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A novel zein-based dry coating tablet design for zero-order release.
Int J Pharm. 2009 Mar 31; 370(1-2):81-6.IJ

Abstract

The purpose of this study was to design zero-order release of dry-coated tablets using pure zein powder, zein granule and zein blend containing two common pharmaceutical excipients such as microcrystalline cellulose (MCC) or starch in different proportions as coating material. The 5-fluorouracil (5-FU) was used as a model drug. The physical characterization and drug release behaviors of dry-coated tablets were investigated. The surface structure of the tablets was examined by a scanning electron microscopy. The correlation coefficient (R) was used as indicator of the best fitting of the zero-order model for drug release. It was found that zein formed a gelatinous layer fast and its network prevented disintegration of the tablet during dissolution process. Zein-based dry coating tablets had good physical properties such as compactibility and friability. All formulations fit the zero-order model well. The mechanism for zero-order release of these dry-coated tablets was solvent penetration into the dosage form and dissolving the drug, the dissolving core formed an apex in the center of the tablets and the drug diffused out. The apex of zein-coated tablets worked as orifice of an osmotic system and released the drug in zero-order profile.

Authors+Show Affiliations

Department of Pharmaceutics, Faculty of Pharmacy, Shandong University, 250012 Jinan, China. hongxia.guo@gmail.comNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

19100825

Citation

Guo, H X., and Y P. Shi. "A Novel Zein-based Dry Coating Tablet Design for Zero-order Release." International Journal of Pharmaceutics, vol. 370, no. 1-2, 2009, pp. 81-6.
Guo HX, Shi YP. A novel zein-based dry coating tablet design for zero-order release. Int J Pharm. 2009;370(1-2):81-6.
Guo, H. X., & Shi, Y. P. (2009). A novel zein-based dry coating tablet design for zero-order release. International Journal of Pharmaceutics, 370(1-2), 81-6. https://doi.org/10.1016/j.ijpharm.2008.11.026
Guo HX, Shi YP. A Novel Zein-based Dry Coating Tablet Design for Zero-order Release. Int J Pharm. 2009 Mar 31;370(1-2):81-6. PubMed PMID: 19100825.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A novel zein-based dry coating tablet design for zero-order release. AU - Guo,H X, AU - Shi,Y P, Y1 - 2008/12/03/ PY - 2008/07/07/received PY - 2008/10/28/revised PY - 2008/11/17/accepted PY - 2008/12/23/entrez PY - 2008/12/23/pubmed PY - 2009/6/24/medline SP - 81 EP - 6 JF - International journal of pharmaceutics JO - Int J Pharm VL - 370 IS - 1-2 N2 - The purpose of this study was to design zero-order release of dry-coated tablets using pure zein powder, zein granule and zein blend containing two common pharmaceutical excipients such as microcrystalline cellulose (MCC) or starch in different proportions as coating material. The 5-fluorouracil (5-FU) was used as a model drug. The physical characterization and drug release behaviors of dry-coated tablets were investigated. The surface structure of the tablets was examined by a scanning electron microscopy. The correlation coefficient (R) was used as indicator of the best fitting of the zero-order model for drug release. It was found that zein formed a gelatinous layer fast and its network prevented disintegration of the tablet during dissolution process. Zein-based dry coating tablets had good physical properties such as compactibility and friability. All formulations fit the zero-order model well. The mechanism for zero-order release of these dry-coated tablets was solvent penetration into the dosage form and dissolving the drug, the dissolving core formed an apex in the center of the tablets and the drug diffused out. The apex of zein-coated tablets worked as orifice of an osmotic system and released the drug in zero-order profile. SN - 1873-3476 UR - https://www.unboundmedicine.com/medline/citation/19100825/A_novel_zein_based_dry_coating_tablet_design_for_zero_order_release_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0378-5173(08)00780-1 DB - PRIME DP - Unbound Medicine ER -