Paramagnetic Nanoparticles Research Articles

In-Vitro Assessment of Magnetic Dextran-Spermine Nanoparticles for Capecitabine Delivery to Cancerous Cells.

Cationic polymeric nanoparticles have great potential for developing drug delivery systems with limited side effects for tumor medication. The goal of this research is investigation of cationic dextran-spermine polymer (DS) efficacy for improvement of hydrophilic drug delivery to negatively charged cancerous cells. Capecitabine (as a hydrophilic antineoplastic drug) was loaded into the magnetic dextran-spermine nanoparticles (DS-NPs) via ionic gelation. Design of experiments was applied to specify how the significant factors affect size, surface charge and capecitabine entrapment efficiency of the DS-NPs. Physicochemical properties, in-vitro release profile and cellular studies of the optimized DS-NPs were evaluated. The experimental results indicated that DS-NPs with favorable properties can be achieved at an optimized condition of 2 mg/mL DS and 0.75 mg/mL tri-polyphosphate (TPP) concentrations, TPP addition rate of 35 mL/min, pH 3 of DS solution and super paramagnetic iron oxide nanoparticles (SPION)/DS mass ratio of 0.5. The entrapment efficiency of capecitabine was 26.1% at optimum condition and drug release at neutral pH after 24 h and acidic pH within 3 h was 56 and 98%, respectively. The cytotoxicity assessment exhibited that capecitabine loaded DS-NPs was more toxic than corresponding free drug as control. Significant cellular uptake of capecitabine loaded DS-NPs by U87MG glioblastoma cells were proved by Prussian blue staining and TEM, qualitatively. DS-NPs are suitable candidates for delivery of the hydrophilic drugs in cancer treatment and due to positive charge of the dextran-spermine, the uptake of the hydrophilic drugs by the cancerous cells was improved.

Magnetic properties of crystalline nickel and low phosphorus amorphous Ni1-XPx nanoparticles

This paper explores how synthesis parameters can affect the size, composition and crystallinity degree of the Ni1-xPx nanoparticles and describes the process for preparing nanoparticles with tunable ferromagnetic, superparamagnetic and paramagnetic properties. Ni1-xPx nanoparticles of different sizes, compositions and crystallinities were synthesized through microemulsion method and by variation of micellar ratio, type of reducing agent and process pH. The results of particle size analysis (PSA), transmission electron microscopy (TEM), atomic absorption spectroscopy (AAS) and X-ray diffraction (XRD) confirmed successful synthesis of Ni1-xPx nanoparticles. While pure and crystalline nickel nanoparticles can be synthesized in the presence of hydrazine, phosphorus is doped on the structure of nanoparticles synthesized by sodium hypophosphite reducing agent. In this case, lower bath pH caused to synthesis of amorphous nanoparticles with higher phosphorous concentrations. It was shown that ferromagnetic nickel nanoparticles can be transferred to superparamagnetic ones if their particle size reduces to less than 14 nm. As well, crystalline to amorphous transition by phosphorus addition led to preparation of paramagnetic nanoparticles. Magnetic properties measurement using vibrating sample magnetometer (VSM) suggested interesting relationship between the magnetic properties and characteristics of nanoparticles. Moreover, the results indicated that synthesis method is flexible for preparation of nanoparticles with tunable magnetic properties from ferromagnetic to paramagnetic.

Magnetic Resonance Imaging of Alginate Beads Containing Pancreatic Beta Cells and Paramagnetic Nanoparticles

Microencapsulation is being investigated as a means to avoid rejection of transplanted pancreatic islets. Monitoring bead distribution and stability in vivo is an important step toward improving microencapsulated islet transplantation strategies. Islet co-encapsulation with gadolinium-labeled mesoporous silica nanoparticles (Gd-MSNs) could allow bead visualization while immobilizing and limiting the potential internalization of the contrast agent. The porous nature of the MSNs could also be used to locally release anti-inflammatory, angiogenic, or anti-apoptotic factors. Mouse insulinoma 6 (MIN6) beta cells were co-encapsulated with Gd-MSNs in alginate beads produced by emulsification and internal gelation. Gd-MSN alginate beads appeared brighter in T1-weighted imaging sequences (detection threshold of 0.016 mM Gd; relaxometric ratio r2/r1 = 1.45) than beads without Gd-MSNs. No leaching of Gd3+ from the hydrogels was detected over the course of 3 months. MIN6 cells co-encapsulated with Gd-MSNs were viable without significant differences in cell growth rate compared to encapsulated controls without Gd-MSNs. This study paves the way for microencapsulated islet tracking via MRI using co-encapsulated paramagnetic nanomaterials.

On-Demand Disassembly of Paramagnetic Nanoparticle Chains for Microrobotic Cargo Delivery

Paramagnetic nanoparticles are considered as attractive building blocks, particularly for robotic delivery of drugs. Although paramagnetic nanoparticles can be effectively gathered and transported using external magnetic fields, the disassembly process is yet to be fully investigated to avoid the formation of aggregations. In this paper, we report a novel method of controllable disassembly of paramagnetic nanoparticle chains using a predefined dynamic magnetic field. The dynamic field is capable of performing spreading and fragmentation of the particle chains simultaneously. Using the magnetic dipole–dipole repulsive forces, the final area covered by the particle chains swells up to 545% of the initial area. The final length distribution presents a strong relationship with the frequency of the dynamic field in deionized (DI) water and two kinds of biofluids. An analytical model of phase lag is proposed, which shows good agreement with the experimental results. Furthermore, we also present an assembly process using a rotating magnetic field, indicating that the assembly disassembly process is reversible. In addition, batch-cargo delivery of polystyrene microbeads using the nanoparticle chains as swarm-like nanorobots is demonstrated.

Centrifugation-Free Magnetic Isolation of Functional Mitochondria Using Paramagnetic Iron Oxide Nanoparticles.

Subcellular fractionation techniques are essential for cell biology and drug development studies. The emergence of organelle-targeted nanoparticle (NP) platforms necessitates the isolation of target organelles to study drug delivery and activity. Mitochondria-targeted NPs have attracted the attention of researchers around the globe, since mitochondrial dysfunctions can cause a wide range of diseases. Conventional mitochondria isolation methods involve high-speed centrifugation. The problem with high-speed centrifugation-based isolation of NP-loaded mitochondria is that NPs can pellet even if they are not bound to mitochondria. We report development of a mitochondria-targeted paramagnetic iron oxide nanoparticle, Mito-magneto, that enables isolation of mitochondria under the influence of a magnetic field. Isolation of mitochondria using Mito-magneto eliminates artifacts typically associated with centrifugation-based isolation of NP-loaded mitochondria, thus producing intact, pure, and respiration-active mitochondria. © 2017 by John Wiley & Sons, Inc.

MRI-guided targeting delivery of doxorubicin with reduction-responsive lipid-polymer hybrid nanoparticles.

In recent years, there has been increasing interest in developing a multifunctional nanoscale platform for cancer monitoring and chemotherapy. However, there is still a big challenge for current clinic contrast agents to improve their poor tumor selectivity and response. Herein, we report a new kind of Gd complex and folate-coated redox-sensitive lipid-polymer hybrid nanoparticle (Gd-FLPNP) for tumor-targeted magnetic resonance imaging and therapy. Gd-FLPNPs can simultaneously accomplish diagnostic imaging, and specific targeting and controlled release of doxorubicin (DOX). They exhibit good monodispersity, excellent size stability, and a well-defined core-shell structure. Paramagnetic nanoparticles based on gadolinium-diethylenetriaminepentaacetic acid-bis-cetylamine have paramagnetic properties with an approximately two-fold enhancement in the longitudinal relaxivity compared to clinical used Magnevist. For targeted and reduction-sensitive drug delivery, Gd-FLPNPs released DOX faster and enhanced cell uptake in vitro, and exhibited better antitumor effect both in vitro and in vivo.

Synthesis and characterization of ZnS@Fe3O4 fluorescent-magnetic bifunctional nanospheres

Herein, we synthesized and characterized fluorescent and super paramagnetic ZnS@Fe3O4 nanospheres. First, (3-mercaptopropyl) trimethoxysilane (MPS) capped ZnS quantum dots (QDs) and SiO2 coated Fe3O4 nanoparticles were synthesized separately by using solution growth and co-precipitation techniques. After synthesis and characterization of these two nanoparticles, they were conglutinated together in a nano sized sphere. The QDs were attached to the surface of the Fe3O4 nanoparticles by SiOSi bonds and so SiOSi bonds created a SiO2 network around the nanoparticles during the formation of the ZnS@Fe3O4 nanospheres. The synthesized MPS capped ZnS fluorescent QDs, SiO2 coated magnetite super paramagnetic nanoparticles and ZnS@Fe3O4 fluorescent-magnetic bifunctional nanospheres were characterized by using UV–Vis Absorption Spectroscopy, Fluorescence Spectroscopy, X-ray analysis, Vibrating Sample Magnetometer analysis, Attenuated Total Reflection-Fourier Transform Infrared Spectroscopy, Scanning Electron Microscope and Energy-dispersive X-ray spectroscopy. ZnS@Fe3O4 bifunctional nanospheres were shown to retain the magnetic properties of magnetite, while exhibiting the luminescent optical properties of ZnS nanoparticles. The combination of fluorescent and magnetic behaviors of nano composites make them useful for potential applications in the field of bio-medical and environmental.

Excellent alkene epoxidation catalytic activity of macrocyclic‐based complex of dioxo‐Mo(VI) on supermagnetic separable nanocatalyst

A phenoxybutane‐based Schiff base complex of cis‐dioxo‐Mo(VI) was supported on paramagnetic nanoparticles and characterized using powder X‐ray diffraction, infrared, diffuse reflectance and atomic absorption spectroscopies, scanning and transmission electron microscopies and vibrating sample magnetometry. The separable nanocatalyst was tested for the selective epoxidation of cyclohexene, cyclooctene, styrene, indene, α‐pinene, 1‐octene, 1‐heptene, 1‐dodecene and trans‐stilbene using tert‐butyl hydroperoxide (80% in di‐tert‐butyl peroxide–water, 3:2) as oxidant in chloroform. The catalyst was efficient for oxidation of cyclooctene with 100% selectivity for epoxidation with 98% conversion in 10 min. We were able to separate magnetically the nanocatalyst using an external magnetic field and used the catalyst at least six successive times without significant decrease in conversion. The turnover frequency of the catalyst was remarkable (2556 h−1 for cyclooctene). The proposed nanomagnetic catalyst has advantages in terms of catalytic activity, selectivity, catalytic reaction time and reusability by easy separation.

Enhancement in dielectric and magnetic properties of Mg2+ substituted highly porous super paramagnetic nickel ferrite nanoparticles with Williamson-Hall plots mechanistic view

Abstract In our present investigation, we have reported the fabrication of a low-cost, magnetically separable, Highly Conductive Magnesium substituted nickel ferrite (Ni 1−x Mg x Fe 2 O 4 with x = 0.2, 0.4, 0.6, 0.8, 1.0) nanoparticles by Simple co-precipitation method. The structural, dielectric and magnetic properties of the synthesized nanoparticles were investigated by XRD, SEM, VSM, and FTIR. XRD pattern confirms the formation of single phase face centred cubic structured nanoparticles. The crystallite size of Ni 1−x Mg x Fe 2 O 4 was found to decrease from 28 nm to 10 nm with increase in Mg content. SEM results show the agglomerated spherical morphology. The Coercivity (Hc) and remnant Magnetization (Mr) decreases and Saturation magnetization (Ms) increases with increase in Mg content as indicated by VSM. Dielectric properties decreases and electrical conductivity increases with increasing frequency and increasing Mg concentration, this was in good agreement with the SEM, TEM and VSM studies. The mean size and strain within Ni 1−x Mg x Fe 2 O 4 have been calculated successfully from Williamson-Hall plots.

Toxicity and T₂-Weighted Magnetic Resonance Imaging Potentials of Holmium Oxide Nanoparticles.

In recent years, paramagnetic nanoparticles (NPs) have been widely used for magnetic resonance imaging (MRI). This paper reports the fabrication and toxicity evaluation of polyethylene glycol (PEG)-functionalized holmium oxide (Ho2O3) NPs for potential T2-weighted MRI applications. Various characterization techniques were used to examine the morphology, structure and chemical properties of the prepared PEG–Ho2O3 NPs. MRI relaxivity measurements revealed that PEG–Ho2O3 NPs could generate a strong negative contrast in T2-weighted MRI. The pilot cytotoxicity experiments showed that the prepared PEG–Ho2O3 NPs are biocompatible at concentrations less than 16 μg/mL. Overall, the prepared PEG–Ho2O3 NPs have potential applications for T2-weighted MRI imaging.

Biodegradation of LDPE with Mixed Consortium in presence of Super Paramagnetic Iron Oxide Nanoparticle (SPION) as the Enhancer for Biodegradation by Accelerating Growth Profiling of Microbes

Biodegradation of LDPE with Mixed Consortium in presence of Super Paramagnetic Iron Oxide Nanoparticle (SPION) as the Enhancer for Biodegradation by Accelerating Growth Profiling of Microbes

Preparation of water-soluble magnetic nanoparticles with controllable silica coating

Abstract This work provides a general method for preparing monodisperse, water-soluble and paramagnetic magnetic nanoparticles which are easy to be modified. Firstly, magnetic silica with core-shell structure was prepared according to a previous work. Then, the magnetic silica was treated with alkali solution to afford magnetic nanoparticles. With the increase of calcination temperature for the preparation of magnetic silica, the crystallinity and the magnetic responsibility of magnetic silica strengthened, meanwhile, the corresponding magnetic nanoparticles kept monodisperse without any aggregation. The magnetic nanoparticles are comprised of cobalt ferrite and a silica coating. The silica coating on the cobalt ferrite facilitates the magnetic nanoparticles well-dissolved and monodisperse in water, and easily modified.

Modeling and Simulation Study for Solid Particles Detection in Gas–Oil Pipelines Using Field Free Line in Magnetic Particle Imaging and Its Hardware Realization

This paper suggests a new magnetic particle imaging (MPI) technique for 2-D tomographic imaging to detect the presence of flowing solid particles (i.e., black powder, which consist of paramagnetic nanoparticles) passing through gas-oil pipelines. The hardware consists of a ring of a modified Halbach array of 24 permanent magnets, in addition to two surrounding Helmholtz coil pairs, and a receiving coil, which are evenly distributed across a cross section of the probe. With the application of static and dynamically moving drive fields, the MPI utilizes the full benefit of superparamagnetic iron oxide nanoparticles (SPIONs) by providing a linear response when they are exposed to a relatively low magnetic field and no response when they are saturated. The scanning of region of interest with the field-free line (FFL) instead of the field-free point (FFP) is motivated by the fact that a high-intensity dc current is required for FFP, which is not tolerated in oil-gas pipelines where the maximal current should not exceed few amperes. With the presence of an oscillatory magnetic field, SPIONs react with a nonlinear magnetization response, which is further measured by the receiving coil. A 2-D image reconstruction is then performed using the frequency-based image reconstruction process. The hardware design, specifically the sizing of permanent magnets with regard to their relative position and dimensions, was refined following an optimization technique based on the particle swarm optimization technique. The assessment of the system using finite-element method indicates that the system can reconstruct the 2-D profile of the SPION with a mean absolute error of prediction of less than 4% and 12% using FFL and FFP methods, respectively.

Albumin and Hyaluronic Acid-Coated Superparamagnetic Iron Oxide Nanoparticles Loaded with Paclitaxel for Biomedical Applications.

Super paramagnetic iron oxide nanoparticles (SPION) were augmented by both hyaluronic acid (HA) and bovine serum albumin (BSA), each covalently conjugated to dopamine (DA) enabling their anchoring to the SPION. HA and BSA were found to simultaneously serve as stabilizing polymers of Fe3O4·DA-BSA/HA in water. Fe3O4·DA-BSA/HA efficiently entrapped and released the hydrophobic cytotoxic drug paclitaxel (PTX). The relative amount of HA and BSA modulates not only the total solubility but also the paramagnetic relaxation properties of the preparation. The entrapping of PTX did not influence the paramagnetic relaxation properties of Fe3O4·DA-BSA. Thus, by tuning the surface structure and loading, we can tune the theranostic properties of the system.

Enhanced electrical conductivity of collagen films through long-range aligned iron oxide nanoparticles

The development of biocompatible collagen substrates able to conduct electric current along specific pathways represent an appealing issue in tissue engineering, since it is well known that electrical stimuli significantly affects important cell behaviour, such as proliferation, differentiation, directional migration, and, therefore, tissue regeneration. In this work, a cheap and easy approach was proposed to produce collagen-based films exhibiting enhanced electrical conductivity, through the simple manipulation of a weak external magnetic trigger. Paramagnetic iron oxide nanoparticles (NPs) capped by a biocompatible polyethylene-glycol coating were synthetized by a co-precipitation and solvothermic method and sprayed onto a collagen suspension. The system was then subjected to a static external magnetic field in order to conveniently tune NPs organization. Under the action of the external stimulus, NPs were induced to orient along the magnetic field lines, forming long-range aligned micropatterns within the collagen matrix. Drying of the substrate following water evaporation permanently blocked the magnetic architecture produced, thereby preserving NPs organization even after magnetic field removal. Electrical conductivity measurements clearly showed that the presence of such a magnetic framework endowed collagen with marked conductive properties in specific directions. The biocompatibility of the paramagnetic collagen films was also demonstrated by MTT cell cytotoxicity test.

Construction of an Acetylcholinesterase Sensor Based on Synthesized Paramagnetic Nanoparticles, a Simple Tool for Neurotoxic Compounds Assay.

Magnetic particles (MPs) have been widely used in biological applications in recent years as a carrier for various molecules. Their big advantage is in repeated use of immobilized molecules including enzymes. Acetylcholinesterase (AChE) is an enzyme playing crucial role in neurotransmission and the enzyme is targeted by various molecules like Alzheimer’s drugs, pesticides and warfare agents. In this work, an electrochemical biosensor having AChE immobilized onto MPs and stabilized through glutaraldehyde (GA) molecule was proposed for assay of the neurotoxic compounds. The prepared nanoparticles were modified by pure AChE and they were used for the measurement anti-Alzheimer’s drug galantamine and carbamate pesticide carbofuran with limit of detection 1.5 µM and 20 nM, respectively. All measurements were carried out using screen-printed sensor with carbon working, silver reference, and carbon auxiliary electrode. Standard Ellman’s assay was used for validation measurement of both inhibitors. Part of this work was the elimination of reversible inhibitors represented by galantamine from the active site of AChE. For this purpose, we used a lower pH to get the original activity of AChE after inhibition by galantamine. We also observed decarbamylation of the AChE-carbofuran adduct. Influence of organic solvents to AChE as well as repeatability of measurement with MPs with AChE was also established.

Preparation, Optimization and Toxicity Evaluation of (SPION-PLGA) ±PEG Nanoparticles Loaded with Gemcitabine as a Multifunctional Nanoparticle for Therapeutic and Diagnostic Applications.

The aim of this study was to develop a novel multifunctional nanoparticle, which encapsulates SPION and Gemcitabine in PLGA ± PEG to form multifunctional drug delivery system. For this aim, super paramagnetic iron oxide nanoparticles (SPIONs) were simultaneously synthesized and encapsulated with Gemcitabine (Gem) in PLGA ± PEG copolymers via W/O/W double emulsification method. Optimum size and encapsulation efficiency for radiosensitization, hyperthermia and diagnostic applications were considered and the preparation parameters systematically were investigated and physicochemical characteristics of optimized nanoparticle were studied. Then SPION-PLGA and PLGA-Gem nanoparticles were prepared with the same optimized parameters and the toxicity of these nanoparticles was compared with Gemcitabine in human breast cancer cell line (MCF-7). The optimum preparation parameters were obtained with Gem/polymer equal to 0.04, SPION/polymer equal to 0.8 and 1% sucrose per 20 mg of polymer. The hydrodynamic diameters of all nanoparticles were under 200 nm. Encapsulation efficiency was adjusted between 13.2% to 16.1% for Gemcitabine and 48.2% to 50.1% for SPION. In-vitro Gemcitabine release kinetics had controlled behavior. Enhancement ratios for PLGA-Gem and SPION-PLGA-Gem at concentration of nanoparticles equal to IC50 of Gemcitabine were 1.53 and 1.89 respectively. The statistical difference was significant (p-value = 0.006 for SPION-PLGA-Gem and p-value = 0.015 for PLGA-Gem compared with Gemcitabine). In conclusion, we have successfully developed a Gemcitabine loaded super paramagnetic PLGA-Iron Oxide multifunctional drag delivery system. Future work includes in-vitro and in-vivo investigation of radiosensitization and other application of these nanoparticles.

Nickel-Salen supported paramagnetic nanoparticles for 6-His-target recombinant protein affinity purification

In this research, a simple, efficient, inexpensive, rapid and high yield method for the purification of 6×histidine-tagged recombinant protein was developed. For this purpose, manganese ferrite magnetic nanoparticles (MNPs) were synthesized through a co-precipitation method and then they were conveniently surface-modified with tetraethyl orthosilicate (TEOS) in order to prevent oxidation and form high density of hydroxyl groups. Next, the salen ligand was prepared from condensation reaction of salicylaldehyde and 3-aminopropyl (trimethoxy) silane (APTMS) in 1:1 molar ratio; followed by complexation with Ni(OAc)2.4H2O. Finally, the prepared Ni(II)-salen complex conjugated to silica coated MNPs and MnFe2O4@SiO2@Ni-Salen complex nanoparticles were obtained. The functionalized nanoparticles were spherical with an average diameter around 70nm. The obtained MNPs had a saturation magnetization about 54 emu/g and had super paramagnetic character. These MNPs were used efficiently to enrich recombinant histidine-tagged (His-tagged) protein-A from bacterial cell lysate. In about 45min, highly pure His-tagged recombinant protein was obtained, as judged by SDS-PAGE analysis and silver staining. The amount of target protein in flow through and washing fractions was minimal denoting the high efficiency of purification process. The average capacity of the matrix was found to be high and about 180±15mgg−1 (protein/MnFe2O4@SiO2@Ni-Salen complex). Collectively, purification process with MnFe2O4@SiO2@Ni-Salen complex nanoparticles is rapid, efficient, selective and whole purification can be carried out in only a single tube without the need for expensive systems.

Thermally tunable grating using thermo-responsive magnetic fluid

We report a thermally tunable grating prepared using poly(N-isopropylacrylamide) and super paramagnetic iron oxide nanoparticles. The array spacing is reversibly tuned by varying the temperature between 5 and 38 °C. Here, the ability of thermo-responsive polymer brushes to alter their conformation at an interface is exploited to control the grating spacing in nanoscale. The underlying mechanism for the temperature dependent conformational changes are studied by measuring the subtle intermolecular forces between the polymer covered interfaces. It is observed that the interparticle forces are repulsive and exponentially decaying with distance. The thermo-responsive grating is simple to use and offers a wide range of applications.

Magnetic-field measurement and simulation of a field-free line magnetic-particle scanner

AbstractIn 2005, B. Gleich and J. Weizenecker initially presented the tracer based medical imaging modality Magnetic Particle Imaging (MPI). It uses the nonlinear magnetization behavior of super paramagnetic iron oxide nanoparticles (SPIONs). MPI has the potential to perform real-time imaging in the sub millimeter-range without the use of harmful radiation. To acquire a particle signal from the tracer, an alternating homogenous magnetic field (drive field) is applied. Due to the nonlinearity of the particle magnetization, the magnetic field is distorted and higher harmonics are generated that indicate a particle concentration within the field of view (FOV). For the spatial distribution, another magnetic field that exhibits a high gradient (selection field) is applied simultaneously. Basically, there are two different types of selection fields containing either a field- free point (FFP) or a field-free line (FFL). Because of magnetic saturation, only SPIONs within the close vicinity of the FFP or FFL contribute to the particle signal. As the FFP is moved by the drive field through the FOV a spatial distribution of the SPIONs can be obtained. In the other encoding concept, the FFL rotates and is additionally translated by the drive field to obtain one dimensional projections for various angles. In this work, the currently world’s largest FFL MPI Scanner is investigated. Single components of the generated magnetic field are measured precisely to accomplish an accurate simulation of a translating and rotating FFL.