Determination of 16 antineoplastic drugs by capillary electrophoresis with UV detection: Applications in quality control

被引:19
作者
Guichard, Nicolas [1 ,2 ]
Ogereau, Marie [1 ]
Falaschi, Ludivine [1 ]
Rudaz, Serge [2 ]
Schappler, Julie [2 ]
Bonnabry, Pascal [1 ,2 ]
Fleury-Souverain, Sandrine [1 ]
机构
[1] Geneva Univ Hosp, Pharm, Geneva, Switzerland
[2] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, Geneva, Switzerland
关键词
Antineoplastic drugs; Capillary electrophoresis; Micellar electrokinetic chromatography (MEKC); Quality control; QUANTITATIVE ANALYTICAL PROCEDURES; THIN-LAYER-CHROMATOGRAPHY; SFSTP PROPOSAL; PHARMACEUTICAL PRODUCTS; STRATEGIES; HARMONIZATION; VALIDATION; IDENTIFICATION; PLASMA;
D O I
10.1002/elps.201800007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two capillary electrophoresis (CE) methods were developed for the analysis of 16 antineoplastic drugs contained in injectable pharmaceutical formulations. A capillary zone electrophoresis (CZE) method coupled to UV was developed with a background electrolyte (BGE) made of a 100 mM phosphate buffer at pH 2.5 containing 50% v/v of acetonitrile and dynamic coating of capillaries with Ceofix (R). This method allowed the analysis of doxorubicin, epirubicin, idarubicin, daunorubicin, irinotecan, topotecan, vincristine, vindesine, vinblastine, and vinorelbine in less than 8 min. A micellar electrokinetic chromatography (MEKC) method coupled to UV was also developed for the determination of methotrexate, pemetrexed, etoposide, etoposide phosphate, fludarabine phosphate, and 5-fluorouracil. A run time of 16min was obtained with a BGE made of 50mM borate buffer at pH 9.2 with 80mM of sodium dodecyl sulfate (SDS) and 20% v/v of acetonitrile. For both methods, the applied voltage was 30kV and the sample injection was performed in the hydrodynamic mode. All analyses were carried out in fused silica capillaries with an internal diameter of 50m and a total length of 64.5cm. Both methods were validated and trueness values between 99.4 and 101.3% were obtained with repeatability and intermediate precision values of 0.5-1.8% for all drugs. These methods were found appropriate for controlling injectable pharmaceutical formulations containing antineoplastic drugs and successfully applied in quality control.
引用
收藏
页码:2512 / 2520
页数:9
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