Li Hanlin, Sluggett Gregory W
Pfizer Global Research and Development, Eastern Point Road, MS 8118D-3041, Groton, CT 06340, USA.
J Pharm Biomed Anal. 2005 Sep 15;39(3-4):486-94. doi: 10.1016/j.jpba.2005.04.042.
A direct injection gas chromatographic method utilizing selected-ion monitoring (SIM) mode mass selective detection was developed and validated for the trace analysis of an impurity, carbonic acid chloromethyl tetrahydro-pyran-4-yl ester (CCMTHP), present in a beta-lactam active pharmaceutical ingredient (API). A variety of analytical techniques including LC-MS, GC-FID, GC-ECD and GC-MS were evaluated during the method development. GC-MS with SIM at m/z=49 demonstrated the best detection sensitivity. A 10 ppm (5 pg on column) limit of quantitation (LOQ) was attained and the linearity of the method was demonstrated in the range of 10-1000 ppm. Accurate and precise quantitation of the impurity in drug substance was achieved with external standardization. A 10:1 split injection was applied to limit the amount of non-volatile API loading onto the column. The effects of injection and detection parameters such as split ratio, liner type, injection temperature and number of mass ions monitored were studied. Full validation proved the accuracy, precision and specificity of the method, which was successfully employed to analyze many pilot lots of the API.
建立了一种利用选择离子监测(SIM)模式质量选择性检测的直接进样气相色谱法,并对其进行了验证,用于分析一种β-内酰胺类活性药物成分(API)中存在的杂质氯甲基四氢吡喃-4-基碳酸酯(CCMTHP)。在方法开发过程中评估了包括LC-MS、GC-FID、GC-ECD和GC-MS在内的多种分析技术。在m/z = 49处进行SIM的GC-MS显示出最佳的检测灵敏度。实现了10 ppm(柱上5 pg)的定量限(LOQ),并且该方法在10 - 1000 ppm范围内具有线性。通过外标法实现了原料药中杂质的准确和精确定量。采用10:1分流进样以限制非挥发性API进入色谱柱的量。研究了进样和检测参数如分流比、衬管类型、进样温度和监测的质量离子数的影响。全面验证证明了该方法的准确性、精密度和特异性,该方法已成功用于分析许多中试批次的API。