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Keywords = magneto-polymersome

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12 pages, 21595 KiB  
Article
Coarse-Grained Molecular Dynamics Modelling of a Magnetic Polymersome
by Aleksandr Ryzhkov and Yuriy Raikher
Nanomaterials 2018, 8(10), 763; https://doi.org/10.3390/nano8100763 - 27 Sep 2018
Cited by 11 | Viewed by 3821
Abstract
A coarse-grained molecular dynamics framework is proposed to investigate the equilibrium structure and quasi-static deformational response of a magnetic polymersome, a hollow object whose magnetoactive part is its shell (membrane). In the developed scheme, the shell is modelled as a pair of two [...] Read more.
A coarse-grained molecular dynamics framework is proposed to investigate the equilibrium structure and quasi-static deformational response of a magnetic polymersome, a hollow object whose magnetoactive part is its shell (membrane). In the developed scheme, the shell is modelled as a pair of two concentric interfaces, between which a layer of a linearly viscous fluid filled with magnetic nanoparticles is confined; the thickness of this layer slightly exceeds the nanoparticle diameter. The shell boundaries possess weak bending elasticity, very high surface tension and are impermeable for the nanoparticles. The nanoparticles bear permanent magnetic moments and are translationally and rotationally free inside the layer. The factors favoring the particle aggregation are the magneto-dipole coupling and Zeeman interaction with the external field; the impeding factors are thermal motion and steric restrictions imposed by the boundaries. The volume content of magnetic phase in the shell is sufficiently small (below 11 vol.%) to enable one to clearly observe structure patterns occurring in the basic state and under an applied magnetic field. As shown, both the particle concentration and the level of interparticle interaction strongly affect the extent and type of the aggregation that, in turn, causes overall deformation of the polymersome: stretching along the applied field and shrinking in the transverse plane. Full article
(This article belongs to the Special Issue Magnetic Nanoparticles in Biological Applications)
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17 pages, 5595 KiB  
Article
Fluorescent Magnetopolymersomes: A Theranostic Platform to Track Intracellular Delivery
by Oliver Bixner, Noga Gal, Christoph Zaba, Andrea Scheberl and Erik Reimhult
Materials 2017, 10(11), 1303; https://doi.org/10.3390/ma10111303 - 13 Nov 2017
Cited by 6 | Viewed by 4339
Abstract
We present a potential theranostic delivery platform based on the amphiphilic diblock copolymer polybutadiene-block-poly (ethylene oxide) combining covalent fluorescent labeling and membrane incorporation of superparamagnetic iron oxide nanoparticles for multimodal imaging. A simple self-assembly and labeling approach to create the fluorescent [...] Read more.
We present a potential theranostic delivery platform based on the amphiphilic diblock copolymer polybutadiene-block-poly (ethylene oxide) combining covalent fluorescent labeling and membrane incorporation of superparamagnetic iron oxide nanoparticles for multimodal imaging. A simple self-assembly and labeling approach to create the fluorescent and magnetic vesicles is described. Cell uptake of the densely PEGylated polymer vesicles could be altered by surface modifications that vary surface charge and accessibility of the membrane active species. Cell uptake and cytotoxicity were evaluated by confocal microscopy, transmission electron microscopy, iron content and metabolic assays, utilizing multimodal tracking of membrane fluorophores and nanoparticles. Cationic functionalization of vesicles promoted endocytotic uptake. In particular, incorporation of cationic lipids in the polymersome membrane yielded tremendously increased uptake of polymersomes and magnetopolymersomes without increase in cytotoxicity. Ultrastructure investigations showed that cationic magnetopolymersomes disintegrated upon hydrolysis, including the dissolution of incorporated iron oxide nanoparticles. The presented platform could find future use in theranostic multimodal imaging in vivo and magnetically triggered delivery by incorporation of thermorepsonsive amphiphiles that can break the membrane integrity upon magnetic heating via the embedded superparamagnetic nanoparticles. Full article
(This article belongs to the Special Issue Polymeric Materials for Medical Applications)
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14 pages, 1857 KiB  
Article
Triggered Release from Thermoresponsive Polymersomes with Superparamagnetic Membranes
by Oliver Bixner, Steffen Kurzhals, Mudassar Virk and Erik Reimhult
Materials 2016, 9(1), 29; https://doi.org/10.3390/ma9010029 - 6 Jan 2016
Cited by 29 | Viewed by 7470
Abstract
Magnetic polymersomes were prepared by self-assembly of the amphiphilic block copolymer poly(isoprene-b-N-isopropylacrylamide) with monodisperse hydrophobic superparamagnetic iron oxide nanoparticles (SPION). The specifically designed thermoresponsive block copolymer allowed for efficient incorporation of the hydrophobic nanoparticles in the membrane core and [...] Read more.
Magnetic polymersomes were prepared by self-assembly of the amphiphilic block copolymer poly(isoprene-b-N-isopropylacrylamide) with monodisperse hydrophobic superparamagnetic iron oxide nanoparticles (SPION). The specifically designed thermoresponsive block copolymer allowed for efficient incorporation of the hydrophobic nanoparticles in the membrane core and encapsulation of the water soluble dye calcein in the lumen of the vesicles. Magnetic heating of the embedded SPIONs led to increased bilayer permeability through dehydration of the thermoresponsive PNIPAM block. The entrapped calcein could therefore be released in controlled doses solely through exposure to pulses of an alternating magnetic field. This hybrid SPION-polymersome system demonstrates a possible direction for release applications that merges rational polymersome design with addressed external magnetic field-triggered release through embedded nanomaterials. Full article
(This article belongs to the Section Advanced Composites)
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14 pages, 3899 KiB  
Article
Synthesis of ABA Tri-Block Co-Polymer Magnetopolymersomes via Electroporation for Potential Medical Application
by Jennifer Bain, Matthew E. Berry, Catherine E. Dirks and Sarah S. Staniland
Polymers 2015, 7(12), 2558-2571; https://doi.org/10.3390/polym7121529 - 2 Dec 2015
Cited by 5 | Viewed by 9389
Abstract
The ABA tri-block copolymer poly(2-methyloxazoline)–poly(dimethylsiloxane)–poly(2-methyloxazoline) (PMOXA–PDMS–PMOXA) is known for its capacity to mimic a bilayer membrane in that it is able to form vesicular polymersome structures. For this reason, it is the subject of extensive research and enables the development of more robust, [...] Read more.
The ABA tri-block copolymer poly(2-methyloxazoline)–poly(dimethylsiloxane)–poly(2-methyloxazoline) (PMOXA–PDMS–PMOXA) is known for its capacity to mimic a bilayer membrane in that it is able to form vesicular polymersome structures. For this reason, it is the subject of extensive research and enables the development of more robust, adaptable and biocompatible alternatives to natural liposomes for biomedical applications. However, the poor solubility of this polymer renders published methods for forming vesicles unreproducible, hindering research and development of these polymersomes. Here we present an adapted, simpler method for the production of PMOXA–PDMS–PMOXA polymersomes of a narrow polydispersity (45 ± 5.8 nm), via slow addition of aqueous solution to a new solvent/polymer mixture. We then magnetically functionalise these polymersomes to form magnetopolymersomes via in situ precipitation of iron-oxide magnetic nanoparticles (MNPs) within the PMOXA–PDMS–PMOXA polymersome core and membrane. This is achieved using electroporation to open pores within the membrane and to activate the formation of MNPs. The thick PMOXA–PDMS–PMOXA membrane is well known to be relatively non-permeable when compared to more commonly used di-block polymer membranes due a distinct difference in both size and chemistry and therefore very difficult to penetrate using standard biological methods. This paper presents for the first time the application of electroporation to an ABA tri-block polymersome membrane (PMOXA–PDMS–PMOXA) for intravesicular in situ precipitation of uniform MNPs (2.6 ± 0.5 nm). The electroporation process facilitates the transport of MNP reactants across the membrane yielding in situ precipitation of MNPs. Further to differences in length and chemistry, a tri-block polymersome membrane structure differs from a natural lipid or di-block polymer membrane and as such the application and effects of electroporation on this type of polymersome is entirely novel. A mechanism is hypothesised to explain the final structure and composition of these biomedically applicable tri-block magnetopolymersomes. Full article
(This article belongs to the Special Issue Polymers and Polymeric Nanoparticles for Therapy and Imaging)
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