LC Evaluation of In Vitro Release of AZT from Microemulsions

被引:8
作者
Carvalho, Flavia Chiva [1 ]
Barbi, Mariana da Silva [1 ]
Daflon Gremiao, Maria Palmira [1 ]
机构
[1] Sao Paulo State Univ, UNESP, Coll Pharmaceut Sci, Araraquara, Brazil
关键词
Column liquid chromatography; In vitro drug release; Drug delivery system; Zidovudine; PERFORMANCE LIQUID-CHROMATOGRAPHY; HUMAN PLASMA; ZIDOVUDINE GLUCURONIDE; 3'-AZIDO-3'-DEOXYTHYMIDINE; QUANTIFICATION; METABOLITES; URINE; SERUM;
D O I
10.1365/s10337-009-1015-1
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
A reversed phase LC method was developed and validated to analyze the in vitro release of AZT from microemulsions. A mobile phase of acetonitrile:water (15:85) was used. The method validation showed good selectivity and linearity (r = 0.9993) for sample concentrations ranging from 0.6 to 100.0 mu g mL(-1). The RSD values (0.7-4.3%) and percentage recovery (88.1-109.8%) were within acceptable limits. The limit of detection (LOD) and limit of quantitation (LOQ) were found to be 0.012 and 0.041 mu g mL(-1). Quantitative analysis of the values obtained in the drug release assay indicates that the microemulsions used promote sustained release of AZT, which follows a Fickian diffusion mechanism.
引用
收藏
页码:207 / 211
页数:5
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