Liang Yan, Liu Ai-hua, Qin Song, Sun Jiang-hao, Yang Min, Li Ping, Guo De-an
Department of Pharmacognosy and Pharmaceutical Botany, China Pharmaceutical University, Nanjing 210009, PR China.
J Pharm Biomed Anal. 2008 Feb 13;46(3):442-8. doi: 10.1016/j.jpba.2007.11.001. Epub 2007 Nov 9.
A sensitive and rapid solid-phase extraction-high performance liquid chromatography (SPE-HPLC) method has been developed for the determination of five bufadienolides, arenobufagin, teliocinobufagin, cinobufotalin, cinobufagin and resibufogenin in rat plasma and applied to a pharmacokinetic study in rats after oral administration of Chansu extract (Venenum Bufonis). Plasma samples were pretreated with solid-phase extraction using Extract-Clean cartridges, and the extracts were analyzed by a reversed-phase C(18) column on a HPLC system with photodiode array detection (DAD). The calibration curves were linear over the range of 0.10-1.66 microg/ml for arenobufagin, 0.03-1.20 microg/ml for telocinobufagin, 0.01-0.62 microg/ml for cinobufotalin, 0.03-0.70 microg/ml for cinobufagin and 0.02-2.57 microg/ml for resibufogenin, respectively. The limit of quantification was 1.1 ng/ml for arenobufagin, 0.3 ng/ml for telocinobufagin, 9.7 ng/ml for cinobufotalin, 8.8 ng/ml for cinobufagin, 7.7 ng/ml for resibufogenin, respectively. The established method could be easily applied to the determination and pharmacokinetic studies of five bufadienolides in rat plasma after oral administration of Chansu extract.
已建立一种灵敏、快速的固相萃取-高效液相色谱法(SPE-HPLC),用于测定大鼠血浆中5种蟾蜍二烯羟酸内酯,即华蟾酥毒基、日本蟾蜍它灵、脂蟾毒配基、蟾毒灵和远华蟾毒精,并将其应用于大鼠口服蟾酥提取物(蟾酥)后的药代动力学研究。血浆样品采用Extract-Clean柱进行固相萃取预处理,提取物在配备光电二极管阵列检测(DAD)的HPLC系统上通过反相C18柱进行分析。华蟾酥毒基的校准曲线在0.10 - 1.66μg/ml范围内呈线性,日本蟾蜍它灵在0.03 - 1.20μg/ml范围内,脂蟾毒配基在0.01 - 0.62μg/ml范围内,蟾毒灵在0.03 - 0.70μg/ml范围内,远华蟾毒精在0.02 - 2.57μg/ml范围内。华蟾酥毒基的定量限为1.1 ng/ml,日本蟾蜍它灵为0.3 ng/ml,脂蟾毒配基为9.7 ng/ml,蟾毒灵为8.8 ng/ml,远华蟾毒精为7.7 ng/ml。所建立的方法可轻松应用于大鼠口服蟾酥提取物后血浆中5种蟾蜍二烯羟酸内酯的测定和药代动力学研究。