Microfluidic Production of Alginate Hydrogel Particles for Antibody Encapsulation and Release

Macromol Biosci. 2015 Dec;15(12):1641-6. doi: 10.1002/mabi.201500226. Epub 2015 Jul 21.

Abstract

Owing to their biocompatibility and reduced side effects, natural polymers represent an attractive choice for producing drug delivery systems. Despite few successful examples, however, the production of monodisperse biopolymer-based particles is often hindered by high viscosity of polymer fluids. In this work, we present a microfluidic approach for production of alginate-based particles carrying encapsulated antibodies. We use a triple-flow micro-device to induce hydrogel formation inside droplets before their collection off-chip. The fast mixing and gelation process produced alginate particles with a unique biconcave shape and dimensions of the mammalian cells. We show slow and fast dissolution of particles in different buffers and evaluate antibody release over time.

Keywords: alginate particles; antibody; droplet microfluidics; drug delivery system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alginates* / chemistry
  • Alginates* / pharmacokinetics
  • Animals
  • Delayed-Action Preparations / chemistry
  • Delayed-Action Preparations / pharmacokinetics
  • Glucuronic Acid / chemistry
  • Glucuronic Acid / pharmacokinetics
  • Hexuronic Acids / chemistry
  • Hexuronic Acids / pharmacokinetics
  • Hydrogels* / chemistry
  • Hydrogels* / pharmacokinetics
  • Immobilized Proteins / chemistry
  • Immobilized Proteins / pharmacokinetics
  • Immunoglobulin G / chemistry*
  • Lab-On-A-Chip Devices*
  • Mice
  • Microfluidic Analytical Techniques / methods*

Substances

  • Alginates
  • Delayed-Action Preparations
  • Hexuronic Acids
  • Hydrogels
  • Immobilized Proteins
  • Immunoglobulin G
  • Glucuronic Acid