Physical Sciences Inc. proposes to develop a new, integrated multimodal adaptive optics small animal imager, including AO-OCT and AO scanning laser fluorescence (fAOSLO), and to demonstrate its applications to detecting pathology in the retinas of rodent models of eye disease. The imaging platform includes novel design elements such as adaptable wavefront sensing methods enabling dynamic and static AO correction in selected layers;integrated Badal optometer system with path-length-locked OCT reference arm for flexible AO-OCT-guided imaging, and co-scanning AO-OCT/fAOSLO rasters for enhanced fluorescence sensitivity and co-registration in anesthetized rodents. Together with collaborators at Children's Hospital Boston (CHB), we propose to demonstrate the imaging platform in a GFP mouse (B6.129P-Cx3cr1tm1Litt/J mice) model of STZ-induced diabetic retinopathy. The rapidly growing array of small animal models of human eye disease has significantly increased the need for new in vivo animal fundus imaging modalities with cellular resolution. However, there are currently no commercial AO platforms for high resolution in vivo imaging which can exploit such features. A successful Phase I program will result in a multimodal adaptive optics small animal imaging (MAOSI) platform with simultaneous AO- OCT, fAOSLO, and improved AO control for 3D structural and functional imaging. Such a device has immediate research and drug discovery applications and markets.

Public Health Relevance

Small animal models have proven to be powerful tools in the study of the pathogenesis of eye disease. Transgenic mouse models have been developed for many forms of retinal degeneration including glaucoma, diabetic retinopathy, inherited vision disorders and anterior segment disease. The use of these models and new cellular resolution imaging tools will continue to be an important part of new research, from basic vision research to commercial drug discovery. The investigation of the detailed relationships between structure and function in the living eye is made possible by advanced cellular resolution in vivo imaging modalities and by many new animal models. The wealth of information inherent in simultaneous AO-OCT scan volumes and AOSLO/fAOSLO images in such models will lead to better understanding of both normal visual function and disease processes, as well as improvements in human AO imaging diagnostics and new therapies. The proposed research program and subsequent commercial development will result in new, small animal multimodal AO imaging platforms with immediate research applications and markets.

National Institute of Health (NIH)
National Eye Institute (NEI)
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
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Special Emphasis Panel (ZRG1-SBIB-T (10))
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Wujek, Jerome R
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Physical Sciences, Inc
United States
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