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Validation and statistical analysis of two high performance liquid chromatography methods for the determination of indinavir sulfate raw material and capsules

机译:两种高效液相色谱法测定硫酸茚地那韦原料药和胶囊剂的验证和统计分析

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Two high performance liquid chromatography (HPLC) methods for the quantitative determination of indinavir sulfate were tested, validated and statistically compared. Assays were carried out using as mobile phases mixtures of dibutylammonium phosphate buffer pH 6.5 and acetonitrile (55:45) at 1 mL/min or citrate buffer pH 5 and acetonitrile (60:40) at 1 mL/min, an octylsilane column (RP-8) and a UV spectrophotometric detector at 260 nm. Both methods showed good sensitivity, linearity, precision and accuracy. The statistical analysis using the t-student test for the determination of indinavir sulfate raw material and capsules indicated no statistically significant difference between the two methods.
机译:测试,验证和统计比较了两种用于定量测定茚地那韦硫酸盐的高效液相色谱(HPLC)方法。使用辛基硅烷柱(RP -8)和260 nm的紫外分光光度检测器。两种方法均显示出良好的灵敏度,线性,精度和准确性。使用t型学生检验确定硫酸茚地那韦原料药和胶囊的统计分析表明,两种方法之间没有统计学上的显着差异。

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