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[荧光素给药后在手术显微镜下使用荧光成像检测脑肿瘤的实验研究]

[Experimental study of detection of brain tumor at surgery using fluorescent imaging under a surgical microscope after fluorescein administration].

作者信息

Kabuto M, Kubota T, Kobayashi H, Ishii H, Nakagawa T, Kawai H, Kitai R, Kodera T, Kaneko M

机构信息

Department of Neurosurgery, Fukui Medical School, Japan.

出版信息

No To Shinkei. 1997 Mar;49(3):261-5.

PMID:9125731
Abstract

Total resection is the optimal treatment for malignant gliomas. However, we sometimes find an unexpected residual tumor mass on magnetic resonance imaging performed after an operation because of a macroscopically unclear margin of the tumor during operation. This study was designed to evaluate the effect of fluorescein sodium on imaging of glioma in combination with a surgical microscope for detection of the tumor at surgery in a rat glioma model. For this study, we produced two filters for the excitation and emission of fluorescein that can be easily fitted to and removed from a surgical microscope manually during the operation. For the in vivo study, Wistar rat brains bearing C6 glioma were removed at appropriate intervals after the intravenous administration of 10-20 mg/kg body weight of fluorescein sodium, and their surface and coronal sections through the tumor were observed using a surgical microscope with the filters. For the in vitro study, the cultured C6 glioma cells were exposed to 5 micrograms/ml of fluorescein sodium for 2 hours and then observed by confocal laser scanning microscopy. In the in vivo study, the C6 glioma itself and the brain within 2-3 mm of the gross surface of the tumor (probably indicating part of the perifocal edema) were well stained a brilliant yellowish green for a few hours. The normal brain was not stained. The intensity of the fluorescence was dose-dependent and was stronger under the xenon than under the halogen lamp. The in vitro study demonstrated almost no uptake of fluorescein by the C6 glioma cells. This fact indicates that the fluorescein in the stained tumor exists in extracellular spaces due to the disruption of the blood-brain barrier. These results suggest that this staining technique using fluorescein sodium and a surgical microscope with special filters during the operation may be the intravenous administration of 10 useful for detection of gliomas and warrants evaluation of clinical application.

摘要

全切除是恶性胶质瘤的最佳治疗方法。然而,由于手术中肿瘤边界在肉眼下不清晰,我们有时会在术后磁共振成像中发现意外的残留肿瘤肿块。本研究旨在评估荧光素钠联合手术显微镜在大鼠胶质瘤模型手术中对胶质瘤成像以检测肿瘤的效果。在本研究中,我们制作了两个用于荧光素激发和发射的滤光片,在手术过程中可轻松手动安装到手术显微镜上并从其上取下。在体内研究中,静脉注射10 - 20毫克/千克体重的荧光素钠后,在适当的时间间隔取出携带C6胶质瘤的Wistar大鼠大脑,使用带有滤光片的手术显微镜观察其表面和通过肿瘤的冠状切片。在体外研究中,将培养的C6胶质瘤细胞暴露于5微克/毫升的荧光素钠中2小时,然后通过共聚焦激光扫描显微镜观察。在体内研究中,C6胶质瘤本身以及肿瘤大体表面2 - 3毫米内的脑组织(可能指示部分瘤周水肿)在数小时内被染成鲜艳的黄绿色。正常脑组织未被染色。荧光强度呈剂量依赖性,在氙灯下比在卤素灯下更强。体外研究表明C6胶质瘤细胞几乎不摄取荧光素。这一事实表明,由于血脑屏障的破坏,染色肿瘤中的荧光素存在于细胞外间隙。这些结果表明,在手术过程中使用荧光素钠和带有特殊滤光片的手术显微镜的这种染色技术可能有助于胶质瘤的检测,值得评估其临床应用价值。

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