UHPLC-MS/MS method for the quantification of aloin-A in rat plasma and its application to a pharmacokinetic study

被引:12
|
作者
Niu, Chao [1 ,2 ]
Ye, Weijian [1 ,2 ]
Cui, Xiao [1 ,2 ]
Sun, Jia [3 ]
Xiao, Shuyi [1 ,2 ]
Chen, Gen [3 ]
Bao, Shihui [1 ,2 ]
Chen, Ruijie [1 ,2 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou 325027, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325027, Peoples R China
[3] Wenzhou Med Univ, Sch Pharmaceut Sci, Wenzhou 325000, Peoples R China
基金
中国国家自然科学基金;
关键词
Aloin-A; Quantification; UHPLC-MS/MS; Pharmacokinetics; PERFORMANCE LIQUID-CHROMATOGRAPHY; ANTIVIRAL ACTIVITY; EMODIN; VERA; ANTHRAQUINONES; BREAST; VIRUS; CELLS; ARRAY;
D O I
10.1016/j.jpba.2019.112928
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Aloin-A (also known as barbaloin), the main bioactive anthraquinone-C-glycoside of Aloe species, exhibits various beneficial pharmacological effects. However, the determination and pharmacokinetic study of aloin-A in rat plasma need to be improved and systematically demonstrated. In the present study, a simple, robust and sensitive ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method for rapid quantification of aloin-A in rat plasma was developed. Plasma preparation was conducted by a single step protein precipitation with obtusin serving as an internal standards (IS) followed by separation of the analytes using an Agilent C18 column with a gradient mobile phase comprised of acetonitrile and formic acid aqueous solution. Negative ion electrospray was used and multiple reaction monitoring transitions were m/z 417.1 -> 297.0 for aloin-A and m/z 343.1 -> 328.1 for IS, respectively. The developed method was validated with linear range of 1-1000 ng/mL. All validation parameters were well within the acceptance criteria based on the guidance of FDA. The validated approach was successfully applied to analyze samples from a pharmacokinetic study in healthy rats following intravenous and oral administration. Aloin-A was found to be quickly absorbed, extensively distributed and rapidly eliminated. The absolute bioavailability of aloin-A was 5.79%. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页数:6
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