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Safety and efficacy of quercetin as an alternative to riboflavin in collagen cross-linking treatment

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Volume Title

dc.identifier.issn

0181-5512
1773-0597

dc.identifier.doi

10.1016/j.jfo.2025.104667

dc.identifier.other

dc.description.volume

48

dc.description.issue

9

Publisher

MASSON EDITEUR

DOI

10.1016/j.jfo.2025.104667
10.1016/j.jfo.2025.104667

Abstract

Purpose. - To evaluate the safety and efficacy of quercetin as an alternative to riboflavin in collagen cross-linking (CXL) treatment. Methods. - Australia-New Zealand rabbits (n = 60) were divided into four groups: a control group (C group; no UVA exposure), a Tween 20 buffer group (T group; UVA irradiated), a riboflavin group (R group; UVA irradiated with riboflavin), and a quercetin group (Q group; UVA irradiated with quercetin). The corneal tissues were analyzed histologically and biomechanically on days 7 and 42 post-treatment. Results. - The biomechanical tests demonstrated a 50% increase in Young's modulus and a 21% increase in tensile strength in the R group compared to controls (P < 0.05), confirming significant corneal stiffening. In contrast, the Q group showed an 18% increase in Young's modulus, but this was not statistically significant compared to controls (P > 0.05). Histological analysis revealed no inflammation, corneal edema, or endothelial damage in any group. Keratocyte apoptosis was detected in the anterior stroma of the Rand Q groups at day 7, with repopulation occurring by day 42. Conclusion. - While quercetin demonstrated some biomechanical effects; its impact on corneal stiffening was significantly lower than that of riboflavin, indicating its inefficacy as a photo-induced cross-linking agent. (c) 2025 Elsevier Masson SAS. All rights are reserved, including those for text and data mining, AI training, and similar technologies.

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