A potentiometric titration method for the crystallization of drug-like organic molecules

被引:2
|
作者
Du-Cuny, Lei
Huwyler, Joerg
Fischer, Holger
Kansy, Manfred [1 ]
机构
[1] F Hoffmann La Roche & Co Ltd, Discovery Chem Mol Properties & Struct Property C, CH-4070 Basel, Switzerland
[2] Univ Appl Sci NW Switzerland, Inst Pharma Technol, CH-4132 Muttenz, Switzerland
关键词
crystal; crystallization; solubility; potentiometric titration;
D O I
10.1016/j.ijpharm.2007.05.030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It is generally accepted, that crystalline solids representing a low energy polymorph should be selected for development of oral dosage forms. As a consequence, efficient and robust procedures are needed at an early stage during drug discovery to prepare crystals from drug-like organic molecules. In contrast to the use of supersaturated solutions, we present a potentiometric crystallization procedure where saturated solutions are prepared in a controlled manner by pH-titration. Crystallization is carried out under defined conditions using the sample concentration and experimental pK(a) values as input parameters. Crystals of high quality were obtained for I I drugs selected to demonstrate the efficiency and applicability of the new method. Technical improvements are suggested to overcome practical limitations and to enhance the possibility of obtaining crystals from molecules in their uncharged form. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:161 / 167
页数:7
相关论文
共 50 条
  • [31] How accurate are continuum solvation models for drug-like molecules?
    Jacob Kongsted
    Pär Söderhjelm
    Ulf Ryde
    Journal of Computer-Aided Molecular Design, 2009, 23 : 395 - 409
  • [32] Generative Network Complex for the Automated Generation of Drug-like Molecules
    Gao, Kaifu
    Duc Duy Nguyen
    Tu, Meihua
    Wei, Guo-Wei
    JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2020, 60 (12) : 5682 - 5698
  • [33] A structure-permeability study of small drug-like molecules
    Fichert, T
    Yazdanian, M
    Proudfoot, JR
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (04) : 719 - 722
  • [34] A Robust Force Field Based Method for Calculating Conformational Energies of Charged Drug-Like Molecules
    Poehlsgaard, Jacob
    Harpsoe, Kasper
    Jorgensen, Flemming Steen
    Olsen, Lars
    JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2012, 52 (02) : 409 - 419
  • [35] Automation of the Charmm General Force Field for Drug-Like Molecules
    Vanommeslaeghe, Kenno
    Ghosh, Jayeeta
    Polani, Narendra K.
    Sheetz, Michael
    Pamidighantam, Sudhakar V.
    Connolly, John W. D.
    MacKerell, Alexander D., Jr.
    BIOPHYSICAL JOURNAL, 2011, 100 (03) : 611 - 611
  • [36] Modeling quinone formation of drug-like molecules with machine learning
    Hughes, Tyler B.
    Le Dang, Na
    Swamidass, S. Joshua
    DRUG METABOLISM REVIEWS, 2016, 48 : 107 - 107
  • [37] How accurate are continuum solvation models for drug-like molecules?
    Kongsted, Jacob
    Soderhjelm, Par
    Ryde, Ulf
    JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 2009, 23 (07) : 395 - 409
  • [38] POTENTIOMETRIC METHOD FOR DIFFERENTIATED TITRATION OF ORGANIC BASES IN A METHYLETHYLKETONE MEDIUM
    KRESHKOV, AP
    BYKOVA, LN
    SHEMET, NS
    DOKLADY AKADEMII NAUK SSSR, 1960, 134 (01): : 96 - 99
  • [39] The impact of physical organic chemistry on the control of drug-like properties
    Davis, AM
    Riley, R
    DRUG DESIGN: CUTTING EDGE APPROACHES, 2002, (279): : 106 - 123
  • [40] Aqueous and cosolvent solubility data for drug-like organic compounds
    Erik Rytting
    Kimberley A. Lentz
    Xue-Qing Chen
    Feng Qian
    Srini Venkatesh
    The AAPS Journal, 7