A sensitive bioanalytical ultra-high-performance liquid chromatography-tandem mass spectrometry method for the simultaneous quantitation of lactone and carboxylate forms of topotecan in plasma and vitreous

被引:4
|
作者
Mudrova, Barbora [1 ]
Hrabakova, Katerina [1 ]
Kozlik, Petr [1 ]
Hobzova, Radka [2 ]
Sirc, Jakub [2 ]
Bosakova, Zuzana [1 ]
机构
[1] Charles Univ Prague, Fac Sci, Dept Analyt Chem, Albertov 2030, Prague 2, Czech Republic
[2] Inst Macromol Chem, Prague, Czech Republic
关键词
anti-cancer drug topotecan; carboxylate form; lactone form; topotecan stability; UHPLC-MS/MS; HPLC METHOD; I INHIBITOR; PHARMACOKINETICS; CAMPTOTHECIN; PHARMACOLOGY; STABILITY; INJECTION; 104864-A; ASSAY;
D O I
10.1002/jssc.202400181
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Topotecan (TPT) is used in the treatment of retinoblastoma, the most common malignant intraocular tumor in children. TPT undergoes pH-dependent hydrolysis of the lactone ring to the ring-opened carboxylate form, with the lactone form showing antitumor activity. A selective, and highly sensitive ultra-high-performance liquid chromatography-tandem mass spectrometry method was developed for the determination of both forms of TPT in one mobile phase composition in plasma and vitreous humor matrices. The method showed an excellent linear range of 0.375-120 ng/mL for the lactone. For the carboxylate, the linear range was from 0.75 to 120 ng/mL. The matrix effect and the recovery for the lactone ranged from 98.5% to 106.0% in both matrices, for the carboxylate form, it ranged from 94.9% to 101.2%. The dynamics of the transition between TPT lactone and TPT carboxylate were evaluated at different pH environments. The stability of TPT forms was assessed in plasma and vitreous humor at 8 and 37 degrees C and a very fast conversion of lactone to carboxylate form occurred at 37 degrees C in both matrices. The method developed facilitates the investigation of TPT pharmacodynamics and the release kinetics in the development of the innovative local drug delivery systems.
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页数:13
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