首页|15%虫螨腈·氯虫苯甲酰胺悬浮剂的超高效液相色谱分析

15%虫螨腈·氯虫苯甲酰胺悬浮剂的超高效液相色谱分析

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目的 建立测定15%虫螨腈·氯虫苯甲酰胺悬浮剂中2种有效成分含量的超高效液相色谱分析方法.方法 样品经乙腈超声提取,过滤后使用Waters ACQUITY UPLC ® BEH C18色谱柱和二极管阵列检测器,以乙腈-水(体积比60∶40)为流动相,流速0.2 mL/min,在196 nm波长下,对虫螨腈和氯虫苯甲酰胺进行分析.外标法定量.结果 方法的线性范围为20~100 mg/L,虫螨腈和氯虫苯甲酰胺线性相关系数分别为0.999 4和0.999 9.平均加标回收率分别为99.58%和99.81%,变异系数为2.92%和1.26%(n=6).虫螨腈和氯虫苯甲酰胺的定量限分别为6.71×10-3、9.23×10-3 mg/L(以信噪比为10计).结论 该方法具有简便、快速、精确度和准确度高、线性关系好的优点,是理想的分析方法.
Analysis of chlorfenapyr and chlorantraniliprole 15%SC by ultra performance liquid chromatography
Objective To establish the method to detect the chlorfenapyr and chlorantraniliprole 15%SC by ultra performance liquid chromatography(UPLC).Methods The sample was extracted by acetonitrile ultrasonically.Quantitative analysis of the active ingredient was conducted using a Waters ACQUITY UPLC ® BEH C18 chromatographic column and variable wavelength photodiode array detection(PDA).The mobile phase was acetonitrile-water(60∶40,by vol),the mobile speed was 0.2 mL/min and the detecting wavelength was 196 nm.The quantitative analysis was performed using external standard calibration curve.Results The linear range for the method was 20~100 mg/L(r2=0.999 4 and 0.999 9).The average recovery rates were 99.58%and 99.81%,respectively.The coefficient of variations were 2.92%and 1.26%(n=6).The quantitative limits of chlorfenapyr and chlorantraniliprole were 6.71×10-3and 9.23×10-3 mg/L,respectively(10S/N).Conclusion The method is an ideal analysis method with the advantages of simple,fast,high precision and good linear correlations.

UPLCchlorfenapyrchlorantraniliproleanalysis

彭凯俊、熊先贵、于洋、贾慧娴、陈阳、杨文锋、曾小虎、张亮、徐静

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成都市白蚁防治研究中心,四川 成都 610016

四川众安居有害生物防制有限公司,四川成都 610016

超高效液相色谱 虫螨腈 氯虫苯甲酰胺 分析

2024

中华卫生杀虫药械
南京军区疾病预防控制中心

中华卫生杀虫药械

CSTPCD
影响因子:0.566
ISSN:1671-2781
年,卷(期):2024.30(6)