Measurement of <sup>227</sup> Ac by Isotopic Ratio with <sup>225</sup> Ac Using ICP-MS

A method is reported for the measurement of <sup>227</sup>Ac using inductively coupled plasma mass spectrometry (ICP-MS) and isotope ratio analysis. The method has application for the quality testing of <sup>225</sup>Ac produced as an active pharmaceutical ingredient (API). The <sup>225</sup>Ac/<sup>227</sup>Ac isotope ratio is measured directly from ICP-MS count rate data and converted to an <sup>225</sup>Ac/<sup>227</sup>Ac activity ratio by using basic nuclear decay equations. The activity ratio, which is itself a measure of radioisotopic purity, is coupled with an orthogonal measurement of <sup>225</sup>Ac activity to obtain an absolute <sup>227</sup>Ac activity. Thus, the method may be used to report the <sup>227</sup>Ac content of an <sup>225</sup>Ac API in absolute or relative terms. The methodology was evaluated against appropriate validation criteria (e.g., linearity, accuracy, precision, specificity) by analyzing a series of solutions containing known quantities of <sup>225</sup>Ac and <sup>227</sup>Ac. Accuracy was evaluated using a spike recovery study. The spike recoveries were 100-108% for samples with 0.100 to 2.00 ng L<sup>-1</sup> of <sup>227</sup>Ac and 74-91% for 0.025 ng L<sup>-1</sup> of <sup>227</sup>Ac. Intermediate precision was measured as 4.1% using replicate measurements (<i>n</i> = 12, two instruments) of <sup>227</sup>Ac spiked samples (0.5 ng L<sup>-1</sup>). The instrumental detection limits for <sup>227</sup>Ac were shown to be as low as 23 Bq L<sup>-1</sup> (0.0086 ng L<sup>-1</sup>), which is lower than comparable methods for the quantification of <sup>227</sup>Ac in <sup>225</sup>Ac APIs. Actinium-225 samples are analyzed under this method without any need for <sup>225</sup>Ac decay or <sup>227</sup>Ac daughter in-growth. Sample preparation involves simple dilution of the <sup>225</sup>Ac API in 3% HCl/1% HNO<sub>3</sub>. The analysis takes as little as 2 h using equipment common to radioanalytical laboratories. Thus, the measurement of <sup>227</sup>Ac by this method can be performed as part of routine <sup>225</sup>Ac API quality testing and reported on release documents. This is a significant advantage over radiometric methods reported for the quantification of <sup>227</sup>Ac in <sup>225</sup>Ac APIs, which require days to weeks before reportable results can be obtained. The measurement of <sup>227</sup>Ac by ICP-MS and isotope ratio analysis is rapid, accurate, and sensitive. The implementation of this method for <sup>225</sup>Ac API quality testing will help <sup>225</sup>Ac producers and end-users ensure product quality and demonstrate regulatory compliance.

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Journal
ACS Omega
Published
2025-11-11
DOI
https://doi.org/10.1021/acsomega.5c09343
Citations
1
Primary Topic
Radiopharmaceutical Chemistry and Applications
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article
Field-Weighted Citation Impact
1.36
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article

Measurement of 227 Ac by Isotopic Ratio with 225 Ac Using ICP-MS

Cory A. Hawkins, D.J. de Vries, Jakob E. Baumeister, John W. N. Brown et al.
1 citations
ACS Omega
Radiopharmaceutical Chemistry and Applications
1.36
article

Measurement of 227 Ac by Isotopic Ratio with 225 Ac Using ICP-MS

Cory A. Hawkins, D.J. de Vries, Jakob E. Baumeister, John W. N. Brown, Joshua B. McCormick, Miguel Toro-González, Benjamin W. Puffer
article en
1 citations

Abstract

A method is reported for the measurement of <sup>227</sup>Ac using inductively coupled plasma mass spectrometry (ICP-MS) and isotope ratio analysis. The method has application for the quality testing of <sup>225</sup>Ac produced as an active pharmaceutical ingredient (API). The <sup>225</sup>Ac/<sup>227</sup>Ac isotope ratio is measured directly from ICP-MS count rate data and converted to an <sup>225</sup>Ac/<sup>227</sup>Ac activity ratio by using basic nuclear decay equations. The activity ratio, which is itself a measure of radioisotopic purity, is coupled with an orthogonal measurement of <sup>225</sup>Ac activity to obtain an absolute <sup>227</sup>Ac activity. Thus, the method may be used to report the <sup>227</sup>Ac content of an <sup>225</sup>Ac API in absolute or relative terms. The methodology was evaluated against appropriate validation criteria (e.g., linearity, accuracy, precision, specificity) by analyzing a series of solutions containing known quantities of <sup>225</sup>Ac and <sup>227</sup>Ac. Accuracy was evaluated using a spike recovery study. The spike recoveries were 100-108% for samples with 0.100 to 2.00 ng L<sup>-1</sup> of <sup>227</sup>Ac and 74-91% for 0.025 ng L<sup>-1</sup> of <sup>227</sup>Ac. Intermediate precision was measured as 4.1% using replicate measurements (<i>n</i> = 12, two instruments) of <sup>227</sup>Ac spiked samples (0.5 ng L<sup>-1</sup>). The instrumental detection limits for <sup>227</sup>Ac were shown to be as low as 23 Bq L<sup>-1</sup> (0.0086 ng L<sup>-1</sup>), which is lower than comparable methods for the quantification of <sup>227</sup>Ac in <sup>225</sup>Ac APIs. Actinium-225 samples are analyzed under this method without any need for <sup>225</sup>Ac decay or <sup>227</sup>Ac daughter in-growth. Sample preparation involves simple dilution of the <sup>225</sup>Ac API in 3% HCl/1% HNO<sub>3</sub>. The analysis takes as little as 2 h using equipment common to radioanalytical laboratories. Thus, the measurement of <sup>227</sup>Ac by this method can be performed as part of routine <sup>225</sup>Ac API quality testing and reported on release documents. This is a significant advantage over radiometric methods reported for the quantification of <sup>227</sup>Ac in <sup>225</sup>Ac APIs, which require days to weeks before reportable results can be obtained. The measurement of <sup>227</sup>Ac by ICP-MS and isotope ratio analysis is rapid, accurate, and sensitive. The implementation of this method for <sup>225</sup>Ac API quality testing will help <sup>225</sup>Ac producers and end-users ensure product quality and demonstrate regulatory compliance.

ACS OmegaVol. 10(46)
Japan Radioisotope Association (JP)
Openalex Percentile: Top 14%
Radiopharmaceutical Chemistry and Applications
1.36
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