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Journal Abstract Search


506 related items for PubMed ID: 17826364

  • 1. Normal phase and reverse phase HPLC-UV-MS analysis of process impurities for rapamycin analog ABT-578: application to active pharmaceutical ingredient process development.
    Chen Y, Brill GM, Benz NJ, Leanna MR, Dhaon MK, Rasmussen M, Zhou CC, Bruzek JA, Bellettini JR.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Oct 15; 858(1-2):106-17. PubMed ID: 17826364
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Simultaneous separation and determination of coenzyme Q(10) and its process related impurities by NARP-HPLC and atmospheric pressure chemical ionization-mass spectrometry (APCI-MS).
    Nageswara Rao R, Kumar Talluri MV, Shinde DD.
    J Pharm Biomed Anal; 2008 Jun 09; 47(2):230-7. PubMed ID: 18243624
    [Abstract] [Full Text] [Related]

  • 4. Development of a validated RP-LC/ESI-MS-MS method for separation, identification and determination of related substances of tamsulosin in bulk drugs and formulations.
    Nageswara Rao R, Kumar Talluri MV, Narasa Raju A, Shinde DD, Ramanjaneyulu GS.
    J Pharm Biomed Anal; 2008 Jan 07; 46(1):94-103. PubMed ID: 17951020
    [Abstract] [Full Text] [Related]

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  • 7. Characterization of impurities in semi-synthetic vinorelbine bitartrate by HPLC-MS with mass spectrometric shift technique.
    Cao X, Tai Y, Sun C, Wang K, Pan Y.
    J Pharm Biomed Anal; 2005 Sep 01; 39(1-2):39-45. PubMed ID: 16085133
    [Abstract] [Full Text] [Related]

  • 8. Separation and characterization of synthetic impurities of triclabendazole by reversed-phase high-performance liquid chromatography/electrospray ionization mass spectrometry.
    Zhou H, Tai Y, Sun C, Pan Y.
    J Pharm Biomed Anal; 2005 Feb 07; 37(1):97-107. PubMed ID: 15664748
    [Abstract] [Full Text] [Related]

  • 9. New gradient high-performance liquid chromatography method for determination of donepezil hydrochloride assay and impurities content in oral pharmaceutical formulation.
    Kafkala S, Matthaiou S, Alexaki P, Abatzis M, Bartzeliotis A, Katsiabani M.
    J Chromatogr A; 2008 May 02; 1189(1-2):392-7. PubMed ID: 18206895
    [Abstract] [Full Text] [Related]

  • 10. Identification, characterization and quantification of new impurities by LC-ESI/MS/MS and LC-UV methods in rivastigmine tartrate active pharmaceutical ingredient.
    Thomas S, Shandilya S, Bharati A, Paul SK, Agarwal A, Mathela CS.
    J Pharm Biomed Anal; 2012 Jan 05; 57():39-51. PubMed ID: 21880452
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. LC-MS characterization of trace impurities contained in calcium folinate.
    Francese G, Corana F, Meneghetti O, Marazza F.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):757-63. PubMed ID: 15927438
    [Abstract] [Full Text] [Related]

  • 13. The use of LC/MS, GC/MS, and LC/NMR hyphenated techniques to identify a drug degradation product in pharmaceutical development.
    Pan C, Liu F, Ji Q, Wang W, Drinkwater D, Vivilecchia R.
    J Pharm Biomed Anal; 2006 Feb 24; 40(3):581-90. PubMed ID: 16242883
    [Abstract] [Full Text] [Related]

  • 14. Use of high resolution LC-MSn analysis in conjunction with mechanism-based stress studies: identification of asarinin, an impurity from sesame oil in an animal health product.
    Wang X, Peng Y, Li M, Rustum AM.
    J Pharm Biomed Anal; 2009 Dec 05; 50(5):1015-21. PubMed ID: 19631486
    [Abstract] [Full Text] [Related]

  • 15. High-performance liquid chromatography analysis of anti-inflammatory pharmaceuticals with ultraviolet and electrospray-mass spectrometry detection in suspected counterfeit homeopathic medicinal products.
    Panusa A, Multari G, Incarnato G, Gagliardi L.
    J Pharm Biomed Anal; 2007 Mar 12; 43(4):1221-7. PubMed ID: 17127029
    [Abstract] [Full Text] [Related]

  • 16. Identification of novel rapamycin derivatives as low-level impurities in active pharmaceutical ingredients.
    Zech SG, Carr M, Mohemmad QK, Narasimhan NI, Murray C, Rozamus LW, Dalgarno DC.
    J Antibiot (Tokyo); 2011 Sep 12; 64(9):649-54. PubMed ID: 21792211
    [Abstract] [Full Text] [Related]

  • 17. Investigation on the photochemical stability of lercanidipine and its determination in tablets by HPLC-UV and LC-ESI-MS/MS.
    Fiori J, Gotti R, Bertucci C, Cavrini V.
    J Pharm Biomed Anal; 2006 Apr 11; 41(1):176-81. PubMed ID: 16378707
    [Abstract] [Full Text] [Related]

  • 18. Trace level detection and quantitation of ethyl diazoacetate by reversed-phase high performance liquid chromatography and UV detection.
    Axe BP.
    J Pharm Biomed Anal; 2006 Jun 07; 41(3):804-10. PubMed ID: 16495031
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Simultaneous quantification of both triterpenoid and steroidal saponins in various Yunnan Baiyao preparations using HPLC-UV and HPLC-MS.
    Liu XX, Wang L, Chen XQ, Deng XT, Cao Y, Wang Q.
    J Sep Sci; 2008 Dec 01; 31(22):3834-46. PubMed ID: 19021166
    [Abstract] [Full Text] [Related]


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