127 related articles for article (PubMed ID: 35831974)
1. Unique liquid chromatography technique for the determination of mirabegron in the presence of polymers; robustness by Design Expert in the light of Quality by Design.
Konduru N; Kowtharapu LP; Gundla R
Biomed Chromatogr; 2022 Oct; 36(10):e5449. PubMed ID: 35831974
[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. 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]
4. 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]
5. Development and validation of stability indicating RP-HPLC method for simultaneous estimation of silodosin and mirabegron in synthetic mixture.
Mishra S; Surekha N; Chauhan A
Ann Pharm Fr; 2024 Mar; 82(2):243-262. PubMed ID: 38163458
[TBL] [Abstract][Full Text] [Related]
6. A combined qualitative and quantitative method development and validation of vancomycin hydrochloride injection formulation by HPLC and UV involving quality by design.
Sasikala L; Koteswara Rao V; Katari NK; Kowtharapu LP
Biomed Chromatogr; 2023 Mar; 37(3):e5568. PubMed ID: 36517962
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Unique green chromatography method for the determination of serotonin receptor antagonist (Ondansetron hydrochloride) related substances in a liquid formulation, robustness by quality by design-based design of experiments approach.
Kowtharapu LP; Katari NK; Sandoval CA; Muchakayala SK; Rekulapally VK
J Sep Sci; 2022 May; 45(10):1711-1726. PubMed ID: 35279949
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Development and validation of a stability-indicating RP-HPLC method for the determination of febuxostat (a xanthine oxidase inhibitor).
Mukthinuthalapati MA; Bandaru SP; Bukkapatnam V; Mohapatro C
J Chromatogr Sci; 2013; 51(10):931-8. PubMed ID: 23204011
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. An analytical quality by design approach towards a simple and novel HPLC-UV method for quantification of the antifibrotic peptide N-acetyl-seryl-aspartyl-lysyl-proline.
Ho HMK; Sembi S; Abukhamees S; Day RM; Craig DQM
Anal Biochem; 2022 Oct; 654():114793. PubMed ID: 35750251
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. User-Friendly HPLC Method Development and Validation for Determination of Enalapril Maleate and Its Impurities in Enalapril Tablets.
Koppala S; Ranga Reddy V; Anireddy JS
J Chromatogr Sci; 2017 Nov; 55(10):979-988. PubMed ID: 28985272
[TBL] [Abstract][Full Text] [Related]
17. Stability-indicating HPLC method development and validation of rivaroxaban impurities and identification of forced degradation products using LC-MS/MS.
Cholleti V; Ravindra Kumar Y; Pasula A; Surya PRP
Biomed Chromatogr; 2022 Sep; 36(9):e5424. PubMed ID: 35697473
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Using an innovative Quality-by-Design approach for development of a stability indicating UHPLC method for ebastine in the API and pharmaceutical formulations.
Schmidt AH; Molnár I
J Pharm Biomed Anal; 2013 May; 78-79():65-74. PubMed ID: 23454599
[TBL] [Abstract][Full Text] [Related]
20. Development of a validated liquid chromatographic method for quantification of sorafenib tosylate in the presence of stress-induced degradation products and in biological matrix employing analytical quality by design approach.
Sharma T; Khurana RK; Jain A; Katare OP; Singh B
Biomed Chromatogr; 2018 May; 32(5):e4169. PubMed ID: 29244215
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
