BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 21370250)

  • 21. Determination and characterization of degradation products of anastrozole by LC-MS/MS and NMR spectroscopy.
    Sitaram C; Rupakula R; Reddy BN
    J Pharm Biomed Anal; 2011 Dec; 56(5):962-8. PubMed ID: 21890298
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Stability Indicating Method Development and Validation for Separation of Process Related Impurities and Characterization of Unknown Impurities of Tyrosine Kinase Inhibitor Ibrutinib Using QbD Approach by RP-HPLC, NMR Spectroscopy and ESI-MS.
    Gopireddy RR; Maruthapillai A; Mahapatra S
    J Chromatogr Sci; 2021 Sep; 59(9):830-846. PubMed ID: 33420506
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Development and validation of a stability-indicating RP-HPL C-CAD method for gabapentin and its related impurities in presence of degradation products.
    Ragham PK; Chandrasekhar KB
    J Pharm Biomed Anal; 2016 Jun; 125():122-9. PubMed ID: 27018505
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Characterization of forced degradation products of ketorolac tromethamine using LC/ESI/Q/TOF/MS/MS and in silico toxicity prediction.
    Kalariya PD; Raju B; Borkar RM; Namdev D; Gananadhamu S; Nandekar PP; Sangamwar AT; Srinivas R
    J Mass Spectrom; 2014 May; 49(5):380-91. PubMed ID: 24809899
    [TBL] [Abstract][Full Text] [Related]  

  • 25. LC and LC-MS study of stress decomposition behaviour of isoniazid and establishment of validated stability-indicating assay method.
    Bhutani H; Singh S; Vir S; Bhutani KK; Kumar R; Chakraborti AK; Jindal KC
    J Pharm Biomed Anal; 2007 Mar; 43(4):1213-20. PubMed ID: 17118610
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Forced degradation and impurity profiling: recent trends in analytical perspectives.
    Jain D; Basniwal PK
    J Pharm Biomed Anal; 2013 Dec; 86():11-35. PubMed ID: 23969330
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Isolation and characterization of process related impurities and degradation products of bicalutamide and development of RP-HPLC method for impurity profile study.
    Nageswara Rao R; Narasa Raju A; Narsimha R
    J Pharm Biomed Anal; 2008 Feb; 46(3):505-19. PubMed ID: 18162355
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. LC-MS/MS method for the characterization of the forced degradation products of Entecavir.
    Ramesh T; Rao PN; Rao RN
    J Sep Sci; 2014 Feb; 37(4):368-75. PubMed ID: 24323372
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Study of forced degradation behaviour of florfenicol by LC and LC-MS and development of a validated stability-indicating assay method.
    Mistiri F; Louati K; Grissa O; Kallel M; Safta F
    Ann Pharm Fr; 2012 Nov; 70(6):333-47. PubMed ID: 23177560
    [TBL] [Abstract][Full Text] [Related]  

  • 31. RP-HPLC separation and characterization of unknown impurities of a novel HIV-protease inhibitor Darunavir by ESI-MS and 2D NMR spectroscopy.
    Nageswara Rao R; Ramachandra B; Santhakumar K
    J Pharm Biomed Anal; 2013 Mar; 75():186-91. PubMed ID: 23266664
    [TBL] [Abstract][Full Text] [Related]  

  • 32. LC-MS/MS characterization of forced degradation products of zofenopril.
    Ramesh T; Nageswara Rao P; Nageswara Rao R
    J Pharm Biomed Anal; 2014 Jan; 88():609-16. PubMed ID: 24211724
    [TBL] [Abstract][Full Text] [Related]  

  • 33. LC-MS/MS structural characterization of stress degradation products including the development of a stability indicating assay of Darunavir: An anti-HIV drug.
    Rao RN; Ramachandra B; Sravan B; Khalid S
    J Pharm Biomed Anal; 2014 Feb; 89():28-33. PubMed ID: 24252722
    [TBL] [Abstract][Full Text] [Related]  

  • 34. HPLC method for the determination of emtricitabine and related degradation substances.
    Hamarapurkar PD; Parate AN
    J Chromatogr Sci; 2013; 51(5):419-24. PubMed ID: 23051064
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Development and validation of a stability-indicating RP-HPLC method for the simultaneous estimation of process related impurities and degradation products of rasagiline mesylate in pharmaceutical formulation.
    Reddy PS; Sudhakar Babu K; Kumar N
    J Chromatogr Sci; 2013 Mar; 51(3):242-9. PubMed ID: 22988002
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Reverse phase-HPLC and HPTLC methods for determination of gemifloxacin mesylate in human plasma.
    Rote AR; Pingle SP
    J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Nov; 877(29):3719-23. PubMed ID: 19716354
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification and characterization of stressed degradation products of prulifloxacin using LC-ESI-MS/Q-TOF, MSn experiments: development of a validated specific stability-indicating LC-MS method.
    Raju B; Ramesh M; Srinivas R; Raju SS; Venkateswarlu Y
    J Pharm Biomed Anal; 2011 Nov; 56(3):560-8. PubMed ID: 21783336
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Development of a Forced Degradation Profile of Alosetron by Single Mode Reversed-Phase HPLC, LC-MS, and its Validation.
    Karthik Y; Babu B; Meyyanathan SN
    Sci Pharm; 2015; 83(2):311-20. PubMed ID: 26839817
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Development and Validation of a Stability-Indicating RP-HPLC Method for the Quantitative Analysis of Anagrelide Hydrochloride.
    Pujeri SS; Khader AM; Seetharamappa J
    Sci Pharm; 2012; 80(3):567-79. PubMed ID: 23008806
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification and Characterization of an Oxidative Degradation Product of Fexofenadine, Development and Validation of a Stability-Indicating RP-UPLC Method for the Estimation of Process Related Impurities and Degradation Products of Fexofenadine in Pharmaceutical Formulations.
    Vaghela B; Rao SS; Reddy AM; Venkatesh P; Kumar N
    Sci Pharm; 2012; 80(2):295-309. PubMed ID: 22896817
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.