Skip to main content
Have a personal or library account? Click to login
Liquisolid technique as a tool for enhancement of poorly water-soluble drugs and evaluation of their physicochemical properties Cover

Liquisolid technique as a tool for enhancement of poorly water-soluble drugs and evaluation of their physicochemical properties

Acta Pharmaceutica
Volume 57 (2007): Issue 1 (March 2007)
By: ,  ,   and    
Open Access
|Feb 2007
References

References

  1. S. G. Kapsi and J. W. Ayres, Processing factors in development of solid solution formulation of itraconazole for enhancement of drug dissolution and bioavailability,229 (2001) 193-203.
    Open DOISearch in Google Scholar
  2. A. J. Aguiar, A. J. Zelmer and A. W. Kinkel, Deagglomeration behavior of relatively insoluble benzoic acid and its sodium salt,56 (1967) 1243-1252.
    Open DOISearch in Google Scholar
  3. P. Finholt and S. Solvang, Dissolution kinetics of drugs in human gastric juice; the role of surface tension,57 (1968) 1322-1326.
    Open DOISearch in Google Scholar
  4. S. L. Lin, J. Menig and L. Lachman, Interdependence of physiological surfactant and drug particle size on the dissolution behavior of water insoluble drugs,57 (1968) 2143-2146.
    Open DOISearch in Google Scholar
  5. S. Spireas and S. Sadu, Enhancement of prednisolone dissolution properties using liquisolid compacts,166 (1998) 177-188.
    Open DOISearch in Google Scholar
  6. S. Spireas, S. Sadu and R. Grover, In vitro release evaluation of hydrocortisone liquisolid tablets,87 (1998) 867-872.
    Open DOISearch in Google Scholar
  7. S. Spireas, T. Wang and R. Grover, Effect of powder substrate on the dissolution properties of methchrothiazide liquisolid compacts,25 (1999) 163-168.
    Open DOISearch in Google Scholar
  8. K. Y. Yang, R. Glemza and C. I. Jarowski, Effect of amorphous silicon dioxide on drug dissolution,68 (1979) 560-565.
    Open DOISearch in Google Scholar
  9. C. Liao and C. I. Jarowski, Dissolution rates of corticoid solutions dispersed on silicas,73 (1984) 401-403.
    Open DOISearch in Google Scholar
  10. A. Nokhodchi, Y. Javadzadeh, M. R. Siahi and M. Barzegar-Jalali, The effect of type and concentration of vehicles on the dissolution rate of a poorly soluble drug (indomethacin) from liquisolid compacts,8 (2005) 18-25.
    Search in Google Scholar
  11. , USP Convention, Rockville 2003.
    Search in Google Scholar
  12. P. Costa, An alternative method to the evaluation of similarity factor in dissolution testing,220 (2001) 77-83.
    Open DOISearch in Google Scholar
  13. P. Costa and J. M. S. Lobo, Modelling and comparison of dissolution profiles,13 (2001) 123-133.
    Open DOISearch in Google Scholar
  14. K. A. Khan, Concept of dissolution efficiency,27 (1975) 48-49.
    Open DOISearch in Google Scholar
  15. H. Abdou, Effect of the physicochemical properties of the drug on dissolution in Dissolution, Bioavailability and Bioequivalence (Ed. H. Abdou), Edison Mack Publishing Co., Easton, PA 1989, pp. 53-72.
    Search in Google Scholar
  16. N. Kaneniwa, M. Otsuka and T. Hayashi, Physicochemical characterization of indomethacin polymorphs and transformation kinetics in ethanol,33 (1985) 3447-3455.
    Open DOISearch in Google Scholar
  17. H. Imaizumi, N. Nambu and T. Nagai, Stability of several physical properties of amorphous and crystalline forms of indomethacin,28 (1980) 2565-2569.
    Open DOISearch in Google Scholar
  18. L. Borka, Polymorphism of indomethacin. New modifications, their melting behavior and solubility,11 (1974) 295-303.
    Search in Google Scholar
  19. M. Otsuka, F. Kato and Y. Matsuda, Determination of indomethacin polymorphic contents by chemometric near-infrared spectroscopy and conventional powder X-ray diffractometry,126 (2001) 1578-1582.
    Open DOISearch in Google Scholar
  20. M. Yoshioka, B.C. Hancock and G. Zografi, Crystallization of indomethacin from the amorphous state below and above its glass transition temperature,83 (1994) 1700-1705.
    Open DOISearch in Google Scholar
  21. H. Imaizumi, N. Nambu and T. Nagai, Stabilization of amorphous state of indomethacin by solid dispersions in polyvinylpyrolidone,31 (1983) 2510-2512.
    Open DOISearch in Google Scholar
DOI: https://doi.org/10.2478/v10007-007-0008-6 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Journal RSS Feed
Language: English
Page range: 99 - 109
Published on: Feb 28, 2007
Published by: Croatian Pharmaceutical Society
In partnership with: Paradigm Publishing Services
Keywords:
indomethacin,
liquisolid compacts,
dissolution rate,
aging,
DSC,
XPD
Related subjects:
Pharmacy,
Pharmacy, other

© 2007 Yousef Javadzadeh, Mohammad Siahi, Solmaz Asnaashari, Ali Nokhodchi, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons License.

Volume 57 (2007): Issue 1 (March 2007)
Previous article
Next article