Femtosecond laser generation of bimetallic oxide nanoparticles with potential X-ray absorbing and magnetic functionalities for medical imaging applications

Bimetallic nanoparticles have gained vivid attention due to their unique and synergistic properties. They can be used in fields such as solar cells, optics, sensing, as well as medicine. The generation of bimetallic nanoparticles, containing oxide phases of both magnetic and X-ray attenuating metals for bioimaging applications has been challenging with traditional chemical synthesis methods. An alternative is the generation of nanoparticles from binary oxide ceramics by laser ablation in liquid. However, the applicability of this technique for production of hybrid nanoparticles consisting of magnetic and X-ray absorbing elements has not been demonstrated yet. In this work, novel ceramics composed of bimetallic oxide phases of iron-tantalum, iron-tungsten, and ironbismuth were produced by a reaction-sintering method. The bulk samples were characterized with scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffractometry. Nanoparticles were produced in aqueous and ethanol solutions by employing a femtosecond laser and characterized with transmission electron microscopy, selected area electron diffraction, and energy dispersive X-ray spectroscopy. The results demonstrated that the production of binary oxide bulk ceramics and their subsequent laser ablation in liquids leads to the successful generation of bimetallic oxide nanoparticles, without a core-shell morphology. In addition, it was found that the ablation threshold fluence of bulk samples as well as the crystallinity of the synthesized nanoparticles is governed by both the nature of the metallic oxide ceramics and the employed liquid. The results pave the way for a single step generation of well-defined bimetallic nanoparticles by laser ablation that could potentially exhibit X-ray and magnetic absorption properties suitable for multimodal imaging applications.This research has been partially funded by the Spanish Ministerio de Ciencia e Innovacion through the research project MAT2015-67354R (MINECO-FEDER). Funding through a Marie Sklodowska-Curie Individual Fellowships (MSCA-IF 2014, 656908-NIMBLIS-ESR) of the Horizon 2020 program, and the Project PI-0030-2017 of the Junta de Andalucia in the framework of the integrated territorial initiative 20142020 for research and innovation in biomedicine and health sciences in the province of Cadiz is also greatly appreciated. The authors acknowledge support for scanning electron microscopy by Dr. Stephan Puchegger and the faculty center for nanostructure research at the University of Vienna

Comparison of different methodologies for obtaining nickel nanoferrites

Nickel nanoferrites were obtained by means of four different synthetic wet-routes: co-precipitation (CP), sonochemistry (SC), sonoelectrochemistry (SE) and electrochemistry (E). The influence of the synthesis method on the structural and magnetic properties of nickel ferrite nanoparticles is studied. Although similar experimental conditions such as temperature, pH and time of synthesis were used, a strong dependence of composition and microstructure on the synthesis procedure is found, as electron microscopy, X-ray diffraction and Mössbauer spectroscopy studies reveal. Whereas by means of the CP and SC methods particles of a small size around 5–10 nm, respectively, and composed by different phases are obtained, the electrochemical routes (E and SE) allow obtaining monodisperse nanoparticles, with sizes ranging from 30 to 40 nm, and very close to stoichiometry. Magnetic characterization evidences a superparamagnetic behavior for samples obtained by CP and SC methods, whereas the electrochemical route leads to ferromagnetic ferrite nanoparticles

Pursuit of optimal synthetic conditions for obtaining colloidal zero-valent iron nanoparticles by scanning pulsed laser ablation in liquids

Liquid-Assisted Pulsed Laser Ablation (LA-PLA) is a promising top-down method to directly synthesize colloidal dispersions of nanoparticles in a eco-friendly manner. However, the role of LA-PLA synthesis parameters is not yet fully agreed. This work seeks to optimize the production of nanoscale zero-valent iron (nZVI) particles suitable for biomedical or environmental applications using nanosecond LA-PLA on iron targets with different ablation media, laser and target scanning parameters. The use of alcohols as solvents produces iron-iron oxide core-shell nanoparticles with amorphous cores, except for a small crystalline fraction corresponding to the biggest core sizes. Decreasing carbon chain length and complexity leads to a thinning of the carbonaceous material coatings and an increase of the colloidal stability and the nanoparticle productivity. Moreover, a decrease of solvent density and surface tension allows obtaining reduced sizes and polydispersity values. Among, laser and scanning parameters, the pulse accumulation per spot displayed a clear effect in boosting size and productivity. As main outcome, aqueous dispersions with suitable colloidal properties are obtained, either by transferring to water of optimized nZVI particles produced in ethanol, or by direct formation of nZVI particles and in situ coating with hydrophilic molecules in aqueous solutions of these moleculesThis research has been funded by the Spanish Ministry of Economy and Competitiveness (MINECO) and FEDER [research projects MAT2015-67354R, MAT2014-53961-R, and MAT2017- 86826-R] and by the Aragón government (DGA) [grant for consolidated group PLATON E31_17R]. OBM thanks the financial support from the “Ramón y Cajal Program” [research project RYC2010-07332] of the Spanish Ministry of Economy and Competitiveness (MINECO) and the H2020 Action H2020-MSCA-IF-2014_ST [grant 656908-NIMBLIS] of the Executive Agency for Research Manages of EU Commissio

A new ex vivo method to evaluate the performance of candidate MRI contrast agents: a proof-of-concept study

BACKGROUND: Magnetic resonance imaging (MRI) plays an important role in tumor detection/diagnosis. The use of exogenous contrast agents (CAs) helps to improve the discrimination between lesion and neighbouring tissue, but most of the currently available CAs are non-specific. Assessing the performance of new, selective CAs requires exhaustive assays and large amounts of material. Accordingly, in a preliminary screening of new CAs, it is important to choose candidate compounds with good potential for in vivo efficiency. This screening method should reproduce as close as possible the in vivo environment. In this sense, a fast and reliable method to select the best candidate CAs for in vivo studies would minimize time and investment cost, and would benefit the development of better CAs. RESULTS: The post-mortem ex vivo relative contrast enhancement (RCE) was evaluated as a method to screen different types of CAs, including paramagnetic and superparamagnetic agents. In detail, sugar/gadolinium-loaded gold nanoparticles (Gd-GNPs) and iron nanoparticles (SPIONs) were tested. Our results indicate that the post-mortem ex vivo RCE of evaluated CAs, did not correlate well with their respective in vitro relaxivities. The results obtained with different Gd-GNPs suggest that the linker length of the sugar conjugate could modulate the interactions with cellular receptors and therefore the relaxivity value. A paramagnetic CA (GNP (E_2)), which performed best among a series of Gd-GNPs, was evaluated both ex vivo and in vivo. The ex vivo RCE was slightly worst than gadoterate meglumine (201.9 ± 9.3% versus 237 ± 14%, respectively), while the in vivo RCE, measured at the time-to-maximum enhancement for both compounds, pointed to GNP E_2 being a better CA in vivo than gadoterate meglumine. This is suggested to be related to the nanoparticule characteristics of the evaluated GNP. CONCLUSION: We have developed a simple, cost-effective relatively high-throughput method for selecting CAs for in vivo experiments. This method requires approximately 800 times less quantity of material than the amount used for in vivo administrations

Solvothermal synthesis and characterization of ytterbium/iron mixed oxide nanoparticles with potential functionalities for applications as multiplatform contrast agent in medical image techniques

A solvothermal route to prepare Glutathione capped hybrid ytterbium/iron oxide nanoparticles with potential applications as multiplatform contrast agent in medical image techniques has been developed. The influence of ytterbium/iron molar ratio used as precursor, as well as the degree of the autoclave filling on the structural and morphological characteristics of the obtained nanoparticles has been extensively studied. Although all nanoparticles present similar composition, with YbFeO3 being the majority phase, size and morphology of the as synthetized nanoparticles are highly influenced by the critical temperature and by the over -saturation reached during the solvothermal process. We have demonstrated that glutathione properly functionalizes the hybrid nanoparticles, increasing their colloidal stability and decreasing their cytotoxicity. Additionally, they show good imaging in magnetic resonance and X-ray computerized tomography, thereby indicating promising potential as a dual contrast agent. This work presents, for the first time, glutathione functionalized ytterbium/iron oxide nanoparticles with potential applications in Biomedicine. © 2022 Elsevier Ltd and Techna Group S.r.l

Scanning pulsed laser ablation in liquids: An alternative route to obtaining biocompatible YbFe nanoparticles as multiplatform contrast agents for combined MRI and CT imaging

Ytterbium ferrites are being used in many promising applications, such as visible-light photocatalysis, solar cells, magnetooptic devices, electro-magnetic equipment, etc., due to their fantastic ferroelectric and ferromagnetic properties. However, despite their good magnetic and radiopaque features, the use of ytterbium ferrites as multiplatform contrast agents in magnetic resonance imaging (MRI) and X-ray computed tomography (CT) is still under-developed. This is mainly due to difficulties in obtaining stable and biocompatible aqueous colloidal dispersions of ytterbium ferrite nanoparticles. In order to overcome this limitation, this work explores an eco-friendly method to directly synthesize such dispersions by liquid-assisted pulsed laser ablation of ytterbium ferrite massive targets. First, orthorhombic bulk YbFeO3 targets were obtained by a reaction-sintering method. Then, colloidal dispersions of nanoparticles were produced directly in both distilled water and ethanol by irradiating the bulk YbFeO3 targets with high-power infrared nanosecond lasers pulses. A battery of techniques has been used to characterize the as synthesized YbFeO3 targets and colloidal dispersions of YbFe nanoparticles to determine their composition, structure, magnetic properties, X-ray attenuation potentials, and colloidal properties. Moreover, the biocompatibility of the systems was also analysed by MTT cell viability assay. Results indicated that the use of distilled water as ablation medium yields colloidal dispersions consisted mainly of paramagnetic ytterbium ferrite nanoparticles. Contrarily, the use of ethanol as solvent leads to colloidal dispersions of polycrystalline nanoparticles with both ferromagnetic and paramagnetic behaviour, due to the coexistence, in each nanoparticle, of ytterbium ferrite, ytterbium oxide, and iron oxide crystalline phases. Both colloidal dispersions exhibit also high biocompatibility and suitable X-ray attenuation properties. Moreover, they show bio-safe hydrodynamic sizes (lower than 200 nm) with acceptable overall hydrodynamic polydispersity index values (under 0.4), being stable in water for several weeks. These results pave the way for the future evaluation of Yb–Fe based nanoparticles as multiplatform contrast agents in multimodal MRI and CT imaging.This research has been funded by the Spanish Ministry of Economy and Competitiveness (MINECO) and FEDERthrough the research project MAT2015-67354R, and a MSCA-IF postdoctoral fellowship from the Marie Curie action 2014 [grant 656908-NIMBLIS] of the H2020 program of the Executive Agency for Research Manages of EU Commission. Additionally, this research has been funded throught a research project (research project ULST-NANO) of the Proyectos Integradores MdM-IMEYMAT, call 2020, as well as the researcg project PID2020-118329RB-I00 funded by Spanish MCIN/AEI/10.13039/501100011033 action. Moreover, this research was also co-financed through two regional research projects funded by the Junta de Andalucía, specifically, the research project PECART-0096-2020 (Consejería Salud y Familias. JA Spain) and the research project P20_01293 (Consejería Economía, Conocimiento, Empresas y Universidad. JA Spain). In addition, Dr. Monserrat Llaguno-Munive is grateful for the funding received through the post-doctoral grant of the Consejo Nacional de Ciencia y Tecnología from Mexico (CONACYT, no 619639). In addition, we acknowledge the received technical assistance from the SC-ICYT of the University of Cádiz and the Servicio General de Apoyo a la Investigación-SAI, Universidad de Zaragoza. We also acknowledge to the Networking Research Centre on Bioengineering, Biomaterials, and Nanomedicine (CIBERBBN) (which is financed by the Instituto de Salud Carlos III (ISCIII) with assistance from the European Regional Development Fund (ERDF)) and the ICTS “NANBIOSIS”, specifically the FVPR/U20 (http://www.nanbiosis.es/portfolio/u20-in-vivo-experimentalplatform/) for providing access to the micro-CT. Finally, we want to thank the company LASING S.L. its technical support in the development of the NANO-GLAS laser system where the LA-PLA experiments were carried out.Peer reviewe

Synthesis of Magnetic Nanocrystals by Thermal Decomposition in Glycol Media: Effect of Process Variables and Mechanistic Study

The nucleation and growth of water dispersible iron-oxide nanoparticles synthesized by high temperature decomposition of iron­(III) acetylacetonate in the presence of different solvents has been studied. A battery of techniques was used to characterize the products obtained under different conditions and to elucidate the synthesis mechanism. Results show that the synthesis of iron-oxide nanoparticles in triethylene glycol (TEG) proceeds through a multistep process whose first stage is likely to be the formation of an intermediate TEG-iron-complex that evolves into a low-crystallinity iron-oxide-organic precursor during aging at 180 °C. Raising the temperature above 240 °C caused the thermal decomposition of the precursor and the sudden nucleation of small iron-oxide nanocrystals. Keeping the reactant mixture at 280 °C led to the growth of iron-oxide nanocrystals, as did increasing the time at reflux temperature, the amount of initial iron precursor or the use high boiling point solvents. The particle size could be reproducibly controlled between 1.5 and 13 nm, with a relatively narrow size distribution. Larger particles could also be obtained using a solvothermal method in an autoclave reactor

Scanning pulsed laser ablation in liquids: An alternative route to obtaining biocompatible YbFe nanoparticles as multiplatform contrast agents for combined MRI and CT imaging

Ytterbium ferrites are being used in many promising applications, such as visible-light photocatalysis, solar cells, magnetooptic devices, electro-magnetic equipment, etc., due to their fantastic ferroelectric and ferromagnetic properties. However, despite their good magnetic and radiopaque features, the use of ytterbium ferrites as multiplatform contrast agents in magnetic resonance imaging (MRI) and X-ray computed tomography (CT) is still under-developed. This is mainly due to difficulties in obtaining stable and biocompatible aqueous colloidal dispersions of ytterbium ferrite nanoparticles. In order to overcome this limitation, this work explores an eco-friendly method to directly synthesize such dispersions by liquid-assisted pulsed laser ablation of ytterbium ferrite massive targets. First, orthorhombic bulk YbFeO3 targets were obtained by a reaction-sintering method. Then, colloidal dispersions of nanoparticles were produced directly in both distilled water and ethanol by irradiating the bulk YbFeO3 targets with high-power infrared nanosecond lasers pulses. A battery of techniques has been used to characterize the as synthesized YbFeO3 targets and colloidal dispersions of YbFe nanoparticles to determine their composition, structure, magnetic properties, X-ray attenuation potentials, and colloidal properties. Moreover, the biocompatibility of the systems was also analysed by MTT cell viability assay. Results indicated that the use of distilled water as ablation medium yields colloidal dispersions consisted mainly of paramagnetic ytterbium ferrite nanoparticles. Contrarily, the use of ethanol as solvent leads to colloidal dispersions of polycrystalline nanoparticles with both ferromagnetic and paramagnetic behaviour, due to the coexistence, in each nanoparticle, of ytterbium ferrite, ytterbium oxide, and iron oxide crystalline phases. Both colloidal dispersions exhibit also high biocompatibility and suitable X-ray attenuation properties. Moreover, they show bio-safe hydrodynamic sizes (lower than 200 nm) with acceptable overall hydrodynamic polydispersity index values (under 0.4), being stable in water for several weeks. These results pave the way for the future evaluation of Yb–Fe based nanoparticles as multiplatform contrast agents in multimodal MRI and CT imaging