Preclinical trials of remote noninvasive electromagnetic therapy of purulent wounds on experimental animals
https://doi.org/10.21518/akh2025-047
Abstract
Introduction. The development of new methods for the treatment of purulent wounds of various etiologies in surgical practice is an urgent task.
Aim. Тo study the effect of noninvasive electromagnetic therapy on the healing process of purulent wounds in rabbits.
Materials and methods. The experiment was conducted on the 14 mongrel rabbits. After modeling purulent skin wounds, rabbits were divided into 2 equal groups on day 5. The control group of animals underwent only local wound treatment with saline solution, the experimental group – this manipulation was combined with electromagnetic therapy. The duration of the experiment was 17 days, and the follow-up was 30 days. Clinical monitoring of the animals’ condition was carried out, clinical blood analysis was monitored, and wound discharge was seeded. Wound healing was assessed using the planimetric method. Biometric values were determined in the statistical analysis of the results, and the R.B. Strelkov table was used.
Results and discussion. By day 9 of the experiment, normothermia was noted in the animals in the experimental group, while hyperthermia persisted in 14.3% of the rabbits in the control group. On day 7, in 57.14% of the animals in the control group, the wound decreased by 1.0 cm, and in the experimental group, a decrease from 0.5 to 1.0 cm was detected in 71.42%. On day 14, in the experimental group, in contrast to the control group, no microflora was detected in the wound. On day 5, leukocytosis exceeded the norm by 3.0% in the control group and by 67.7% in the experimental group. In the experimental group, thrombocytosis was observed throughout the experiment, which exceeded the initial values by 70.78% by the end of the experiment.
Conclusions. The use of noninvasive electromagnetic therapy in the treatment of purulent wounds in rabbits accelerates their healing processes.
About the Authors
L. G. AistovaRussian Federation
Lyubov G. Aistova, Postgraduate Student of the Department of Pathology, Morphology and Physiology,
86, Politechnicheskaya St., Blagoveshchensk-on-Amur, 675005
A. O. Fedorova
Russian Federation
Anastasia O. Fedorova, Dr. Sci. (Biol.), Associate Professor of the Department of Pathology, Morphology and Physiology,
86, Politechnicheskaya St., Blagoveshchensk-on-Amur, 675005
T. V. Miller
Russian Federation
Tatyana V. Miller, Cand. Sci. (Biol.), Associate Professor of the Department of Pathology, Morphology and Physiology,
86, Politechnicheskaya St., Blagoveshchensk-on-Amur, 675005
O. V. Gruzdova
Russian Federation
Olesya V. Gruzdova, Cand. Sci. (Biol.), Head of the Department of Pathology, Morphology and Physiology,
86, Politechnicheskaya St., Blagoveshchensk-on-Amur, 675005
E. V. Bondarchuk
Russian Federation
Elena V. Bondarchuk, Vice President,
31, Bldg. 2, Gogolevsky Boulevard, 119019, Moscow
A. G. Vaganov
Russian Federation
Alexey G. Vaganov, Cand. Sci. (Med.), Associate Professor, Department of Hospital Surgery,
173, Chernyshevsky St., Nalchik, 360004
I. F. Turkanov
Russian Federation
Igor F. Turkanov, Head,
31, Bldg. 2, Gogolevsky Boulevard, 119019, Moscow
V. G. Gryaznov
Russian Federation
Valery G. Gryaznov, Cand. Sci. (Phys-Math.), Deputy Head,
31, Bldg. 2, Gogolevsky Boulevard, 119019, Moscow
E. A. Galkina
Russian Federation
Ekaterina A. Galkina, Head of the Laboratory of Electrobiophysical and Chemical Research,
31, Bldg. 2, Gogolevsky Boulevard, 119019, Moscow
G. A. Flaks
Russian Federation
Gregory A. Flaks, Medical Adviser,
31, Bldg. 2, Gogolevsky Boulevard, 119019, Moscow
A. D. Aslanov
Russian Federation
Akhmed D. Aslanov, Dr. Sci. (Med.), Professor, Head of the Department of Hospital Surgery at the Medical Academy,
173, Chernyshevsky St., Nalchik, 360004
M. A. Gotyzhev
Russian Federation
Murat A. Gotyzhev, Assistant Professor at the Department of Hospital Surgery, Faculty of Medicine,
173, Chernyshevsky St., Nalchik, 360004
A. M. Nogmov
Russian Federation
Akhmed M. Nogmov, Lecturer at the Department of Hospital Surgery, Faculty of Medicine,
173, Chernyshevsky St., Nalchik, 360004
References
1. Heal CF, Banks JL, Lepper PD, Kontopantelis E, van Driel ML. Topical antibiotics for preventing surgical site infection in wounds healing by primary intention. Cochrane Database Syst Rev. 2016;11(11):CD011426. https://doi.org/10.1002/14651858.CD011426.pub2.
2. Peel T, Astbury S, Cheng AC, Paterson D, Buising K, Spelman T et al. Multicentre randomised double-blind placebo controlled trial of combination vancomycin and cefazolin surgical antibiotic prophylaxis: the Australian surgical antibiotic prophylaxis (ASAP) trial. BMJ Open. 2019;9(11):e033718. https://doi.org/10.1136/bmjopen-2019-033718.
3. Li Y, Zhang ZB, Liu JS, Wu ZM, Sun XC, Zhao YT, Zhang XZ. Analysis of the therapeutic effect of artificial leather embedding combined with fascial sleeve flap transplantation on chronic wounds oflower limbs with bone and plate exposure. BMC Surg. 2022;22(1):69. https://doi.org/10.1186/s12893-022-01521-2.
4. Norman G, Dumville JC, Mohapatra DP, Owens GL, Crosbie EJ. Antibiotics and antiseptics for surgical wounds healing by secondary intention. Cochrane Database Syst Rev. 2016;3(3):CD011712. https://doi.org/10.1002/14651858.CD011712.pub2. 5. Diao W, Li P, Jiang X, Zhou J, Yang S. Progress in copper-based materials for wound healing. Wound Repair Regen. 2024;32(3):314–322. https://doi.org/10.1111/wrr.13122.
5. Аndreeva AA, Glukhov AA, Ostroushko AP, Boev SN, Laptieva AY, Grigor’eva EV et al. Simulation of Mechanical and Thermal Wounds of Soft Tissues. Bull Exp Biol Med. 2022;173(3):287–292. https://doi.org/10.1007/s10517-022-05535-x.
6. Babushkina IV, Gladkova EV, Belova SV, Norkin IA. Application of Preparations Containing Copper Nanoparticles for the Treatment of Experimental Septic Wounds. Bull Exp Biol Med. 2017;164(2):162–164. https://doi.org/10.1007/s10517-017-3948-y.
7. Adams B, Petruccione F. Nature’s Novel Materials: A Review of Quantum Biology. In: Chakraborty T (еd.). Encyclopedia of Condensed Matter Physics 2nd ed. Academic Press: Oxford, UK; 2024. Vol. 3, pp. 593–604. https://doi.org/10.1016/B978-0-323-90800-9.00268-7.
8. Amini A, Pouriran R, Abdollahifar MA, Abbaszadeh HA, Ghoreishi SK, Chien S, Bayat M. Stereological and molecular studies on the combined effects of photobiomodulation and human bone marrow mesenchymal stem cell conditioned medium on wound healing in diabetic rats. J Photochem Photobiol B. 2018;182:42–51. https://doi.org/10.1016/j.jphotobiol.2018.03.010.
9. Dastgheib M, Shaddel M, Saba V, Homayouni MM, Fereydoni A. Role of magnetic Field in the Healing of Cutaneous Leishmaniasis Lesions in Mice. Arch Razi Inst. 2020;75(2):227–232. https://doi.org/10.22092/ari.2019.123403.1246.
10. Li Y, Nie L, Jin S, Sun C, Lu X. The Effect of Plasma on Bacteria and Normal Cells in Infected Wound. Oxid Med Cell Longev. 2022;2022:1838202. https://doi.org/10.1155/2022/1838202.
11. Usselman RJ, Chavarriaga C, Castello PR, Procopio M, Ritz T, Dratz EA et al. The Quantum Biology of Reactive Oxygen Species Partitioning Impacts Cellular Bioenergetics. Sci Rep. 2016;6:38543. https://doi.org/10.1038/srep38543.
12. Kouhkheil R, Fridoni M, Piryaei A, Taheri S, Chirani AS, Anarkooli IJ et al. The effect of combined pulsed wave low-level laser therapy and mesenchymal stem cell-conditioned medium on the healing of an infected wound with methicillin-resistant Staphylococcal aureus in diabetic rats. J Cell Biochem. 2018;119(7):5788–5797. https://doi.org/10.1002/jcb.26759.
13. Bagheri M, Amini A, Abdollahifar MA, Ghoreishi SK, Piryaei A, Pouriran R et al. Effects of Photobiomodulation on Degranulation and Number of Mast Cells and Wound Strength in Skin Wound Healing of Streptozotocin-Induced Diabetic Rats. Photomed Laser Surg. 2018;36(8):415–423. https://doi.org/10.1089/pho.2018.4453.
14. Gurhan H, Bruzon R, Kandala S, Greenebaum B, Barnes F. Effects Induced by a Weak Static Magnetic Field of Different Intensities on HT-1080 Fibrosarcoma Cells. Bioelectromagnetics. 2021;42(3):212–223. https://doi.org/10.1002/bem.22332.
15. Bunkin NF, Bolotskova PN, Bondarchuk EV, Gryaznov VG, Kozlov VA, Okuneva MA et al. Dynamics of Polymer Membrane Swelling in Aqueous Suspension of Amino-acids with Different Isotopic Composition; Photoluminescence Spectroscopy Experiments. Polymers. 2021;13(16):2635. https://doi.org/10.3390/polym13162635.
16. Fatenkov OV, Davydkin IL, Yashkov AV, Gubareva EYu, Komarova MV, Bondarchuk EV et al. Efficacy of the TOR Non-invasive electromagnetic Therapy Device for the Remote Treatment of COVID-19 Clearance: Phase II Clinical Trial Results. Bulletin of the Medical Institute of Сontinuing Education. 2024;4(4):25–34. (In Russ.) https://doi.org/10.36107/2782-1714_2024-4-4-25-34.
17. Ploskonos MV, Zulbalaeva DF, Kurbangalieva NR, Ripp SV, Neborak EV, Blagonravov ML et al. Assessing the biological effects of microwave irradiation on human semen in vitro and determining the role of seminal plasma polyamines in this process. Biomed Rep. 2022;16(5):38. https://doi.org/10.3892/br.2022.1521.
Review
For citations:
Aistova L.G., Fedorova A.O., Miller T.V., Gruzdova O.V., Bondarchuk E.V., Vaganov A.G., Turkanov I.F., Gryaznov V.G., Galkina E.A., Flaks G.A., Aslanov A.D., Gotyzhev M.A., Nogmov A.M. Preclinical trials of remote noninvasive electromagnetic therapy of purulent wounds on experimental animals. Ambulatornaya khirurgiya = Ambulatory Surgery (Russia). 2025;22(2):107-115. (In Russ.) https://doi.org/10.21518/akh2025-047
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