衍生化分光光度法快速测定卡托普利片中主药的含量  

Determination of the Main Component of Captopril Tablets by Derivative Spectrophotometry

作　　者：熊正平[1] 黄开顺[1] 朱链链[1] 陈志琼[1] 

机构地区：[1]重庆医科大学药物分析教研室,重庆市400016

出　　处：《中国药房》2010年第13期1226-1228,共3页China Pharmacy

基　　金：国家自然科学基金资助项目(30371632);重庆医科大学资助项目(XB200332)

摘　　要：目的:建立以衍生化分光光度法快速测定卡托普利片中主药含量的方法。方法:在氢氧化钠碱性条件下,采用2,4-二硝基氟苯作为衍生化试剂,与卡托普利在水浴40℃暗处反应后,以342nm为检测波长,通过紫外-可见分光光度法测定卡托普利的含量。结果:卡托普利检测浓度线性范围为1.0～14.0μg·mL-1(r=0.9999),平均回收率为99.61%,RSD=1.27%(n=9),日内、日间RSD均小于2%。结论:该方法稳定、可靠,操作简便、快速,可用于卡托普利片中主药的含量测定。OBJECTIVE： To establish derivative spectrophotometry for the determination of the main component of Captopril tablets. METHODS： Under the alkaline condition of sodium hydroxide, 2, 4-dinitrofluorobenzene was used as derivatization reagent to react with captopril at 40℃ in the water bath. Then UV spectrophotometry was adopted to detect the content of captopril with detection wavelength set at 342 urn. RESULTS： The linear range of captopril was 1.0- 14.0μg·mL^-1（r= 0.999 9） with an average recovery of 99.61% （RSD=l.27%, n=9）. The RSD of intra-day and inter-day both were less than 2%. CONCLUSION： This method is stable, reliable, rapid and simple for the determination of the main components of Captopril tablets.

关 键 词：卡托普利片 衍生化分光光度法 2 4-二硝基氟苯 含量测定 

分 类 号：R927.2[医药卫生—药学] R972.4