Development and validation of LC-MS/MS method for the detection and quantification of CpG oligonucleotides 107 (CpG ODN107) and its metabolites in mice plasma

被引:18
作者
Cen, Yanyan [1 ]
Li, Xiaoli [1 ]
Liu, Dan [1 ]
Pan, Feng [2 ]
Cai, Yongqing [3 ]
Li, Bin [1 ]
Peng, Wei [1 ]
Wu, Chong [1 ]
Jiang, Weiwei [1 ]
Zhou, Hong [1 ]
机构
[1] Third Mil Med Univ, Coll Pharm, Dept Pharmacol, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Biomed Anal Ctr, Chongqing 400038, Peoples R China
[3] Third Mil Med Univ, Southwestern Hosp, Dept Pharm, Chongqing 400038, Peoples R China
关键词
CpG ODN107; Metabolites; Solid-phase extraction; Pharmacokinetics; LC-MS/MS; PERFORMANCE LIQUID-CHROMATOGRAPHY; ALPHA ANTISENSE OLIGONUCLEOTIDE; MASS-SPECTROMETRY; SOLID-PHASE; PHOSPHOROTHIOATE OLIGODEOXYNUCLEOTIDES; IN-VIVO; PHARMACOKINETICS; QUANTITATION; ELECTROPHORESIS; GROWTH;
D O I
10.1016/j.jpba.2012.06.022
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
CpG oligodeoxynucleotide 107 (CpG ODN107) could be used as a novel radiosensitizer for glioma. Herein, a novel and sensitive reversed-phase HPLC coupled with electrospray triple quadrupole mass spectrometry (LC-MS/MS) following a one-step 08 solid-phase extraction (SPE) for biological matrix removal was developed and fully validated for the determination of CpG ODN107 and its metabolites such as 5'N-1, 3'N-1, 3'N-2, and 3'N-3 in mouse plasma. The analytes were separated on an Extend-C18 analytical column (150 mm x 2.1 mm, 3.5 mu m) using an eluent of acetonitrile-0.05% aqueous NH3 (20:80, v/v) and detected by electrospray ionization (ESI) mass spectrometry in the negative multiple reaction monitoring mode (MRM). The assay was specific, and it showed a good linearity with a determination coefficient (r(2)) that was greater than or equal to 0.998 for CpG ODN107 and its metabolites in the biological matrices. The precision, accuracy, and relative recovery values were found to be <15%, +/-15%, and 95-105%, respectively. This method was successfully applied to measure the concentrations of CpG ODN107 and its metabolites in the plasma following the intravenous administration of 15.0 mg/kg of CpG ODN107 in mice; therefore, the method was suitable for preclinical pharmacokinetic studies on CpG ODN107 and its metabolites. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:447 / 455
页数:9
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