Abstract:We report the synthesis and characterization of size-tunable MnxFe3−xO4 ferrite nanoclusters of different sizes ranging from ∼30 to ∼120 nm. The nanoclusters synthesized via a hydrothermal polyol process show high crystallinity and a narrow size distribution. The magnetic properties of the nanoclusters demonstrate well-behaved magnetization and low-coercivity characteristics, ferrimagnetically at a large size, and superparamagnetically at a small size.
“…From a structural point of view, the introduction of Mn determines a decrease in size of both the nanoclusters and the primary nanocrystals, which is reflected in the variations observed in saturation magnetisation: for lower doping regimes (0 o x o 0.5) the net magnetisation is increased due to the Mn contribution, while for higher doping regimes (x Z 0.5) the effects of size reduction prevail and cause its overall decrease. 28,32 Thus, our choice of introducing a low Mn doping content is intended as a conservative approach to boost the net magnetisation without heavily affecting the size of the nanocrystals and nanoclusters. In order to assess the effect of Mn-doping on our clusters, the DC magnetic susceptibility was measured as a function of temperature at low fields according to the ZFC-FC (Zero-Field Cooled-Field Cooled) protocols, while isothermal hysteresis loops were recorded at 5 K and body temperature (310 K).…”
Section: Magnetic Structure Of the Mn-doped Iron Oxide Clustersmentioning
confidence: 99%
“…Although the doping of the clusters can occur during an easy step of one-pot, rapid chemical synthesis, only few cases of relevant preliminary chemical studies have been reported so far. 28,29 In our experiments, Mn-doped iron oxide CNCs have been prepared and evaluated as MRI contrast agents as well as heating probes in magnetic fluid hyperthermia. These nanomaterials may hold a great potential for biomedical applications and highlight the need of more synthetic efforts to enrich the library of functional doped-CNCs.…”
A simple, one pot method to synthesize water-dispersible Mn doped iron oxide colloidal clusters constructed of nanoparticles arranged into secondary flower-like structures was developed. This method allows the successful incorporation and homogeneous distribution of Mn within the nanoparticle iron oxide clusters. The formed clusters retain the desired morphological and structural features observed for pure iron oxide clusters, but possess intrinsic magnetic properties that arise from Mn doping. They show distinct performance as imaging contrast agents and excellent characteristics as heating mediators in magnetic fluid hyperthermia. It is expected that the outcomes of this study will open up new avenues for the exploitation of doped magnetic nanoparticle assemblies in biomedicine.
“…From a structural point of view, the introduction of Mn determines a decrease in size of both the nanoclusters and the primary nanocrystals, which is reflected in the variations observed in saturation magnetisation: for lower doping regimes (0 o x o 0.5) the net magnetisation is increased due to the Mn contribution, while for higher doping regimes (x Z 0.5) the effects of size reduction prevail and cause its overall decrease. 28,32 Thus, our choice of introducing a low Mn doping content is intended as a conservative approach to boost the net magnetisation without heavily affecting the size of the nanocrystals and nanoclusters. In order to assess the effect of Mn-doping on our clusters, the DC magnetic susceptibility was measured as a function of temperature at low fields according to the ZFC-FC (Zero-Field Cooled-Field Cooled) protocols, while isothermal hysteresis loops were recorded at 5 K and body temperature (310 K).…”
Section: Magnetic Structure Of the Mn-doped Iron Oxide Clustersmentioning
confidence: 99%
“…Although the doping of the clusters can occur during an easy step of one-pot, rapid chemical synthesis, only few cases of relevant preliminary chemical studies have been reported so far. 28,29 In our experiments, Mn-doped iron oxide CNCs have been prepared and evaluated as MRI contrast agents as well as heating probes in magnetic fluid hyperthermia. These nanomaterials may hold a great potential for biomedical applications and highlight the need of more synthetic efforts to enrich the library of functional doped-CNCs.…”
A simple, one pot method to synthesize water-dispersible Mn doped iron oxide colloidal clusters constructed of nanoparticles arranged into secondary flower-like structures was developed. This method allows the successful incorporation and homogeneous distribution of Mn within the nanoparticle iron oxide clusters. The formed clusters retain the desired morphological and structural features observed for pure iron oxide clusters, but possess intrinsic magnetic properties that arise from Mn doping. They show distinct performance as imaging contrast agents and excellent characteristics as heating mediators in magnetic fluid hyperthermia. It is expected that the outcomes of this study will open up new avenues for the exploitation of doped magnetic nanoparticle assemblies in biomedicine.
“…25 The peak shift is accompanied with a lattice expansion (Table S1), indicating the successful incorporation of Zn 2+ and Mn 2+ ions into the γ-Fe2O3 crystal lattice. 23,35 Furthermore, no diffraction peaks corresponding to pure zinc oxide or manganese oxide were observed. The average crystallite size (dXRD) was about 14 nm for both γ-Fe2O3 and Zn0.5Fe2.5O4 and 18 nm for Mn0.5Fe2.5O4 (Figure 2a).…”
Superparamagnetic iron oxide nanoparticles (SPIONs) generate heat upon exposure to an alternating magnetic field (AMF) which has been studied for hyperthermia treatment and triggered drug release. This study introduces a novel application of magnetic hyperthermia to induce amorphization of a poorly aqueous soluble drug, celecoxib, in situ in tablets for oral administration. In situ amorphization can overcome the drug development hurdle of poor aqueous solubility by molecularly dispersing the drug in a polymeric network inside a tablet. However, current shortcomings of this approach include low drug loading in the tablets, toxicity of enabling excipients, and drug degradation. Here, SPIONs produced by flame spray pyrolysis are compacted with polyvinylpyrolidone and celecoxib, and exposed to an AMF. The degree of amorphization is strongly linked to the maximum tablet temperature achieved during AMF exposure, which depends on SPION composition and content in the tablets. Manganese ferrites exhibit no toxicity in human intestinal Caco-2 cell lines and are more effective than zinc ferrites in inducing complete amorphization of celecoxib. The resulting rapid dissolution and high solubility of in situ amorphized celecoxib in biorelevant intestinal fluid demonstrates the promising capability of SPIONs as enabling excipients to magnetically induce amorphization in situ in oral dosage forms.
“…The magnetic saturation value is increased with increasing cluster size effects. 31 Both FT-IR and NMR spectra show that corresponding results of the modification of PCMNCs. The original form of polysorbate 80 contains a CO stretching vibration band at 1735 cm −1 , which is slightly shifted to 1733 cm −1 for the modified form; this is due to the presence of negatively charged tricarboxylate groups on the PCMNCs (Figure 2D).…”
mentioning
confidence: 99%
“…The magnetic hysteresis loop of MNPs and PCMNCs were analyzed using a vibration sample magnetometer at 298 K. The magnetic saturation values at 15T are measured to be 67.7 and 68.3 emu g –1 for MNPs and PCMNCs, respectively (Figure S3). The magnetic saturation value is increased with increasing cluster size effects . Both FT-IR and NMR spectra show that corresponding results of the modification of PCMNCs.…”
Early diagnosis of infectious diseases is important for treatment; therefore, selective and rapid detection of pathogenic bacteria is essential for human health. We report a strategy for highly selective detection and rapid separation of pathogenic microorganisms using magnetic nanoparticle clusters. Our approach to develop probes for pathogenic bacteria, including Salmonella, is based on a theoretically optimized model for the size of clustered magnetic nanoparticles. The clusters were modified to provide enhanced aqueous solubility and versatile conjugation sites for antibody immobilization. The clusters with the desired magnetic property were then prepared at critical micelle concentration (CMC) by evaporation-induced self-assembly (EISA). Two different types of target-specific antibodies for H- and O-antigens were incorporated on the cluster surface for selective binding to biological compartments of the flagella and cell body, respectively. For the two different specific binding properties, Salmonella were effectively captured with the O-antibody-coated polysorbate 80-coated magnetic nanoclusters (PCMNCs). The synergistic effect of combining selective targeting and the clustered magnetic probe leads to both selective and rapid detection of infectious pathogens.
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