Venkataramana D, Krishna D R
University College of Pharmaceutical Sciences, Kakatiya University, Warangal, India.
J Chromatogr. 1992 Mar 13;575(1):167-70. doi: 10.1016/0378-4347(92)80520-z.
A high-performance liquid chromatographic method for the determination of usnic acid in human plasma using diclofenac sodium as internal standard is described. Plasma proteins were precipitated with methanol. A 250 mm x 4 mm I.D. Nucleosil. C18 (5 microns) column with a mobile phase consisting of methanol-phosphate buffer (pH 7.4) (70:30, v/v) was used. Chromatography was performed at ambient temperature with flow-rate of 1 ml min-1 and ultraviolet detection at 280 nm. Each analysis required no longer than 7 min. Quantification was achieved by measurement of the peak-height ratio and the absolute recovery varied from 93.8 to 97.3%. The limit of quantitation of usnic acid in plasma was 0.25 micrograms ml-1. The intra-day relative standard deviation (R.S.D.) ranged from 1.24 to 4.53% and the inter-day R.S.D. from 2.23 to 8.25% at three different concentrations. The method was applied to the determination of plasma levels of usnic acid after intravenous and oral administration to study its disposition in a healthy male rabbit.
描述了一种以双氯芬酸钠为内标物测定人血浆中松萝酸的高效液相色谱法。用甲醇沉淀血浆蛋白。使用内径为4 mm、长250 mm的Nucleosil C18(5微米)柱,流动相为甲醇 - 磷酸盐缓冲液(pH 7.4)(70:30,v/v)。在室温下进行色谱分析,流速为1 ml min-1,在280 nm处进行紫外检测。每次分析所需时间不超过7分钟。通过测量峰高比进行定量,绝对回收率在93.8%至97.3%之间。血浆中松萝酸的定量限为0.25微克ml-1。在三种不同浓度下,日内相对标准偏差(R.S.D.)范围为1.24%至4.53%,日间R.S.D.范围为2.23%至8.25%。该方法应用于健康雄性兔静脉注射和口服后血浆中松萝酸水平的测定,以研究其体内处置情况。