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Detection of 9α-OH-AD prepared by biotransformation

机译:检测通过生物转化制备的9α-OH-AD

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Detection of 9α-OH-AD prepared by biotransformation by RP-HPLC directly was studied. The detection is performed on a Kromasil 100-5C18 (4.6×250 mm) column, using methanol: water (7:3, v/v) as mobile phase, 0.8 mL·min~(-1) flow rate and external standard method, detected at 242 nm. There is a good line correlation between peak area and content in range of 0.01-0.20 g/L, the correlation coefficient is 0.9942, the average recovery is 99.09% with a relative stand deviation of 0.89% (n=5). The method is simple, stable, accurate and reliable for quality control of 9α-OH-AD.
机译:研究了通过RP-HPLC通过RP-HPLC进行的9α-OH-AD直接进行。 使用甲醇:水(7:3,v / v)作为流动相,0.8ml·min〜(-1)流量和外标方法对检测进行检测。流速和外标方法 ,在242 nm处检测到。 峰面积与0.01-0.20g / L范围内的良好的线相关性,相关系数为0.9942,平均回收率为99.09%,相对支架偏差为0.89%(n = 5)。 该方法简单,稳定,准确可靠,对9α-OH-AD的质量控制。

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