TY - JOUR
T1 - Erratum
T2 - Chelating Rare-Earth Metals (Ln3+) And 225Ac3+ With The Dual-Size-Selective Macrocyclic Ligand Py2‑Macrodipa (Inorganic Chemistry (2022) 61:32 (12847-12855) DOI: 10.1021/acs.inorgchem.2c01998)
AU - Hu, Aohan
AU - Simms, Megan E.
AU - Kertesz, Vilmos
AU - Wilson, Justin J.
AU - Thiele, Nikki A.
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/11/7
Y1 - 2022/11/7
N2 - Page 12852 and 12853. In Figure 5 of the paper and Table S3 of the Supporting Information, the radiochemical yields (RCYs) from the complexation of 225Ac by DOTA at 25 °C were reported incorrectly as <5% across the entire range of chelator concentrations investigated (10−3−10−8 M). Subsequent experiments revealed that the iTLC-silica gel (iTLC-SG, Agilent) method employed to analyze the radiolabeling reactions is ineffective at separating DOTA-complexed 225Ac from uncomplexed 225Ac, regardless of whether a mobile phase of EDTA (0.05 M, pH 6) or sodium citrate (0.4 M, pH 4, with 10% MeOH) is used. Separation of the 225Ac−DOTA complex from free 225Ac can instead be achieved using aluminum-backed silica TLC plates (TLC-SG, silica gel 60, F254, Merck) in conjunction with a mobile phase of sodium citrate (0.4 M, pH 4) containing 10% MeOH. Under these conditions, the 225Ac−DOTA complex remains at the baseline (Rf = 0) and free 225Ac migrates with the solvent front (Rf = 1). Using this chromatographic separation system, the RCYs for 225Ac radiolabeling of DOTA were determined to be above 10% at chelator concentrations of 10−3 and 10−4 M. The corrected RCYs at both the 5 and 60 min reaction times are provided in the revised Figure 5 and Table S3 below. These corrections do not affect the conclusions presented in the published paper. (Table Presented).
AB - Page 12852 and 12853. In Figure 5 of the paper and Table S3 of the Supporting Information, the radiochemical yields (RCYs) from the complexation of 225Ac by DOTA at 25 °C were reported incorrectly as <5% across the entire range of chelator concentrations investigated (10−3−10−8 M). Subsequent experiments revealed that the iTLC-silica gel (iTLC-SG, Agilent) method employed to analyze the radiolabeling reactions is ineffective at separating DOTA-complexed 225Ac from uncomplexed 225Ac, regardless of whether a mobile phase of EDTA (0.05 M, pH 6) or sodium citrate (0.4 M, pH 4, with 10% MeOH) is used. Separation of the 225Ac−DOTA complex from free 225Ac can instead be achieved using aluminum-backed silica TLC plates (TLC-SG, silica gel 60, F254, Merck) in conjunction with a mobile phase of sodium citrate (0.4 M, pH 4) containing 10% MeOH. Under these conditions, the 225Ac−DOTA complex remains at the baseline (Rf = 0) and free 225Ac migrates with the solvent front (Rf = 1). Using this chromatographic separation system, the RCYs for 225Ac radiolabeling of DOTA were determined to be above 10% at chelator concentrations of 10−3 and 10−4 M. The corrected RCYs at both the 5 and 60 min reaction times are provided in the revised Figure 5 and Table S3 below. These corrections do not affect the conclusions presented in the published paper. (Table Presented).
UR - http://www.scopus.com/inward/record.url?scp=85141889720&partnerID=8YFLogxK
U2 - 10.1021/acs.inorgchem.2c03483
DO - 10.1021/acs.inorgchem.2c03483
M3 - Comment/debate
C2 - 36282271
AN - SCOPUS:85141889720
SN - 0020-1669
VL - 61
SP - 17924
EP - 17925
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 44
ER -