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Development and Validation of HPTLC and RP-HPLC Methods for the Estimation of Berberine in Coscinium Fenestratum Extract and its Formulation

机译:HPTLC和RP-HPLC方法在F药提取物中黄连素含量估算及其配方中的开发与验证

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ABSTRACT Two simple, sensitive and precise HPTLC and RP-HPLC methods were developed for the estimation of berberine from Coscinium fenestratum, and its formulation. For the determination of berberine by HPTLC method, precoated silicagel 60F254 on aluminium sheets and a mobile phase system comprising of n-butanol: glacial acetic acid : water (8:1:1 % v/v/v ) was selected. After development the plate was scanned and quantified at 350 nm. Linearity was found in the concentration range of 10 to 50 ng/spot (r=0.9992). Limit of detection was found to be 5 ng/spot and limit of quantification was found to be 10 ng/spot. In RP-HPLC method, separation was achieved on a Phenomenex, Luna, C18 column (150 x 4.6mm internal diameter, 5µ particle size) using a mobile phase consisting of potassium dihydrogen phosphate (pH - 2.5) (A)  : acetonitrile (B), where B was run in gradient programme (20% for 0.01-20min, 50% for 20-25min, 50% for 25-26min, 20% for 26-30min), at a flow rate of 1ml/min and the elute was monitored at 220nm. The calibration curve was obtained in the range of 100 - 500 µg/mL. The slope, intercept and correlation coefficient values were found to be 57588, 6041and 0.9959, respectively. The method was validated in compliance with ICH guidelines. Low relative standard deviation and good % recovery values of both the methods showed that the developed methods were highly precise, accurate and can be employed for the routine analysis of formulations containing berberine. Keywords: Coscinium fenestratum, Berberine, HPTLC, RP-HPLC, Frok capsules, Validation.
机译:摘要开发了两种简单,灵敏和精确的HPTLC和RP-HPLC方法,用于从齿s骨中估计小ber碱及其配方。为了通过HPTLC方法测定小ber碱,选择了铝板上的预涂硅胶60F254和包含正丁醇:冰醋酸:水(8:1:1%v / v / v)的流动相系统。显影后,将板扫描并在350nm下定量。发现线性范围为10至50 ng / spot(r = 0.9992)。发现检测限为5 ng /点,定量限为10 ng /点。在RP-HPLC方法中,使用由磷酸二氢钾(pH-2.5)组成的流动相在Phenomenex,Luna,C18色谱柱(150 x 4.6mm内径,5μ粒径)上进行分离(A):乙腈(B ),其中B以1ml / min的流速和洗脱液以梯度程序(20%进行0.01-20min,50%进行20-25min,50%进行25-26min,20%进行26-30min)运行在220nm处被监测。获得的校准曲线范围为100-500 µg / mL。斜率,截距和相关系数值分别为57588、6041和0.9959。该方法已按照ICH指南进行了验证。两种方法的相对标准偏差低,回收率%良好,表明所开发的方法非常准确,准确,可用于含有小containing碱的配方的常规分析。关键字:茴香s,小Ber碱,HPTLC,RP-HPLC,Frok胶囊,验证。

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