Implications on emergence of antimicrobial resistance as a critical aspect in the design of oral sustained release delivery systems of antimicrobials

Pharm Res. 2008 Mar;25(3):667-71. doi: 10.1007/s11095-007-9373-6. Epub 2007 Oct 16.

Abstract

Purpose: To assess the effects of the unabsorbed fraction of an orally administered antimicrobial drug which enters the colon on the emergence of resistance among the natural microflora, a phenomenon largely overlooked so far despite its clinical importance, especially when sustained release formulations are used.

Methods: Effects of an orally administered model beta-lactam antibiotic (amoxicillin) on emergence of resistant bacteria were assessed using a microbiological assay for qualitative and quantitative determination of resistant bacteria in fecal samples of rats following gastric administration of the drug to rats for 4 consecutive days. Time- and site-controlled administration of a beta-lactamase to the rat colon was assessed as a potential strategy for prevention the emergence of resistant bacteria following oral administration of incompletely absorbed antimicrobials.

Results: Emergence of resistant bacteria was demonstrated following oral administration of amoxicillin to rats, whereas de-activation of the beta-lactam prior to entering the colon, by infusion of a beta-lactamase into the lower ileum, was shown to prevent the emergence of resistant colonic bacteria.

Conclusions: This study illustrates the need to consider the emergence of antimicrobial resistance as a goal equally important to microbiological and clinical cure, when designing oral sustained-release delivery systems of antimicrobial drugs.

MeSH terms

  • Administration, Oral
  • Amoxicillin / administration & dosage
  • Amoxicillin / chemistry
  • Amoxicillin / metabolism
  • Amoxicillin / pharmacology*
  • Animals
  • Anti-Infective Agents / administration & dosage
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / metabolism
  • Anti-Infective Agents / pharmacology*
  • Chemistry, Pharmaceutical
  • Colon / drug effects
  • Colon / microbiology
  • Colony Count, Microbial
  • Delayed-Action Preparations
  • Drug Compounding
  • Drug Design*
  • Drug Resistance, Bacterial / drug effects*
  • Feces / microbiology
  • Gastrointestinal Transit
  • Ileum / drug effects
  • Ileum / microbiology
  • Intestinal Absorption
  • Intestinal Mucosa / metabolism
  • Intestines / drug effects*
  • Intestines / microbiology
  • Intubation, Gastrointestinal
  • Male
  • Rats
  • Rats, Wistar
  • Time Factors
  • beta-Lactamases / administration & dosage*
  • beta-Lactamases / metabolism

Substances

  • Anti-Infective Agents
  • Delayed-Action Preparations
  • Amoxicillin
  • beta-Lactamases