实验2 高效液相色谱法测定栀子药材中栀子苷的含量

实验2 高效液相色谱法测定栀子药材中栀子苷的含量

学时分配：6学时

实验目的和要求

1.掌握高效液相色谱法的基本原理及操作步骤；

2.熟悉高效液相色谱法在中草药有效成分测定中的应用。

实验原理

高效液相色谱法是用高压输液泵将具有不同极性的单一溶剂或不同比例的混合溶剂、缓冲液等流动相，泵入装有固定相的色谱柱，经进样阀注入供试品，由流动相带入色谱柱，在柱内各组分被分离后,依次进入检测器，色谱信号由记录仪或积分仪记录。

所用的仪器为高效液相色谱仪。色谱柱的填充剂和流动相的组分应按待测组分的性质而定，常用的色谱柱填充剂有硅胶和化学键合硅胶，后者以十八烷基键合硅胶最为常用，辛基硅烷键合硅胶次之，氰基或氨基键合硅胶也有使用。除另有规定外，柱温为室温，检测器有紫外检测器，二极管阵列检测器，示差折光检测器等。

影响色谱分离效率有两大主要因素，其一为热力学因素, 如不同组分容量因子(K’)，其二是动力学因素, 如色谱峰的展宽。反映这些物理过程的指标是保留时间和理论塔板数(N)。

其中K’=t R-t o / t o ；n = 5.54(t R / W1/2)2

密切注视和努力解决这两个因素引起的矛盾，组分间的分离就成功了，分离的表现指标是分离度“R”。

R = 2 (t2 - t1) / (W b1+W b2)

实验条件

1.仪器：高效液相色谱仪，超声波清洗器，Zorbax C18柱（4.6×250mm）。

2.试剂：栀子苷对照品，乙睛，甲醇，水。

实验内容

1.色谱条件：色谱柱：Zorbax C18柱（4.6×250mm）；流动相：乙睛—水（15:85）；检测波长：238nm，流速：1mL/min。

2.对照品溶液的制备和标准曲线的绘制：精密称取栀子苷对照品适量，加甲

醇制成每1mL含100μg的溶液，摇匀后，分别取该液1，2，3，4，5mL，置10mL容量瓶中，加甲醇稀释至刻度，摇匀后，分别进样20μl，按上述色谱条件测定，以峰面积为纵坐标，浓度为横坐标绘制标准曲线，计算回归方程和相关系数。

3.供试品溶液的制备：取本品粉末0.1g，精密称定，置25mL量瓶中，精密加入甲醇20mL，超声处理30min s。放冷，加甲醇至刻度，摇匀，滤过。精密量取续滤液10mL，置25mL容量瓶中，加甲醇至刻度，摇匀，过微孔滤膜，取续滤液，作为供试品溶液。

4.测定法：吸取供试品溶液20μl注入液相色谱仪，测定。由标准曲线法或

一点法计算样品中栀子苷的含量（C

17H

24

O

10

）。

五实验记录

1.扼要说明操作步骤及实验结果；

2.绘制标准曲线图，及回归方程，相关系数；

六思考题

1.在仪器操作过程中，应重点注意哪些方面？

2.用HPLC法测定中药中有效成分含量的主要优势是什么？

Experiment 3 Determination of Gardenoside in Fructus Gardeniae by HPLC

Class hour: 3

Objectives

1. Master the principles and operational method of HPLC through this experiment.

2. Be familiar with the use of HPLC in determination of components in traditional Chinese medicine.

Principles

In high performance liquid chromatography, the mobile phase, a solvent or a solvent mixture of suitable polarity (or a buffer solution of suitable ion strength), is pumped into a column containing the stationary phase. While the sample is injected into an injector and carried into the column by the mobile phase, the components are separated on the stationary phase and each component passes through the detector in succession and thus a chromatogram is record.

The stationary phase and the component part of the mobile phase should be in accordance with the qualities of test samples. Silica gel and chemically bonded silica gel are commonly used as the bulking agent. For chemically bonded silica gel, octadecylsilane type is most frequently used, followed by the octylsilane type, and the cyano and amino group bonded silica gel are occasionally used. The column is maintained at room temperature. The type of detector includes UV, DAD, SPD and so on.

There are two important factors responsible for chromatographic separation efficiency. One is the thermodynamic factor, such as the capacity factor of different components (k’), the other is the dynamic factor, such as the width of peak. The indexes to reflect these physical processes are retention time (t R) and the number of theoretical plates of column (n). Calculate the value of k’ and n as follows:

k’ = (t R－t o) / t o; n = 5.54 (t R / w1/2)2

The separation of different components will be successful if close attention is paid and great effort is taken to solve the contradiction caused by the above factors. The