SPECT-CT study of directed drug delivery using /sup 111/In-labeled liposomes in a murine mammary carcinoma model

E. Izaguirre, Mingshan Sun, D. Drummond, D. Kirpotin, T. Funk, S. Thompson, J. Carver, M. Hayes, M. Wendland, M. Knudsen, B. Hasegawa
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引用次数: 2

Abstract

Liposomal drugs offer the promise of an improved therapeutic index due to improvements in the specific delivery of anti-cancer agents to tumors. The presented work concentrates on imaging the tumor uptake of /sup 111/In-labeled liposomes noninvasively as a specific tumor drug delivery carrier in a murine cancer model. The tumor uptake of liposomes has been imaged using a microSPECT/microCT small animal dedicated scanner prototype constructed at our laboratory. The imaging system consists of a high resolution SPECT (700 /spl mu/m) and high resolution CT (70 /spl mu/m). The SPECT subsystem consists in specially designed CZT gamma cameras shielded for energies up to 250 keV. The mice were injected with liposomes and scanned at the time of maximum tumor uptake (24 h). The total activity of the mouse samples was of the order of 250 uCi, and with tumor sizes of 1000-1500 mm/sup 3/. The imaging geometries in the CT and SPECT acquisitions were selected to obtain high magnification and high efficiency to image the tumor located within the torso. The SPECT and CT projections were taken sequentially. The acquired images show that necrotic tumors can de imaged with high resolution to observe liposome inhomogeneous uptake.
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使用/sup 111/ in标记脂质体在小鼠乳腺癌模型中定向给药的SPECT-CT研究
由于改善了抗癌药物对肿瘤的特异性递送,脂质体药物提供了改善治疗指数的希望。目前的工作集中在成像肿瘤摄取/sup 111/ in标记脂质体作为一个特定的肿瘤药物递送载体在小鼠癌症模型中无创。肿瘤对脂质体的摄取使用我们实验室构建的微spect /微ct小动物专用扫描仪原型进行了成像。成像系统由高分辨率SPECT (700 /spl mu/m)和高分辨率CT (70 /spl mu/m)组成。SPECT子系统包括特别设计的CZT伽玛相机屏蔽能量高达250千伏特。给小鼠注射脂质体,并在最大肿瘤摄取时间(24 h)进行扫描。小鼠样品的总活性约为250 uCi,肿瘤大小为1000-1500 mm/sup 3/。选择CT和SPECT成像几何形状以获得高倍率和高效率来成像位于躯干内的肿瘤。依次进行SPECT和CT投影。获得的图像显示,坏死肿瘤可以用高分辨率成像,观察脂质体的不均匀摄取。
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