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Updated: Sep 11, 2025

Optimized Minimally Invasive Transscleral Subretinal Injection Technique in Mouse
Published on: July 25, 2025
Optimized Minimally Invasive Transscleral Subretinal Injection Technique in Mouse
Lauren Y Cao1, Lindsey A Chew2, Stella Finkelstein1
1Department of Ophthalmology, Duke University School of Medicine.
We optimized a minimally invasive transscleral injection technique for subretinal delivery in mice. This method preserves retinal function and minimizes damage, improving therapeutic efficacy assessments for retinal diseases.
Area of Science:
- Ophthalmology
- Retinal Surgery
- Gene Therapy Delivery
Background:
- Conventional subretinal injections in mice cause significant retinal damage.
- This damage introduces variability in functional outcome measures, complicating therapeutic assessments.
- Existing methods hinder the development of treatments for retinal and macular diseases.
Purpose of the Study:
- To optimize a minimally invasive transscleral subretinal injection technique in mice.
- To compare the functional and anatomical outcomes of this new technique against the conventional transretinal method.
- To establish a more reliable method for delivering therapeutics to the subretinal space.
Main Methods:
- Developed a transscleral injection technique accessing the superior fornix.
- Utilized a custom eyelid speculum, diamond knife for sclerotomy, and microinjection pump.
- Assessed subretinal bleb with optical coherence tomography (OCT) and retinal function via electroretinogram (ERG).
Main Results:
- Transscleral injection preserved retinal function, with ERG results comparable to uninjected controls.
- Conventional transretinal injections resulted in significant ERG signal reduction.
- The optimized technique minimized anatomical damage to the retina.
Conclusions:
- Optimized minimally invasive transscleral subretinal injection is a robust technique for mice.
- This method significantly reduces retinal damage and preserves visual function.
- It provides a more reliable platform for evaluating gene therapies for retinal diseases.
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