Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, China.
School of Food Science and Biotechnology, Zhejiang Gongshang University, Xuezheng Street No. 18, Hangzhou 310018, China.
J Pharm Biomed Anal. 2018 Sep 5;158:262-268. doi: 10.1016/j.jpba.2018.06.002. Epub 2018 Jun 4.
Reported here is a simple and rapid static headspace gas chromatography (SHS-GC) method for the determination of trace solvents including ethanol, isopropanol, n-butanol, 1,4-dioxane, tetrahydrofuran, acetonitrile, methanol and acetone which commonly used in drug production process. Natural deep eutectic solvents (NADESs) are firstly used as the matrix medium for this method, which provided high sensitivity for residual solvents detection. With the optimized method, validation experiments were performed and the data showed excellent linearity for all the solvents (R ≥ 0.999, n = 7). The limits of detection (LOD) for ethanol, isopropanol, n-butanol, 1,4-dioxane, tetrahydrofuran, acetonitrile, methanol and acetone are 0.09, 0.08, 0.07, 0.11, 0.06, 0.10, 0.12 and 0.08 μg g, respectively. Accuracy was checked by a recovery experiment at three different levels, and the recoveries of the tested solvents were ranged from 94.3% to 105.4%. The relative standard deviation (RSD) of each solvent for intra- and inter-day precision is in the range of 0.85 to 3.65 and 1.51 to 4.53, respectively. The developed approach can be readily used for determination of the residual solvents in six active pharmaceutical ingredients including pramipexole dihydrochloride, rivaroxaban, lisinopril, ramipril, imatinib mesylate and sitagliptin.
本文报道了一种简单快速的静态顶空气相色谱(SHS-GC)法,用于测定药物生产过程中常用的痕量溶剂,包括乙醇、异丙醇、正丁醇、1,4-二恶烷、四氢呋喃、乙腈、甲醇和丙酮。该方法首次将天然深共晶溶剂(NADESs)用作基质介质,为残留溶剂检测提供了高灵敏度。采用优化后的方法进行验证实验,结果表明所有溶剂均具有良好的线性(R≥0.999,n=7)。乙醇、异丙醇、正丁醇、1,4-二恶烷、四氢呋喃、乙腈、甲醇和丙酮的检测限(LOD)分别为 0.09、0.08、0.07、0.11、0.06、0.10、0.12 和 0.08μg g。通过在三个不同水平进行回收实验来检查准确性,测试溶剂的回收率在 94.3%至 105.4%之间。各溶剂的日内和日间精密度的相对标准偏差(RSD)分别在 0.85%至 3.65%和 1.51%至 4.53%之间。该方法可用于测定六种活性药物成分中残留溶剂,包括盐酸普拉克索、利伐沙班、赖诺普利、雷米普利、甲磺酸伊马替尼和西他列汀。