Vincent Motto-Ros

Long-term in vivo clearance of gadolinium-based AGuIX nanoparticles and their biocompatibility after systemic injection.

We previously reported the synthesis of gadolinium-based nanoparticles (NPs) denoted AGuIX (activation and guiding of irradiation by X-ray) NPs and demonstrated their potential as an MRI contrast agent and their efficacy as radiosensitizing particles during X-ray cancer treatment. Here we focus on the elimination kinetics of AGuIX NPs from the subcellular to whole-organ scale using original and complementary methods such as laser-induced breakdown spectroscopy (LIBS), intravital two-photon microscopy, inductively coupled plasma optical emission spectrometry (ICP-OES), transmission electron microscopy (TEM), and electrospray ionization mass spectrometry (ESI-MS). This combination of techniques allows the exact mechanism of AGuIX NPs elimination to be elucidated, including their retention in proximal tubules and their excretion as degraded or native NPs. Finally, we demonstrated that systemic AGuIX NP administration induced moderate and transient effects on renal function. These results provide useful and promising preclinical information concerning the safety of theranostic AGuIX NPs.

Ultraviolet versus infrared: Effects of ablation laser wavelength on the expansion of laser-induced plasma into one-atmosphere argon gas

Laser-induced plasma from an aluminum target in one-atmosphere argon background has been investigated with ablation using nanosecond ultraviolet (UV: 355 nm) or infrared (IR: 1064 nm) laser pulses. Time- and space-resolved emission spectroscopy was used as a diagnostics tool to have access to the plasma parameters during its propagation into the background, such as optical emission intensity, electron density, and temperature. The specific feature of nanosecond laser ablation is that the pulse duration is significantly longer than the initiation time of the plasma. Laser-supported absorption wave due to post-ablation absorption of the laser radiation by the vapor plume and the shocked background gas plays a dominant role in the propagation and subsequently the behavior of the plasma. We demonstrate that the difference in absorption rate between UV and IR radiations leads to different propagation behaviors of the plasma produced with these radiations. The consequence is that higher electron density and tem...

Convoluted effect of laser fluence and pulse duration on the property of a nanosecond laser-induced plasma into an argon ambient gas at the atmospheric pressure

We studied the behavior of the plasma induced by a nanosecond infrared (1064 nm) laser pulse on a metallic target (Al) during its propagation into argon ambient gas at the atmospheric pressure and especially over the delay interval ranging from several hundred nanoseconds to several microseconds. In such interval, the plasma is particularly interesting as a spectroscopic emission source for laser-induced plasma spectroscopy (LIBS). We show a convoluted effect between laser fluence and pulse duration on the structure and the emission property of the plasma. With a relatively high fluence of about 160 J/cm2 where a strong plasma shielding effect is observed, a short pulse of about 4 ns duration is shown to be significantly more efficient to excite the optical emission from the ablation vapor than a long pulse of about 25 ns duration. While with a lower fluence of about 65 J/cm2, a significantly more efficient excitation is observed with the long pulse. We interpret our observations by considering the post-a...

Ultrasmall Nanoplatforms as Calcium‐Responsive Contrast Agents for Magnetic Resonance Imaging

The preparation of ultrasmall and rigid platforms (USRPs) that are covalently coupled to macrocycle-based, calcium-responsive/smart contrast agents (SCAs), and the initial in vitro and in vivo validation of the resulting nanosized probes (SCA-USRPs) by means of magnetic resonance imaging (MRI) is reported. The synthetic procedure is robust, allowing preparation of the SCA-USRPs on a multigram scale. The resulting platforms display the desired MRI activity—i.e., longitudinal relaxivity increases almost twice at 7 T magnetic field strength upon saturation with Ca(2+). Cell viability is probed with the MTT assay using HEK-293 cells, which show good tolerance for lower contrast agent concentrations over longer periods of time. On intravenous administration of SCA-USRPs in living mice, MRI studies indicate their rapid accumulation in the renal pelvis and parenchyma. Importantly, the MRI signal increases in both kidney compartments when CaCl2 is also administrated. Laser-induced breakdown spectroscopy experiments confirm accumulation of SCA-USRPs in the renal cortex. To the best of our knowledge, these are the first studies which demonstrate calcium-sensitive MRI signal changes in vivo. Continuing contrast agent and MRI protocol optimizations should lead to wider application of these responsive probes and development of superior functional methods for monitoring calcium-dependent physiological and pathological processes in a dynamic manner.

Experimental investigation of the structure and the dynamics of nanosecond laser-induced plasma in 1-atm argon ambient gas

We have investigated the structure and the dynamics of the plasma induced on a metallic target in 1-atm argon ambient by a nanosecond laser pulse with irradiance in the range of 10 GW/cm2. The structure is revealed to be sensitively dependent on the laser wavelength. A layered structure of different species characterizes the plasma induced by ultraviolet 355 nm pulse, while an effective mixing between the ablation vapor and the shocked ambient gas is observed with infrared 1064 nm pulse. The absorption property of the shocked gas is found to be crucial for determining the structure of the plasma.

On the performance of laser-induced breakdown spectroscopy for quantitative analysis of minor and trace elements in glass

The analytical figures of merit of laser-induced breakdown spectroscopy (LIBS) for elemental analysis of glass have been evaluated using a laboratory prototype of the LIBS instrument for the quantification of 4 elements, Ti, Cr, Ca and Ba. Two sets of samples were prepared or collected for the assessment. The first one consisted of 10 laboratory-prepared fused beads with the elemental content determined by X-ray fluorescence (XRF), an established analytical technique which was considered in our study as the reference technique for the assessment of the LIBS technique. Among them, 8 were used as reference samples and 2 as “unknown” samples for test. The calibration curves were thus established with the references. The counter calibration led to the determination of the elemental content in the unknown samples. Such a calibration procedure allowed assessing the figures of merit of LIBS together with the used setup and measurement protocol about a certain number of key parameters, such as the correlation with a linear regression of the calibration data, limit of detection (LoD), repeatability, reproducibility and relative accuracy. The second set of samples was collected from different origins and consisted of 8 bottle glass fragments, which were different in appearance (color and surface) and in content for the 4 analyzed elements. Their elemental concentrations were first determined using XRF. The LIBS calibration curves established with the fused beads were thus used to perform the analysis of 2 glass fragments with elemental contents lying around the range of the calibration concentration. Further analysis of the ensemble of glass fragments allowed assessing the matrix effect introduced by the different types of glasses and extending the calibration curves over a very large concentration range from several ppm to several percent. We show that the self-absorption effect observed over such a large concentration range can be taken into account by using quadratic regression.

Laser-induced breakdown spectroscopy for elemental characterization of calcitic alterations on cave walls

Cave walls are affected by different kinds of alterations involving preservative issues in the case of ornate caves, in particular regarding the rock art covering the walls. In this context, coralloids correspond to a facies with popcorn-like aspect belonging to the speleothem family, mostly composed of calcium carbonate. The elemental characterization indicates the presence of elements that might be linked to the diagenesis and the expansion of the alterations as demonstrated by prior analyses on stalagmites. In this study, we report the use of laser-induced breakdown spectroscopy (LIBS) to characterize the elemental composition of one coralloid sample with a portable instrument allowing punctual measurements and a laboratory mapping setup delivering elemental images with spatial resolution at the micrometric scale, being particularly attentive to Mg, Sr, and Si identified as elements of interest. The complementarity of both instruments allows the determination of the internal structure of the coralloid. Although a validation based on a reference technique is necessary, LIBS data reveal that the external layer of the coralloid is composed of laminations correlated to variations of the LIBS signal of Si. In addition, an interstitial layer showing high LIBS signals for Fe, Al, and Si is interpreted to be a detrital clay interface between the external and the internal part of the coralloid. These preliminary results sustain a possible formation scenario of the coralloid by migration of the elements from the bedrock.

Evaluation of a compact VUV spectrometer for elemental imaging by laser-induced breakdown spectroscopy: application to mine core characterization

This work introduces a new approach to perform LIBS elemental imaging in the vacuum ultraviolet (VUV) wavelength range by using an argon purged probe coupled to a compact spectrometer. In spite of several important elements for geological and industrial applications such as S, P, As, B, C, or Zn presenting strong lines in the VUV range, the need for using specific optics and working under oxygen-free conditions has limited the extension of LIBS systems available for such a range. Herein, we present an adaptation of our LIBS imaging instrumentation to access the VUV while operating under ambient conditions. The proposed detection system is based on an optical probe directly coupled to a Maya2000Pro compact spectrometer (Ocean Optics), all purged with argon. The technical design along with a detailed evaluation of the VUV probe is addressed. The possibility of using this VUV probe for LIBS imaging is also investigated by studying a Canadian mine core sample with special emphasis on the detection of sulfur. In addition to sulfur, more than 15 elements including P, As, C, Ca, Si, Mo, B, and Zn have also been detected. Elemental images covering sample surfaces in the range of cm2 with a micrometric spatial resolution (10 μm) are presented. A detection limit of 0.2 wt% for sulfur is demonstrated in a single shot configuration. These results open new perspectives for both conventional LIBS and LIBS-based imaging in various application fields.

Characterization of foreign materials in paraffin-embedded pathological specimens using in situ multi-elemental imaging with laser spectroscopy

Pathologists typically encounter many disparate exogenous materials in clinical specimens during their routine histopathological examinations, especially within the skin, lymph nodes, and lungs. These foreign substances may be free extracellular deposits or induce several clinical abnormalities or histopathological patterns. However, pathologists almost never investigate or report the chemical nature of exogenous metals in clinical specimens due to a lack of convenient and available technologies. In this paper, a novel strategy based on laser-induced breakdown spectroscopy (LIBS) technology is evaluated for in situ multi-elemental tissue imaging. The improved procedures allow visualization of the presence of chemical elements contained within paraffin-embedded specimens of medical interest with elemental images that are stackable with conventional histology images. We selected relevant medical situations for which the associated pathology reports were limited to the presence of lymphohistiocytic and inflammatory cells containing granules (a granuloma and a pseudolymphoma) or to lymph nodes or skin tissues containing pigments or foreign substances. Exogenous elements such as aluminum, titanium, copper, and tungsten were identified and localized within the tissues. The all-optical LIBS elemental imaging instrument that we developed is fully compatible with conventional optical microscopy used for pathology analysis. When combined with routine histopathological analysis, LIBS is a versatile technology that might help pathologists establish or confirm diagnoses for a wide range of medical applications, particularly when the nature of external agents present in tissues needs to be investigated.

Exploration of megapixel hyperspectral LIBS images using principal component analysis

Laser-Induced Breakdown Spectroscopy (LIBS) has achieved promising performance as an elemental imaging technology, and considerable progress has been achieved in the development of LIBS over the last several years, which has led to great interest in the use of LIBS in various fields of applications. LIBS is a highly attractive technology that is distinguished by its table top instrumentation, speed of operation, and operation in ambient atmosphere, able to produce megapixel multi-elemental images with micrometric resolution (10 μm) and ppm-scale sensitivity. However, the points that limit the development of LIBS are undeniably the expertise and the time required to extract a relevant signal from the LIBS dataset. The complexity of the emission spectra (e.g., elemental responses, structure of the baseline), the high dynamic range of measurement (i.e., possibility to image major to trace elements), and the large number of spectra to process require new data analysis strategies. Such new strategies are particularly critical for multi-phase materials. In this paper, we report a new methodology based on the well-known Principal Component Analysis (PCA) approach for the multivariate hyperspectral analysis of LIBS images. The proposed methodology is designed for large, raw, and potentially complex series of LIBS spectra, that allows various and exhaustive levels of information to be extracted (including the characterization of mineral phases, assessment of the measurement and identification of isolated elements) and facilitates the manipulation of such hyperspectral datasets.