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Localization of near-infrared contrast agents in tumors by intravital microscopy

机译:通过球衣显微镜检查肿瘤中近红外造影剂的定位

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In this contribution we use intravital microscopy to study the dynamics of extravasation into normal and tumor tissue of several hydrophilic cyanine dyes used as near-infrared (NIR) contrast agents. The technique provides information about the angiographic properties of the dyes and about their interaction with tumor tissue under dynamic conditions in vivo. In our previous work we demonstrated that several NIR- absorbing fluorescent dyes enable in vivo fluorescence detection of tumors in mice and rats. However, the mechanism leading to dye accumulation and enhanced fluorescence in tumors is not fully understood. Increased extravasation of dyes into tumor tissue due to pathologically altered tumor vessels may be an important factor in this process. Indocyanine green (ICG) displayed predominantly intravascular distribution and rapid elimination resulting in enhanced fluorescence signal of vessels during the first 15 min after administration only. No elevated extravasation into tumor tissue was observed with ICG. A hydrophilic indotricarbocyanine derivative with a high molecular weight displayed prolonged intravascular distribution and increased fluorescence signal of the vasculature compared to surrounding tissue for up to five hours. Rapid extravasation and accumulation in tumor areas, yielding elevated contrast of tumors up to 15 min after administration, was observed with hydrophilic, low molecular weight indotricarbocyanine derivatives.
机译:在这一贡献中,我们使用流体显微镜检查将外渗的动力学研究到几种亲水性青色染料的正常和肿瘤组织中用作近红外(NIR)造影剂。该技术提供有关染料的血管造影性质的信息以及关于它们在体内动态条件下与肿瘤组织的相互作用。在我们以前的工作中,我们证明了几种NIR吸收荧光染料能够在小鼠和大鼠中的肿瘤体内荧光检测。然而,导致染料积累和增强肿瘤中荧光的机制尚不完全理解。由于病理改变的肿瘤血管,将染料渗入肿瘤组织的外渗可能是该方法的重要因素。吲哚菁绿(ICG)主要显示出在给药后的前15分钟后血管血管内分布和快速消除,导致血管的增强荧光信号。用ICG观察到肿瘤组织没有升高的渗入肿瘤组织。与周围组织相比,具有高分子量的亲水性吲哚甘油衍生物,延长血管内分布延长,血管系统的荧光信号增加,最多五小时。用亲水性的低分子量吲哚碳碳碳碳糖胺衍生物观察到肿瘤区域的快速外渗和积累在肿瘤区域产生高达15分钟的肿瘤的对比度。

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