北方药学
北方藥學
북방약학
JOURNAL OF NORTH PHARMACY
2015年
1期
19-19,20
,共2页
赛那%金蓉%顾艳丽%贾颖
賽那%金蓉%顧豔麗%賈穎
새나%금용%고염려%가영
紫外分光光度法%阿替洛尔缓释微囊%含量测定
紫外分光光度法%阿替洛爾緩釋微囊%含量測定
자외분광광도법%아체락이완석미낭%함량측정
UV spectrophotometry%Atenolol sustained-release microcapsules%Determination of content
目的:建立以紫外分光光度法测定阿替洛尔缓释微囊含量的方法。方法:将阿替洛尔缓释微囊研磨破碎,转移至容量瓶中,稀释后,在224nm处进行含量测定。结果:阿替洛尔在224nm处有最大吸收,辅料对测定无干扰。标准曲线方程:A=0.0355C+0.0014,线性范围为2.5~20.0μg·ml-1。回收率98.81%~99.36%,精密度和稳定性RSD均在2%以内,符合《中国药典》的要求。
目的:建立以紫外分光光度法測定阿替洛爾緩釋微囊含量的方法。方法:將阿替洛爾緩釋微囊研磨破碎,轉移至容量瓶中,稀釋後,在224nm處進行含量測定。結果:阿替洛爾在224nm處有最大吸收,輔料對測定無榦擾。標準麯線方程:A=0.0355C+0.0014,線性範圍為2.5~20.0μg·ml-1。迴收率98.81%~99.36%,精密度和穩定性RSD均在2%以內,符閤《中國藥典》的要求。
목적:건립이자외분광광도법측정아체락이완석미낭함량적방법。방법:장아체락이완석미낭연마파쇄,전이지용량병중,희석후,재224nm처진행함량측정。결과:아체락이재224nm처유최대흡수,보료대측정무간우。표준곡선방정:A=0.0355C+0.0014,선성범위위2.5~20.0μg·ml-1。회수솔98.81%~99.36%,정밀도화은정성RSD균재2%이내,부합《중국약전》적요구。
Objective: to establish a method for determination of atenolol sustained-release microcapsules content by ultraviolet spectrophotometry. Methods:to grind the atenolol sustained-release microcapsules, transferred to a volumetric flask, determining content at 224nm. Results: the atenolol has maximum absorption at 224nm, excipients do not interfere with the determination. standard curve equation: A=0.0355C+0.0014, linear range is 2.5~20.0μg·ml-1. The rate of recovery is 98.81%~99.36%, the precision and stability of RSD are within 2%.