Ming Hui,Gao Jingmei,Fang Lei,Li Chengxia,Ji Yanhui,Shen Yiming,Hu Yiming,Chang Jin,Li Wei,Tan Jian.Evaluation of SPECT/CT imaging and internal therapeutic effectiveness of 131I-RGD-BSA-PCL in the lung cancer mouse model[J].Chinese Journal of Radiological Medicine and Protection,2016,36(9):641-647
Evaluation of SPECT/CT imaging and internal therapeutic effectiveness of 131I-RGD-BSA-PCL in the lung cancer mouse model
Received:March 31, 2016  
DOI:10.3760/cma.j.issn.0254-5098.2016.09.001
KeyWords:Radioiodine  Arg-Gly-Asp (RGD)  Nano-liposome  NSCLC
FundProject:国家自然科学基金(81301244)
Author NameAffiliationE-mail
Ming Hui Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China  
Gao Jingmei Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China  
Fang Lei Tianjin University, School of Life Sciences, Tianjin 300072, China  
Li Chengxia Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China  
Ji Yanhui Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China  
Shen Yiming Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China  
Hu Yiming Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China  
Chang Jin Tianjin University, School of Life Sciences, Tianjin 300072, China  
Li Wei Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China weiwei_tianjin@foxmail.com 
Tan Jian Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China  
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Abstract::
      Objective To investigate the SPECT/CT imaging of non-small-cell lung carcinoma (NSCLC) mice models and the internal irradiation biological effects and therapeutic effectiveness of nanoliposome 131I-RGD-BSA-PCL. Methods RGD-BSA-PCL and BSA-PCL were constructed. The target binding and cellular uptake in H460 cell line were observed by fluorescence confocal microscopy in vitro. The nanoliposome with 131I were labeled using the Chloramine-T method. Apoptosis analyses was performed using flow cytometry. By construcing tumor xenografts, the biological distribution, change of tumor volume and the SPECT/CT imaging were discussed. Results Confocal microscopy revealed significant uptake of RGD-BSA-PCL or BSA-PCL in NCI-H460 cell after nanolipsome incubated for 1 and 8 h. The early apoptosis rates of Na131I, 131I-BSA-PCL and 131I-RGD-BSA-PCL were (33.3±12.5)%, (68.4±8.0)% and (70.5±12.2)%, respectively. The tumor uptake levels of 131I-BSA-PCL were higher than that of 131I-BSA-PCL (t=9.53, 5.03, P<0.01). There was a significant difference of tumor volume between the treatment group and the control group, and the tumor volume inhibition was most obvious in the 131I-RGD-BSA-PCL group on day 23 post-treatment (t=126.44, P<0.01). SPECT/CT tomography showed that 131I-RGD-BSA-PCL and 131I-BSA-PCL groups had obvious accumulation in the tumor on day 21 post-treatment, and intensity of radiation signal of 131I-RGD-BSA-PCL group was stronger than that of 131I-BSA-PCL group. Conclusions Radionuclide therapy using 131I-RGD-BSA-PCL, which showed excellent targeted cell killing and suppressed tumor growth, exhibited favorable intracellular retention of 131I.
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