Determination of Ecliptasaponin A in Rat Plasma by using UPLC-MS/MS and its Pharmacokinetics Application

被引:0
作者
Pan, Qing [1 ]
Sun, Jinghai [2 ]
Zhang, Lin [3 ]
Tian, Jingkui [3 ]
Ma, Luyu [4 ]
机构
[1] Shandong Acad Med Sci, Shandong Prov Inst Dermatol & Venereol, Jinan, Shandong, Peoples R China
[2] Jinan Matern & Child Care Hosp, Jinan, Shandong, Peoples R China
[3] Zhejiang Univ, Dept Biomed Engn, Hangzhou, Zhejiang, Peoples R China
[4] Shandong Acad Med Sci, Jinan, Shandong, Peoples R China
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2018年 / 37卷 / 10期
关键词
eclipta; ecliptasaponin A; pharmacokinetics; rat plasma; UPLC-MS/MS; LC-MS/MS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Eclipta (Eclipta prostrata L.) is a widely used Chinese medicinal plant that mainly contains saponins. Ultra-high performance liquid chromatography tandem mass spectrometry is a rapid, selective and sensitive method for the determination and pharmacokinetic investigation of ecliptasaponin A in rat plasma with notoginsenoside R1 as the internal standard (IS). Plasma sample preparation was achieved through a one-step liquid-liquid extraction method. Plasma samples were analyzed by using a COSMOSIL 5C18-MS-II packed column (2.0 x 50 mm, 5 mu m) with a line gradient elution using acetonitrile and 0.1 % acetic acid as the mobile phase. All analytes and notoginsenoside R1 were detected in negative ionization mode by using multiple reaction monitoring (MRM) of the transitions at m/z 633.2 -> 587.2 (ecliptasaponin A) and m/z 931.6 -> 637.2 (IS), respectively. The method was linear for all analytes over the investigated ranges, with all correlation coefficients > 0.997. The intra- and inter-day precisions (RSD, %) were < 9.0 %, and accuracy (RE, %) ranged from 5.6 to 11.3 %, which were within the acceptable limits. The mean extraction recoveries of the analytes from rat plasma were within the range of 96.9-104.4 %, and no notable matrix effect was observed. This validated method was successfully utilized in a pharmacokinetic study of an ecliptasaponin A extract via oral and intravenous administration.
引用
收藏
页码:2079 / 2085
页数:7
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