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首页> 外文期刊>Graefe's archive for clinical and experimental ophthalmology: Albrecht von Graefes Archiv fur klinische und experimentelle Opthalmologie >In vivo retinal and choroidal hypoxia imaging using a novel activatable hypoxia-selective near-infrared fluorescent probe
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In vivo retinal and choroidal hypoxia imaging using a novel activatable hypoxia-selective near-infrared fluorescent probe

机译:使用新型可激活的缺氧选择性近红外荧光探针进行体内视网膜和脉络膜缺氧成像

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摘要

Retinal hypoxia plays a crucial role in ocular neovascular diseases, such as diabetic retinopathy, retinopathy of prematurity, and retinal vascular occlusion. Fluorescein angiography is useful for identifying the hypoxia extent by detecting non-perfusion areas or neovascularization, but its ability to detect early stages of hypoxia is limited. Recently, in vivo fluorescent probes for detecting hypoxia have been developed; however, these have not been extensively applied in ophthalmology. We evaluated whether a novel donor-excited photo-induced electron transfer (d-PeT) system based on an activatable hypoxia-selective near-infrared fluorescent (NIRF) probe (GPU-327) responds to both mild and severe hypoxia in various ocular ischemic diseases animal models.
机译:视网膜缺氧在诸如糖尿病性视网膜病,早产儿视网膜病和视网膜血管阻塞等眼部新生血管疾病中起着至关重要的作用。荧光素血管造影可用于通过检测非灌注区域或新血管形成来确定缺氧程度,但其检测早期缺氧的能力有限。最近,已经开发出了用于检测缺氧的体内荧光探针。但是,这些在眼科中尚未得到广泛应用。我们评估了基于可激活的缺氧选择性近红外荧光(NIRF)探针(GPU-327)的新型供体激发的光诱导电子转移(d-PeT)系统是否对多种眼缺血性中的轻度和重度缺氧作出反应疾病动物模型。

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