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Journal Abstract Search

135 related items for PubMed ID: 20022725

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Development and validation of RP-HPLC method for the analysis of metformin.
    Arayne MS, Sultana N, Zuberi MH.
    Pak J Pharm Sci; 2006 Jul; 19(3):231-5. PubMed ID: 16935831
    [Abstract] [Full Text] [Related]

  • 3. Development and validation of RP-HPLC method to determine letrozole in different pharmaceutical formulations and its application to studies of drug release from nanoparticles.
    Mondal N, Pal TK, Ghosal SK.
    Acta Pol Pharm; 2009 Jul; 66(1):11-7. PubMed ID: 19226963
    [Abstract] [Full Text] [Related]

  • 4. Characterisation of protein stability in rod-insert vaginal rings.
    Pattani A, Lowry D, Curran RM, McGrath S, Kett VL, Andrews GP, Malcolm RK.
    Int J Pharm; 2012 Jul 01; 430(1-2):89-97. PubMed ID: 22486955
    [Abstract] [Full Text] [Related]

  • 5. Sustained release dosage forms dissolution behavior prediction: a study of matrix tablets using NIR spectroscopy.
    Tabasi SH, Moolchandani V, Fahmy R, Hoag SW.
    Int J Pharm; 2009 Dec 01; 382(1-2):1-6. PubMed ID: 19660535
    [Abstract] [Full Text] [Related]

  • 6. Quantitation of buclizine hydrochloride in pharmaceutical formulations and human serum by RP-HPLC.
    Arayne MS, Sultana N, Siddiqui FA.
    Pak J Pharm Sci; 2006 Oct 01; 19(4):326-9. PubMed ID: 17105713
    [Abstract] [Full Text] [Related]

  • 7. In-vitro and in-vivo evaluation of enteric-coated starch-based pellets prepared via extrusion/spheronisation.
    Dukić-Ott A, De Beer T, Remon JP, Baeyens W, Foreman P, Vervaet C.
    Eur J Pharm Biopharm; 2008 Sep 01; 70(1):302-12. PubMed ID: 18579353
    [Abstract] [Full Text] [Related]

  • 8. Quantitative determination of insulin entrapment efficiency in triblock copolymeric nanoparticles by high-performance liquid chromatography.
    Xu X, Fu Y, Hu H, Duan Y, Zhang Z.
    J Pharm Biomed Anal; 2006 Apr 11; 41(1):266-73. PubMed ID: 16303273
    [Abstract] [Full Text] [Related]

  • 9. Permeability assessment for solid oral drug formulations based on Caco-2 monolayer in combination with a flow through dissolution cell.
    Motz SA, Schaefer UF, Balbach S, Eichinger T, Lehr CM.
    Eur J Pharm Biopharm; 2007 May 11; 66(2):286-95. PubMed ID: 17156983
    [Abstract] [Full Text] [Related]

  • 10. Simple and reliable HPLC analysis of fexofenadine hydrochloride in tablets and its application to dissolution studies.
    Oliveira DC, Weigch A, Rolim CM.
    Pharmazie; 2007 Feb 11; 62(2):96-100. PubMed ID: 17341026
    [Abstract] [Full Text] [Related]

  • 11. A stability-indicating HPLC method for the determination of glucosamine in pharmaceutical formulations.
    Shao Y, Alluri R, Mummert M, Koetter U, Lech S.
    J Pharm Biomed Anal; 2004 May 28; 35(3):625-31. PubMed ID: 15137989
    [Abstract] [Full Text] [Related]

  • 12. Freeze drying of human serum albumin (HSA) nanoparticles with different excipients.
    Anhorn MG, Mahler HC, Langer K.
    Int J Pharm; 2008 Nov 03; 363(1-2):162-9. PubMed ID: 18672043
    [Abstract] [Full Text] [Related]

  • 13. Validated RP-hPLC method for the assay of zalcitabine in drug substance, formulated products and human serum.
    Uslu B, Savaşer A, Ozkan SA, Ozkan Y.
    Pharmazie; 2004 Aug 03; 59(8):604-7. PubMed ID: 15378847
    [Abstract] [Full Text] [Related]

  • 14. Simultaneous determination of pioglitazone and glimepiride in bulk drug and pharmaceutical dosage form by RP-HPLC method.
    A K, G S, C MR, Bhat K, A R, P M, M S, K K, N U.
    Pak J Pharm Sci; 2008 Oct 03; 21(4):421-5. PubMed ID: 18930865
    [Abstract] [Full Text] [Related]

  • 15. Isocratic RP-HPLC method for rutin determination in solid oral dosage forms.
    Kuntić V, Pejić N, Ivković B, Vujić Z, Ilić K, Mićić S, Vukojević V.
    J Pharm Biomed Anal; 2007 Jan 17; 43(2):718-21. PubMed ID: 16920326
    [Abstract] [Full Text] [Related]

  • 16. A validated RP-HPLC method for the determination of mosapride citrate in bulk drug samples and pharmaceutical formulations.
    Krishnaiah YS, Murthy TK, Sankar DG, Satyanarayana V.
    Pharmazie; 2002 Dec 17; 57(12):814-6. PubMed ID: 12561242
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Determination of gentamicin in different matrices by a new sensitive high-performance liquid chromatography-mass spectrometric method.
    Lecároz C, Campanero MA, Gamazo C, Blanco-Prieto MJ.
    J Antimicrob Chemother; 2006 Sep 15; 58(3):557-63. PubMed ID: 16787953
    [Abstract] [Full Text] [Related]

  • 19. A validated method for the analysis of diltiazem in raw materials and pharmaceutical formulations by rp-HPLC.
    Sultana N, Arayne MS, Shafi N.
    Pak J Pharm Sci; 2007 Oct 15; 20(4):284-90. PubMed ID: 17604250
    [Abstract] [Full Text] [Related]

  • 20. Development and validation of reversed phase high performance liquid chromatography method for determination of dexpanthenol in pharmaceutical formulations.
    Kulikov AU, Zinchenko AA.
    J Pharm Biomed Anal; 2007 Feb 19; 43(3):983-8. PubMed ID: 17049793
    [Abstract] [Full Text] [Related]

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