Alternative strategies for the synthesis of [11C]ER176 for PET imaging of neuroinflammation

[11C]ER176 is a next generation PET radioligand for imaging 18 kDa translocator protein, a biomarker for neuroinflammation. The goal of this work was to investigate alternative strategies for the radiochemical synthesis, purification, and formulation of [11C]ER176. An optimized tri-solvent high-perf...

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Veröffentlicht in:Applied radiation and isotopes 2021-12, Vol.178, p.109954-109954, Article 109954
Hauptverfasser: Mixdorf, Jason C., Murali, Dhanabalan, Xin, Yangchun, DiFilippo, Alexandra H., Aluicio-Sarduy, Eduardo, Barnhart, Todd E., Engle, Jonathan W., Ellison, Paul A., Christian, Bradley T.
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Sprache:eng
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Zusammenfassung:[11C]ER176 is a next generation PET radioligand for imaging 18 kDa translocator protein, a biomarker for neuroinflammation. The goal of this work was to investigate alternative strategies for the radiochemical synthesis, purification, and formulation of [11C]ER176. An optimized tri-solvent high-performance liquid chromatography (HPLC) protocol is described to separate the hydro-de-chlorinated byproduct from [11C]ER176. A newly implemented solid phase extraction work-up efficiently removed HPLC solvent while maintaining chemical purity and overall radiochemical yield and purity. This new HPLC purification and final formulation was completed within 40 min, providing 2.7 ± 0.5 GBq of [11C]ER176 at end of synthesis with 1400 ± 300 GBq/μmol molar activity while meeting all specifications for radiopharmaceutical quality control tests for human research use. •New ternary isocratic semi-preparative HPLC providing improved resolution of [11C]ER176 from non-radioactive impurity.•Identification of non-radioactive impurity that elutes proximal to [11C]ER176 and preliminary mechanistic investigation of its formation.•Purification of [11C]ER176 utilizing solid-phase extraction (SPE) for removal of semi-preparatory HPLC mobile phase.•Production of [11C]ER176 within 40 min, providing 2.7 ± 0.5 GBq at end of synthesis with 1400 ± 300 GBq/μmol molar activity.
ISSN:0969-8043
1872-9800
DOI:10.1016/j.apradiso.2021.109954