Literature DB >> 12791824

Safety, biodistribution, and dosimetry of 99mTc-HYNIC-annexin V, a novel human recombinant annexin V for human application.

Gerrit J Kemerink1, Xuan Liu, Davy Kieffer, Sarah Ceyssens, Luc Mortelmans, Alfons M Verbruggen, Neil D Steinmetz, Jean-Luc Vanderheyden, Allan M Green, Kristin Verbeke.   

Abstract

UNLABELLED: 99mTc-hydrazinonicotinamido (HYNIC)-annexin V is a novel tracer for in vivo imaging of apoptosis. The present study on humans was performed to investigate the safety of (99m)Tc-HYNIC-annexin V and to quantify the biodistribution and radiation dose.
METHODS: Six healthy, male volunteers participated in the study. A dual-head gamma camera was used to acquire conjugate anterior and posterior views. Imaging started with a transmission scan using a (57)Co-flood source to obtain a map of the local thickness of the volunteer. Approximately 250 MBq of (99m)Tc-HYNIC-annexin V were injected intravenously, directly followed by a 30-min dynamic study. Whole-body scans were obtained at about 30 min, 3 h, 6 h, and 24 h after injection. Organ uptake was determined after correction for background, scatter, and attenuation. The MIRDOSE3.1 program was used to calculate organ-absorbed doses and effective dose. Signs of adverse effects were investigated by monitoring renal and liver function, hematology, blood coagulation, and vital signs (blood pressure, pulse, respiration rate, temperature, and electrocardiogram).
RESULTS: The kidneys accumulated 49.7 +/- 8.1 percentage injected dose (%ID) at 3 h after injection; the liver, 13.1 +/- 1.0 %ID; the red marrow, 9.2 +/- 1.8 %ID; and the spleen, 4.6 +/- 1.6 %ID. More than 90% of the blood activity was cleared with a half-life of 24 +/- 3 min. The biologic half-life of the activity registered over the total body was long (69 +/- 7 h). Excretion of the activity was almost exclusively through the urine (22.5 +/- 3.5 %ID at 24 h), and hardly any activity was seen in the bowel or feces. Absorbed doses were found to be 196 +/- 31 micro Gy/MBq for the kidneys, 41 +/- 12 micro Gy/MBq for the spleen, 16.9 +/- 1.3 micro Gy/MBq for the liver, and 8.4 +/- 0.9 micro Gy/MBq for the red marrow. The effective dose was 11.0 +/- 0.8 micro Sv/MBq, or 2.8 +/- 0.2 mSv for the average injected activity of 250 MBq. No adverse effects were observed.
CONCLUSION: (99m)Tc-HYNIC-annexin V is a safe radiopharmaceutical, having a favorable biodistribution for imaging of apoptosis in the abdominal as well as thoracic area with an acceptable radiation dose.

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Year:  2003        PMID: 12791824

Source DB:  PubMed          Journal:  J Nucl Med        ISSN: 0161-5505            Impact factor:   10.057


  35 in total

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2.  Engineered annexin A5 variants have impaired cell entry for molecular imaging of apoptosis using pretargeting strategies.

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7.  Mapping of treatment-induced apoptosis in normal structures: 99mTc-Hynic-rh-annexin V SPECT and CT image fusion.

Authors:  Marina S Kartachova; Renato A Valdés Olmos; Rick L M Haas; Frank J P Hoebers; Michiel W van den Brekel; Nico van Zandwijk; Marcel van Herk; Marcel Verheij
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Review 8.  Pre-clinical and clinical evaluation of nuclear tracers for the molecular imaging of vulnerable atherosclerosis: an overview.

Authors:  L M Riou; A Broisat; J Dimastromatteo; G Pons; D Fagret; C Ghezzi
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9.  Evaluation of [(18)F]-CP18 as a PET imaging tracer for apoptosis.

Authors:  Helen Su; Gang Chen; Umesh Gangadharmath; Luis F Gomez; Qianwa Liang; Fanrong Mu; Vani P Mocharla; A Katrin Szardenings; Joseph C Walsh; Chun-Fang Xia; Chul Yu; Hartmuth C Kolb
Journal:  Mol Imaging Biol       Date:  2013-12       Impact factor: 3.488

10.  In vitro and in vivo evaluation of the caspase-3 substrate-based radiotracer [(18)F]-CP18 for PET imaging of apoptosis in tumors.

Authors:  Chun-Fang Xia; Gang Chen; Umesh Gangadharmath; Luis F Gomez; Qianwa Liang; Fanrong Mu; Vani P Mocharla; Helen Su; A Katrin Szardenings; Joseph C Walsh; Tieming Zhao; Hartmuth C Kolb
Journal:  Mol Imaging Biol       Date:  2013-12       Impact factor: 3.488

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