A validated chiral LC method for the enantiomeric separation of AT13148 on polysaccharide-based chiral stationary phase

被引:1
作者
Xia, Yong [1 ,2 ]
Liu, Zhihao [1 ,2 ]
Huang, Yong [3 ]
Huang, Xiaojun [4 ]
Liao, Mengya [5 ]
Zhang, Yiwen [1 ,2 ]
Ma, Xuelei [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Canc Ctr, Chengdu 610041, Sichuan, Peoples R China
[2] Collaborat Innovat Ctr, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Taihuatang Pharmaceut Co Ltd, 18,Sect 4,Nanchang Rd, Guanghan 618300, Peoples R China
[4] Jinan Univ, Shenzhen Peoples Hosp, Clin Med Coll 2, Dept Hepatobiliary & Pancreas Surg, Shenzhen 518020, Peoples R China
[5] Sichuan Nursing Vocat Coll, Chengdu 610100, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Column liquid chromatography; Chiral separation; Enantiomeric purity; AT13148; AGC KINASE INHIBITOR; SIGNALING PATHWAY; CANCER; HPLC; VANCOMYCIN; MECHANISMS;
D O I
10.1007/s13738-017-1270-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A sensitive and accurate LC method for the determination of AT13148 enantiomeric purity has been developed and validated. Baseline separation with a resolution higher than 1.8 was accomplished within 15 min using a Chiralpak AD-H column (250 x 4.6 mm; particle size 5 mu m) and n-hexane: 2-propanol: diethylamine (85:15:0.1, v/v) as mobile phase at a flow rate of 1 mL min(-1). Eluted analytes were monitored by UV absorption at 254 nm. The effects of mobile phase components, temperature and flow rate on enantiomeric selectivity and resolution of enantiomers were investigated. Calibration curves were plotted within the concentration range between 7 and 500 mu g mL(-1) (n = 11), and the recoveries between 98.24 and 100.99% were obtained, with relative standard deviation lower than 1.32%. LOD and LOQ for AT13148 were 2.46 and 7.38 mu g mL(-1) and for its enantiomer were 2.54 and 7.49 mu g mL(-1), respectively. It was demonstrated that the developed method was accurate, robust and sensitive for the determination of enantiomeric purity of AT13148, especially for the analysis of bulk samples.
引用
收藏
页码:711 / 717
页数:7
相关论文
共 20 条
[1]   MULTIPLE ENANTIOSELECTIVE RETENTION MECHANISMS ON DERIVATIZED CYCLODEXTRIN GAS-CHROMATOGRAPHIC CHIRAL STATIONARY PHASES [J].
BERTHOD, A ;
LI, WY ;
ARMSTRONG, DW .
ANALYTICAL CHEMISTRY, 1992, 64 (08) :873-879
[2]   Growth signalling pathways in Arabidopsis and the AGC protein kinases [J].
Bögre, L ;
Ökrész, L ;
Henriques, R ;
Anthony, RG .
TRENDS IN PLANT SCIENCE, 2003, 8 (09) :424-431
[3]   Reversed-phase high-performance liquid chromatographic separation of some 2-arylpropionic acids using vancomycin as chiral stationary phase [J].
Bouchair, Nabila ;
Righezza, Michel ;
Hamdi, Abderrezak .
JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2015, 12 (06) :921-928
[4]   AKT Inhibition Relieves Feedback Suppression of Receptor Tyrosine Kinase Expression and Activity [J].
Chandarlapaty, Sarat ;
Sawai, Ayana ;
Scaltriti, Maurizio ;
Rodrik-Outmezguine, Vanessa ;
Grbovic-Huezo, Olivera ;
Serra, Violeta ;
Majumder, Pradip K. ;
Baselga, Jose ;
Rosen, Neal .
CANCER CELL, 2011, 19 (01) :58-71
[5]   The PI3K Pathway As Drug Target in Human Cancer [J].
Courtney, Kevin D. ;
Corcoran, Ryan B. ;
Engelman, Jeffrey A. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (06) :1075-1083
[6]   Chiral separation of enantiomers of amino acid derivatives by high-performance liquid chromatography on a norvancomycin-bonded chiral stationary phase [J].
Ding, GS ;
Liu, Y ;
Cong, RZ ;
Wang, JD .
TALANTA, 2004, 62 (05) :997-1003
[7]   Determination of AR-42 enantiomeric purity by HPLC on chiral stationary phase [J].
Fang, Aiping ;
Zhang, Yue ;
Shen, Jiang ;
Sun, Shijin ;
Zou, Junyi ;
Yao, Yuqin .
JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2017, 14 (09) :1909-1915
[8]   Enantioselective potential of chiral stationary phases based on immobilized polysaccharides in reversed phase mode [J].
Geryk, Radim ;
Kalikova, Kveta ;
Vozka, Jiri ;
Plecita, Denisa ;
Schmid, Martin G. ;
Tesarova, Eva .
JOURNAL OF CHROMATOGRAPHY A, 2014, 1363 :155-161
[9]   The Dictyostelium kinome -: Analysis of the protein kinases from a simple model organism [J].
Goldberg, Jonathan M. ;
Manning, Gerard ;
Liu, Allen ;
Fey, Petra ;
Pilcher, Karen E. ;
Xu, Yanji ;
Smith, Janet L. .
PLOS GENETICS, 2006, 2 (03) :291-303
[10]   Targeting the phosphoinositide 3-kinase pathway in cancer [J].
Liu, Pixu ;
Cheng, Hailing ;
Roberts, Thomas M. ;
Zhao, Jean J. .
NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (08) :627-644