BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 34496550)

  • 21. Validation and application of high performance liquid chromatographic method for the estimation of metoclopramide hydrochloride in plasma.
    Khan A; Khan J; Irfan M; Naqvi SBS; Khan GM; Shoaib MH; Yousaf RI; Khan A
    Pak J Pharm Sci; 2017 Jan; 30(1):143-147. PubMed ID: 28603124
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Quantitative Determination of Related Substances in Formoterol Fumarate and Tiotropium in Tiomate Transcaps
    Gondhale PS; Varghese Cheriyan B
    Turk J Pharm Sci; 2022 Feb; 19(1):35-47. PubMed ID: 35227048
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Ultraviolet-photodiode array and high-performance liquid chromatographic/mass spectrometric studies on forced degradation behavior of glibenclamide and development of a validated stability-indicating method.
    Bansal G; Singh M; Jindal KC; Singh S
    J AOAC Int; 2008; 91(4):709-19. PubMed ID: 18727528
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Systematic Development and Validation of a RP-HPLC Method for Estimation of Abiraterone Acetate and its Degradation Products.
    Beg S; Malik AK; Afzal O; Altamimi ASA; Kazmi I; Al-Abbasi FA; Almalki WH; Barkat MA; Kawish SM; Pradhan DP; Rahman M
    J Chromatogr Sci; 2021 Jan; 59(1):79-87. PubMed ID: 33169159
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Development and Validation of Two Robust Stability-Indicating Chromatographic Methods for Determination of Metolazone in Drug Substance and Pharmaceutical Dosage Form in the Presence of Its Degradation Products and Characterization of Main Degradation Products Based on LC-MS.
    Zaazaa HE; Abdel-Ghany R; Abdelkawy M; Sayed M
    J Chromatogr Sci; 2020 Apr; 58(3):251-261. PubMed ID: 31879759
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Development of a validated liquid chromatographic method for quantification of sorafenib tosylate in the presence of stress-induced degradation products and in biological matrix employing analytical quality by design approach.
    Sharma T; Khurana RK; Jain A; Katare OP; Singh B
    Biomed Chromatogr; 2018 May; 32(5):e4169. PubMed ID: 29244215
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A validated stability-indicating liquid chromatographic method for the determination of retapamulin in topical dosage form.
    Nalwade S; Reddy VR
    J Chromatogr Sci; 2014 Mar; 52(3):238-45. PubMed ID: 23510782
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Simultaneous determination of gatifloxacin and ambroxol hydrochloride from tablet dosage form using reversed-phase high performance liquid chromatography.
    Shahed M; Nanda R; Dehghan MH; Nasreen H; Feroz S
    Se Pu; 2008 May; 26(3):358-61. PubMed ID: 18724676
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Stability-indicating method for simultaneous estimation of olmesartan medoxomile, amlodipine besylate and hydrochlorothiazide by RP-HPLC in tablet dosage form.
    Jain PS; Patel MK; Gorle AP; Chaudhari AJ; Surana SJ
    J Chromatogr Sci; 2012 Sep; 50(8):680-7. PubMed ID: 22593253
    [TBL] [Abstract][Full Text] [Related]  

  • 30. High performance liquid chromatographic method development for simultaneous analysis of doxofylline and montelukast sodium in a combined form.
    Revathi R; Ethiraj T; Thenmozhi P; Saravanan VS; Ganesan V
    Pharm Methods; 2011 Oct; 2(4):223-8. PubMed ID: 23781461
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Simultaneous liquid chromatographic determination of ezetimibe and simvastatin in pharmaceutical products.
    Oliveira PR; Barth T; Todeschini V; Dalmora SL
    J AOAC Int; 2007; 90(6):1566-72. PubMed ID: 18193733
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Microemulsion liquid chromatographic method for simultaneous determination of simvastatin and ezetimibe in their combined dosage forms.
    Hammouda ME; Abu El-Enin MA; El-Sherbiny DT; El-Wasseef DR; El-Ashry SM
    J Anal Methods Chem; 2013; 2013():132836. PubMed ID: 24282651
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Validation and method development of Tadalafil in bulk and tablet dosage form by RP-HPLC.
    Bojanapu A; Subramaniam AT; Munusamy J; Dhanapal K; Chennakesavalu J; Sellappan M; Jayaprakash V
    Drug Res (Stuttg); 2015 Feb; 65(2):82-5. PubMed ID: 24782284
    [TBL] [Abstract][Full Text] [Related]  

  • 35. High performance liquid chromatographic assay of amlodipine, valsartan and hydrochlorothiazide simultaneously and its application to pharmaceuticals, urine and plasma analysis.
    Shaikh JSA; Raut S; Abdul A; Pathan MAAK
    J Chromatogr B Analyt Technol Biomed Life Sci; 2020 Oct; 1155():122295. PubMed ID: 32771968
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Simultaneous RPHPLC Determination of Nitazoxanide and Ofloxacin in Combined Tablet Dosage Form.
    Kalta RR; Sharma R; Chaturvedi SC
    Indian J Pharm Sci; 2008; 70(4):491-4. PubMed ID: 20046777
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Development and validation of RP-HPLC method for simultaneous estimation of docetaxel and ritonavir in PLGA nanoparticles.
    Kumbhar PS; Diwate SK; Mali UG; Shinde TU; Disouza JI; Manjappa AS
    Ann Pharm Fr; 2020 Sep; 78(5):398-407. PubMed ID: 32681903
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Stability indicating liquid chromatographic method for the simultaneous determination of rosuvastatin and ezetimibe in pharmaceutical formulations.
    Mukthinuthalapati MA; Bukkapatnam V; Bandaru SP
    Adv Pharm Bull; 2014 Dec; 4(4):405-11. PubMed ID: 25436199
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Application of QbD based approach in development and validation of RP-HPLC method for simultaneous estimation of methotrexate and baicalin in dual-drug-loaded liposomes.
    Adin SN; Gupta I; Aqil M; Mujeeb M
    Biomed Chromatogr; 2023 Apr; 37(4):e5581. PubMed ID: 36609805
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.