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A transpupillary approach for crosslinking Guinea pig sclera using WST11 and near-infrared light
A transpupillary approach for crosslinking Guinea pig sclera using WST11 and near-infrared light
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A transpupillary approach for crosslinking Guinea pig sclera using WST11 and near-infrared light
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A transpupillary approach for crosslinking Guinea pig sclera using WST11 and near-infrared light
A transpupillary approach for crosslinking Guinea pig sclera using WST11 and near-infrared light

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A transpupillary approach for crosslinking Guinea pig sclera using WST11 and near-infrared light
A transpupillary approach for crosslinking Guinea pig sclera using WST11 and near-infrared light
Journal Article

A transpupillary approach for crosslinking Guinea pig sclera using WST11 and near-infrared light

2026
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Overview
Crosslinking strengthens the sclera and holds potential as a treatment for myopia. This study aims to identify optimal crosslinking parameters in guinea pigs using WST11 with dextran followed by near-infrared (NIR) illumination. Guinea pig eyes were incubated in WST11 with 2, 5 or 10% dextran, and penetration depth was assessed by fluorescence microscopy. Crosslinking efficacy was measured as thermal stability using a thermal degradation assay, following incubation in WST11 + 10% dextran (WST-D) for 30 min and NIR irradiation at 10 mW/cm 2 or 20 mW/cm 2 for 10, 20 and 30 min. The optimized parameters were then applied in vivo in 6-month-old guinea pigs. Ex vivo treatment using the optimal crosslinking parameters (WST-D, 30 min; NIR, 10 mW/cm 2 , 30 min) resulted in the highest thermal degradation midpoint ( ΔT 50 : 6.8), significantly higher than untreated controls ( p  = 0.0006), with WST-D penetration limited to the sclera. Efficacy was greater in eyes obtained from older compared to younger guinea pigs ( p  = 0.02). In vivo , WST-D/NIR treatment resulted in significant crosslinking compared to untreated controls (equatorial, ΔT 50 : 3.7, p  < 0.0001; posterior, ΔT 50 : 3.4, p  = 0.01). WST-D/NIR treatment effectively induces scleral crosslinking, with age-related differences suggesting the need for personalized treatment.

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