BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 35279949)

  • 1. 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]  

  • 2. Green Liquid Chromatography Method for the Determination of Related Substances Present in Olopatadine HCl Nasal Spray Formulation, Robustness by Design Expert.
    Kowtharapu LP; Katari NK; Sandoval CA; Muchakayala SK; Rekulapally VK
    J AOAC Int; 2022 Sep; 105(5):1247-1257. PubMed ID: 35686891
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Quality by Design and green LC technique for the determination of mast cell stabilizer and histamine receptor antagonist (Olopatadine HCl) in multiple formulations.
    Kowtharapu LP; Katari NK; Ch S; Sandoval CA; Muchakayala SK; Konduru N
    Biomed Chromatogr; 2022 Jun; 36(6):e5359. PubMed ID: 35203103
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Eco-Friendly Stability-Indicating HPLC Method for Related Compounds in Pemetrexed Ditromethamine (Antineoplastic Agent) for Injection.
    Nekkalapudi AR; Navuluri S; Pippalla S
    J AOAC Int; 2024 May; 107(3):415-429. PubMed ID: 38310337
    [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. 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]  

  • 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. Green Chromatographic Method for Determination of Active Pharmaceutical Ingredient, Preservative, and Antioxidant in an Injectable Formulation: Robustness by Design Expert.
    Kowtharapu LP; Katari NK; Sandoval CA; Rekulapally VK; Jonnalagadda SB
    ACS Omega; 2022 Sep; 7(38):34098-34108. PubMed ID: 36188248
    [TBL] [Abstract][Full Text] [Related]  

  • 9. AQbD based green UPLC method to determine mycophenolate mofetil impurities and Identification of degradation products by QToF LCMS.
    Muchakayala SK; Katari NK; Saripella KK; Schaaf H; Marisetti VM; Kowtharapu LP; Jonnalagadda SB
    Sci Rep; 2022 Nov; 12(1):19138. PubMed ID: 36352016
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel and rapid validated stability-indicating UPLC method of related substances for dorzolamide hydrochloride and timolol maleate in ophthalmic dosage form.
    Sharma N; Rao SS; Reddy AM
    J Chromatogr Sci; 2012 Oct; 50(9):745-55. PubMed ID: 22562819
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A quality-by-design evaluated liquid chromatography method development and validation for the separation and quantification of nitroxoline and its impurities.
    Lankalapalli SP; Rachel KV; Chintala V; Kowtharapu LP; Katari NK
    J Sep Sci; 2024 Jan; 47(1):e2300760. PubMed ID: 38135885
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Implementation of analytical quality by design and green chemistry principles to develop an ultra-high performance liquid chromatography method for the determination of Fluocinolone Acetonide impurities from its drug substance and topical oil formulations.
    Muchakayala SK; Katari NK; Saripella KK; Schaaf H; Marisetti VM; Ettaboina SK; Rekulapally VK
    J Chromatogr A; 2022 Aug; 1679():463380. PubMed ID: 35970050
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Simultaneous determination of benzydamine hydrochloride and five impurities in an oral collutory as a pharmaceutical formulation by high-performance liquid chromatography.
    Carlucci G; Iuliani P; Di Federico L
    J Chromatogr Sci; 2010 Nov; 48(10):854-9. PubMed ID: 21044418
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Stability-indicating reversed-phase-HPLC method development and validation for sacubitril/valsartan complex in the presence of impurities and degradation products: Robustness by quality-by-design approach.
    Subramanian VB; Katari NK; Ponnam V; Konduru N; Dongala T; Marisetti VM; Vyas G
    Biomed Chromatogr; 2022 Jan; 36(1):e5240. PubMed ID: 34486750
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Quality by design with design of experiments approach for development of a stability-indicating LC method for enzalutamide and its impurities in soft gel dosage formulation.
    Katakam LNR; Dongala T; Ettaboina SK
    Biomed Chromatogr; 2021 May; 35(5):e5062. PubMed ID: 33410554
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analytical method development and validation for the analysis of verapamil hydrochloride and its related substances by using ultra perfomance liquid chromatography.
    Vijayabaskar S; Mahalingam V; Kalaivani
    J Pharm Biomed Anal; 2017 Apr; 137():189-195. PubMed ID: 28131058
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New gradient high-performance liquid chromatography method for determination of donepezil hydrochloride assay and impurities content in oral pharmaceutical formulation.
    Kafkala S; Matthaiou S; Alexaki P; Abatzis M; Bartzeliotis A; Katsiabani M
    J Chromatogr A; 2008 May; 1189(1-2):392-7. PubMed ID: 18206895
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Development, stability-indicating assessment, and evaluation of influential method conditions using a full factorial design for the determination of Nintedanib esylate-related impurities.
    Yenda P; Katari NK; Satheesh B; Gundla R; Muchakayala SK; Rekulapally VK
    J Sep Sci; 2023 Jun; 46(11):e2200770. PubMed ID: 36976154
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.