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Conventional micro-particle manipulation technologies have been used for various biomedical applications using dynamics on a plane without vertical movement. In this case, irregular topographic structures on surfaces could be a factor that causes the failure of the intended control. Here, we demonstrated a novel colloidal particle manipulation mediated by the topographic effect generated by the "micro hill" and "surface gradient" around a micro-magnet. The magnetic landscape, matter orbital, created by periodically arranged circular micro-magnets, induces a symmetric orbit of magnetic particle flow under a rotating magnetic field. The topographic effect can break this symmetry of the energy distribution by controlling the distance between the source of the driving force and target particles by several nanometers on the surface morphology. The origin symmetric orbit of colloidal flow can be distorted by modifying the symmetry in the energy landscape at the switching point without changing the driving force. The enhancement of the magnetic effect of the micro-magnet array can lead to the recovery of the symmetry of the orbit. Also, this effect on the surfaces of on-chip-based devices configured by symmetry control was demonstrated for selective manipulation, trapping, recovery, and altering the direction using a time-dependent magnetic field. Hence, the developed technique could be used in various precise lab-on-a-chip applications, including where the topographic effect is required as an additional variable without affecting the existing control method.

Recently, miniaturized electrochemical biosensors have the advantage of real-time monitoring and label-free detection of biomarkers. However, controlled manipulation of reagent samples for specific immobilization of biomarkers remains a challenge to attend high-resolution microfluidic biosensor. Here, we designed a microfluidic channel and valves integrated electrochemical biosensor for the detection of β-amyloid (1–42) biomarker, one of the most neurotoxic peptides present in the cerebrospinal fluid, and a possible marker for the detection of Alzheimer's disease. The formation of the antibody-antigen complexes on gold microelectrode integrated inside the fluidic chambers was presented in the developed biosensor, and all the measurements are carefully controlled using pneumatic valves integrated with the device. The demonstrated microfluidic electrochemical biosensor exhibits a linear response towards various β-amyloid antigen concentrations from 2.2 pM to 22 μM, with an enhanced detection limit of 1.62 pM. The developed technology offers an advantage of minimal reagent sample and suitable environment for miniaturized and sensitive detection of biomarkers, could also be used for the detection of other biomarkers with high efficiency.

Herein, we have developed a novel high-resolution electrochemical biosensor for the detection of the microRNA-122 (miRNA-122) using gold nanoparticles dotted reduced graphene oxide (rGO/Au) nanocomposite. The natural soapnut solution was used as a reducing agent for the synthesis of the nanocomposite. The naturally reduced rGO/Au nanocomposite was confirmed through various characterization techniques. When rGO/Au nanocomposite was coated on to the gold electrode and checked the electrochemical performance, the nanocomposite shows superior analytical performance. The probe DNA was anchored onto the binding sites of rGO/Au nanocomposite through thiol linker and recognized the target miRNA-122. The developed rGO/Au based electrochemical biosensor demonstrated a linear response for various target miRNA-122 concentrations with a range from 10 μM to 10 pM and, with a detection limit of 1.73 pM. The developed biosensor also shows good stability and reproducibility, could be used for the detection of miRNA-122 and, also can be used for the basic research and clinical studies. Besides, the demonstrated rGO/Au nanocomposite-based sensing strategy could be used to detect various miRNA and protein biomarkers. Furthermore, the green synthesis approach could also be useful for the synthesis of various nanomaterials and nanocomposites for various biomedical applications.

We demonstrated a simple one-pot synthesis approach for the controlled composition of homogeneous FePt and phase-controlled heterostructured FePt/Fe3O4 nanocubes (NCs) utilizing 1,2-hexadecanediol and 1-octadecene as the reducing agents, respectively. When the Fe : Pt precursor ratio was varied from 1 : 1 to 4 : 1 and 1,2-hexadecanediol was utilized as the reducing agent, homogeneous FePt NCs were formed, whereas the heterostructures of FePt/Fe3O4 NCs were obtained when utilizing 1-octadecene as the reducing agent at Fe : Pt ratio of 4 : 1. The initial domination of nucleation of Pt-rich species and the subsequent deposition of Fe atoms leads to the formation of homogeneous FePt NCs. Heterostructured FePt/Fe3O4 NCs were obtained by the initial FePt seed formation, which was then followed by the heterogeneous growth of Fe3O4. The heterostructured FePt/Fe3O4 NCs exhibited two phases, i.e., FePt phase with a (111) facet of the fcc and Fe3O4 phase with an inverse cubic spinel structure. Moreover, both the FePt and the FePt/Fe3O4 NCs demonstrated almost negligible coercivity, which confirmed a typical superparamagnetic behavior. Furthermore, the cell viability tests of the FePt and FePt/Fe3O4 NCs demonstrated excellent biocompatibilities. Hence, the NCs could be useful for various biomedical applications, including MRI contrast agents, hyperthermia, and as a label in magnetic biochips.

Herein, we have reported the real-time photodegradation of methylene blue (MB), an organic pollutant, in the presence of sunlight at an ambient temperature using a platinum-decorated reduced graphene oxide (rGO/Pt) nanocomposite. The photocatalyst was prepared via a simple, one-pot and green approach with the simultaneous reduction of GO and Pt using aqueous honey as a reducing agent. Moreover, the honey not only simultaneously reduced Pt ions and GO but also played a key role in the growth and dispersion of Pt nanoparticles on the surface of rGO. Various rGO/Pt nanocomposites with different percentages of Pt nanoparticles loaded on rGO were obtained by tuning the concentration of the Pt source. The high percentage of Pt nanoparticles with an average size of 2.5 nm dispersed on rGO has shown excellent electrochemical performance. The photocatalytic activity of the rGO/Pt composite was enhanced by increasing the weight percent of the Pt particles on rGO, which led to the formation of a highly efficient photocatalyst. The optimized photocatalyst exhibited remarkable photocatalytic activity and degraded 98% MB in 180 minutes; thus, it can be used for industrial and environmental applications.

Simple Summary The development of new approaches in the field of drug delivery systems is primarily based on increasing the accuracy and precision of the targeted site and improving the stability of the drug by preventing the phagocytosis process inside the body. Among many other methods used to fulfill the above-mentioned requirements, the use of magnetotactic bacteria (MTB) is proven to be a promising solution, as it is self-propelling in nature, and can also be controlled by an external magnetic field. For the present work, we developed an MTB/PEG–biotin complex by exploiting the process of covalent bond formation between bacteria and a biotin–PEG–NHS polymer. In addition to this, attachment efficacy and stability were also determined. In biological applications, cytotoxicity assay of THP-1 cells was performed, showing the MTB/PEG–biotin complex to be less harmful to the cells; meanwhile, to explore the stealth properties of the complex, we performed a cell association assay. With these results, we provide a significant contribution to the field of potential drug delivery system development. Abstract The early removal of drug delivery agents before reaching the affected target remains an area of interest to researchers. Several magnetotactic bacteria (MTB) have been used as self-propelled drug delivery agents, and they can also be controlled by an external magnetic field. By attaching the PEG–biotin polymer, the bacteria are turned into a stealth material that can escape from the phagocytosis process and reach the area of interest with the drug load. In the study, we developed a potential drug carrier by attaching the PEG–biotin to the MTB-through-NHS crosslinker to form a MTB/PEG–biotin complex. The attachment stability, efficacy, and bacterial viability upon attachment of the PEG–biotin polymer were investigated. Biological applications were carried out using a cytotoxicity assay of THP-1 cells, and the results indicate that the MTB/PEG–biotin complex is less harmful to cell viability compared to MTB alone. Along with cytotoxicity, an assay for cell association was also evaluated to assess the complex as a potential stealth material. The development of these complexes focuses on an easy, time-saving, and stable technique of polymer attachment with the bacteria, without damaging the cell’s surface, so as to make it a strong and reliable delivery agent.

In article number 2100532, Sri Ramulu Torati, CheolGi Kim, and co‐workers develop the magnetophoretic decoupler for the disaggregation and inter‐particle distance control of magnetic bead cluster for higher efficiency of bio‐carrier role. This magnetophoretic decoupler can split the multiple bead pairs in different directions using single driving force, and linearly control the inter‐particle distance between them through the angle of the external field. [Image: see text]

Manipulating and separating single label-free cells without biomarker conjugation have attracted significant interest in the field of single-cell research, but digital circuitry control and multiplexed individual storage of single label-free cells remain a challenge. Herein, by analogy with the electrical circuitry elements and electronical holes, we develop a pseudo-diamagnetophoresis (PsD) mattertronic approach in the presence of biocompatible ferrofluids for programmable manipulation and local storage of single PsD holes and label-free cells. The PsD holes conduct along linear negative micro-magnetic patterns. Further, eclipse diode patterns similar to the electrical diode can implement directional and selective switching of different PsD holes and label-free cells based on the diode geometry. Different eclipse heights and junction gaps influence the switching efficiency of PsD holes for mattertronic circuitry manipulation and separation. Moreover, single PsD holes are stored at each potential well as in an electrical storage capacitor, preventing multiple occupancies of PsD holes in the array of individual compartments due to magnetic Coulomb-like interaction. This approach may enable the development of large programmable arrays of label-free matters with high throughput, efficiency, and reliability as multiplex cell research platforms., Here, the authors present a pseudo-diamagnetophoresis mattertronic approach for programmable manipulation of label-free cells. Immersed in biocompatible ferrofluids, single cells are moved along linear negative micromagnetic patterns, switched at eclipse diode patterns and stored in potential wells.

Herein, we have reported the real-time photodegradation of methylene blue (MB), an organic pollutant, in the presence of sunlight at an ambient temperature using a platinum-decorated reduced graphene oxide (rGO/Pt) nanocomposite. The photocatalyst was prepared

The development of environmentally benign, low-processing and low-cost approaches to the large-scale preparation of advanced nanomaterials based on the use of biological materials is currently attracting great interest. Here, we report the discovery that aqueous honey solutions reduce graphene oxide in a low-cost and an eco-friendly manner, yielding highly water dispersive functionalized reduced graphene sheets. The roles of honey in the reduction of graphene oxide of as-prepared graphene are demonstrated. The possible mechanism for the de-epoxidation of graphene oxide is elucidated. The fabricated a honey-reduced graphene oxide-based field-effect transistor exhibited ambipolar transfer characteristics, thereby demonstrating that the developed material may therefore have applications in electronic devices and sensors.

Cell clustering techniques are important to produce artificial cell clusters for in vitro models of intercellular mechanisms at the single-cell level. The analyses considering physical variables such as the shape and size of cells have been very limited. In addition, the precise manipulation of cells and control of the physical variables are still challenging. In this paper, a magnetophoretic device consisting of a trampoline micromagnet and active elements that enable the control of individual selective jumping motion and positioning of a micro-object is proposed. Based on a numerical simulation under various conditions, automatic separation or selective clustering of micro-objects according to their sizes is performed by parallel control and programmable manipulation. This method provides efficient control of the physical variables of cells and grouping of cells with the desired size and number, which can be a milestone for a better understanding of the intercellular dynamics between clustered cells at the single-cell level for future cell-on-chip applications.

A facile and cost effective chemical reduction method is employed for the preparation of reduced graphene oxide/hydroxyapatite (rGO/HAp) nanocomposites. The transmission electron microscopy images revealed that the HAp flakes are well decorated on the surface of rGO. The morphological structure of the as-synthesized rGO/HAp nanocomposites was confirmed through X-ray diffraction, Fourier transform infrared spectroscopy and Raman spectroscopy, while the composition and thermal stability were analyzed by energy dispersive spectra and thermogravimetric analysis, respectively. Furthermore, the effect of rGO/HAp nanocomposites for the proliferation of Human Mesenchymal Stem Cell (hMSC) was performed to confirm the biocompatibility. A selective chemical sensor based on rGO/HAp modified glassy carbon electrode (GCE) for sensitive detection of Bis-phenol A (BPA) has been developed. Several important parameters controlling the performance of the BPA chemi-sensor were investigated and optimized at room conditions. The rGO/HAp/Nafion/GCE sensor offers a fast response and highly sensitive BPA detection. Under the optimal conditions, a linear range from 0.2 nmol L−1 to 2.0 mmol L−1 for the detection of BPA was observed with the detection limit of 60.0 pmol L−1 (signal-to-noise ratio, at an SNR of 3) and sensitivity of 18.98 × 104 μA.L/μmol.m2. Meanwhile, the fabricated chemi-sensor showed an excellent, specific and selective recognition to target BPA molecules among coexistence of other analytes in the buffer system. This novel effort initiated a well-organized way of efficient rGO/HAp/Nafion/GCE sensor development and practically analyzed the real hazardous environmental pollutants at room conditions.

Gold nanostructures (GNs) modified electrode, which was fabricated by simple, cost–effective one–step electrochemical technique, was used for the development of an electrochemical immunosensor for the detection of CA125 antigen. The morphology of the GNs modified electrodes was easily controlled by changing the pH of the source gold electrolyte and the electrodeposition time. The GNs electrode has shown excellent electrochemical performance compared with flat bare Au electrode. Hence, the GNs electrode was used for the fabrication electrochemical immunosensor. The immobilization and sensing properties of the GNs modified bioelectrode is characterized by cyclic voltammetry, electrochemical impedance spectroscopy and differential pulse voltammetry with Fe(CN)63−/4− as an electrochemical redox indicator. The developed GNs based electrochemical immunosensor offers good response for the detection of CA125 antigen with a linear range (10–100 U mL−1), low detection limit (5.5 U mL−1). Thus, the fabricated immunosensor have potential applications as an enhance biosensing platform for biomolecules immobilization and detection.

Polyethylene glycol mediated reduced graphene oxide/zinc oxide (r-GO/ZnO) nanocomposites were synthesized by simple and cost-effective chemical reduction method using graphene oxide and zinc acetate as the precursors. The crystalline structure, morphology and thermal decomposition of the as-prepared r-GO/ZnO nanocomposites were characterized by X-ray diffraction, transmission electron microscopy and thermogravimetric analysis, respectively. Elemental composition was analyzed by energy dispersive spectra and mapping. A selective 2-nitrophenol (2-NP) sensor onto glassy carbon electrode (GCE) was fabricated with a thin-layer of synthesized r-GO/ZnO composites. Improved electrochemical responses with high sensitivity including large dynamic range and long-term stability towards the selective 2-NP were acquired using the fabricated r-GO/ZnO/GCE sensor. The calibration curve was found linear ( r 2 : 0.9916) over a wide range of 2-NP concentrations (10.0 nM–10.0 mM). The detection limit and the sensitivity were calculated as 0.27 nM and 5.8 μA·mM − 1 cm − 2 respectively based on 3 N/S (Signal-to-Noise ratio). In this approach, 2-NP was detected by I-V method using r-GO/ZnO composites modified GCE electrode with very high sensitivity compared to various nanocomposites reported earlier. The synthesis of r-GO/ZnO composites using chemical reduction process is a good way of establishing sensor based r-GO/ZnO composites for toxic and carcinogenic chemicals.

Ni1− x Fe x ( x = 0.20, 0.40, and 0.80) alloy nanoparticles (NPs) with tunable magnetization were synthesized by a simple sonofragmentation process, a facile one-step technique to produce NPs directly from bulk powders. The X-ray diffraction (XRD) patterns show the crystalline structure of the alloy samples, and the sizes of the particles are 35 nm from the Scherrer equation. Scanning electron microscopy reveals the aggregation or cluster of spherical NPs with wide size distribution from 20 to 30 nm for all compositions of Ni-Fe nanoalloys. Magnetization versus field curves exhibit superparamagnetic behavior. The saturation magnetization for the Ni0.80Fe0.20, Ni0.60Fe0.40, and Ni0.20Fe0.80 alloy NPs are 57, 66, and 105 emu g−1, respectively, increasing with Fe content. Such tunability has potential technological applications.

We synthesized three types of magnetic nanowires (Co-Ni-P, Co-Pt-P, and Co-Fe-P) by electrochemical deposition in polycarbonate membranes for use in magnetic barcodes. The nanowires were about 50 nm in diameter and 6 μm in length. The Co-Pt-P nanowires had the highest coercivity and remanence. We used finite elements to calculate the spatial distribution of the stray magnetic fields produced by the barcodes. The Co-Pt-P had the greatest spatial variation which makes it the best composition for the hard magnetic segment of barcode nanowires. These barcode nanowires may be used for magnetic multiplexing detection.

Programmable delivery of biological matter is indispensable for the massive arrays of individual objects in biochemical and biomedical applications. Although a digital manipulation of single cells has been implemented by the integrated circuits of micromagnetophoretic patterns with current wires, the complex fabrication process and multiple current operation steps restrict its practical application for biomolecule arrays. Here, a convenient approach using multifarious transit gates is proposed, for digital manipulation of biofunctionalized microrobotic particles that can pass through the local energy barriers by a time-dependent pulsed magnetic field instead of multiple current wires. The multifarious transit gates including return, delay, and resistance linear gates, as well as dividing, reversed, and rectifying T-junction gates, are investigated theoretically and experimentally for the programmable manipulation of microrobotic particles. The results demonstrate that, a suitable angle of the gating field at a suitable time zone is crucial to implement digital operations at integrated multifarious transit gates along bifurcation paths to trap microrobotic particles in specific apartments, paving the way for flexible on-chip arrays of biomolecules and cells.

We present a protein-assisted method for the facile and scalable synthesis of Cobalt sulfide (CoS) nanostructures with various morphologies using bovine serum albumin (BSA) as a stabilizing agent. The CoS samples prepared from 10:1 volume ratio of Cobalt (Co):Sulfur (S) and 1:10 volume ratio of Co:S at 0.01% w/v amount of BSA shows 3D flowers with an average diameter of 510 nm and hollow spheres about 900 nm in average diameter, respectively. The CoS samples prepared from 0.01, 0.1 and 0.5% w/v amounts of BSA at 1:1 volume ratio of Co:S shows nanosheet based porous clusters, nanosheet based partially porous clusters and aggregated spheres, respectively. Fourier transform infrared spectroscopy study confirms that the obtained BSA stabilized CoS nanostructures are stabilized by hydroxyl and amine groups present in the BSA molecules.

The manipulation of superparamagnetic beads has attracted various lab on a chip and magnetic tweezer platforms for separating, sorting, and labeling cells and bioentities, but the irreversible aggregation of beads owing to magnetic interactions has limited its actual functionality. Here, an efficient solution is developed for the disaggregation of magnetic beads and interparticle distance control with a magnetophoretic decoupler using an external rotating magnetic field. A unique magnetic potential energy distribution in the form of an asymmetric magnetic thin film around the gap is created and tuned in a controlled manner, regulated by the size ratio of the bead with a magnetic pattern. Hence, the aggregated beads are detached into single beads and transported in one direction in an array pattern. Furthermore, the simultaneous and accurate spacing control of multiple magnetic bead pairs is performed by adjusting the angle of the rotating magnetic field, which continuously changes the energy well associated with a specific shape of the magnetic patterns. This technique offers an advanced solution for the disaggregation and controlled manipulation of beads, can allow new possibilities for the enhanced functioning of lab on a chip and magnetic tweezers platforms for biological assays, intercellular interactions, and magnetic biochip systems., This study reports the real‐time disaggregation and interdistance control of the magnetic beads using magnetophoretic decoupler fabricated with permalloy thin film pattern. The application of a rotating magnetic field creates a unique magnetic potential energy distribution around the decoupler at multiple points, and thus, separates the aggregated beads and transported them on the pattern to the desired direction.

We demonstrate a separation method for complex mixture of superparamagnetic beads using half-disk pathways, under an in-plane rotating magnetic field, which is highly sensitive to the bead size and magnetic susceptibility. The non-linear dynamics of the beads moving along the half-disk pathways at multiple frequencies can be divided into three regimes: a phase-locked regime at low driving frequencies, a phase-slipping regime above the first critical frequency f c1 , and a phase-insulated regime above the second critical frequency f c2 in which the beads just hop at the gaps between two half-disks. Hence, based on the dynamical motions, the beads with varied sizes or heterogenic magnetic properties can be separated efficiently. Furthermore, a bio-selective separation of bead plus human monocytic leukemia (THP-1) cell complexes from bare beads has been achieved due to the increased drag force on the complexes, resulting in a decreased critical frequency.

Monodisperse Mn x Zn 1− x Fe 2 O 4 ( x = 0.2, 0.5 and 0.8) nanoparticles have been synthesized using two different routes namely sonochemical and polyol methods, and the shape and size along with physiochemical properties of the nanoparticles were compared in detail. In both the routes, the synthesis was performed in a single reaction without the use of any surfactant and deoxygenated conditions. The reaction kinetics and surface adsorption characteristics of nanoparticles were observed by thermogravimetric analysis and Fourier transform infrared spectroscopy measurements. X-ray diffraction patterns confirmed the formation of a pure ferrite phase with cubic spinel structure, and the patterns further clearly indicate that the sonochemical method produces highly crystalline particles without any post calcination reaction, comparing with the polyol process. Transmission electron microscopy results reveal that the nanoparticles synthesized by polyol method are mostly aggregated and spherical in nature whereas the nanoparticles produced by sonochemical method are monodisperse large particles with cubic like shapes. The overall studies demonstrated that the sonochemical method is facile, reliable, rapid and very attractive for the aqueous synthesis of highly crystalline and high magnetic moment (84.5 emu/g) monodisperse superparamagnetic Mn–Zn ferrite nanoparticles which considered as potential materials for various applications.

Sri Ramulu Torati,1 Venu Reddy,1 Seok Soo Yoon,2 CheolGi Kim1 1Department of Emerging Materials Science, Daegu Gyeongbuk Institute of Science and Technology, Daegu, South Korea; 2Department of Physics, Andong National University, Andong, South Korea Abstract: CoFe nanowires have been synthesized by the electrodeposition technique into the pores of a polycarbonate membrane with a nominal pore diameter of 50 nm, and the composition of CoFe nanowires varying by changing the source concentration of iron. The synthesized nanowire surfaces were functionalized with amine groups by treatment with aminopropyltriethoxysilane (APTES) linker, and then conjugated with streptavidin-Cy3 protein via ethyl (dimethylaminopropyl) carbodiimideand N-hydroxysuccinimide coupling chemistry. The oxide surface of CoFe nanowire is easily modified with aminopropyltriethoxysilane to form an amine terminating group, which is covalently bonded to streptavidin-Cy3 protein. The physicochemical properties of the nanowires were analyzed through different characterization techniques such as scanning electron microscope, energy dispersive spectroscopy, and vibrating sample magnetometer. Fluorescence microscopic studies and Fourier transform infrared studies confirmed the immobilization of protein on the nanowire surface. In addition, the transmission electron microscope analysis reveals the thin protein layer which is around 12–15 nm on the nanowire surfaces. Keywords: electrodeposition, biofunctionalization, streptavidin

Recent years have seen an increasing range of planar Hall resistive (PHR) sensor applications in the field of magnetic sensing. This study describes a new application of the PHR sensor to monitor a current. Initially, thermal drift experiments of the PHR sensor are performed, to determine the accuracy of the PHR signal output. The results of the thermal drift experiments show that there is no considerable drift in the signals attained from 0.1, 0.5, 1 and 2 mA current. Consequently, the PHR sensor provides adequate accuracy of the signal output, to perform the current monitoring experiments. The performances of the PHR sensor with bilayer and trilayer structures are then tested. The minimum detectable currents of the PHR sensor using bilayer and trilayer structures are 0.51 µA and 54 nA, respectively. Therefore, the PHR sensor having trilayer structure is the better choice to detect ultra low current of few tens nanoampere.

This erratum corrects scanning electron microscopy images and a magnetization curve that appeared in an article by the authors.

We investigate the non-linear dynamics of bio-functionalized beads moving around the periphery of patterned magnetic disks in the presence of an in-plane rotating magnetic field.

The manipulation ability of individual cells has significant applications for gene sequencing, protein and bio-content analysis in single cell level for their heterogeneity related with drug resistance aiming to lab-on-organ and new drug development. Even though, various single cell platforms are exit, it is still challenge and complex to collect rare cells and their digital manipulation in large-scale operation. In recent years the flexibility of magnetic transport technology using nano/micro scale magnets for the digital magnetophoresis has experienced tremendous advances and has been used for a wide variety of single cells manipulation tasks such as selection, capture, transport, encapsulation, transfection, or lysing of magnetically labeled and un-labeled cells. The magnetic transport technology, which can be integrated within microfluidic channels, relies on both magnetic energy and force tunability and remote control implemented by micro-and nano-patterned magnetic structures. Here, we demonstrate a class of integrated magnetic track circuits for executing sequential and parallel, timed operations on an ensemble of single particles and cells. The magnetic circuitry tracks are designed by conventional lift-off technology and were used for the passive control of cells/particles similar concept to electrical conductor, diodes and capacitor. When the magnetic tracks are combined into arrays and driven by rotating magnetic field, the single cells are precisely control for multiplexed analysis. In addition, the concentric cell translocation and separation were performed by the assembly of this magnetic track into a novel architecture, resembled with spider web network, where all the cells are concentrated into one position and then transported to apartments array for the single cell analysis.

A novel method based on remotely controlled magnetic forces of bio-functionalized superparamagnetic colloids using micromagnet arrays was devised to measure frictional force at the sub-picoNewton (pN) scale for bio-nano-/micro-electromechanical system (bio-NEMS/MEMS) interfaces in liquid. The circumferential motion of the colloids with phase-locked angles around the periphery of the micromagnets under an in-plane rotating magnetic field was governed by a balance between tangential magnetic force and drag force, which consists of viscous and frictional forces. A model correlating the phase-locked angles of the steady colloid rotation was formulated and validated by measuring the angles under controlled magnetic forces. Hence, the frictional forces on the streptavidin/Teflon interface between the colloids and the micromagnet arrays were obtained using the magnetic forces at the phase-locked angles. The friction coefficient for the streptavidin/Teflon interface was estimated to be approximately 0.036 regardless of both vertical force in the range of a few hundred pN and velocity in the range of a few tenths of μm s(-1).

The precise delivery of biofunctionalized matters is of great interest from the fundamental and applied viewpoints. In spite of significant progress achieved during the last decade, a parallel and automated isolation and manipulation of rare analyte, and their simultaneous on-chip separation and trapping, still remain challenging. Here, a universal micromagnet junction for self-navigating gates of microrobotic particles to deliver the biomolecules to specific sites using a remote magnetic field is described. In the proposed concept, the nonmagnetic gap between the lithographically defined donor and acceptor micromagnets creates a crucial energy barrier to restrict particle gating. It is shown that by carefully designing the geometry of the junctions, it becomes possible to deliver multiple protein-functionalized carriers in high resolution, as well as MCF-7 and THP-1 cells from the mixture, with high fidelity and trap them in individual apartments. Integration of such junctions with magnetophoretic circuitry elements could lead to novel platforms without retrieving for the synchronous digital manipulation of particles/biomolecules in microfluidic multiplex arrays for next-generation biochips.

The template assisted electrochemical deposition technique was used for the synthesis of gold nanotubes array (AuNTsA). The morphological structure of the synthesized AuNTsA was observed by scanning electron microscopy and found that the individual nanotubes are around 1.5 μm in length with a diameter of 200 nm. Nanotubes are vertically aligned to the Au thick film, which is formed during the synthesis process of nanotubes. The electrochemical performance of the AuNTsA was compared with the bare Au electrode and found that AuNTsA has better electron transfer surface than bare Au electrode which is due to the high surface area. Hence, the AuNTsA was used as an electrode for the fabrication of DNA hybridization biosensor for detection of Mycobacterium Tuberculosis DNA. The DNA hybridization biosensor constructed by AuNTsA electrode was characterized by cyclic voltammetry technique with Fe(CN)63−/4− as an electrochemical redox indicator. The selectivity of the fabricated biosensor was illustrated by hybridization with complementary DNA and non-complementary DNA with probe DNA immobilized AuNTsA electrode using methylene blue as a hybridization indicator. The developed electrochemical DNA biosensor shows good linear range of complementary DNA concentration from 0.01 ng/μL to 100 ng/μL with high detection limit.

A novel sonochemical approach was developed for the synthesis of different core/shell structures of Fe3O4/SiO2/Ag nanocubes and SiO2/Ag nanospheres. The total reaction time of the three sonochemical steps for the synthesis of Fe3O4/SiO2/Ag nanocubes is shorter than that of the previously reported methods. A proposed reaction mechanism for the sonochemical functionalization of the silica and the silver on the surface of magnetic nanocubes was discussed in detail. Transmission electron microscopy revealed that the surface of Fe3O4/SiO2 nanocubes was decorated with small Ag nanoparticles of approximately 10–20 nm in size, and the energy dispersive spectroscopy mapping analysis confirmed the morphology of the structure. Additionally, X-ray diffraction data were used to confirm the formation of both phases of a cubic inverse spinel structure for Fe3O4 and bcc structures for Ag in the core/shell structure of the Fe3O4/SiO2/Ag nanocubes. The as-synthesized Fe3O4/SiO2/Ag nanocubes showed a high efficiency in the catalytic reduction reaction of 4-nitroaniline to 4-phenylenediamine and a better performance than both Ag and SiO2/Ag nanoparticles. The grafted silver catalyst was recycled and reused at least fifteen times without a significant loss of catalytic efficiency.

A lab-on-a-chip (LOC) magnetophoretic system for the remotely controllable transport of magnetic particles actuated by thin permalloy magnetic tracks has been developed as a novel architecture composed of radii and spiral tracks resembling a spider web network, where the network tracks have the asymmetric and anisotropic magnetic properties for the directional transportation of particles (cargos). A planar Hall resistance (PHR) sensor is integrated with the web networks, and the manipulation and detection are achieved via superparamagnetic particles with dual functions as a biomolecule cargo for transportation and labels for monitoring. The streptavidin protein-coated magnetic particles are precisely manipulated toward the PHR sensor surface via the radii and spiral tracks by applying an external rotating magnetic field. The stray field was analyzed in terms of the particle coverage on the sensor surface, where the sensor signal linearly varies with the number of particles on the sensor surface. This allows the effective collection of low-density biomolecule carriers to one specific point and monitors the accumulated carriers. The developed novel technology could affect multiple fields, including bioassays, cell manipulation and separation and biomechanics. Arranging linear and spiral-shaped magnetic tracks in a web-like network enables simultaneous monitoring and manipulation of biomolecules. As lab-on-a-chip devices get increasingly smaller, it is becoming more difficult to move tiny liquid droplets in them. CheolGi Kim of the Daegu Gyeongbuk Institute of Science and Technology in South Korea and co-workers has developed a way to precisely transport proteins and label them for biosensing. They used streptavidin proteins coated superparamagnetic carriers and then manipulated them on a magnetic surface that resembled a microscale spider web, consisting of concentric tracks centred on a central magnetoresistive sensor. Applying an external rotating magnetic field enabled on-demand movement of the particles towards the sensor, where they were quantified. This could enhance the sensitivity of biosensing schemes by collecting biomolecules, even when they are present in low densities. Novel magnetophoretic device resembling a spider web network, being integrated with planar Hall resistance sensor, has been developed for the simultaneous concentric transportation and monitoring of superparamagnetic streptavidin-loaded cargos (particles). The multilayer sensor and permalloy network tracks have been fabricated by successive micropatterning processes of film deposition and photolithography. The transporting particles are precisely manipulated on the magnetic tracks towards the sensor by an external magnetic field, where the sensor signal varies with the accumulated particle number. This effective collection and monitoring platform could open novel bioassays overcoming limitation of Brownian transportation of biomolecules to the sensor surface.

An on-chip magnetometer was fabricated by integrating a planar Hall magnetoresistive (PHR) sensor with microfluidic channels. The measured in-plane field sensitivities of an integrated PHR sensor with NiFe/Cu/IrMn trilayer structure were extremely high at 8.5 μV Oe(-1). The PHR signals were monitored during the oscillation of 35 pL droplets of magnetic nanoparticles, and reversed profiles for the positive and negative z-fields were measured, where magnitudes increased with the applied z-field strength. The measured PHR signals for 35 pL droplets of magnetic nanoparticles versus applied z-fields showed excellent agreement with magnetization curves measured by a vibrating sample magnetometer (VSM) of 3 μL volume, where a PHR voltage of 1 μV change is equivalent to 0.309 emu cc(-1) of the volume magnetization with a magnetic moment resolution of ~10(-10) emu.