PET imaging of sterile inflammation with a 18F-labeled bis(zinc(II)-dipicolylamine) complex

被引:0
作者
Hongliang Wang
Ganghua Tang
Kongzhen Hu
Tingting Huang
Xiang Liang
Sijin Li
Zhifang Wu
机构
[1] The First Affiliated Hospital of Shanxi Medical University,Department of Nuclear Medicine
[2] The First Affiliated Hospital of Sun Yat-Sen University,Department of Nuclear Medicine
来源
Journal of Radioanalytical and Nuclear Chemistry | 2014年 / 302卷
关键词
Positron emission tomography; Sterile inflammation; Phosphatidylserine; Zinc(II)-dipicolylamine; Cell death;
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摘要
Small-molecular probe 18F-labeled bis(zinc(II)-dipicolylamine) complex (18F-FB-DPAZn2) was evaluated for PET imaging of sterile inflammation. In comparison with 18F-2-deoxy-β-d-glucose (18F-FDG), 18F-radiolabeled Annexin V (18F-FB-Annexin V) showed rapid clearance of radioactivity from the kidney and low uptake in most tissues. Both the lower radioactivity accumulation in brain and heart and the higher uptakes in the lung, liver, and intestine were observed for the biodistribution of 18F-FB-DPAZn2. In PET imaging, 18F-FDG showed significantly higher tumor and inflammation uptake than did of 18F-FB-DPAZn2 and 18F-FB-Annexin V in the S-180 fibrosarcoma mouse model and sterile inflammation mouse model. Both 18F-FB-DPAZn2 and 18F-FB-Annexin V performed the specifically localization in inflammation, and the ratios of inflammatory lesion-to-muscle and tumor-to-muscle were 1.83 ± 0.20 and 0.90 ± 0.12 (P < 0.05) for 18F-FB-DPAZn2, and 1.51 ± 0.14 and 1.21 ± 0.12 (P > 0.05) for 18F-FB-Annexin V, respectively. Terminal deoxynucleotide end-labeling (TUNEL) assays performed on the dissected tissues showed the significantly more TUNEL-positive nuclei in the inflammatory muscle than in tumor and normal muscle, and these TUNEL results correlated with the uptake of 18F-FB-DPAZn2 in dissected tissues. Biodistribution and PET imaging studies showed that the 18F-FB-DPAZn2 is suitable for imaging sterile inflammation in vivo and is capable of the differentiating tumor from inflammation.
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页码:273 / 280
页数:7
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共 240 条
[1]  
Kennedy AD(2009)Neutrophil apoptosis and the resolution of infection Immunol Res 43 25-61
[2]  
DeLeo FR(2006)Neutrophil apoptosis: a marker of disease severity in sepsis and sepsis-induced acute respiratory distress syndrome Crit Care 10 R155-698
[3]  
Fialkow L(2008)Caspase-8 is activated by cathepsin D initiating neutrophil apoptosis during the resolution of inflammation J Exp Med 205 685-1064
[4]  
Fochesatto Filho L(2006)Cyclin-dependent kinase inhibitors enhance the resolution of inflammation by promoting inflammatory cell apoptosis Nat Med 12 1056-91
[5]  
Bozzetti MC(1998)Interleukin-8 delays spontaneous and tumor necrosis factor-alpha-mediated apoptosis of human neutrophils Kidney Int 53 84-26165
[6]  
Milani AR(1997)Appearance of phosphatidylserine on apoptotic cells requires calcium-mediated nonspecific flip-flop and is enhanced by loss of the aminophospholipid translocase J Biol Chem 272 26159-95S
[7]  
Rodrigues Filho EM(2008)In vivo detection of apoptosis J Nucl Med 49 81S-1688
[8]  
Ladniuk RM(2008)Site-specific labeling of annexin V with F-18 for apoptosis imaging Bioconjug Chem 19 1684-964
[9]  
Pierozan P(2011)Annexin A5-conjugated polymeric micelles for dual SPECT and optical detection of apoptosis J Nucl Med 52 958-2220
[10]  
de Moura RM(2005)Fluorescent detection of apoptotic cells by using zinc coordination complexes with a selective affinity for membrane surfaces enriched with phosphatidylserine ChemBioChem 6 2214-69