Enzyme-powered synthetic colloidal motors hold promising potential for medical applications because of their unique features such as self-propulsion, sub-micrometer size, fuel bioavailability, and structural and functional versatility. However, the key parameters influencing the propulsion efficiency of enzyme-powered colloidal motors still remain unclear. Here, we report the effect of the neck length of urease-powered pentosan flask-like colloidal motors on their kinematic behavior resembling the role of bacterial flagella. The sub-micrometer-sized and streamlined pentosan flask-like colloidal motors with variable neck lengths are synthesized through a facile interfacial dynamic assembly and polymerization strategy. The urease molecules are loaded through vacuum infusion technology and thus the urease-triggered catalytic reaction can propel the pentosan flask-like colloidal motors to move autonomously in the urea solution. The self-propelled speed of these pentosan flask-like colloidal motors significantly increases with the elongating neck lengths. The mechanism of the relationship between the neck length and self-propelled motion is that a longer neck can provide a larger self-propelled force due to the larger force area and stabilize the rotation because of the increased rotational friction. This research can provide guidance for the design of biomedical colloidal motors.
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http://dx.doi.org/10.1039/d4sm01294a | DOI Listing |
J Colloid Interface Sci
January 2025
School of Materials Science and Engineering, Harbin Institute of Technology (Shenzhen), Shenzhen, Guangdong 518055, China. Electronic address:
Active colloids driven out of thermal equilibrium serve as building blocks for smart materials with tunable structures and functions. Using chemical energy to drive colloids is advantageous but requires precise control over chemical release. To address this, we developed colloidal ionogels-polymer microspheres infused with ionic liquids-that show controlled assembly and self-propulsion upon tunable swelling.
View Article and Find Full Text PDFACS Nano
January 2025
School of Medicine and Health, Harbin Institute of Technology, Harbin 150080, China.
Modularly organizing active micromachines into high-grade metamachines makes a great leap for operating the microscopic world in a biomimetic way. However, modulating the nonreciprocal interactions among different colloidal motors through chemical reactions to achieve the controllable construction of active colloidal metamachines with specific dynamic properties remains challenging. Here, we report the phototactic active colloidal metamachines constructed by shape-directed dynamic self-assembly of chemically driven peanut-shaped TiO colloidal motors and Janus spherical Pt/SiO colloidal motors.
View Article and Find Full Text PDFJ Nanobiotechnology
January 2025
Department of Orthopedics, Huashan Hospital, Fudan University, No. 12, Middle Wulumuqi Road, Jing'an District, Shanghai, 200040, China.
Background: Spinal cord injury (SCI) treatment remains a formidable challenge, as current therapeutic approaches provide only marginal relief and fail to reverse the underlying tissue damage. This study aims to develop a novel composite material combining enzymatic nanoparticles and nerve growth factor (NGF) to modulate the immune microenvironment and enhance SCI repair.
Methods: CeMn nanoparticles (NP) and CeMn NP-polyethylene glycol (PEG) nanozymes were synthesized via sol-gel reaction and DSPE-mPEG modification.
Nature
January 2025
Department of Chemistry, University of Manchester, Manchester, UK.
Cells display a range of mechanical activities generated by motor proteins powered through catalysis. This raises the fundamental question of how the acceleration of a chemical reaction can enable the energy released from that reaction to be transduced (and, consequently, work to be done) by a molecular catalyst. Here we demonstrate the molecular-level transduction of chemical energy to mechanical force in the form of the powered contraction and powered re-expansion of a cross-linked polymer gel driven by the directional rotation of artificial catalysis-driven molecular motors.
View Article and Find Full Text PDFSoft Matter
January 2025
School of Medicine and Health, Harbin Institute of Technology, XiDaZhi Street 92, Harbin, 150001, China.
Enzyme-powered synthetic colloidal motors hold promising potential for medical applications because of their unique features such as self-propulsion, sub-micrometer size, fuel bioavailability, and structural and functional versatility. However, the key parameters influencing the propulsion efficiency of enzyme-powered colloidal motors still remain unclear. Here, we report the effect of the neck length of urease-powered pentosan flask-like colloidal motors on their kinematic behavior resembling the role of bacterial flagella.
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