On the Colonic Bacterial Metabolism of Azo‐Bonded Prodrugsof 5‐Aminosalicylic Acid. Issue 10 (4th August 2014)

• Record Type: Journal Article
• Authors: Sousa, Tiago; Yadav, Vipul; Zann, Vanessa; Borde, Anders; Abrahamsson, Bertil; Basit, Abdul W.
• Is Part Of: Journal of pharmaceutical sciences. Volume 103:Issue 10(2014:Oct.)
• Page Start: 3171
• Page End: 3175
• Publication Date: 2014-08-04
• Subjects: Pharmacy -- Periodicals; 615.1
• DOI: 10.1002/jps.24103
• Languages: English
• ISSNs: 0022-3549

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Azo‐bonded prodrugs of 5‐aminosalicylic acid (mesalazine)—sulfasalazine, balsalazide, and olsalazine, which are used in the treatment of ulcerative colitis, rely on colonic bacteria to cleave the azo bond and liberate the active drug in the large intestine. The aim of this study was to use an <italic>in vitro</italic> colonic simulator to determine the rates of metabolism of these three prodrugs in the presence of colonic bacteria, and to link the data to results obtained previously in humans. In individual fecal slurries prepared from five different donors, sulfasalazine degradation was rapid and virtually complete within 4 h, confirming the ubiquitous nature of azo‐reduction between individuals. In pooled fecal slurry, the rate of degradation of sulfasalazine was faster (<italic>t</italic><sub>1/2</sub>, 32.8 min) than balsalazide (<italic>t</italic><sub>1/2</sub>, 80.9 min) and olsalazine (<italic>t</italic><sub>1/2</sub>, 145.1 min). These results are in agreement with data in humans, where it was found that sulfasalazine was more extensively metabolized on passage through the human colon than the other two drugs. These findings indicate that other than the azo bond itself, the broader chemical structure of the molecules play a role in the degradation of this class of compound, and highlight the utility of this <italic>in vitro</italic> model to evaluate the metabolism of drugs in the presence of colonic microbiota. © 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 103:3171–3175, 2014</p> </abstract>