Development of radiolabeled bis(zinc(II)-dipicolylamine) complexes for cell death imaging

被引:10
作者
Aoki, Miho [1 ]
Odani, Akira [1 ]
Ogawa, Kazuma [1 ,2 ]
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Kakuma Machi, Kanazawa, Ishikawa 9201192, Japan
[2] Kanazawa Univ, Inst Frontier Sci Initiat, Kakuma Machi, Kanazawa, Ishikawa 9201192, Japan
关键词
Zinc(II)-dipicolylamine; Phosphatidylserine; Cell death imaging; Technetium; IN-VIVO DETECTION; COORDINATION-COMPLEXES; MEMBRANE SURFACES; APOPTOTIC CELLS; PHOSPHATIDYLSERINE; PROBE; BISPHOSPHONATE; RECOGNITION; BIOMARKERS; PEPTIDES;
D O I
10.1007/s12149-019-01339-8
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
PurposeAlthough it has been traditionally surmised that phosphatidylserine (PS) externalization is a hallmark of apoptosis, most other non-apoptotic modes of cell death, such as necrosis, are also associated with PS externalization. Bis(zinc-dipicolylamine) (ZnDPA) complexes have been reported to exhibit affinity for PS. The present study aimed to develop novel radiolabeled ZnDPA derivatives for cell death imaging in tumor after treatment with anticancer drugs.Methods[I-125]IB-EG(2)-ZnDPA and [Tc-99m]Tc-MAG3-EG(2)-ZnDPA were designed and prepared. The stabilities of these radiotracers were determined in 0.1M phosphate buffer (pH 7.4) or murine plasma at 37 degrees C, and their 1-octanol/water partition coefficients (logP) were measured. The uptake of radioactivity in cancer cells, which were preincubated in a normal medium or in a medium containing 5-FU, was measured after incubation with radiotracers. Accumulation of [Tc-99m]Tc-MAG3-EG(2)-ZnDPA in the tumor was evaluated in tumor-bearing mice treated with or without 5-FU, and then TUNEL staining was performed to detect dead cells in the tumor tissue sections.ResultsThe radiochemical purities of [I-125]IB-EG(2)-ZnDPA and [Tc-99m]Tc-MAG3-EG(2)-ZnDPA exceeded 95%. Although [I-125]IB-EG(2)-ZnDPA gradually decomposing with time, more than 90% of [Tc-99m]Tc-MAG3-EG(2)-ZnDPA remained in its intact form in phosphate buffer through 6h of incubation. Neither [I-125]IB-EG(2)-ZnDPA nor [Tc-99m]Tc-MAG3-EG(2)-ZnDPA decomposed so much after 6-h incubation in murine plasma. [I-125]IB-EG(2)-ZnDPA could not specifically recognize PS on the cell surface because of its high lipophilicity. Conversely, [Tc-99m]Tc-MAG3-EG(2)-ZnDPA accumulated in cancer cells after treatment with an anticancer drug both in vitro and in vivo, and its accumulation was correlated with the number of TUNEL-positive cells. However, the biodistribution of [Tc-99m]Tc-MAG3-EG(2)-ZnDPA was not suitable for imaging because of its low accumulation in tumor and high uptake in abdomen organs.Conclusion[Tc-99m]Tc-MAG3-EG(2)-ZnDPA could be useful for the early detection of treatment effects after chemotherapy. Since the signal-to-noise ratio is not enough for single photon emission computed tomography imaging, further modification is needed to improve its biodistribution and affinity for PS.
引用
收藏
页码:317 / 325
页数:9
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