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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 21168299)

  • 1. A validated ultra high pressure liquid chromatographic method for qualification and quantification of folic acid in pharmaceutical preparations.
    Deconinck E; Crevits S; Baten P; Courselle P; De Beer J
    J Pharm Biomed Anal; 2011 Apr; 54(5):995-1000. PubMed ID: 21168299
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A validated Ultra High Pressure Liquid Chromatographic method for the characterisation of confiscated illegal slimming products containing anorexics.
    Deconinck E; Verlinde K; Courselle P; Beer JO
    J Pharm Biomed Anal; 2012 Feb; 59():38-43. PubMed ID: 22075376
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A fast ultra high pressure liquid chromatographic method for qualification and quantification of pharmaceutical combination preparations containing paracetamol, acetyl salicylic acid and/or antihistaminics.
    Deconinck E; Sacré PY; Baudewyns S; Courselle P; De Beer J
    J Pharm Biomed Anal; 2011 Sep; 56(2):200-9. PubMed ID: 21665401
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HPLC-DAD method for the simultaneous determination of zofenopril and hydrochlorothiazide in oral pharmaceutical formulations.
    Carlucci G; Di Federico L; Iuliani P
    J Sep Sci; 2010 Jun; 33(12):1717-22. PubMed ID: 20437414
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Development, optimization and validation of a sub-minute analytical enantioselective high performance liquid chromatographic separation for a folic acid precursor in normal phase mode.
    Frühauf D; Juza M
    J Chromatogr A; 2012 Dec; 1269():242-54. PubMed ID: 23102632
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Using an innovative Quality-by-Design approach for development of a stability indicating UHPLC method for ebastine in the API and pharmaceutical formulations.
    Schmidt AH; Molnár I
    J Pharm Biomed Anal; 2013 May; 78-79():65-74. PubMed ID: 23454599
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Microemulsion high performance liquid chromatography (MELC) method for the determination of terbutaline in pharmaceutical preparation.
    Althanyan MS; Assi KH; Clark BJ; Hanaee J
    J Pharm Biomed Anal; 2011 Jun; 55(3):397-402. PubMed ID: 21371845
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The use of partially porous particle columns for the routine, generic analysis of biological samples for pharmacokinetic studies in drug discovery by reversed-phase ultra-high performance liquid chromatography-tandem mass spectrometry.
    Mallett DN; Ramírez-Molina C
    J Pharm Biomed Anal; 2009 Jan; 49(1):100-7. PubMed ID: 19019615
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Separation and quantification of two diastereomers of a Drug Candidate in rat plasma by ultra-high pressure liquid chromatography/mass spectrometry.
    Wang H; Edom RW; Kumar S; Vincent S; Shen Z
    J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Jul; 854(1-2):26-34. PubMed ID: 17442640
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rapid quantitative determination of fat-soluble vitamins and coenzyme Q-10 in human serum by reversed phase ultra-high pressure liquid chromatography with UV detection.
    Paliakov EM; Crow BS; Bishop MJ; Norton D; George J; Bralley JA
    J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Jan; 877(1-2):89-94. PubMed ID: 19041283
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Using of HPLC coupled with coulometric detector for the determination of biotin in pharmaceuticals.
    Zerzanová A; Zizkovský V; Kucera R; Klimes J; Jesenský I; Dohnal J; Barrón D
    J Pharm Biomed Anal; 2007 Dec; 45(5):730-5. PubMed ID: 17920225
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Development and validation of a high-performance liquid chromatographic method for the determination of buspirone in pharmaceutical preparations.
    Zaxariou M; Panderi I
    J Pharm Biomed Anal; 2004 Apr; 35(1):41-50. PubMed ID: 15030878
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Development of a validated HPLC method for the determination of B-complex vitamins in pharmaceuticals and biological fluids after solid phase extraction.
    Chatzimichalakis PF; Samanidou VF; Verpoorte R; Papadoyannis IN
    J Sep Sci; 2004 Oct; 27(14):1181-8. PubMed ID: 15537074
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Raman spectroscopic method for the determination of medroxyprogesterone acetate in a pharmaceutical suspension: validation of quantifying abilities, uncertainty assessment and comparison with the high performance liquid chromatography reference method.
    De Beer TR; Baeyens WR; Vermeire A; Broes D; Remon JP; Vervaet C
    Anal Chim Acta; 2007 Apr; 589(2):192-9. PubMed ID: 17418181
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 1189(1-2):392-7. PubMed ID: 18206895
    [TBL] [Abstract][Full Text] [Related]  

  • 16. HPLC separation technique for analysis of bufuralol enantiomers in plasma and pharmaceutical formulations using a vancomycin chiral stationary phase and UV detection.
    Hefnawy MM; Sultan MA; Al-Shehri MM
    J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Sep; 856(1-2):328-36. PubMed ID: 17681871
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lipophilicity determination of highly lipophilic compounds by liquid chromatography.
    Guillot A; Henchoz Y; Moccand C; Guillarme D; Veuthey JL; Carrupt PA; Martel S
    Chem Biodivers; 2009 Nov; 6(11):1828-36. PubMed ID: 19937824
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Development of an ion-pairing reversed-phase liquid chromatography method using a double detection analysis (UV and evaporative light scattering detection) to monitor the stability of Alimta(®)-pemetrexed preparations: identification and quantification of L-glutamic acid as a potential degradation product.
    Respaud R; Tournamille JF; Croix C; Laborie H; Elfakir C; Viaud-Massuard MC
    J Pharm Biomed Anal; 2011 Jan; 54(2):411-6. PubMed ID: 20869830
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Methotrexate determination in pharmaceuticals by enantioselective HPLC.
    el-Hady DA; el-Maali NA; Gotti R; Bertucci C; Mancini F; Andrisano V
    J Pharm Biomed Anal; 2005 Apr; 37(5):919-25. PubMed ID: 15862667
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The use of HPLC method for determination of the folic acid in multi-component vitamin preparations.
    Kłaczkow G; Anuszewska E
    Acta Pol Pharm; 2000; 57(4):257-60. PubMed ID: 11126612
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.