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Journal Abstract Search

329 related items for PubMed ID: 21440101

  • 1. Stress degradation study on sulfadimethoxine and development of a validated stability-indicating HPLC assay.
    Louati K, Mistiri F, Kallel M, Safta F.
    Ann Pharm Fr; 2011 Mar; 69(2):91-9. PubMed ID: 21440101
    [Abstract] [Full Text] [Related]

  • 2. Validation of a liquid chromatography method for the simultaneous determination of sulfadimethoxine and trimethoprim and application to a stability study.
    Louati K, Mistiri F, Kallel M, Safta F.
    Ann Pharm Fr; 2010 Mar; 68(2):113-26. PubMed ID: 20434600
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. ICH guidance in practice: validated stability-indicating HPLC method for simultaneous determination of ampicillin and cloxacillin in combination drug products.
    Kumar V, Bhutani H, Singh S.
    J Pharm Biomed Anal; 2007 Jan 17; 43(2):769-73. PubMed ID: 16959462
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. A validated stability-indicating LC method for acetazolamide in the presence of degradation products and its process-related impurities.
    Srinivasu P, Subbarao DV, Vegesna RV, Sudhakar Babu K.
    J Pharm Biomed Anal; 2010 May 01; 52(1):142-8. PubMed ID: 20053517
    [Abstract] [Full Text] [Related]

  • 7. RP-HPLC method for simultaneous estimation of bisoprolol fumarate and hydrochlorothiazide in tablet formulation.
    Joshi SJ, Karbhari PA, Bhoir SI, Bindu KS, Das C.
    J Pharm Biomed Anal; 2010 Jul 08; 52(3):362-71. PubMed ID: 19926421
    [Abstract] [Full Text] [Related]

  • 8. Stress degradation studies on ezetimibe and development of a validated stability-indicating HPLC assay.
    Singh S, Singh B, Bahuguna R, Wadhwa L, Saxena R.
    J Pharm Biomed Anal; 2006 Jun 07; 41(3):1037-40. PubMed ID: 16495029
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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 12; 43(4):1213-20. PubMed ID: 17118610
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. A validated stability indicating rapid LC method for duloxetine HCl.
    Srinivasulu P, Srinivas KS, Reddy RS, Mukkanti K, Buchireddy R.
    Pharmazie; 2009 Jan 05; 64(1):10-3. PubMed ID: 19216224
    [Abstract] [Full Text] [Related]

  • 13. A validated stability-indicating RP-HPLC method for levofloxacin in the presence of degradation products, its process related impurities and identification of oxidative degradant.
    Lalitha Devi M, Chandrasekhar KB.
    J Pharm Biomed Anal; 2009 Dec 05; 50(5):710-7. PubMed ID: 19632800
    [Abstract] [Full Text] [Related]

  • 14. Determination of duloxetine hydrochloride in the presence of process and degradation impurities by a validated stability-indicating RP-LC method.
    Raman NV, Harikrishna KA, Prasad AV, Reddy KR, Ramakrishna K.
    J Pharm Biomed Anal; 2010 Mar 11; 51(4):994-7. PubMed ID: 20005658
    [Abstract] [Full Text] [Related]

  • 15. A stability-indicating high performance liquid chromatographic assay for the determination of orlistat in capsules.
    Mohammadi A, Haririan I, Rezanour N, Ghiasi L, Walker RB.
    J Chromatogr A; 2006 May 26; 1116(1-2):153-7. PubMed ID: 16603170
    [Abstract] [Full Text] [Related]

  • 16. A validated stability indicating ion-pair RP-LC method for zoledronic acid.
    Rao BM, Srinivasu MK, Rani ChP, kumar SS, Kumar PR, Chandrasekhar KB, Veerender M.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):781-90. PubMed ID: 15922532
    [Abstract] [Full Text] [Related]

  • 17. Development and validation of a HPLC-UV method for the determination in didanosine tablets.
    de Oliveira AM, Löwen TC, Cabral LM, dos Santos EM, Rodrigues CR, Castro HC, dos Santos TC.
    J Pharm Biomed Anal; 2005 Jul 15; 38(4):751-6. PubMed ID: 15967304
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Fesoterodine stress degradation behavior by liquid chromatography coupled to ultraviolet detection and electrospray ionization mass spectrometry.
    Sangoi MS, Todeschini V, Steppe M.
    Talanta; 2011 May 30; 84(4):1068-79. PubMed ID: 21530781
    [Abstract] [Full Text] [Related]

  • 20. Determination of nelfinavir mesylate as bulk drug and in pharmaceutical dosage form by stability indicating HPLC.
    Jing Q, Shen Y, Tang Y, Ren F, Yu X, Hou Z.
    J Pharm Biomed Anal; 2006 Jun 07; 41(3):1065-9. PubMed ID: 16545536
    [Abstract] [Full Text] [Related]

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