^99mTc-labeled annexin V fragments: a potential SPECT radiopharmaceutical for imaging cell death

Abstract 

Introduction

Annexin V is a protein that binds to phosphatidylserine exposed on dying cells. The phosphatidylserine-specific sequence is attributed to a chain on the N-terminal of annexin consisting of 13 amino acid sequence. Radiolabeled annexin V is used for imaging apoptosis.

Methods

With an aim to synthesize a probe that can detect cell death akin to annexin V but smaller in size, annexin-13 fragments were derivatized to contain cysteine, cysteine–cysteine and histidine in their sequence at N terminal and were labeled with ^99mTc via nitrido and carbonyl precursors. The ^99mTc-labeled annexin-13 derivatives were characterized by HPLC and studied for their stability. In vitro and in vivo studies were carried out in apoptotic HL-60 cells and fibrosarcoma tumor-bearing Swiss mice, respectively.

Results

The ^99mTc complexes were formed in high yields and were found to be stable. HPLC pattern of ^99mTc nitrido complex of cysteine–cysteine–annexine 13 (CC-Anx13) and ^99mTc carbonyl complex of histdine–annexin 13 (H-Anx13) revealed the formation of single species. In vitro cell uptake studies with ^99mTc nitrido complex of cysteine–cysteine–annexin 13 fragment showed 6.5% uptake in apoptotic HL-60 cells. The uptake was found to be specific on testing with apoptotic HL-60 cells. Biodistribution studies of ^99mTc nitrido complex with CC-Anx13 in fibrosarcoma tumor-bearing Swiss mice revealed optimum tumor uptake of 0.52 (0.17) %ID/g at 1 h pi.

Conclusion

^99mTc(N)-CC-anx13 showed specific uptake in apoptotic tumor cells and warrants further evaluation.

Keywords: Annexin V, Apoptosis, ^99mTc nitrido, Carbonyl precursors