中华核医学杂志
中華覈醫學雜誌
중화핵의학잡지
CHINESE JOURNAL OF NUCLEAR MEDICINE
2011年
4期
259-262
,共4页
刘红霞%章英剑%张勇平%谢集照%徐俊彦%姚之丰%赵庆
劉紅霞%章英劍%張勇平%謝集照%徐俊彥%姚之豐%趙慶
류홍하%장영검%장용평%사집조%서준언%요지봉%조경
乙酸盐类%氟放射性同位素%化学合成
乙痠鹽類%氟放射性同位素%化學閤成
을산염류%불방사성동위소%화학합성
Acetates%Fluorine radioisotopes%Chemical synthesis
目的 探讨18F-氟乙酸盐(FAC)及其前体化合物2-甲磺酸基乙酸乙酯(EOMG)的合成和进行质量分析.方法 改进前体化合物EOMG的合成方法,利用HPLC法测定该前体化合物的化学纯度,并通过各种光谱学手段对其结构进行鉴定.以EOMG为前体,用Explora GN模块合成18F-FAC,再用ExploraLC除去其中的化学杂质,HPLC法和放射性薄层色谱(TLC)法检测其放化纯、化学纯度和比活度.结果 合成并鉴定了前体化合物EOMG,产率为70%,化学纯度为97.0%(按色谱峰面积计算).合成了18F-FAC,放化纯>98%,且无明显的化学杂质,比活度为236.5 MBq/μmol.结论 该研究为制备有效、质量可控的18F-FAC提供了依据.
目的 探討18F-氟乙痠鹽(FAC)及其前體化閤物2-甲磺痠基乙痠乙酯(EOMG)的閤成和進行質量分析.方法 改進前體化閤物EOMG的閤成方法,利用HPLC法測定該前體化閤物的化學純度,併通過各種光譜學手段對其結構進行鑒定.以EOMG為前體,用Explora GN模塊閤成18F-FAC,再用ExploraLC除去其中的化學雜質,HPLC法和放射性薄層色譜(TLC)法檢測其放化純、化學純度和比活度.結果 閤成併鑒定瞭前體化閤物EOMG,產率為70%,化學純度為97.0%(按色譜峰麵積計算).閤成瞭18F-FAC,放化純>98%,且無明顯的化學雜質,比活度為236.5 MBq/μmol.結論 該研究為製備有效、質量可控的18F-FAC提供瞭依據.
목적 탐토18F-불을산염(FAC)급기전체화합물2-갑광산기을산을지(EOMG)적합성화진행질량분석.방법 개진전체화합물EOMG적합성방법,이용HPLC법측정해전체화합물적화학순도,병통과각충광보학수단대기결구진행감정.이EOMG위전체,용Explora GN모괴합성18F-FAC,재용ExploraLC제거기중적화학잡질,HPLC법화방사성박층색보(TLC)법검측기방화순、화학순도화비활도.결과 합성병감정료전체화합물EOMG,산솔위70%,화학순도위97.0%(안색보봉면적계산).합성료18F-FAC,방화순>98%,차무명현적화학잡질,비활도위236.5 MBq/μmol.결론 해연구위제비유효、질량가공적18F-FAC제공료의거.
Objective To synthesize and analyze sodium 18F-fluoroacetate (FAC) and its precursor ethyl O-mesylglycolate (EOMG). Methods EOMG was synthesized using modified method. Its chemical purity was checked by HPLC and its structure was elucidated on the basis of spectral analyses. Final product of 18F-FAC was synthesized based on general nucleophilic reactions module Explora GN using EOMG as a precursor. Liquid chromatography Explora LC was applied to get rid of its chemical impurities.Then HPLC and radio-thin layer chromatography were used to assay its radiochemical purity, chemical purity and specific activity. Results EOMG was synthesized and identified. Its yield was 70% and its chemical purity was 97.0% (calculated by chromatographic peak area). The radiochemical purity of 18F-FAC was more than 98%, and its specific activity was 236. 5 MBq/μmol. Conclusion This synthetic method for 18F-FAC and its precursor can be defined as effective and highly quality-controlled.