Determination of apatinib and its three active metabolites by UPLC-MS/MS in a Phase IV clinical trial in NSCLC patients

被引:3
作者
Guan, Shaoxing [1 ]
Shi, Wei [2 ,3 ,4 ]
Zhao, Zerui [2 ]
Wang, Fei [5 ]
Jiang, Fulin [1 ]
Zhang, Caibin [1 ]
Jin, Zhongming [1 ]
Guan, Yanping [1 ]
Liu, Dihan [2 ]
Zhong, GuoPing [1 ]
Huang, Min [1 ]
Long, Hao [2 ]
Wang, Xueding [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Lab Drug Metab & Pharmacokinet, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Canc Ctr, State Key Lab Oncol South China, Dept Thorac Oncol, 651 Dongfeng East Rd, Guangzhou 510080, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Canc Ctr, State Key Lab Oncol South China, Collaborat Innovat Ctr Canc Med,Dept Med Oncol, 651 Dongfeng East Rd, Guangzhou 510080, Guangdong, Peoples R China
[4] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau 999078, Peoples R China
[5] Qingxi Hosp, Dept Pharm, Dongguan 510080, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
active metabolites; apatinib; therapeutic drug monitoring; UPLC-MS/MS; GASTRIC-CANCER; INHIBITOR;
D O I
10.4155/bio-2019-0214
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aim: To develop and validate a simple method using UPLC-MS/MS for determination of apatinib and its three active metabolites in a Phase IV clinical trial. Materials & methods: All compounds were separated on a Hypersil GOLD (TM) aQ C18 Polar Endcapped LC column (50 x 2.1 mm, 1.9 mu m, Thermo) using 5 mmol/l ammonium acetate with 0.1% formic acid:acetonitrile (20:80, v/v) as the mobile phase after a rapid liquid-liquid extraction. This method was validated over the linear concentration range of 1.00-1000 ng/ml for each compound. Results: The interassay precision and accuracy were less than +/- 15%. The validated method was successfully applied to determine concentrations of clinical samples in non-small-cell lung cancer patients.
引用
收藏
页码:2049 / 2060
页数:12
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