Department of Pharmacy, Urumqi General Hospital of PLA, Urumqi Xinjiang, P. R. China.
J Sep Sci. 2011 Jan;34(2):160-8. doi: 10.1002/jssc.201000382. Epub 2010 Dec 20.
A simple, rapid and specific method based on cloud-point extraction (CPE) was developed to determine ampelopsin in rat plasma after oral administration by reversed-phase high-performance liquid chromatography. The non-ionic surfactant Genapol X-080 was chosen as the extract solvent. Some important parameters affecting the CPE efficiency, such as the nature and concentration of surfactant, extraction temperature and time, centrifuge time and salt effect, were investigated and optimized. Separation was accomplished using a C(18) column by gradient elution with a acetonitrile-phosphate buffer solution as the mobile phase. The detection wavelength was set at 290 nm. Under optimum conditions, the linear range of ampelopsin in rat plasma was 20-2000 ng/mL (r(2)=0.9996). The limit of detection was 6 ng/mL (S/N=3) with the limit of quantification being 20 ng/mL (S/N=10). The proposed method has been successfully applied for pharmacokinetic studies of ampelopsin from rat plasma after oral administration.
建立了一种基于浊点萃取(CPE)的简单、快速、专属性强的方法,用于反相高效液相色谱法测定大鼠灌胃后血浆中的蛇葡萄素。选用非离子表面活性剂 Genapol X-080 作为萃取溶剂。考察并优化了影响 CPE 效率的一些重要参数,如表面活性剂的种类和浓度、萃取温度和时间、离心时间和盐效应等。采用 C(18)柱,以乙腈-磷酸盐缓冲溶液为流动相进行梯度洗脱,检测波长为 290nm。在最佳条件下,大鼠血浆中蛇葡萄素的线性范围为 20-2000ng/mL(r(2)=0.9996)。检测限为 6ng/mL(S/N=3),定量下限为 20ng/mL(S/N=10)。该方法已成功应用于大鼠灌胃后蛇葡萄素的药代动力学研究。