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Journal Abstract Search

629 related items for PubMed ID: 19103562

  • 1. Use of chemometrics for development and validation of an RP-HPLC method for simultaneous determination of haloperidol and related compounds.
    Petkovska R, Dimitrovska A.
    Acta Pharm; 2008 Sep; 58(3):243-56. PubMed ID: 19103562
    [Abstract] [Full Text] [Related]

  • 2. C(18) columns for the simultaneous determination of oxytetracycline and its related substances by reversed-phase high performance liquid chromatography and UV detection.
    Smyrniotakis CG, Archontaki HA.
    J Pharm Biomed Anal; 2007 Jan 17; 43(2):506-14. PubMed ID: 16989968
    [Abstract] [Full Text] [Related]

  • 3. 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 01; 52(1):19-29. PubMed ID: 20045275
    [Abstract] [Full Text] [Related]

  • 4. Development and validation of a HPLC method for the determination of buprenorphine hydrochloride, naloxone hydrochloride and noroxymorphone in a tablet formulation.
    Mostafavi A, Abedi G, Jamshidi A, Afzali D, Talebi M.
    Talanta; 2009 Feb 15; 77(4):1415-9. PubMed ID: 19084658
    [Abstract] [Full Text] [Related]

  • 5. Development of an enhanced separation of erythromycin and its related substances by liquid chromatography.
    Deubel A, Holzgrabe U.
    J Pharm Biomed Anal; 2007 Jan 17; 43(2):493-8. PubMed ID: 16935448
    [Abstract] [Full Text] [Related]

  • 6. Development and validation of an LC method for the determination of emtricitabine and related compounds in the drug substance.
    Ashenafi D, Verbeek A, Hoogmartens J, Adams E.
    J Sep Sci; 2009 Jun 17; 32(11):1823-30. PubMed ID: 19425024
    [Abstract] [Full Text] [Related]

  • 7. Stability indicating validated HPLC method for quantification of levothyroxine with eight degradation peaks in the presence of excipients.
    Shah RB, Bryant A, Collier J, Habib MJ, Khan MA.
    Int J Pharm; 2008 Aug 06; 360(1-2):77-82. PubMed ID: 18524511
    [Abstract] [Full Text] [Related]

  • 8. Development and validation of RP-HPLC method for cetrimonium bromide and lidocaine determination.
    Malenovic A, Medenica M, Ivanovic D, Jancic B, Markovic S.
    Farmaco; 2005 Feb 06; 60(2):157-61. PubMed ID: 15752474
    [Abstract] [Full Text] [Related]

  • 9. Multivariate optimization and validation of an analytical methodology by RP-HPLC for the determination of losartan potassium in capsules.
    Bonfilio R, Tarley CR, Pereira GR, Salgado HR, de Araújo MB.
    Talanta; 2009 Nov 15; 80(1):236-41. PubMed ID: 19782220
    [Abstract] [Full Text] [Related]

  • 10. Liquid chromatographic analysis of oxytocin and its related substances.
    Ashenafi D, Van Hemelrijck E, Chopra S, Hoogmartens J, Adams E.
    J Pharm Biomed Anal; 2010 Jan 05; 51(1):24-9. PubMed ID: 19716673
    [Abstract] [Full Text] [Related]

  • 11. Development and validation of a simple stability-indicating high performance liquid chromatographic method for the determination of miconazole nitrate in bulk and cream formulations.
    De Zan MM, Cámara MS, Robles JC, Kergaravat SV, Goicoechea HC.
    Talanta; 2009 Aug 15; 79(3):762-7. PubMed ID: 19576442
    [Abstract] [Full Text] [Related]

  • 12. Development and validation of a gradient HPLC method for the determination of clindamycin and related compounds in a novel tablet formulation.
    Platzer DJ, White BA.
    J Pharm Biomed Anal; 2006 Apr 11; 41(1):84-8. PubMed ID: 16298506
    [Abstract] [Full Text] [Related]

  • 13. Chemometrically assissted optimization and validation of RP-HPLC method for the analysis of itraconazole and its impurities.
    Kasagić I, Malenović A, Jovanović M, Rakić T, Jančić Stojanović B, Ivanović D.
    Acta Pharm; 2013 Jun 11; 63(2):159-73. PubMed ID: 23846140
    [Abstract] [Full Text] [Related]

  • 14. A stability indicating LC method for zolmitriptan.
    Rao BM, Srinivasu MK, Sridhar G, Kumar PR, Chandrasekhar KB, Islam A.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):503-9. PubMed ID: 15899567
    [Abstract] [Full Text] [Related]

  • 15. Developing and optimizing a validated isocratic reversed-phase high-performance liquid chromatography separation of nimodipine and impurities in tablets using experimental design methodology.
    Barmpalexis P, Kanaze FI, Georgarakis E.
    J Pharm Biomed Anal; 2009 Jul 12; 49(5):1192-202. PubMed ID: 19369025
    [Abstract] [Full Text] [Related]

  • 16. Validated stability-indicating HPLC method for the determination of dimethyl-4,4'-dimethoxy-5,6,5',6'-dimethylene dioxybiphenyl-2,2'-dicarboxylate (DDB) and its degradation products.
    Hadad GM.
    J Pharm Biomed Anal; 2008 Aug 05; 47(4-5):695-703. PubMed ID: 18403161
    [Abstract] [Full Text] [Related]

  • 17. A validated reversed phase HPLC method for the determination of process-related impurities in almotriptan malate API.
    Kumar AP, Ganesh VR, Rao DV, Anil C, Rao BV, Hariharakrishnan VS, Suneetha A, Sundar BS.
    J Pharm Biomed Anal; 2008 Mar 13; 46(4):792-8. PubMed ID: 18191357
    [Abstract] [Full Text] [Related]

  • 18. Development and validation of a liquid chromatographic method for the analysis of capreomycin sulfate and its related substances.
    Mallampati S, Huang S, Ashenafi D, Van Hemelrijck E, Hoogmartens J, Adams E.
    J Chromatogr A; 2009 Mar 20; 1216(12):2449-55. PubMed ID: 19185869
    [Abstract] [Full Text] [Related]

  • 19. Effect of system variables involved in packed column supercritical fluid chromatography of stavudine taken as model analyte using response surface methodology along with study of thermodynamic parameters.
    Kaul N, Agrawal H, Paradkar AR, Mahadik KR.
    J Pharm Biomed Anal; 2007 Jan 17; 43(2):471-80. PubMed ID: 16935453
    [Abstract] [Full Text] [Related]

  • 20. LC determination of glimepiride and its related impurities.
    Khan MA, Sinha S, Vartak S, Bhartiya A, Kumar S.
    J Pharm Biomed Anal; 2005 Oct 04; 39(5):928-43. PubMed ID: 16040224
    [Abstract] [Full Text] [Related]

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