Physicochemical properties of enteric films prepared from aqueous dispersions and organic solutions

被引:31
作者
Bando, H [1 ]
McGinity, JW [1 ]
机构
[1] Univ Texas, Coll Pharm, Drug Dynam Inst, Austin, TX 78712 USA
关键词
organic cast films; aqueous cast films; Eudragit((R)) S100; Eudragit((R)) L100; Eudragit((R)) L100-55; triethyl citrate;
D O I
10.1016/j.ijpharm.2006.01.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cast films composed of mixtures of Eudragit((R)) S100:L100 (1:1) and plasticized with triethyl citrate (TEC) were prepared from aqueous dispersions and organic solutions, and the physicochemical properties and the weight loss of cast films during dissolution testing were examined. The tensile strength of the organic cast films was significantly higher and the percent elongation was lower than that of the aqueous cast films. The weight loss of the organic films was also lower than that of the aqueous films. Furthermore, leaching of the TEC from the aqueous films was rapid and the TEC was found to diffuse from the films within one hour at pH 6.0, the pH at which the Eudragit((R)) S 100:L100 (1: 1) films were insoluble. In contrast to the aqueous films, minimal levels of the TEC diffused front the organic cast films, and the disintegration of acrylic polymers occurred simultaneously with the release of TEC from the film during dissolution testing at pH 7.0. For Eudragit((R)) L100-55, which could form films at lower TEC levels than Eudragit((R)) S100:L100, both the organic and aqueous films showed the same weight loss after four hours in pH 5.0 media. These results demonstrated that for Eudragit((R)) S100:L100 cast films, the high levels of TEC needed for film formation from aqueous dispersions resulted in rapid dissolution and disintegration at pH 6.0 and above. While aqueous dispersions are preferred for the coating of solid substrates, for Eudragit((R)) S100:L100 film coatings, a change from organic solutions to aqueous dispersions in the coating process will impact film properties and product performance. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 48
页数:6
相关论文
共 18 条
[12]  
Lehmann K.O.R., 1997, AQUEOUS POLYM COATIN, P101
[13]   Influence of process parameters on sustained-release theophylline pellets coated with aqueous polymer dispersions and organic solvent-based polymer solutions [J].
Lorck, CA ;
Grunenberg, PC ;
Junger, H ;
Laicher, A .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1997, 43 (02) :149-157
[14]   DISPOSITION OF 5-AMINOSALICYLIC ACID BY 5-AMINOSALICYLIC ACID-DELIVERING COMPOUNDS [J].
RIJK, MCM ;
VANSCHAIK, A ;
VANTONGEREN, JHM .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1988, 23 (01) :107-112
[15]   A new 5-aminosalicylic acid multi-unit dosage form for the therapy of ulcerative colitis [J].
Rudolph, MW ;
Klein, S ;
Beckert, TE ;
Petereit, HU ;
Dressman, JB .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2001, 51 (03) :183-190
[16]   Influence of aqueous coatings on the stability of enteric coated pellets and tablets [J].
Thoma, K ;
Bechtold, K .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1999, 47 (01) :39-50
[17]   Drug release from beads coated with an aqueous colloidal ethylcellulose dispersion, Aquacoat®, or an organic ethylcellulose solution [J].
Wesseling, M ;
Bodmeier, R .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1999, 47 (01) :33-38
[18]  
WHEATLEY TA, 1997, AQUEOUS POLYM COATIN, P1