BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 25014125)

  • 1. Computational predictions of glass-forming ability and crystallization tendency of drug molecules.
    Alhalaweh A; Alzghoul A; Kaialy W; Mahlin D; Bergström CA
    Mol Pharm; 2014 Sep; 11(9):3123-32. PubMed ID: 25014125
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Toward in silico prediction of glass-forming ability from molecular structure alone: a screening tool in early drug development.
    Mahlin D; Ponnambalam S; Höckerfelt MH; Bergström CA
    Mol Pharm; 2011 Apr; 8(2):498-506. PubMed ID: 21344945
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Early drug development predictions of glass-forming ability and physical stability of drugs.
    Mahlin D; Bergström CA
    Eur J Pharm Sci; 2013 May; 49(2):323-32. PubMed ID: 23557841
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Is there a correlation between the glass forming ability of a drug and its supersaturation propensity?
    Blaabjerg LI; Lindenberg E; Löbmann K; Grohganz H; Rades T
    Int J Pharm; 2018 Mar; 538(1-2):243-249. PubMed ID: 29341914
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Glass-forming ability of compounds in marketed amorphous drug products.
    Wyttenbach N; Kuentz M
    Eur J Pharm Biopharm; 2017 Mar; 112():204-208. PubMed ID: 27903457
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A classification system to assess the crystallization tendency of organic molecules from undercooled melts.
    Baird JA; Van Eerdenbrugh B; Taylor LS
    J Pharm Sci; 2010 Sep; 99(9):3787-806. PubMed ID: 20623696
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Theoretical Considerations of the Prigogine-Defay Ratio with Regard to the Glass-Forming Ability of Drugs from Undercooled Melts.
    Wyttenbach N; Kirchmeyer W; Alsenz J; Kuentz M
    Mol Pharm; 2016 Jan; 13(1):241-50. PubMed ID: 26587865
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Predicting Glass-Forming Ability of Pharmaceutical Compounds by Using Machine Learning Technologies.
    Jiang J; Ouyang D; Williams RO
    AAPS PharmSciTech; 2023 Apr; 24(5):103. PubMed ID: 37072563
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Understanding the glass-forming ability of active pharmaceutical ingredients for designing supersaturating dosage forms.
    Kawakami K; Usui T; Hattori M
    J Pharm Sci; 2012 Sep; 101(9):3239-48. PubMed ID: 22531946
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications.
    Kawabata Y; Wada K; Nakatani M; Yamada S; Onoue S
    Int J Pharm; 2011 Nov; 420(1):1-10. PubMed ID: 21884771
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular Drivers of Crystallization Kinetics for Drugs in Supersaturated Aqueous Solutions.
    Alhalaweh A; Alzghoul A; Bergström CAS
    J Pharm Sci; 2019 Jan; 108(1):252-259. PubMed ID: 30423342
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An investigation into the influence of counterion on the properties of some amorphous organic salts.
    Towler CS; Li T; Wikström H; Remick DM; Sanchez-Felix MV; Taylor LS
    Mol Pharm; 2008; 5(6):946-55. PubMed ID: 19434850
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Physical stability of drugs after storage above and below the glass transition temperature: Relationship to glass-forming ability.
    Alhalaweh A; Alzghoul A; Mahlin D; Bergström CAS
    Int J Pharm; 2015 Nov; 495(1):312-317. PubMed ID: 26341321
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Influence of preparation pathway on the glass forming ability.
    Blaabjerg LI; Lindenberg E; Rades T; Grohganz H; Löbmann K
    Int J Pharm; 2017 Apr; 521(1-2):232-238. PubMed ID: 28232267
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Long-Term Amorphous Drug Stability Predictions Using Easily Calculated, Predicted, and Measured Parameters.
    Nurzyńska K; Booth J; Roberts CJ; McCabe J; Dryden I; Fischer PM
    Mol Pharm; 2015 Sep; 12(9):3389-98. PubMed ID: 26236939
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Development and validation of in silico models for estimating drug preformulation risk in PEG400/water and Tween80/water systems.
    Crivori P; Morelli A; Pezzetta D; Rocchetti M; Poggesi I
    Eur J Pharm Sci; 2007 Nov; 32(3):169-81. PubMed ID: 17714921
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Amino acids as co-amorphous stabilizers for poorly water soluble drugs--Part 1: preparation, stability and dissolution enhancement.
    Löbmann K; Grohganz H; Laitinen R; Strachan C; Rades T
    Eur J Pharm Biopharm; 2013 Nov; 85(3 Pt B):873-81. PubMed ID: 23537574
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Impact of Intermolecular Interactions, Dimeric Structures on the Glass Forming Ability of Naproxen, and a Series of Its Derivatives.
    Minecka A; Kaminska E; Tarnacka M; Grudzka-Flak I; Bartoszek M; Wolnica K; Dulski M; Kaminski K; Paluch M
    Mol Pharm; 2018 Oct; 15(10):4764-4776. PubMed ID: 30156420
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long-Term Physical (In)Stability of Spray-Dried Amorphous Drugs: Relationship with Glass-Forming Ability and Physicochemical Properties.
    Edueng K; Bergström CAS; Gråsjö J; Mahlin D
    Pharmaceutics; 2019 Aug; 11(9):. PubMed ID: 31438566
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prediction of pH-dependent aqueous solubility of druglike molecules.
    Hansen NT; Kouskoumvekaki I; Jørgensen FS; Brunak S; Jónsdóttir SO
    J Chem Inf Model; 2006; 46(6):2601-9. PubMed ID: 17125200
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.