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出 处:《中国药房》2016年第33期4686-4688,共3页China Pharmacy
基 金:国家自然科学基金资助项目(No.21402012);国家自然科学项目子项目(No.GJZXM201605)
摘 要:目的:建立同时测定尼莫地平缓释片中乙醇和丙酮残留量的方法。方法:采用顶空气相色谱法。色谱柱为以6%氰丙基苯基-94%二甲基聚硅氧烷(DB-624)为固定液的毛细管柱,程序升温,进样口温度为230℃,检测器为氢火焰离子化检测器,检测器温度为250℃,载气为氮气,流速为2.0 ml/min,分流比为5∶1,顶空加热温度为90℃,平衡时间为20 min,顶空进样量为1.0 ml。结果:乙醇、丙酮检测质量浓度线性范围分别为1.25-500.0μg/ml(r=0.999 9)、0.50-202.0μg/ml(r=0.999 2);定量限分别为5.01、2.02μg/ml,检测限分别为1.67、0.67μg/ml;精密度、稳定性、重复性试验的RSD〈3.0%;加样回收率分别为96.81%-102.00%(RSD=1.89%,n=9)、96.64%-102.31%(RSD=1.82%,n=9)。结论:该方法简便、快速、准确,可用于同时测定尼莫地平缓释片中乙醇和丙酮的残留量。OBJECTIVE: To establish a method for the residual determination of ethanol and acetone in Nimodipine sus- tained-release tablet. METHODS: Headspace GC was on the column of capillary column with fixative solution of 6% cyanopropyl phenyl-94% dimethyl polysiloxane (DB-624) by temperature programming, injector temperature was 230 %, detector was a flame ionization detector, detector temperature was 250 %, carrier gas was nitrogen gas, flow rate was 2.0 ml/min, split ratio was 5 : 1, equilibrium temperature was 90℃ , equilibrium time was 20 min, and volume of sample was 1.0 ml. RESULTS: The linear range was 1.25-500.0 μg/ml for ethanol (r=0.999 9) and 0.50-202.0 μg/ml for acetone (r=0.999 2); limits of quantitative were 5.01, 2.02 μg/ml, limits of detection were 1.67, 0.67 μg/ml, respectively; RSDs of precision, stability and reproducibility tests were lower than 3.0% ; recoveries were 96.81% -102.00% (RSD=1.89%, n=9), 96.64% -102.31% (RSD=1.82%, n=9), respectively. CONCLUSIONS: The method is simple, rapid, accurate, and can be used for simultaneous residual determination of ethanol and acetone in Nimodipine sustained-release tablet.
关 键 词:顶空气相色谱法 尼莫地平 乙醇 丙酮 有机溶剂 残留量
分 类 号:R917[医药卫生—药物分析学]
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