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Published on: April 3, 2016
Prevention of ocular scarring post glaucoma filtration surgery using the inflammatory cell and platelet binding
Jeff Min1, Zachary L Lukowski, Monica A Levine
1Department of Ophthalmology, College of Medicine, University of Florida, Gainesville, Florida, United States of America.
Clinical Relevance:
Late complications can occur with use of current antimetabolites to prevent scarring following glaucoma filtration surgery (GFS). Safer, more targeted, anti-fibrosis agents are sought.
Objectives:
The protein saratin has been shown to exhibit anti-fibrotic and anti-thrombotic properties in response to injury, but had not been used for glaucoma surgery. The goal of this study was to compare the efficacy of saratin with that of the widely accepted mitomycin-C (MMC) in prolonging bleb survival following GFS in the rabbit model. Two saratin delivery routes were compared; a single intraoperative topical application versus a combination of intraoperative topical application with two additional postoperative injections.
Methods:
Twenty-four New Zealand White rabbits underwent GFS and received either intraoperative topical saratin, intraoperative topical saratin plus two injections on post-operative days 4 and 8, balanced saline solution (BSS), or MMC. The bleb tissues and their elevation durations were compared based on clinical and histological findings.
Results:
Rabbits receiving topical+injections of saratin had a mean bleb survival of 33.6±8.5 days, significantly higher than the negative BSS controls, which averaged 17.4±6.0 days (p = 0.018). No improvement over BSS was seen for rabbits receiving topical saratin only (15.5±4.8 days, p = 0.749). Rabbits receiving saratin did not develop bleb avascularity and thinning associated with MMC treatment and there were no apparent clinical signs of toxicity.
Conclusions:
Treatment with a single intraoperative topical application plus two additional postoperative injections significantly prolonged bleb elevation comparable to MMC, but without toxicity; however, topical application alone was ineffective.
Insights
Saratin, when applied topically and with injections, significantly prolonged bleb survival after glaucoma surgery in rabbits. This new anti-fibrosis agent offers a safer alternative to mitomycin-C, avoiding toxicity.
Area of Science:
- Ophthalmology
- Regenerative Medicine
- Surgical Innovation
Background:
- Glaucoma filtration surgery (GFS) often requires antimetabolites to prevent scarring, but these can cause late complications.
- Safer, targeted anti-fibrosis agents are needed to improve outcomes after GFS.
- Saratin, a protein with known anti-fibrotic properties, has not been previously studied in the context of glaucoma surgery.
Purpose of the Study:
- To evaluate the efficacy of saratin in prolonging bleb survival following GFS in a rabbit model.
- To compare saratin's performance against mitomycin-C (MMC), a standard anti-scarring agent.
- To assess two different saratin delivery methods: intraoperative topical application alone versus combined topical application with postoperative injections.
Main Methods:
- Twenty-four New Zealand White rabbits underwent GFS.
- Interventions included: intraoperative topical saratin, topical saratin plus two postoperative injections, balanced saline solution (BSS), or MMC.
- Bleb survival and tissue characteristics were assessed clinically and histologically.
Main Results:
- Saratin administered via topical application plus injections significantly increased mean bleb survival to 33.6 days compared to BSS controls (17.4 days, p=0.018).
- Intraoperative topical saratin alone did not improve bleb survival over BSS (15.5 days, p=0.749).
- Saratin treatment did not result in bleb avascularity or thinning, unlike MMC, and showed no signs of toxicity.
Conclusions:
- A regimen of intraoperative topical saratin combined with postoperative injections effectively prolonged bleb survival after GFS, comparable to MMC.
- This saratin treatment strategy demonstrated a favorable safety profile, avoiding the toxicities associated with MMC.
- Topical saratin application alone was insufficient to enhance bleb longevity in this model.
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