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040 _aAIKTC-KRRC
_cAIKTC-KRRC
100 _918077
_aSalode, Vikrant Liladhar
245 _aDevelopment of validated stability indicating method for estimation of vandetanib and characterization of its degradants by LC-ESI-MS
250 _aVol.56(1), Jan-Mar
260 _aKarnataka
_bAssociation of Pharmaceutical Teachers of India (APTI)
_c2022
300 _a232-239p.
520 _aAim: In the current study, stability indicating high performance liquid chromatography method (RP-HPLC) was developed and validated for the determination of Vandetanib, also its major degradants were identified and characterized by Liquid Chromatography- Tandem Mass spectrophotometric method (LC-ESI-MS). Methods and Materials: This method was developed on Nucleosil 100-5, C18 (250×4.6 mm, 5μm) column by using Methanol: Ammonium acetate buffer as Mobile phase in the ratio, 90:10 v/v, having flow rate of 1 ml/min. The estimation was carried out at 249 nm. Further Vandetanib was subjected to various stress condition like acidic, alkali, oxidative, thermal and photolytic degradation. The degradation pathways for major degradants were idenitifed. Results: The method was developed and validated for linearity, robustness, accuracy, precision, linear regression analysis data which indicates the good linear relationship, correlation coefficient was found 0.992 in the concentration range of 1-10 μg/ml. In the stress results, the degradation of drug in alkaline, as well as acidic medium showed significantly. The product degradation was characterized by the LC-MS technique. Conclusion: The developed method was found to be rapid, sensitive, accurate, precise, and robust for the analysis of Vandetanib by which routine analysis of drugs can be done.
650 0 _94639
_aPHARMACEUTICS
700 _918078
_aGame, Madhuri Deorao
773 0 _dBengluru Association of Pharmaceutical Teachers of India (APTI)
_x0019-5464
_tIndian journal of pharmaceutical education and research
856 _uhttps://www.ijper.org/sites/default/files/IndJPhaEdRes-56-1-232.pdf
_yClick here
942 _2ddc
_cAR