Amylose formulations for drug delivery to the colon: a comparison of two fermentation models to assess colonic targeting performance in vitro

被引:59
作者
Siew, LF [1 ]
Man, SM [1 ]
Newton, JM [1 ]
Basit, AW [1 ]
机构
[1] Univ London, Sch Pharm, Dept Pharmaceut, London WC1N 1AX, England
关键词
amylose; colonic delivery; mesalazine; 5-aminosalicylic acid; gastrointestinal microflora; Bacillus licheniformis; fermentation assessment;
D O I
10.1016/j.ijpharm.2003.12.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to develop an enzyme-based fermentation system for the in vitro assessment of colonic digestion of amylose films and coatings, and to compare its performance with a conventional fermentation model inoculated with human faecal bacteria. Amylose and ethylcellulose were mixed in different ratios and cast as isolated films, as well as spray coated onto drug-(5-aminosalicylic acid) loaded pellets. Four commercial amylase enzymes were individually screened for their ability to digest amylose cast films. The enzyme from the bacterium Bacillus ficheniformis was found to be the most active against this substrate. Digestion of mixed amylose and ethylcellulose films was also observed, with the extent of digestion being proportional to the quantity of amylose present in the film. In terms of product performance, drug release from coated pellets was accelerated in the presence of the enzyme. The results with the enzyme system were comparable to those obtained from a faecal-based fermentation model, thereby suggesting that such a system has practical potential for in vitro screening of putative amylose formulations for colonic drug delivery. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 134
页数:6
相关论文
共 19 条
[1]   TARGETING DRUGS TO THE COLON - DELIVERY SYSTEMS FOR ORAL-ADMINISTRATION [J].
ASHFORD, M ;
FELL, JT .
JOURNAL OF DRUG TARGETING, 1994, 2 (03) :241-257
[2]   The use of formulation technology to assess regional gastrointestinal drug absorption in humans [J].
Basit, AW ;
Podczeck, F ;
Newton, JM ;
Waddington, WA ;
Ell, PJ ;
Lacey, LF .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 21 (2-3) :179-189
[3]   Colonic metabolism of ranitidine: implications for its delivery and absorption [J].
Basit, AW ;
Lacey, LF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 227 (1-2) :157-165
[4]  
BASIT AW, 2000, PHARM TECHNOL EUR, V12, P30
[5]  
BLOOR JR, 2002, AAPS PHARMSCI, V4
[6]   In vivo studies of amylose- and ethylcellulose-coated [C-13]glucose microspheres as a model for drug delivery to the colon [J].
Cummings, JH ;
Milojevic, S ;
Harding, M ;
Coward, WA ;
Gibson, GR ;
Botham, RL ;
Ring, SG ;
Wraight, EP ;
Stockham, MA ;
Allwood, MC ;
Newton, JM .
JOURNAL OF CONTROLLED RELEASE, 1996, 40 (1-2) :123-131
[7]  
Finegold S.M., 1983, HUMAN INTESTINAL MIC, P3
[8]   Drug delivery to the colon [J].
Fish, NW ;
Bloor, JR .
EXPERT OPINION ON THERAPEUTIC PATENTS, 1999, 9 (11) :1515-1521
[9]   Review article - Colonic drug targeting [J].
Kinget, R ;
Kalala, W ;
Vervoort, L ;
van den Mooter, G .
JOURNAL OF DRUG TARGETING, 1998, 6 (02) :129-149
[10]   The formation of colonic digestible films of amylose and ethylcellulose from aqueous dispersions at temperatures below 37°C [J].
Leong, CW ;
Newton, JM ;
Basit, AW ;
Podczeck, F ;
Cummings, JH ;
Ring, SG .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2002, 54 (03) :291-297