Photoresponsive Hydrogel Microcrawlers Exploit Friction Hysteresis to Crawl by Reciprocal Actuation.

PNIPAM crawler friction hysteresis hydrogel photothermal

Journal

Soft robotics
ISSN: 2169-5180
Titre abrégé: Soft Robot
Pays: United States
ID NLM: 101623819

Informations de publication

Date de publication:
02 2021
Historique:
pubmed: 23 4 2020
medline: 22 4 2022
entrez: 23 4 2020
Statut: ppublish

Résumé

Mimicking the locomotive abilities of living organisms on the microscale, where the downsizing of rigid parts and circuitry presents inherent problems, is a complex feat. In nature, many soft-bodied organisms (inchworm, leech) have evolved simple, yet efficient locomotion strategies in which reciprocal actuation cycles synchronize with spatiotemporal modulation of friction between their bodies and environment. We developed microscopic (∼100 μm) hydrogel crawlers that move in aqueous environment through spatiotemporal modulation of the friction between their bodies and the substrate. Thermo-responsive poly-n-isopropyl acrylamide hydrogels loaded with gold nanoparticles shrink locally and reversibly when heated photothermally with laser light. The out-of-equilibrium collapse and reswelling of the hydrogel is responsible for asymmetric changes in the friction between the actuating section of the crawler and the substrate. This friction hysteresis, together with off-centered irradiation, results in directional motion of the crawler. We developed a model that predicts the order of magnitude of the crawler motion (within 50%) and agrees with the observed experimental trends. Crawler trajectories can be controlled enabling applications of the crawler as micromanipulator that can push small cargo along a surface.

Identifiants

pubmed: 32320334
doi: 10.1089/soro.2019.0169
doi:

Substances chimiques

Hydrogels 0
Gold 7440-57-5

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

10-18

Auteurs

Ivan Rehor (I)

Van't Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Utrecht, The Netherlands.
Faculty of Chemical Engineering, UCT Prague, Prague, Czech Republic.
Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Prague, Czech Republic.

Charlie Maslen (C)

Van't Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Utrecht, The Netherlands.
Faculty of Chemical Engineering, UCT Prague, Prague, Czech Republic.

Pepijn G Moerman (PG)

Van't Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Utrecht, The Netherlands.

Bas G P van Ravensteijn (BGP)

Netherlands Organization for Applied Scientific Research (TNO), Materials Solutions, Eindhoven, The Netherlands.

Renee van Alst (R)

Van't Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Utrecht, The Netherlands.

Jan Groenewold (J)

Van't Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Utrecht, The Netherlands.
Guangdong Provincial Key Laboratory of Optical Information Materials and Technology and Institute of Electronic Paper Displays, South China Academy of Advanced Optoelectronics, South China Normal University, Guangzhou, China.

Huseyin Burak Eral (HB)

Van't Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Utrecht, The Netherlands.
Process and Energy Laboratory, 3ME Faculty, TU Delft, Delft, The Netherlands.

Willem K Kegel (WK)

Van't Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Utrecht, The Netherlands.

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