Review article: 5-aminosalicylate formulations for the treatment of ulcerative colitis - methods of comparing release rates and delivery of 5-aminosalicylate to the colonic mucosa

被引:55
作者
Lichtenstein, G. R. [1 ]
Kamm, M. A. [2 ]
机构
[1] Univ Penn, Sch Med, Div Gastroenterol, Philadelphia, PA 19104 USA
[2] St Marks Hosp, Dept Gastroenterol, London EC1V 2PS, England
关键词
D O I
10.1111/j.1365-2036.2008.03751.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Many oral 5-aminosalicylic acid (5-ASA) formulations are designed to maximize 5-ASA release in the colon where it acts topically on the colonic mucosa. Delayed-release formulations and azo-prodrugs minimize 5-ASA absorption in the upper gastrointestinal (GI) tract. Aims To review methods for assessing 5-ASA release and colonic distribution from oral formulations, and the potential use of this information for guiding clinical decisions. Methods PubMed and recent conference abstracts were searched for articles describing techniques used to assess 5-ASA release from ulcerative colitis (UC) therapies. Results In-vitro GI models, although unable to simulate more complex aspects of GI physiology, can provide useful data on 5-ASA release kinetics and bioaccessibility. Gamma-scintigraphy is useful for investigating GI disintegration of different formulations, but may not accurately reflect 5-ASA distribution. Plasma pharmacokinetic studies provide data on systemic exposure, but not on colonic distribution or mucosal uptake. Mucosal biopsies provide direct evidence of colonic distribution and may predict clinical efficacy, but must be interpreted cautiously because of considerable inter-subject variability and other confounding factors. Conclusion While assessment of 5-ASA release is important, limitations of individual measurement techniques mean that randomized clinical studies in UC patients remain the best guide for dosing and treatment regimen decisions.
引用
收藏
页码:663 / 673
页数:11
相关论文
共 84 条
[1]   CLINICAL-EVIDENCE SUPPORTING THE RADICAL SCAVENGER MECHANISM OF 5-AMINOSALICYLIC ACID [J].
AHNFELTRONNE, I ;
NIELSEN, OH ;
CHRISTENSEN, A ;
LANGHOLZ, E ;
BINDER, V ;
RIIS, P .
GASTROENTEROLOGY, 1990, 98 (05) :1162-1169
[2]   Bioaccessibility of folic acid and (6S)-5-methyltetrahydrofolate decreases after the addition of folate-binding protein to yogurt as studied in a dynamic in vitro gastrointestinal model [J].
Arkbåge, K ;
Verwei, M ;
Havenaar, R ;
Witthöft, C .
JOURNAL OF NUTRITION, 2003, 133 (11) :3678-3683
[3]   CLINICAL-APPEARANCE AT DIAGNOSIS OF ULCERATIVE-COLITIS AND CROHNS-DISEASE IN A REGIONAL PATIENT GROUP [J].
BOTH, H ;
TORPPEDERSEN, K ;
KREINER, S ;
HENDRIKSEN, C ;
BINDER, V .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1983, 18 (07) :987-991
[4]   MESALAZINE - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES, AND THERAPEUTIC POTENTIAL IN CHRONIC INFLAMMATORY BOWEL-DISEASE [J].
BROGDEN, RN ;
SORKIN, EM .
DRUGS, 1989, 38 (04) :500-523
[5]   5-aminosalicylic acid release from a new controlled-release mesalazine formulation during gastrointestinal transit in healthy volunteers [J].
Brunner, M ;
Lackner, E ;
Exler, PS ;
De Fluiter, HC ;
Kletter, K ;
Tschurlovits, M ;
Dudczak, R ;
Eichler, HG ;
Müller, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2006, 23 (01) :137-144
[6]   Gastrointestinal transit and release of 5-aminosalicylic acid from 153Sm-labelled mesalazine pellets vs. tablets in male healthy volunteers [J].
Brunner, M ;
Greinwald, R ;
Kletter, K ;
Kvaternik, H ;
Corrado, ME ;
Eichler, HG ;
Müller, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (09) :1163-1169
[7]   Gastrointestinal transit and 5-ASA release from a new mesalazine extended-release formulation [J].
Brunner, M ;
Assandri, R ;
Kletter, K ;
Tschurlovits, M ;
Corrado, ME ;
Villa, R ;
Eichler, HG ;
Müller, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (03) :395-402
[8]   Guidelines for the management of inflammatory bowel disease in adults [J].
Carter, MJ ;
Lobo, AJ ;
Travis, SPL .
GUT, 2004, 53 :v1-v16
[9]   Review article: evolutionary advances in the delivery of aminosalicylates for the treatment of ulcerative colitis [J].
Cohen, R. D. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2006, 24 (03) :465-474
[10]  
COLE AT, 1994, ALIMENT PHARM THERAP, V8, P521