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Updated: Jun 18, 2026

In Vivo Imaging of Cx3cr1gfp/gfp Reporter Mice with Spectral-domain Optical Coherence Tomography and Scanning Laser Ophthalmoscopy
Published on: November 11, 2017
Molecular-Specific Optical Coherence Tomography Contrast Agents for High-Sensitivity In Vivo Detection of Corneal
Shuya Liu1, Lubin Han1, Wen Yang1
1New Cornerstone Science Laboratory, MOE Key Laboratory for Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection Technology for Food Safety, College of Chemistry, Fuzhou University, Fuzhou 350116, P. R. China.
None:
Optical coherence tomography (OCT) is a powerful tool for in vivo corneal imaging; however, its diagnostic precision is hampered by a lack of molecular specificity. To overcome this limitation, we designed and synthesized CD44 aptamer-conjugated gold nanoparticles (AP-GNPs) as a molecularly targeted OCT contrast agent for the quantitative assessment of corneal injury. AP-GNPs specifically bind to CD44, a biomarker overexpressed in injured corneal tissue, leading to enhanced signal intensity and prolonged retention at the lesion site compared to nontargeted nanoparticles. In the alkali burn mouse model, AP-GNP-enhanced OCT enabled noninvasive and highly sensitive detection of mild and severe injuries, demonstrating a significant increase in the signal-to-noise ratio from 12 to 24 h postinsult, a feat not achievable by conventional diagnostics such as fluorescein staining. This was quantified by a significant amplification of the signal-to-noise ratio at 12 h by 23.6% for mild injuries and 54.5% for severe injuries, relative to nonenhanced controls. Comprehensive safety profiling confirmed the excellent biocompatibility of the nanoprobes after topical administration. This study establishes an aptamer-based contrast enhancement strategy for OCT, providing the first demonstration of quantitative in vivo improvement in detection sensitivity for corneal pathology and offering a promising platform for both preclinical research and clinical diagnostics.

