Deng Yuan-Xiong, Lu Tong, Xie Lin, Liu Xiao-Dong
Key Laboratory of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Tongjiaxiang 24, Nanjing 210009, Jiangsu, People's Republic of China.
Biomed Chromatogr. 2006 Oct;20(10):1098-102. doi: 10.1002/bmc.649.
A high-performance liquid chromatographic method for the determination of wogonoside in plasma of rats administrated orally with the traditional Chinese medicinal preparation Huang-Lian-Jie-Du decoction was developed. Sample preparation was carried out by protein precipitation with a mixture of acetonitrile and methanol (1:1, v/v). The extracted sample was separated on a Hypersil C(18) (150 x 5 mm i.d., 5 microm) analytical column by linear gradient elution using 0.05% (v/v) phosphoric acid (containing 5 mm sodium dihydrogen phosphate) and acetonitrile as mobile phase at a flow rate of 1.5 mL/min. The eluate was detected using a UV detector at 276 nm. The assay was linear over the range 0.109-7.0 microg/mL (R(2) = 0.9999, n = 5). Mean recovery was determined as 98.39%. Intra- and inter-day precisions (RSD) were < or =7.59%. The limit of quantitation was 0.109 microg/mL. After validation, the HPLC method developed was applied to investigate the preliminary pharmacokinetics of wogonoside in rat after oral administration of Huang-Lian-Jie-Du decoction.
建立了一种高效液相色谱法,用于测定口服中药制剂黄连解毒汤的大鼠血浆中汉黄芩苷的含量。样品制备采用乙腈和甲醇(1:1,v/v)混合液进行蛋白沉淀。提取的样品在Hypersil C(18)(150×5 mm内径,5μm)分析柱上,以0.05%(v/v)磷酸(含5 mM磷酸二氢钠)和乙腈为流动相,通过线性梯度洗脱进行分离,流速为1.5 mL/min。洗脱液用紫外检测器在276 nm处检测。该测定法在0.109 - 7.0μg/mL范围内呈线性(R(2)=0.9999,n = 5)。平均回收率为98.39%。日内和日间精密度(RSD)≤7.59%。定量限为0.109μg/mL。经过验证后,所建立的高效液相色谱法应用于研究大鼠口服黄连解毒汤后汉黄芩苷的初步药代动力学。