Synthesis of magnetic nanoparticles for analytical applications

A simple method based on magnetically assisted chemical separation has been developed for analytical purposes. In this method, morin-modified magnetic nanoparticles were used for the selective extraction and preconcentration of copper ions from aqueous solutions. The influence of different parameters, such as the presence of the morin extractant, the amount of morin extractant loaded on the nanoparticles, the pH, adsorption time and the type and minimum amount of eluent required for elution of the copper from the magnetic nanoparticles, were evaluated. The detection limit of the proposed method followed by ICP–OES was found to be 1.3 µg L^?1 and a dynamic linear range of 10–200 µg L^?1 was obtained. The relative standard deviation was less than 5%. The method was applied to the recovery and determination of copper in real samples.     

Microchip integrating magnetic nanoparticles for allergy diagnosis

We report on the development of a simple and easy to use microchip dedicated to allergy diagnosis. This microchip combines both the advantages of homogeneous immunoassays i.e. species diffusion and heterogeneous immunoassays i.e. easy separation and preconcentration steps. In vitro allergy diagnosis is based on specific Immunoglobulin E (IgE) quantitation, in that way we have developed and integrated magnetic core-shell nanoparticles (MCSNPs) as an IgE capture nanoplatform in a microdevice taking benefit from both their magnetic and colloidal properties. Integrating such immunosupport allows to perform the target analyte (IgE) capture in the colloidal phase thus increasing the analyte capture kinetics since both immunological partners are diffusing during the immune reaction. This colloidal approach improves 1000 times the analyte capture kinetics compared to conventional methods. Moreover, based on the MCSNPs' magnetic properties and on the magnetic chamber we have previously developed the MCSNPs and therefore the target can be confined and preconcentrated within the microdevice prior to the detection step. The MCSNPs preconcentration factor achieved was about 35,000 and allows to reach high sensitivity thus avoiding catalytic amplification during the detection step. The developed microchip offers many advantages: the analytical procedure was fully integrated on-chip, analyses were performed in short assay time (20 min), the sample and reagents consumption was reduced to few microlitres (5 μL) while a low limit of detection can be achieved (about 1 ng mL(-1)).     

Synthesis and characterization of magnetic nanoparticles

Magnetic nanoparticles with average diameter in the range of 6.4-8.3 nni have been synthesized by a chemical co-precipitation of Fe(Ⅱ)and Fe(Ⅲ)salts in 1.5 M NH4OH solution.The size of the magnetic particles is dependent on both temperature and the ionic strength of the iron ion solutions.The magnetic particles formed at higher temperature or lower ionic strength were slightly larger than those formed at lower temperature or higher ionic strength respectively.In spite of the different reaction conditions,all the resultant nanoparticles are nearly spherical and have a similar crystalline structure.At 300 K,such prepared nanoparticles are superparam-agnetic.The saturation magnetizations for 7.8 and 6.4 nm particles are 71 and 63 emu/g respectively,which are only ~ 20-30% less than the saturation magnetization(90 emu/g)of bulk Fe3O4 Our results indicated that a control of the reaction conditions could be used to tailor the size of magnetic nanoparticles in free precipitation.     

Synthesis of trisaccharide-coated magnetic nanoparticles for antibody removal

An efficient strategy for the synthesis of blood group A trisaccharide antigen has been developed. Magnetic nanoparticles having Fe₃O₄-Silica core-shell structure were prepared and functionalized with the prepared blood group A trisaccharide antigen derivative, and its excellent removal ability toward anti-A antibody was explored.     

Synthesis of magnetic nanoparticles and their application to bioassays

Magnetic nanoparticles have been attracting much interest as a labeling material in the fields of advanced biological and medical applications such as drug delivery, magnetic resonance imaging, and array-based assaying. In this review, synthesis of iron oxide magnetic nanoparticles via a reverse micelle system and modification of their surface by an organosilane agent are discussed. Furthermore, as a practical biological assay system, the magnetic detection of biomolecular interactions is demonstrated by using the combination of a patterned substrate modified with a self-assembled monolayer and the magnetic nanoparticles.     

Synthesis of hollow magnetic and luminescent bifunctional composite nanoparticles

Composite nanoparticles consisted of Au-coating Co superparamagnetic cores and CdSe shells have been synthesized. In-situ reduction and cation exchange methods have been applied in the synthetic process. The composite nanoparticles have been characterized by various methods. Experimental results showed that the oxidation of cobalt nanoparticles might be restrained by a gold shell. The as-prepared nanoconjugates exhibited magnetic and luminescent properties. The bifunctional nanoparticles can be used as detecting agent to analyze tumor cell in vitro and in vivo. We believe that the results could be used as a reference by researchers engaged in both fundamental and applied biomedicine.     

Synthesis and electrochemical investigation of spinel cobalt ferrite magnetic nanoparticles for supercapacitor application

Cobalt ferrite magnetic nanoparticles (CoFe₂O₄-MNPs) were synthesized by hydrothermal and co-precipitation methods using different precursors such as nitrates, chlorides, and acetates, at different concentrations with/without surfactant under different growth conditions. The structural and morphological analyses reveal the formation of a single-phase CoFe₂O₄ in nanoplatelet-shaped NPs with average particle size between 11 and 26 nm depending on synthesis condition. The specific surface area of these NPs obtained by hydrothermal method was ~ 34 m² g^?1. Electrochemical performances of the obtained nanoparticles in a three-electrode configuration with a 6 M KOH electrolyte revealed a specific capacitance (C _s) of 429 F/g at 0.5 A/g, with excellent capacitance retention of 98.8% after 6000 cycles at 10 A/g for the electro-active NPs synthesized by hydrothermal method at 200 °C for 18 h.     

Synthesis and characterization of pore size-tunable magnetic mesoporous silica nanoparticles

Magnetic mesoporous silica nanoparticles (M-MSNs) are emerging as one of the most appealing candidates for theranostic carriers. Herein, a simple synthesis method of M-MSNs with a single Fe(3)O(4) nanocrystal core and a mesoporous shell with radially aligned pores was elaborated using tetraethyl orthosilicate (TEOS) as silica source, cationic surfactant CTAB as template, and 1,3,5-triisopropylbenzene (TMB)/decane as pore swelling agents. Due to the special localization of TMB during the synthesis process, the pore size was increased with added TMB amount within a limited range, while further employment of TMB lead to severe particle coalescence and not well-developed pore structure. On the other hand, when a proper amount of decane was jointly incorporated with limited amounts of TMB, effective pore expansion of M-MSNs similar to that of analogous mesoporous silica nanoparticles was realized. The resultant M-MSN materials possessed smaller particle size (about 40-70 nm in diameter), tunable pore sizes (3.8-6.1 nm), high surface areas (700-1100 m(2)/g), and large pore volumes (0.44-1.54 cm(3)/g). We also demonstrate their high potential in conventional DNA loading. Maximum loading capacity of salmon sperm DNA (375 mg/g) was obtained by the use of the M-MSN sample with the largest pore size of 6.1 nm.     

Endosome-escapable magnetic poly(amino acid) nanoparticles for cancer diagnosis and therapy

Endosome-escapable poly(amino acid) nanoparticles composed of iron oxide nanocrystals and anticancer drugs were prepared and demonstrated high T(2) relaxivity coefficients and higher efficacy attributed to the endosomolytic ability of the conjugated histidine moiety.     

Synthesis of cyano-bridged magnetic nanoparticles using room-temperature ionic liquids

A principally new exploit of ionic liquids as an alternative reaction medium in the synthesis of cyano-bridged coordination-polymer nanoparticles is reported. Stable colloid solutions containing nanoparticles of cyano-bridged molecule-based magnets, M)[Fe(CN)6]2/[RMIM][BF4] (M2+=Ni, Cu, Co) and Fe4[Fe(CN)6]3/[RMIM][BF4] (R=1-butyl (BMIM), 1-decyl (DMIM)), were prepared in the corresponding 1-R-3-methylimidazolium tetrafluoroborate [RMIM][BF4], which acts as both a stabilising agent and a solvent. By varying the length of the N-alkyl chain on the imidazolium cation of [RMIM]+ and the temperature, the growing process can be controlled to produce nanoparticles of different sizes. By studying the magnetic properties of frozen colloids it is shown that the relaxation of magnetisation is strongly influenced by interparticle interactions, which leads to the appearance of spin-glass-like dynamics in these systems.     

水溶性CoFe2O4磁性纳米粒子的制备和磁性研究

采用溶剂热法,分别以FeCl3· 6H2O和CoCl2·4H20为铁源和钴源,二甘醇和二乙醇胺为溶剂和配位剂,制备了水溶性CoFe2O4纳米粒子.采用TEM、XRD、FTIR光谱、热重-差热分析等技术对所得纳米粒子进行表征,并研究了材料的磁学性质.结果表明,这种铁酸钴纳米粒子具有超顺磁性,饱和磁化强度M.达53.2em...     

Synthesis,functionalization, and nanomedical applications of functional magnetic nanoparticles

This review summarizes the current synthesis of magnetic nanoparticles (MNPs) preparation, functionalization and stabilization methods. And furthermore it highlights some actual case analyses of these MNPs for disease therapy, drug delivery, hyperthermia, bioseparation and bioimaging applications.     

Advances of nanoparticles as drug delivery systems for disease diagnosis and treatment

Decades have passed since the first nanoparticles-base medicine was approved for human cancer treatment, and the research and development of nanoparticles for drug delivery are always undergoing. Nowadays, the significant advances complicate nanoparticles’ branches, including liposomes, solid lipid nanoparticles, inorganic nanoparticles, micelles, nanovaccines and nano-antibodies, etc. These nanoparticles show numerous capabilities in treatment and diagnosis of stubborn diseases like cancer and neurodegenerative diseases, emerging as novel drug carriers or therapeutic agents in future. In this review, the complicated branches of nanoparticles are classified and summarized, with their property and functions concluded. Besides, there are also some delivery strategies that make nanoparticles smarter and more efficient in drug delivery, and frontiers in these strategies are also summarized in this review. Except these excellent works in newly-produced drug delivery nanoparticles, some points of view and future expectations are made in the end.     

Synthesis,textural and magnetic properties of doped and undoped CuO nanoparticles

We have fabricated undoped CuO, Co_0.1Ni_0.07Zn_0.04Cu_0.79O and Co_0.08Ni_0.07Zn_0.04Mg_0.03Cu_0.78O nanoparticles through thermal decomposition of their respective inorganic copper creatinate hydrazinate and mixed metal doped copper creatinate hydrazinate precursors which were prepared by the co-precipitation method and characterized through EDS, ICP-AES, IR, and TG-DTA analysis. Techniques such as EDS, ICP-AES, FT-IR, XRD, XPS, TEM, SEM, BET, and VSM analysis were employed to characterize the composition, structural phase, chemical state, morphological, textural, and magnetic properties of the nanoparticles.     

Synthesis and surface treatment of magnetite nanoparticles for tuning hydrophobicity and colloidal stability

Post-synthetic surface modification of magnetite nanoparticles synthesized by a modified co-precipitation process was carried out with triethoxy-terminated perfluoropolyether (PFPE) oligomers. The chemisorption of PFPE oligomers on the surface of magnetites was confirmed by ATR-FTIR and TGA analyses. The efficiency of surface modification of the oligomer to prevent the aggregation of magnetite nanoparticles was studied with the dynamic light scattering technique by measuring the hydrodynamic diameter and polydispersity index of the surface treated nanoparticles, together with their zeta potential. Aggregation kinetics profiles were constructed for surface treated nanoparticles. The obtained data was compared with magnetite nanoparticles treated with critic acid, to assess the efficiency of the surface modification with the PFPE oligomers. The comparison showed that the bifunctional PFPE oligomer treated nanoparticles are characterized by improved colloidal stability and hydrophobicity.     

Synthesis,magnetic and ethanol gas sensing properties of semiconducting magnetite nanoparticles

The superparamagnetic magnetite (Fe₃O₄) nanoparticles with an average size of 7 nm were synthesized using a rapid and facile microwave hydrothermal technique. The structure of the magnetite nanoparticles was characterized by X-ray diffraction (X-ray), field effect scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS), and transmission electron microscopy (TEM). The prepared Fe₃O₄ was shown to have a cubic phase of pure magnetite. Magnetization hysteresis loop shows that the synthesized magnetite exhibits no hysteretic features with a superparamagnetic behavior. The ethanol gas sensing properties of the synthesized magnetite were investigated, and it was found that the responsibility time is less than 10 s with good reproducibility for ethanol sensor. Accordingly, it is evaluated that the magnetite nanoparticles can be effectively used as a solid state ethanol sensor in industrial commercial product applications.     

Synthesis of adenosine functionalized metal immobilized magnetic nanoparticles for highly selective and sensitive enrichment of phosphopeptides

A new type of IMAC material, with ATP as the chelating ligand, was synthesized and applied to capture phosphopeptides. For the first time, the approach for phosphopeptide enrichment could provide selectivity under 5000-fold dilution by nonphosphopeptides, and sensitivity of on-target enrichment at 3 amol.     

Synthesis of one-dimensional magnetic Co nanoparticles in a novel solution system

Magnetic Co nanoparticles with different morphologies were synthesized in a novel solution system using a UV irradiation technique. By adjusting the compositions in the solution, long nanowires with different aspect ratios as well as spherical nanoparticles with controllable particle size could be obtained.     

Synthesis of polymer-stabilized magnetic nanoparticles and fabrication of nanocomposite fibers thereof using electrospinning

Polymer-stabilized magnetic nanoparticles were obtained using two biocompatible polyelectrolytes: N-carboxyethylchitosan (CECh) and poly(2-acrylamido-2-methylpropanesulfonic acid) (PAMPS). The size of the particles (mean diameter 10 or 30 nm, respectively) and the stability of the dispersions could be effectively controlled depending on the polyelectrolyte nature. The presence of polyelectrolyte shell was proved by transmission electron microscopy (TEM) studies and confirmed by thermogravimetric analyses. Depending on the polyelectrolyte nature the magnetic nanoparticles existed in different magnetic states - superparamagnetic or intermediate state between superparamagnetic and ferrimagnetic one, as evidenced by the measurements of the magnetization and Mössbauer analyses. Fabrication of nanocomposite magnetic fibers with mean diameter in the range 100-500 nm was achieved using electrospinning of the system CECh/ferrofluid/non-ionogenic polymer.