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117 related items for PubMed ID: 30473499

  • 1. Development and validation of HPLC method for the determination of Candesartan in human plasma.
    Hamid S, Beg AE, Muhammad IN, Hassan S, Hassan A, Akram A, Alladin N.
    Pak J Pharm Sci; 2018 Nov; 31(6):2323-2327. PubMed ID: 30473499
    [Abstract] [Full Text] [Related]

  • 2. HPLC method development and validation for the determination of Cefaclor in human plasma.
    Naz S, Shoaib MH, Bashir L, Yousuf RI, Anjum F, Siddiqui F, Yaseen S.
    Pak J Pharm Sci; 2017 Sep; 30(5):1645-1649. PubMed ID: 29084685
    [Abstract] [Full Text] [Related]

  • 3. Development and validation of HPLC method for the determination of Cefpodoxime Proxetil in human plasma.
    Bashir L, Shoaib MH, Naz S, Yousuf RI, Jabeen S, Israr F, Siddiqui F.
    Pak J Pharm Sci; 2017 Sep; 30(5):1603-1607. PubMed ID: 29084679
    [Abstract] [Full Text] [Related]

  • 4. Simple RP-HPLC method for determination of triple drug combination of valsartan, amlodipine and hydrochlorothiazide in human plasma.
    Sharma RN, Pancholi SS.
    Acta Pharm; 2012 Mar; 62(1):45-58. PubMed ID: 22472448
    [Abstract] [Full Text] [Related]

  • 5. Chromatographic method development and validation for the determination of valsartan in biological fluid.
    Ghayas S, Shoaib MH, Siddiqui F, Yousuf RI, Masood MA, Anjum F, Bushra R, Bashir L, Naz S, Muhammad IN.
    Pak J Pharm Sci; 2017 Nov; 30(6(Supplementary)):2355-2362. PubMed ID: 29188769
    [Abstract] [Full Text] [Related]

  • 6. Determination and validation of ketoprofen, pantoprazole and valsartan together in human plasma by high performance liquid chromatography.
    Koçyiğit-Kaymakçoğlu B, Unsalan S, Rollas S.
    Pharmazie; 2006 Jul; 61(7):586-9. PubMed ID: 16889064
    [Abstract] [Full Text] [Related]

  • 7. Optimization via experimental design of an SPE-HPLC-UV-fluorescence method for the determination of valsartan and its metabolite in human plasma samples.
    Iriarte G, Ferreirós N, Ibarrondo I, Alonso RM, Maguregi MI, Gonzalez L, Jiménez RM.
    J Sep Sci; 2006 Oct; 29(15):2265-83. PubMed ID: 17120810
    [Abstract] [Full Text] [Related]

  • 8. Development and validation of reverse phase HPLC method for determination of angiotensin receptor blocking agent irbesartan in plasma.
    Nisa Z, Ali SI, Rizvi M, Khan MA, Sultan RA, Fatima R, Shaheen N, Zafar F, Kashif SS, Khatian N.
    Pak J Pharm Sci; 2019 Mar; 32(2 (Supplementary)):853-858. PubMed ID: 31103982
    [Abstract] [Full Text] [Related]

  • 9. Quantitative bio-analysis of pitavastatin and candesartan in rat plasma by HPLC-UV: Assessment of pharmacokinetic drug-drug interaction.
    Patel M, Kothari C.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2020 Feb 01; 1138():121962. PubMed ID: 31915110
    [Abstract] [Full Text] [Related]

  • 10. A simple, rapid and fully validated HPLC method for simultaneous quantitative bio-analysis of rosuvastatin and candesartan in rat plasma: Application to pharmacokinetic interaction study.
    Patel M, Kothari C.
    Biomed Chromatogr; 2019 Oct 01; 33(10):e4607. PubMed ID: 31141832
    [Abstract] [Full Text] [Related]

  • 11. Determination of azide impurity in sartans using reversed-phase HPLC with UV detection.
    Gričar M, Andrenšek S.
    J Pharm Biomed Anal; 2016 Jun 05; 125():27-32. PubMed ID: 26999319
    [Abstract] [Full Text] [Related]

  • 12. Determination of candesartan cilexetil, candesartan and a metabolite in human plasma and urine by liquid chromatography and fluorometric detection.
    Stenhoff H, Lagerström PO, Andersen C.
    J Chromatogr B Biomed Sci Appl; 1999 Aug 20; 731(2):411-7. PubMed ID: 10510797
    [Abstract] [Full Text] [Related]

  • 13. Evaluation of gender difference in pharmacokinetics of Candesartan cilexetil in the fasted state by RP-HPLC: A single dose comparative study.
    Nawaz HA, Masood MI, Abbas M, Usman M, Khan AM, Rasheed H, Riffat S.
    Pak J Pharm Sci; 2019 May 20; 32(3):1019-1024. PubMed ID: 31278715
    [Abstract] [Full Text] [Related]

  • 14. Simple and effective HPLC method development and its validation for Clindipine in human drug free plasma.
    Muralidharan S, Kumar Jr, Dhanaraj SA.
    Pak J Pharm Sci; 2015 Jan 20; 28(1):135-8. PubMed ID: 25553676
    [Abstract] [Full Text] [Related]

  • 15. Fast screening method for the determination of angiotensin II receptor antagonists in human plasma by high-performance liquid chromatography with fluorimetric detection.
    González L, López JA, Alonso RM, Jiménez RM.
    J Chromatogr A; 2002 Mar 08; 949(1-2):49-60. PubMed ID: 11999756
    [Abstract] [Full Text] [Related]

  • 16. DEVELOPMENT AND VALIDATION OF HPLC ANALYTICAL METHODS USED-FOR DETERMINATION OF ASSAY, CONTENT UNIFORMITY AND DISSOLUTION OF IMMEDIATE RELEASE CANDESARTAN CILEXETIL 32 MG TABLETS.
    Yuce M, Capan Y.
    Acta Pol Pharm; 2017 Mar 08; 74(2):357-367. PubMed ID: 29624240
    [Abstract] [Full Text] [Related]

  • 17. HPLC determination of irbesartan in human plasma: its application to pharmacokinetic studies.
    Bae SK, Kim MJ, Shim EJ, Cho DY, Shon JH, Liu KH, Kim EY, Shin JG.
    Biomed Chromatogr; 2009 Jun 08; 23(6):568-72. PubMed ID: 19277953
    [Abstract] [Full Text] [Related]

  • 18. Rapid determination of valsartan in human plasma by protein precipitation and high-performance liquid chromatography.
    Macek J, Klíma J, Ptácek P.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Feb 17; 832(1):169-72. PubMed ID: 16426905
    [Abstract] [Full Text] [Related]

  • 19. Improved analytical validation and pharmacokinetics of valsartan using HPLC with UV detection.
    Piao ZZ, Lee ES, Tran HT, Lee BJ.
    Arch Pharm Res; 2008 Aug 17; 31(8):1055-9. PubMed ID: 18787797
    [Abstract] [Full Text] [Related]

  • 20. High-performance liquid chromatographic analysis of angiotensin II receptor antagonist valsartan using a liquid extraction method.
    Daneshtalab N, Lewanczuk RZ, Jamali F.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2002 Jan 25; 766(2):345-9. PubMed ID: 11824822
    [Abstract] [Full Text] [Related]

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