Naveen P, Lingaraju H B, Prasad K Shyam
Analytical Research and Development, Vidya Herbs Pvt. Ltd., Bengaluru, Karnataka, India.
Phytochemistry Lab, Vidya Herbs Pvt. Ltd., Bengaluru, Karnataka, India.
Pharmacognosy Res. 2017 Apr-Jun;9(2):215-219. doi: 10.4103/0974-8490.204652.
Mangiferin, a polyphenolic xanthone glycoside from , is used as traditional medicine for the treatment of numerous diseases. The present study was aimed to develop and validate a reversed-phase high-performance liquid chromatography (RP-HPLC) method for the quantification of mangiferin from the bark extract of . RP-HPLC analysis was performed by isocratic elution with a low-pressure gradient using 0.1% formic acid: acetonitrile (87:13) as a mobile phase with a flow rate of 1.5 ml/min. The separation was done at 26°C using a Kinetex XB-C18 column as stationary phase and the detection wavelength at 256 nm. The proposed method was validated for linearity, precision, accuracy, limit of detection, limit of quantification, and robustness by the International Conference on Harmonisation guidelines. In linearity, the excellent correlation coefficient more than 0.999 indicated good fitting of the curve and also good linearity. The intra- and inter-day precision showed < 1% of relative standard deviation of peak area indicated high reliability and reproducibility of the method. The recovery values at three different levels (50%, 100%, and 150%) of spiked samples were found to be 100.47, 100.89, and 100.99, respectively, and low standard deviation value < 1% shows high accuracy of the method. In robustness, the results remain unaffected by small variation in the analytical parameters, which shows the robustness of the method. Liquid chromatography-mass spectrometry analysis confirmed the presence of mangiferin with M/Z value of 421. The assay developed by HPLC method is a simple, rapid, and reliable for the determination of mangiferin from .
The present study was intended to develop and validate an RP-HPLC method for the quantification of mangiferin from the bark extract of . The developed method was validated for linearity, precision, accuracy, limit of detection, limit of quantification and robustness by International Conference on Harmonization guidelines. This study proved that the developed assay by HPLC method is a simple, rapid and reliable for the quantification of the mangiferin from . : , RP-HPLC: Reversed-phase high-performance liquid chromatography, M/Z: Mass to charge ratio, ICH: International conference on harmonization, % RSD: Percentage of relative standard deviation, ppm: Parts per million, LOD: Limit of detection, LOQ: Limit of quantification.
芒果苷是一种来自[具体来源未给出]的多酚氧杂蒽酮糖苷,被用作治疗多种疾病的传统药物。本研究旨在开发并验证一种反相高效液相色谱(RP - HPLC)方法,用于定量测定[具体来源未给出]树皮提取物中的芒果苷。RP - HPLC分析采用等度洗脱,通过低压梯度,以0.1%甲酸:乙腈(87:13)作为流动相,流速为1.5 ml/min。分离在26°C下进行,使用Kinetex XB - C18柱作为固定相,检测波长为256 nm。所提出的方法按照国际协调会议指南对线性、精密度、准确度、检测限、定量限和稳健性进行了验证。在线性方面,大于0.999的优异相关系数表明曲线拟合良好且线性良好。日内和日间精密度显示峰面积相对标准偏差<1%,表明该方法具有高可靠性和重现性。加标样品在三个不同水平(50%、100%和150%)下的回收率分别为100.47、100.89和100.99,低标准偏差值<1%表明该方法具有高准确度。在稳健性方面,分析参数的小变化对结果没有影响,这表明该方法具有稳健性。液相色谱 - 质谱分析确认了芒果苷的存在,其质荷比(M/Z)值为421。通过HPLC方法开发的该测定法对于测定[具体来源未给出]中的芒果苷而言简单、快速且可靠。
本研究旨在开发并验证一种用于定量测定[具体来源未给出]树皮提取物中芒果苷的RP - HPLC方法。按照国际协调会议指南对所开发的方法进行了线性、精密度、准确度、检测限、定量限和稳健性的验证。本研究证明,通过HPLC方法开发的该测定法对于定量测定[具体来源未给出]中的芒果苷而言简单、快速且可靠。:[具体来源未给出],RP - HPLC:反相高效液相色谱,M/Z:质荷比,ICH:国际协调会议,%RSD:相对标准偏差百分比,ppm:百万分之一,LOD:检测限,LOQ:定量限。