DOI:

10.37988/1811-153X_2026_1_136

Dose-dependent effect of nanosilver on the kinetics of development of clinically significant microorganisms in oral surgery practice: in vitro study

Authors

  • P.A. Panin 1, assistant at the Oral surgery propaedeutics Department
    ORCID: 0009-0009-5511-5415
  • M.S. Podporin 1, PhD in Medical Sciences, senior lecturer of the Microbiology, virology, immunology Department
    ORCID: 0000-0001-6785-0016
  • A.M. Tsitsiashvili 1, Doctor of Science in Medicine, professor of the Oral surgery propaedeutics Department
    ORCID: 0000-0002-4737-8508
  • Ya.N. Karasenkov 2, PhD in Medical Sciences, chief medical officer
    ORCID: 0000-0002-9658-3700
  • V.N. Tsarev 1, Doctor of Science in Medicine, full professor of the Microbiology, virology, immunology Department
    ORCID: 0000-0002-3311-0367
  • A.M. Panin 1, Doctor of Science in Medicine, full professor of the Oral surgery propaedeutics Department
    ORCID: 0000-0001-6073-1591
  • A.A. Berezkina 1, 5th year student at the Dental Faculty
    ORCID: 0009-0009-3441-0546
  • S.V. Akulova 3, 6th year student
    ORCID: 0000-0001-7008-9440
  • 1 Russian University of Medicine, 127994, Moscow, Russia
  • 2 Dental clinic “Rosdent”, 117342, Moscow, Russia
  • 3 Moscow State Academy of Veterinary Medicine and Biotechnology of K.I. Scriabin, 109472, Moscow, Russia

Abstract

Surgical dentistry is associated with a high risk of infectious complications caused by pathogens such as S. aureus, S. constellatus, P. intermedia and C. albicans. Resistance of microorganisms to standard antimicrobial drugs and the formation of biofilms require the search for new effective agents. Nanargol, which has a broad spectrum of action, is of interest for use in the prevention and treatment of postoperative infections. The purpose of the study — to study the dose-dependent antimicrobial activity of antiseptic drug with nanosilver against model pathogens, assessing its effect on the growth kinetics of microorganism populations.
Materials and methods.
The study was conducted on clinical isolates of S. aureus, S. constellatus, P. intermedia and C. albicans using the automated culture system RTS-8. Growth phases (lag, logarithmic, stationary, dying off) and key points (α — maximum growth rate, β — maximum culture density) were assessed. The drug was used in dilutions of 1:5, 1:25 and 1:125.
Results.
Antiseptic drug with nanosilver demonstrated dose-dependent growth inhibition of all studied microorganisms. The highest efficiency was noted for C. albicans: a decrease in α and β points by 34.5% and 41.2%, respectively (p<0.05). In S. aureus, the lag phase increased by 2.5 times (p<0.05). For P. intermedia and S. constellatus, significant changes were observed only at high concentrations (1:5 and 1:25). Growth variability (IQR) decreased by 42.8% in C. albicans and by 34.2% in P. intermedia (p<0.05), indicating stabilization of growth kinetics.
Conclusions.
The dose-dependent inhibitory effect of the studied antiseptic based on silver nanoparticles is due to the pronounced suppression of the growth of all studied microorganisms (S. aureus, S. constellatus, P. intermedia, C. albicans), with the greatest effectiveness observed at maximum concentration (dilution 1:5). In C. albicans, there was a decrease in the key growth points α and β by 34.5% and 41.2%, respectively, and in S. aureus, an elongation of the lag phase by 2.5 times, which confirms the antimicrobial activity of the drug.

Key words:

antimicrobial activity, S. aureus, C. albicans, growth kinetics, oral surgery, nanosilver, infectious complications

For Citation

[1]
Panin P.A., Podporin M.S., Tsitsiashvili A.M., Karasenkov Ya.N., Tsarev V.N., Panin A.M., Berezkina A.A., Akulova S.V. Dose-dependent effect of nanosilver on the kinetics of development of clinically significant microorganisms in oral surgery practice: in vitro study. Clinical Dentistry (Russia).  2026; 29 (1): 136—141. DOI: 10.37988/1811-153X_2026_1_136

References

  1. Gabidullina V.R., Tsitsiashvili A.M., Volkov A.V., Stankova N.V., Zaborovsky A.V., Tsarev V.N., Panin A.M., Podporina V.V. Comprehensive assessment of dental implant procedures: a comparative study on different antibiotic prophylaxis regimens. Parodontologiya. 2024; 2: 113—126 (In Russian). DOI: 10.33925/1683-3759-2024-889
  2. Logan B.E., Rossi R., Ragab A., Saikaly P.E. Electroactive microorganisms in bioelectrochemical systems. Nat Rev Microbiol. 2019; 17 (5): 307—319. PMID: 30846876
  3. van der Weijden G.A. [Use of antimicrobial agents in periodontology]. Ned Tijdschr Tandheelkd. 2019; 126 (10): 533—539 (In Dutch). PMID: 31613283
  4. Avdiushkina I.U. Prevention of infections following surgical interventions in dentistry: analysis of current protocols and their impact on outcomes. Innovation Science. 2024; 12—2: 137—143 (In Russian). eLIBRARY ID: 78325952
  5. Khabadze Z.S., Generalova Y.A., Shubaeva V.S., Abdulkerimova S.M., Bakaev Y.A., Mordanov O.S. Periodonal desiease local antiseptic therapy: problem of efficiency. Literature review. Medical alphabet. 2021; 2: 24—37 (In Russian). eLIBRARY ID: 45663238
  6. Munita J.M., Arias C.A. Mechanisms of antibiotic resistance. Microbiol Spectr. 2016; 4 (2): 10.1128/microbiolspec.VMBF-0016-2015. PMID: 27227291
  7. Kirakosyan L.G., Grachev D.I., Tsarev V.N. Microbial adhesion as the initial stage of biofilm formation on dental prosthesis structural materials: an experimental approach. In: proceedings of the First Russian Congress on Medical Microbiology and Infectious Diseases. Moscow, 2023. Pp. 114—115 (In Russian). eLIBRARY ID: 50475598
  8. Gulati M., Nobile C.J. Candida albicans biofilms: development, regulation, and molecular mechanisms. Microbes Infect. 2016; 18 (5): 310—21. PMID: 26806384
  9. Shulakov V.V., Lashchuk S.Yu., Tsarev V.N., Shipkova T.P. Prognostic significance of bacteria antibiotic resistance in chronic odontogenic maxillary sinusitis. Advances in Medical Mycology. 2023; 24: 148—150 (In Russian). eLIBRARY ID: 54045691
  10. Kampf G. Acquired resistance to chlorhexidine is it time to establish an ‘antiseptic stewardship’ initiative?J Hosp Infect. 2016; 94 (3): 213—227. PMID: 27671220
  11. Ushakov R.V., Nuruev N.N., Ushakova T.V., Karpova V.M., Arutyunjan A.A., Labazanov A.A., Tsarev V.N. Combined antimicrobial chemotherapy (fluoroquinolones and imidazoles) in the complex treatment of inflammatory diseases of the periodontal. Clinical Dentistry (Russia). 2021; 1 (97): 60—65. DOI: 10.37988/1811-153X_2021_1_60
  12. Liñares A., et al. Efficacy of adjunctive measures in the non-surgical treatment of peri-implantitis: A systematic review. J Clin Periodontol. 2023; 50 Suppl 26: 224—243. PMID: 37143407
  13. Podporin M.S., Tsarev V.N., Ippolitov E.V., Tsareva T.V., Vishlenkova V.V., Goldman I.L., Sadchikova E.R. Experimental substantiation of the development of the dosage form of lactoferrin with enamel matrix derivatives for use in periodontology. Clinical Dentistry (Russia). 2022; 4: 74—80 (In Russian). DOI: 10.37988/1811-153X_2022_4_74
  14. Balmasova I.P., et al. Microecology of the Periodontium: The Interrelation of Local and Systemic Effects. Moscow: Prakticheskaya meditsina, 2021. 264 p. (In Russian).
  15. Kao R.T., Nares S., Reynolds M.A. Periodontal regeneration intrabony defects: a systematic review from the AAP Regeneration Workshop. J Periodontol. 2015; 86 (2 Suppl): S77—104. PMID: 25216204

Received

December 18, 2025

Accepted

February 6, 2026

Published on

March 31, 2026