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Multimodality optical coherence tomography and fluorescence confocal scanning laser ophthalmoscopy for image-guided feedback of intraocular injections in mouse models

机译:多模光学相干断层扫描和荧光共聚焦扫描激光眼压镜检查小鼠模型中眼内注射的图像引导反馈

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100-word summary: Rodent models are robust tools for understanding human retinal disease and function because of their similarities with human physiology and anatomy and availability of genetic mutants. Optical coherence tomography (OCT) has been well-established for ophthalmic imaging in rodents and enables depth-resolved visualization of structures and image-based surrogate biomarkers of disease. Similarly, fluorescence confocal scanning laser ophthalmoscopy (cSLO) has demonstrated utility for imaging endogenous and exogenous fluorescence and scattering contrast in the mouse retina. We present a non-contact multimodal OCT+cSLO small animal imaging system with extended working distance to the pupil, which enables imaging during and after intraocular injection. 250-word abstract: Rodent models are robust tools for understanding human retinal disease and function because of their similarities with human physiology and anatomy and availability of genetic mutants. Optical coherence tomography (OCT) has been well-established for ophthalmic imaging in rodents and enables depth-resolved visualization of structures and image-based surrogate biomarkers of disease. Similarly, fluorescence confocal scanning laser ophthalmoscopy (cSLO) has demonstrated utility for imaging endogenous and exogenous fluorescence and scattering contrast in the mouse retina. Complementary volumetric scattering and en face fluorescence contrast from OCT and cSLO, respectively, enables cellular-resolution longitudinal imaging of changes in ophthalmic structure and function. We present a non-contact multimodal OCT+cSLO small animal imaging system with extended working distance to the pupil, which enables imaging during and after intraocular injection. While injections are routinely performed in mice to develop novel models of ophthalmic diseases and screen novel therapeutics, the location and volume delivered is not precisely controlled and difficult to reproduce. Animals were imaged using a custom-bu
机译:100字摘要:啮齿动物模型是理解人类视网膜疾病和功能的强大工具,因为它们与人类生理学和解剖学和遗传突变体的解剖学和可用性的相似性。光学相干断层扫描(OCT)已经为啮齿动物的眼科成像提供了很好的成熟,并且能够实现结构和基于图像的替代生物标志物的深度分辨可视化。类似地,荧光共焦扫描激光眼镜(CSLO)已经证明了用于在小鼠视网膜中进行成像和外源荧光和散射对比的效用。我们介绍了一个非接触式多模式OCT + CSLO小动物成像系统,其与瞳孔延伸的工作距离,这使得眼内注射期间和之后能够成像。 250字摘要:由于其与人类生理学和遗传突变体的解剖和可用性以及遗传突变体的解剖和可用性,啮齿动物模型是理解人类视网膜疾病和功能的强大工具。光学相干断层扫描(OCT)已经为啮齿动物的眼科成像提供了很好的成熟,并且能够实现结构和基于图像的替代生物标志物的深度分辨可视化。类似地,荧光共焦扫描激光眼镜(CSLO)已经证明了用于在小鼠视网膜中进行成像和外源荧光和散射对比的效用。互补的体积散射和抗OCT和CSLO的荧光对比,使得眼科结构和功能变化的细胞分辨率纵向成像。我们介绍了一个非接触式多模式OCT + CSLO小动物成像系统,其与瞳孔延伸的工作距离,这使得眼内注射期间和之后能够成像。虽然在小鼠中常规进行注射以发展新型眼科疾病和筛选新型治疗剂的新型模型,但送达的位置和体积并不精确控制且难以繁殖。使用定制-BU成像动物

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