Issue 105, 2016

Microfluidic fabrication of composite hydrogel microparticles in the size range of blood cells

Abstract

The fabrication of alginate hydrogel microparticles with embedded liposomes and magnetic nanoparticles for radiofrequency controlled release of encapsulated chemical cargo was considered. An extractive gelation process was implemented in a microfluidic device, which enabled the production of uniform composite microparticles of dimensions comparable to those of blood cells (between 5 and 10 μm). The critical parameters that control the extractive gelation process were systematically explored and feasible values that provide microgel particles of a defined size and morphology were identified. First, the initial water-in-oil droplet is formed in a flow-focusing junction whose size is controlled by the flow-rate of the oil phase. Then, the train of droplets is sandwiched between two streams of oil containing calcium ions. In that way, a flux of water molecules from the droplets towards the continuous phase as well as a transport of calcium ions towards the disperse phase are initiated. The final microparticle properties were thus found to be sensitive to three elementary sub-processes: (i) the initial droplet size; (ii) the extraction of water into the oil phase, which was controlled by the volume of the oil phase and its initial moisture content; and (iii) the kinetics of ionic cross-linking of the alginate matrix, which was controlled by the varying calcium concentration. The size and morphology of the final composite microgels were fully characterized.

Graphical abstract: Microfluidic fabrication of composite hydrogel microparticles in the size range of blood cells

Supplementary files

Article information

Article type
Paper
Submitted
14 Sep 2016
Accepted
21 Oct 2016
First published
21 Oct 2016
This article is Open Access
Creative Commons BY license

RSC Adv., 2016,6, 103532-103540

Microfluidic fabrication of composite hydrogel microparticles in the size range of blood cells

A. Pittermannová, Z. Ruberová, A. Zadražil, N. Bremond, J. Bibette and F. Štěpánek, RSC Adv., 2016, 6, 103532 DOI: 10.1039/C6RA23003B

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