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 *

162 related articles for article (PubMed ID: 32590301)

  • 1. Development of a generic reversed-phase liquid chromatography method for protein quantification using analytical quality-by-design principles.
    Kopp J; Zauner FB; Pell A; Hausjell J; Humer D; Ebner J; Herwig C; Spadiut O; Slouka C; Pell R
    J Pharm Biomed Anal; 2020 Sep; 188():113412. PubMed ID: 32590301
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Using Analytical Quality by Design to improve analytical method development in vaccines quality control: Application to an optimized quantitative high-performance anion-exchange chromatographic method.
    Moineau I; Chambon V; Perret C; Gouit L; Zamora I; Macumi M; Fertier-Prizzon S; Pitiot O
    J Chromatogr B Analyt Technol Biomed Life Sci; 2024 Feb; 1233():123946. PubMed ID: 38217970
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analytical quality-by-design (AQbD) approach for comprehensive analysis of bioactive compounds from Citrus peel wastes by UPLC.
    Santana IM; Rostagno MA; Breitkreitz MC
    Anal Bioanal Chem; 2023 Jul; 415(18):4411-4422. PubMed ID: 36853412
    [TBL] [Abstract][Full Text] [Related]  

  • 4. QbD-steered development and validation of an RP-HPLC method for quantification of ferulic acid: Rational application of chemometric tools.
    Saini S; Sharma T; Patel A; Kaur R; Tripathi SK; Katare OP; Singh B
    J Chromatogr B Analyt Technol Biomed Life Sci; 2020 Oct; 1155():122300. PubMed ID: 32771967
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Development of an analytical method for the determination of pimavanserin and its impurities applying analytical quality by design principles as a risk-based strategy.
    Radić I; Runje M; Babić S
    J Pharm Biomed Anal; 2021 Jul; 201():114091. PubMed ID: 33964725
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Increasing Analytical Quality by Designing a Thin-Layer Chromatography Scanner Method for the Determination of the Radiochemical Purity of Radiopharmaceutical Sodium Iodide
    Vasquez-Huaman M; Castro-Luna A; Ramos-Cevallos NJ; Ramos-Perfecto D; Alcarraz-Curi M; Segura-Vasquez J; Cáceres-Antaurco D
    Molecules; 2024 Apr; 29(8):. PubMed ID: 38675702
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Development and optimization of a LC-MS/MS compatible method for quantification of losartan, hydrochlorothiazide and their impurities using AQbD approach and measurement uncertainty evaluation.
    Rocha AL; Lourenço FR
    Talanta; 2023 Jul; 259():124481. PubMed ID: 36989967
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Implementation of QbD Approach to the Development of Chromatographic Methods for the Determination of Complete Impurity Profile of Substance on the Preclinical and Clinical Step of Drug Discovery Studies.
    Gurba-Bryśkiewicz L; Dawid U; Smuga DA; Maruszak W; Delis M; Szymczak K; Stypik B; Moroz A; Błocka A; Mroczkiewicz M; Dubiel K; Wieczorek M
    Int J Mol Sci; 2022 Sep; 23(18):. PubMed ID: 36142622
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Developing a Validated HPLC Method for Quantification of Ceftazidime Employing Analytical Quality by Design and Monte Carlo Simulations.
    Kaur R; Saini S; Patel A; Sharma T; Kaur R; Katare OP; Singh B
    J AOAC Int; 2021 Jun; 104(3):620-632. PubMed ID: 33528003
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analytical quality by design development of an ecologically acceptable enantioselective HPLC method for timolol maleate enantiomeric purity testing on ovomucoid chiral stationary phase.
    Mitrović M; Protić A; Malenović A; Otašević B; Zečević M
    J Pharm Biomed Anal; 2020 Feb; 180():113034. PubMed ID: 31838281
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case study application of AQbD to the re-development and validation of an affinity chromatography analytical procedure for mAb titer quantitation.
    Cernosek T; Dalphin M; Jain N; Lor J; Richter N; Mellal M; Behrens S; Wunderli P
    J Chromatogr B Analyt Technol Biomed Life Sci; 2024 Jul; 1242():124205. PubMed ID: 38880058
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Integrated Analytical Quality by Design (AQbD) Approach for the Development and Validation of Bioanalytical Liquid Chromatography Method for Estimation of Valsartan.
    Bandopadhyay S; Beg S; Katare OP; Sharma T; Singh B
    J Chromatogr Sci; 2020 Jul; 58(7):606-621. PubMed ID: 32706387
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stability kinetics of fusidic acid: Development and validation of stability indicating analytical method by employing Analytical Quality by Design approach in medicinal product(s).
    Sharma G; Thakur K; Raza K; Katare OP
    J Chromatogr B Analyt Technol Biomed Life Sci; 2019 Jul; 1120():113-124. PubMed ID: 31082718
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Risk and DoE-Based DMAIC Principle to the Multipurpose-RP-HPLC Method for Synchronous Estimation of Anti-Hypertensive Drugs Using AQbD Approach.
    Prajapati PB; Patel A; Shah SA
    J AOAC Int; 2021 Sep; 104(5):1442-1452. PubMed ID: 34115124
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Application of analytical quality by design principles for the determination of alkyl p-toluenesulfonates impurities in Aprepitant by HPLC. Validation using total-error concept.
    Zacharis CK; Vastardi E
    J Pharm Biomed Anal; 2018 Feb; 150():152-161. PubMed ID: 29245084
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Rapid Development and Validation of Improved Reversed-Phase High-performance Liquid Chromatography Method for the Quantification of Mangiferin, a Polyphenol Xanthone Glycoside in
    Naveen P; Lingaraju HB; Prasad KS
    Pharmacognosy Res; 2017; 9(2):215-219. PubMed ID: 28539748
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stability-indicating method development for quantification of bromopride, its impurities, and degradation products by ultra-high performance liquid chromatography applying Analytical Quality by Design principles.
    Abreu JC; Mahr AG; do Lago CL
    J Pharm Biomed Anal; 2021 Oct; 205():114306. PubMed ID: 34385016
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analytical Quality by Design as applied to the development of a SEC-HPLC platform procedure for the determination of monoclonal antibody purity without mobile phase additives.
    Cernosek T; Dalphin M; Jain N; Richter N; Beard S; Wang J; Osborne J; Stone T; Mellal M; Behrens S; Wunderli P
    J Pharm Biomed Anal; 2024 Aug; 246():116220. PubMed ID: 38795426
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Discriminative Dissolution Method Development Through an aQbD Approach.
    Chen H; Wang R; McElderry JD
    AAPS PharmSciTech; 2023 Dec; 24(8):255. PubMed ID: 38066324
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.