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 *

105 related articles for article (PubMed ID: 22816264)

  • 1. Development and optimization of an HPLC analysis of citalopram and its four nonchiral impurities using experimental design methodology.
    Tadić S; Nikolić K; Agbaba D
    J AOAC Int; 2012; 95(3):733-43. PubMed ID: 22816264
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development of a novel RP-HPLC method for the efficient separation of aripiprazole and its nine impurities.
    Nikolic K; Filijović ND; Maričić B; Agbaba D
    J Sep Sci; 2013 Oct; 36(19):3165-75. PubMed ID: 23900963
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Quantitative structure -retention relationship modeling of selected antipsychotics and their impurities in green liquid chromatography using cyclodextrin mobile phases.
    Maljurić N; Golubović J; Otašević B; Zečević M; Protić A
    Anal Bioanal Chem; 2018 Apr; 410(10):2533-2550. PubMed ID: 29442144
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The chemometric study and quantitative structure retention relationship modeling of liquid chromatography separation of ziprasidone components.
    Nikolic K; Pavlovic M; Smolinski A; Agbaba D
    Comb Chem High Throughput Screen; 2012 Nov; 15(9):730-44. PubMed ID: 22934948
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isolation and characterization of degradation products of citalopram and process-related impurities using RP-HPLC.
    Rao RN; Raju AN; Narsimha R
    J Sep Sci; 2008 Jun; 31(10):1729-38. PubMed ID: 18481321
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Quantitative structure-retention relationship model for the determination of naratriptan hydrochloride and its impurities based on artificial neural networks coupled with genetic algorithm.
    Mizera M; Krause A; Zalewski P; Skibiński R; Cielecka-Piontek J
    Talanta; 2017 Mar; 164():164-174. PubMed ID: 28107913
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of the trace-level impurities in the bulk drug citalopram by high-performance liquid chromatography/tandem multistage mass spectrometry.
    Sun C; Xu H; Pan Y; Shen Z; Wang D
    Rapid Commun Mass Spectrom; 2007; 21(17):2889-94. PubMed ID: 17663502
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Monitoring of fosinopril sodium impurities by liquid chromatography-mass spectrometry including the neural networks in method evaluation.
    Jancić B; Medenica M; Ivanović D; Janković S; Malenović A
    J Chromatogr A; 2008 May; 1189(1-2):366-73. PubMed ID: 18154978
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rapid Method Development in Hydrophilic Interaction Liquid Chromatography for Pharmaceutical Analysis Using a Combination of Quantitative Structure-Retention Relationships and Design of Experiments.
    Taraji M; Haddad PR; Amos RI; Talebi M; Szucs R; Dolan JW; Pohl CA
    Anal Chem; 2017 Feb; 89(3):1870-1878. PubMed ID: 28208251
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Development and validation of an HPLC method for determination of ziprasidone and its impurities in pharmaceutical dosage forms.
    Pavlovic M; Malesevic M; Nikolic K; Agbaba D
    J AOAC Int; 2011; 94(3):713-22. PubMed ID: 21796998
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Development and validation of a HPLC method for the determination of sertraline and three non-chiral related impurities.
    Ferrarini A; Huidobro AL; Pellati F; Barbas C
    J Pharm Biomed Anal; 2010 Oct; 53(2):122-9. PubMed ID: 20138727
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Use of dual-filtering to create training sets leading to improved accuracy in quantitative structure-retention relationships modelling for hydrophilic interaction liquid chromatographic systems.
    Taraji M; Haddad PR; Amos RIJ; Talebi M; Szucs R; Dolan JW; Pohl CA
    J Chromatogr A; 2017 Jul; 1507():53-62. PubMed ID: 28587779
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Towards a chromatographic similarity index to establish localised quantitative structure-retention relationships for retention prediction. II Use of Tanimoto similarity index in ion chromatography.
    Park SH; Talebi M; Amos RIJ; Tyteca E; Haddad PR; Szucs R; Pohl CA; Dolan JW
    J Chromatogr A; 2017 Nov; 1523():173-182. PubMed ID: 28291517
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Drug impurity profiling: Method optimization on dissimilar chromatographic systems: Part I: pH optimization of the aqueous phase.
    Dumarey M; Sneyers R; Janssens W; Somers I; Vander Heyden Y
    Anal Chim Acta; 2009 Dec; 656(1-2):85-92. PubMed ID: 19932818
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development of the HPLC Method for Simultaneous Determination of Lidocaine Hydrochloride and Tribenoside Along with Their Impurities Supported by the QSRR Approach.
    Plenis A; Konieczna L; Miękus N; Bączek T
    Chromatographia; 2013 Mar; 76(5-6):255-265. PubMed ID: 23482886
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A validated reversed phase HPLC method for the determination of process-related impurities in almotriptan malate API.
    Kumar AP; Ganesh VR; Rao DV; Anil C; Rao BV; Hariharakrishnan VS; Suneetha A; Sundar BS
    J Pharm Biomed Anal; 2008 Mar; 46(4):792-8. PubMed ID: 18191357
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prediction of retention in hydrophilic interaction liquid chromatography using solute molecular descriptors based on chemical structures.
    Taraji M; Haddad PR; Amos RI; Talebi M; Szucs R; Dolan JW; Pohl CA
    J Chromatogr A; 2017 Feb; 1486():59-67. PubMed ID: 28049585
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chemometrics-assisted simultaneous voltammetric determination of ascorbic acid, uric acid, dopamine and nitrite: application of non-bilinear voltammetric data for exploiting first-order advantage.
    Gholivand MB; Jalalvand AR; Goicoechea HC; Skov T
    Talanta; 2014 Feb; 119():553-63. PubMed ID: 24401455
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chemometrically assissted optimization and validation of RP-HPLC method for the analysis of itraconazole and its impurities.
    Kasagić I; Malenović A; Jovanović M; Rakić T; Jančić Stojanović B; Ivanović D
    Acta Pharm; 2013 Jun; 63(2):159-73. PubMed ID: 23846140
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Developing and optimizing a validated isocratic reversed-phase high-performance liquid chromatography separation of nimodipine and impurities in tablets using experimental design methodology.
    Barmpalexis P; Kanaze FI; Georgarakis E
    J Pharm Biomed Anal; 2009 Jul; 49(5):1192-202. PubMed ID: 19369025
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.