稳定性指示反相高效液相色谱法定量测定三种芒果叶提取物中的芒果苷

Y. Retnaningtyas, Nia Kristiningrum, H. D. Renggani, Indah Purnama Sary
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引用次数: 0

摘要

采用反相高效液相色谱法(RP-HPLC)对3种芒果叶(芒果香、芒果叶和芒果叶)中芒果苷的含量进行了定量测定。样品采用甲醇浸泡法提取,旋转蒸发器浓缩。固定相为purrospher RP-18端盖柱(25 cm × 4.6 mm id, 5µm),流动相为甲醇:磷酸0.1% (v/v) (31:69);流量:0.8 mL/min;溶剂甲醇,检测波长258 nm。该方法具有良好的线性度(r2=0.998)、精密度(%RSD=0.649%)、准确度(10.67%)。强迫退化研究是根据国际协调会议的准则进行的。结果表明,降解产物与芒果苷峰完全分离。除基本条件(100%)外,芒果苷的降解极限为5-20%(按ICH指南)。该方法成功地测定了芒果叶、芒果叶和芒果叶提取物中芒果苷的含量。得到的芒果苷含量分别为包皮(9.95%)、kopyor(7.40%)和kweni(芒果香)(2.49%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stability Indicating RP-HPLC for Quantification Mangiferin in Extract of Three Species Mango Leaves
The stability indication of Reversed Phase-High Performance Liquid Chromatography (RP-HPLC) method was validated for quantitative determination of mangiferin on three species mango leaves (Mangifera odorata Griff, Mangifera foetida Lour, and Mangifera indica L.). The samples were extracted by maseration method using methanol and concentrated using rotary evaporator. The method carried out on stationary phase a purospher RP-18 endcapped (25 cm × 4.6 mm i.d., 5 µm) column with a mobile phase consisting of methanol: phosphoric acid 0.1% (v/v) (31:69); flow rate:0.8 mL/min; solvent methanol, detection was carried out at 258 nm. The analytical  performace this measurement is good with the value of linearity (r2=0.998), precision (%RSD=0.649%), and accuration (10.67%). The forced degradation studies were carried out according to the International Conference on Harmonization (ICH) guidelines. The results indicating that the complete separation between degradation products and mangiferin peak occured. The degradation limit of mangiferin 5–20% (according to the guideline of ICH) except in basic condition (100%). The method was succesful applied to determine of the mangiferin in  pakel (Mangifera foetida), kweni (Mangifera indica) and kopyor (Mangifera odorata) extract. The mangiferin content was obtained are pakel (9.95%), kopyor (7.40%) and kweni (Mangifera odorata) (2.49%) respectively.
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