Technetium-99M generator for enriched molybdenum
A method for separating a parent isotope from a daughter isotope is provided, the method comprising supplying irradiated target; dissolving the irradiated target; treating the dissolved irradiated target to a precipitation step to form a first solid phase of the parent isotope and a first liquid phase of the daughter isotope; filtering the first liquid phase of daughter isotope to create a first purified fraction of the daughter isotope to create a second solid phase of the parent isotope and a second liquid phase of the daughter isotope; and filtering the second liquid phase to create a second liquid fraction of the daughter isotope. The process can be repeated until the 99 Mo is exhausted and the enriched target material 98 Mo or 100 Mo can be easily re-used.
1. A method for separating a parent isotope from a daughter isotope, the method comprising:
a) supplying irradiated target material;
b) dissolving the irradiated target material to form an aqueous solution of molybdate salt;
c) treating the dissolved irradiated target with ethanol to form a first solid phase of the parent isotope and a first liquid phase of the daughter isotope;
d) filtering the first liquid phase of the daughter isotope with a guard column to capture residual target material that was not precipitated;
e) capturing the daughter isotope contained in the filtered first liquid phase onto a concentration column;
f) eluting the captured daughter isotope in a low-volume, pharmaceutically suitable matrix;
g) dissolving the first solid phase of parent isotope in water, and;
h) repeating steps c-g wherein the parent isotope is an element selected from the group consisting of molybdenum, tungsten, and combinations thereof and daughter isotope is an element selected from the group consisting of technetium, rhenium, and combinations thereof.
2. The method as recited in claim 1 wherein the first liquid phase of the daughter isotope is repeatedly treated to precipitate bulk amounts of the parent isotope, wherein no pH adjustment is required prior to the precipitation step.
3. The method as recited in claim 1 wherein the first liquid phase of the daughter isotope represents more than 75 percent yield of total daughter isotope present.
4. The method as recited in claim 1 wherein the parent isotope is molybdenum, and the daughter isotope is technetium, and wherein 99 percent of the molybdenum present is precipitated.
5. The method as recited in claim 4 wherein the first solid phase of the parent isotope is solubilized to yield additional liquid phase daughter isotope for subsequent harvesting.
6. The method as recited in claim 4 wherein the yield of the daughter isotope is between 75 percent and 99 percent.
7. The method as recited in claim 1 wherein the step of eluting the first liquid phase of the daughter isotope comprises combining the first liquid phase with a chloride to create a mixture and contacting the mixture with a sorbent to create a purified fraction of the daughter isotope.
8. The method as recited in claim 7 wherein the purified fraction of the daughter isotope resides in a saline solution.
9. The method as recited in claim 8 wherein the saline solution is less than one percent concentrated.
10. The method as recited in claim 1 further comprising resolubilizing the target material residing in steps c and d with hydroxide.
11. The method as recited in claim 5 wherein no pH adjustment is required prior to the subsequent reharvesting of the liquid phase daughter isotope.
12. The method as recited in claim 1 wherein the low volume ranges from between 0.1 ml and 10 ml.
13. The method as recited in claim 7 wherein the purified daughter isotope exhibits 1E+0 to 1E+4 counts ranging from between 50 and 950 keV.