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HPLC法测定阿维菌素缓释注射液中阿维菌素B_1的含量

Determination of avermectin B_1 in avermectin sustained-release injection by HPLC
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摘要 目的:建立阿维菌素(AVM)缓释注射液中阿维菌素B1(AVM B1)的高效液相含量测定方法.方法:采用HPLC方法测定自制的AVM缓释注射液中AVM B1的含量.色谱柱:Hypersil-C18(200 mm×4.6 mm,5 μm),流动相为甲醇-水(85∶15),流速1 ml/min,检测波长245 nm.结果:AVM B1在0.695 8~6.957 5 μg(r=0.999 2)范围内线性关系良好,平均回收率为99.10%(RSD=0.89%),日内及日间精密度RSD分别为0.59%、0.67%.结论: HPLC法操作简单、快速、准确,可用于阿维菌素缓释注射液中AVM B1含量的测定. Objective: To establish a HPLC method for the determination of Avermectin B1 in Avermectin sustained-release injection which was made by ourself. Methods: SHIMADZU VP-ODS(200 mm×4. 6 mm, 5μm) column was used. The mobile phase consisted of methanol-water(85:15,v/v). The flow rate was 1 ml/min. Detection wavelengths was set at 245 nm. Results:The linear range of AVM B1 was 0. 6958-6. 957 5μg (r=0. 999 2). The average recovery was 99.10%(RSD=0.89%). Conclusion: This method is simple, rapid and accurate, and can be used for the determination of Avermectin B1 in Avermectin sustained-release injection.
作者 王萍 陈坚
出处 《新疆医科大学学报》 CAS 2005年第8期783-784,共2页 Journal of Xinjiang Medical University
基金 新疆维吾尔自治区科学研究与技术开发计划项目(No.990101006)
关键词 可维菌素 缓释 注射液 HPLC法 avermectin sustained-release injection HPLC
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  • 1Gogolewski RP, Rugg D, Allerton GR, et al. Demonstration of the sustained anthelmintic activity of a controlled-release capsule formulation of ivermectin in ewes under field conditions in New Zealand[J] . NZ Vet J,1997,45:163-166.
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