BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 30389208)

  • 1. Fast, selective and quantitative protein profiling of adenovirus-vector based vaccines by ultra-performance liquid chromatography.
    van Tricht E; de Raadt P; Verwilligen A; Schenning M; Backus H; Germano M; Somsen GW; Sänger-van de Griend CE
    J Chromatogr A; 2018 Dec; 1581-1582():25-32. PubMed ID: 30389208
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development and validation of RP-HPLC and RP-UPLC methods for quantification of erythropoietin formulated with human serum albumin.
    Rane SS; Ajameri A; Mody R; Padmaja P
    J Pharm Anal; 2012 Apr; 2(2):160-165. PubMed ID: 29403737
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Development and validation of RP-HPLC and RP-UPLC methods for quantification of parathyroid hormones (1-34) in medicinal product formulated with meta-cresol.
    Rane SS; Ajameri A; Mody R; Padmaja P
    J Pharm Anal; 2012 Apr; 2(2):136-142. PubMed ID: 29403733
    [TBL] [Abstract][Full Text] [Related]  

  • 4. UPLC and LC-MS studies on degradation behavior of irinotecan hydrochloride and development of a validated stability-indicating ultra-performance liquid chromatographic method for determination of irinotecan hydrochloride and its impurities in pharmaceutical dosage forms.
    Kumar N; Sangeetha D; Reddy SP
    J Chromatogr Sci; 2012 Oct; 50(9):810-9. PubMed ID: 22661461
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Development of a liquid-chromatography tandem mass spectrometry and ultra-high-performance liquid chromatography high-resolution mass spectrometry method for the quantitative determination of zearalenone and its major metabolites in chicken and pig plasma.
    De Baere S; Osselaere A; Devreese M; Vanhaecke L; De Backer P; Croubels S
    Anal Chim Acta; 2012 Dec; 756():37-48. PubMed ID: 23176738
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A validated stability-indicating UPLC method for the determination of impurities in Maraviroc.
    Chilukuri M; Hussainreddy K; Narayanareddy P; Venkataramana M
    J Chromatogr Sci; 2014 Aug; 52(7):609-16. PubMed ID: 23825352
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Dynamically modified C
    Thirumalai M; Kumar SN; Prabhakaran D; Sivaraman N; Maheswari MA
    J Chromatogr A; 2018 Sep; 1569():62-69. PubMed ID: 30025611
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel validated ultra-performance liquid chromatography Method for separation of eszopiclone impurities and its degradants in drug products.
    Sharma N; Rao SS; Kumar ND; Reddy AM
    J AOAC Int; 2013; 96(5):981-6. PubMed ID: 24282935
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stability-indicating UPLC method for determination of Imatinib Mesylate and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms.
    Nageswari A; Reddy KV; Mukkanti K
    J Pharm Biomed Anal; 2012 Jul; 66():109-15. PubMed ID: 22502910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Development of a stability-indicating UPLC method for determination of isotretinoin in bulk drug.
    Hsi SL; Surman P; Al-Kassas R
    Pharm Dev Technol; 2019 Feb; 24(2):189-198. PubMed ID: 29558234
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Development of a stability-indicating UPLC method for determining olanzapine and its associated degradation products present in active pharmaceutical ingredients and pharmaceutical dosage forms.
    Krishnaiah Ch; Vishnu Murthy M; Kumar R; Mukkanti K
    J Pharm Biomed Anal; 2011 Mar; 54(4):667-73. PubMed ID: 21075576
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Determination of free formaldehyde in cosmetics containing formaldehyde-releasing preservatives by reversed-phase dispersive liquid-liquid microextraction and liquid chromatography with post-column derivatization.
    Miralles P; Chisvert A; Alonso MJ; Hernandorena S; Salvador A
    J Chromatogr A; 2018 Mar; 1543():34-39. PubMed ID: 29478830
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel and rapid validated stability-indicating UPLC method of related substances for dorzolamide hydrochloride and timolol maleate in ophthalmic dosage form.
    Sharma N; Rao SS; Reddy AM
    J Chromatogr Sci; 2012 Oct; 50(9):745-55. PubMed ID: 22562819
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development and validation of a stability-indicating RP-UPLC method for the quantitative analysis of nabumetone in tablet dosage form.
    Sethi N; Anand A; Chandrul KK; Jain G; Srinivas KS
    J Chromatogr Sci; 2012 Feb; 50(2):85-90. PubMed ID: 22298755
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The optimization and establishment of QuEChERS-UPLC-MS/MS method for simultaneously detecting various kinds of pesticides residues in fruits and vegetables.
    Xiu-Ping Z; Lin M; Lan-Qi H; Jian-Bo C; Li Z
    J Chromatogr B Analyt Technol Biomed Life Sci; 2017 Aug; 1060():281-290. PubMed ID: 28649028
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Development and validation of ultra-performance liquid chromatography method for the determination of meloxicam and its impurities in active pharmaceutical ingredients.
    Louati K; Bargaoui I; Safta F
    Ann Pharm Fr; 2018 May; 76(3):187-200. PubMed ID: 29544974
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stability-indicating UPLC method for determining related substances and degradants in dronedarone.
    Pydimarry SP; Cholleti VK; Vangala RR
    J Chromatogr Sci; 2014 Aug; 52(7):666-75. PubMed ID: 23863770
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Development and validation of RP-UPLC method for the determination of darifenacin hydrobromide, its related compounds and its degradation products using design of experiments.
    Murthy MV; Krishnaiah Ch; Srinivas K; Rao KS; Kumar NR; Mukkanti K
    J Pharm Biomed Anal; 2013 Jan; 72():40-50. PubMed ID: 23146225
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Stability-indicating UPLC method for determination of Valsartan and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms.
    Krishnaiah Ch; Reddy AR; Kumar R; Mukkanti K
    J Pharm Biomed Anal; 2010 Nov; 53(3):483-9. PubMed ID: 20646890
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.