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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.
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页数:6
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