A'Keen Camry Vonyae', Mroz Jakub, Joseph Simon Kunta, Baquero Jairo, Cantorias Melchor V, Carberry Patrick
Department of Radiology, New York University Grossman School of Medicine, 660 First Avenue, Room 240, New York, NY 10016, USA.
Pharmaceuticals (Basel). 2023 Nov 17;16(11):1623. doi: 10.3390/ph16111623.
A novel gas chromatography method was developed using automatic injections to identify and quantify the amount of residual solvents or analytes in samples of fluorine-18 and carbon-11 radiopharmaceuticals. This approach evaluates seven analytes in less than 5 versus 13 min of acquisition time. The method additionally includes a 3 min bakeout to aid in the removal and carry-over of higher-boiling impurities. Chromatographic parameters such as column temperature, hold time, column pressure, flow rate, and split ratios were adjusted and optimized to analyze radioactive drug samples containing analytes which include methanol, ethanol, acetone, acetonitrile, triethylamine, ,-dimethylformamide, and dimethyl sulfoxide. The relative standard deviation for each solvent was determined to be no greater than 1.6%. The method limit of detection (LOD) and limit of quantification (LOQ) were between 0.053 and 0.163 and 0.000 (5.791 × 10) and 0.520 mg/mL, respectively. This GC technique, using flame ionization detection (FID), was validated and is currently employed for the routine quality control of all approved IND and RDRC PET radiopharmaceuticals at our center.
开发了一种新型气相色谱法,采用自动进样来鉴定和定量氟 - 18和碳 - 11放射性药物样品中的残留溶剂或分析物含量。该方法在不到5分钟的采集时间内评估七种分析物,而之前的方法需要13分钟。该方法还包括3分钟的烘烤步骤,以帮助去除和减少高沸点杂质的残留。调整并优化了诸如柱温、保留时间、柱压、流速和分流比等色谱参数,以分析含有甲醇、乙醇、丙酮、乙腈、三乙胺、N,N - 二甲基甲酰胺和二甲基亚砜等分析物的放射性药物样品。每种溶剂的相对标准偏差确定不大于1.6%。方法的检测限(LOD)和定量限(LOQ)分别在0.053至0.163以及0.000(5.791×10)至0.520 mg/mL之间。这种使用火焰离子化检测(FID)的气相色谱技术已经过验证,目前用于我们中心所有获批的研究性新药(IND)和放射性药物研究中心(RDRC)正电子发射断层显像(PET)放射性药物的常规质量控制。