These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 35686891)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. QbD-based stability-indicating liquid chromatography (RP-HPLC) method for the determination of flurbiprofen in cataplasm.
    Nathi R; Kowtharapu LP; Muchakayala SK; Konduru N
    Biomed Chromatogr; 2023 Apr; 37(4):e5580. PubMed ID: 36609857
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 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. Stability-Indicating RP-HPLC Method Development and Validation for Eltrombopag Olamine in the Presence of Impurities and Degradation Products. Robustness by Design of Expert Software.
    Dandabattina R; Subramanian VB; Merugu KS; SharathBabu H; Katari NK; Kowtharapu LP
    J AOAC Int; 2023 Mar; 106(2):267-275. PubMed ID: 36416121
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evaluation of analytical greenness metric for an eco-friendly method developed through the integration of green chemistry and quality-by-design for the simultaneous determination of Nebivolol hydrochloride, Telmisartan, Valsartan, and Amlodipine besylate.
    Veerendra YVS; Brahman PK; Mankumare SD; Ch J; C VK
    Heliyon; 2024 Aug; 10(16):e35376. PubMed ID: 39220975
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Quantification of Drospirenone- and Ethinyl Estradiol-Related Impurities in a Combined Pharmaceutical Dosage Form by a Chromatography Method With a QbD Robustness Study.
    Chinta SR; Chintala V; Nandimalla V; Ch R; Ediga SG; Kowtharapu LP; Katari NK
    J AOAC Int; 2024 Jan; 107(1):31-39. PubMed ID: 37758265
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Development and Validation of Stability-Indicating Impurity Profiling Method for Azelastine Hydrochloride and Fluticasone Propionate in Nasal Spray Product Using HPLC with a UV/PDA Detector.
    Musmade B; Korhale R; Sable M; Lokhande S; Padmanabhan S; Bhope S
    J AOAC Int; 2023 Jul; 106(4):866-872. PubMed ID: 36929921
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exquisite integration of quality-by-design and green analytical approaches for simultaneous determination of xylometazoline and antazoline in eye drops and rabbit aqueous humor, application to stability study.
    Hussein OG; Ahmed DA; Rezk MR; Abdelkawy M; Rostom Y
    J Pharm Biomed Anal; 2023 Oct; 235():115598. PubMed ID: 37516064
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Impurity assessment, development and validation of an RP-HPLC method for the determination of eleven potential impurities of eltrombopag precursor.
    Demirhan T; Guksu E; Yazar Y; Keskin E; Bellur Atici E; Özkan SA
    J Pharm Biomed Anal; 2024 Jun; 243():116085. PubMed ID: 38471254
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Validation of a high-performance liquid chromatographic method for the simultaneous determination of tramadol and its impurities in oral drops as a pharmaceutical formulation.
    Zecević M; Stanković Z; Zivanović Lj; Jocić B
    J Chromatogr A; 2006 Jun; 1119(1-2):251-6. PubMed ID: 16386751
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.