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Radiolabeling and Quantitative In Vivo SPECT/CT Imaging Study of Liposomes Using the Novel Iminothiolane-99mTc-Tricarbonyl Complex

机译:使用新型Iminothiolane-99mTc-Tri羰基复合物对脂质体进行放射性标记和体内SPECT / CT定量成像研究

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摘要

The in vivo biodistribution of liposomal formulations greatly influences the pharmacokinetics of these novel drugs; therefore the radioisotope labeling of liposomes and the use of nuclear imaging methods for in vivo studies are of great interest. In the present work, a new procedure for the surface labeling of liposomes is presented using the novel 99mTc-tricarbonyl complex. Liposomes mimicking the composition of two FDA approved liposomal drugs were used. In the first step of the labeling, thiol-groups were formed on the surface of the liposomes using Traut's reagent, which were subsequently used to bind 99mTc-tricarbonyl complex to the liposomal surface. The labeling efficiency determined by size exclusion chromatography was 95%, and the stability of the labeled liposomes in bovine serum was found to be 94% over 2 hours. The obtained specific activity was 50 MBq per 1 μmol lipid which falls among the highest values reported for 99mTc labeling of liposomes. Quantitative in vivo SPECT/CT biodistribution studies revealed distinct differences between the labeled liposomes and the free 99mTc-tricarbonyl, which indicates the in vivo stability of the labeling. As the studied liposomes were non-PEGylated, fast clearance from the blood vessels and high uptake in the liver and spleen were observed.
机译:脂质体制剂的体内生物分布极大地影响了这些新药的药代动力学。因此,脂质体的放射性同位素标记以及在体内研究中使用核成像方法引起了人们的极大兴趣。在目前的工作中,提出了使用新型的 99m Tc-三羰基复合物进行脂质体表面标记的新方法。使用模仿两种FDA批准脂质体药物组成的脂质体。在标记的第一步中,使用Traut's试剂在脂质体表面形成硫醇基,然后将其用于将 99m Tc-三羰基复合物结合到脂质体表面。通过尺寸排阻色谱法测定的标记效率为95%,并且在2小时内发现标记的脂质体在牛血清中的稳定性为94%。所获得的比活为每1μmol脂质50μMqq,属于脂质体 99m Tc标记的最高值。体内定量SPECT / CT生物分布研究表明,标记的脂质体与游离的99mTs-三羰基脂质之间存在明显差异,这表明标记的体内稳定性。由于所研究的脂质体是非聚乙二醇化的,因此可从血管中快速清除,并观察到肝脏和脾脏的高摄取。

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