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那西肽预混剂组分HPLC检测方法的建立 被引量:3

The Establishment of The HPLC Method to Determine Component in Nosiheptide Premix
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摘要 为了建立那西肽预混剂组分测定的高效液相检查法,采用十八烷基键合硅胶为填充剂,以0.025%磷酸水溶液-乙腈(50:50)为流动相,检测波长为241 nm,并以该色谱条件对来自7个厂家的14批不同规格的那西肽预混剂进行了测定。综合结果给出组分的建议限度为:那西肽组分A的峰面积不得少于那西肽组分A与组分B峰面积之和的88.0%。该方法具有专属性强、耐用性好、操作简便等优点。 The HPLC method of component determination for Nosiheptide premix was established. The operation conditions were performed on C18 column with a mobile phase of 0. 025% phosphoric acid solution -acetonitrile (50:50). The detection wavelength was 241 nm. According to this method, the component of 14 batches of Nosiheptide premix from 7 manufacturers was determined. Based on the results, a proposed limitation of the component was given: the peak area of Nosiheptide component A can not less than 88.0% of the total peak area of component A and B. This method has special property, good durability and simple operation.
出处 《中国兽药杂志》 北大核心 2015年第10期27-31,共5页 Chinese Journal of Veterinary Drug
关键词 那西肽预混剂 组分 高效液相色谱法 Nosiheptide premix component HPLC method
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