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作 者:宋更申[1] 杜旭召[2] 庞文哲[1] 姜建国[1] 闫凯[1]
机构地区:[1]河北省药品检验所,石家庄市050011 [2]石药集团中奇制药技术(石家庄)有限公司,石家庄市050051
出 处:《中国药房》2010年第45期4296-4297,共2页China Pharmacy
摘 要:目的:建立顶空气相色谱法测定药用辅料羧甲基淀粉钠中乙醇、异丙醇残留量的方法。方法:采用顶空气相色谱法,以水为溶解介质,色谱柱为DB-1301石英毛细管柱,柱温80℃,检测器为氢火焰离子化检测器,检测器温度为250℃,进样口温度为150℃。结果:乙醇、异丙醇的检测浓度的线性范围分别为0.025~2.0mg·mL-1(r=0.9999)和0.025~2.0mg·mL-1(r=0.9999);平均回收率分别为99.5%(RSD=0.9%)和99.2%(RSD=1.2%);定量限分别为4.85、2.95μg·mL-1;3批样品中乙醇和异丙醇残留量均符合《中国药典》要求。结论:本方法简单、准确、灵敏度高、重复性好,可用于羧甲基淀粉钠中有机溶剂残留量的测定。OBJECTIVE: To establish the headspace capillary GC method for the content determination of residual organic solvents (alcohol and isopropyl alcohol) in pharmaceutical excipients carbonyl methyl starch. METHODS: The residual organic solvents were separated on DB-1301 capillary column by headspace GC. The samples were dissolved in water. FID detector was adopted and the column temperature was 80 %. The detector temperature was 250 %. The inlet temperature was 150 %. RESULTS: The linear ranges of alcohol and isopropyl alcohol were 0.025-2.0 mg·mL^-1 (r=0.999 9) and 0.025-2.0 mg·mL^-1 (r=0.999 9), respectively; the average recoveries were 99.5% (RSD=0.9%) and 99.2% (RSD= 1.2%); the determination limits were 4.85 μg· mL^-1 and 2.95 μg·mL^-1. 2 kinds of residual organic solvents in 3 batches of samples were all up to the standard stated in Chinese Pharmacopeia. CONCLUSION: The method is simple, accurate, sensitive and reproducible, and it can be used for the content determination of the residual organic solvents in carbonyl methyl starch.
关 键 词:羧甲基淀粉钠 顶空毛细管气相色谱法 溶剂 残留量
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