Polymeric bile acid sequestrants: Review of design, in vitro binding activities, and hypocholesterolemic effects

Eur J Med Chem. 2018 Jan 20:144:300-317. doi: 10.1016/j.ejmech.2017.12.015. Epub 2017 Dec 6.

Abstract

Polymeric bile acid sequestrants (BAS) have recently attracted much attention as lipid-lowering agents. These non-absorbable materials specifically bind bile acids (BAs) in the intestine, preventing bile acid (BA) reabsorption into the blood through enterohepatic circulation. Therefore, it is important to understand the structure-property relationships between the polymer sequestrant and its ability to bind specific BAs molecules. In this review, we describe pleiotropic effects of bile acids, and we focus on BAS with various molecular architectures that result in different mechanisms of BA sequestration. Here, we present 1) amphiphilic polymers based on poly(meth)acrylates, poly(meth)acrylamides, polyalkylamines and polyallylamines containing quaternary ammonium groups, 2) cyclodextrins, and 3) BAS prepared via molecular imprinting methods. The synthetic approaches leading to individual BAS preparation, as well as results of their in vitro BA binding activities and in vivo lipid-lowering activities, are discussed.

Keywords: Bile acid sequestrant; Cholestyramine; Cyclodextrin; Molecular imprinting; Pleiotropic effect; Review.

Publication types

  • Review

MeSH terms

  • Animals
  • Anticholesteremic Agents / chemical synthesis
  • Anticholesteremic Agents / chemistry
  • Anticholesteremic Agents / pharmacology*
  • Bile Acids and Salts / chemical synthesis
  • Bile Acids and Salts / chemistry
  • Bile Acids and Salts / pharmacology*
  • Binding Sites / drug effects
  • Drug Design*
  • Humans
  • Hypercholesterolemia / drug therapy*
  • Molecular Structure
  • Polymers / chemical synthesis
  • Polymers / chemistry
  • Polymers / pharmacology*

Substances

  • Anticholesteremic Agents
  • Bile Acids and Salts
  • Polymers