Čes. slov. farm. 2007, 56(5):235-242
Effect of thermal curing of the ethyl cellulose film on the rapidity of release of diclofenac sodium from pellets
- 1 Veterinární a farmaceutická univerzita Brno, Ústav technologie léků
- 2 Zentiva a. s., Praha
Coated pellets controlling drug release are a very popular dosage form which is widely used in medical practice. At present the coatings of water-insoluble polymers formed from aqueous dispersions are preferred. However, film formation from an aqueous polymeric dispersion is different from that from their organic solutions. A stable film on the pellets surface is produced by coalesces of discrete latex particles at an optimum temperature. The present experimental paper studied the changes of diclofenac sodium dissolution profiles from coated pellets, when their coatings from an aqueous polymeric dispersion of ethyl cellulose were cured for different time periods (1-72 hours) and a temperature of 60 °C. Drug release rate was decreasing with the increasing time of the layer curing up to 24 hours. At this time the dissolution curve was similar to a strait line. When the curing time further increased, the drug release was again faster. All prepared samples (with or without seal coat, cured for a period of 24 hour or uncured) were filled into hard gelatine capsules and stored in blisters in three different stability boxes (25 °C/60 % RH, 30 °C/65 % RH, 40 °C/75 % RH) for 6 or 12 months. The best drug dissolution profile and stability were observed for the pellets with the seal coat and ethyl cellulose coating cured for 24 hours.
Keywords: pellets; water dispersion of ethyl cellulose; curing; drug dissolution profile; stability
Received: May 28, 2007; Accepted: June 29, 2007; Published: May 1, 2007 Show citation
References
- Wade, A., Weller, P. J.: Handbook of pharmaceutical excipients. London, The Pharmaceutical Press, 1994, 651 s.
- Poter, S. C.: Drug Dev. Ind. Pharm., 1989; 15), 1495-1521
Go to original source...
- Wallace, J. W.: In: Encyclopedia of pharmaceutical technology (Swarbrick, J., Boylan, J. C.), vol. 2. New York, Marcel Dekker, 1996, 319-337.
- Hogan, J. E.: In: Pharmaceutical coating technology (Cole, G., Hogan, J., Aulton, M.). London and Bristol, Taylor and Francis, 1995, s. 409-438.
- Hogan, J. E.: In: Pharmaceutical coating technology (Cole, G., Hogan, J., Aulton, M.). London and Bristol 1995, s. 6-52.
- Porter, S. C., Bruno, CH. H.: In: Pharmaceutical dosage forms: Tablets (Lieberman, H. A., Lachman, L., Schwartz, J. B.), vol. 3, second edition. New York and Basel, Marcel Dekker, 1990, 77-159.
- Fukumori, Y.: In: Multiparticulate oral drug delivery (Ghebre-Sellasie, I.). New York and Basel, Marcel Dekker, 1989, 79-111.
- Dressman, J. B. et al.: J. Control. Release, 1995; 36, 251-260.
Go to original source...
- Sadeghi, F., Ford, J. L., Rajabi-Siahboomi, A.: Int. J. Pharm., 2003; 254, 123-135.
Go to original source...
Go to PubMed...
- Wesseling, M., Bodmeier, R.: Eur. J. Pharm. Biopharm., 1999; 47, 33-38
Go to original source...
Go to PubMed...
- firemní materiály Colorcon
- Bertocci, P. et al.: J. Pharm. Biomed. Anal., 2005; 37, 679-685
Go to original source...
- Deasy, P. B., Law, M. F. L.: Int. J. Pharm., 1997; 148, 201-209.
Go to original source...
- Vertommen, J., Kinget, R.: Drug Dev. Ind. Pharm., 1997; 23, 39-46.
Go to original source...
- Lippold, B. H, Sutter, B. K., Lippold, B. C.: Int. J. Pharm., 1989; 54, 15-25.
Go to original source...
- Kincl, M., Vrečer, F., Veber, M.: Analytica Chimica Acta, 2004; 502,107-113.
Go to original source...