19.10.2015 Views

Yttrium-90 and Rhenium-188 Radiopharmaceuticals for Radionuclide Therapy

Pub1662web-89688003

Pub1662web-89688003

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

adionuclidic purity of the <strong>90</strong> Y solution, the ‘BARC technique’ was also used.<br />

This method was a combination of solvent EPC [10.20] wherein Whatman No. 1<br />

(18 cm × 2 cm) paper chromatographic strips impregnated with KSM-17 at the<br />

point of spotting were used. On development with normal saline, <strong>90</strong> Sr moved to<br />

the solvent front, while <strong>90</strong> Y was retained at the point of spotting. The activity at<br />

the solvent front was estimated by cutting the chromatograms into 1 cm strips <strong>and</strong><br />

measuring radioactivity in a dose calibrator. Radionuclidic purity was calculated<br />

as a percentage of the total activity spotted.<br />

10.4.3. Results <strong>and</strong> discussion<br />

10.4.3.1. Electrochemical separation of <strong>90</strong> Y<br />

Although there are different methods of separation of <strong>90</strong> Y from the parent<br />

radionuclide <strong>90</strong> Sr reported in the literature [10.19], the <strong>90</strong> Sr/ <strong>90</strong> Y generator used an<br />

electrochemical method <strong>for</strong> separation of <strong>90</strong> Y. The electrolysis was carried out in<br />

an electrolytic quartz cell, prepared in the Laboratory <strong>for</strong> Radioisotopes, Vinča<br />

Institute of Nuclear Sciences (see Fig. 10.15(a)), as potentiostatic electrolysis with<br />

potential –2.500 ± 0.055 V with respect to the SCE. During the first electrolysis,<br />

the current was increased from 730 to 745 mA. The electrolytic potential at the<br />

platinum cathode was stable during the electrolysis, but could not be maintained<br />

at –2.50 V. It fell to –2.39 V, but was within the accepted limits of ± 0.2% plus<br />

5 mV, in constant voltage mode. The pH was adjusted to 2.7 ± 0.2.<br />

The second electrolysis was accomplished with a stable potential of –2.50 V<br />

on the platinum cathode <strong>and</strong> a constant current of 100 mA during the electrolysis.<br />

The solution was warmed up during electrolysis, <strong>and</strong> hence subsequent cooling<br />

of the electrolysis cell was necessary. Separation of H 2 gas was also detected<br />

(see Fig. 10.15(b)) <strong>and</strong>, there<strong>for</strong>e, stirring during the process was not required.<br />

These conditions ensured that the deposition yield was ><strong>90</strong>%.<br />

10.4.3.2. Quality control of <strong>90</strong> Y<br />

<strong>Yttrium</strong>-<strong>90</strong> exists in secular equilibrium with its parent isotope <strong>90</strong> Sr, which<br />

is a product of the fission reaction. Many impurities must be removed, <strong>and</strong> pure<br />

<strong>90</strong> Y has to be converted into an appropriate chemical <strong>for</strong>m <strong>for</strong> application in<br />

medicine therapy. Radioactive <strong>90</strong> Sr, as <strong>90</strong> Sr(NO 3 ) in equilibrium with <strong>90</strong> Y in 1M<br />

HNO 3 from POLATOM, had a high radionuclidic purity (>99.5%), as well as a<br />

high RCP. Strontium-<strong>90</strong> breakthrough was the major problem often encountered<br />

with the <strong>90</strong> Sr/ <strong>90</strong> Y generator. Because <strong>90</strong> Sr is a bone seeker <strong>and</strong> the upper limit of<br />

201

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!