In silico and in vitro methods to optimize the performance of experimental gastroretentive floating mini-tablets

Drug Dev Ind Pharm. 2016;42(5):808-17. doi: 10.3109/03639045.2015.1078350. Epub 2015 Aug 25.

Abstract

Context: Development of floating drug delivery systems (FDDS) is challenging. To facilitate this task, an evaluation method was proposed, which allows for a combined investigation of drug release and flotation.

Objective: It was the aim of the study to use functionalized calcium carbonate (FCC)-based lipophilic mini-tablet formulations as a model system to design FDDS with a floating behavior characterized by no floating lag time, prolonged flotation and loss of floating capability after complete drug release.

Materials and methods: Release of the model drug caffeine from the mini-tablets was assessed in vitro by a custom-built stomach model. A cellular automata-based model was used to simulate tablet dissolution. Based on the in silico data, floating forces were calculated and analyzed as a function of caffeine release.

Results and discussion: Two floating behaviors were identified for mini-tablets: linear decrease of the floating force and maintaining of the floating capability until complete caffeine release. An optimal mini-tablet formulation with desired drug release time and floating behavior was developed and tested.

Conclusion: A classification system for a range of varied floating behavior of FDDS was proposed. The FCC-based mini-tablets had an ideal floating behavior: duration of flotation is defined and floating capability decreases after completion of drug release.

Keywords: Drug release; floating force; flotation; functionalized calcium carbonate; mini-tablet formulations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caffeine / chemistry
  • Calcium Carbonate / chemistry
  • Chemistry, Pharmaceutical / methods
  • Computer Simulation
  • Delayed-Action Preparations / chemistry*
  • Drug Delivery Systems / methods
  • Drug Liberation
  • Excipients / chemistry
  • Gastric Mucosa / metabolism*
  • In Vitro Techniques / methods*
  • Solubility
  • Tablets / chemistry*
  • Technology, Pharmaceutical / methods*

Substances

  • Delayed-Action Preparations
  • Excipients
  • Tablets
  • Caffeine
  • Calcium Carbonate