Effects of Subconjunctival Bevacizumab and Ranibizumab on Corneal and Systemic Oxidative Stress Biomarkers in an Alkali Injury Model

ArticleAçık Erişim

Özet

The study tests the efficacy of subconjunctival ranibizumab and bevacizumab treatments in determining the oxidant and antioxidant levels during alkali-induced corneal neovascularisation. The researchers assigned 24 New Zealand White rabbits into four different groups, which included a healthy control, an alkali-injured control, a BV-treated group, and an RN-treated group, with six rabbits per group. All animals received alkali injury treatment except for the HC group. The AC group received six doses of subconjunctival saline 24 h after their injury, while the BV group and RN group received one dose of 0.5 mg of their respective treatment. The researchers conducted 14-day assays on normal tissue, blood plasma, and erythrocytes to determine total antioxidant status and total oxidant status. The researchers performed biochemical assays for total antioxidant status TAS and total oxidant status TOS on samples that were collected after the 14-day observation period. The corneal TOS levels increased in all injured groups when matched against the HC group. The RN group showed the highest corneal TOS levels, but the difference between the RN and AC and BV groups did not reach statistical significance. The injured groups showed higher corneal TAS levels than HC (p = 0.002), but the AC, BV, and RN groups showed no differences. The injured groups showed a significant decrease in erythrocyte TAS compared with HC (p < 0.001), but the injured groups showed lower plasma TOS levels than HC (p < 0.001). The researchers found no other systemic differences between the groups that received anti-VEGF treatment. The study results show that alkali injury leads to both local and systemic changes in redox status. The two anti-VEGF agents caused numerical changes in corneal oxidative parameters, but these changes did not achieve statistical significance. The research requires further investigation to understand potential agent-related effects on corneal redox balance, which should take place in larger, more detailed studies. © 2026 by the authors.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/10483Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.3390/life16030488Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorYarbağ, Abdulhekim
dc.contributor.authorBardaş Özkan, Ebru
dc.contributor.authorUlaş, Mustafa
dc.contributor.authorArslan, Yusuf Kemal
dc.date.accessioned2026-10-18T20:25:41.687430496Z
dc.date.available2026-10-18T20:25:41.687430496Z
dc.date.issued2026
dc.description.abstractThe study tests the efficacy of subconjunctival ranibizumab and bevacizumab treatments in determining the oxidant and antioxidant levels during alkali-induced corneal neovascularisation. The researchers assigned 24 New Zealand White rabbits into four different groups, which included a healthy control, an alkali-injured control, a BV-treated group, and an RN-treated group, with six rabbits per group. All animals received alkali injury treatment except for the HC group. The AC group received six doses of subconjunctival saline 24 h after their injury, while the BV group and RN group received one dose of 0.5 mg of their respective treatment. The researchers conducted 14-day assays on normal tissue, blood plasma, and erythrocytes to determine total antioxidant status and total oxidant status. The researchers performed biochemical assays for total antioxidant status TAS and total oxidant status TOS on samples that were collected after the 14-day observation period. The corneal TOS levels increased in all injured groups when matched against the HC group. The RN group showed the highest corneal TOS levels, but the difference between the RN and AC and BV groups did not reach statistical significance. The injured groups showed higher corneal TAS levels than HC (p = 0.002), but the AC, BV, and RN groups showed no differences. The injured groups showed a significant decrease in erythrocyte TAS compared with HC (p < 0.001), but the injured groups showed lower plasma TOS levels than HC (p < 0.001). The researchers found no other systemic differences between the groups that received anti-VEGF treatment. The study results show that alkali injury leads to both local and systemic changes in redox status. The two anti-VEGF agents caused numerical changes in corneal oxidative parameters, but these changes did not achieve statistical significance. The research requires further investigation to understand potential agent-related effects on corneal redox balance, which should take place in larger, more detailed studies. © 2026 by the authors.
dc.identifier.doi10.3390/life16030488
dc.identifier.eissn2075-1729
dc.identifier.issn2075-1729
dc.identifier.issue3
dc.identifier.pmcidPMC13027824
dc.identifier.pmid41901006
dc.identifier.scopus2-s2.0-105034021681
dc.identifier.startpage488
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/10483
dc.identifier.volume16
dc.identifier.wosWOS:001727363000001
dc.language.isoen
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.ispartofLife
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectalkali burn
dc.subjectbevacizumab
dc.subjectcorneal neovascularisation
dc.subjectoxidative stress
dc.subjectrabbit model
dc.subjectranibizumab
dc.subjectTAS
dc.subjectTOS
dc.subjectVEGF
dc.subjectalkali
dc.subjectantioxidant
dc.subjectbiological marker
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectdrug efficacy
dc.subjecteffect size
dc.subjectexperimental design
dc.subjecthypothesis
dc.subjectLeporidae
dc.subjectlight dark cycle
dc.subjectneovascularization (pathology)
dc.subjectnonhuman
dc.subjectpost hoc analysis
dc.subjectsample size
dc.titleEffects of Subconjunctival Bevacizumab and Ranibizumab on Corneal and Systemic Oxidative Stress Biomarkers in an Alkali Injury Model
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus1
rdl.citation.wos1
rdl.departmentDepartment of Physiology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan 24100, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)