Vincenzo Amendola

Silver Nanoparticles with Broad Multiband Linear Optical Absorption

Keywords: thiols ; cluster compounds ; luminescence ; quantum dots ; surface plasmon resonance Reference EPFL-ARTICLE-166610doi:10.1002/anie.200900298 Record created on 2011-06-06, modified on 2017-05-10

Controlled size manipulation of free gold nanoparticles by laser irradiation and their facile bioconjugation

The average size of gold nanoparticles (AuNP), obtained by laser ablation in solution, is reduced to a few nanometers or increased to tens of nanometers using laser treatments with different strategies. The techniques do not require any stabilizing molecules and the AuNP surface is free from strongly linked ligands. This allowed one-step, immediate and very efficient functionalization of AuNP with commonly used proteins like bovine serum albumin (BSA), which can be detected, using small nanoparticles, down to 3 picomoles and with a 1 : 10 concentration ratio of BSA : AuNP.

Cell up-take control of gold nanoparticles functionalized with a thermoresponsive polymer

Surface decoration of gold nanoparticles with thermoresponsive polymers endows a temperature tunable colloidal system switchable for enhanced intracellular up-take. Gold nanoparticles (AuNP, 18 ± 11 nm-diameter) produced by laser ablation synthesis in liquid solution were surface coated with thermoresponsive thiol terminated poly-N-isopropylacrylamide-co-acrylamide co-polymer possessing a lower critical solution temperature (LCST) at 37 °C. Under selected conditions about 3800 polymer chains were conjugated per particle. The polymer coated nanoparticles were found to display thermosensitive properties, as in solution they exhibited reversible aggregation/deaggregation above and below the LCST, respectively. Cell culture studies showed that the polymer decorated AuNP were located into human breast adenocarcinoma MCF7 cells treated at 40 °C (12000 AuNP/cell) with more than 80-fold greater up-take compared to cells treated at 34 °C with the same particles (140 AuN/cell). This difference is attributable to a ‘switching’ of the polymer coating to a globule state at 37 °C and an increased hydrophobicity of the particles with a simultaneous loss of the ‘stealth’ properties of the polymer coating. By contrast, cell up-take of uncoated AuNP (about 6000 AuNP/cell) did not depend on the incubation temperature. These data show that good control of the AuNP cell up-take can be obtained with the new polymer-gold nanoconjugates, and suggest that these systems might find use for targeting cellsin vitro by a small temperature change or in vivo in body sites, such as inflamed or tumour tissues, where a temperature variation is already present.

Surface plasmon resonance in gold nanoparticles: a review

In the last two decades, plasmon resonance in gold nanoparticles (Au NPs) has been the subject of intense research efforts. Plasmon physics is intriguing and its precise modelling proved to be challenging. In fact, plasmons are highly responsive to a multitude of factors, either intrinsic to the Au NPs or from the environment, and recently the need emerged for the correction of standard electromagnetic approaches with quantum effects. Applications related to plasmon absorption and scattering in Au NPs are impressively numerous, ranging from sensing to photothermal effects to cell imaging. Also, plasmon-enhanced phenomena are highly interesting for multiple purposes, including, for instance, Raman spectroscopy of nearby analytes, catalysis, or sunlight energy conversion. In addition, plasmon excitation is involved in a series of advanced physical processes such as non-linear optics, optical trapping, magneto-plasmonics, and optical activity. Here, we provide the general overview of the field and the background for appropriate modelling of the physical phenomena. Then, we report on the current state of the art and most recent applications of plasmon resonance in Au NPs.

Plasmon-enhanced optical trapping of gold nanoaggregates with selected optical properties.

We show how light forces can be used to trap gold nanoaggregates of selected structure and optical properties obtained by laser ablation in liquid. We measure the optical trapping forces on nanoaggregates with an average size range 20-750 nm, revealing how the plasmon-enhanced fields play a crucial role in the trapping of metal clusters featuring different extinction properties. Force constants of the order of 10 pN/nmW are detected, the highest measured on a metal nanostructure. Finally, by extending the transition matrix formalism of light scattering theory to the optical trapping of metal nanoaggregates, we show how the plasmon resonances and the fractal structure arising from aggregation are responsible for the increased forces and wider trapping size range with respect to individual metal nanoparticles.

Magneto‐Plasmonic Au‐Fe Alloy Nanoparticles Designed for Multimodal SERS‐MRI‐CT Imaging

Diagnostic approaches based on multimodal imaging are needed for accurate selection of the therapeutic regimens in several diseases, although the dose of administered contrast drugs must be reduced to minimize side effects. Therefore, large efforts are deployed in the development of multimodal contrast agents (MCAs) that permit the complementary visualization of the same diseased area with different sensitivity and different spatial resolution by applying multiple diagnostic techniques. Ideally, MCAs should also allow imaging of diseased tissues with high spatial resolution during surgical interventions. Here a new system based on multifunctional Au-Fe alloy nanoparticles designed to satisfy the main requirements of an ideal MCA is reported and their biocompatibility and imaging capability are described. The MCAs show easy and versatile surface conjugation with thiolated molecules, magnetic resonance imaging (MRI) and computed X-ray tomography (CT) signals for anatomical and physiological information (i.e., diagnostic and prognostic imaging), large Raman signals amplified by surface enhanced Raman scattering (SERS) for high sensitivity and high resolution intrasurgical imaging, biocompatibility, exploitability for in vivo use and capability of selective accumulation in tumors by enhanced permeability and retention effect. Taken together, these results show that Au-Fe nanoalloys are excellent candidates as multimodal MRI-CT-SERS imaging agents.

Top-down synthesis of multifunctional iron oxide nanoparticles for macrophage labelling and manipulation

Multifunctional iron oxide (FeOx) magnetic nanoparticles (MNPs) are promising items for biomedical applications. They are studied as theranostic agents for cancer treatment, selective probes for bioanalytical assays, controllable carriers for drug delivery and biocompatible tools for cell sorting or tissue repair. Here we report a new method for the synthesis in water of FeOx–MNPsvia a top-down physical technique consisting in Laser Ablation Synthesis in Solution (LASiS). LASiS is a green method that does not require chemicals or stabilizers, because nanoparticles are directly obtained in water as a stable colloidal system. A gamut of characterization techniques was used for investigating the structure of FeOx–MNPs that have a polycrystalline structure prevalently composed of magnetite (ca. 75%) and hematite (ca. 22%). The FeOx–MNPs exhibit very good magnetic properties if compared to what is usually reported for iron oxide nanoparticles, with saturation magnetization close to the bulk value (ca. 80 emu g−1) and typical signatures of the coexistence of ferrimagnetic and antiferromagnetic phases in the same particle. The functionalization of FeOx–MNPs after the synthesis was possible with a variety of ligands. In particular, we succeeded in the functionalization of FeOx–MNPs with carboxylated phosphonates, fluorescent alkylamines, fluorescent isothiocyanates and bovine serum albumin. Our FeOx–MNPs showed excellent biocompatibility. Multifunctional FeOx–MNPs were exploited for macrophage cell labelling with fluorescent probes as well as for cell sorting and manipulation by external magnetic fields.

Coexistence of plasmonic and magnetic properties in Au89Fe11 nanoalloys

We describe an environmentally friendly, top-down approach to the synthesis of Au89Fe11 nanoparticles (NPs). The plasmonic response of the gold moiety and the magnetism of the iron moiety coexist in the Au89Fe11 nanoalloy with strong modification compared to single element NPs, revealing a non-linear surface plasmon resonance dependence on the iron fraction and a transition from paramagnetic to a spin-glass state at low temperature. These nanoalloys are accessible to conjugation with thiolated molecules and they are promising contrast agents for magnetic resonance imaging.

LDI-MS assisted by chemical-free gold nanoparticles: enhanced sensitivity and reduced background in the low-mass region.

Gold nanoparticles (AuNPs) assisted laser desorption ionization mass spectrometry (LDI-MS) emerged as an effective technique for the detection of analytes with high sensitivity. The surface chemistry and the size of AuNPs are the crucial parameters for lowering the detection limits and increasing the selectivity of LDI-MS. Here we show that chemical-free size selected AuNPs, obtained by laser ablation synthesis in solution (LASiS), have very low background in the low mass region (<500 Da), contrary to citrate stabilized AuNPs (citrate-AuNPs) and dihydroxyacetophenone (DHAP). This allowed better performances for the picomole detection of low mass analytes like arginine, fructose, atrazine, anthracene and paclitaxel. The results suggest that chemical-free LASiS-AuNPs can be an excellent matrix for nanoparticle-assisted LDI-MS.

Magnetic iron oxide nanoparticles with tunable size and free surface obtained via a “green” approach based on laser irradiation in water

Crystalline structure, size and surface coating are the relevant parameters influencing the catalytic and magnetic properties of iron oxide nanoparticles (FeOxNPs). The development of a “green” method for the synthesis of FeOxNPs with good crystallinity, controlled size and uncontaminated surface all at the same time is challenging. Here we show that laser ablation in water can be combined with laser irradiation at 355 nm to obtain FeOxNPs with average size tunable in the 10–30 nm range and a percentage of ferrimagnetic phase up to the 94% of crystalline phases, while maintaining the particles surface free from stabilizers or other chemical by-products and without using harmful or toxic reagents. The final FeOxNPs show good magnetization values and have the typical magnetic behaviour of exchange bias systems, due to their highly polycrystalline structure and small (ca. 3 nm) crystalline domains. The one-step coating with phosphonate ligands conferred long time stability in physiological medium to FeOxNPs.