Imparting magnetic dipole heterogeneity to internalized iron oxide nanoparticles for microorganism swarm control

Tetrahymena pyriformis is a single cell eukaryote that can be modified to respond to magnetic fields, a response called magnetotaxis. Naturally, this microorganism cannot respond to magnetic fields, but after modification using iron oxide nanoparticles, cells are magnetized and exhibit a constant magnetic dipole strength. In experiments, a rotating field is applied to cells using a two-dimensional approximate Helmholtz coil system. Using rotating magnetic fields, we characterize discrete cells’ swarm swimming which is affected by several factors. The behavior of the cells under these fields is explained in detail. After the field is removed, relatively straight swimming is observed. We also generate increased heterogeneity within a population of cells to improve controllability of a swarm, which is explored in a cell model. By exploiting this straight swimming behavior, we propose a method to control discrete cells utilizing a single global magnetic input. Successful implementation of this swarm control method would enable teams of microrobots to perform a variety of in vitro microscale tasks impossible for single microrobots, such as pushing objects or simultaneous micromanipulation of discrete entities.     

铝电解槽内电-磁-流场的耦合仿真方法及应用

基于电磁流体力学的基本理论,应用等效电阻网络法与有限元相结合计算铝电解槽电流场,标量电位法和双标量磁位法计算铝电解槽磁场,k-ε双方程模型计算电磁力驱动下的铝液流动,并与工业测试结果进行比较.对200 kA侧部四点进电的铝电解槽进行计算与测试,其结果吻合良好;水平磁场形成一个顺时针的漩涡,垂直磁场沿长轴和短轴呈反对分布;铝液流动呈现出沿长轴方向排列的4个漩涡.仿真磁场误差小于10.0%,流场误差不超过5.0%.     

Synthetic and biogenic magnetite nanoparticles for tracking of stem cells and dendritic cells

Accurate delivery of cells to target organs is critical for success of cell-based therapies with stem cells or immune cells such as antigen-presenting dendritic cells (DC). Labeling with contrast agents before implantation provides a powerful means for monitoring cellular migration using magnetic resonance imaging (MRI). In this study, we investigated the uptake of fully synthesized or bacterial magnetic nanoparticles (MNPs) into hematopoietic Flt3⁺ stem cells and DC from mouse bone marrow. We show that (i) uptake of both synthetic and biogenic nanoparticles into cells endow magnetic activity and (ii) low numbers of MNP-loaded cells are readily detected by MRI.     

Numerical simulation of biomagnetic fluid in a channel with thrombus

Biomagnetic fluid dynamics is the study of the interaction of biological fluids with an applied steady magnetic field. Recently, several medical applications begin to utilize magnetic labeling of specific cells and targeted drug delivery using magnets. The magnetically labeled cells and the drug encapsulates are usually loaded in the blood stream and are directed toward a specific site by use of a magnet. In this paper, numerical simulation of biomagnetic fluid in the presence of a thrombus when exposed to magnetic field is presented. The finite analytic method is used to obtain the numerical simulation. It is found that the magnetic force causes a drastic change in the fluid behavior and the friction coefficient increases as the magnetic field strength increases.     

Computational model investigating the effect of magnetic field on neural-astrocyte microcircuit

Extremely low-frequency magnetic field is widely used as a noninvasive stimulation method in clinical practice and basic research. Electrical field induced from magnetic pulse can decrease or increase neuronal electrical activity. However, the cellular mechanism underlying the effects of magnetic field is not clear from experimental data. Recent studies have demonstrated that "non-neuronal" cells, especially astrocytes, may be the potential effector for transcranial magnetic stimulation (TMS). In the present study, we implemented a neural-astrocyte microcircuit computational model based on hippocampal architecture to investigate the biological effects of different magnetic field frequencies on cells. The purpose of the present study is to elucidate the main influencing factors of MS to allow a better understanding of its mechanisms. Our model reproduced the basic characteristics of the neuron and astrocyte response to different magnetic stimulation. The results predict that interneurons with lower firing thresholds were more active in magnetic fields by contrast to pyramidal neurons. And the synaptic coupling strength between the connected neurons may be one of the critical factor to affect the effect of magnetic field on cells. In addition, the simulations show that astrocytes can decrease or increase slow inward currents (SICs) to finely tune neuronal excitation, which suggests their key role in excitatory-inhibitory balance. The interaction between neurons and astrocytes may represent a novel target for effective therapeutic strategies involving magnetic stimulation.     

Uptake of magnetic nanoparticles into cells for cell tracking

A challenge for future applications in nanotechnology is the functional integration of nano-sized materials into cellular structures. Here we investigated superparamagnetic Fe₃O₄ iron oxide nanoparticles coated with a lipid bilayer for uptake into cells and for targeting subcellular compartments. It was found that magnetic nanoparticles (MNPs) are effectively taken up into cells and make cells acquire magnetic activity. Biotin-conjugated MNPs were further functionalized by binding of the fluorescent tag streptavidin–fluorescein isothiocyanate (FITC) and, following uptake into cells, shown to confer magnetic activity and fluorescence labeling. Such FITC-MNPs were localized in the lysosomal compartment of cells which suggests a receptor-mediated uptake mechanism.     

Magnetic Relaxometry with an Atomic Magnetometer and SQUID Sensors on Targeted Cancer Cells

Magnetic relaxometry methods have been shown to be very sensitive in detecting cancer cells and other targeted diseases. Superconducting Quantum Interference Device (SQUID) sensors are one of the primary sensor systems used in this methodology because of their high sensitivity with demonstrated capabilities of detecting fewer than 100,000 magnetically-labeled cancer cells. The emerging technology of atomic magnetometers (AM) represents a new detection method for magnetic relaxometry with high sensitivity and without the requirement for cryogens. We report here on a study of magnetic relaxometry using both AM and SQUID sensors to detect cancer cells that are coated with superparamagnetic nanoparticles through antibody targeting. The AM studies conform closely to SQUID sensor results in the measurement of the magnetic decay characteristics following a magnetization pulse. The AM and SQUID sensor data are well described theoretically for superparamagnetic particles bound to cells and the results can be used to determine the number of cells in a cell culture or tumor. The observed fields and magnetic moments of cancer cells are linear with the number of cells over a very large range. The AM sensor demonstrates very high sensitivity for detecting magnetically labeled cells does not require cryogenic cooling and is relatively inexpensive.     

Internal structure of magnetic endosomes

The internal structure of biological vesicles filled with magnetic nanoparticles is investigated using the following complementary analyses: electronic transmission microscopy, dynamic probing by magneto-optical birefringence and structural probing by Small Angle Neutron Scattering (SANS). These magnetic vesicles are magnetic endosomes obtained via a non-specific interaction between cells and anionic magnetic iron oxide nanoparticles. Thanks to a magnetic purification process, they are probed at two different stages of their formation within HeLa cells: (i) adsorption of nanoparticles onto the cellular membrane and (ii) their subsequent internalisation within endosomes. Differences in the microenvironment of the magnetic nanoparticles at those two different stages are highlighted here. The dynamics of magnetic nanoparticles adsorbed onto cellular membranes and confined within endosomes is respectively 3 and 5 orders of magnitude slower than for isolated magnetic nanoparticles in aqueous media. Interestingly, SANS experiments show that magnetic endosomes have an internal structure close to decorated vesicles, with magnetic nanoparticles locally decorating the endosome membrane, inside their inner-sphere. These results, important for future biomedical applications, suggest that multiple fusions of decorated vesicles are the biological processes underlying the endocytosis of that kind of nanometric materials.     

21世纪物理学和生物学交叉的热点--生物电磁学

介绍了神经科学、经络的研究、脉冲梯度磁场治疗癌症和方法论。用电镜观测脉冲梯度磁场抑制鼠Ｓ－１８０肉瘤生长和加强免疫细胞溶癌作用。文章作者观测到磁场能影响癌细胞的代谢;磁场能降低癌细胞的恶性程度,抑制其高 异形生长;磁场能抑制癌细胞的分裂和ＤＮＡ倍性;磁场能提高细胞免疫功能,加强淋巴细胞、浆细胞反应。     

Thermal Stability of Triangular Ferromagnetic Nanowire Arrays under Magnetic Field

The thermal stability of a triangular nanowire array under an external magnetic field is studied by the damage spreading technique. The results show that stability of the system may be enhanced by decreasing the spacing of magnetic cells (or increasing the storage density). The existence of an external magnetic field is another way to hinder the damage spreading.     

Discrete model of a dynamo with diffusion

A model of magnetic field generation by the turbulent motions of a highly conducting fluid is constructed. It is assumed that the field is generated in individual cells of space in a statistically independent manner. A coupling between the cells is realized by magnetic diffusion. The rates of growth of the field and its moments are calculated. The field distribution generated by this mechanism possesses an intermittent nature in both time and space.     

Microscopic calculation of the magnetic field of neutron stars

Based on the Dirac equation describing an electron moving in a uniform and cylindrically symmetric magnetic field which may be the result of the self-consistent mean field of the electrons themselves in a neutron star, we have obtained the eigen solutions and the orbital magnetic moments of electrons in which each eigen orbital can be calculated. From the eigen energy spectrum we find that the lowest energy level is the highly degenerate orbitals with the quantum numbers pZ=0, n=0, and m≥0. At the ground state, the electrons fill the lowest eigen states to form many Landau magnetic cells and each cell is a circular disk with the radius λfree and the thickness λe, where λfree is the electron mean free path determined by Coulomb cross section and electron density and λe is the electron Compton wavelength. The magnetic moment of each cell and the number of cells in the neutron star are calculated, from which the total magnetic moment and magnetic field of the neutron star can be calculated. The results are compared with the observational data and the agreement is reasonable.     

Use of a SQUID array to detect T-cells with magnetic nanoparticles in determining transplant rejection

Acute rejection in organ transplant is signaled by the proliferation of T-cells that target and kill the donor cells requiring painful biopsies to detect rejection onset. An alternative non-invasive technique is proposed using a multi-channel superconducting quantum interference device (SQUID) magnetometer to detect T-cell lymphocytes in the transplanted organ labeled with magnetic nanoparticles conjugated to antibodies specifically attached to lymphocytic ligand receptors. After a magnetic field pulse, the T-cells produce a decaying magnetic signal with a characteristic time of the order of a second. The extreme sensitivity of this technique, 10(5) cells, can provide early warning of impending transplant rejection and monitor immune-suppressive chemotherapy.     

Model for Influences of Magnetic Fields on Intracellular Calcium Oscillations

Based on the model of the two calcium stores developed by Goldbeter, the influence of external magnetic field on the calcium concentration has been discussed. We believe that the cell membrane is a major site of interaction for extremely-low-frequency (ELF) electromagnetic fields, and the permeability of ions can be changed with the changing electromagnetic fields. It is shown that magnetic field initiatesintracellular calcium oscillation with a threshold in flux density, and that the calcium oscillations do not occur if the density of magnetic field is below the threshold. The results of theoretical calculation are consistent with that of the experiment. The intracellular free calcium concentrations of different cells exposed to the same magnetic fields are different from each other. It is indicated that the different behaviors such as oscillation, rise and invariability of calcium concentration are associated with the sort of cells.     

Quadrupole magnetic field-flow fractionation: A novel technique for the characterization of magnetic nanoparticles

Quadrupole magnetic field-flow fractionation (MgFFF) is an analytical separation and characterization technique for nano- and micro-sized magnetic particles. It fractionates particles according to their content of magnetite or other magnetic material. The potential and versatility of MgFFF for separation and characterization of magnetic nanoparticles, such as those used for immunospecific labeling of biological cells for magnetic separation, is demonstrated. A broadly polydisperse sample of dextran-coated magnetite nanoparticles was eluted under programmed field decay conditions, and quantitative data concerning the distribution of magnetite content were determined from the elution profile using a data reduction method.     

Magnetic fields: a tool for the study of organic solar cells

Charge transfer in polymer devices represents a crucial, though highly inaccessible stage of photocurrent generation. In this article we propose studying the properties and behaviour of organic solar cells through the modification of photocurrent generation when an external magnetic field is applied. By allowing the parameters of our theoretical model not to be constrained to any specific material, we are able to show that not only a modest external magnetic field leads to a significant increase in photocurrent intensity, but also how such magnetic field can be used to study in detail the energy levels and transition rates within the polymer compound. Systematic exploration of key properties in organic composites thus can lead to highly optimised devices in which a magnetic field produces an enhancement in the efficiency of polymer solar cells.     

Application of magnetic poly(styrene-glycidyl methacrylate) microspheres for immunomagnetic separation of bone marrow cells

Surface-functionalized magnetic poly(styrene-glycidyl methacrylate) (PS-GMA) microspheres were prepared and coupled with Sca-1 antibody for cell selection from murine bone marrow mononuclear cells (MNCs). Biotinylated Sca-1 antibody could be directly coupled to avidin-bound magnetic microspheres. Alternatively, oxidized goat anti-mouse antibody was covalently bound onto the amino group-containing magnetic microspheres in a site-directed manner, and the resultant conjugate was coupled with non-modified Sca-1 antibody. Using the indirect antibody-bound magnetic microspheres, the purity of isolated Sca-1⁺ cells increased with bead-to-cell ratio. Using a bead-to-cell ratio of 10 beads/cell, a purity of 85% Sca-1⁺ cells corresponding to a 17-fold enrichment was achieved.     

Application of pulsed-magnetic field enhances non-viral gene delivery in primary cells from different origins

Primary cell lines are more difficult to transfect when compared to immortalized/transformed cell lines, and hence new techniques are required to enhance the transfection efficiency in these cells. We isolated and established primary cultures of synoviocytes, chondrocytes, osteoblasts, melanocytes, macrophages, lung fibroblasts, and embryonic fibroblasts. These cells differed in several properties, and hence were a good representative sample of cells that would be targeted for expression and delivery of therapeutic genes in vivo. The efficiency of gene delivery in all these cells was enhanced using polyethylenimine-coated polyMAG magnetic nanoparticles, and the rates (17–84.2%) surpassed those previously achieved using other methods, especially in cells that are difficult to transfect. The application of permanent and pulsating magnetic fields significantly enhanced the transfection efficiencies in synoviocytes, chondrocytes, osteoblasts, melanocytes and lung fibroblasts, within 5 min of exposure to these magnetic fields. This is an added advantage for future in vivo applications, where rapid gene delivery is required before systemic clearance or filtration of the gene vectors occurs.     

Combined confocal and magnetic resonance microscopy

Confocal fluorescence optical microscopy and magnetic resonance microscopy are each used to study live cells in a minimally invasive way. Both techniques provide complementary information. Therefore, by examining cells simultaneously with both methodologies, more detailed information is obtained than is possible with each microscope individually. In this paper two configurations of a combined confocal and magnetic resonance microscope are described. The first configuration is capable of studying large single cells or three-dimensional cell agglomerates, whereas the second configuration is designed for the investigation of monolayers of mammalian cells. In both cases the sample compartment is part of a temperature regulated perfusion system. Images obtained with the combined system are shown forXenopus laevis oocytes, model JB6 tumor spheroids, and a single layer of Chinese hamster ovary cells. Finally, potential applications of the combined microscope are discussed.     

Pulsed electric discharges in water as a source of magnetic nanoparticles for transportation of microorganisms

The distinguishing property of magnetic nanoparticles that determines the increasing interest in these objects is their mobility under the action of a magnetic field, which can be used for their directional transportation, deposition, and concentration in a preset region. It is shown that nanoparticles consisting of iron oxide can be used as magnetoactive agents for converting the cells of microorganisms into microaggregates for their directional transportation or concentration in liquid media under the action of a magnetic field.