Karsten Bamminger, Lukas Nics, Marcus Hacker, Cécile Philippe, Marius Ozenil
{"title":"[11C]醋酸酯和[11C]醋酸酯的明确分析分离及改进合成。","authors":"Karsten Bamminger, Lukas Nics, Marcus Hacker, Cécile Philippe, Marius Ozenil","doi":"10.1186/s41181-025-00412-0","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>[<sup>11</sup>C]Acetate and [<sup>11</sup>C]acetoacetate are PET radiotracers widely used to assess oxidative metabolism and ketone body utilization, respectively. This study aimed to establish robust, high-yield syntheses of both tracers using a GE TRACERlab FX2 C module, with an emphasis on improving radiochemical purity (RCP), radiochemical yield (RCY), optimizing operational parameters, and developing accurate quality control methods. [<sup>11</sup>C]Acetate was synthesized via Grignard carboxylation using [<sup>11</sup>C]CO<sub>2</sub> and purified with a cartridge-based system. [<sup>11</sup>C]Acetoacetate was produced via in-loop [<sup>11</sup>C]CO<sub>2</sub> carboxylation of a lithium enolate precursor, followed by semi-preparative reversed-phase HPLC purification. Quality control was performed by reported ion-exchange chromatography (IEX-HPLC) and novel reversed-phase HPLC (RP-HPLC). A systematic literature review was conducted to evaluate prior quality control methods for [<sup>11</sup>C]acetoacetate.</p><h3>Results</h3><p>Omission of helium flow during [<sup>11</sup>C]CO<sub>2</sub> trap bake-out significantly improved activity recovery from the [<sup>11</sup>C]CO<sub>2</sub> trap (from 63 to 89%) and reduced release time (from 4.8 to 3.1 min). [<sup>11</sup>C]Acetate and [<sup>11</sup>C]acetoacetate were synthesized with mean isolated activities of 30.2 GBq and 3.24 GBq and mean RCPs of 96.9% and 97.1%, respectively. The final formulations met all European Pharmacopoeia criteria. While the widely-used IEX-HPLC method failed to differentiate [<sup>11</sup>C]acetate from [<sup>11</sup>C]acetoacetate, the newly-developed RP-HPLC method enabled unambiguous separation. Literature analysis revealed that most published studies on [<sup>11</sup>C]acetoacetate likely overlooked [<sup>11</sup>C]acetate as a radiochemical impurity due to insufficient analytical separation.</p><h3>Conclusions</h3><p>Reliable synthesis protocols for [<sup>11</sup>C]acetate and [<sup>11</sup>C]acetoacetate were established on the GE TRACERlab FX2 C, with significant improvements in [<sup>11</sup>C]CO<sub>2</sub> handling and product purification. Inclusion of the proposed RP-HPLC method enables a more accurate and specific assessment of RCP compared to IEX-HPLC alone and should be considered for a valid quality control of [<sup>11</sup>C]acetoacetate.</p></div>","PeriodicalId":534,"journal":{"name":"EJNMMI Radiopharmacy and Chemistry","volume":"11 1","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1186/s41181-025-00412-0.pdf","citationCount":"0","resultStr":"{\"title\":\"Unambiguous analytical separation and improved syntheses of [11C]acetate and [11C]acetoacetate\",\"authors\":\"Karsten Bamminger, Lukas Nics, Marcus Hacker, Cécile Philippe, Marius Ozenil\",\"doi\":\"10.1186/s41181-025-00412-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>[<sup>11</sup>C]Acetate and [<sup>11</sup>C]acetoacetate are PET radiotracers widely used to assess oxidative metabolism and ketone body utilization, respectively. This study aimed to establish robust, high-yield syntheses of both tracers using a GE TRACERlab FX2 C module, with an emphasis on improving radiochemical purity (RCP), radiochemical yield (RCY), optimizing operational parameters, and developing accurate quality control methods. [<sup>11</sup>C]Acetate was synthesized via Grignard carboxylation using [<sup>11</sup>C]CO<sub>2</sub> and purified with a cartridge-based system. [<sup>11</sup>C]Acetoacetate was produced via in-loop [<sup>11</sup>C]CO<sub>2</sub> carboxylation of a lithium enolate precursor, followed by semi-preparative reversed-phase HPLC purification. Quality control was performed by reported ion-exchange chromatography (IEX-HPLC) and novel reversed-phase HPLC (RP-HPLC). A systematic literature review was conducted to evaluate prior quality control methods for [<sup>11</sup>C]acetoacetate.</p><h3>Results</h3><p>Omission of helium flow during [<sup>11</sup>C]CO<sub>2</sub> trap bake-out significantly improved activity recovery from the [<sup>11</sup>C]CO<sub>2</sub> trap (from 63 to 89%) and reduced release time (from 4.8 to 3.1 min). [<sup>11</sup>C]Acetate and [<sup>11</sup>C]acetoacetate were synthesized with mean isolated activities of 30.2 GBq and 3.24 GBq and mean RCPs of 96.9% and 97.1%, respectively. The final formulations met all European Pharmacopoeia criteria. While the widely-used IEX-HPLC method failed to differentiate [<sup>11</sup>C]acetate from [<sup>11</sup>C]acetoacetate, the newly-developed RP-HPLC method enabled unambiguous separation. Literature analysis revealed that most published studies on [<sup>11</sup>C]acetoacetate likely overlooked [<sup>11</sup>C]acetate as a radiochemical impurity due to insufficient analytical separation.</p><h3>Conclusions</h3><p>Reliable synthesis protocols for [<sup>11</sup>C]acetate and [<sup>11</sup>C]acetoacetate were established on the GE TRACERlab FX2 C, with significant improvements in [<sup>11</sup>C]CO<sub>2</sub> handling and product purification. Inclusion of the proposed RP-HPLC method enables a more accurate and specific assessment of RCP compared to IEX-HPLC alone and should be considered for a valid quality control of [<sup>11</sup>C]acetoacetate.</p></div>\",\"PeriodicalId\":534,\"journal\":{\"name\":\"EJNMMI Radiopharmacy and Chemistry\",\"volume\":\"11 1\",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-12-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1186/s41181-025-00412-0.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EJNMMI Radiopharmacy and Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.1186/s41181-025-00412-0\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EJNMMI Radiopharmacy and Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1186/s41181-025-00412-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Unambiguous analytical separation and improved syntheses of [11C]acetate and [11C]acetoacetate
Background
[11C]Acetate and [11C]acetoacetate are PET radiotracers widely used to assess oxidative metabolism and ketone body utilization, respectively. This study aimed to establish robust, high-yield syntheses of both tracers using a GE TRACERlab FX2 C module, with an emphasis on improving radiochemical purity (RCP), radiochemical yield (RCY), optimizing operational parameters, and developing accurate quality control methods. [11C]Acetate was synthesized via Grignard carboxylation using [11C]CO2 and purified with a cartridge-based system. [11C]Acetoacetate was produced via in-loop [11C]CO2 carboxylation of a lithium enolate precursor, followed by semi-preparative reversed-phase HPLC purification. Quality control was performed by reported ion-exchange chromatography (IEX-HPLC) and novel reversed-phase HPLC (RP-HPLC). A systematic literature review was conducted to evaluate prior quality control methods for [11C]acetoacetate.
Results
Omission of helium flow during [11C]CO2 trap bake-out significantly improved activity recovery from the [11C]CO2 trap (from 63 to 89%) and reduced release time (from 4.8 to 3.1 min). [11C]Acetate and [11C]acetoacetate were synthesized with mean isolated activities of 30.2 GBq and 3.24 GBq and mean RCPs of 96.9% and 97.1%, respectively. The final formulations met all European Pharmacopoeia criteria. While the widely-used IEX-HPLC method failed to differentiate [11C]acetate from [11C]acetoacetate, the newly-developed RP-HPLC method enabled unambiguous separation. Literature analysis revealed that most published studies on [11C]acetoacetate likely overlooked [11C]acetate as a radiochemical impurity due to insufficient analytical separation.
Conclusions
Reliable synthesis protocols for [11C]acetate and [11C]acetoacetate were established on the GE TRACERlab FX2 C, with significant improvements in [11C]CO2 handling and product purification. Inclusion of the proposed RP-HPLC method enables a more accurate and specific assessment of RCP compared to IEX-HPLC alone and should be considered for a valid quality control of [11C]acetoacetate.