153 related articles for article (PubMed ID: 34523747)
1. Determination of progesterone (steroid drug) in the semi-solid dosage form (vaginal gel) using a stability-indicating method by RP-HPLC/PDA detector.
Konduru N; Kethe VB; Gundla R; Katari NK; Mallavarapu R
Biomed Chromatogr; 2022 Jan; 36(1):e5246. PubMed ID: 34523747
[TBL] [Abstract][Full Text] [Related]
2. Favipiravir (SARS-CoV-2) degradation impurities: Identification and route of degradation mechanism in the finished solid dosage form using LC/LC-MS method.
Vemuri DK; Gundla R; Konduru N; Mallavarapu R; Katari NK
Biomed Chromatogr; 2022 Jun; 36(6):e5363. PubMed ID: 35292997
[TBL] [Abstract][Full Text] [Related]
3. A validated stability-indicating reversed-phase-HPLC method for dipyridamole in the presence of degradation products and its process-related impurities in pharmaceutical dosage forms.
Mallavarapu R; Katari NK; Dongala T; Rekulapally VK; Marisetti VM; Vyas G
Biomed Chromatogr; 2022 Jan; 36(1):e5247. PubMed ID: 34541698
[TBL] [Abstract][Full Text] [Related]
4. Determination of stress-induced degradation products of cetirizine dihydrochloride by a stability-indicating RP-HPLC method.
Flórez Borges P; Pérez Lozano P; García Montoya E; Miñarro M; Ticó JR; Jo E; Suñe Negre JM
Daru; 2014 Dec; 22(1):82. PubMed ID: 25487685
[TBL] [Abstract][Full Text] [Related]
5. UPLC and LC-MS studies on degradation behavior of irinotecan hydrochloride and development of a validated stability-indicating ultra-performance liquid chromatographic method for determination of irinotecan hydrochloride and its impurities in pharmaceutical dosage forms.
Kumar N; Sangeetha D; Reddy SP
J Chromatogr Sci; 2012 Oct; 50(9):810-9. PubMed ID: 22661461
[TBL] [Abstract][Full Text] [Related]
6. A rapid RP-HPLC stability-indicating method development and validation of moxifloxacin hydrochloride-related substances in finished dosage forms.
Vankalapati KR; Algete P; Boodida S
Biomed Chromatogr; 2021 Nov; 35(11):e5192. PubMed ID: 34110029
[TBL] [Abstract][Full Text] [Related]
7. Development and validation of apalutamide-related substances method in solid dosage forms using HPLC.
Bandaru LGR; Konduru N; Kowtharapu LP; Regulagadda S; Kanuparthy PR; Gundla R
Biomed Chromatogr; 2023 Apr; 37(4):e5576. PubMed ID: 36573285
[TBL] [Abstract][Full Text] [Related]
8. Development and validation of novel RP-HPLC method for midostaurin determination using analytical quality by design approach from regulatory perspective and determination of major degradation compounds of midostaurin using LC-MS.
Reddy Saddala MP; Konduru N; Gundla R; Kowtharapu LP
Biomed Chromatogr; 2022 Dec; 36(12):e5486. PubMed ID: 36001450
[TBL] [Abstract][Full Text] [Related]
9. Development and validation of a stability-indicating UPLC method for the determination of olmesartan medoxomil, amlodipine and hydrochlorothiazide degradation impurities in their triple-combination dosage form using factorial design of experiments.
Marisetti VM; Katakam P; Siddhani VK; Katari NK
Biomed Chromatogr; 2021 Nov; 35(11):e5194. PubMed ID: 34110035
[TBL] [Abstract][Full Text] [Related]
10. A simple isocratic LC method for quantification of trace-level inorganic degradation impurities (ferricyanide, ferrocyanide, nitrite, and nitrate) in sodium nitroprusside injection and robustness by quality using design approach.
Yenda P; Katari NK; Dongala T; Vyas G; Katakam LNR; Ettaboina SK
Biomed Chromatogr; 2022 Feb; 36(2):e5269. PubMed ID: 34693546
[TBL] [Abstract][Full Text] [Related]
11. Unique Quality by Design Approach for Developing HPLC and LC-MS Method for Estimation of Process and Degradation Impurities in Pibrentasvir, Antiviral Agent for Hepatitis C.
Vemuri DK; Akshinthala P; Konduru N; Kowtharapu LP; Katari NK; Jonnalagadda SB; Gundla R
ACS Omega; 2022 Dec; 7(51):47650-47661. PubMed ID: 36591161
[TBL] [Abstract][Full Text] [Related]
12. An Eco-Friendly RP-HPLC Method Development and Validation for Quantification of Favipiravir in Bulk and Tablet Dosage Form Followed by Forced Degradation Study.
Sangani MB; Patel N
J Chromatogr Sci; 2024 May; 62(5):432-438. PubMed ID: 38266038
[TBL] [Abstract][Full Text] [Related]
13. A validated stability-indicating liquid chromatographic method for the determination of retapamulin in topical dosage form.
Nalwade S; Reddy VR
J Chromatogr Sci; 2014 Mar; 52(3):238-45. PubMed ID: 23510782
[TBL] [Abstract][Full Text] [Related]
14. A Stability-Indicating UPLC Method for the Determination of Potential Impurities and Its Mass by a New QDa Mass Detector in Daclatasvir Drug Used to Treat Hepatitis C Infection.
Jagadabi V; Nagendra Kumar PV; Mahesh K; Pamidi S; Ramaprasad LA; Nagaraju D
J Chromatogr Sci; 2019 Jan; 57(1):44-53. PubMed ID: 30169761
[TBL] [Abstract][Full Text] [Related]
15. A stability-indicating, reversed-phase HPLC method for quantification of assay and organic impurities in doxycycline hyclate bulk and parenteral dosage forms.
Pippalla S; Nekkalapudi AR; Jillellamudi SB; Reddy MP; Kumar CV
Biomed Chromatogr; 2023 Jun; 37(6):e5626. PubMed ID: 36930874
[TBL] [Abstract][Full Text] [Related]
16. A simple and rapid HPLC method for determination of parabens and their degradation products in pharmaceutical dosage forms.
Katakam LNR; Ettaboina SK; Dongala T
Biomed Chromatogr; 2021 Oct; 35(10):e5152. PubMed ID: 33931875
[TBL] [Abstract][Full Text] [Related]
17. Stability-indicating RP-HPLC method development and validation for determination of nine impurities in apixaban tablet dosage forms. Robustness study by quality by design approach.
Subramanian VB; Katari NK; Dongala T; Jonnalagadda SB
Biomed Chromatogr; 2020 Jan; 34(1):e4719. PubMed ID: 31634417
[TBL] [Abstract][Full Text] [Related]
18. Development and validation of a stability-indicating column high-performance liquid chromatographic assay method for determination of nebivolol in tablet formulation.
Kachhadia PK; Doshi AS; Joshi HS
J AOAC Int; 2008; 91(3):557-61. PubMed ID: 18567301
[TBL] [Abstract][Full Text] [Related]
19. RP-HPLC stability-indicating assay method for talinolol and characterization of its degradation products.
Sinha VR; Ghai D
J Chromatogr Sci; 2011; 49(10):786-95. PubMed ID: 22080807
[TBL] [Abstract][Full Text] [Related]
20. Development and validation of a stability indicating RP-HPLC method for the simultaneous determination of related substances of albuterol sulfate and ipratropium bromide in nasal solution.
Kasawar GB; Farooqui M
J Pharm Biomed Anal; 2010 May; 52(1):19-29. PubMed ID: 20045275
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
