2022
DOI: 10.1039/d2cp00617k
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Morphological transitions of micelles induced by the block arrangements of copolymer blocks: dissipative particle dynamics simulation

Abstract: Polymer micelles with distinct morphologies and unique microphase separation microstructures can exhibit different properties and functions, holding the great promises for a range of biomedical applications. In current work, the...

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Cited by 2 publications
(2 citation statements)
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“…Block copolymers undergo microphase separation in bulk and tend toward the self-assembly in solution and the formation of internally ordered microparticles. 185,186 Common block copolymers undergo microphase separation in selective solvents to form micelles. If A is a solvophilic block, an AB diblock copolymer in a selective solvent for the A block is self-organized in spherical micelles, worm-like micelles or vesicles.…”
Section: Multicompartment Polymer Micelles and Related Structuresmentioning
confidence: 99%
“…Block copolymers undergo microphase separation in bulk and tend toward the self-assembly in solution and the formation of internally ordered microparticles. 185,186 Common block copolymers undergo microphase separation in selective solvents to form micelles. If A is a solvophilic block, an AB diblock copolymer in a selective solvent for the A block is self-organized in spherical micelles, worm-like micelles or vesicles.…”
Section: Multicompartment Polymer Micelles and Related Structuresmentioning
confidence: 99%
“…Since computational simulations have been demonstrated to be a powerful support and supplement for experimental systems, in this work, dissipative particle dynamics (DPD) simulations, a mesoscopic stochastic coarse-grained method proposed by Hoogerbrugge and Koelman in 1992 34 suitable for complex multiphase systems, was employed to optimize the molecular structure of the polymers and the drug-loading proportion of the mixed micelles, [35][36][37][38] as well as to investigate the relationship between the mesoscopic structure and macroscopic properties of the drug-loaded mixed polymeric micelles. Then, the target polymers PEG-PDEAEMA, FA-PEG-PDEAEMA and PEG-SS-PCL were experimentally synthesized and characterized, and their mixed micelles were applied for doxorubicin (DOX) delivery.…”
Section: Introductionmentioning
confidence: 99%