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采用HPLC-ESI-MS法同时测定大鼠口服中药制剂黄连解毒汤后血浆中小檗碱和巴马汀含量及其药代动力学应用

Simultaneous determination of berberine and palmatine in rat plasma by HPLC-ESI-MS after oral administration of traditional Chinese medicinal preparation Huang-Lian-Jie-Du decoction and the pharmacokinetic application of the method.

作者信息

Lu Tong, Liang Yan, Song Jue, Xie Lin, Wang Guang Ji, Liu Xiao Dong

机构信息

Center of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China.

出版信息

J Pharm Biomed Anal. 2006 Mar 18;40(5):1218-24. doi: 10.1016/j.jpba.2005.09.023. Epub 2005 Nov 15.

Abstract

A sensitive and specific liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) method has been developed and validated for the identification and quantification of berberine and palmatine in rat plasma. After the addition of the internal standard (IS) and alkalization with 0.5M sodium hydroxide solution, plasma samples were extracted by ethyl ether and separated by HPLC on a Shim-pack ODS (4.6 microm, 150 mm x 2.0mm i.d.) column using a mobile phase composed of A (0.08% formic acid and 2 mmol/l ammonium acetate) and B (acetonitrile) with linear gradient elution. Analysis was performed on a Shimadzu LC/MS-2,010A in selected ion monitoring (SIM) mode with a positive electrospray ionization (ESI) interface. M=336 for berberine; 352 for palmatine and M+H=340 for IS were selected as detecting ions, respectively. The method was validated over the concentration range of 0.31-20 ng/ml for berberine and palmatine. Inter- and intra-CV precision (R.S.D.%) were all within 15% and accuracy (%bias) ranged from -5 to 5%. The lower limits of quantification were 0.31 ng/ml for both analytes. The extraction recovery was on average 68.6% for berberine, 64.2% for palmatine. The validated method was used to study the pharmacokinetic profile of berberine and palmatine in rat plasma after oral administration of Huang-Lian-Jie-Du decoction.

摘要

已开发并验证了一种灵敏且特异的液相色谱 - 电喷雾电离 - 质谱(LC - ESI - MS)方法,用于鉴定和定量大鼠血浆中的小檗碱和巴马汀。加入内标(IS)并用0.5M氢氧化钠溶液碱化后,血浆样品用乙醚萃取,并在Shim - pack ODS(4.6微米,150mm×2.0mm内径)柱上通过HPLC分离,流动相由A(0.08%甲酸和2mmol / l醋酸铵)和B(乙腈)组成,采用线性梯度洗脱。在配备正电喷雾电离(ESI)接口的Shimadzu LC / MS - 2010A上以选择离子监测(SIM)模式进行分析。小檗碱的M=336;巴马汀的M=352,内标的M + H=340分别被选为检测离子。该方法在小檗碱和巴马汀浓度范围为0.31 - 20 ng/ml内进行了验证。批间和批内变异系数(R.S.D.%)均在15%以内,准确度(%偏差)范围为 - 5至5%。两种分析物的定量下限均为0.31 ng/ml。小檗碱的萃取回收率平均为68.6%,巴马汀为64.2%。经验证的方法用于研究大鼠口服黄连解毒汤后血浆中小檗碱和巴马汀的药代动力学特征。

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