Impression cytology in assessing the dynamics of corneal regeneration after acid burn treated with biostimulating films

Authors

DOI:

https://doi.org/10.31279/2949-4796-2026-16-1-41-54

Keywords:

cornea, acid burn, ophthalmic medicinal films, biostimulator, regeneration, impression cytology, rabbits
284 368

Abstract

Introduction. Chemical burns of the cornea of acid etiology represent one of the most challenging pathologies in veterinary ophthalmology, often leading to irreversible vision loss. The high prevalence of eye injuries in agricultural and domestic animals, as well as the tendency of the process toward chronization and secondary infection, necessitate the search for new effective and safe therapeutic agents devoid of the disadvantages of existing drugs (presence of antibiotics, high cost). A promising direction is the development of prolonged-release dosage forms based on biogenic stimulators.
Aim. To study the cytological processes of corneal regeneration in rabbits after experimental acid burn against the background of the application of ophthalmic medicinal films (OMF) based on a biostimulator (BSB) from bovine brain tissue.
Materials and Methods. The experiment was performed on 30 sexually mature rabbits of the Gray Giant breed, divided into two equal groups. Animals of the first group received daily applications of OMF based on BSB after burn modeling; animals of the second group served as controls (without treatment). Corneal impression smears were obtained on days 3, 7, 14, 21, and 28, stained with azure-eosin according to the Romanowsky-Giemsa method, and examined by light microscopy.
Results. We established that the application of OMF based on BSB promotes a regular sequence of wound healing phases: acute inflammation (days 3–7) is followed by proliferation (day 14), culminating in the phase of epithelial differentiation and maturation by days 21–28. Cytologically, this was expressed in a reduction of dystrophic changes, an increase in the size of epithelial cell nuclei, normalization of cellular composition, and complete disappearance of inflammatory cells by the end of observation. In the control group, a protracted course with chronization of inflammation, massive microbial contamination (Streptococcus, Corynebacterium, Bacillus, Streptobacillus), persistence of neutrophilic infiltration, and absence of signs of complete regeneration by day 28 were noted.
Conclusion. Ophthalmic medicinal films based on BSB possess pronounced regenerative potential, arrest inflammation, reduce the risk of secondary infection, and can be recommended for further study as a therapeutic agent for chemical corneal burns in veterinary practice.

References

Niaki R.I., Pedram M.S., Abarkar M., et al. The Effect of Limbal Tissue with Conjunctival Flap and Bovine Amniotic Membrane on Alkaline Burn Corneal Wound: experimental study in rabbits. Experimental Eye Research. 2025;260:110597. https://doi.org/10.1016/j.exer.2025.110597

Sharifipanah I., Abdolmaleki Z., Abarkar M. Investigating the effect of alpha-lipoic acid and retinoic acid eye drops on re-epithelialization, inflammation, and angiogenesis in a rabbit model of corneal wound healing through ICAM-1 and MMP-9 pathways. Experimental Eye Research. 2026;263:110808. https://doi.org/10.1016/j.exer.2025.110808

Yingwei W., Liling X., Jupeng Z., et al. Reconstructing auto tissue engineering lamellar cornea with aspartic acid modified acellular porcine corneal stroma and preconditioned limbal stem cell for corneal regeneration. Biomaterials. 2022;289:121745 https://doi.org/10.1016/j.biomaterials.2022.121745

Purnama L.O.M. J. , Fristiohady A., Payuhakrit W., et al. Effect of thermoresponsive quercetin-nanoemulgel eye drop on VEGF-A–induced corneal neovascularization: In vitro and in vivo. Journal of Drug Delivery Science and Technology. 2026;116:107968 https://doi.org/10.1016/j.jddst.2025.107968

Singha S.K., Goswami D.G., Wright H.N., et al. Effect of supersaturated oxygen emulsion treatment on chloropicrin-induced chemical injury in ex vivo. Toxicology Letters. 2021;349(1):124-133. https://doi.org/10.1016/j.toxlet.2021.06.015

Silva R.O., Costa B.L., Silva C.N., et al. The proteolytic fraction from Vasconcellea cundinamarcensis accelerates wound healing after corneal chemical burn in rabbits. Burns. 2020;46(4):928-936. https://doi.org/10.1016/j.burns.2019.10.005

Regu V.R., Gohel V., Gaur M., et al. Tamarind seed polysaccharide-metformin insert: Higher ocular retention, slow-release, and efficacy against corneal burn. International Journal of Pharmaceutics. 2024;659:124265. https://doi.org/10.1016/j.ijpharm.2024.124265

Dıaz N.M., Sun X., Gelder R.N.V., et al. Opsin 5 mediates violet light-accelerated wound healing in mammalian corneas. Cell Reports. 2025;44(8):116045. https://doi.org/10.1016/j.celrep.2025.116045

Sun X., Song W., Tengi L., et al. MiRNA 24-3p-rich exosomes functionalized DEGMA-modified hyaluronic acid hydrogels for corneal epithelial healing. Bioactive Materials. 2023;25:640-656. https://doi.org/10.1016/j.bioactmat.2022.07.011

Li Y., Wang X., Wu M., et al. Micelle-integrated hydrogel combined with pH-response boosts eye burns therapy by inhibiting neovascularization, regulating inflammation and bacteriostasis. Biomaterials Advances. 2026;183:214732. https://doi.org/10.1016/j.bioadv.2026.214732

Zhang H., Lan L.-M., Hu H.-J., et al. Cannabidiol-loaded hydrogel contact lenses for on-demand pH regulation and enhanced corneal alkali burn repair. Journal of Controlled Release. 2025;383:113859. https://doi.org/10.1016/j.jconrel.2025.113859

Wang J., Wanga X., Mab X., et al. Mesenchymal stem cells derived extracellular vesicles modified PLGA electrospinning nanofibrous scaffolds for corneal and retinal repair. Materials and Design. 2024;247:113389. https://doi.org/10.1016/j.matdes.2024.113389

Semenov S.A., Khasanova G.R. The influence of risk factors associated with medical care on Streptococcus pneumoniae resistance to penicillin (meta-analysis). Medicine. 2025;13(4):72-89. (In Russ.)

Butsel A.Ch., Maximenya G.G. The forgotten group of antibacterial drugs. Military medicine. 2021;4(61):94-100. https://doi.org/10.51922/2074-5044.2021.4.94 (In Russ.)

Gorokhova M.M., Shulunova A.N., Fedota N.V., Kvochko A.N. Patent № 2811124 C1, Russian Federation. Ophthalmic medicinal films based on a biostimulant from bovine brain tissue with the addition of silver nanoparticles. № 2022126920: filed on 17.10.2022: published on 11.01.2024, applicant Stavropol State Agrarian University. (In Russ.)

Skripkin V.S., Fedota N.V., Kvochko A.N., et al. Simulation of a cornea burn with an acetic acid solution. Agrarian Bulletin of the North Caucasus. 2023;4(52):18-21. https://doi.org/10.31279/2949-4796-2023-4-52-18-21 (In Russ.)

Gorokhova M.M., Fedota N.V., Shulunova A.N. Patent № 2836425 C1, Russian Federation. Method for simulating chemical corneal burn in rabbits. Appl. 02.08.2024: Publ. 14.03.2025; Applicant: Stavropol State Agrarian University. (In Russ.)

Park S.K., Ha M., Kim E.J., et al. Hyaluronic acid hydrogels crosslinked via blue light-induced thiol-ene reaction for the treatment of rat corneal alkali burn. Regenerative Therapy. 2022;20:51-60. https://doi.org/10.1016/j.reth.2022.03.005

Gong Y., Gao J., Li M., et al. URP20 improves corneal injury caused by alkali burns combined with pathogenic bacterial infection in rats. Experimental Eye Research. 2024;238:109739. https://doi.org/10.1016/j.exer.2023.109739

Sugioka K., Fukuda K., Nishida T., et al. The fibrinolytic system in the cornea: A key regulator of corneal wound healing and biological defense. Experimental Eye Research. 2021;204:108459. https://doi.org/10.1016/j.exer.2021.108459

Published

2026-03-31

Issue

Section

Animal Husbandry and Veterinary Medicine

How to Cite

Agarkova , M. M., Agarkov , N. V., Kvochko , A. N., Skripkin , V. S., & Dilekova , O. V. (2026). Impression cytology in assessing the dynamics of corneal regeneration after acid burn treated with biostimulating films. Agrarian Bulletin of the North Caucasus, 16(1), 41-54. https://doi.org/10.31279/2949-4796-2026-16-1-41-54