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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

661 related items for PubMed ID: 19111423

  • 1. Development and validation of an anion-exchange LC-UV method for the quantification and purity determination of the DNA plasmid pDERMATT.
    Quaak SG, Nuijen B, Haanen JB, Beijnen JH.
    J Pharm Biomed Anal; 2009 Feb 20; 49(2):282-8. PubMed ID: 19111423
    [Abstract] [Full Text] [Related]

  • 2. Development and validation of an LC-UV method for the quantification and purity determination of the novel anticancer agent C1311 and its pharmaceutical dosage form.
    den Brok MW, Nuijen B, Hillebrand MJ, Grieshaber CK, Harvey MD, Beijnen JH.
    J Pharm Biomed Anal; 2005 Sep 01; 39(1-2):46-53. PubMed ID: 15899571
    [Abstract] [Full Text] [Related]

  • 3. GMP production of pDERMATT for vaccination against melanoma in a phase I clinical trial.
    Quaak SG, van den Berg JH, Toebes M, Schumacher TN, Haanen JB, Beijnen JH, Nuijen B.
    Eur J Pharm Biopharm; 2008 Oct 01; 70(2):429-38. PubMed ID: 18606527
    [Abstract] [Full Text] [Related]

  • 4. LC-UV method development and validation for the investigational anticancer agent imexon and identification of its degradation products.
    den Brok MW, Nuijen B, Hillebrand MJ, Lutz C, Opitz HG, Beijnen JH.
    J Pharm Biomed Anal; 2005 Jul 15; 38(4):686-94. PubMed ID: 15967296
    [Abstract] [Full Text] [Related]

  • 5. Validation of a HPLC method for the quantification and purity determination of SK3530 in drug substance and tablet.
    Oh JG, Jang WJ, Chi SC.
    J Pharm Biomed Anal; 2007 Feb 19; 43(3):1179-84. PubMed ID: 17134866
    [Abstract] [Full Text] [Related]

  • 6. Long term stability of lyophilized plasmid DNA pDERMATT.
    van der Heijden I, Beijnen JH, Nuijen B.
    Int J Pharm; 2013 Sep 10; 453(2):648-50. PubMed ID: 23792100
    [Abstract] [Full Text] [Related]

  • 7. Development and validation of a stability-indicating high performance liquid chromatographic (HPLC) assay for biperiden in bulk form and pharmaceutical dosage forms.
    Mohammadi A, Mehramizi A, Moghaddam FA, Jabarian LE, Pourfarzib M, Kashani HN.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Jul 01; 854(1-2):152-7. PubMed ID: 17466605
    [Abstract] [Full Text] [Related]

  • 8. Determination of piperazine in pharmaceutical drug substances using capillary electrophoresis with indirect UV detection.
    Denis CM, Baryla NE.
    J Chromatogr A; 2006 Mar 31; 1110(1-2):268-71. PubMed ID: 16504199
    [Abstract] [Full Text] [Related]

  • 9. A validated stability-indicating normal phase LC method for clopidogrel bisulfate and its impurities in bulk drug and pharmaceutical dosage form.
    Durga Rao D, Kalyanaraman L, Sait SS, Venkata Rao P.
    J Pharm Biomed Anal; 2010 May 01; 52(1):160-5. PubMed ID: 20074888
    [Abstract] [Full Text] [Related]

  • 10. A chromatographic method for determination of supercoiled plasmid DNA concentration in complex solutions.
    Bennemo M, Blom H, Emilsson A, Lemmens R.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Aug 15; 877(24):2530-6. PubMed ID: 19616488
    [Abstract] [Full Text] [Related]

  • 11. A novel validated LC method for quantitation of lopinavir in bulk drug and pharmaceutical formulation in the presence of its potential impurities and degradation products.
    Seshachalam U, Haribabu B, Chandrasekhar K.
    Biomed Chromatogr; 2007 Jul 15; 21(7):716-23. PubMed ID: 17370253
    [Abstract] [Full Text] [Related]

  • 12. Stability-indicating UPLC method for determination of Valsartan and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms.
    Krishnaiah Ch, Reddy AR, Kumar R, Mukkanti K.
    J Pharm Biomed Anal; 2010 Nov 02; 53(3):483-9. PubMed ID: 20646890
    [Abstract] [Full Text] [Related]

  • 13. Development and validation of a stability-indicating HPLC-UV method for the determination of alizapride and its degradation products.
    Tamaro I, Aprile S, Giovenzana GB, Grosa G.
    J Pharm Biomed Anal; 2010 Apr 06; 51(5):1024-31. PubMed ID: 19962264
    [Abstract] [Full Text] [Related]

  • 14. Development and validation of a capillary electrophoresis method for the determination of sulfate in effervescent tablets.
    Sung HH, Laborde-Kummer E, Gaudin K, Dubost JP.
    Eur J Pharm Biopharm; 2006 Aug 06; 64(1):33-7. PubMed ID: 16750356
    [Abstract] [Full Text] [Related]

  • 15. Indirect UV detection in HPLC determination of UV-transparent non-electrolytes in pharmaceutical dosage forms.
    Massaccesi M.
    Farmaco; 1992 May 06; 47(5 Suppl):753-67. PubMed ID: 1524624
    [Abstract] [Full Text] [Related]

  • 16. Stability indicating reversed-phase liquid chromatographic determination of metronidazole benzoate and diloxanide furoate as bulk drug and in suspension dosage form.
    Mishal A, Sober D.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):819-23. PubMed ID: 16055294
    [Abstract] [Full Text] [Related]

  • 17. Achiral liquid chromatography with circular dichroism detection for the determination of carnitine enantiomers in dietary supplements and pharmaceutical formulations.
    de Andrés F, Castañeda G, Ríos A.
    J Pharm Biomed Anal; 2010 Jan 20; 51(2):478-83. PubMed ID: 19303234
    [Abstract] [Full Text] [Related]

  • 18. Stability indicating method for famotidine in pharmaceuticals using porous graphitic carbon column.
    Helali N, Monser L.
    J Sep Sci; 2008 Feb 20; 31(2):276-82. PubMed ID: 18172920
    [Abstract] [Full Text] [Related]

  • 19. Chiral purity assay for Flindokalner using tandem mass spectrometry: method development, validation, and benchmarking.
    Young BL, Cooks RG, Madden MC, Bair M, Jia J, Aubry AF, Miller SA.
    J Pharm Biomed Anal; 2007 Apr 11; 43(5):1602-8. PubMed ID: 17298872
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 34.