Coated dosage forms for colon-specific drug delivery

被引:78
作者
Leopold, CS [1 ]
机构
[1] Univ Dusseldorf, Dept Pharmaceut Technol, D-40225 Dusseldorf, Germany
来源
PHARMACEUTICAL SCIENCE & TECHNOLOGY TODAY | 1999年 / 2卷 / 05期
关键词
D O I
10.1016/S1461-5347(99)00151-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Coating materials used in the manufacture of colon-specific solid oral dosage forms include polymers with a pH-dependent solubility that rely on the difference in pH between the small and the distal large intestine (pH-controlled release), polymers with a slow or pH-dependent rate of swelling, dissolution or erosion that take advantage of the constant small intestinal transit time (time-controlled release), polymers that are degradable by the microbial enzymes in the colon (enzyme-controlled release) and polymers that form firm layers that are destroyed by an increase of the luminal pressure in the colon caused by peristaltic waves (pressure-controlled release). This review gives an overview of coated dosage forms that have been developed to achieve colon specificity.
引用
收藏
页码:197 / 204
页数:8
相关论文
共 88 条
[1]  
ABRAMOWITZ R, 1996, Patent No. 5536507
[2]  
[Anonymous], 1978, Intestinal Bacteria and Health
[3]   AN INVITRO INVESTIGATION INTO THE SUITABILITY OF PH-DEPENDENT POLYMERS FOR COLONIC TARGETING [J].
ASHFORD, M ;
FELL, JT ;
ATTWOOD, D ;
WOODHEAD, PJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 91 (2-3) :241-245
[4]   AN EVALUATION OF PECTIN AS A CARRIER FOR DRUG TARGETING TO THE COLON [J].
ASHFORD, M ;
FELL, J ;
ATTWOOD, D ;
SHARMA, H ;
WOODHEAD, P .
JOURNAL OF CONTROLLED RELEASE, 1993, 26 (03) :213-220
[5]   AN IN-VIVO INVESTIGATION INTO THE SUITABILITY OF PH DEPENDENT POLYMERS FOR COLONIC TARGETING [J].
ASHFORD, M ;
FELL, JT ;
ATTWOOD, D ;
SHARMA, H ;
WOODHEAD, PJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 95 (1-3) :193-199
[6]  
BAUER KH, 1993, Patent No. 4209160
[7]  
BETZING J, 1992, PZ WISSENSCHAFT, V137, P131
[8]  
Bragger Janine L., 1997, Pharmaceutical Research (New York), V14, pS656
[9]   Investigations into the azo reducing activity of a common colonic microorganism [J].
Bragger, JL ;
Lloyd, AW ;
Soozandehfar, SH ;
Bloomfield, SC ;
Marriott, C ;
Martin, GP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 157 (01) :61-71
[10]   HYDROGELS FOR SITE-SPECIFIC ORAL-DRUG DELIVERY - SYNTHESIS AND CHARACTERIZATION [J].
BRONDSTED, H ;
KOPECEK, J .
BIOMATERIALS, 1991, 12 (06) :584-592