摘要
A high performance liquid chromatographic method was used for the simultaneous identification and qualitative evaluation of 12 bufadienolides（resibufogenin, einobufagin, cinobufaginol, arenobufagin, bufalin, bufotalin, gamabufotalin, cinobufotalin, ψ-bufaranogin, desacetylcinobufagin, telocinobufagin and resibufogenol） in Venenum Bufonis. The chromatographic separation was performed on a Dikma C18 analytical column via gradient elution with an aqueous solution of acetonitrile and 0.3% acetic acid at a flow rate of 0.8 mL/min. The method was validated to be acceptable in consideration of linearity（r2 〉 0.9992） and recovery（ranged from 98.9% to 102.0%）. The limits of detection of the bufadienolides were from 0.48 ng for bufalin to 6.00 ng for cinobufotalin. The intra-day and inter-day precisions of the method were evaluated and were less than 3.0%. The method was successfully used to analyze 19 batches of Venenum Bufonis, and the similarity values between batches were calculated by Similarity Evaluation System for Chromatographic Fingerprint of TCM（Version 2004A, Chinese Pharmacopoeia Committee, Beijing）. The results show that the contents of bufadienolides in the medicine and the similarity values based on these bufadienolides varied significantly from batch to batch. This proposed method could be utilized to qualify and control Venenum Bufonis to ensure its safety and efficacy in application.
A high performance liquid chromatographic method was used for the simultaneous identification and qualitative evaluation of 12 bufadienolides（resibufogenin, einobufagin, cinobufaginol, arenobufagin, bufalin, bufotalin, gamabufotalin, cinobufotalin, ψ-bufaranogin, desacetylcinobufagin, telocinobufagin and resibufogenol） in Venenum Bufonis. The chromatographic separation was performed on a Dikma C18 analytical column via gradient elution with an aqueous solution of acetonitrile and 0.3% acetic acid at a flow rate of 0.8 mL/min. The method was validated to be acceptable in consideration of linearity（r2 〉 0.9992） and recovery（ranged from 98.9% to 102.0%）. The limits of detection of the bufadienolides were from 0.48 ng for bufalin to 6.00 ng for cinobufotalin. The intra-day and inter-day precisions of the method were evaluated and were less than 3.0%. The method was successfully used to analyze 19 batches of Venenum Bufonis, and the similarity values between batches were calculated by Similarity Evaluation System for Chromatographic Fingerprint of TCM（Version 2004A, Chinese Pharmacopoeia Committee, Beijing）. The results show that the contents of bufadienolides in the medicine and the similarity values based on these bufadienolides varied significantly from batch to batch. This proposed method could be utilized to qualify and control Venenum Bufonis to ensure its safety and efficacy in application.
基金
Supported by the National Basic Researeh Program of China(No.2007CB507400)
the National High Technology Research and Development Program(No.2006AA02Z338)
Program for Changjiang Scholars and Innovative Research Team in Universities of China(PCSIRT)
Partly Supported by the Scientific Foundation of Shanghai City,China(Nos.05DZ19733,06DZ19717,06DZ19005)
