Amphiphilic Block Copolymers: A Novel Substance for Bitter-Masking in Aqueous Solutions

Mol Pharm. 2020 May 4;17(5):1586-1595. doi: 10.1021/acs.molpharmaceut.9b01296. Epub 2020 Mar 30.

Abstract

It is a challenging task to suppress the bitterness of liquid preparations, especially for children. Bitter molecules are highly dispersible in liquids, leading to a strong and instant stimulation of the bitter receptors. At present, there is no effective way to correct this issue except for adding sweeteners, resulting in an unsatisfying taste. Based on the three-point contact theory, which is a universally accepted mechanism of bitterness formation, a new idea and application of amphiphilic block copolymers (ABCs) for bitterness suppression was proposed for the first time. We found that ABCs could widely inhibit the bitterness of four typical bitter substances. The mechanism is that ABCs self-assemble to form association colloids, which attract bitter components and reduce their distribution in the molecular form in solution. The bitter components were demonstrated to automatically embed in the spiral hydrophobic cavity of the hydrophobic chain of the ABCs, and their special interaction dispersed the positive electrostatic potential of bitter groups. The combination did not affect the pharmacokinetic parameters and pharmacodynamics of bitter drugs. These findings highlight the novel application of ABCs for the inhibition of bitterness and illuminate the underlying inhibition mechanisms.

Keywords: amphiphilic block copolymers; bitter receptors; bitter-masking; pharmaceutics principle; self-assembled micelles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Berberine / pharmacology
  • Male
  • Mice
  • Micelles
  • Molecular Docking Simulation
  • Polyesters / pharmacology
  • Polyethylene Glycols / pharmacology
  • Polymers / pharmacology*
  • Solutions
  • Taste / drug effects*

Substances

  • Micelles
  • Polyesters
  • Polymers
  • Solutions
  • methoxy poly(ethylene glycol-co-epsilon-caprolactone)
  • Berberine
  • Polyethylene Glycols
  • poly(lactide)