Design of Remote-Controllable\nDiels–Alder Platform\non Magnetic Nanoparticles via Layer-by-Layer Assembly for AC Magnetic\nField-Triggered Drug Release

Diels–Alder\nchemistry was exploited to develop a remote-controllable\ndrug release platform on magnetic nanoparticles (MNPs). For this purpose,\nMNPs were decorated with anionic poly(styrenesulfonic acid-<i>co</i>-furfuryl methacrylate) (poly(SS-<i>co</i>-FMA))\nand cationic poly(allylamine hydrochloride) by layer-by-layer assembly.\nThe decorated MNPs successfully underwent DA reaction to produce covalent\nbonding between FMA (diene) and maleimide (dienophile)-terminated\nmodel drug. Thermal treatment above 80 °C caused the retro Diels–Alder\nreaction (rDA) between FMA and the drug, resulting in drug release.\nThe retro DA could be also achieved by applying an alternating-current\n(AC) magnetic field to the decorated MNPs. This could spatially limit\nthe heat generation around MNP without heating entire system. Drug\nrelease could be also accelerated with the irradiation time when a\nthreshold temperature was met or exceeded the required energy for\nrDA reaction. Our results highlight the potential of DA chemistry\nas a new strategy to provide a remote controllable drug release platform\nfor improving the therapeutic efficiency.

Publication Details

Journal
Figshare
Published
2024-11-02
DOI
https://doi.org/10.1021/acs.langmuir.4c02998.s001
Primary Topic
Rangeland Management and Livestock Ecology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Design of Remote-Controllable\nDiels–Alder Platform\non Magnetic Nanoparticles via Layer-by-Layer Assembly for AC Magnetic\nField-Triggered Drug Release

Figshare
Rangeland Management and Livestock Ecology
article

Design of Remote-Controllable\nDiels–Alder Platform\non Magnetic Nanoparticles via Layer-by-Layer Assembly for AC Magnetic\nField-Triggered Drug Release

article en

Abstract

Diels–Alder\nchemistry was exploited to develop a remote-controllable\ndrug release platform on magnetic nanoparticles (MNPs). For this purpose,\nMNPs were decorated with anionic poly(styrenesulfonic acid-<i>co</i>-furfuryl methacrylate) (poly(SS-<i>co</i>-FMA))\nand cationic poly(allylamine hydrochloride) by layer-by-layer assembly.\nThe decorated MNPs successfully underwent DA reaction to produce covalent\nbonding between FMA (diene) and maleimide (dienophile)-terminated\nmodel drug. Thermal treatment above 80 °C caused the retro Diels–Alder\nreaction (rDA) between FMA and the drug, resulting in drug release.\nThe retro DA could be also achieved by applying an alternating-current\n(AC) magnetic field to the decorated MNPs. This could spatially limit\nthe heat generation around MNP without heating entire system. Drug\nrelease could be also accelerated with the irradiation time when a\nthreshold temperature was met or exceeded the required energy for\nrDA reaction. Our results highlight the potential of DA chemistry\nas a new strategy to provide a remote controllable drug release platform\nfor improving the therapeutic efficiency.

Figshare
Affordable and clean energy
Openalex Percentile: Top 47%
Rangeland Management and Livestock Ecology
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.