The ApoCorrect assay: a novel, rapid method to determine the biological functionality of radiolabeled and fluorescent Annexin A5.

Abstract We have demonstrated that imaging of programmed cell death (PCD) in patients is possible using 99m Tc-Annexin A5. Because of the short half-life of the technetium label it is important to limit the time span between the preparation of 99m Tc-Annexin A5 and its administration into the patient. Therefore methods of quality control that determine the biological active fraction in the 99m Tc-Annexin A5 should be not only accurate and precise but also rapid. We report the development and validation of a rapid, simple assay measuring the biological active fraction of 99m Tc-Annexin A5. The assay is based on a solid phase of paramagnetic beads which are coated with phospholipids. Annexin A5 binds to these beads with high affinity if phosphatidyl serine is present within the phospholipid coat. Furthermore the binding depends on Ca 2+ ions and functional Ca 2+ /phospholipid binding sites of Annexin A5. The bead assay is specific, stability-indicating, repeatable, and reproducible. It allows one to determine within 25 min the biological active fraction of a 99m Tc-Annexin A5 preparation. We dubbed this assay the ApoCorrect assay.