三氯苯达唑中有机溶剂残留量测定方法学验证
投稿时间:2003-10-28    点此下载全文
引用本文:韩加怡,郑国钢.三氯苯达唑中有机溶剂残留量测定方法学验证[J].药学实践杂志,2003,(6):355~357
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作者单位
韩加怡 浙江省药品检验所, 浙江 杭州 310004 
郑国钢 浙江省药品检验所, 浙江 杭州 310004 
中文摘要:目的 用气相色谱法测定三氯苯达唑中有机溶剂残留量。方法 采用高效毛细管色谱柱INNOWAX(30m×0.32mm×0.25μm),检测器为FID,应用程序升温,直接进样法检测。结果 两个测定系统中乙醇、DMF、乙酸与所用内标、溶剂互不干扰,分离度及检出灵敏度均达到要求,三成分的最小检出浓度分别为2.03μg/mL、2.21μg/mL与3.75μg/mL。结论 本方法能准确控制样品中残留溶剂,控制产品的质量。
中文关键词:气相色谱法  三氯苯达唑  残留量
 
Method verify on quantity of organic solvents remaining
Abstract:OBJECTIVE To establish a GC method for the determination of organic solvents remaining. METHODS The methods was approved by high efficiency chlomatogram column of INNOWAX(30m×0.32mm×0.25μm),with a detector of FID using direct injection. RESULTS:There is no interfere of every component between ethanol,DMF,acetic acid inside standard and solven. The resolution and sensitivity were acceptable. The detection limit of the three components were 2.03μg/mL, 2.21μg/mL, 3.75μg/mL respectively. CONCLUSIONS This method is accurate to control the organic solvents remaining.
keywords:GC  quantity of organic solvents  remaining
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