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作 者:汤洁[1]
机构地区:[1]安徽医科大学第一附属医院药剂科,安徽合肥230022
出 处:《安徽医药》2007年第2期125-126,共2页Anhui Medical and Pharmaceutical Journal
摘 要:目的建立法罗培南钠片的溶出度考察方法,以有效控制药品质量。方法以水1000ml为溶出介质,转速为75r·min^-1,30min时取样,在306am波长处测其吸收度计算溶出量。结果法罗培南钠在浓度为4.27~42.66mg·L^-1吸收度与浓度呈良好线性关系,Y=0.0180X-0.O004,相关系数r=0.9999,平均加样回收率为99.8%,RSD=0.80%,3批样品的30min溶出度均在90%以上。结论方法简便、准确,结果可靠。可用于法罗培南钠片的溶出度测定。Aim To determine the dissolution of faropenem sodium tablets. Methods The dissolution was calculated according to Chinese Pharmacopeia( 2005 ) with water as the solvent. UV spectrophotometry was used, and the detection wavelength was 306 nm. Results The method showed a good linear relationship in the range of 4.27 - 42.66 mg ~ L- 1 ( r = 0. 9999 ). The average recovery was 99. 8% ,and RSD was 0.80%. The dissolutions of 3 batches of samples were all above 90%. Conclusion The method is simple, accurate, and can be used as the quality control method for determing the dissolution of faropenem sodium tablets.
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