A Validated Stability-Indicating HPTLC Method for the Estimation of Capecitabine in its Tablet Dosage Form

被引:2
|
作者
Thorat, Sonali [1 ]
Chikhale, Rupesh [2 ]
Rode, Vanita [1 ]
Tajne, Madhukar [1 ]
机构
[1] Rasthrast Tukadoji Maharaj Nagpur Univ, Dept Pharmaceut Sci, Nagpur 440033, MS, India
[2] Tata Mem Hosp, ACTREC, Mumbai 410210, MS, India
关键词
Capecitabine; prodrug; high-performance thin-layer chromatography; stability-indicating stress degradation; tablet dosage; anticancer drug; LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; METABOLITES; PHARMACOKINETICS; HPLC;
D O I
10.2174/1573412913666171023154934
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Capecitabine is an orally available prodrug of 5-flurouracil used in the treatment of breast cancer, metastatic colorectal cancer and stage III colorectal cancer. Various studies have reported the HPLC, HPLC-MS, MS/MS methods for estimation of capecitabine. However, till date HPTLC method for estimation of capecitabine and its validation is not reported in tablet dosage form. Introduction: Presented study deals with the development and validation of stability indicating high performance thin layer chromatography method for the determination of Capecitabine in tablet dosage form. Methods: The method was developed using precoated HPTLC plates with silica gel 60 F254 as stationary phase and toluene-methanol the ratio of 7.5:2.5 v/v as the mobile phase. Capecitabine (RF 0.48 +/- 0.03) and its degradation products were well resolved. The wavelength selected for study was 240 nm. The method was linear in the concentration range 50-550 ng/band with a correlation coefficient of 0.994. The repeatability for six samples was 1.25% RSD. The intraday and interday precisions were 1.46-1.71%RSD and 1.31-1.67% RSD, respectively. The accuracy (recovery) was found to be in the range of 99.10-101.23% with LOD and LOQ were found to be 0.650 and 1.765 mg/band. The mean content of drug in tablet dosage form was found to be 101.51% with a % RSD of 1.20. The drug was subjected to stress conditions such as hydrolysis, oxidation, photolysis, and heat. Results: Degradation products produced as a result of the stress conditions did not interfere with the detection of Capecitabine; therefore, the proposed technique can be considered stability-indicating. Capecitabine did not degrade under thermal and photolytic conditions but showed degradation under acidic and alkaline conditions with 15 and 11% decompositions respectively. Conclusion: The developed method was found to be facile, simple, specific, precise, and stability-indicating. It can be employed for the routine analysis of capecitabine in tablet dosage form.
引用
收藏
页码:61 / 66
页数:6
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