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Comprehensive evaluation of copper-coated intraosseous structures implantation in experimental conditions with deep gram-negative hip infection in animals

https://doi.org/10.17238/issn2226-2016.2025.4.112-118

Abstract

Introduction: The resistance of pathogenic microorganisms to antibacterial therapy in cases of periprosthetic infection is the cause of the chronic course and the inability to stop the inflammatory process. The use of antibacterial coated implants opens up new opportunities for the prevention and effective treatment of postoperative complications of an infectious nature during operations using non-biotic implants.

Purpose. To carry out a comprehensive assessment of clinical and paraclinical indicators in animals with modeled gram-negative periimplant infection of the femur using intramedullary titanium rods without coating and with copper-containing coating based on amorphous nanocarbon.

Materials and methods. The research material included indicators of the severity of disorders of static-dynamic function, the severity of local signs of inflammation, the dynamics of animal body weight, as well as the pathomorphological picture of the disease course of two compared groups of animals (each group included 16 individuals) with a model of periimplant deep hip infection with an etiotropic agent in the form of a museum strain of P. aeruginosa. The evaluation of treatment outcomes took into account the sum of criteria. The criterion was expressed in scores from 0 to 4. In experimental operations, intramedullary titanium alloy implants were used without coating (control group) and coated with amorphous nanocarbon containing microparticles of copper in a certain concentration (main group). The studies were conducted on days 3, 7, 14, and 28. Clinical, electron microscopic, radiation and statistical research methods were used.

Results. It has been revealed that the use of innovative copper-coated implants for gram-negative osteomyelitis of the femur in laboratory rats achieves optimal treatment results in the absence of physical inactivity, weight loss, extensive osteolysis and an array of necrotic tissues. The total assessment of the result in animals of the control group was 11.7 points (unsatisfactory outcome), in the main group — 4.7 points (good result). Statistical calculation of the difference determined their significant reliable difference (t=11.32; df=30, p=0.01).

Conclusions. A comprehensive study of the inflammatory response when using coated implants based on amorphous nanocarbon with copper particles in conditions of experimental gram-negative infection allows us to consider this type of implant as a promising tool for solving the problems of treatment and prevention of periprosthetic infection and osteomyelitis in clinical practice.

About the Authors

G. K. Sergeev
Tyumen State Medical University
Russian Federation

Grigory K. Sergeev - Assistant Professor, Department of Traumatology and Orthopedics, Tyumen State Medical University.

625023, Tyumen



V. A. Malchevsky
Tyumen State Medical University
Russian Federation

Vladimir A. Malchevsky - Doctor of Medical Sciences, Professor, Department of Mobilization Training and Emergency Medicine, Tyumen State Medical University.

625023, Tyumen



K. S. Sergeev
Tyumen State Medical University
Russian Federation

Konstantin S. Sergeev - Doctor of Medical Sciences, Head of the Department of Traumatology and Orthopedics, Tyumen State Medical University.

625023, Tyumen



I. A. Lebedev
Tyumen State Medical University
Russian Federation

Ilya A. Lebedev - Doctor of Medical Sciences, Professor, Department of Nervous Diseases, Tyumen State Medical University.

625023, Tyumen



A. B. Vladimirov
Institute of Metal Physics, Ural Branch of the Russian Academy of Sciences
Russian Federation

Alexander B. Vladimirov - Researcher, Institute of Metal Physics, Ural Branch of the Russian Academy of Sciences.

620108, Yekaterinburg



V. I. Arkhipenko
Regional Clinical Hospital №2
Russian Federation

Vitaly I. Arkhipenko - PhD in Medicine, Head of the Center for Combined Trauma and Reconstructive Surgery, Regional Clinical Hospital №2.

625048, Tyumen



M. S. Alfayyumi
Tyumen State Medical University
Russian Federation

Malek S. Alfayyumi - PhD student, Department of Traumatology and Orthopedics, Tyumen State Medical University.

625023, Tyumen



References

1. Trampuz A., Zimmerli W. Diagnosis and treatment of implant-associated septic arthritis and osteomyelitis. Curr Infect Dis Rep. 2008; 10: 394-403. https://doi.org/10.1007/s11908-008-0064-1

2. del Pozo J.L., Patel R. The challenge of treating biofilm-associated bacterial infections. Clin Pharmacol Ther. 2007;82:204-9. https://doi.org/10.1038/sj.clpt.6100247

3. Arciola C.R., Campoccia D., Montanaro L. Implant infections: adhesion, biofilm formation and immune evasion. Nat Rev Microbiol. 2018; 16(7): 397-409. https://doi.org/10.1038/s41579-018-0019-y

4. Cerioli M., Batailler C., Conrad A., Roux S., Perpoint T., Becker A., et al. Pseudomonas aeruginosa Implant-Associated Bone and Joint Infections: Experience in a Regional Reference Center in France. Front Med. 2020; 7: 513242. https://doi.org/10.3389/fmed.2020.513242

5. Zimmerli W., Trampuz A., Ochsner P.E. Prosthetic-joint infections. N Engl J Med. 2004; 351: 1645-54. https://doi.org/10.1056/NEJMra040181

6. Murillo O., Grau I., Lora-Tamayo J., Gomez-Junyent J., Ribera A., Tubau F., et al. The changing epidemiology of bacteraemic osteoarticular infections in the early 21st century. Clin Microbiol Infect. 2015; 21: 254.e1-8. https://doi.org/10.1016/j.cmi.2014.09.007

7. Moran E., Masters S., Berendt A.R., McLardy-Smith P., Byren I., Atkins B.L. Guiding empirical antibiotic therapy in orthopaedics: the microbiology of prosthetic joint infection managed by debridement, irrigation and prosthesis retention. J Infect. 2007; 55: 1-7. https://doi.org/10.1016/j.jinf.2007.01.007

8. Hsieh PH, Lee MS, Hsu KY, Chang YH, Shih HN, Ueng SW. Gram-negative prosthetic joint infections: risk factors and outcome of treatment. Clin Infect Dis. 2009; 49: 1036-43. https://doi.org/10.1086/605593

9. Pliska N.N. Microorganisms isolated in cases of suspected periprosthetic infection, their sensitivity. Farmakologiya, klinicheskaya farmakologiya. 2023; 22(2): 34-42 (In Russ.). https://doi.org/10.37903/vsgma.2023.2.5

10. Sudduth J.D., Moss J.A., Spitler C.A., Pham V.H., Jones L.C., Brown J.T., et al. Open fractures: are we still treating the same types of infections? Surg Infect. 2020. https://doi.org/10.1089/sur.2019.140

11. Legout L., Senneville E., Stern R., Yazdanpanah Y., Savage C., Roussel-Delvalez M., et al. Treatment of bone and joint infections caused by Gram-negative bacilli with a cefepime-fluoroquinolone combination. Clin Microbiol Infect. 2006; 12: 1030-3. https://doi.org/10.1111/j.1469-0691.2006.01523.x

12. Zmistowski B., Fedorka C.J., Sheehan E., Deirmengian G., Austin M.S., Parvizi J. Prosthetic joint infection caused by gram-negative organisms. J Arthroplasty. 2011; 26(6 Suppl): 104-8. https://doi.org/10.1016/j.arth.2011.03.044

13. Sculco TP. The economic impact of infected joint arthroplasty. Orthopedics. 1995; 18: 871-3.

14. Triffault-Fillit C., Ferry T., Laurent F., Pradat P., Dupieux C., Conrad A., et al. Microbiologic epidemiology depending on time to occurrence of prosthetic joint infection: a prospective cohort study. Clin Microbiol Infect. 2018; 25: 353-8. https://doi.org/10.1016/j.cmi.2018.04.035

15. Pestrak MJ, Chaney SB, Eggleston HC, Dellos-Nolan S, Dixit S, Mathew-Steiner SS, et al. Pseudomonas aeruginosa rugose small-colony variants evade host clearance, are hyper-inflammatory, and persist in multiple host environments. PLoS Pathog. 2018; 14: e1006842. https://doi.org/10.1371/journal.ppat.1006842

16. Skleenova E.Y., Azizov I.S., Shek E.A., Edelstein M.V., Kozlov R.S., Dekhnich A.V. Pseudomonas aeruginosa in the Russian Federation: history of one of the most successful nosocomial pathogens. Klinicheskaya mikrobiologiya i antimikrobnaya khimioterapiya. 2018; 20(3): 164-171 (In Russ.). https://doi.org/10.36488/cmac.2018.3.164-171

17. Esmaeilnejad A., Mahmoudi P., Zamanian A., Mozafari M. Synthesis of titanium oxide nanotubes and their decoration by MnO nanoparticles for biomedical applications. Ceram Int. 2019; 45(15): 19275-19282. https://doi.org/10.1016/j.ceramint.2019.06.170

18. Atefyekta S., Ercan B., Karlsson J., Taylor E., Chung S., Webster T.J., Andersson M. Antimicrobial performance of mesoporous titania thin films: role of pore size, hydrophobicity, and antibiotic release. Int J Nanomed. 2016; 11: 977-990. https://doi.org/10.2147/IJN.S92605

19. Li B., Xia X., Guo M., Jiang Y., Li Y., Zhang Z., et al. Biological and antibacterial properties of the micro-nanostructured hydroxyapatite/chitosan coating on titanium. Sci Rep. 2019; 9(1): 14. https://doi.org/10.1038/s41598-018-36436-6

20. Akhtar M.A., Ilyas K., Dlouhy I., Siska F., Boccaccini A.R. Electrophoretic deposition of copper(II)-Chitosan complexes for antibacterial coatings. Int J Mol Sci. 2020; 21(7): 2637. https://doi.org/10.3390/ijms21072637

21. Malcher M., Volodkin D., Heurtault B., Andre P., Schaaf P., Mohwald H., et al. Embedded silver ions-containing liposomes in polyelectrolyte multilayers: cargos films for antibacterial agents. Langmuir. 2008; 24(18): 10209-10215. https://doi.org/10.1021/la8014755

22. Arkusz K., Paradowska E., Nycz M., Mazurek-Popczyk J., Baldy-Chudzik K. Evaluation of the antibacterial activity of Ag-and Au nanoparticles loaded TiO2 nanotubes. J Biomed Nanotechnol. 2020; 16(9): 1416-1425. https://doi.org/10.1166/jbn.2020.2976

23. Ding Z., Wang Y., Zhou Q., Ding Z., Wu Y., Zhu Y., et al. The preparation and properties of multilayer Cu-MTa2O5 composite coatings on Ti6Al4V for biomedical applications. Nanomaterials. 2019; 9(10): 1498. https://doi.org/10.3390/nano9101498

24. Vu A.A., Robertson S.F., Ke D., Bandyopadhyay A., Bose S. Mechanical and biological properties of ZnO, SiO2, and Ag2O doped plasma sprayed hydroxyapatite coating for orthopaedic and dental applications. Acta Biomater. 2019; 92: 325-335. https://doi.org/10.1016/j.actbio.2019.05.020

25. de Bie P., Muller P., Wijmenga C., Klomp L.W. Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes. J Med Genet. 2007; 44(11): 673-688. https://doi.org/10.1136/jmg.2007.052746

26. Avdeeva E.Y., Slizovskij G.V., Skorohodova M.G., et al. Modeling traumatic osteomyelitis in rats in experiment. Bulletin of Experimental Biology and Medicine. 2016; 161(1): 157-160 (In Russ.). EDN: VHIAHB.

27. Ovchinnikov E.N., Dyuryagina O.V., Stogov M.V., et al. Model of osteomyelitis in rats. Bulletin of Experimental Biology and Medicine. 2022; 173(3): 395-399 (In Russ.). https://doi.org/10.47056/03655-9615-2022-173-3-395-399

28. Rissing J.P., Buxton T.B., Weinstein R.S., Shockley R.K. Model of experimental chronic osteomyelitis in rats. Infection and Immunity. 1985; 47(3): 581-586. https://doi.org/10.1128/iai.47.3.581-586.1985

29. Tiemann A., Hofmann G.O., Krukemeyer M.G., Krenn V., Langwald S. Histopathological Osteomyelitis Evaluation Score (HOES) an innovative approach to histopathological diagnostics and scoring of osteomyelitis. GMS Interdisciplinary Plastic and Reconstructive Surgery DGPW. 2014; 3: Doc08. https://doi.org/10.3205/iprs00004


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For citations:


Sergeev G.K., Malchevsky V.A., Sergeev K.S., Lebedev I.A., Vladimirov A.B., Arkhipenko V.I., Alfayyumi M.S. Comprehensive evaluation of copper-coated intraosseous structures implantation in experimental conditions with deep gram-negative hip infection in animals. Department of Traumatology and Orthopaedics. 2025;(4):112-118. (In Russ.) https://doi.org/10.17238/issn2226-2016.2025.4.112-118

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ISSN 2226-2016 (Print)