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采用液相色谱法同时测定中药制剂六神丸中的蟾毒配基。

Simultaneous determination of bufadienolides in the traditional Chinese medicine preparation, liu-shen-wan, by liquid chromatography.

作者信息

Hong Z, Chan K, Yeung H W

机构信息

Chinese Medicinal Materials Research Centre.

出版信息

J Pharm Pharmacol. 1992 Dec;44(12):1023-6. doi: 10.1111/j.2042-7158.1992.tb07086.x.

Abstract

The bufadienolide compounds (bufalin, cinobufagin and resibufogenin), major constituents of Chansu in Liu-Shen-Wan (LSW), were determined by reverse phase high performance liquid chromatography. The procedure involves a preliminary extraction of the bufadienolides from LSW with chloroform using ultrasonication and subsequent evaporation to dryness of the chloroform extract. The residue of the chloroform extract was dissolved in methanol and separated on a Merck LiChrosorb RP-18 column. Methanol: water (74:26) was used as mobile phase. The compounds were satisfactorily separated with good chromatographic peaks. Good coefficients of correlation (r > 0.999) were obtained from the calibration of peak areas with concentrations for the 3 bufadienolides. Results of analysis showed that there were differences between the contents of bufadienolides in 11 LSW samples of different origin available to the public in Hong Kong where at present there is no legal control over the sale of traditional Chinese medicines. The variability of quantities of bufadienolides in Chansu may be a hazard to the public.

摘要

采用反相高效液相色谱法测定了六神丸中蟾酥的主要成分蟾蜍二烯羟酸内酯类化合物(蟾毒灵、华蟾酥毒基和脂蟾毒配基)。该方法包括先用氯仿对六神丸中的蟾蜍二烯羟酸内酯类化合物进行超声提取,然后将氯仿提取物蒸发至干。氯仿提取物的残渣用甲醇溶解,并在默克LiChrosorb RP - 18柱上进行分离。以甲醇∶水(74∶26)作为流动相。这些化合物得到了满意的分离,色谱峰良好。通过对3种蟾蜍二烯羟酸内酯类化合物的峰面积与浓度进行校准,获得了良好的相关系数(r > 0.999)。分析结果表明,在香港市面上可获得的11种不同产地的六神丸样品中,蟾蜍二烯羟酸内酯类化合物的含量存在差异,目前香港对中药销售没有法律管制。蟾酥中蟾蜍二烯羟酸内酯类化合物含量的变异性可能对公众构成危害。

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