. R.; Cho, A.; Weon, S.; Lee, S.; Lee, J.; Han, J. W.; Kim, D. P.; Choi, W. Modified carbon nitride nanozyme as bifunctional glucose oxidase-peroxidase for metal-free bioinspired cascade photocatalysis. Nat. Commun. 2019, 10, 940.

DOI Google Scholar

210

Wang, J. N.; Bao, M. Y.; Wei, T. X.; Wang, Z. Y.; Dai, Z. H. Bimetallic metal-organic framework for enzyme immobilization by biomimetic mineralization: Constructing a mimic enzyme and simultaneously immobilizing natural enzymes. Anal. Chim. Acta 2020, 1098, 148–154.

DOI Google Scholar

211

Xu, W. Q.; Jiao, L.; Yan, H. Y.; Wu, Y.; Chen, L. J.; Gu, W. L.; Du, D.; Lin, Y. H.; Zhu, C. Z. Glucose oxidase-integrated metalorganic framework hybrids as biomimetic cascade nanozymes for ultrasensitive glucose biosensing. ACS Appl. Mater. Interfaces 2019, 11, 22096–22101.

DOI Google Scholar

212

Xu, B. L.; Wang, H.; Wang, W. W.; Gao, L. Z.; Li, S. S.; Pan, X. T.; Wang, H. Y.; Yang, H. L.; Meng, X. Q.; Wu, Q. W. et al. A single-atom nanozyme for wound disinfection applications. Angew. Chem. , Int. Ed. 2019, 58, 4911–4916.

DOI Google Scholar

213

Zhong, X.; Xia, H.; Huang, W. Q.; Li, Z. X.; Jiang, Y. B. Biomimetic metal-organic frameworks mediated hybrid multienzyme mimic for tandem catalysis. Chem. Eng. J. 2020, 381, 122758.

DOI Google Scholar

214

Hu, D. F.; Li, H.; Wang, B. L.; Ye, Z.; Lei, W. X.; Jia, F.; Jin, Q.; Ren, K. F.; Ji, J. Surface-adaptive gold nanoparticles with effective adherence and enhanced photothermal ablation of methicillinresistant Staphylococcus aureus biofilm. ACS Nano 2017, 11, 9330–9339.

DOI Google Scholar

215

Teng, W. S. Y.; Zhang, Z. J.; Wang, Y. K.; Ye, Y. X.; Yinwang, E.; Liu, A.; Zhou, X. Z.; Xu, J. X.; Zhou, C. W.; Sun, H. X. et al. Iodine immobilized metal-organic framework for NIR-triggered antibacterial therapy on orthopedic implants. Small 2021, 17, 2102315.

DOI Google Scholar

216

Yang, Y. Q.; Huang, K.; Wang, M. Q.; Wang, Q. S.; Chang, H. S.; Liang, Y. K.; Wang, Q.; Zhao, J.; Tang, T. T.; Yang, S. B. Ubiquitination flow repressors: Enhancing wound healing of infectious diabetic ulcers through stabilization of polyubiquitinated hypoxia-inducible factor-1α by theranostic nitric oxide nanogenerators. Adv. Mater. 2021, 33, 2103593.

DOI Google Scholar

217

Yu, Y.; Tan, L.; Li, Z. Y.; Liu, X. M.; Zheng, Y. F.; Feng, X. B.; Liang, Y. Q.; Cui, Z. D.; Zhu, S. L.; Wu, S. L. Single-atom catalysis for efficient sonodynamic therapy of methicillin-resistant Staphylococcus aureus-infected osteomyelitis. ACS Nano 2021, 15, 10628–10639.

DOI Google Scholar

218

Chilakamarthi, U.; Giribabu, L. Photodynamic therapy: Past, present and future. Chem. Rec. 2017, 17, 775–802.

DOI Google Scholar

219

Lu, K. D.; He, C. B.; Lin, W. B. Nanoscale metal-organic framework for highly effective photodynamic therapy of resistant head and neck cancer. J. Am. Chem. Soc. 2014, 136, 16712–16715.

DOI Google Scholar

220

Ethirajan, M.; Chen, Y. H.; Joshi, P.; Pandey, R. K. The role of porphyrin chemistry in tumor imaging and photodynamic therapy. Chem. Soc. Rev. 2011, 40, 340–362.

DOI Google Scholar

221

Guo, J.; Wan, Y.; Zhu, Y. F.; Zhao, M. T.; Tang, Z. Y. Advanced photocatalysts based on metal nanoparticle/metal-organic framework composites. Nano Res. 2021, 14, 2037–2052.

DOI Google Scholar

222

Cheng, L.; Wang, C.; Feng, L. Z.; Yang, K.; Liu, Z. Functional nanomaterials for phototherapies of cancer. Chem. Rev. 2014, 114, 10869–10939.

DOI Google Scholar

223

Agostinis, P.; Berg, K.; Cengel, K. A.; Foster, T. H.; Girotti, A. W.; Gollnick, S. O.; Hahn, S. M.; Hamblin, M. R.; Juzeniene, A.; Kessel, D. et al. Photodynamic therapy of cancer: An update. CA Cancer J. Clin. 2011, 61, 250–281.

DOI Google Scholar

224

Castano, A. P.; Demidova, T. N.; Hamblin, M. R. Mechanisms in photodynamic therapy: Part one-photosensitizers, photochemistry and cellular localization. Photodiagn. Photodyn. Ther. 2004, 1, 279–293.

DOI Google Scholar

225

Ge, J. C.; Lan, M. H.; Zhou, B. J.; Liu, W. M.; Guo, L.; Wang, H.; Jia, Q. Y.; Niu, G. L.; Huang, X.; Zhou, H. Y. et al. A graphene quantum dot photodynamic therapy agent with high singlet oxygen generation. Nat. Commun. 2014, 5, 4596.

DOI Google Scholar

226

Tan, L.; Li, J.; Liu, X. M.; Cui, Z. D.; Yang, X. J.; Yeung, K. W. K.; Pan, H. B.; Zheng, Y. F.; Wang, X. B.; Wu, S. L. In situ disinfection through photoinspired radical oxygen species storage and thermal-triggered release from black phosphorous with strengthened chemical stability. Small 2018, 14, 1703197.

DOI Google Scholar

227

Hong, L.; Liu, X. M.; Tan, L.; Cui, Z. D.; Yang, X. J.; Liang, Y. Q.; Li, Z. Y.; Zhu, S. L.; Zheng, Y. F; Yeung, K. W. K. et al. Rapid biofilm elimination on bone implants using near-infrared-activated inorganic semiconductor heterostructures. Adv. Healthc. Mater. 2019, 8, 1900835.

DOI Google Scholar

228

Yang, X. Y.; Wang, D. Y.; Shi, Y. H.; Zou, J. H.; Zhao, Q. S.; Zhang, Q.; Huang, W.; Shao, J. J.; Xie, X. J.; Dong, X. C. Black phosphorus nanosheets immobilizing Ce6 for imaging-guided photothermal/photodynamic cancer therapy. ACS Appl. Mater. Interfaces 2018, 10, 12431–12440.

DOI Google Scholar

229

Yin, Z. H.; Chen, D. P.; Zou, J. H.; Shao, J. J.; Tang, H.; Xu, H.; Si, W. L.; Dong, X. C. Tumor microenvironment responsive oxygenself-generating nanoplatform for dual-imaging guided photodynamic and photothermal therapy. Chemistryselect 2018, 3, 4366–4373.

DOI Google Scholar

230

Li, L.; Chen, Y. S.; Chen, W. J.; Tan, Y.; Chen, H. Y.; Yin, J. Photodynamic therapy based on organic small molecular fluorescent dyes. Chin. Chem. Lett. 2019, 30, 1689–1703.

DOI Google Scholar

231

Dai, X. M.; Zhao, Y.; Yu, Y. J.; Chen, X. L.; Wei, X. S.; Zhang, X. G.; Li, C. X. Single continuous near-infrared laser-triggered photodynamic and photothermal ablation of antibiotic-resistant bacteria using effective targeted copper sulfide nanoclusters. ACS Appl. Mater. Interfaces 2017, 9, 30470–30479.

DOI Google Scholar

232

Liang, S.; Deng, X. R.; Chang, Y.; Sun, C. Q.; Shao, S.; Xie, Z. X.; Xiao, X.; Ma, P.; Zhang, H. Y.; Cheng, Z. Y. et al. Intelligent hollow Pt-CuS janus architecture for synergistic catalysis-enhanced sonodynamic and photothermal cancer therapy. Nano Lett. 2019, 19, 4134–4145.

DOI Google Scholar

233

Huo, M. F.; Wang, L. Y.; Wang, Y. W.; Chen, Y.; Shi, J. L. Nanocatalytic tumor therapy by single-atom catalysts. ACS Nano 2019, 13, 2643–2653.

DOI Google Scholar

234

Yumita, N.; Nishigaki, R.; Umemura, K.; Umemura, S. I. Hematoporphyrin as a sensitizer of cell-damaging effect of ultrasound. Jpn. J. Cancer Res. 1989, 80, 219–222.

DOI Google Scholar

235

Wang, X. N.; Ip, M.; Leung, A. W.; Xu, C. S. Sonodynamic inactivation of methicillin-resistant Staphylococcus aureus in planktonic condition by curcumin under ultrasound sonication. Ultrasonics 2014, 54, 2109–2114.

DOI Google Scholar

236

Wang, X. N. ; Ip, M. ; Leung, A. W. ; Yang, Z. R. ; Wang, P. ; Zhang, B. T. ; Ip, S. ; Xu, C. S. Sonodynamic action of curcumin on foodborne bacteria Bacillus cereus and Escherichia coli. Ultrasonics 2015, 62, 75–79.https://doi.org/10.1016/j.ultras.2015.05.003

DOI

237

Nakonechny, F.; Nisnevitch, M.; Nitzan, Y.; Nisnevitch, M. Sonodynamic excitation of rose bengal for eradication of grampositive and gram-negative bacteria. BioMed Res. Int. 2013, 2013, 684930.

DOI Google Scholar

238

Wang, X. N. ; Ip, M. ; Leung, A. W. ; Wang, P. ; Zhang, H. W. ; Hua, H. Y. ; Xu, C. S. Sonodynamic action of hypocrellin B on methicillin-resistant Staphylococcus aureus. Ultrasonics 2016, 65, 137–144.https://doi.org/10.1016/j.ultras.2015.10.008

DOI

239

Xu, C. S. ; Dong, J. H. ; Ip, M. ; Wang, X. N. ; Leung, A. W. Sonodynamic action of chlorin e6 on Staphylococcus aureus and Escherichia coli. Ultrasonics 2016, 64, 54–57.https://doi.org/10.1016/j.ultras.2015.07.010

DOI

240

Zhuang, D. S. ; Hou, C. Y. ; Bi, L. J. ; Han, J. L. ; Hao, Y. R. ; Cao, W. W. ; Zhou, Q. Sonodynamic effects of hematoporphyrin monomethyl ether on Staphylococcus aureus in vitro. FEMS Microbiol. Lett. 2014, 361, 174–180.https://doi.org/10.1111/1574-6968.12628

DOI

241

Huo, M. F.; Wang, L. Y.; Chen, Y.; Shi, J. L. Tumor-selective catalytic nanomedicine by nanocatalyst delivery. Nat. Commun. 2017, 8, 357.

DOI Google Scholar

242

Li, W. P.; Su, C. H.; Chang, Y. C.; Lin, Y. J.; Yeh, C. S. Ultrasoundinduced reactive oxygen species mediated therapy and imaging using a fenton reaction activable polymersome. ACS Nano 2016, 10, 2017–2027.

DOI Google Scholar

Recent advances in metal-organic framework-based materials for anti-staphylococcus aureus infection

Recent advances in metal-organic framework-based materials for anti-staphylococcus aureus infection

Abstract

References(242)

Publication history

Copyright