Have a personal or library account? Click to login
Dissolution rate enhancement of gliclazide by ordered mixing Cover

Dissolution rate enhancement of gliclazide by ordered mixing

Open Access
|Sep 2011

References

  1. V. A. Saharan, V. Kukkar, M. Kataria, V. Kharb and P. Choudhury, Ordered mixing: mechanism, process and applications in pharmaceutical formulations, Asian J. Pharm. Sci. 3 (2008) 240-259.
  2. V. A. Saharan, M. Kataria, V. Kukkar, M. Gera and P. K. Choudhury, Dissolution enhancement of drugs Part II: Effect of carriers, Int. J. Health Res. 2 (2009) 207-223.
  3. V. A. Saharan, M. Kataria, V. Kukkar, M. Gera and P. K. Choudhury, Dissolution enhancement of drugs Part I: Technologies and effect of carriers, Int. J. Health Res. 2 (2009) 107-124.
  4. C. M. Wassvik, A. G. Holmen, C. A. Bergstrom, I. Zamora and P. Artursson, Contribution of solid-state properties to the aqueous solubility of drugs, Eur. J. Pharm. Sci. 29 (2006) 294-305; DOI: 10.1016/j.ejps.2006.05.013.10.1016/j.ejps.2006.05.013
  5. H. Allaboun, K. A. Alkhamis and W. Y. AlMomani, The application of the convective diffusion model and the film equilibrium model to surfactant-facilitated dissolution of gliclazide, Eur. J. Pharm. Sci. 19 (2003) 231-236; DOI: 10.1016/S0928-0987(03)00107-6.10.1016/S0928-0987(03)00107-6
  6. S. Biswal, J. Sahoo, P. N. Murthy, R. P. Giradkar and J. G. Avari, Enhancement of dissolution rate of gliclazide using solid dispersions with polyethylene glycol 6000, AAPS PharmSciTech 9 (2008) 563-570; DOI: 10.1208/s12249-008-9079-z.10.1208/s12249-008-9079-z
  7. S. Asyarie and H. Rachmawati, In vivo and in vitro evaluation of a solid dispersion system of gliclazide: PEG 6000, PDA J. Pharm. Sci. Technol. 61 (2007) 400-410.
  8. M. P. Patil and N. J. Gaikwad, Preparation and characterization of gliclazide-polyethylene glycol 4000 solid dispersions, Acta Pharm. 59 (2009) 57-65; DOI: 10.2478/v10007-009-0001-3.10.2478/v10007-009-0001-3
  9. R. Talari, A. Nokhodchi, S. A. Mostafavi and J. Varshosaz, Dissolution enhancement of gliclazide using pH change approach in the presence of twelve stabilizers with various physico-chemical properties, J. Pharm. Pharm. Sci. 12 (2009) 250-265.10.18433/J31P4P
  10. R. Talari, J. Varshosaz, S. A. Mostafavi and A. Nokhodchi, Gliclazide microcrystals prepared by two methods of in situ micronization: Pharmacokinetic studies in diabetic and normal rats, AAPS PharmSciTech 11 (2010) 786-792; DOI: 10.1208/s12249-010-9441-9.10.1208/s12249-010-9441-9
  11. M. Barzegar-Jalalia, H. Valizadeha, M.-R. S. Shadbada, K. Adibkiaa, G. Mohammadia, A. Farahania, Z. Arasha and A. Nokhodchi, Cogrinding as an approach to enhance dissolution rate of a poorly water-soluble drug (gliclazide), Powder Technol. 197 (2010) 150-158; DOI: 10.1016/j.powtec.2009.09.008.10.1016/j.powtec.2009.09.008
  12. Y. K. Lo, C. J. Chen, T. R. Tsai and T. M. Cham, Comparison of the solubility and dissolution rate between gliclazide solid complex and its nanospheres, Drug Dev. Ind. Pharm. 33 (2007) 301-309; DOI: 10.1080/03639040600920622.10.1080/03639040600920622
  13. United States Pharmacopeia XXIV, National Formulary XIX USO Convention, Rockville (MD) 1999.
  14. P. Costa and J. Lobo, Modeling and comparison of dissolution profiles, Eur. J. Pharm. Sci. 13 (2001) 123-133; DOI: 10.1016/S0928-0987(01)00095-1.10.1016/S0928-0987(01)00095-1
  15. M. Westerberg and C. Nystrom, Physicochemical aspects of drug release. Part 18: Use of a surfactant and a disintegrant for improving drug dissolution rate from ordered mixtures, STPPharm Sci. 3 (1993) 142-147.
DOI: https://doi.org/10.2478/v10007-011-0021-7 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Language: English
Page range: 323 - 334
Published on: Sep 26, 2011
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Related subjects:

© 2011 Vikas Saharan, Pratim Choudhury, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons License.

Volume 61 (2011): Issue 3 (September 2011)