Quality by design tool–evaluated stability‐indicating ultra‐performance liquid chromatography method for the determination of drugs (ritonavir and darunavir) used to treat the human immunodeficiency virus/acquired immunodeficiency syndromeJyothsna Menda, Surya Prakash Rao Pydimarry, Santhosh Kumar Ettaboina et al.|Biomedical Chromatography|2023Cited by 13
Development and validation of apalutamide‐related substances method in solid dosage forms using HPLCLova Gani Raju Bandaru, Rambabu Gundla, Phani Raja Kanuparthy et al.|Biomedical Chromatography|2022Cited by 12
Quality by Design Tool Assessed Ultraperformance Liquid Chromatography Method for the Analysis of Remogliflozin and Teneligliptin in Oral Dosage FormJyothsna Menda, Sreekantha B. Jonnalagadda, Vaishnavi Chintala et al.|ACS Omega|2024Cited by 11
Unique Research for Developing a Full Factorial Design Evaluated Liquid Chromatography Technique for Estimating Budesonide and Formoterol Fumarate Dihydrate in the Presence of Specified and Degradation Impurities in Dry Powder InhalationLova Gani Raju Bandaru, Naresh Kumar Katari, Naresh Konduru et al.|Biomedical Chromatography|2025Cited by 10
Quality by design tool evaluated green stability-indicating UPLC content determination method for the Olanzapine and Samidorphan dosage formJyothsna Menda, Naresh Kumar Katari, Surya Prakash Rao Pydimarry et al.|Microchemical Journal|2023Cited by 9