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Characterization of forced degradants of Tegafur, Gimeracil, and Oteracil potassium by Liquid Chromatographic-Electrospray Ionization-Mass Spectrometry and simultaneous estimation of triple combination in drug substance and finished pharmaceutical Dosage Form | ||
| Archives of Razi Institute | ||
| مقاله 7، دوره 79، شماره 2، خرداد و تیر 2024، صفحه 287-302 اصل مقاله (790.08 K) | ||
| نوع مقاله: Original Articles | ||
| شناسه دیجیتال (DOI): 10.32592/ARI.2024.79.2.287 | ||
| نویسندگان | ||
| Ashish Kumar Pal* ؛ Raja Sundararajan | ||
| Department of Pharmaceutical Analysis, GITAM Institute of Pharmacy, GITAM (Deemed to be University), Gandhi Nagar, Rushikonda, Visakhapatnam, Pin code: 530 045, Andhra Pradesh (State), India. | ||
| چکیده | ||
| Tegafur, gimeracil, and oteracil potassium are widely used pharmaceuticals to treat lung cancers of the gastrointestinal tract like the oral cavity, esophagus, colon and rectum, pancreas, and also non-small cell lung cancers. Literature review revealed that no study has yet offered a completely stability-demonstrating, validated liquid chromatography-mass spectrometric approach for the concurrent estimation of tegafur, gimeracil, and oteracil potassium along with all known degradation products. The simultaneous detection of tegafur, gimeracil, and oteracil potassium, and their forced degradation products characterization, necessitated the invention of a simple, faster, and less expensive method. The goal of the study was to follow ICH method validation standards to develop and validate a fast, easy, and rugged liquid chromatography-mass spectrometry (LC-MS) technique for the concurrent estimation of Tegafur, gimeracil, and oteracil potassium in drug substance and finished dosage form according to ICH method validation guidelines. Tegafur, gimeracil, and oteracil potassium were examined on Waters HPLC Alliance system coupled to SCIEX QTRAP 5500 mass spectrometer endowed with an interface capable of carryout electrospray ionization. The tegafur, gimeracil, and oteracil peaks eluted at retention times of 2.338 min., 3.756 min., and 5.338 min. respectively. The limit of detection (LOD) values of tegafur, gimeracil, and oteracil were detected to be 0.6, 0.174, and 0.474 μg/mL, respectively however the results for quantification limit (LOQ) were calculated to be 2.0, 0.58, 1.58 µg/mL concentration, respectively. Tegafur, gimeracil, and oteracil had linear ranges of 50-300 µg/ml, 14.5-87 µg/ml, and 39.5-237 µg/ml, respectively, with regression coefficients of 0.99956, 0.99986, and 0.999479. Accuracy values for tegafur, gimeracil, and oteracil in the ranges of 50%, 100% and 150% for each were respectively, were determined to be 99.9%, 99.9%, and 99.4%. The % RSD for six replicates was less than 2% for precision. According to ICH Q2 guidelines, this approach was effectively evaluated with LC-MS to validate the chemical structures of freshly created tegafur, gimeracil, and oteracil degradation products. An accurate and sensitive LC-MS technique was developed and validated for the concurrent quantification of tegafur, gimeracil, and oteracil potassium in drug material and medicinal dosage form. | ||
| کلیدواژه‌ها | ||
| Tegafur؛ Gimeracil؛ Oteracil؛ liquid chromatography mass-spectrometry (LC-MS) technique؛ degradation study | ||
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