4.8 Article

Preparation and characterization of a magnetic microsphere synthesized from sucrose allyl ether for transcatheter arterial embolization

Journal

MATERIALS TODAY CHEMISTRY
Volume 24, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.mtchem.2022.100772

Keywords

Magnetic nanoparticles; Sucrose polymers; Allyl monomers; Photopolymerization; Targeted embolization

Funding

  1. National Natural Science Foundation of China [21274032]
  2. Natural Science Foundation of Guangdong Province [2014A030313500]
  3. Science and Technology Projects in Guangzhou [202102080199]
  4. Guangzhou Medical University [2021A083]

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In this study, Fe3O4 sucrose allyl ether (Fe3O4@SAE) magnetic microspheres were prepared using photodriven radical-mediated cyclization reaction (PRMC). These microspheres showed good morphology, performance, and cell compatibility, making them suitable for use as embolic agents.
The polymerization of allyl monomers has been reported as notoriously difficult because of degradative chain transfer induced by the allyl radical as a primary radical with resonance-stabilized structure. A favorable approach is to produce polymers from inert monomers by using photodriven radical-mediated cyclization reaction (PRMC). In this study, Fe3O4 at sucrose allyl ether (Fe3O4@SAE) magnetic micro spheres with sucrose as the skeleton and encapsulated nanomagnetic particles was prepared by PRMC. Its morphology and performance were characterized by using microscope, infrared, thermogravimetric and differential scanning calorimetry, scanning electron microscope/energy-dispersive spectrometer, and vibrating sample magnetometer. The feasibility as an embolic agent was evaluated by catheter transportability and cell compatibility. The results show that Fe3O4@SAE (sucrose allyl ether) magnetic microspheres have an average particle size of 371 mm, regular spherical shape, good dispersion, basically non-toxicity, and good cell compatibility. It has a certain degree of magnetism and can use alternating magnetic fields to achieve targeted embolization. (C) 2022 Elsevier Ltd. All rights reserved.

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