TY - JOUR
T1 - Preparation of high specific activity 86Y using a small biomedical cyclotron
AU - Yoo, Jeongsoo
AU - Tang, Lucie
AU - Perkins, Todd A.
AU - Rowland, Douglas J.
AU - Laforest, Richard
AU - Lewis, Jason S.
AU - Welch, Michael J.
N1 - Funding Information:
This work was supported by a grant from the U.S. Department of Energy (grant DE FG02-87ER60512). The production of yttrium-86 at Washington University is supported by a grant from the National Cancer Institute (grant R24 CA86307).
Funding Information:
This work was supported by the National Cancer Institute (NCI R24 CA86307) and the United States Department of Energy (DE-FG02-87ER60512). The authors would like to thank Bill Margenau, Pat Margenau and Grainne Biddlecombe for cyclotron operation and technical support.
PY - 2005/11
Y1 - 2005/11
N2 - 86Y is an attractive PET radionuclide due to its intermediate half-life. 86Y was produced via the 86Sr(p,n) 86Y nuclear reaction. Enriched SrCO3 or SrO was irradiated with 2-6 μA of beam current for <4 h on a CS-15 cyclotron. It was shown that the SrO target could withstand at least 6 μA of beam current, a significant improvement over a maximum of 2 μA on the SrCO3 target. Average yields of 4.5 mCi/μA•h were achieved with SrO, which represent 71% of the theoretical yield, compared to 2.3 mCi/μA•h with SrCO3. The radioisotopic contaminants were 86mY (220%), 87Y (0.27%), 87mY (0.43%) and 88Y (0.024%). 86Y was isolated in an electrochemical cell consisting of three Pt electrodes. The solution was electrolyzed at 2000 mA (40 min) using two Pt plate electrodes. A second electrolysis (230 mA for 20 min) was performed using one Pt plate and a Pt wire. On average, 97.1% of the 86Y was recollected on the Pt wire after a second electrolysis. The 86Y was collected from the Pt wire using 2.8 M HNO3/EtOH (3:1). After evaporation, 86Y was reconstituted in 100 μl of 0.1 M HCl. Target materials were recovered as SrCO3 and then converted to SrO by thermal decomposition at 1150°C. Specific activity of 86Y was determined to be 29±19 mCi/μg via titration of 86Y(OAc)3 with DOTA or DTPA. We have established techniques for the routine, economical production of high purity, high specific activity 86Y on a small biomedical cyclotron that are translatable to other institutions.
AB - 86Y is an attractive PET radionuclide due to its intermediate half-life. 86Y was produced via the 86Sr(p,n) 86Y nuclear reaction. Enriched SrCO3 or SrO was irradiated with 2-6 μA of beam current for <4 h on a CS-15 cyclotron. It was shown that the SrO target could withstand at least 6 μA of beam current, a significant improvement over a maximum of 2 μA on the SrCO3 target. Average yields of 4.5 mCi/μA•h were achieved with SrO, which represent 71% of the theoretical yield, compared to 2.3 mCi/μA•h with SrCO3. The radioisotopic contaminants were 86mY (220%), 87Y (0.27%), 87mY (0.43%) and 88Y (0.024%). 86Y was isolated in an electrochemical cell consisting of three Pt electrodes. The solution was electrolyzed at 2000 mA (40 min) using two Pt plate electrodes. A second electrolysis (230 mA for 20 min) was performed using one Pt plate and a Pt wire. On average, 97.1% of the 86Y was recollected on the Pt wire after a second electrolysis. The 86Y was collected from the Pt wire using 2.8 M HNO3/EtOH (3:1). After evaporation, 86Y was reconstituted in 100 μl of 0.1 M HCl. Target materials were recovered as SrCO3 and then converted to SrO by thermal decomposition at 1150°C. Specific activity of 86Y was determined to be 29±19 mCi/μg via titration of 86Y(OAc)3 with DOTA or DTPA. We have established techniques for the routine, economical production of high purity, high specific activity 86Y on a small biomedical cyclotron that are translatable to other institutions.
KW - Biomedical cyclotron
KW - Electrochemical separation
KW - Electrodeposition
KW - Y
UR - http://www.scopus.com/inward/record.url?scp=27144451415&partnerID=8YFLogxK
U2 - 10.1016/j.nucmedbio.2005.06.007
DO - 10.1016/j.nucmedbio.2005.06.007
M3 - Article
C2 - 16253815
AN - SCOPUS:27144451415
SN - 0969-8051
VL - 32
SP - 891
EP - 897
JO - Nuclear Medicine and Biology
JF - Nuclear Medicine and Biology
IS - 8
ER -