浏览全部资源
扫码关注微信
目的:建立胆木叶药材的质量标准。方法:采用显微鉴别法和薄层色谱法(TLC)对药材进行定性鉴别;测定药材水分、灰分;采用高效液相色谱法测定药材中异长春花苷内酰胺含量:色谱柱为Lichrospher C18,流动相为乙腈-0.1%磷酸溶液(梯度洗脱),流速为1 mL/min,检测波长为226 nm,柱温为30 ℃,进样量为10 μL。结果:胆木叶的显微鉴别特征性强,TLC图斑点清晰,分离度好,阴性对照无干扰。异长春花苷内酰胺检测质量浓度线性范围为0.010 5~0.21 mg/mL(r=0.999 5);精密度、稳定性、重复性试验的RSD<2.0%;加样回收率为96.25%~101.82%(RSD=1.86%,n=9)。测得药材样品总灰分为5.27%~6.44%,酸不溶性灰分为0.23%~0.36%,水分为9.48%~11.46%,异长春花苷内酰胺含量为0.124%~1.003%。结论:该研究所建标准可用于胆木叶药材的质量控制。
OBJECTIVE: To establish the quality standard for the leaves of Nauclea officinalis. METHODS: Microscopic identification and TLC methods were used for qualitative identification of N. officinalis. The moisture and ash of medicinal materials were determined. HPLC method was adopted to determine the content of strictosamide in medicinal materials. The determination was performed on Lichrospher C18 column with mobile phase consisted of acetonitrile-0.1% phosphoric acid solution (gradient elution) at the flow rate of 1 mL/min, injection volume was 10 μL. The detection wavelength was set at 226 nm, and the column temperature was 30 ℃. RESULTS: Microscopic identification of the leaves of N. officinalis had strong characteristics, and TLC sports were clear and well-separated without interference from negative control. The linear range of strictosamide were 0.010 5-0.21 mg/mL(r=0.999 5); RSDs of precision, stability and reproducibility tests were all lower than 2.0%. Average recoveries were 96.25-101.82%(RSD=1.86%,n=9). Total ash of medicinal materials was 5.27%-6.44%, acid insoluble ash was 0.23%-0.36%,water content was 9.48%-11.46%, strictosamide was 0.124%-1.003%. CONCLUSIONS: Established standard can be used for quality evaluation of N. officinalis.
胆木叶质量标准显微鉴别法薄层色谱法含量测定高效液相色谱法
Leaves of Nauclea officinalisQuality standardMicroscopic identificationTLCContent determinationHPLC
0
浏览量
7
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构