How to improve the storage stability of aqueous polymeric film coatings

被引:43
作者
Siepmann, F. [1 ]
Muschert, S. [1 ]
Leclercq, B. [2 ]
Carlin, B. [3 ]
Siepmann, J. [1 ]
机构
[1] Univ Lille, JE 2491, Coll Pharm, F-59006 Lille, France
[2] FMC BioPolymer, B-1200 Brussels, Belgium
[3] FMC BioPolymer, Princeton, NJ 08543 USA
关键词
storage stability; coating; ethylcellulose; aqueous dispersion; pellet;
D O I
10.1016/j.jconrel.2007.10.018
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
The major aim of this study was to identify an easy tool to improve the long term stability of polymeric film coatings applied from aqueous dispersions. Drug release profiles from ethylcellulose-coated theophylline pellets were monitored during 6 months open storage under ambient and stress conditions ["room temperature/ambient relative humidity (RH)" and "40 degrees C/75%RH"]. The pellets were cured for I or 2 d at 60 degrees C or for 1 or 2 d at 60 degrees C/75%RH (followed by 1 d at 60 degrees C for drying). Drug release was measured in 0.1 M HCl and in phosphate buffer pH 7.4. Interestingly, the addition of only small amounts of poly(vinyl alcohol)-poly(ethylene glycol) graft copolymer provided stable drug release profiles under all the investigated conditions, irrespective of the type of release medium, coating level, polymer blend ratio and curing conditions. The addition of small amounts of propylene glycol alginate resulted in unaltered drug release kinetics during open storage under ambient conditions, but decreasing theophylline release rates during open storage under stress conditions, due to further gradual polymer particle coalescence. When adding small amounts of carrageenan to the ethylcellulose coatings, essentially stable theophylline release patterns (with slight variations) were obtained. As coating conditions were not optimized for each system, further work is necessary to distinguish polymer from process effects. The observed stabilizing effects of the investigated added polymers might be attributable to their hydrophilic nature, trapping water within the coatings during film formation and, thus, facilitating polymer particle coalescence. This new concept can be used to overcome one of the major practical obstacles associated with aqueous polymeric film coatings today: storage instability. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:26 / 33
页数:8
相关论文
共 16 条
[1]
Amighi K, 1996, EUR J PHARM BIOPHARM, V42, P29
[2]
EVALUATION OF BIODEGRADABLE POLY(LACTIDE) PELLETS PREPARED BY DIRECT COMPRESSION [J].
BODMEIER, R ;
CHEN, HG .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1989, 78 (10) :819-822
[3]
Aqueous ethyl cellulose dispersion containing plasticizers of different water solubility and hydroxypropyl methyl-cellulose as coating material for diffusion pellets II:: properties of sprayed films [J].
Frohoff-Hülsmann, MA ;
Lippold, BC ;
McGinity, JW .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1999, 48 (01) :67-75
[4]
Aqueous ethyl cellulose dispersions containing plasticizers of different water solubility and hydroxypropyl methylcellulose as coating material for diffusion pellets I.: Drug release rates from coated pellets [J].
Frohoff-Hülsmann, MA ;
Schmitz, A ;
Lippold, BC .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 177 (01) :69-82
[5]
HOFFART V, 2005, 2005 AAPS ANN M EXP
[6]
Lippold BC, 2001, PHARMAZIE, V56, P5
[7]
MCGINITY JW, 1997, AQUEOUS POLYMERIC CO, V2
[8]
pH-sensitive film coatings: Towards a better understanding and facilitated optimization [J].
Siepmann, F. ;
Wahle, C. ;
Leclercq, B. ;
Carlin, B. ;
Siepmann, J. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 68 (01) :2-10
[9]
How to adjust desired drug release patterns from ethylcellulose-coated dosage forms [J].
Siepmann, F. ;
Hoffmann, A. ;
Leclercq, B. ;
Carlin, B. ;
Siepmann, J. .
JOURNAL OF CONTROLLED RELEASE, 2007, 119 (02) :182-189
[10]
SIEPMANN F, IN PRESS BIOMACROMOL