BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

679 related articles for article (PubMed ID: 27262107)

  • 1. Development and validation of a selective, sensitive and stability indicating UPLC-MS/MS method for rapid, simultaneous determination of six process related impurities in darunavir drug substance.
    A VBR; Yusop Z; Jaafar J; Aris AB; Majid ZA; Umar K; Talib J
    J Pharm Biomed Anal; 2016 Sep; 128():141-148. PubMed ID: 27262107
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development and validation of a systematic UPLC-MS/MS method for simultaneous determination of three phenol impurities in ritonavir.
    Venugopal N; Vijaya Bhaskar Reddy A; Madhavi G
    J Pharm Biomed Anal; 2014 Mar; 90():127-33. PubMed ID: 24366213
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Simultaneous determination of imperatorin and its metabolite xanthotoxol in rat plasma and urine by LC-MS/MS and its application to pharmacokinetic studies.
    Ngo L; Tran P; Ham SH; Cho JH; Cho HY; Lee YB
    J Chromatogr B Analyt Technol Biomed Life Sci; 2017 Feb; 1044-1045():30-38. PubMed ID: 28064067
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Development and validation of a novel stability-indicating HPLC method for the quantitative determination of eleven related substances in ezetimibe drug substance and drug product.
    Luo Z; Deng Z; Liu Y; Wang G; Yang W; Hou C; Tang M; Yang R; Zhou H
    Talanta; 2015 Jul; 139():67-74. PubMed ID: 25882410
    [TBL] [Abstract][Full Text] [Related]  

  • 5. RP-HPLC separation and characterization of unknown impurities of a novel HIV-protease inhibitor Darunavir by ESI-MS and 2D NMR spectroscopy.
    Nageswara Rao R; Ramachandra B; Santhakumar K
    J Pharm Biomed Anal; 2013 Mar; 75():186-91. PubMed ID: 23266664
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A selective and sensitive UPLC-MS/MS approach for trace level quantification of four potential genotoxic impurities in zolmitriptan drug substance.
    Vijaya Bhaskar Reddy A; Venugopal N; Madhavi G; Gangadhara Reddy K; Madhavi V
    J Pharm Biomed Anal; 2013 Oct; 84():84-9. PubMed ID: 23816589
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Development and validation of a rapid ultra high performance liquid chromatography with tandem mass spectrometry method for the simultaneous determination of darunavir, ritonavir, and tenofovir in human plasma: Application to human pharmacokinetics.
    Reddy AV; Jaafar J; Aris AB; Majid ZA; Umar K; Talib J; Madhavi G
    J Sep Sci; 2015 Aug; 38(15):2580-7. PubMed ID: 25989063
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Development and validation of a reversed-phase ultra-performance liquid chromatographic method for assay of lacidipine and related substances.
    Mohan A; Patel HB; Saravanan D
    J AOAC Int; 2011; 94(6):1800-6. PubMed ID: 22320087
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Simultaneous determination of nineteen major active compounds in Qiangshen tablet by UPLC-ESI-MS/MS.
    Gao J; Qiu Y; Chen J; Mu S; Sun L
    J Pharm Biomed Anal; 2016 Sep; 128():519-527. PubMed ID: 27416474
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Simultaneous determination of fourteen main active components in Gumiganghwal-tang tablet by using a newly developed UPLC-ESI-MS/MS method.
    Jeong SH; Jang JH; Lee GY; Yang SJ; Cho HY; Lee YB
    J Chromatogr B Analyt Technol Biomed Life Sci; 2019 Sep; 1126-1127():121743. PubMed ID: 31401451
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Simultaneous quantification of 5 main components of Psoralea corylifolia L. in rats' plasma by utilizing ultra high pressure liquid chromatography tandem mass spectrometry.
    Gao Q; Xu Z; Zhao G; Wang H; Weng Z; Pei K; Wu L; Cai B; Chen Z; Li W
    J Chromatogr B Analyt Technol Biomed Life Sci; 2016 Feb; 1011():128-35. PubMed ID: 26773881
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Forced degradation and impurity profiling: recent trends in analytical perspectives.
    Jain D; Basniwal PK
    J Pharm Biomed Anal; 2013 Dec; 86():11-35. PubMed ID: 23969330
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel stability-indicating UPLC method development and validation for the determination of seven impurities in various diclofenac pharmaceutical dosage forms.
    Azougagh M; Elkarbane M; Bakhous K; Issmaili S; Skalli A; Iben Moussad S; Benaji B
    Ann Pharm Fr; 2016 Sep; 74(5):358-69. PubMed ID: 27475309
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Determination and pharmacokinetics of chinensinaphthol methyl ether in rat urine by a sensitive and specific UFLC-ESI-MS/MS method.
    Qin J; Luo J; Zhao H; Zhang S; Zhang X; Yang M
    J Chromatogr B Analyt Technol Biomed Life Sci; 2016 Oct; 1033-1034():311-316. PubMed ID: 27595651
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A rapid method for the simultaneous determination of L-ascorbic acid and acetylsalicylic acid in aspirin C effervescent tablet by ultra performance liquid chromatography-tandem mass spectrometry.
    Wabaidur SM; Alothman ZA; Khan MR
    Spectrochim Acta A Mol Biomol Spectrosc; 2013 May; 108():20-5. PubMed ID: 23454710
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Development of a stability- indicating HPLC method for simultaneous determination of ten related substances in vonoprazan fumarate drug substance.
    Luo Z; Liu A; Liu Y; Wang G; Chen X; Wang H; Li M; Zhang H; Qiu Y; Zhai H
    J Pharm Biomed Anal; 2018 Feb; 149():133-142. PubMed ID: 29112902
    [TBL] [Abstract][Full Text] [Related]  

  • 19. UPLC-MS/MS assay of 21-aminosteroid (lazaroid U74389G) for application in pharmacokinetic study.
    Gadgil P; Ibrahim F; Chow DS
    J Pharm Biomed Anal; 2016 Apr; 122():90-7. PubMed ID: 26848737
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Forced degradation of nepafenac: Development and validation of stability indicating UHPLC method.
    Runje M; Babić S; Meštrović E; Nekola I; Dujmić-Vučinić Ž; Vojčić N
    J Pharm Biomed Anal; 2016 May; 123():42-52. PubMed ID: 26871279
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 34.