High efficiency continuous-flow production of radioisotopes
US-2017337998-A1 · Nov 23, 2017 · US
US9449726B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9449726-B2 |
| Application number | US-201414293599-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 2, 2014 |
| Priority date | May 31, 2013 |
| Publication date | Sep 20, 2016 |
| Grant date | Sep 20, 2016 |
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Methods of synthesizing 100 Mo 2 C and 99m TcO 4 − are disclosed. Methods of 100 Mo 2 C generation involve thermally carburizing 100 MoO 3 . Methods of 99m TcO 4 generation involve proton bombardment of 100 Mo 2 C in a cyclotron. Yields of 99m TcO 4 can be increased by sintering 100 Mo 2 C prior to bombardment. The methods also include recycling of 100 Mo 2 C to form 100 MoO 3 . SPECT images obtained using 99m TcO 4 generated by the disclosed methods are also presented.
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What is claimed is: 1. A method of synthesizing pertechnetate ( 99 TcO 4 − ), the method comprising: synthesizing 100 MO 2 C by thermally carburizing 100 MoO 3 ; and bombarding the 100 Mo 2 C with protons in a cyclotron to yield 99 TcO 4 − . 2. A method of synthesizing pertechnetate ( 99m TcO 4 − ) in accordance with claim 1 , further comprising purifying the 99m TcO 4 − by thermo-chromatography. 3. A method of synthesizing pertechnetate ( 99 TcO 4 − ) in accordance with claim 1 , wherein the thermally carburizing comprises: (i) converting 100 MoO 3 to ammonium heptamolybdate tetrahydrate ((NH 4 ) 6 Mo 7 O 24 .4H 2 O) with 28% NH 3 (aq), (ii) converting (NH 4 ) 6 Mo 7 O 24 .4H 2 O to a hexamethyltetramine (HMT)-molybdate complex ((NH 4 ) 4 (HMT) 2 Mo 7 O 24 .4H 2 O) by reacting the (NH 4 ) 6 Mo 7 O 24 .4H 2 O with NH 3 (aq) and HMT and (iii) heating the dried HMT-molybdate complex in argon atmosphere to yield 100 Mo 2 C. 4. A method of synthesizing 99m Tc pertechnetate in accordance with claim 1 , wherein the bombarding the 100 Mo 2 C comprises bombarding the 100 Mo 2 C at a current of from about 1 μA, 1 μA up to 20 μA, or about 20 μA. 5. A method of synthesizing 99m Tc pertechnetate in accordance with claim 1 , wherein the bombarding the 100 Mo 2 C comprises bombarding the 100 Mo 2 C for about 45 minutes, from 45 minutes to 2 hours, or for about 2 hours. 6. A method of synthesizing 99m Tc pertechnetate in accordance with claim 1 , wherein the bombarding the 100 Mo 2 C comprises bombarding the 100 Mo 2 C at a current of about 20 μA for about 2 hours. 7. A method of synthesizing 99m Tc pertechnetate in accordance with claim 1 , further comprising collecting the 99m Tc 4 − in NaOH. 8. A method of synthesizing 99m Tc pertechnetate in accordance with claim 2 , wherein the thermo-chromatography comprises: (i) conditioning the column with acidified water, (ii) passing NaOH containing 99m TcO 4 − through an ion-exchange column and (iii) eluting the column with a saline solution. 9. A method of synthesizing 99m Tc pertechnetate in accordance with claim 8 , wherein the acidified water has a pH of about 2. 10. A method of synthesizing 99m Tc pertechnetate in accordance with claim 1 , further comprising recycling the 100 Mo 2 C to form 100 MoO 3 . 11. A method of synthesizing 99m Tc pertechnetate in accordance with claim 10 , wherein the recycling comprises: (i) washing the 100 Mo 2 C with 28% NH 3 (aq); and (ii) applying the solution from (i) to synthesis of (NH 4 ) 6 Mo 7 O 24 .4H 2 O. 12. A method of synthesizing pertechnetate ( 99m TcO 4 − ) in accordance with claim 1 , further comprising: prior to the bombarding, pressing the 100 Mo 2 C to form a compact powder; and sintering the compact powder. 13. A method of synthesizing pertechnetate ( 99m TcO 4 − ) in accordance with claim 12 , wherein the sintering the compact powder comprises heating the compact powder under vacuum at about 600° C.
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