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 *

182 related articles for article (PubMed ID: 29403903)

  • 21. Study of degradation behavior of besifloxacin, characterization of its degradation products by LC-ESI-QTOF-MS and their in silico toxicity prediction.
    Salunke N; Kharkar PS; Pandita N
    Biomed Chromatogr; 2019 Jun; 33(6):e4489. PubMed ID: 30652327
    [TBL] [Abstract][Full Text] [Related]  

  • 22. High-Performance Liquid Chromatography and Liquid Chromatography/Mass Spectrometry Studies on Stress Degradation Behavior of Sulfapyridine and Development of a Validated, Specific, Stability-Indicating HPLC Assay Method.
    Kapoor B; Gupta R; Gulati M; Singh SK; Khatik GL; Chawla M; Nagappan KV; Khursheed R; Kumar R
    Assay Drug Dev Technol; 2020 Apr; 18(3):119-133. PubMed ID: 32267712
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Validated stability indicating assay method of olaparib: LC-ESI-Q-TOF-MS/MS and NMR studies for characterization of its new hydrolytic and oxidative forced degradation products.
    Thummar M; Kuswah BS; Samanthula G; Bulbake U; Gour J; Khan W
    J Pharm Biomed Anal; 2018 Oct; 160():89-98. PubMed ID: 30075398
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Forced degradation study of baricitinib and structural characterization of its degradation impurities by high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy.
    Chaganti S; Dhiman V; Madhyanapu Golla V; K R R; Khemchandani R; Samanthula G
    Rapid Commun Mass Spectrom; 2023 Sep; 37(18):e9605. PubMed ID: 37580847
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Stress degradation studies and development of a validated stability-indicating-assay-method for determination of diacerein in presence of degradation products.
    Hamrapurkar P; Patil P; Desai M; Phale M; Pawar S
    Pharm Methods; 2011 Jan; 2(1):30-5. PubMed ID: 23781427
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Development and validation of a simple, sensitive, selective and stability-indicating RP-UPLC method for the quantitative determination of ritonavir and its related compounds.
    Koppala S; Panigrahi B; Raju SV; Padmaja Reddy K; Ranga Reddy V; Anireddy JS
    J Chromatogr Sci; 2015; 53(5):662-75. PubMed ID: 25186277
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Isolation and characterization of a degradation product in leflunomide and a validated selective stability-indicating HPLC-UV method for their quantification.
    Saini B; Bansal G
    J Pharm Anal; 2015 Jun; 5(3):207-212. PubMed ID: 29403933
    [TBL] [Abstract][Full Text] [Related]  

  • 28. LC-MS-MS Characterization of Forced Degradation Products of Fidarestat, a Novel Aldose Reductase Inhibitor: Development and Validation of a Stability-Indicating RP-HPLC Method.
    Talluri MV; Khatoon L; Kalariya PD; Chavan BB; Ragampeta S
    J Chromatogr Sci; 2015 Oct; 53(9):1588-96. PubMed ID: 26014964
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Development and validation of a stability-indicating high performance liquid chromatographic assay for determination of cariprazine in bulk form and in drug product.
    Toujani E; Mejri W; Lassoued HE; Toujani S; Fliss O; Cheikh MHB; Safta F
    Ann Pharm Fr; 2023 Jan; 81(1):83-93. PubMed ID: 36037933
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Forced degradation of fingolimod: effect of co-solvent and characterization of degradation products by UHPLC-Q-TOF-MS/MS and 1H NMR.
    Patel PN; Kalariya PD; Gananadhamu S; Srinivas R
    J Pharm Biomed Anal; 2015 Nov; 115():388-94. PubMed ID: 26279369
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Development and validation of stability indicating assay method for mitapivat: Identification of novel hydrolytic, photolytic, and oxidative forced degradation products employing quadrupole-time of flight mass spectrometry.
    Bagul MA; Patil Y; Mane SS; Kunnath Shaji A; Das P; Ranjan OP; Dengale SJ
    J Sep Sci; 2024 Jul; 47(14):e2400173. PubMed ID: 39054589
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Impurity profile of macitentan in tablet dosage form using a stability-indicating high performance liquid chromatography method and forced degradation study].
    Lakka NS; Kuppan C; Rangasamy P
    Se Pu; 2019 Jan; 37(1):100-110. PubMed ID: 30693716
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Characterization of stress degradation products of duloxetine hydrochloride employing LC-UV/PDA and LC-MS/TOF studies.
    Chadha R; Bali A; Bansal G
    J Pharm Biomed Anal; 2016 Mar; 121():39-55. PubMed ID: 26775018
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Selective separation and characterisation of stress degradation products and process impurities of prucalopride succinate by LC-QTOF-MS/MS.
    Mahamuni BS; Jajula A; Awasthi A; Kalariya PD; Talluri MV
    J Pharm Biomed Anal; 2016 Jun; 125():219-28. PubMed ID: 27037978
    [TBL] [Abstract][Full Text] [Related]  

  • 36. HPLC and LC-MS studies on stress degradation behaviour of tinidazole and development of a validated specific stability-indicating HPLC assay method.
    Bakshi M; Singh S
    J Pharm Biomed Anal; 2004 Jan; 34(1):11-8. PubMed ID: 14738914
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Column liquid chromatography-ultraviolet and column liquid chromatography/mass spectrometry evaluation of stress degradation behavior of escitalopram oxalate.
    Dhaneshwar SR; Mahadik MV; Kulkarni MJ
    J AOAC Int; 2009; 92(1):138-47. PubMed ID: 19382571
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Identification of stress degradation products of iloperidone using liquid chromatography coupled with an Orbitrap mass spectrometer.
    Pandeti S; Rout TK; Tadigoppula N; Thota JR
    Rapid Commun Mass Spectrom; 2017 Aug; 31(16):1324-1332. PubMed ID: 28556266
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification and characterization of stress degradation products of dronedarone hydrochloride employing LC-UV/PDA, LC-MS/TOF and MS(n) studies.
    Chadha R; Bali A; Bansal G
    J Pharm Biomed Anal; 2016 Jan; 118():139-148. PubMed ID: 26547261
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.