Methods and kits for preparing radionuclide complexes

1. A method for preparing a complex comprising a radioisotope of gallium for use in radiotherapy or in a medical imaging procedure, said method comprising adding a gallium radioisotope eluate obtained directly from a gallium radionuclide generator without additional purification or concentration steps to a chelator composition comprising a pharmaceutically acceptable buffer in amounts sufficient to increase the pH to a level in the range of 3 to 8, and a chelator that is able to chelate radioactive gallium within said pH range and at a temperature of 10 to 30 ° C., said chelator being linked to a biological targeting agent, wherein said chelator is selected from desferrioxamine-B (DFO), bis(2-hydroxybenzyl)ethylenediaminediacetic acid (HBED), 1,4,7-triazacyclononane macrocycle substituted with phosphonic groups at the amines (NOTP), or a compound of formula (I)

or a salt thereof; wherein one of X and Y is C=0 and the other is NR; wherein each m and p are independently selected from 0 to 6; wherein R 1 is a chelating group capable of chelating a radionuclide and is selected from:

wherein R, R 2 , R 3 and R 4 independently hydrogen or an optionally substituted C 1-7 alkyl group; and where Z is hydrogen or a group of formula —B′—H, —B′-A, or a group —B′-A*-T, where T is a targeting group capable of binding to a target of interest in a subject;

A is a reactive group allowing coupling to the group T,

A* is a reacted reactive group A;

B′ is a linker group for linking the chelating group to a reactive group A, and is represented by the formula:

wherein each Q is independently selected from a group consisting of —NR 5 —, —C(O)NR 5 —, —C(O)O, —NR 5 C(O)NR 5 —, —NR 5 C(S)NR 5 — and —O—, each R 5 is independently hydrogen or an optionally substituted C 1-7 alkyl group, each q and s are independently selected from 0 to 6 and each r is independently selected from 1 to 6,

wherein said chelator, buffer are in lyophilized or freeze-dried form, and

wherein said chelator composition does not include agents inhibiting metals other than gallium.

2. The method of claim 1 , wherein the gallium radioisotope eluate is at a pH of less than 2.

3. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable basic reagent selected from sodium hydroxide, potassium hydroxide, a carbonate and bicarbonate.

4. The method of claim 1 , wherein the chelator is linked to a biological targeting agent that targets a cancer specific marker.

5. The method of claim 1 , wherein the pharmaceutically acceptable buffer is a phosphate buffer, bicarbonate or carbonate buffer, succinate buffer, borate buffer, cacodylate buffer, citrate buffer, a zwitterionic buffer, a tris(hydroxymethyl)aminomethane (TRIS) buffer, morpholine propanesulphonic acid (MOPS), N-(2-hydroxyethyl) piperazine-N′(2- ethanesulfonic acid) (HEPES), tartaric add, arginine or an acetate buffer.

6. The method of claim 4 , wherein the cancer specific marker is prostate specific membrane antigen (PSMA).

7. The method of claim 1 , wherein the gallium radioisotope eluate is obtained by eluting a 68 Ga radionuclide column with an inorganic acid.