| QbD based development of HPLC method for simultaneous quantification of Telmisartan and Hydrochlorothiazide impurities in tablets dosage form AK Palakurthi, T Dongala, LNR Katakam Practical Laboratory Medicine 21, e00169, 2020 | 38 | 2020 |
| Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines T Dongala, NK Katari, AK Palakurthi, SB Jonnalagadda Biomedical Chromatography 33 (11), e4641, 2019 | 31 | 2019 |
| Simultaneous determination of related organic impurities of ibuprofen and paracetamol in combination solid dosage form by Rp‐Hplc with Qbd approach PA Kumar, D Thirupathi, YR Kumar, A Jayashree Oriental Journal of Chemistry 33 (3), 1461-1468, 2017 | 27 | 2017 |
| Stability‐indicating HPLC method for simultaneous quantification of 14 impurities in excedrin tablet formulations and identification of new impurity by LC–MS in accelerated … T Dongala, NK Katari, AK Palakurthi, SB Jonnalagadda Biomedical Chromatography 33 (10), e4608, 2019 | 26 | 2019 |
| RP-HPLC stability indicating method development and validation of pseudoephedrine sulfate and related organic impurities in tablet dosage forms, robustness by QbD approach T Dongala, LNR Katakam, AK Palakurthi, NK Katari Analytical Chemistry Letters 9 (5), 697-710, 2019 | 24 | 2019 |
| A novel UPLC-PDA isocratic method for the quantification fulvestrant in oil-based pre-filled syringe injection matrix formulations T Dongala, AK Palakurthi, Y Vytla, NK Katari Journal of Analytical Science and Technology 10, 1-12, 2019 | 22 | 2019 |
| Stability indicating LC method development for hydroxychloroquine sulfate impurities as available for treatment of COVID-19 and evaluation of risk assessment prior to method … T Dongala, NK Katari, AK Palakurthi, LNR Katakam, VM Marisetti Chromatographia 83 (10), 1269-1281, 2020 | 21 | 2020 |
| Development and validation of a stability-indicating LC-method for the simultaneous estimation of levodropropizine, chloropheniramine, methylparaben, propylparaben, and … PA Kumar, TVR Raju, D Thirupathi, R Kumar, J Shree Scientia Pharmaceutica 81 (1), 139-150, 2013 | 19 | 2013 |
| QbD‐based development of an extraction procedure for simultaneous quantification of telmisartan, amlodipine besylate and chlorthalidone in combination complex matrix formulation AK Palakurthi, T Dongala, RK Yalavarthi, J Anireddy Biomedical chromatography 34 (2), e4755, 2020 | 14 | 2020 |
| HPLC-UV method development for the determination of EDTA in oxycodone HCl oral liquids with derivatization technique. Robustness by design of experiments approach AK Palakurthi, T Dongala Analytical Chemistry Letters 9 (5), 594-607, 2019 | 12 | 2019 |
| Development and validation of RP-HPLC method for simultaneous determination of diclofenac potassium and its process related impurities in solid Oral dosage form T Dongala, AK Palakurthi, KK Velaveni, NK Katari J Chromatogr Sep Tech 9 (412), 2, 2018 | 12 | 2018 |
| Development and validation of liquid chromatography–tandem mass spectrometry method for the estimation of a potential genotoxic impurity 2‐(2‐chloroethoxy) ethanol in hydroxyzine NS Lakka, C Kuppan, P Ravinathan, AK Palakurthi Biomedical Chromatography 36 (5), e5325, 2022 | 11 | 2022 |
| Stability-indicating LC method for the simultaneous determination of methyl paraben, propyl paraben, butylated hydroxytoluene and alpha-tocopherol contents in marijuana capsules T Dongala, AK Palakurthi Journal of the Iranian Chemical Society 17, 631-638, 2020 | 9 | 2020 |
| Stability‐indicating liquid chromatography method development and validation for impurity profiling of montelukast sodium in bulk drug and tablet dosage form M Pasham, SB Haridasyam, NP Boppy, M Venkatanarayana, ... Biomedical Chromatography 36 (4), e5330, 2022 | 6 | 2022 |
| DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING RP-HPLC METHOD FOR THE ESTIMATION OF ERLOTINIB IMPURITIES BY QbD APPROACH PA Kumar, YR Kumar, A Jayashree RASAYAN J Chemistry 9 (2), 180-188, 2016 | 5 | 2016 |
| A RP-HPLC method development and validation for the estimation of febuxostat in bulk and pharmaceutical dosage forms RS Kumar, BR Kumar, PA Kumar International research journal of pharmacy 3, 205-208, 2012 | 5 | 2012 |
| Quantification of SSRR impurity of orlistat in orlistat capsules by normal phase HPLC UV detector AK Palakurthi, RB Vinta Int Res J Pharm 3, 350-5, 2012 | 4 | 2012 |
| Estimation of ramipril and telmisartan in human plasma by LC–MS/MS: Application in pharmacokinetic study AK Palakurthi, T Dongala, SSR Yadlapalli Separation Science Plus 3 (6), 191-199, 2020 | 2 | 2020 |
| Simultaneous Estimation of Acetaminophen, Chlorpheniramine Maleate, Methyl Paraben, Propyl Paraben, Sodium Benzoate and Related Impurities in Over-the-Counter Syrup Formulation AK Palakurthi, T Dongala Pharmaceutical Chemistry Journal 56 (3), 421-427, 2022 | 1 | 2022 |
Dr.Naresh Kumar KatariGITAM deemed to be University HyderabadVerified email at gitam.edu
Dr.Naresh Kumar KatariGITAM deemed to be University HyderabadVerified email at gitam.edu