Krüger, Andreas J. D.;
Bakirman, Onur;
Guerzoni, Luis. P. B.;
Jans, Alexander;
Gehlen, David B.;
Rommel, Dirk;
Haraszti, Tamás;
Kuehne, Alexander J. C.;
De Laporte, Laura
Compartmentalized Jet Polymerization as a High‐Resolution Process to Continuously Produce Anisometric Microgel Rods with Adjustable Size and Stiffness
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Media type:
E-Article
Title:
Compartmentalized Jet Polymerization as a High‐Resolution Process to Continuously Produce Anisometric Microgel Rods with Adjustable Size and Stiffness
Contributor:
Krüger, Andreas J. D.;
Bakirman, Onur;
Guerzoni, Luis. P. B.;
Jans, Alexander;
Gehlen, David B.;
Rommel, Dirk;
Haraszti, Tamás;
Kuehne, Alexander J. C.;
De Laporte, Laura
imprint:
Wiley, 2019
Published in:Advanced Materials
Language:
English
DOI:
10.1002/adma.201903668
ISSN:
0935-9648;
1521-4095
Origination:
Footnote:
Description:
<jats:title>Abstract</jats:title><jats:p>In the past decade, anisometric rod‐shaped microgels have attracted growing interest in the materials‐design and tissue‐engineering communities. Rod‐shaped microgels exhibit outstanding potential as versatile building blocks for 3D hydrogels, where they introduce macroscopic anisometry, porosity, or functionality for structural guidance in biomaterials. Various fabrication methods have been established to produce such shape‐controlled elements. However, continuous high‐throughput production of rod‐shaped microgels with simultaneous control over stiffness, size, and aspect ratio still presents a major challenge. A novel microfluidic setup is presented for the continuous production of rod‐shaped microgels from microfluidic plug flow and jets. This system overcomes the current limitations of established production methods for rod‐shaped microgels. Here, an <jats:italic>on‐chip</jats:italic> gelation setup enables fabrication of soft microgel rods with high aspect ratios, tunable stiffness, and diameters significantly smaller than the channel diameter. This is realized by exposing jets of a microgel precursor to a high intensity light source, operated at specific pulse sequences and frequencies to induce ultra‐fast photopolymerization, while a change in flow rates or pulse duration enables variation of the aspect ratio. The microgels can assemble into 3D structures and function as support for cell culture and tissue engineering.</jats:p>