A generic static headspace gas chromatography method for determination of residual solvents in drug substance

被引:67
作者
Cheng, Chang [2 ]
Liu, Shaorong [2 ]
Mueller, Bradford J. [1 ]
Yan, Zimeng [1 ]
机构
[1] AstraZeneca Pharmaceut LP, Analyt Dev, Wilmington, DE 19850 USA
[2] Univ Oklahoma, Dept Chem & Biochem, Norman, OK 73019 USA
关键词
Headspace gas chromatography; Residual solvents; Drug substance; Method validation; PHARMACEUTICALS; PRODUCTS;
D O I
10.1016/j.chroma.2010.08.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In order to increase productivity of drug analysis in the pharmaceutical industry, an efficient and sensitive generic static headspace gas chromatography (HSGC) method was successfully developed and validated for the determination of 44 classes 2 and 3 solvents of International Conference of Harmonization (ICH) guideline Q3C, as residual solvents in drug substance. In order to increase the method sensitivity and efficiency in sample equilibration, dimethylsulfoxide(DMSO)was selected as the sample diluent based on its high capacity of dissolving drug substance, stability and high boiling point. The HS sample equilibration temperature and equilibration time are assessed in ranges of 125-150 degrees C and 8-15 min, respectively. The results indicate that the residual solvents in 200 mg of drug substance can be equilibrated efficiently in HS sampler at 140 degrees C for 10 min. The GC parameters, e.g. sample split ratio, carrier flow rate and oven temperature gradient are manipulated to enhance the method sensitivity and separation efficiency. The two-stage gradient GC run from 35 to 240 degrees C, using an Agilent DB-624 capillary column (30m long, 0.32 mm I.D., 1.8 mu m film thickness), is suitable to determine 44ICH classes 2 and 3 solvents in 30 min. The method validation results indicate that the method is accurate, precise, linear and sensitive for solvents assessed. The recoveries of most of these solvents from four drug substances are greater than 80% within the method determination ranges. However, this method is not suitable for the 10 remaining ICH classes 2 and 3 solvents, because they are too polar (e.g. formic acid and acidic acid), or have boiling points higher than 150 degrees C, (e.g. anisol and cumene). In comparison with the previous published methods, this method has a much shorter sample equilibration time, a better separation for many solvents, a higher sensitivity and a broader concentration range. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:6413 / 6421
页数:9
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