Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest 1117, Hungary.
Department of Biophysics and Radiation Biology, Semmelweis University, Budapest 1094, Hungary.
Contrast Media Mol Imaging. 2017 May 31;2017:4693417. doi: 10.1155/2017/4693417. eCollection 2017.
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 Tc-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 Tc-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 mol lipid which falls among the highest values reported for Tc labeling of liposomes. Quantitative in vivo SPECT/CT biodistribution studies revealed distinct differences between the labeled liposomes and the free Tc-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.
脂质体制剂的体内生物分布极大地影响这些新型药物的药代动力学;因此,脂质体的放射性同位素标记以及使用核成像方法进行体内研究非常重要。在本工作中,提出了一种使用新型 Tc-三羰基配合物对脂质体进行表面标记的新方法。使用模拟两种已获 FDA 批准的脂质体药物组成的脂质体。在标记的第一步中,使用 Traut 试剂在脂质体表面形成巯基,随后将 Tc-三羰基配合物结合到脂质体表面。通过尺寸排阻色谱法确定的标记效率为 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%。获得的比活度为每 1mol 脂质 50MBq,属于 Tc 标记脂质体报道的最高值之一。定量的体内 SPECT/CT 生物分布研究表明,标记的脂质体与游离 Tc-三羰基之间存在明显差异,这表明标记的体内稳定性。由于研究的脂质体是非聚乙二醇化的,因此观察到从血管快速清除和在肝脏和脾脏中高摄取。