首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >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.
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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.

机译:黄连解毒汤口服后HPLC-ESI-MS同时测定大鼠血浆中小ber碱和棕榈碱的含量,并在药代动力学中应用。

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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.
机译:已经开发了一种灵敏而特异性的液相色谱-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ber碱和棕榈碱。加入内标(IS)并用0.5M氢氧化钠溶液碱化后,用乙醚萃取血浆样品,并在Shim-pack ODS(4.6 microm,150 mm x 2.0mm id)色谱柱上使用HPLC分离血浆流动相由A(0.08%甲酸和2 mmol / l乙酸铵)和B(乙腈)组成,线性梯度洗脱。在具有正电喷雾电离(ESI)接口的选定离子监测(SIM)模式下,对Shimadzu LC / MS-2,010A进行了分析。小M碱的[M](+)= 336;分别选择棕榈碱352和离子对[M + H](+)= 340作为检测离子。该方法在小1碱和棕榈碱的浓度范围为0.31-20 ng / ml时得到验证。 CV内和CV内精度(R.S.D.%)都在15%以内,精度(%bias)介于-5到5%之间。两种分析物的定量下限均为0.31 ng / ml。小ber碱的提取回收率平均为68​​.6%,巴马汀的提取回收率平均为64.2%。验证的方法用于研究黄连解毒汤口服后小plasma碱和棕榈碱在大鼠血浆中的药代动力学特征。

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