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Asian Journal of Pharmaceutical Analysis
Year : 2022, Volume : 12, Issue : 3
First page : ( 166) Last page : ( 172)
Print ISSN : 2231-5667. Online ISSN : 2231-5675.
Article DOI : 10.52711/2231-5675.2022.00028

Analytical method development and validation of teriflunomide active pharmaceutical ingredient by RP-UHPLC

Kashid Arun Maruti1,*, Polshettiwar Pranali Prakash2, Bhosale Kshitija Maruti2

1Department of Pharmaceutical Chemistry, Sinhgad Institute of Pharmacy, Narhe, Pune, Maharashtra, India - 41

2Department of Pharmaceutical Quality Assurance, Sinhgad Institute of Pharmacy, Narhe, Pune, Maharashtra, India - 41

*Corresponding Author E-mail: arunkashid2006@gmail.com

Online published on 22 February, 2023.

Abstract

Drug analysis is crucial in the discovery, production, and therapeutic use of pharmaceuticals. Standard analytical procedures for newer medications or formulations may not be available in Pharmacopoeias; thus, newer analytical methods that are accurate, precise, specific, linear, simple, and rapid must be developed. A rapid, simple, sensitive, precise, and cost-effective RP-UHPLC method was developed and validated for the determination of Teriflunomide Active Pharmaceutical Ingredient (API) in this study. The method involved determination of Teriflunomide by resolving on RP-UHPLC using Sunniest C18 (250mm × 4.6mm, 5μm) column, utilizing a mobile phase of ACN: Water in the ratio of 60:40 v/v. The mobile phase was delivered with an isocratic flow rate of 1.0ml/minute. Ultra violet detection was carried out at 210nm. The retention time was optimized to 4. 4 minutes. The linearity range of Teriflunomide 35 to 247μg/ml was found to obey linearity with a correlation coefficient of 0.999. The LOD and LOQ were found to be 1.61μg/ml and 4.90μg/ml respectively and precision data was found to be <2 %RSD. The percentage recovery range was found to be satisfied which is represented in the results. The robustness studies were performed by changing the flow rate and mobile phase compositions. The method was validated for system suitability, specificity, linearity, precision, accuracy, Limit of Detection, Limit of Quantification and robustness. The developed method can be applied for the quality control of commercial teriflunomide API.

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Keywords

Teriflunomide, Method development, UPLC, Validation, ICH guidelines.

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