Magnetic Polymer Research Articles

Fabrication of a Nanomagnetic Smart Polymer Carrier as a Potential Candidate for a Drug Delivery System

We developed an intelligent device capable of controlled release of anti-cancer drugs. The nano-carrier consists of two key components: firstly, magnetic nanoparticles were synthesized through co-precipitation and then functionalized for attaching anti-cancer drugs; secondly, a polymer (poly(N-isopropylacrylamide-co-acrylic acid)) sensitive to pH and temperature was synthesized and employed to encapsulate the drug-loaded magnetic nanoparticles. This responsive polymer exhibits a lower critical solution temperature (LCST) of 38.5 °C, indicating a phase transition behavior. Numerous techniques and analyses, including Fourier transform infrared spectroscopy, thermogravimetric analysis, zeta potentials, scanning electron microscope, and transmission electron microscopy, were employed to confirm the successful execution of the aforementioned process. In vitro release assessments of the anti-cancer drug, doxorubicin, were conducted across various media (pH 5–8 and temperatures ranging from 20 to 40 °C). The outcomes revealed higher drug releases at temperatures exceeding the LCST (40 °C) and at slightly acidic pH levels (5–5.3). Notably, compared to the effectiveness of the unloaded drug, the magnetic smart polymer loaded with DOX exhibited a more potent cytotoxic effect. Considering these results, this nano-carrier emerges as a promising candidate for targeted therapeutic delivery to cancerous tissues.

Green synthesis of magnetic azo-linked porous organic polymers with recyclable properties for enhanced Bisphenol-A adsorption from aqueous solutions

Porous organic polymers (POPs) present superior adsorption performance to steroid endocrine disruptors. However, the effective recovery and high cost have been a big limitation for their large-scale applications. Herein, magnetic azo-linked porous polymers (Fe3O4@SiO2/ALP-p) were designed and prepared in a green synthesis approach using low-price materials from phloroglucinol and pararosaniline via a diazo-coupling reaction under standard temperature and pressure conditions, which embedded with Fe3O4@SiO2 nanoparticles to form three-dimensional interlayer network structure with flexible-rigid interweaving. The saturated adsorption capacity to bisphenol-A (BPA) was 485.09 mg/g at 298 K, which increased by 1.4 times compared with ALP-p of relatively smaller mass density. This enhanced adsorption was ascribed to increment from surface adsorption and pore filling with 2.3 times of specific surface area and 2.6 times of pore volume, although the total organic functional groups decreased with Fe3O4@SiO2 amendment. Also, the adsorption rate increased by about 1.1 and 1.5-fold due to enhancement in the initial stage of surface adsorption and subsequent stage pore diffusion, respectively. Moreover, this adsorbent could be used in broad pH (3.0–7.0) and salinity adaptability (<0.5 mol/L). The loss of adsorption capacity and magnetic recovery were lower than 1.1% and 0.8% in each operation cycle because of the flexible-rigid interweave. This excellent performance was contributed by synergistic effects from physisorption and chemisorption, such as pore filling, electrostatic attraction, π–π stacking, hydrogen bonding, and hydrophobic interaction. This study offered a cost-effective, high-performing, and ecologically friendly material along with a green preparation method.

Hyperthermia and Photocatalytic Performance of Magnetic Polyvinyl Alcohol under External Magnetic Field

The promising physical and chemical properties of components of magnetic polymers could enable extending their intelligent behaviors to material applications. Indeed, investigation into magnetic nanofillers to ensure their uniform dispersion within the polymer matrix remains a great challenge at present. In this work, polyvinyl alcohol-stabilized iron oxide nanoparticles (PVA@IONPs) were prepared using ultrasonic-assisted coprecipitation at room temperature. It is possible to produce PVA@IONPs with desirable shapes and sizes, which would enable the control of their hyperthermia and photocatalytic performance under an external magnetic field. The saturation magnetization of PVA@IONPs (45.08 emu g−1) was enhanced to the level of IONPs (41.93 emu g−1). The PVA@IONPs showed good photocatalytic and outstanding self-heating behavior. The hydrogen yield was 60 mmole min−1 g−1 for photocatalyst PVA@IONPs under visible light with magnetic force. In addition, the PVA@IONPs exhibited a higher specific absorption rate (SAR) than IONPs under the same magnetic field conditions. The PVA@IONPs displayed superior self-heating and photocatalytic performances, rendering them appropriate materials for biomedical and environmental applications.

Mesoporous Magnetic/Polymer Hybrid Nanoabsorbent for Rapid and Efficient Removal of Heavy Metal Ions from Wastewater.

As an advanced water purification technology, magnetic nanoabsorbents are highly attractive for their sustainability, robustness, and energy efficiency. However, magnetic responsiveness and high adsorptive capacity are irreconcilable during the design and synthesis of a high-performance magnetic nanoabsorbent. Here, we address this issue by designing a kind of mesoporous magnetic polymer hybrid microspheres, where functional polymers such as polyrhodanine and polypyrrole were attached to the pore walls in the interior of mesoporous Fe3O4 microspheres through in situ polymerization. Due to the integrated large saturation magnetic moment, porous structure, and dense polymer layer, the mesoporous magnetic polymer hybrid microspheres demonstrated fast magnetic responsiveness, excellent recycling performance, and high adsorption capacities toward Pb(II) ions (189 mg g-1) for polyrhodanine and Cr(VI) ions (199 mg g-1) for polypyrrole. Furthermore, their potential application in wastewater treatment was verified by a self-made magnetic separation column, where the designed magnetic nanoabsorbent exhibits significant advantages including rapid separation of heavy metal ions and high outflow. This study provided a promising magnetic polymer hybrid nanoabsorbent for realizing efficient removal of heavy metal ions from wastewater.

Microsized uniform magnetic polymer microspheres with carboxyl groups

Microsized uniform magnetic polymer microspheres with carboxyl groups

Synthesis and Modification of a Natural Polymer with the Participation of Metal Nanoparticles, Study of Their Composition and Properties.

A magnetic polymer material based on natural polymers-humic acids and magnetite, pre-configured for the sorption of a metal ion-was obtained. The magnetic polymer material was obtained via the interaction of a natural polymer, magnetite nanoparticles and sorbed metal ions that were used as a template. Moreover, the formation of a pre-polymerization complex was followed by copolycondensation with an amine in the presence of a crosslinking agent and further removal of metal ions from the crosslinked copolymer. The physicochemical properties of the resulting materials were determined using various physical methods. The composition of the resulting magnetic polymer materials was characterized by elemental analysis using an Elementar Unicube elemental analyzer. It was found that the carbon content increases by 8.28% and nitrogen by 0.42% for the polymer material Fe3O4:HA:T:AA; for the polymer material Fe3O4:HA:AA, the carbon content increases by 14.61% and nitrogen by 3.01%. Based on the IR spectra data, it is clear that magnetic polymer materials have much in common before hydrolysis (Fe3O4:HA:T:AA) and after hydrolysis (Fe3O4:HA:AA). The structure of the resulting polymer materials was studied using electron microscopy. Micrographs show the presence of pores in magnetic polymer materials after acid hydrolysis, indicating the formation of imprints. The results of the study of the sorption properties of magnetic polymer materials showed that after acid hydrolysis, the sorption capacity of a customized magnetic polymer material increases two times and it can act as a magnetic sorption material.

Effectiveness and advantages of ablative method of surgical removal of focies of verrucous leukoplakia of the oral mucosa with dental diode laser

The article presents clinical and diagnostic aspects of leukoplakia of the oral mucosa and red border of the lips and approaches to the treatment of the verrucous form of leukoplakia. The effectiveness of laser thermal ablation and adhesive balm with magnetic polymers, hexethidine, cytylpyridinium chloride and hyaluronic acid has been shown, which opens up new possibilities in the treatment of this pathology with minimal risk of complications.

Magnetorheological liquid-crystalline polymers with magnetic tetrachloroferrate ions based on polyvinyl chloride

ABSTRACT Novel magnetic ionic polymers based on polyvinyl chloride ([PVCs][FeCl4]) with liquid-crystalline (LC) ordering were synthetised and characterised. The [PVCs][FeCl4] containing magnetic tetrachloroferrate ions were prepared with PVC, pyridyl LC monomers and FeCl3. Various devices and instruments were used to characterise the chemical structure, thermal behaviour, magnetic properties, and LC properties. The synthetised [PVCs][FeCl4] showed smectic LC phase and presented excellent thermal stability. Several magnetorheological (MR) fluids were prepared using [PVCs][FeCl4] as particles and silicone oil as carrier fluid. MR Effects and settlement stability were investigated. Under the condition of external magnetic field, the MR fluids showed Bingham flow characteristics, and the MR effect was enhanced with increasing FeCl4 − content in the systems. Under the condition of magnetic field intensity of 80 kA/m and shear rate of 2.5 s−1, the magnetorheological efficiency of [PVCs][FeCl4] based MR fluids with particle concentration of 20% can reach up to 14.7. The excellent MR effect of [PVCs][FeCl4] was due to the strong coupling between the magnetic moment of the FeCl4 − anion and the orientation of cationic LC primitive under the action of an applied magnetic field. Furthermore, the good settling stability of the MR fluids was due to the introduction of organic mesogens, PVC main-chains and the ionic components for the [PVCs][FeCl4] particles.

Developing a novel magnetic organic polymer for selective extraction and determination of 16 macrolides in water and honey samples.

A novel magnetic organic polymer Fe3O4@SiO2@Tb-PDAN was designed and synthesized, which was used as an adsorbent for magnetic solid-phase extraction (MSPE) of 16 macrolides (MALs) in water and honey. The synthesized adsorbent was characterized using techniques including scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD). Then several parameters of the extraction process were further optimized. Under the optimized conditions, an MSPE-LC-MS/MS method was established for extraction and determination of 16 MALs, which showed good linearity (r ≥ 0.999), low limits of detection (0.001-0.012 μg L-1 for water and 0.001-0.367 μg kg-1 for honey) and satisfactory recoveries (70.02-118.91%) with the relative standard deviations (RSDs) lower than 10.0%. This established method was then successfully applied to detect MALs in real samples, which suggested that Fe3O4@SiO2@Tb-PDAN was a potential magnetic adsorbent for efficient extraction and analysis of MALs.

Fiber optic cadmium ion sensors based on functionalization of a magnetic ion-imprinted polymer.

Cadmium poisoning is a chronic accumulation process, and long-term drinking of even low cadmium content water will cause kidney damage, so an ultra-low detection limit is particularly important. However, at the present stage, the traditional detection method cannot reach a sufficiently low detection limit, the response time is too long, and the cost of detection is very high, so that real-time measurement cannot be realized. Therefore, the traditional cadmium ion detection method has a slow response and an insufficient detection limit. This paper presents a fiber optic cadmium ion sensor functionalized based on an Fe3O4@SiO2@CS magnetic ion imprinting polymer (M-IIP). The sensor is based on the coupling characteristics of the optical microfiber coupler (OMC) cone region to achieve a highly sensitive response to the change in the cadmium ion concentration. M-IIP materials were prepared by surface imprinting polymerization to achieve low cross-sensitivity and thus improve the detection limit of the sensor. The results show that the developed fiber sensor has high specificity and a rapid response to cadmium ions. The experimental limit of detection (LOD) reached 0.051 nM within 0-1 μM with a response time of less than 50 s. Moreover, the proposed fiber cadmium ion sensor exhibits excellent performance in terms of sensitivity, stability, repeatability and biocompatibility.

Magnetic polyvinylpolypyrrolidone polymer composite-supported copper(i) catalyst: an efficient and easily reusable catalyst for sustainable synthesis of 1,2,3-triazoles in water

Highlighting the efficiency and sustainable use of magnetic polyvinylpolypyrrolidone polymer composite-supported copper(i) catalyst for the synthesis of 1,4-disubstituted-1,2,3-triazoles in water.

Facile synthesis of multifunctional magnetic porous organic polymers with high catalytic performance and dye adsorption capacity

Multifunctional magnetic porous organic polymers (MOPs) rich in sulfide and free phenolic hydroxyl groups were synthesized. The MOPs exhibit a large surface area and can interact strongly with metal ions and cationic dyes, including methylene blue.

On the Evaluation of the Hyperthermic Efficiency of Magnetic Scaffolds.

Goal: Deep-seated tumors (DST) can be treated using thermoseeds exposed to a radiofrequency magnetic field for performing local interstitial hyperthermia treatment (HT). Several research efforts were oriented to the manufacturing of novel biocompatible magnetic nanostructured thermo-seeds, called magnetic scaffolds (MagS). Several iron-doped bioceramics or magnetic polymers in various formulations are available. However, the crucial evaluation of their heating potential has been carried out with significantly different, lab specific, variable experimental conditions and protocols often ignoring the several error sources and inaccuracies estimation. Methods: This work comments and provides a perspective analysis of an experimental protocol for the estimation methodology of the specific absorption rate (SAR) of MagS for DST HT. Numerical multiphysics simultions have been performed to outline the theoretical framework. After the in silico analysis, an experimental case is considered and tested. Results: From the simulations, we found that large overestimation in the SAR values can be found, due to the axial misplacement in the radiofrequency coil, while the radial misplacement has a lower impact on the estimated SAR value. Conclusions: The averaging of multiple temperature records is needed to reliably and effectively estimate the SAR of MagS for DST HT.

Prediction of pure carbon crystals with intrinsic antiferromagnetism: polymerized from C20 fullerenes.

Pure carbon materials with magnetic properties have attracted considerable research interest due to their advantages over traditional magnetic materials. Nevertheless, such materials are exceedingly rare. Disrupting the Kekulé valence structures in carbon materials potentially leads to the emergence of magnetism. In this study, using first principles calculations, we developed a range of pure carbon allotropes derived from the smallest fullerene C20 which potentially disrupts the Kekulé valence structures after polymerization. The results indicate that some of the allotropes disrupting the Kekulé valence structures exhibit intrinsic antiferromagnetic ordering, and the magnetism originates from the presence of isolated three-fold coordinated C atoms. The other allotropes adhering to the Kekulé valence structures show non-magnetism with all three-fold coordinated C atoms forming dimers. In all magnetic polymers, magnetism arises from unpaired electrons on the isolated three-fold coordinated carbon atoms, with magnetic moments of about 0.40μB at these sites. The adsorption of dopant atoms can significantly alter the magnetic properties of polymers, for instance, the C20-71 polymer with Immm symmetry undergoes a transition from non-magnetic to anti-magnetic ordering upon adsorption of hydrogen atoms. Electronic calculations indicate that these polymers display a range of electronic properties, encompassing both metallic and semiconducting characteristics. Notably, certain magnetic phases exhibit superhard properties, with the hardness value exceeding 40 GPa. This study presents a potential method for designing magnetic carbon materials. Specifically, certain compounds address the gap in magnetic superhard materials composed of light elements, and can be utilized in the field of spintronics where traditional superhard materials are unsuitable.

Facile synthesis of a magnetic molecularly-imprinted polymer adsorbent for solid-phase extraction of diclofenac from water.

Numerous pollutants endanger the safety and purity of water, making water pollution a major worldwide concern. The health of people and aquatic ecosystems are at risk from these contaminants, which include hazardous microbes, industrial waste, and agricultural runoff. Fortunately, there appears to be a viable option to address this problem with adsorptive water treatment techniques. The present study presents a magnetic adsorbent (MMIP) based on molecularly imprinted polyaniline and magnetite nanoparticles for the solid-phase extraction of diclofenac, an anti-inflammatory medication, from industrial wastewater. The adsorbent nanomaterial was characterized using dynamic light scattering, zeta potential measurement, vibrating sample magnetometry, X-ray diffraction, and scanning electron microscopy. The MMIP demonstrated a particle size of 86.3 nm and an adsorption capacity of 139.7 mg g-1 at 600 mg L-1 of diclofenac and after a 200 min incubation period. The highest %removal was attained at pH range of 3-7. The adsorption process follows the pseudo-second order kinetic model. In addition, it was found that the adsorption process is enthalpy-driven and may occur via hydrogen bonding and/or van der Waals interactions.

Purely organic-derived polymeric magnets: a brief review on polyradicals with intrinsic magnetism

This mini-review summarizes the recent progress in the research field of polyradicals that are designed and prepared to obtain strong ferromagnetic coupling.

Long-term in vivo dissolution of thermo- and pH-responsive, 19F magnetic resonance-traceable and injectable polymer implants.

19F magnetic resonance (19F MR) tracers stand out for their wide range of applications in experimental and clinical medicine, as they can be precisely located in living tissues with negligible fluorine background. This contribution demonstrates the long-term dissolution of multiresponsive fluorinated implants designed for prolonged release. Implants were detected for 14 (intramuscular injection) and 20 (subcutaneous injection) months by 19F MR at 4.7 T, showing favorable MR relaxation times, biochemical stability, biological compatibility and slow, long-term dissolution. Thus, polymeric implants may become a platform for long-term local theranostics.

Effects of iron oxide and carbon nanotube contents on mechanical properties and shape memory behavior of biocompatible and biodegradable shape memory polymers

AbstractThe shape memory polymers (SMPs) is a potential alternative material for conventional shape memory alloys (SMAs) in various fields. Previous studies have focused on the application of SMPs materials as an alternative to SMAs. However, considering problems such as the poor mechanical properties, its application has been limited. This study developed a biodegradable, magnetically responsive SMPs material that can be used for medical implants with shape memory behavior under magnetic force and improved mechanical properties by adding nanoparticles. Moreover, effect of the added nanoparticle was investigated due to contents ratio. Nanocomposite was synthesized with polycaprolactone which has shape memory properties, Fe3O4 that generates heat under magnetic field, and carbon nanotubes with reinforcing effect. The morphology analysis confirmed the homogeneous dispersion of the Fe3O4/Carbon‐nanotubes (CNTs) in polymer matrix. The tensile test shows that tensile strength (14.9–17.6 MPa) increased when Fe3O4 (0–20 wt%) was included and that it did not increase significantly when CNTs (0–0.8 wt%) were included. The shape memory test result confirmed that developed composite had a shape memory under a magnetic field. It was confirmed that even if Fe3O4 was incorporated into polycaprolactone, did not lose its exothermic properties under magnetic field. The developed polymer showed high shape memory ratio (91%–98%) in all the nanoparticle content rates. With regard to biodegradability, weight loss occurred over time in the phosphate‐buffered saline solution. Therefore, the biocompatible, biodegradable, magnetic response shape memory polymer developed in this study might applied to various medical implant as advanced shape memory materials.

4D printed biocompatible magnetic nanocomposites toward deployable constructs

Herein, an alternating magnetic field-triggered shape memory polymer composite has been 3D printed as a tissue scaffold that can be remotely deployed at physiological temperatures and can be extended to soft robotics.

Bottom-up data integration in polymer models of chromatin organisation

Cellular functions crucially depend on the precise execution of complex biochemical reactions taking place on the chromatin fiber in the tightly packed environment of the cell nucleus. Despite the availability of large data sets probing this process from multiple angles, bottom-up frameworks which allow the incorporation of the sequence-specific nature of biochemistry in a unified model of 3D chromatin structure remain scarce. Here we propose SEMPER (Sequence Enhanced Magnetic PolymER), a novel stochastic polymer model which naturally incorporates observational data about sequence-driven biochemical processes, such as binding of transcription factor proteins, in a 3D model of chromatin structure. We introduce a novel approximate Bayesian algorithm to quantify a posteriori the relative importance of various factors, including the polymeric nature of DNA, in determining chromatin epigenetic state, thus providing a transparent way to generate biological hypotheses. While accurate prediction of contact frequencies (a problem already extensively studied in the literature) is not our main aim, as a byproduct of the inference procedure and without additional input from the genome 3D structure, our model can predict with reasonable accuracy some notable and nontrivial conformational features of chromatin folding within the nucleus. Our work highlights the importance of introducing physically realistic statistical models for predicting chromatin states from epigenetic data and opens the way to a new class of more systematic approaches to interpreting epigenomic data.