Affiliation:
1. Department of Biomedical Engineering University of Michigan Ann Arbor Michigan USA
2. Department of Ophthalmology and Visual Sciences University of Michigan Ann Arbor Michigan USA
3. Institute for Bioengineering Research and Department of Mechanical Engineering University of Kansas Lawrence Kansas USA
Abstract
AbstractBackgroundAge‐related macular degeneration (AMD) is a major cause of irreversible central vision loss. The main reason for lost vision due to AMD is choroidal neovascularization (CNV). In the clinic, current treatments for CNV include photodynamic therapy, laser photocoagulation, and anti‐vascular endothelial growth factor (VEGF) therapy.PurposeThis study evaluates a novel treatment technique combining synchronized nanosecond laser pulses and ultrasound bursts, namely photo‐mediated ultrasound therapy (PUT) as a potential treatment method for CNV, for its efficacy and safety in the treatment of CNV via the experiments in a clinically‐relevant rabbit model in vivo.MethodsCNV was created by subretinal injection of Matrigel and vascular endothelial growth factor (M&V) in 10 New Zealand white rabbits. Six rabbits were used in the PUT group. In the control groups, two rabbits were treated by laser‐only, and two rabbits were treated by ultrasound‐only. The treatment efficacy was evaluated through fundus photography and fluorescein angiography (FA) longitudinally for up to 4 weeks. Rabbits were sacrificed for histopathology 3 months after treatment to examine the safety of PUT.ResultsThe fluorescein leakage on FA was quantified to longitudinally evaluate treatment outcome. Compared with baseline, the relative intensity index was reduced by 26.57% ± 8.66% at 3 days after treatment, 27.24% ± 6.21% at 1 week after treatment, 27.79% ± 2.61% at 2 weeks after treatment, and 32.12% ± 3.23% at 4 weeks after treatment, all with a statistically significant difference of p < 0.01. The comparison between the relative intensity indexes from the two control groups (laser‐only treatment and ultrasound‐only treatment) did not show any statistically significant difference at all time points. Safety evaluation at 3 months with histopathology demonstrated that the PUT did not result in morphologic changes to the neurosensory retina.ConclusionsThis study introduces PUT for the first time for the treatment of CNV. The results demonstrated good efficacy and safety of PUT to treat CNV in a clinically‐relevant rabbit model. With a single session of treatment, PUT can safely reduce the leakage of CNV for at least 1 month after treatment.
Funder
National Institutes of Health
Alliance for Vision Research
Research to Prevent Blindness
National Eye Institute
Cited by
2 articles.
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