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Journal Abstract Search

247 related items for PubMed ID: 18207706

  • 1. High throughput UV method for the estimation of thermodynamic solubility and the determination of the solubility in biorelevant media.
    Bard B, Martel S, Carrupt PA.
    Eur J Pharm Sci; 2008 Mar 03; 33(3):230-40. PubMed ID: 18207706
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  • 3. Biological assay challenges from compound solubility: strategies for bioassay optimization.
    Di L, Kerns EH.
    Drug Discov Today; 2006 May 03; 11(9-10):446-51. PubMed ID: 16635808
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  • 4. A high throughput solubility assay for drug discovery using microscale shake-flask and rapid UHPLC-UV-CLND quantification.
    Lin B, Pease JH.
    J Pharm Biomed Anal; 2016 Apr 15; 122():126-40. PubMed ID: 26855285
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  • 6. Automated approach to couple solubility with final pH and crystallinity for pharmaceutical discovery compounds.
    Seadeek C, Ando H, Bhattachar SN, Heimbach T, Sonnenberg JL, Blackburn AC.
    J Pharm Biomed Anal; 2007 Apr 11; 43(5):1660-6. PubMed ID: 17270379
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  • 14. Development of a high throughput equilibrium solubility assay using miniaturized shake-flask method in early drug discovery.
    Zhou L, Yang L, Tilton S, Wang J.
    J Pharm Sci; 2007 Nov 11; 96(11):3052-71. PubMed ID: 17722003
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  • 15. Kinetic and thermodynamic solubility values of some bioactive compounds.
    Shoghi E, Fuguet E, Ràfols C, Bosch E.
    Chem Biodivers; 2009 Nov 11; 6(11):1789-95. PubMed ID: 19937816
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  • 18. Advances in the design of fasted state simulating intestinal fluids: FaSSIF-V3.
    Fuchs A, Leigh M, Kloefer B, Dressman JB.
    Eur J Pharm Biopharm; 2015 Aug 11; 94():229-40. PubMed ID: 26032292
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  • 19. Use of (1)H NMR to facilitate solubility measurement for drug discovery compounds.
    Lin M, Tesconi M, Tischler M.
    Int J Pharm; 2009 Mar 18; 369(1-2):47-52. PubMed ID: 19073245
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