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Indocyanine green: physicochemical factors affecting its fluorescence in vivo.

机译:吲哚菁绿:影响其体内荧光的理化因素。

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This study reinvestigates the spectral properties of ICG (Indocyanine green) in vivo, the role of quenching, and the possibility of an interaction of ICG with blood components and/or vessel walls. ICG quenching as a function of concentration was studied by spectrophotometry on whole blood samples from golden hamsters. Fluorescence ICG characteristics were evaluated by front-face fluorometry. In vivo, fluorescence measurements were performed on the femoral artery of golden hamsters. In vitro, on whole blood samples, fluorescence intensity is modified by ICG quenching as concentration increases above 80 microgram/ml. The maximum fluorescence peak is not affected and remains centered at 832 nm. The in vivo measurements display a similar fluorescence intensity shape, which is affected only by ICG concentrations. However, the maximum fluorescence emission peak is modified significantly with time. Between 0 and 120 min, four phases can be distinguished in which a wavelength shift from 826 to 835 nm is observed. The wavelength shift with change in fluorescence intensity observed in vivo could be due to a localization of ICG molecules in sites more hydrophobic than serum proteins. It is possible to hypothesize the presence of an endothelium-bound form with a specific fluorescence spectrum. The amphiphilic properties of ICG are consistent with fixation of some ICG molecules on sites other than plasmatic proteins after injection. The process of fixation of ICG molecules on surface components or within the vascular endothelium could be due to a change in the microenvironment of some ICG molecules. Copyright 1998 Academic Press.
机译:这项研究重新研究了ICG(吲哚菁绿)在体内的光谱特性,猝灭作用以及ICG与血液成分和/或血管壁相互作用的可能性。通过分光光度法对来自金黄仓鼠的全血样品研究了ICG淬灭作为浓度的函数。通过正面荧光法评估荧光ICG特性。在体内,对金黄仓鼠的股动脉进行荧光测量。在体外,在全血样品上,当浓度增加到80微克/毫升以上时,ICG淬灭会改变荧光强度。最大荧光峰不受影响,并保持在832 nm为中心。体内测量显示相似的荧光强度形状,仅受ICG浓度影响。但是,最大荧光发射峰随时间显着改变。在0到120分钟之间,可以区分四个相位,其中观察到波长从826到835 nm。在体内观察到的随着荧光强度变化而发生的波长偏移可能是由于ICG分子位于比血清蛋白疏水性更高的位点所致。可以假设存在具有特定荧光光谱的内皮结合形式。 ICG的两亲特性与注射后某些ICG分子固定在血浆蛋白以外的其他部位上是一致的。 ICG分子在表面组件上或在血管内皮内的固定过程可能是由于某些ICG分子的微环境变化所致。版权所有1998学术出版社。

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