Determination of manassantin B in rat plasma using a high performance liquid chromatography with fluorescence detection and its quantitative application to pharmacokinetic study

被引:6
|
作者
Lee, Jae-Young [1 ,2 ]
Song, Jae-Hyoung [3 ]
Yoon, In-Soo [4 ,5 ]
Ko, Hyun-Jeong [3 ]
Kim, Dae-Duk [1 ,2 ]
Cho, Hyun-Jong [3 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[2] Seoul Natl Univ, Pharmaceut Sci Res Inst, Seoul 151742, South Korea
[3] Kangwon Natl Univ, Coll Pharm, 1 Kangwondaehak Gil, Chunchon 200701, South Korea
[4] Mokpo Natl Univ, Coll Pharm, Jeonnam 534729, South Korea
[5] Mokpo Natl Univ, Nat Med Res Inst, Jeonnam 534729, South Korea
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2016年 / 1011卷
基金
新加坡国家研究基金会;
关键词
Manassantin B; Validation; HPLC; Fluorescence detection; Pharmacokinetics; SAURURUS-CHINENSIS; EXTRACT; CELLS; INHIBITORS; LIGNANS; ROOTS;
D O I
10.1016/j.jchromb.2015.12.058
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple, sensitive, rapid, and reproducible analytical method of manassantin B in rat plasma by high performance liquid chromatography with fluorescence detection (HPLC-FL) was developed for its application to pharmacokinetic study in rats. Valsartan (VST) was used as an internal standard (IS) in this quantitative analytical method. Manassantin B and VST were extracted by simple and efficient protein precipitation method. Manassantin B was detected at 282/322 nm (excitation/emission) wavelengths using FL detector. The chromatographic separation was obtained with reverse phase C18 column and the mobile phase composed of potassium phosphate buffer containing 0.025% trifluoroacetic acid (pH 2.5; 5 mM) and acetonitrile including 0.025% trifluoroacetic acid (20:80, v/v) at 1.0 mL/min flow rate. The linearity was established at 25.0-10000 ng/mL and the lower limit of detection (LLOD) was 7 ng/mL. The intra- and inter-day accuracy and precision values of manassantin B were within +/- 15% of the theroretical values and <9% from the nominal concentrations, respectively. Accuracy and precision values of manassantin B after stability tests were also within the acceptable ranges. Developed assay was also successfully applied to pharmacokinetic study after intravenous administration of manassantin B in rats. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:121 / 127
页数:7
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