摘要
目的建立同时测定痔康泰(ZKT)纳米粒中5种大黄蒽醌成分总量的方法。方法采用RP—HPLC法,色谱柱为Agilent Zorbax C18(250mm×4.6mm,5um)柱,流动相为甲醇-0.1%磷酸梯度洗脱,流速为1.0ml·min^-1,柱温为30℃,检测波长为254nm。结果各成分达到基线分离,峰形良好。芦荟大黄素、大黄酸、大黄素、大黄酚和大黄素甲醚的线性范围分别为8.76~87.60(r=0.9999)、7.85—78.50(r=0.9999)、7.48~74.80(r=0.9999)、8.24~82.40(r=0.9999)、5.58~55.80ug·ml^-1(r=0.9998)。平均加样回收率分别为99.76%(RSD=1.92%)、101.53%(RSD=1.73%)、98.47%(RSD:1.59%)、103.62%(RSD=1.75%)、102.94%(RSD=1.63%)。结论所建方法简便可行、重复性好,可用于评价和控制ZKT纳米粒的质量。
OBJECTIVE To establish a method for the determination of total content of five rhubarb anthraquinones in Zhi Kangtai nanoparticles. METHODS RP - HPLC was adopted. Rhubarb anthraquinones were simultaneously separated and determined with an Agilent Zorbax C18 column(250 mm ×4.6 mm,5 um)by gradient elution using methanol-0. 1% phosphoric acid solution as the mobile phase. The flow rate was 1.0 ml. min^-1 and the detective wavelength was set at 254 nm with column temperature of 30℃. RESULTS The five rhubarb anthraquinones were completely separated and were not interfered by other components. Every rhubarb anthraquinone' s linearity range, correlation coefficient and average recoveries were showed respectively as follows : linearity range of aloe - emodin:8.76 - 87.6 ug·ml^-1 ( r = 0. 9999 ), average recovery 99.76% with RSD of 1.92% ; linearity range of rhein:7.85 - 78. 5 ug. ml^-1 ( r = 0. 9999), average recovery 101.53 % with RSD of 1.73 % ; linearity range of emodin : 7.48 - 74.8ug. ml^-1 ( r = 0. 9999), average recovery 98.47 % with RSD of 1.59 % ; linearity range of chrysophanol : 8.24 - 82.4ug. ml^-1( r = 0.9999), average recovery 103.62% with RSD of 1.75% ;linearity range of physcion :5. 58 - 55.8ug. ml^-1 (r =0. 9998) ,average recovery 102.94 % with RSD of 1.63%. CONCLUSION This method is simple, feasible and reproducible. It can be used for the quality control of Zhi Kang tai nanoparticles.
出处
《华西药学杂志》
CAS
CSCD
北大核心
2009年第3期288-290,共3页
West China Journal of Pharmaceutical Sciences