Rapidly liver-clearable rare-earth core-shell nanoprobe for dual-modal breast cancer imaging in the second near-infrared window.

BACKGROUND: Fluorescence imaging as the beacon for optical navigation has wildly developed in preclinical studies due to its prominent advantages, including noninvasiveness and superior temporal resolution. However, the traditional optical methods based on ultraviolet (UV, 200-400 nm) and visible light (Vis, 400-650 nm) limited by their low penetration, signal-to-noise ratio, and high background auto-fluorescence interference. Therefore, the development of near-infrared-II (NIR-II 1000-1700 nm) nanoprobe attracted significant attentions toward in vivo imaging. Regrettably, most of the NIR-II fluorescence probes, especially for inorganic NPs, were hardly excreted from the reticuloendothelial system (RES), yielding the anonymous long-term circulatory safety issue. RESULTS: Here, we develop a facile strategy for the fabrication of Nd3+-doped rare-earth core-shell nanoparticles (Nd-RENPs), NaGdF4:5%Nd@NaLuF4, with strong emission in the NIR-II window. What's more, the Nd-RENPs could be quickly eliminated from the hepatobiliary pathway, reducing the potential risk with the long-term retention in the RES. Further, the Nd-RENPs are successfully utilized for NIR-II in vivo imaging and magnetic resonance imaging (MRI) contrast agents, enabling the precise detection of breast cancer. CONCLUSIONS: The rationally designed Nd-RENPs nanoprobes manifest rapid-clearance property revealing the potential application toward the noninvasive preoperative imaging of tumor lesions and real-time intra-operative supervision.

Effect of the dose on the toxicokinetics of a quaternary mixture of rare earth elements administered to rats.

Large human biomonitoring studies are starting to assess exposure to rare earth elements (REEs). Yet, there is a paucity of data on the toxicokinetics of these substances to help interpret biomonitoring data. The objective of the study was to document the effect of the administered dose on the toxicokinetics of REEs. Male Sprague-Dawley rats were injected intravenously with 0.3, 1 or 10 mg/kg body weight (bw) of praseodynium chloride (PrCl3), cerium chloride (CeCl3), neodymium chloride (NdCl3) and yttrium chloride (YCl3) administered together as a mixture. Serial blood samples were withdrawn up to 72 h following injection, and urine and feces were collected at predefined time intervals up to 7 days post-dosing. The REEs were measured by Inductively Coupled Plasma Mass Spectrometry (ICP-MS). For a given REE dose, the time courses in blood, urine and feces were similar for all four REEs. However, the REE dose administered significantly impacted their kinetics, as lower cumulative excretion in urine and feces was associated with higher REE doses. The fraction of REE remaining in rat tissues at the terminal necropsy on post-dosing day 7 also increased with the dose administered, most notably in the lungs and spleen at the 10 mg/kg bw dose. The toxicokinetic parameters calculated from the blood concentration-time profiles further showed significant increases in the mean residence time (MRTIV) for all four REEs at the 10 mg/kg bw dose. The shift in the REE kinetics at high dose may be explained by a higher retention in lysosomes, the main organelle responsible for accumulation of these REEs in different tissues.

Synthesis and application of alginate immobilised banana peels nanocomposite in rare earth and radioactive minerals removal from mine water.

This study describes the preparation, characterisation and application of pelletised immobilised alginate/montmorillonite/banana peels nanocomposite (BPNC) in a fixed-bed column for continuous adsorption of rare earth elements and radioactive minerals from water. The materials was characterised by Fourier transform infrared, X-ray diffraction and scanning electron microscopy analyses. Analyses indicated that the pellets are porous and spherical in shape. FT-IR analysis showed that the functional groups responsible for the coordination of metal ions were the carboxylic (-COO-) and siloxane (Si-O-Si and Si-O-Al) groups. XRD analysis showed two additional peaks which were attributed to alginate and montmorillonite. The influence of the initial concentration, bed depth and flow rate were investigated using synthetic and real mine water in order to determine the breakthrough behaviour of both minerals. The processed bed volume, adsorbent exhaustion rate and service time, were also explored as performance indices for the adsorbent material. Furthermore, the breakthrough data were fitted to both the Thomas and Bohart-Adams models. The BPNC exhibited high affinity for U, Th, Gd and La in the real mine water sample. However, studies may still be required using waters from different environments in order to determine the robustness of BPNC.

Seasonal changes in concentrations of trace elements and rare earth elements in shoot samples of Juncus effusus L. collected from natural habitats in the Holy Cross Mountains, south-central Poland.

Selected trace elements (Ag, As, Ba, Bi, Cd, Co, Cr, Mn, Cu, Fe, Ni, Pb, Tl, U, Zn) and rare earth elements were determined in 13 samples of Juncus effusus collected from three investigation sites in the Holy Cross Mts., south-central Poland. Sampling was carried out four times during a vegetative season of 2014. Almost all the elements examined showed different seasonal trends in their concentrations, except for Ag, Co and Ni. Maximum concentrations of Ag in samples of three investigation sites were found in May (0.068, 0.062, 0.047 mg/kg) whereas Co (0.124, 0.070, 0.079 mg/kg) and Ni (1.8, 0.998, 2.8 mg/kg) in July, respectively. Mean concentrations of Mn and Cd were higher in shoots (558 and 2.35 mg/kg) than in roots (435 and 1.7 mg/kg). Both these elements revealed much higher concentrations in J. effusus than their typical contents in plant samples. Principal component method allowed us to allocate Ni, Ba, Cd and Cu to one group with the highest positive loadings. The most probable explanation for this correlation is that bioavailability of these metals is increased by J. effusus through a release of oxygen to the rhizosphere. Light rare earth elements concentrations predominate over heavy rare earth elements in the samples examined. A fractionation of lanthanides occurs during their transport from roots to shoots, although this transport is rather limited. All shoot samples have a strong positive Eu anomaly.

Phytotoxicity of individual and binary mixtures of rare earth elements (Y, La, and Ce) in relation to bioavailability.

Rare earth elements (REEs) are typically present as mixtures in the environment, but a quantitative understanding of mixture toxicity and interactions of REEs is still lacking. Here, we examined the toxicity to wheat (Triticum aestivum L.) of Y, La, and Ce when applied individually and in combination. Both concentration addition (CA) and independent action (IA) reference models were used for mixture toxicity analysis because the toxicity mechanisms of REEs remain obscure. Upon single exposure, the EC50s of Y, La, and Ce, expressed as dissolved concentrations, were 1.73 ±â€¯0.24 µM, 2.59 ±â€¯0.23 µM, and 1.50 ±â€¯0.22 µM, respectively. The toxicity measured with relative root elongation followed La < Y ≈ Ce, irrespective of the dose descriptors. The use of CA and IA provided similar estimates of REE mixture interactions and toxicity. When expressed as dissolved metal concentrations, nearly additive effects were observed in Y-La and La-Ce mixtures, while antagonistic interactions were seen in Y-Ce mixtures. When expressed as free metal activities, antagonistic interactions were found for all three binary mixtures. This can be explained by a competitive effect of REEs ions for binding to the active sites of plant roots. The application of a more elaborate MIXTOX model in conjunction with the free ion activities, which incorporates the non-additive interactions and bioavailability-modifying factors, well predicted the mixture toxicity (with >92% of toxicity variations explained). Our results highlighted the importance of considering mixture interactions and subsequent bioavailability in assessing the joint toxicity of REEs.

Biouptake of a rare earth metal (Nd) by Chlamydomonas reinhardtii - Bioavailability of small organic complexes and role of hardness ions.

A green alga, Chlamydomonas reinhardtii, was used to verify whether a simple Biotic Ligand Model (BLM) could be used to predict carefully controlled short-term biouptake for the lanthanide, Nd. In the absence of ligands or competitors, Nd biouptake was well described by a Michaelis-Menten equation with an affinity constant, KNd, of 106.8 M-1 and a maximum internalization flux of Jmax = 1.70 × 10-14 mol cm-2 s-1. For bi-metal mixtures containing Nd and Ca, Mg, Sm or Eu, Nd uptake could also be well modelled by assigning experimentally determined affinity constants of KCa = 102.6 M-1, KMg = 103.4 M-1, KSm = 106.5 M-1 and KEu = 106.5 M-1. The similar values of Km and Jmax for the three rare earth elements (REEs): Sm, Eu and Nd is consistent with them sharing a common metal uptake site. On the other hand, in the presence of the small organic ligands (citric or malic acid), neither, free or total Nd concentrations could be used to quantitatively predict Nd internalization fluxes. In other words, in order to predict biouptake by simple BLM determinations, it was necessary to consider that the Nd complexes were bioavailable. The data strongly suggest that risk evaluations of the REE will require a new paradigm and new tools for evaluating bioavailability.

A novel approach for acid mine drainage pollution biomonitoring using rare earth elements bioaccumulated in the freshwater clam Corbicula fluminea.

Lanthanide series have been used as a record of the water-rock interaction and work as a tool for identifying impacts of acid mine drainage (lixiviate residue derived from sulphide oxidation). The application of North-American Shale Composite-normalized rare earth elements patterns to these minority elements allows determining the origin of the contamination. In the current study, geochemical patterns were applied to rare earth elements bioaccumulated in the soft tissue of the freshwater clam Corbicula fluminea after exposure to different acid mine drainage contaminated environments. Results show significant bioaccumulation of rare earth elements in soft tissue of the clam after 14 days of exposure to acid mine drainage contaminated sediment (ΣREE=1.3-8µg/gdw). Furthermore, it was possible to biomonitor different degrees of contamination based on rare earth elements in tissue. The pattern of this type of contamination describes a particular curve characterized by an enrichment in the middle rare earth elements; a homologous pattern (EMREE=0.90) has also been observed when applied NASC normalization in clam tissues. Results of lanthanides found in clams were contrasted with the paucity of toxicity studies, determining risk caused by light rare earth elements in the Odiel River close to the Estuary. The current study purposes the use of clam as an innovative "bio-tool" for the biogeochemical monitoring of pollution inputs that determines the acid mine drainage networks affection.

Rare earth elements in human and animal health: State of art and research priorities.

BACKGROUND: A number of applications have been developed using rare earth elements (REE), implying several human exposures and raising unsolved questions as to REE-associated health effects. METHODS: A MedLine survey was retrieved from early reports (1980s) up to June 2015, focused on human and animal exposures to REE. Literature from animal models was selected focusing on REE-associated health effects. RESULTS: Some REE occupational exposures, in jobs such as glass polishers, photoengravers and movie projectionists showed a few case reports on health effects affecting the respiratory system. No case-control or cohort studies of occupational REE exposures were retrieved. Environmental exposures have been biomonitored in populations residing in REE mining areas, showing REE accumulation. The case for a iatrogenic REE exposure was raised by the use of gadolinium-based contrast agents for nuclear magnetic resonance. Animal toxicity studies have shown REE toxicity, affecting a number of endpoints in liver, lungs and blood. On the other hand, the use of REE as feed additives in livestock is referred as a safe and promising device in zootechnical activities, possibly suggesting a hormetic effect both known for REE and for other xenobiotics. Thus, investigations on long-term exposures and observations are warranted. CONCLUSION: The state of art provides a limited definition of the health effects in occupationally or environmentally REE-exposed human populations. Research priorities should be addressed to case-control or cohort studies of REE-exposed humans and to life-long animal experiments.

Biotic ligand model does not predict the bioavailability of rare Earth elements in the presence of organic ligands.

Due to their distinct physicochemical properties, rare earth elements (REEs) are critical to high-tech and clean-energy industries; however, their bioavailability is still largely unexplored. In this paper, the bioavailability of several REEs has been carefully examined for the freshwater alga, Chlamydomonas reinhardtii. In the presence of organic ligands (L), the biouptake of REEs was much higher than that predicted by the biotic ligand model (BLM). Enhancement of the biouptake flux was observed for six ligands (metal = thulium) and six REEs (ligand = citric acid), indicating that this could be a common feature for these metals. In order to explore the mechanism for the enhanced uptake, Tm internalization was carefully evaluated. The Tm internalization flux (Jint) followed first-order (Michaelis-Menten) kinetics with a calculated maximum internalization flux (Jmax) of (1.1 ± 0.08) × 10(-14) mol · cm(-2) · s(-1) and an affinity constant for the reaction of the metal with the transport sites (KTm-R) of 10(7.1) M(-1). In the presence of citric acid, malic acid, or NTA, the Jint for Tm was more than 1 order of magnitude higher than that predicted by the BLM when algae were exposed to a constant 10(-9) M Tm(3+). The bioavailability of the metal complexes could not be explained by a piggyback internalization (through an anion channel) or the contribution of labile complexes. The enhanced biouptake was attributed to the formation of a ternary Tm complex {L-Tm-R} at the metal transport site. In the natural environment where organic ligands are ubiquitous, classic models are unlikely to predict the bioavailability of REEs to aquatic organisms.

Accumulation of rare earth elements by siderophore-forming Arthrobacter luteolus isolated from rare earth environment of Chavara, India.

In this study, Arthrobacter luteolus, isolated from rare earth environment of Chavara (Quilon district, Kerala, India), were found to produce catechol-type siderophores. The bacterial strain accumulated rare earth elements such as samarium and scandium. The siderophores may play a role in the accumulation of rare earth elements. Catecholate siderophore and low-molecular-weight organic acids were found to be present in experiments with Arthrobacter luteolus. The influence of siderophore on the accumulation of rare earth elements by bacteria has been extensively discussed.

Ethylene diamine tetramethylene phosphonic acid labeled with various ß(-)-emitting radiometals: labeling optimization and animal biodistribution.

Skeletal uptake of ß(-)-emitting radionuclides may be used for bone pain palliation or myeloablation. The physical characteristics of the ß(-) particles required for the two conditions are, however, different, that is, higher energies are favorable for destruction of bone marrow. In this study, the labeling conditions of ethylene diamine tetramethylene phosphonic acid (EDTMP) with three rare earth metals (90Y, 166Ho, and 177Lu) having ß(-) particles of diverse physical characteristics were optimized, and their animal biodistributions were studied and compared with 153Sm-EDTMP. All the four radiometals (X = 90Y, 166Ho, 177Lu, and 153Sm) were produced from n,γ reactions of their respective precursors (89Y, 165Ho, 176Lu, and 152Sm). They were labeled with EDTMP at varying degrees of pH and molar ratios, and labeling yields were determined by paper chromatography at each data point. The complexes with optimal labeling yields and their chloride forms (XCl3) were then studied for biodistributions in 66 Sprague-Dawley male rats at 30 minutes, 2 hours, and 24 hours after injection. All the radiopharmaceuticals gave ∼98% complex yields at pH 8. At optimum pH level, good labeling was achieved at X:EDTMP molar ratios of 1:5, 1:8, and 1:20 for 90Y, 166Ho, and 177Lu complexes, respectively. 177Lu-EDTMP showed the best biodistribution results among all the complexes, with a total skeletal uptake of 70.2% ± 2.4% at 24 hours ((153)Sm-EDTMP = 59.1% ± 2.6%). 90Y-EDTMP had skeletal accumulation significantly higher than (166)Ho-EDTMP (45.5% ± 2.9% and 27.4% ± 3.6%, respectively). Blood activity of all the agents disappeared promptly through the kidneys. This study demonstrates higher localization of 177Lu-EDTMP in skeleton than 153Sm-EDTMP and shows that the localization of 90Y-EDTMP is better among the high-energy radiometals studied.

Accumulation of rare earth elements in human bone within the lifespan.

For the first time, the contents of rare earth elements (REEs) in a rib bone of a healthy human were determined. The mean value of the contents of Ce, Dy, Er, Gd, La, Nd, Pr, Sm, Tb, and Yb (10 elements out of 17 total REEs), as well as the upper limit of means for Ho, Lu, Tm, and Y (4 elements) were measured in the rib bone tissue of 38 females and 42 males (15 to 55 years old) using inductively coupled plasma mass spectrometry (ICP-MS). We found age-related accumulation of REEs in the bone tissue of healthy individuals who lived in a non-industrial region. It was calculated that during a lifespan the content of REEs in a skeleton of non-industrial region residents may increase by one to two orders of magnitude. Using our results as indicative normal values and published data we estimated relative Gd accumulation in the bone tissue of patients according to magnetic resonance imaging with contrast agent and La accumulation in the bone tissue of patients receiving hemodialysis after treatment with lanthanum carbonate as a phosphate binder. It was shown that after such procedures contents of Gd and La in the bone tissue of patients are two to three orders of magnitude higher than normal levels. In our opinion, REEs incorporation may affect bone quality and health similar to other potentially toxic trace metals. The impact of elevated REEs content on bone physiology, biochemistry and morphology requires further investigation.

Particle deposition in the lung of the Göttingen minipig.

We report on particle deposition in the tracheobronchial and pulmonary regions of the respiratory tract of the minipig and its dependence on particle size. Four animals breathing spontaneously via the nose were exposed for 1 h to known concentrations of three different polydisperse dry aerosols composed of bovine serum albumin (BSA) and an oxide of a rare earth element: Y2O3, Sm2O3, and Er2O3. The mass size distributions of the rare earth elements of the three test aerosols have mass median aerodynamic diameters of 0.9, 2.5, and, 4.3 microm, and geometric standard deviations of sigma(g) = 2.0, 1.8, and, 1.7. The extrathoracic, tracheobronchial, and pulmonary regions of the respiratory tract were dissected, separately lyophilized, and chemically digested by microwave-assisted high pressure digestion. The tracer element in each compartment was determined by inductively coupled plasma mass spectrometry. A mass balance equation relating the tracer mass found in the lung compartments to the tracer mass inhaled was solved by linear regression to obtain the deposition fraction as function of particle sizes for the tracheobronchial and the pulmonary lung region. Estimated values for the respiratory minute volume were used in this context. For coarse particles > 6 microm, the deposition fraction is < 5% for both compartments. The deposition fraction for particles with aerodynamic diameter of approximately 3 microm is 21% in the tracheobronchial airways and 40% in the pulmonary airways.

[Study on the characteristics of content and distribution of light rare earth elements in rat testes].

OBJECTIVE: To study the characteristics of content and distribution of light Rare Earth Elements (LREEs) in rat testes. METHODS: Based on animal weight, 60 healthy male SD rats were randomly divided into two control groups and four experimental groups. After four week treat, the testes were collected except High-II . The High- II group was freely fed for another four week without the Citrate REEs. The LREE concentrations in the testes were determined by the inductively coupled plasma mass spectrometer (ICP-MS). RESULTS: (1) The concentrations of LREEs in testes increased with the increase of the doses. The concentrations of LREEs of High-II were much lower than those of High-I significantly (P < 0.05). (2) The distribution patterns of La, Ce, Pr in the testes approximated to the Odd Harkin's rule, but the Nd was an exception (negative deviation). 3. The correlation coefficients of LREEs concentrations between hair and testis were about 0.4, while those between blood and testis were much lower and have no significance. CONCLUSION: (1) Dose response relationship could exist in the accumulation of LREEs in the rat testes. (2) Testis could have its own distribution pattern of LREEs. (3) The accumulation of LREEs in testis could be reversible. (4) As it was, a biomarker of the LREEs in hair could be much better than that of blood.

[Correlation of light rare earth elements in rats hair, blood and organs].

OBJECTIVE: To study the correlation of rare earth elements (REEs) in the rats' hair, blood and organs. METHODS: Based on the level of animal weights, 50 healthy male SD rats were randomly divided into five groups including control group and four Citrate REEs level groups (low, middle, high-I and high-II). Before the experiment, the hair of rats' back was eliminated. After the rats were fed for four weeks, the fresh hair of the rats was collected. Except the high-II group, the blood and organs of the others were collected. The high-II group was fed for other four weeks without Citrate REEs. At the end of eighth week, hair, blood and organs of the high-II group were collected. Determination of light REEs concentration in the rats' hair, blood, liver, spleen and bone by ICP-MS. RESULTS: The correlation coefficients of REEs concentration between hair and organs (such as liver, spleen and bone) were more than 0.5, while those of REEs concentration between blood and organs (such as liver spleen and bond) were less than 0.5. In the group H- Il, the Rees concentration in blood, hair, liver, spleen and bone were all decrease, and the REEs concentration of blood was close to that of the control groups. CONCLUSION: The concentrations of REEs in these organs were different. And hair was better than blood as a biomarker to reflect body exposure of REEs.

Selective accumulation of light or heavy rare earth elements using gram-positive bacteria.

The accumulation of samarium from a solution only containing samarium by Arthrobacter nicotianae was examined. The amount of accumulated samarium was strongly affected by the concentration of samarium and pH of the solution. The accumulation of samarium by the strain was very rapid and reached equilibrium within 3h. The accumulation of samarium-europium or europium-gadolinium from the solution containing the two metals using various actinomycetes and gram-positive bacteria was also examined. Most of the tested strains could accumulate similar amounts of samarium and europium; however, most of the tested strains could accumulate a greater amount of europium than gadolinium. Especially, the amounts of accumulated europium using gram-positive bacteria were higher than those using actinomycetes. The selective accumulations of light or heavy rare earth elements (REEs) using A. nicotianae and Streptomyces albus were also examined. The amounts of accumulated samarium and europium were higher than those of the other light REEs using both microorganisms. S. albus can accumulate greater lutetium than other REEs from a solution containing yttrium and eight heavy REEs. On the other hand, A. nicotianae can accumulate higher amounts of terbium and ytterbium than that of the other heavy REEs from the same solution. A. nicotianae can also accumulated higher amounts of Sm than other REEs from a solution containing six light REEs.

Structural differences between light and heavy rare earth element binding chlorophylls in naturally grown fern: Dicranopteris linearis.

Chloroplasts and chlorophylls were isolated from the leaves of Dicranopteris linearis, a natural perennial fern sampled at rare earth element (REE) mining areas in the South-Jiangxi region (southern China). The inductively coupled plasma-mass spectrometry (ICP-MS) results indicated that REEs were present in the chloroplasts and chlorophylls of D. linearis. The in vivo coordination environment of light REE (lanthanum) or heavy REE (yttrium) ions in D. linearis chlorophyll-a was determined by the extended X-ray absorption fine structure (EXAFS). Results revealed that there were eight nitrogen atoms in the first coordination shell of the lanthanum atom, whereas there were four nitrogen atoms in the first coordination shell of yttrium. It was postulated that the lanthanum-chlorophyll-a complex might have a double-layer sandwich-like structure, but yttrium-binding chlorophyll-a might be in a single-layer form. Because the content of REE-binding chlorophylls in D. linearis chlorophylls was very low, it is impossible to obtain structural characteristics of REE-binding chlorophylls by direct analysis of the Fourier transform infrared (FTIR) and ultraviolet (UV)-visible spectra of D. linearis chlorophylls. In order to acquire more structural information of REE-binding chlorophyll-a in D. linearis, lanthanum - and yttrium-chlorophyll-a complexes were in vitro synthesized in acetone solution. Element analyses and EXAFS results indicated that REE ions (lanthanum or yttrium) of REE-chlorophyll-a possessed the same coordination environment whether in vivo or in vitro. The FTIR spectra of the REE-chlorophyll-a complexes indicated that REEs were bound to the porphyrin rings of chlorophylls. UV-visible results showed that the intensity ratios of Soret to the Q-band of REE-chlorophyll-a complexes were higher than those of standard chlorophyll-a and pheophytin-a, indicating that REE-chlorophyll-a might have a much stronger ability to absorb the ultraviolet light. The MCD spectrum in the Soret band region of lanthanum-chlorophyll-a showed a special peak, but yttrium-chlorophyll-a did not have this special peak, corresponding well to their double-layer and single-layer structure, respectively.

Distribution characteristics of rare earth elements in children's scalp hair from a rare earths mining area in southern China.

In order to demonstrate the validity of using scalp hair rare earth elements (REEs) content as a biomarker of human REEs exposure, data were collected on REEs exposure levels from children aged 11-15 years old and living in an ion-adsorptive type light REEs (LREEs) mining and surrounding areas in southern China. Sixty scalp hair samples were analyzed by ICP-MS for 16 REEs (La Lu, Y and Sc). Sixteen REEs contents in the samples from the mining area (e.g., range: La: 0.14-6.93 microg/g; Nd: 0.09-5.27 microg/g; Gd: 12.2-645.6ng/g; Lu: 0.2-13.3 ng/g; Y: 0.03-1.27 microg/g; Sc: 0.05-0.30 microg/g) were significantly higher than those from the reference area (range: La: 0.04-0.40 microg/g; Nd: 0.04-0.32 microg/g; Gd: 8.3-64.6 ng/g; Lu: 0.4-3.3ng/g; Y: 0.03-0.29 microg/g; Sc: 0.11-0.36 microg/g) and even much higher than those published in the literature. The distribution pattern of REEs in scalp hair from the mining area was very similar to that of REEs in the mine and the atmosphere shrouding that area. In conclusion, the scalp hair REEs contents may indicate not only quantitatively but also qualitatively (distribution pattern) the absorption of REEs from environmental exposure into human body. The children living in this mining area should be regarded as a high-risk group with REEs (especially LREEs) exposure, and their health status should be examined from a REEs health risk assessment perspective.

Application of microwave extraction for the evaluation of bioavailability of rare earth elements in soils.

A single microwave extraction procedure was conducted to investigate the bioavailability of rare earth elements (REEs) by using different extractants of 0.05 M EDTA, 0.10 M CH3COOH, 0.10 M HCl, and 0.05 M CaCl2. The experimental conditions of heating time and microwave power were optimized. A microwave power of 60% and extraction time of 30 min were adopted. Compared to the conventional single extraction schemes reported in the literature, the recommended technique shortened the operational time, simplified the experimental task, improved the precision, and obtained consistent results with those obtained by using the conventional methods. In addition, the suggested microwave extraction method has been successfully used to evaluate the bioavailability of REEs in soils. Soil samples collected from 15 sites in China were extracted by four different extractants with microwave ancillary. Extractable REEs from soils were well correlated with REEs contents in shoots of wheat (Troticum aestivum L.) under the greenhouse conditions. The correlation coefficients were 0.6514-0.8996, 0.4522-0.7783, 0.6506-0.8671, 0.4869-0.7014 between the extractable REEs in soils and their concentrations in wheat shoots for the extractants of CaCl2, EDTA, CH3COOH and HCl, respectively.

Labile rhizosphere soil solution fraction for prediction of bioavailability of heavy metals and rare earth elements to plants.

A labile rhizosphere soil solution fraction has been recommended to predict the bioavailability of heavy metals and rare earth elements to plants. This method used moist rhizosphere soil in combination with a mixture of 0.01 mol L(-1) of low-molecular-weight organic acids (LMWOAs) as extractant. The extracted soil solutions were fractionated into two colloidal fractions of <0.45 microm (F(3)) and <0.2 microm (F(2)), and one truly dissolved fraction including free metal ions and inorganic and organic complexes (fractionr(0.2 microm, LMWOAs) approximately r(0.45 microm, LMWOAs). In the case of rare earth elements the good correlation was obtained for both the wheat roots and shoots. Generally, the correlation coefficients obtained by LMWAOs were better than that obtained by the first step of BCR method. Therefore, LMWAOs and F(lrss) were strongly recommended to predict the bioavailability of metals in soil pools to plants.