The Chelator makes the difference

The in-vivo imaging of a biomolecule (peptide, protein, antibody, …) often requires the grafting of a chelator prior to the radiometallation step. Recent litterarure emphasized that a small modification of the chelator can significantly alter the pharmacokinetic of the conjugate. It is especially the case when the biological molecule  is a small peptide or an antibody fragment.
DOTA is a gold standard to complex most of the radiometals. However, it is by far not always the ideal candidate. It is important to find the right combination between the chelating agent and the biovector. Many factors such as the size, the geometry, the lipophilicity and the charge of the metal complex can affect the pharmacokinetic of the drug.
During the design phase of a new radiopharmaceutical, it is crucial to screen very early, which chelate will be the most adapted in order to find the ideal system: chelator/radiometal/biovector.
All these considerations lead us to provide you several samples packs in order to give you the opportunity to test different chelating agents in a cost effective way.

Maleimide Pack

Chelating agents bearing Maleimide function. Specific reactivity toward SH group such as cysteine.

50 mg Maleimide-DOTA

50 mg Maleimide-DOTA-GA

50 mg Maleimide-NOTA

50 mg Maleimide-NODA-GA

50 mg Maleimide-DTPA

Activated Esters Pack

Chelating agents bearing NHS ester or anhydride groups. Specific reactivity toward NH2 group such as lysine.

50 mg DOTA-NHS ester

50 mg NOTA-NHS ester

50 mg NODA-GA-NHS ester

50 mg DOTA-GA- anhydride

50 mg DTPA anhydride

Protected Chelators Pack

Selectively (tBu) ester protected chelating agents.

100 mg DOTA-tris(tBu)ester

100 mg DOTA-GA-t(Bu)4

100 mg NOTA-bis(tBu)ester

100 mg NODA-GA-tris(tBu)ester

100 mg DTPA-tetra(tBu) ester