Application of magnetic iron oxide nanoparticles prepared from microemulsions for protein purification

BACKGROUND: Magnetic nanoparticles are of immense interest for their applications in biotechnology. This paper reports the synthesis of magnetic iron oxide nanoparticles from two different water‐in‐oil microemulsion systems (ME‐MIONs), their characterization and also their use in purification of coagulant protein. RESULTS: ME‐MIONs have demonstrated to be an efficient binder in the purification of Moringa oleifera protein when compared with the superparamagnetic iron oxide nanoparticles prepared from coprecipitation in aqueous media. The size and morphology of the ME‐MIONs were studied by transmission electron microscopy (TEM) while the structural characteristics were studied by X‐ray diffraction (XRD). The microemulsion magnetic iron oxide nanoparticles (ME 1‐MION and ME 2‐MION) obtained have a size range 7–10 nm. The protein and ME‐MIONs interaction was investigated by Fourier transform infrared spectroscopy (FT‐IR); the presence of three peaks at 2970, 2910 and 2870 cm^?1 respectively, confirms the binding of the protein. The purification and molecular weight of the coagulant protein was 6.5 kDa as analyzed by SDS‐PAGE. CONCLUSION: The ME‐MIONs have the advantage of being easily tailored in size, are highly efficient as well as magnetic, cost effective and versatile; they are, thus, very suitable for use in a novel purification technique for protein or biomolecules that possess similar characteristics to the Moringa oleifera coagulant protein. Copyright © 2011 Society of Chemical Industry     

Controlled release of protein from magnetite–chitosan nanoparticles exposed to an alternating magnetic field

In this research, the controlled release of proteins from magnetite (Fe₃O₄)–chitosan (CS) nanoparticles exposed to an alternating magnetic field is reported. Fe₃O₄–CS nanoparticles were synthesized with sodium tripolyphosphate (TPP) molecules as a crosslinking reagent. Bovine serum albumin (BSA) was used as a model protein, and its controlled release studied through the variation of the frequency of an alternating magnetic field. The results show the successful coating of CS and BSA on the Fe₃O₄ nanoparticles with an average diameter of 50 nm. Intermolecular interactions of TPP with CS and BSA were confirmed by Fourier transform infrared spectroscopy. The application of low‐frequency alternating magnetic fields to such magnetic CS nanoparticles enhanced the protein release properties, in which the external magnetic fields could switch on the unloading of these nanoparticles. We concluded that enhanced BSA release from nanoparticles exposed to an alternating magnetic field is a promising method for achieving both the targeted delivery and controlled release of proteins. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43335.     

Controlled aggregation of amphiphilic aggregation-induced emission polycation and superparamagnetic iron oxide nanoparticles as fluorescence/magnetic resonance imaging probes

Fluorescence/magnetic resonance (MR) dual-mode imaging, which combines the excellent single-cell sensitivity of fluorescence imaging and the high spatial resolution of MR imaging, has been applied to different biomedical applications. However, the aggregation-caused quenching characteristic of most fluorescence molecules often put limits in their applications. Herein, a fluorescence/MR dual-mode imaging probe [polyethylene glycol-polyethylenimine-tetraphenylethene (PEG-PEI-TPE)/superparamagnetic iron oxide (SPIO)] with aggregation-induced emission characteristic is prepared by coupling poly(acrylic acid)-coated SPIO with PEG-PEI-TPE. The fluorescence intensity and lifetime of PEG-PEI-TPE/SPIO is higher than PEG-PEI-TPE especially at lower polymer concentrations (≤0.2 mg mL⁻¹). Moreover, the fluorescence intensity of PEG-PEI-TPE/SPIO gradually increased along with the decline of the pH from 9.0 to 4.0, which is beneficial for studying intracellular organelles. The T₂ relaxivity of PEG-PEI-TPE/SPIO is 212.3 Fe mM⁻¹ s⁻¹ under a 3.0 T MR scanner. Cell labeling experiment shows that PEG-PEI-TPE/SPIO can effectively label RAW 264.7 and Hela cells, and labeled cells are visible under both fluorescence and clinical MR examinations. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48760.     

两种表面活性剂在制备纳米氧化铁过程的影响研究

以Fe Cl3和尿素为原料,分别以十二烷基磺酸钠和亚油酸钠为分散剂,采用均匀沉淀法制备纳米Fe2O3,研究了两种表面活性剂在制备纳米Fe2O3过程的影响。用XRD、FESEM对纳米氧化铁的晶体结构、晶粒度和形貌进行表征。用红外光谱仪对前驱物氢氧化铁与表面活性剂的作用进行表征。结果表明亚油酸根与Fe3+存在化学键合作用,能够有效改进制备过程中一次粒子易团聚成大颗粒的问题,制得的Fe2O3为α-Fe2O3,呈球形、晶粒度25.2nm且分散性好;十二烷基磺酸钠与Fe3+不存在化学键合作用,制得的Fe2O3晶粒度65.7nm且分散性差。     

Graphene oxide impregnated with iron oxide nanoparticles for the removal of atrazine from the aqueous medium

ABSTRACT

The present study proposes development of an adsorbent based on combination of graphene oxide (GO) and iron oxide (α-γ-Fe₂O₃) nanoparticles for atrazine removal from water. The synthesized adsorbent (GO@ α-γ-Fe₂O₃) was characterized using different techniques. Magnetic measurements proved that the adsorbent has superparamagnetic characteristics, thus facilitating its magnetic separation from the working suspensions. The maximum adsorption capacity was 42.5 mg g^?1. The Langmuir isotherm and the pseudo-second order kinetic models correlated adequately with the experimental data. The thermodynamic data showed that atrazine adsorption was spontaneous, endothermic and thermodynamically favorable.     

Enhanced hydrophilic polysulfone hollow fiber membranes with addition of iron oxide nanoparticles

Membranes are at the heart of hemodialysis treatment functions to remove excess metabolic waste such as urea. However, membranes made up of pure polymers and hydrophilic polymers such as polyvinylpyrrolidone suffer problems of low flux and bio‐incompatibility. Hence, this study aimed to improve polysulfone (PSf ) membrane surface properties by the addition of iron oxide nanoparticles (IONPs ). The membrane surface properties and separation performance of neat PSf membrane and membrane filled with IONPs at a loading of 0.2 wt% were investigated and compared. The membranes were characterized in terms of morphology, pure water permeability (PWP ) and protein rejection using bovine serum albumin (BSA ). A decrease in contact angle value from 66.62° to 46.23° for the PSf /IONPs membrane indicated an increase in surface hydrophilicity that caused positive effects on the PWP and BSA rejection of the membrane. The PWP increased by 40.74% to 57.04 L m^?2 h^?1 bar^?1 when IONPs were incorporated due to the improved interaction with water molecules. Furthermore, the PSf /IONPs membrane rejected 96.43% of BSA as compared to only 91.14% by the neat PSf membrane. Hence, the incorporation of IONPs enhanced the PSf hollow fiber membrane hydrophilicity and consequently improved the separation performance of the membrane for hemodialysis application. © 2017 Society of Chemical Industry     

复印墨粉用四氧化三铁的制备

主要研究了在碱性条件下，由经过处理的工业级硫酸亚铁和氢氧化钠通过氧化沉淀的方法，制备适合复印墨粉用高档四氧化三铁磁粉。介绍了硫酸亚铁和氢氧化钠的反应原理、工艺流程以及不同的m（Fe）／m（NaOH）、加料方式、反应体系的pH、鼓气量、鼓气时间、以及分散剂对产品性能的影响。制备的四氧化三铁磁粉纯度高，颗粒大小均匀，磁性能好，价格低廉，能够满足国内复印机市场需求。     

pH‐Responsive PEGylated nanoparticles based on amphiphilic polyaspartamide: preparation,physicochemical characterization and in vitro evaluation

A series of amphiphilic graft copolymers based on polyaspartamide were synthesized by successive aminolysis reactions of polysuccinimide using 2‐diisopropylaminoethyl (DIP), O‐(2‐aminoethyl)‐O′‐methylpolyethylene glycol (PEG) and lauryl amine as pH‐sensitive, hydrophilic and hydrophobic groups, respectively. The pH‐dependent self‐assembly behavior of the aqueous copolymer solution was investigated. Nano‐aggregation, which was induced by a hydrophilic/hydrophobic shift of the DIP group in solution, occurred at a pH in the vicinity of the pK_a of the DIP group. The mean diameter of the nano‐aggregate could be modulated by changing the compositions of both pendants. The mean diameter of the nanoparticles increased with increasing solution pH from 6.5 to 8. The dissolution of paclitaxel into these amphiphilic nanoparticles was attempted and the pH‐dependent release behavior was examined using a solvent‐casting method. The results showed a significantly faster release of paclitaxel at pH = 6.5, which is a tumoral acidic pH, than at neutral physiological pH. These pH‐sensitive PEGylated polyaspartamide derivatives have potential use as a tumor‐targeting delivery system.     

BSA修饰Fe_3O_4纳米颗粒用于苦瓜提取液中活性成分的筛选

用一步法直接合成了表面氨基化修饰的Fe3O4纳米颗粒(NH2-MION),通过双功能团试剂戊二醛将牛血清白蛋白(BSA)固定在NH2-MION表面,将BSA-MION用于苦瓜提取液中活性成分的筛选,利用气相色谱-质谱联用技术鉴定出了3种与BSA作用较强的活性成分。     

Fabrication and characterization of zinc oxide nanoparticle coated magnetic iron oxide: Effect of S-layers adsorption on surface of oxide

Mixed zinc oxide nanoparticle coated magnetic iron oxide has been prepared by a sol–gel and co-precipitation routes. Magnetic iron oxide nanoparticles were synthesized by co-precipitation of ferric and ferrous ions with ammonia, and then zinc oxide was coated onto the surface of magnetic iron oxide by hydrolysis of zinc precursors. As a result, zinc oxide coated magnetic iron oxide nanoparticles with an average size of 68 nm were obtained. The crystalline bacterial cell surface layer)S-layer (used in this study was isolated from Lactobacillus helveticus ATCC 12046. The S-layer was adsorbed onto the surface of zinc oxide nanoparticle coated magnetic iron oxide. The nanoparticles were analyzed by X-ray powder diffractometry (XRD), infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and field emission scanning electron microscopy (FESEM) were used to characterize the structural and the chemical features of the nanocomposites. The infrared spectra indicate that the S-layer-nanoparticle interaction occurs. This novel nanoparticle showed admirable potential in adsorption of S-layers on the surface of oxides for drug delivery.     

The cytotoxicity evaluation of magnetic iron oxide nanoparticles on human aortic endothelial cells

One major obstacle for successful application of nanoparticles in medicine is its potential nanotoxicity on the environment and human health. In this study, we evaluated the cytotoxicity effect of dimercaptosuccinic acid-coated iron oxide (DMSA-Fe₂O₃) using cultured human aortic endothelial cells (HAECs). Our results showed that DMSA-Fe₂O₃ in the culture medium could be absorbed into HAECs, and dispersed in the cytoplasm. The cytotoxicity effect of DMSA-Fe₂O₃ on HAECs was dose-dependent, and the concentrations no more than 0.02 mg/ml had little toxic effect which were revealed by tetrazolium dye assay. Meanwhile, the cell injury biomarker, lactate dehydrogenase, was not significantly higher than that from control cells (without DMSA-Fe₂O₃). However, the endocrine function for endothelin-1 and prostacyclin I-2, as well as the urea transporter function, was altered even without obvious evidence of cell injury in this context. We also showed by real-time PCR analysis that DMSA-Fe₂O₃ exposure resulted in differential effects on the expressions of pro- and anti-apoptosis genes of HAECs. Meanwhile, it was noted that DMSA-Fe₂O₃ exposure could activate the expression of genes related to oxidative stress and adhesion molecules, which suggested that inflammatory response might be evoked. Moreover, we demonstrated by in vitro endothelial tube formation that even a small amount of DMSA-Fe₂O₃ (0.01 and 0.02 mg/ml) could inhibit angiogenesis by the HAECs. Altogether, these results indicate that DMSA-Fe₂O₃ have some cytotoxicity that may cause side effects on normal endothelial cells.     

Effect of iron oxide nanoparticles on the morphological properties of isotactic polypropylene

Isotactic polypropylene (iPP) and iron oxide (Fe₃O₄) nanocomposites were mixed by masterbatch blending technique in a single screw extruder machine. The concentrations of Fe₃O₄ in the iPP/Fe₃O₄ nanocomposites were 0.5, 1, 2, and 5% by weight. The influence of Fe₃O₄ nanoparticles on the effectiveness of nucleation, morphology, mode of crystallization, and crystallinity of iPP were studied by differential scanning calorimetry (DSC) and polarized light microscopy (PLM). The introduction of Fe₃O₄ nanoparticles in the iPP matrix inhibited the formation of β crystals, and caused a shift in the melting point to higher values. The magnitude of the shift was up to 20–21°C which indicates that using the masterbatch technique leads to an enhancement of the dispersion process of the Fe₃O₄ nanoparticle and the formation of less agglomerates in the iPP/Fe₃O₄ nanocomposites. The percentage crystallinity, X_c, increased at the low cooling rates of 1 and 2°C/min. At higher cooling rates of 5, 10, and 20°C/min, the masterbatch technique produced nanocomposites of X_c with nonuniform trends. The overall crystallization rate enhancement for the iPP/Fe₃O₄ nanocomposites is attributed to the presence of Fe₃O₄ nanoparticles as a nucleating agent which have no significant effect on the growth rate of iPP crystals. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Preparation of magnetic poly(glycidyl methacrylate) microspheres by emulsion polymerization in the presence of sterically stabilized iron oxide nanoparticles

With the aim to synthesize water‐dispersible superparamagnetic nanoparticles, iron oxide was precipitated in aqueous solution of dextran, (carboxymethyl) dextran (CM‐dextran), (DEAE‐dextran), or D ‐mannose. Glycidyl methacrylate (GMA) was emulsion‐polymerized in the presence of the nanoparticles and the effect of iron oxide modification on the product properties was investigated. The main factors affecting the morphology, size, and size distribution of the latex particles are the type and concentration of emulsifier (Disponil AES 60, Tween 20, Triton X‐100) and initiator [ammonium persulfate (APS) and 4,4′‐azobis(4‐cyanovaleric acid) (ACVA)]. Disponil AES 60 and ACVA are the preferred emulsifier and initiator, respectively, because oxirane groups hydrolyzed during the APS‐initiated polymerization. Up to some 5 wt % of iron was found in poly(glycidyl methacrylate) (PGMA) microspheres obtained by emulsion polymerization in the presence of dextran‐coated iron oxide and emulsified with Disponil AES 60. The size of magnetic PGMA microspheres could be controlled in the range ? 70–400 nm. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4348–4357, 2006     

利用氧化铁红厂废水制备氧化铁红晶种的研究

针对氧化铁红生产过程产生的废水二价铁含量高、pH低的特点,开辟了利用氧化铁红厂含亚铁盐酸性废水处理产生的污泥制备氧化铁红晶种的新工艺。研究表明：每吨废水投加质量分数为30%的工业烧碱溶液2.8 L,可使出水pH至6~9、二价铁离子去除率达到99.5%、色度≤40倍,满足GB 18918-2002《城镇污水处理厂污染物排放标准》的二级标准;生成的氢氧化亚铁和氢氧化铁混合污泥可用于制备氧化铁红晶种并进一步生产氧化铁红产品,最终产品三氧化二铁质量分数达到96.8%,满足GB/T 1863-2008《氧化铁颜料》的标准。     

KFS2型复合氧化铁脱硫剂的制备与性能评价

以硫酸亚铁为原料与碳酸氢氨等碱性物质反应,制备不溶性铁的氧化物,将其与活性氧化锌和特殊助剂混合,经混碾和挤条成型工艺制得以氧化铁、氧化锌为活性组分的KFS2型复合氧化铁脱硫剂,并与某常温氧化锌脱硫剂进行性能比较。结果表明,在相同评价条件下,KFS2型复合氧化铁脱硫剂性能明显优于对比剂。     

Crystallization and magnetic property of iron oxide nanoparticles precipitated in silica glass matrix

Crystallization and magnetic property of Fe₂O₃ nanoparticle precipitated in SiO₂ matrix was investigated. Fe₂O₃/SiO₂ nanocomposite thin film was obtained by annealing of the amorphous Fe-Si-O thin film deposited by RF-magnetron sputtering of (α-Fe₂O₃)_1−x/(SiO₂)_x composite targets. The Fe₂O₃ crystallite size increased with decreasing SiO₂ area ratio, x of the target and increasing annealing temperature. ?-Fe₂O₃ with the crystallite size of 20-30 nm was obtained after annealing the film deposited in SiO₂ area ratio, x = 0.33-0.42 at 900 °C. Lower SiO₂ area ratio (x) than 0.25 and higher annealing temperature resulted in precipitation of α-Fe₂O₃ with the larger crystallite size than 40 nm. In the case of SiO₂ area ratio, x ≥ 0.50, the annealed film was amorphous and showed higher magnetization and smaller coercivity due to the precipitation of very small crystalline γ-Fe₂O₃. The ?-Fe₂O₃/SiO₂ composite thin film showed ferromagnetic hysteresis with coercive force of 0.14 T.     

Composites of polymeric gels and magnetic nanoparticles: Preparation and drug release behavior

The article is concerned with the preparation of polymer–iron oxide nanocomposites and the study as drug‐delivery matrices under the influence of applied magnetic field. Biocompatible materials were prepared by incorporating an aqueous ferrofluid in poly(vinyl alcohol) and scleroglucan (SCL) hydrogels, loaded with theophylline as model drug for release studies. The in vitro release profile was obtained using a flat Franz cell and the kinetic parameters were derived applying a semiempirical power law. A magnetic characterization of nanoparticles contained in the ferrofluid was performed by obtaining the magnetization curve. For both systems, the observed drug release profiles decreased when a uniform external magnetic field is applied suggesting they can be used as environmental responsive matrices for biomedical applications. Dynamic rheological measurements show that a higher storage modulus and a more compact structure are obtained by incorporating the ferrofluid into the hydrogels. These rheological results and environmental electron scanning microscopy micrographs point to an understanding of release behavior once the magnetic field is applied. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007