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040 _aAIKTC-KRRC
_cAIKTC-KRRC
100 _926281
_aTadi, Vinay
245 _aDevelopment of a new stability indicating RP-HPLC method for the determination of tofacitinib and to develop the validated method
250 _aVol.14(4), Oct-Dec
260 _aRaipur
_bAsian Pharma Press
_c2024
300 _a207-210p.
520 _aWe have validated a RP HPLC method to accurately quantify Tofacitinib, a pharmaceutical compound. For separation we used a Kromosil C18 column measuring 4.8mm× 150mm with particle size of 5µm. The mobile phase consisted of a mixture of methanol and water in a ratio of 45:55% v/v. throughout the analysis the mobile phase flowed at a rate of 1.0mL/min. we. Quantified Tofacitinib using a UV detector set to monitor absorbance at 254nm. Importantly Tofacitinib retention time, in this system was determined to be 4.35 minutes ensuring efficient analysis. We thoroughly assessed the linearity of the method across concentrations ranging from 15 to 90µg/mL which revealed an exceptional correlation coefficient of 0.999. This high level of linearity demonstrates the methods suitability for quantifying Tofacitinib over a concentration range. Additionally, we achieved a recovery rate for Tofacitinib at 99.24% further validating the accuracy and precision of the method. Significantly this developed method adheres to validation standards outlined in the International Council, for Harmonization (ICH) guidelines confirming its selectivity, precision and accuracy according to prescribed criteria. As a result the suggested RP HPLC technique serves as a sturdy method to conduct regular quality control tests on Tofacitinib in pharmaceutical products. This ensures that the medication maintains a trustworthy dosage, for usage.
650 0 _94639
_aPHARMACEUTICS
700 _926284
_aVijayasri, K.
773 0 _x2231-5667
_dRaipur A & V Publications
_tAsian journal of pharmaceutical analysis
856 _uhttps://ajpaonline.com/AbstractView.aspx?PID=2024-14-4-1
_yClick here
942 _2ddc
_cAR