# Tranexamic Acid-Associated Hyaluronic Acid Exhibits Enhanced Oxidative Stability: A Comparative Rheological Study

**Authors:** Thierry Conrozier, Guillaume Darsy, Jérômine Mercier, Alexandre Guerry, Jérémy Patarin, Anne Lohse

PMC · DOI: 10.3390/biom16030361 · Biomolecules · 2026-02-28

## TL;DR

This study shows that combining hyaluronic acid with tranexamic acid improves its resistance to oxidative damage, preserving its viscoelastic properties in joint treatments.

## Contribution

The novel finding is that tranexamic acid enhances hyaluronic acid's oxidative stability without chemical cross-linking.

## Key findings

- HA–TXA showed a modest decrease in complex viscosity and minimal increase in phase angle after oxidative stress.
- HA–TXA's stability exceeded hybrid and linear HA and approached cross-linked HA in preserving viscoelastic properties.
- The study suggests TXA protects HA through mechanisms distinct from chemical cross-linking.

## Abstract

Background: The clinical performance of intra-articular hyaluronic acid (HA) is strongly dependent on its resistance to oxidative degradation within the inflamed osteoarthritic joint. Reactive oxygen species induce HA chain scission, leading to a loss of molecular entanglement and a shift from elastic-dominant to viscous-dominant behavior. Tranexamic acid (TXA), a lysine analogue with documented anti-inflammatory and anti-proteolytic properties, has been combined with HA with the hypothesis that it may limit oxidative-induced rheological degradation. Objective: This study aims to determine whether an HA–TXA formulation preserves viscoelastic integrity under oxidative stress and how its behavior compares with linear, hybrid, and cross-linked HA viscosupplements. Methods: Four HA-based formulations were evaluated using stress-controlled rotational rheometry compliant with ISO 3219 standards. Complex modulus (G*), complex viscosity (η*), and phase angle (tan δ) were measured within the linear viscoelastic domain. Oxidative challenge was induced with hydrogen peroxide (5.4% v/v), and time-dependent rheological changes were recorded over 30 min. Resistance to degradation was defined by relative variations in rheological parameters from baseline. Results: Baseline measurements revealed distinct viscoelastic profiles among the HA formulations. After oxidative exposure, the HA–TXA formulation showed a modest decrease in η* (−17.0%) and limited increase in tan δ (+4.0%), indicating preserved viscoelastic organization. Its stability exceeded that of hybrid (−40%; +12.6%) and linear HA (−53%; +25.6%) and approached that of cross-linked HA (−25.4%; +5.6%). The magnitude of microstructural alteration remained minimal despite chemical stress. Conclusions: The association of TXA with HA confers a marked protection against oxidative-induced viscoelastic degradation, preserving macromolecular network integrity and elastic behavior. These findings suggest that TXA modulates oxidative stress-related rheological failure of HA through mechanisms distinct from chemical cross-linking.

## Linked entities

- **Chemicals:** tranexamic acid (PubChem CID 5526), hydrogen peroxide (PubChem CID 784)
- **Diseases:** osteoarthritis (MONDO:0005178)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** HA (MESH:D006820), HA-TXA (-), hydrogen peroxide (MESH:D006861), lysine (MESH:D008239), Reactive oxygen species (MESH:D017382), TXA (MESH:D014148)

## Full text

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023906/full.md

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Source: https://tomesphere.com/paper/PMC13023906