Preclinical evaluation of Manganese-52 labelled cyclodextrin: a prostaglandin E2 affine imaging probe

Prostaglandin E2 (PGE2) is implicated in several tumor-related biological processes, making it a promising biomarker for molecular imaging. In nuclear medicine, radiolabelled cyclodextrins have emerged as potential probes to target PGE2 in various cancer types. Hereafter, we aimed to specify the pharmacokinetics of a novel Manganese-52-labelled randomly methylated β-cyclodextrin ([<sup>52</sup>Mn]Mn-DOTAGA-RAMEB) by performing multiple time-point positron emission tomography and ex vivo biodistribution studies in PGE2 positive BxPC-3 pancreatic adenocarcinoma xenografts. In line with the ex vivo findings, [<sup>52</sup>Mn]Mn-DOTAGA-RAMEB showed early and specific tumor uptake (30 and 60 min after injection), followed by rapid wash-out and renal clearance. Our experimental data demonstrate the feasibility of <sup>52</sup>Mn-labelled RAMEB cyclodextrin to identify PGE2 expressing tumors, although further pharmacokinetic optimization is required to enhance tumor retention and fully exploit its diagnostic potential.

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Publication Details

Journal
European Journal of Pharmaceutical Sciences
Published
2025-10-21
DOI
https://doi.org/10.1016/j.ejps.2025.107344
Primary Topic
Radiopharmaceutical Chemistry and Applications
Type
article
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article

Preclinical evaluation of Manganese-52 labelled cyclodextrin: a prostaglandin E2 affine imaging probe

István Jószai, István Hajdu, Gábor Opposits, Zita Képes et al.
European Journal of Pharmaceutical Sciences
Radiopharmaceutical Chemistry and Applications
article

Preclinical evaluation of Manganese-52 labelled cyclodextrin: a prostaglandin E2 affine imaging probe

István Jószai, István Hajdu, Gábor Opposits, Zita Képes, Miklós Emri, Ferenc Fenyvesi, Dezső Szikra, István Kertész, Anikó Fekete, György Trencsényi, Judit P. Szabó, András Berzi, Renáta Adél Dienes, Lili Anna Komor
article en

Abstract

Prostaglandin E2 (PGE2) is implicated in several tumor-related biological processes, making it a promising biomarker for molecular imaging. In nuclear medicine, radiolabelled cyclodextrins have emerged as potential probes to target PGE2 in various cancer types. Hereafter, we aimed to specify the pharmacokinetics of a novel Manganese-52-labelled randomly methylated β-cyclodextrin ([<sup>52</sup>Mn]Mn-DOTAGA-RAMEB) by performing multiple time-point positron emission tomography and ex vivo biodistribution studies in PGE2 positive BxPC-3 pancreatic adenocarcinoma xenografts. In line with the ex vivo findings, [<sup>52</sup>Mn]Mn-DOTAGA-RAMEB showed early and specific tumor uptake (30 and 60 min after injection), followed by rapid wash-out and renal clearance. Our experimental data demonstrate the feasibility of <sup>52</sup>Mn-labelled RAMEB cyclodextrin to identify PGE2 expressing tumors, although further pharmacokinetic optimization is required to enhance tumor retention and fully exploit its diagnostic potential.

European Journal of Pharmaceutical SciencesVol. 215
University of Debrecen (HU)
Openalex Percentile: Top 56%
Radiopharmaceutical Chemistry and Applications
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