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Tolordava E.R.

P.N. Lebedev Physical Institute of RAS;
N.F. Gamaleya National Research Center

Nastulyavichus A.A.

P.N. Lebedev Physical Institute of RAS

Ulturgasheva E.V.

P.N. Lebedev Physical Institute of RAS

Shelygina S.N.

P.N. Lebedev Physical Institute of RAS

Saraeva I.N.

P.N. Lebedev Physical Institute of RAS

Kudryashov S.I.

P.N. Lebedev Physical Institute of RAS

Antibacterial activity of metal nanoparticles in ex vivo wound infection model

Authors:

Tolordava E.R., Nastulyavichus A.A., Ulturgasheva E.V., Shelygina S.N., Saraeva I.N., Kudryashov S.I.

More about the authors

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To cite this article:

Tolordava ER, Nastulyavichus AA, Ulturgasheva EV, Shelygina SN, Saraeva IN, Kudryashov SI. Antibacterial activity of metal nanoparticles in ex vivo wound infection model. Molecular Genetics, Microbiology and Virology. 2024;42(3):37‑42. (In Russ.)
https://doi.org/10.17116/molgen20244203137

References:

  1. Wibbenmeyer L., Danks R., Faucher L., Amelon M., Latenser B., Kealey G. P., Herwaldt L. A. Prospective analysis of nosocomial infection rates, antibiotic use, and patterns of resistance in a burn population. J Burn Care Res. 2006;27:152-160.  https://doi.org/10.1097/01.BCR.0000203359.32756.F7
  2. Bowler P.G., Duerden B.I., Armstrong D.G. Wound microbiology and associated approaches to wound management. Clin. Microbiol. Rev. 2001;14:244-269.  https://doi.org/10.1128/CMR.14.2.244-269.2001
  3. Lebeaux D., Chauhan A., Rendueles O., Beloin C. From in vitro to in vivo models of bacterial biofilm-related infections. Pathogens. 2013;2:288-356.  https://doi.org/10.3390/pathogens2020288
  4. Alves D.R., Booth S.P., Scavone P., Schellenberger P., Salvage J., Dedi C., et al. Development of a High-Throughput ex-Vivo Burn Wound Model Using Porcine Skin, and Its Application to Evaluate New Approaches to Control Wound Infection. Front. Cell. Infect. Microbiol. 2018;8:15.  https://www.frontiersin.org/articles/10.3389/fcimb.2018.00196
  5. Mah T.-F.C., O Toole G.A. Mechanisms of biofilm resistance to antimicrobial agents. Trends Microbiol. 2001;9:34-39.  https://doi.org/10.1016/S0966-842X(00)01913-2
  6. Ryan R.P., Dow J.M. Diffusible signals and interspecies communication in bacteria. Microbiology 2008;154:1845-1858. https://doi.org/10.1099/mic.0.2008/017871-0
  7. Glushchenko N.N. Reduction of bacterial resistance to antibiotics due to their synergism with copper, Biotechnology: state and development prospects. Proceedings of the II Moscow International Congress: Abstracts of reports. — part 1. — Moscow, 2003. — p. 88 
  8. Nastulyavichus A., Tolordava E., Kudryashov S., Khmelnitskii R., Ionin A. Laser-induced transferred antibacterial nanoparticles for mixed-species bacteria biofilm inactivation. Materials. 2023;16:10.  https://doi.org/10.3390/ma16124309
  9. Nastulyavichus A., Khaertdinova L., Tolordava E., Yushina Y., Ionin A., Semenova A., Kudryashov S. Additive nanosecond laser-induced forward transfer of high antibacterial metal nanoparticle dose onto foodborne bacterial biofilms. Micromachines. 2022;13:12.  https://doi.org/10.3390/mi13122170
  10. Nastulyavichus A., Tolordava E., Rudenko A., Zazymkina D., Shakhov P., Busleev N., et al. In vitro destruction of pathogenic bacterial biofilms by bactericidal metallic nanoparticles via laser-induced forward transfer. Nanomaterials. 2020;10:11.  https://doi.org/10.3390/nano10112259
  11. Semaltianos N., Logothetidis S., Frangis N., Tsiaoussis I., Perrie W., Dearden G., Watkins K. A route to synthesize nanoparticles of titanium monoxide Laser ablation in water. Chem. Phys. Lett. 2010; 496: 113-116.  https://doi.org/10.1016/j.cplett.2010.07.023

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