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兔模型中使用双硅2,3-萘酞菁对眼黑色素瘤进行光动力治疗。

Photodynamic therapy of ocular melanoma with bis silicon 2,3-naphthalocyanine in a rabbit model.

作者信息

Hill R A, Reddi S, Kenney M E, Ryan J, Liaw L H, Garrett J, Shirk J, Cheng G, Krasieva T, Berns M W

机构信息

Department of Ophthalmology, University of California, Irvine 92717, USA.

出版信息

Invest Ophthalmol Vis Sci. 1995 Nov;36(12):2476-81.

PMID:7591637
Abstract

PURPOSE

To investigate bis (tri-n-hexylsiloxy) silicon 2,3-naphthalocyanine (SINc; 0.5 mg/kg) for photodynamic therapy of an experimental ocular melanoma in pigmented rabbits.

METHODS

SINc was dissolved in canola oil by heating, emulsified with Tween 80, and administered by ear vein. Pharmacokinetics were studied in frozen tumor sections by fluorescence microscopy using a charge coupled device, camera-based, low-light detection system with digital image processing at 1 and 24 hours. A Ti:sapphire laser and a microlens were used to deliver the light (770 nm; 40 mW/cm2; 20 J/cm2). A control rabbit received light without SINc.

RESULTS

Localization studies of SINc showed intravascular distribution shifting to a tumor stromal and perivascular distribution 24 hours after treatment. Tissue thermal damage after irradiation was minimal in the control. Exudative retinal detachments were not observed. Tumor destruction was observed, with sharp demarcation to a depth of 3.5 mm.

CONCLUSIONS

Tumor light penetration was good at 770 nm, and thermal effects from the exciting light alone were minimal. Photodynamic therapy with SINc resulted in localized tumor destruction reflecting the light beam path without damage to adjacent tissue or intraocular complications.

摘要

目的

研究双(三正己基硅氧基)硅2,3-萘酞菁(SINc;0.5毫克/千克)用于色素兔实验性眼黑色素瘤的光动力治疗。

方法

将SINc通过加热溶解于菜籽油中,用吐温80乳化,并经耳静脉给药。在1小时和24小时时,使用基于电荷耦合器件、带有数字图像处理的相机式低光检测系统,通过荧光显微镜在冷冻肿瘤切片中研究药代动力学。使用钛宝石激光器和微透镜来传递光(770纳米;40毫瓦/平方厘米;20焦/平方厘米)。一只对照兔接受无光敏剂的光照。

结果

SINc的定位研究显示,治疗后24小时,血管内分布转变为肿瘤基质和血管周围分布。对照中照射后组织热损伤最小。未观察到渗出性视网膜脱离。观察到肿瘤破坏,与周围组织界限清晰,深度达3.5毫米。

结论

在770纳米处肿瘤光穿透良好,仅激发光产生的热效应最小。用SINc进行光动力治疗导致局部肿瘤破坏,反映出光束路径,且未对相邻组织造成损伤或引发眼内并发症。

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