Abstract: Classical photo-induced fluorescence methods are conducted in two steps: a UV irradiation step in order to form a photo-induced compound followed by its fluorimetric determination. Automated flow injection methods are frequently used for these analyses. In this work, we propose a new method of direct laser photo-induced fluorescence analysis. This new method is based on direct irradiation of the analyte in a fluorimetric cell in order to form a photo-induced fluorescent compound and its direct fluorimetric detection during a short irradiation time. Irradiation is performed with a tuneable Nd:YAG laser to select the optimal excitation wavelength and to improve the specificity. It has been applied to the determination of bisphenol A, an endocrine disrupter compound that may be a potential contaminant for food. Irradiation of bisphenol A at 230 nm produces a photo-induced compound with a much higher fluorescence quantum yield and specific excitation/emission wavelengths. In tap water, the fluorescence of bisphenol A increases linearly versus its concentration and, its determination by direct laser photo-induced fluorescence permits to obtain a low limit of detection of 17 μg L(-1).
Abstract: The synthesis of cationic lipo-thiophosphoramidates, a new family of cationic lipids designed for gene delivery, is reported herein. This new class of lipids is less polar than its oxygenated equivalent the lipo-phosphoramidates. Fluorescence anisotropy and FRET were used to determine the fluidity and fusogenicity of the lipo-phosphoramidates 3a-b and lipo-thiophosphoramidates 7a-b. The determination of both the size and the zeta potential of the nano-objects (liposomes and lipoplexes) and the determination of the DNA binding ability of the liposomes have completed the physico-chemical characterizations of the cationic lipids studied. Finally, the cationic lipids 3a-b and 7a-c have been evaluated as synthetic vectors for gene transfection into a variety of mammalian cell lines. The lipo-thiophosphoramidate 7a proved to be an efficient and low toxicity synthetic vector even when used at low lipid to DNA charge ratios.
Abstract: This work presents spectroscopic properties of some Endocrine Disrupting Compounds (EDCs), frequently found in food and in natural water. Studied molecules belong to the groups of phenolic and phthalate EDCs. In a first part, we have examined their absorption and fluorescence properties. Fluorescence emission wavelengths are about 300 nm for phenolic compounds and 360 nm for phtalate compounds; main excitation wavelengths being comprised between 210 nm and 230 nm. Fluorescence lifetimes measured are short (about 4 ns) and the fluorescence quantum yield has been determined. In a second part, to avoid the time consuming solvent extraction step, an analytical application to evaluate the performance of a direct analysis by laser induced fluorescence spectroscopy of ECDs traces in tap water and in raw water is presented. Good detection limits have been obtained, i.e.: 0.35 µg.L(-1) of chlorophenol in tap water, which are always lower than the reported Predictive Non Efficient Concentration (PNEC).
Abstract: In this study, direct determination of mercury at the nanogram per liter level in the complex seawater matrix by imaging time-resolved electrothermal atomization laser-excited atomic fluorescence spectrometry (ITR-ETA-LEAFS) is described. In the case of mercury, the use of a nonresonant line for fluorescence detection with only one laser excitation is not possible. For measurements at the 253.652 nm resonant line, scattering phenomena have been minimized by eliminating the simultaneous vaporization of salts and by using temporal resolution and the imaging mode of the camera. Electrothermal conditions (0.1 M oxalic acid as matrix modifier, low atomization temperature) have been optimized in order to suppress chemical interferences and to obtain a good separation of specific signal and seawater background signal. For ETA-LEAFS, a specific response has been obtained for Hg with the use of time resolution. Moreover, an important improvement of the detection limit has been obtained by selecting, from the furnace image, pixels collecting the lowest number of scattered photons. Using optimal experimental conditions, a detection limit of 10 ng L(-1) for 10 μL of sample, close to the lowest concentration level of total Hg in the open ocean, has been obtained.
Abstract: Two methods available for direct determination of total Fe in seawater at low concentration level have been examined: electrothermal atomization atomic absorption spectrometry (ETAAS) and electrothermal atomization laser excited atomic fluorescence spectrometry (ETA-LEAFS). In a first part, we have optimized experimental conditions of ETAAS (electrothermal program, matrix chemical modification) for the determination of Fe in seawater by minimizing the chemical interference effects and the magnitude of the simultaneous background absorption signal. By using the best experimental conditions, a detection limit of 80 ng L(-1) (20 microL, 3sigma) for total Fe concentration was obtained by ETAAS. Using similar experimental conditions (electrothermal program, chemical modification), we have optimized experimental conditions for the determination of Fe by LEAFS. The selected experimental conditions for ETA-LEAFS: excitation wavelength (296.69 nm), noise attenuation and adequate background correction led to a detection limit (3sigma) of 3 ng L(-1) (i.e. 54 pM) for total Fe concentration with the use a 20 microL seawater sample. For the two methods, concentration values obtained for the analysis of Fe in a NASS-5 (0.2 microg L(-1)) seawater sample were in good agreement with the certified values.
Abstract: This study examined the potential metal pollution induced by the accidental spill of different acids into seawater. The acids sink to the bottom according to their densities and subsequently react with marine sediments. The acids selected for this study were acetic, hydrochloric, nitric, sulfuric, and phosphoric acids; the metallic elements selected were Cr, Cu, Fe, Mn, Pb and Zn. The sediment was collected in Brest Harbour. The percentages of metals released from this sediment in the presence of various concentrations of acids in seawater were important; concentrations of approximately 7 mg L(-1) for Mn and 60 mg L(-1) for Zn were observed under our experimental conditions. We also examined the rate of release of these metals from the sediment into the seawater in the presence of the different acids and under different experimental conditions. We found that most of the metallic elements were released from the sediments into the seawater during the first fifteen minutes of exposure. After this time, a high degree of pollution was induced if acids leached into seawater were not rapidly diluted.
Abstract: Cationic lipophosphoramidates constitute a class of cationic lipids we have previously reported to be efficient for gene transfection. Here, we synthesized and studied a novel lipophosphoramidate derivative characterized by an arsonium headgroup linked, via a phosphoramidate linker, to an unconventional lipidic moiety consisting of two diunsaturated linoleic chains. Physicochemical studies allowed us to comparatively evaluate the specific fluidity and fusogenicity properties of the liposomes formed. Although corresponding lipoplexes exhibited significant but relatively modest in vitro transfection efficiencies, they showed a remarkably efficient and reproducible ability to transfect mouse lung, with in vivo transfection levels higher than those observed with a monounsaturated analogue previously described. Thus, these results demonstrate that this diunsaturated cationic lipophosphoramidate constitutes an efficient and versatile nonviral vector for gene transfection. They also invite further evaluations of the transfection activity, especially in vivo, of gene delivery systems incorporating the lipid reported herein and/or other lipids bearing polyunsaturated chains.
Abstract: We report here a study on the physicochemical properties of cationic phospholipids liposomes used for lipoplex formulation and DNA transfer. The original cationic phospholipids synthesized in our laboratory are first presented with the liposome formulation process. The second part deals with the liposomes fusogenic properties studied by fluorescence resonant energy transfer (FRET). The nature of the cationic polar head and the formulation with or without a neutral colipid have a great influence on the FRET signal. The third part reports the study of the viscosity of the liposome by fluorescence anisotropy measurements. It has been observed that the vectors having a saturated lipid chain exhibit a more pronounced anisotropy than those having unsaturated lipid chains. Finally, liposomes formed by a mixture of phospholipids and DC-Chol (a rigid lipid) leads to increase the anisotropy denoting a more rigid liposome.
Abstract: The behaviour of three South African coals in water and, particularly in seawater, was examined. A sequential speciation procedure used to evaluate trace metal partitioning in coal has shown that trace metals will not be easily released from these coals into environmental ecosystems. Only a few trace elements are slightly leached from these coals into water or seawater at pH around 8. On the other hand, Mn is highly leached from these coals into water or seawater. It has been clearly shown that Mn concentrations are highly correlated to sulfate and calcium concentrations indicating that Mn is mainly solubilized into water simultaneously to gypsum; the leaching efficiency being severely reduced for coal having a high calcite content. The leaching percentage of Mn into seawater is enhanced by the presence of seawater salts that increases gypsum solubility. The leaching process of Mn from coal into water or seawater is governed by gypsum solubilization and is relatively rapid during the first thirty minutes, then very slow. In this study, it has been also shown that, depending on their physico-chemical properties, trace metals may be removed from seawater solutions in the presence of coal having a high calcite content. In this work, it has been also shown that some elements, particularly Fe, are greatly solubilized into seawater in the presence of a strong chelating agent like EDTA. Like for Mn, the leaching rate of metals from coal in the presence of EDTA is relatively rapid during the first 30 min then much slower, suggesting a solubilization process simultaneously to gypsum or/and calcite solubilization.
Abstract: Whenever immersed in seawater after a collier accident, a fossil fuel such as coal could become a source of pollution to the marine environment. To study the effect of such a contamination, four coal samples from different origins were used. A first analysis on those coals enabled us to determine the content of polycyclic aromatic hydrocarbons. Seawater was then mixed with coal to study the organic matter released from coal into seawater. Fluorescence was used for its sensitivity to aromatic compounds, with the additional purpose of evaluating the relevance of using an immersed fluorescence probe to monitor water pollution. Excitation-emission matrices were recorded and the excitation-emission wavelength range corresponding to the highest fluorescence intensity was 230 nm/[370 nm; 420 nm]. The samples with coal happened to fluoresce more than the coal-free samples, the difference depending on the coal origin. The fluorescence intensity increased with coal mass, up to some limit. The particle size also influenced the fluorescence intensity, the finest particles releasing more fluorescing substances, due to their higher exchange surface. When seawater percolated through coal, the samples fluoresced highly at the beginning, and then the fluorescence intensity decreased and reached the seawater level. However, even with a 10 ns acquisition time shift, the fluorescence spectra were not specific enough to show the presence of PAHs in the samples, which were too diluted to be detected, whenever released from coal into seawater. The lifetimes of the seawater and of the coal samples were respectively 4.7 and 3.8 ns, indicating that the substances released from coal mainly consisted of short-lived fluorescing substances, such as natural humic or fulvic substances. Consequently, the presence of coal does not seem to be too detrimental to the marine environment, and a direct fluorescence probe could be used to monitor the seawater organic charge increase due to the immersion of coal in seawater.
Abstract: The DNA compacting properties of polyamines (especially spermine) are well-known, hence the use of spermine as the cationic part in several synthetic DNA carriers. Here, we describe the synthesis of modified spermines, with a "lipophosphoramidate" as the lipidic part, and their use for efficient in vitro transfection. Physicochemical measurements (particle size, zeta potentials, pKa determination) and gel retardation assays were also performed. Theoretical membrane-disrupting ability was established by FRET. Taken together, our results indicate that lipophosphoramidates constitute an interesting alternative to "classical" lipidic parts of cationic lipids used as DNA carriers.
Abstract: Coal is currently becoming an increasingly interesting fossil energy resource and that is the reason why its maritime transport, and hence the risk of collier accidents, increase. In this work, the environmental impact of an accidental coal immersion at sea is studied: the physicochemical effects are estimated using innovative experimental setups--a laboratory seawater canal called "polludrome" is used to evaluate the behaviour of coal particles submitted to a seawater flow, and a specifically designed tub is used to study the physicochemical consequences induced when coal is introduced into continuously renewed seawater. When coal is introduced into seawater, the most easily visible consequences are physical: fine coal particles reduce the daylight penetration up to 100% and move along with the flow, and coal chunks accumulate on the floor. Chemical effects are also measured: humic matters are dissolved from coal into seawater (up to 2 mg L(-1)), but no release of polycyclic aromatic hydrocarbons is evidenced. Some inorganic compounds are dissolved, among which manganese, whose concentrations can reach 1 microg L(-1). Fortunately, the results show that the environmental impact of this type of accident would remain limited.
Abstract: The absorption and fluorescence spectra of carbaryl (CB), carbofuran (CF) and carbendazim (MBC) have been studied. Fluorescence lifetime and fluorescence quantum yields are also reported as well as the influence of pH, solvent and presence of humic acids on fluorescence. The limit of detection (LD) of the three compounds has been measured by direct analysis by laser-induced fluorescence (LIF) using a pulsed YAG laser with an Optical Parametric Oscillator (OPO) as excitation source and an Intensified Charged Coupled Device (ICCD) camera for the fluorescence detection. Instrumental LD found for CB, for MBC and for CF are respectively 4, 50 and 1000 ng L(-1). In tap water, the LD obtained is 800 ng L(-1) for MBC and 20,000 ng L(-1) for CF. For CB, the use of a time shift between excitation and emission allows to reach a LD of 20 ng L(-1) in tap water.
Abstract: Fluorescence was induced by coupling a laser with an optical parametric oscillator (OPO) to develop an analytical method for the direct determination of lead content, at ultra-trace level, in seawater by electrothermal atomization-laser-excited atomic fluorescence (ETA-LEAF). The optimization of atomization conditions, laser pulse energy, and mainly temporal parameters allowed us to reach a 3 fg detection limit (0.3 ng L(-1)) despite the low repetition rate of the device. The expected error on predicted concentrations of lead, at trace levels, in seawater was below 15%.
Abstract: This paper presents a synthesis of some analytical potentialities of an equipment designed for both laser induced molecular and atomic fluorescence in the field of ultra-trace analysis (ng l(-1)). Excitation of fluorescence was performed with a pulsed Nd:Yag laser coupled to an optical parametric oscillator (OPO). Fluorescence spectra were recorded with a spectrograph and an intensified charge-coupled device (ICCD). The high energy and the tunability of the excitation combined with the sensitivity of the ICCD and the time-resolution provide better limit of detection (LOD) and selectivity. By molecular fluorescence, some major organic contaminants in the environment were studied, i.e. polycyclic aromatic hydrocarbons (PAHs) (benzo[a]pyrene and hydroxypyrene) and a pesticide (carbaryl). The LODs achieved by direct analysis were far below the restricted European values for tap water. Analysis was performed in water containing humic acids using time resolution to avoid the matrix fluorescence. By electro thermal atomisation-laser excited atomic fluorescence (ETA-LEAF), we detected traces of aluminium and lead in seawater. Some general considerations about the signal to noise ratio optimisation are reported. LODs reached the femtogram level.
Abstract: This study deals with the optimisation and application of a method for direct analysis of trace pollutants in water by laser-induced fluorescence. The arrangement used consisted of an Nd:YAG Laser coupled with an optical parametric oscillator (LYOPO) and connected to a spectrophotometer and a high-sensitivity camera. Optimisation was achieved by developing an experimental design methodology to maximise the signal-to-noise ratio and reduce the limit of detection. The technique was then applied to the detection of benzo[ a]pyrene in water. The experimental results were evidence of its high sensitivity and time-resolution potential. The detection limit for benzo[ a]pyrene was 0.7 ng L(-1) in drinking water and 4 ng L(-1) in raw water containing 1 mg L(-1) humic acids.
