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1.
Metallomics ; 15(6)2023 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-37193668

RESUMEN

Aluminium, gallium, and indium are group 13 metals with similar chemical and physical properties. While aluminium is one of the most abundant elements in the Earth's crust, gallium and indium are present only in trace amounts. However, the increased use of the latter metals in novel technologies may result in increased human and environmental exposure. There is mounting evidence that these metals are toxic, but the underlying mechanisms remain poorly understood. Likewise, little is known about how cells protect themselves from these metals. Aluminium, gallium, and indium are relatively insoluble at neutral pH, and here we show that they precipitate in yeast culture medium at acidic pH as metal-phosphate species. Despite this, the dissolved metal concentrations are sufficient to induce toxicity in the yeast Saccharomyces cerevisiae. By chemical-genomic profiling of the S. cerevisiae gene deletion collection, we identified genes that maintain growth in the presence of the three metals. We found both shared and metal-specific genes that confer resistance. The shared gene products included functions related to calcium metabolism and Ire1/Hac1-mediated protection. Metal-specific gene products included functions in vesicle-mediated transport and autophagy for aluminium, protein folding and phospholipid metabolism for gallium, and chorismate metabolic processes for indium. Many of the identified yeast genes have human orthologues involved in disease processes. Thus, similar protective mechanisms may act in yeast and humans. The protective functions identified in this study provide a basis for further investigations into toxicity and resistance mechanisms in yeast, plants, and humans.


Asunto(s)
Galio , Humanos , Galio/toxicidad , Indio/toxicidad , Saccharomyces cerevisiae/genética , Aluminio/toxicidad , Genómica
2.
ACS Appl Mater Interfaces ; 14(1): 104-122, 2022 Jan 12.
Artículo en Inglés | MEDLINE | ID: mdl-34958199

RESUMEN

In orthopedic surgery, metals are preferred to support or treat damaged bones due to their high mechanical strength. However, the necessity for a second surgery for implant removal after healing creates problems. Therefore, biodegradable metals, especially magnesium (Mg), gained importance, although their extreme susceptibility to galvanic corrosion limits their applications. The focus of this study was to control the corrosion of Mg and enhance its biocompatibility. For this purpose, surfaces of magnesium-calcium (MgCa1) alloys were modified with calcium phosphate (CaP) or CaP doped with zinc (Zn) or gallium (Ga) via microarc oxidation. The effects of surface modifications on physical, chemical, and mechanical properties and corrosion resistance of the alloys were studied using surface profilometry, goniometry, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), nanoindentation, and electrochemical impedance spectroscopy (EIS). The coating thickness was about 5-8 µm, with grain sizes of 43.1 nm for CaP coating and 28.2 and 58.1 nm for Zn- and Ga-doped coatings, respectively. According to EIS measurements, the capacitive response (Yc) decreased from 11.29 to 8.72 and 0.15 Ω-1 cm-2 sn upon doping with Zn and Ga, respectively. The Ecorr value, which was -1933 mV for CaP-coated samples, was found significantly electropositive at -275 mV for Ga-doped ones. All samples were cytocompatible according to indirect tests. In vitro culture with Saos-2 cells led to changes in the surface compositions of the alloys. The numbers of cells attached to the Zn-doped (2.6 × 104 cells/cm2) and Ga-doped (6.3 × 104 cells/cm2) coatings were higher than that on the surface of the undoped coating (1.0 × 103 cells/cm2). Decreased corrosivity and enhanced cell affinity of the modified MgCa alloys (CaP coated and Zn and Ga doped, with Ga-doped ones having the greatest positive effect) make them novel and promising candidates as biodegradable metallic implant materials for the treatment of bone damages and other orthopedic applications.


Asunto(s)
Aleaciones/química , Fosfatos de Calcio/química , Materiales Biocompatibles Revestidos/química , Implantes Absorbibles , Aleaciones/toxicidad , Animales , Calcio/química , Calcio/toxicidad , Fosfatos de Calcio/toxicidad , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Materiales Biocompatibles Revestidos/toxicidad , Corrosión , Módulo de Elasticidad , Galio/química , Galio/toxicidad , Humanos , Magnesio/química , Magnesio/toxicidad , Ensayo de Materiales , Ratones , Humectabilidad , Zinc/química , Zinc/toxicidad
3.
Pharmacol Res ; 170: 105698, 2021 08.
Artículo en Inglés | MEDLINE | ID: mdl-34058327

RESUMEN

The emergence of pan-resistant strains in nosocomial settings underscores the urgent need of novel therapies targeting vital bacterial functions. Bacterial iron metabolism is a fascinating target for new antimicrobials. Iron mimetic metal Ga(III) has been repurposed as an antimicrobial drug, in pre-clinical studies and recent clinical studies have raised the possibility of using Ga(III) for the treatment of P. aeruginosa pulmonary infection. Ga(III) has been approved by FDA for the treatment of cancer, autoimmune and bone resorption disorders. However, some critical issues affect the therapeutic schedule of Ga(III), principally the intra-venous (i.v.) administration, and the nephrotoxicity caused by prolonged administration. Ga(III) aerosolization could represent a viable alternative for treatment of lung infections, since delivery of antimicrobial agents to the airways maximizes drug concentration at the site of infection, improves the therapeutic efficacy, and alleviates systemic toxic effects. We demonstrate the advantage of inhaled vs i.v. administered Ga(III), in terms of bio-distribution and lung acute toxicity, by using a rat model. In vivo results support the use of Ga(III) for inhalation since intra-tracheal Ga(III) delivery improved its persistence in the lung, while the i.v. administration caused rapid clearance and did not allow to attain a significant Ga(III) concentration in this organ. Moreover, local and systemic acute toxicity following intra-tracheal administration was not observed, since no significant signs of inflammation were found. At this stage of evidence, the direct administration of Ga(III) to the lung appears feasible and safe, boosting the development of Ga(III)-based drugs for inhalation therapy.


Asunto(s)
Antibacterianos/administración & dosificación , Galio/administración & dosificación , Pulmón/metabolismo , Administración por Inhalación , Administración Intravenosa , Aerosoles , Animales , Antibacterianos/farmacocinética , Antibacterianos/toxicidad , Disponibilidad Biológica , Galio/farmacocinética , Galio/toxicidad , Masculino , Ratas Wistar , Distribución Tisular
4.
Sci Total Environ ; 759: 143943, 2021 Mar 10.
Artículo en Inglés | MEDLINE | ID: mdl-33340855

RESUMEN

The emerging contaminants gallium (Ga) and indium (In) are extensively used in advanced industries and are considered as toxic to humans. Limited information is available on the dynamics of Ga and In in soil-upland crop systems. Therefore, this study aimed to investigate the effects of Ga and In on the growth and uptake of Ga and In by wheat plants grown in Ga- and In-contaminated soils. The wheat seedlings were planted in soils of different properties spiked with various Ga and In concentrations (50, 100, 200, and 400 mg kg-1). The plant-available Ga, In, and Al in the soils were extracted by 0.02 M CaCl2, and their concentrations in plant tissues of wheat seedlings and plant biomass were determined after harvesting. The results indicated that the Al toxicity of wheat seedlings increased with Ga and In concentrations in acidic soils. Indium phytotoxicity was found in both neutral and acidic soils. Plant analysis results indicated that the concentration of Ga and In in roots was approximately one order of magnitude higher than that in the shoots of wheat seedlings, and the capability for Ga translocation from roots to shoots was higher than for In. The results of this study suggest that the dynamics of Ga and In in soil-upland crop systems is strongly dependent on the soil properties, such as pH and Al availability.


Asunto(s)
Galio , Contaminantes del Suelo , Galio/toxicidad , Humanos , Indio/toxicidad , Raíces de Plantas/química , Plantones/química , Suelo , Contaminantes del Suelo/análisis , Contaminantes del Suelo/toxicidad , Triticum
5.
Toxicol In Vitro ; 71: 105064, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33279584

RESUMEN

Gallium antimonide (GaSb) is a group III-V compound semiconductor with a comparatively narrow band gap energy (0.73 eV at 300 K) that allows efficient operation in the near-infrared region. This property may be useful in developing new biomedical instruments such as epidermal optoelectronic devices. The present study investigated the absorption of GaSb in pig skin in vitro for 24 h using Franz cells. A donor solution was prepared by soaking GaSb thin films in synthetic sweat. The results showed that both gallium and antimony penetrated the skin, and permeation and resorption occurred for gallium. Histopathological findings showed no inflammatory responses in pig skin exposed to GaSb for 24 h. Cytotoxicity was significantly elevated after 3 and 7 days, and pro-inflammatory cytokines and IL-8 levels were low after 1 and 3 days but elevated 7 days following the direct culturing of human dermal fibroblasts (HDF) on GaSb thin films. These results demonstrate that the short-term cytotoxicity and pro-inflammatory effect of GaSb on HDF were relatively low.


Asunto(s)
Antimonio/administración & dosificación , Fibroblastos/efectos de los fármacos , Galio/administración & dosificación , Semiconductores , Absorción Cutánea , Piel/metabolismo , Animales , Antimonio/toxicidad , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Difusión , Fibroblastos/metabolismo , Galio/toxicidad , Humanos , Interleucina-8/metabolismo , Piel/citología , Porcinos
6.
Environ Toxicol Pharmacol ; 80: 103437, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-32565349

RESUMEN

Gallium arsenide (GaAs) and indium oxide (In2O3) are used in electronic industries at high and increasing tonnages since decades. Gallium oxide (Ga2O3) is an emerging wide-bandgap transparent conductive oxide with as yet little industrial use. Since GaAs has received critical attention due to the arsenic ion, it seemed reasonable to compare its toxicology with the respective endpoints of Ga2O3 and In2O3 toxicology in order to find out if and to what extent arsenic contributes. In addition, the toxicology of Ga2O3 has not yet been adequately reviewed, Therefore, this review provides the first evaluation of all available toxicity data on Ga2O3. The acute toxicity of all three compounds is rather low. Subchronic inhalation studies in rats and mice revealed persistent pulmonary alveolar proteinosis (PAP) and/or alveolar histiocytic infiltrates down to the lowest tested concentration in rats and mice, i.e. 0.16 mg Ga2O3/m3. These are also the predominant effects after GaAs and In2O3 exposure at similarly low levels, i.e. 0.1 mg/m3 each. Subchronic Ga2O3 exposure caused a minimal microcytic anemia with erythrocytosis in rats (at 6.4 mg/m3 and greater) and mice (at 32 and 64 mg/m3), a decrease in epididymal sperm motility and concentration as well as testicular degeneration at 64 mg/m3. At comparable concentrations the hematological effects and male fertility of GaAs were much stronger. The stronger effects of GaAs are due to its better solubility and presumed higher bioavailability. The database for In2O3 is too small and subchronic testing was at very low levels to allow conclusive judgements if blood/blood forming or degrading and male fertility organs/tissues would also be targets.


Asunto(s)
Galio/toxicidad , Indio/toxicidad , Pruebas de Toxicidad/métodos , Animales , Arsenicales/administración & dosificación , Arsenicales/química , Femenino , Galio/administración & dosificación , Galio/química , Indio/administración & dosificación , Indio/química , Masculino , Ratones , Especificidad de Órganos , Ratas , Factores Sexuales , Especificidad de la Especie
7.
Sci Rep ; 10(1): 8685, 2020 05 26.
Artículo en Inglés | MEDLINE | ID: mdl-32457348

RESUMEN

Extensive use of gallium arsenide (GaAs) has led to increased exposure to humans working in the semiconductor industry. This study employed physicochemical characterization of GaAs obtained from a workplace, cytotoxicity analysis of damage induced by GaAs in 16HBE cells, RNA-seq and related bioinformatic analysis, qRT-PCR verification and survival analysis to comprehensively understand the potential mechanism leading to lung toxicity induced by GaAs. We found that GaAs-induced abnormal gene expression was mainly related to the cellular response to chemical stimuli, the regulation of signalling, cell differentiation and the cell cycle, which are involved in transcriptional misregulation in cancer, the MAPK signalling pathway, the TGF-ß signalling pathway and pulmonary disease-related pathways. Ten upregulated genes (FOS, JUN, HSP90AA1, CDKN1A, ESR1, MYC, RAC1, CTNNB1, MAPK8 and FOXO1) and 7 downregulated genes (TP53, AKT1, NFKB1, SMAD3, CDK1, E2F1 and PLK1) related to GaAs-induced pulmonary toxicity were identified. High expression of HSP90AA1, RAC1 and CDKN1A was significantly associated with a lower rate of overall survival in lung cancers. The results of this study indicate that GaAs-associated toxicities affected the misregulation of oncogenes and tumour suppressing genes, activation of the TGF-ß/MAPK pathway, and regulation of cell differentiation and the cell cycle. These results help to elucidate the molecular mechanism underlying GaAs-induced pulmonary injury.


Asunto(s)
Regulación hacia Abajo/efectos de los fármacos , Galio/toxicidad , ARN/metabolismo , Regulación hacia Arriba/efectos de los fármacos , Arsenicales , Bronquios/citología , Línea Celular , Supervivencia Celular/efectos de los fármacos , Células Epitelioides/citología , Células Epitelioides/efectos de los fármacos , Células Epitelioides/metabolismo , Humanos , Lesión Pulmonar/metabolismo , Lesión Pulmonar/patología , Mapas de Interacción de Proteínas/efectos de los fármacos , Proteínas Proto-Oncogénicas c-fos/genética , Proteínas Proto-Oncogénicas c-fos/metabolismo , ARN/química , Análisis de Secuencia de ARN , Transducción de Señal , Proteína p53 Supresora de Tumor/genética , Proteína p53 Supresora de Tumor/metabolismo
8.
Int J Toxicol ; 39(3): 218-231, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32228215

RESUMEN

The semiconductor manufacturing sector plans to introduce III/V film structures (eg, gallium arsenide (GaAs), indium arsenide (InAs) onto silicon wafers due to their high electron mobility and low power consumption. Aqueous solutions generated during chemical and mechanical planarization of silicon wafers can contain a mixture of metal oxide nanoparticles (NPs) and soluble indium, gallium, and arsenic. In this work, the cytotoxicity induced by Ga- and In-based NPs (GaAs, InAs, Ga2O3, In2O3) and soluble III-V salts on human bronchial epithelial cells (16HBE14o-) was evaluated using a cell impedance real-time cell analysis (RTCA) system. The RTCA system provided inhibition data at different concentrations for multiple time points, for example, GaAs (25 mg/L) caused 60% inhibition after 8 hours of exposure and 100% growth inhibition after 24 hours. Direct testing of As(III) and As(V) demonstrated significant cytotoxicity with 50% growth inhibition concentrations after 16-hour exposure (IC50) of 2.4 and 4.5 mg/L, respectively. Cell signaling with rapid rise and decrease in signal was unique to arsenic cytotoxicity, a precursor of strong cytotoxicity over the longer term. In contrast with arsenic, soluble gallium(III) and indium(III) were less toxic. Whereas the oxide NPs caused low cytotoxicity, the arsenide compounds were highly inhibitory (IC50 of GaAs and InAs = 6.2 and 68 mg/L, respectively). Dissolution experiments over 7 days revealed that arsenic was fully leached from GaAs NPs, whereas only 10% of the arsenic was leached out of InAs NPs. These results indicate that the cytotoxicity of GaAs and InAs NPs is largely due to the dissolution of toxic arsenic species.


Asunto(s)
Células Epiteliales/efectos de los fármacos , Galio/toxicidad , Indio/toxicidad , Nanopartículas del Metal/toxicidad , Óxidos/toxicidad , Arsenicales/química , Bronquios/citología , Línea Celular , Supervivencia Celular/efectos de los fármacos , Liberación de Fármacos , Impedancia Eléctrica , Endocitosis , Células Epiteliales/metabolismo , Células Epiteliales/ultraestructura , Galio/química , Humanos , Indio/química , Nanopartículas del Metal/química , Microscopía Electrónica de Transmisión
9.
Artículo en Inglés | MEDLINE | ID: mdl-31607225

RESUMEN

III-V semiconductor materials such as gallium arsenide (GaAs) and indium arsenide (InAs) are increasingly used in the fabrication of electronic devices. There is a growing concern about the potential release of these materials into the environment leading to effects on public and environmental health. The waste effluents from the chemical mechanical planarization process could impact microorganisms in biological wastewater treatment systems. Currently, there is only limited information about the inhibition of gallium- and indium-based nanoparticles (NPs) on microorganisms. This study evaluated the acute toxicity of GaAs, InAs, gallium oxide (Ga2O3), and indium oxide (In2O3) particulates using two microbial inhibition assays targeting methanogenic archaea and the marine bacterium, Aliivibrio fischeri. GaAs and InAs NPs were acutely toxic towards these microorganisms; Ga2O3 and In2O3 NPs were not. The toxic effect was mainly due to the release of soluble arsenic species and it increased with decreasing particle size and with increasing time due to the progressive corrosion of the NPs in the aqueous bioassay medium. Collectively, the results indicate that the toxicity exerted by the arsenide NPs under environmental conditions will vary depending on intrinsic properties of the material such as particle size as well as on the dissolution time and aqueous chemistry.


Asunto(s)
Aliivibrio fischeri/efectos de los fármacos , Galio/toxicidad , Indio/toxicidad , Nanopartículas/toxicidad , Contaminantes Químicos del Agua/toxicidad , Aliivibrio fischeri/metabolismo , Arsenicales/química , Galio/química , Indio/química , Metano/biosíntesis , Nanopartículas/química , Tamaño de la Partícula , Semiconductores , Aguas del Alcantarillado/microbiología , Propiedades de Superficie , Contaminantes Químicos del Agua/química , Purificación del Agua/métodos
10.
Nanoscale ; 11(6): 2655-2667, 2019 Feb 07.
Artículo en Inglés | MEDLINE | ID: mdl-30601530

RESUMEN

To date, photothermal sensitizers include organic and inorganic nanomaterials for biomedical applications. However, the impediments of low biodegradability and potential toxicity hinder their further applications in clinics. Liquid metal nanospheres show superior photothermal effects under near-infrared laser irradiation, in addition, a transformation in shape can be triggered, which also promotes biodegradability that helps to avoid potential systemic toxicity. Here, we fabricated tunable liquid metal nanoparticles having sphere-shaped to rod-shaped characteristics, resulting in good biocompatibility, favorable photothermal conversion efficiency, and targeting capability to tumors. The synthesis strategy is easy to achieve through one-step sonication. We systematically evaluated the photothermal properties of these liquid metal nanoparticles as well as their destructive effects on tumors in a quantitative way both in vitro and in vivo under laser exposure. Results have shown for the first time in mice that gallium nanorods, regulated and controlled through the production of GaO(OH), displayed outstanding photothermal conversion efficiency and exhibited distinct temperature elevation compared to gallium nanospheres and gallium-indium alloy nanorods. These shape transformable and biocompatible gallium nanorods establish the basis for the future laser ablation of tumors to achieve enhanced therapeutic outcomes. This shape tunability of a smart nano-liquid metal directly contributes to enhanced photothermal therapy in mice and opens new opportunities for potential applications with tumor therapy and imaging.


Asunto(s)
Técnicas de Ablación/métodos , Galio/química , Nanopartículas del Metal/química , Nanotubos/química , Fototerapia/métodos , Animales , Antineoplásicos/química , Antineoplásicos/farmacología , Antineoplásicos/toxicidad , Apoptosis/efectos de los fármacos , Línea Celular Tumoral , Femenino , Galio/farmacología , Galio/toxicidad , Humanos , Receptores de Hialuranos , Nanopartículas del Metal/toxicidad , Ratones , Ratones Desnudos , Nanotubos/toxicidad , Ensayos Antitumor por Modelo de Xenoinjerto
11.
Genes (Basel) ; 10(1)2019 01 09.
Artículo en Inglés | MEDLINE | ID: mdl-30634525

RESUMEN

The diagnostic and therapeutic agent gallium offers multiple clinical and commercial uses including the treatment of cancer and the localization of tumors, among others. Further, this metal has been proven to be an effective antimicrobial agent against a number of microbes. Despite the latter, the fundamental mechanisms of gallium action have yet to be fully identified and understood. To further the development of this antimicrobial, it is imperative that we understand the mechanisms by which gallium interacts with cells. As a result, we screened the Escherichia coli Keio mutant collection as a means of identifying the genes that are implicated in prolonged gallium toxicity or resistance and mapped their biological processes to their respective cellular system. We discovered that the deletion of genes functioning in response to oxidative stress, DNA or iron⁻sulfur cluster repair, and nucleotide biosynthesis were sensitive to gallium, while Ga resistance comprised of genes involved in iron/siderophore import, amino acid biosynthesis and cell envelope maintenance. Altogether, our explanations of these findings offer further insight into the mechanisms of gallium toxicity and resistance in E. coli.


Asunto(s)
Antibacterianos/farmacología , Farmacorresistencia Bacteriana , Escherichia coli/genética , Galio/farmacología , Antibacterianos/toxicidad , Escherichia coli/efectos de los fármacos , Proteínas de Escherichia coli/genética , Galio/toxicidad
12.
Ecotoxicol Environ Saf ; 165: 349-356, 2018 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-30216893

RESUMEN

A novel bioassay is presented that allows for the estimation of the chronic toxicity of contaminants in receiving tropical marine environments. Relevant procedures to identify contaminants of concern and evaluate hazards associated with contamination in these environments have long remained inadequate. The 6-day bioassay is conducted using freshly hatched planktonic larvae of the hermit crab Coenobita variabilis and is targeted at generating environmentally relevant, chronic toxicity data. The developmental endpoint demonstrated consistently high control performance and was validated through the use of copper as a reference toxicant. In addition, the biological effects of aluminium, gallium and molybdenum were assessed. The endpoint expressed high sensitivity to copper (EC10 = 24 µg L-1) and moderate sensitivity to aluminium (EC10 = 312 µg L-1), whereas gallium and molybdenum elicited no obvious effects, even at high concentrations (EC10 > 6000 µg L-1), providing valuable information on the toxicity of these elements in tropical marine waters for derivation of water quality guidelines or testing of compliance limits.


Asunto(s)
Aluminio/toxicidad , Anomuros , Bioensayo/métodos , Cobre/toxicidad , Galio/toxicidad , Molibdeno/toxicidad , Animales , Larva/efectos de los fármacos , Larva/crecimiento & desarrollo , Contaminantes Químicos del Agua/toxicidad
13.
Environ Sci Pollut Res Int ; 25(26): 26592-26602, 2018 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-29998444

RESUMEN

Revised water quality guideline values (WQGVs) are presented for the metals aluminium (Al), gallium (Ga) and molybdenum (Mo) in receiving marine environments. These elements are commonly found in elevated concentrations in alumina refinery waste streams, yet current WQGVs fail to accurately assess the environmental risk. Here, chronic biological effects data we have generated over the course of several years were combined with toxicity data from the open literature to construct species sensitivity distributions (SSDs) which enabled the computation of revised WQGVs for Al, Ga and Mo in marine environments. These procedures are in accordance with internationally recommended derivation procedures, and newly computed WQGVs may be incorporated in regulatory frameworks aimed at sustainable exploitation of environmental resources and ongoing protection of the marine estate. Where the available datasets allowed such distinction, separate SSDs were constructed for temperate and tropical environments and zone-specific WQGVs derived. Extrapolated from the SSDs, WQGVs of 56 µg Al L-1, 800 µg Ga L-1 and 3.88 mg Mo L-1 (in the 0.45-µm filtered fraction) for 95% species protection were recommended for implementation in both temperate and tropical receiving environments. Currently, there is insufficient validation to separate the tropical from the temperate data and in most cases, application of the generic WQGVs is recommended.


Asunto(s)
Aluminio/análisis , Monitoreo del Ambiente/métodos , Galio/análisis , Molibdeno/análisis , Contaminantes Químicos del Agua/análisis , Calidad del Agua/normas , Aluminio/toxicidad , Animales , Organismos Acuáticos/efectos de los fármacos , Organismos Acuáticos/crecimiento & desarrollo , Galio/toxicidad , Guías como Asunto , Molibdeno/toxicidad , Agua de Mar/química , Especificidad de la Especie , Pruebas de Toxicidad Crónica , Clima Tropical , Contaminantes Químicos del Agua/toxicidad
14.
J Hazard Mater ; 344: 274-282, 2018 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-29055200

RESUMEN

Limited information exists on the effects of emerging contaminants gallium (Ga) and indium (In) on rice plant growth. This study investigated the effects on growth and uptake of Ga and In by rice plants grown in soils with different properties. Pot experiment was conducted and the rice seedlings were grown in two soils of different pH (Pc and Cf) spiked with various Ga and In concentrations. The results showed concentrations of Ga, In, and Al in soil pore water increased with Ga- or In-spiking in acidic Pc soils, significantly decreasing growth indices. According to the dose-response curve, we observed that the EC50 value for Ga and In treatments were 271 and 390mgkg-1 in Pc soils, respectively. The context of previous hydroponic studies suggests that growth inhibition of rice seedlings in Ga-spiked Pc soils is mainly due to Al toxicity resulting from enhanced Al release through competitive adsorption of Ga, rather than from Ga toxicity. In-spiked Pc soils, both In and Al toxicity resulted in growth inhibition, while no such effect was found in Cf soils due to the low availability of Ga, In and Al under neutral pH conditions.


Asunto(s)
Aluminio/toxicidad , Galio/toxicidad , Indio/toxicidad , Oryza/efectos de los fármacos , Contaminantes del Suelo/toxicidad , Oryza/crecimiento & desarrollo , Oryza/metabolismo , Raíces de Plantas/efectos de los fármacos , Raíces de Plantas/crecimiento & desarrollo , Raíces de Plantas/metabolismo , Brotes de la Planta/efectos de los fármacos , Brotes de la Planta/crecimiento & desarrollo , Brotes de la Planta/metabolismo , Plantones/efectos de los fármacos , Plantones/crecimiento & desarrollo , Plantones/metabolismo
15.
Int J Pharm ; 532(2): 686-695, 2017 Nov 05.
Artículo en Inglés | MEDLINE | ID: mdl-28705622

RESUMEN

The ZnGa1.995Cr0.005O4 persistent luminescence nanoparticles offer the promise of revolutionary tools for biological imaging with applications such as cell tracking or tumor detection. They can be re-excited through living tissues by visible photons, allowing observations without any time constraints and avoiding the undesirable auto-fluorescence signals observed when fluorescent probes are used. Despite all these advantages, their uses demand extensive toxicological evaluation and control. With this purpose, mice were injected with a single intravenous administration of hydroxylated or PEGylated persistent luminescence nanoparticles at different concentrations and then a set of standard tests were carried out 1day, 1 month and 6 months after the administration. High concentrations of hydroxylated nanoparticles generate structural alterations at histology level, endoplasmic reticulum damage and oxidative stress in liver, as well as rising in white blood cells counts. A mechanism involving the endoplasmic reticulum damage could be the responsible of the observed injuries in case of ZGO-OH. On the contrary, no toxicological effects related to PEGylated nanoprobes treatment were noted during our in vivo experiments, denoting the protective effect of PEG-functionalization and thereby, their potential as biocompatible in vivo diagnostic probes.


Asunto(s)
Cromo/toxicidad , Nanopartículas/toxicidad , Óxidos/toxicidad , Zinc/toxicidad , Animales , Recuento de Células Sanguíneas , Ensayo Cometa , Galio/toxicidad , Hidroxilación , Inyecciones Intravenosas , Riñón/efectos de los fármacos , Hígado/efectos de los fármacos , Hígado/patología , Hígado/ultraestructura , Luminiscencia , Pulmón/efectos de los fármacos , Masculino , Ratones Endogámicos BALB C , Óxido Nítrico/metabolismo , Polietilenglicoles/química , Bazo/efectos de los fármacos , Bazo/ultraestructura
16.
Ecotoxicol Environ Saf ; 140: 30-36, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28231503

RESUMEN

III-V materials such as indium arsenide (InAs) and gallium arsenide (GaAs) are increasingly used in electronic and photovoltaic devices. The extensive application of these materials may lead to release of III-V ionic species during semiconductor manufacturing or disposal of decommissioned devices into the environment. Although arsenic is recognized as an important contaminant due to its high toxicity, there is a lack of information about the toxic effects of indium and gallium ions. In this study, acute toxicity of As(III), As(V), In(III) and Ga(III) species was evaluated using two microbial assays testing for methanogenic activity and O2 uptake, as well as two bioassays targeting aquatic organisms, including the marine bacterium Aliivibrio fischeri (bioluminescence inhibition) and the crustacean Daphnia magna (mortality). The most noteworthy finding was that the toxicity is mostly impacted by the element tested. Secondarily, the toxicity of these species also depended on the bioassay target. In(III) and Ga(III) were not or only mildly toxic in the experiments. D. magna was the most sensitive organism for In(III) and Ga(III) with 50% lethal concentrations of 0.5 and 3.4mM, respectively. On the other hand, As(III) and As(V) caused clear inhibitory effects, particularly in the methanogenic toxicity bioassay. The 50% inhibitory concentrations of both arsenic species towards methanogens were about 0.02mM, which is lower than the regulated maximum allowable daily effluent discharge concentration (2.09mg/L or 0.03mM) for facilities manufacturing electronic components in the US. Overall, the results indicate that the ecotoxicity of In(III) and Ga(III) is much lower than that of the As species tested. This finding is important in filling the knowledge gap regarding the ecotoxicology of In and Ga.


Asunto(s)
Arseniatos/toxicidad , Arsenitos/toxicidad , Galio/toxicidad , Indio/toxicidad , Semiconductores , Aliivibrio fischeri/efectos de los fármacos , Animales , Arseniatos/análisis , Arsenicales/análisis , Arsenitos/análisis , Bioensayo/métodos , Daphnia/efectos de los fármacos , Ecotoxicología , Galio/análisis , Indio/análisis , Iones , Pruebas de Toxicidad Aguda
17.
Ecotoxicol Environ Saf ; 135: 32-39, 2017 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-27677080

RESUMEN

Limited information is available on the effects of gallium (Ga) and indium (In) on the growth of paddy rice. The Ga and In are emerging contaminants and widely used in high-tech industries nowadays. Understanding the toxicity and accumulation of Ga and In by rice plants is important for reducing the effect on rice production and exposure risk to human by rice consumption. Therefore, this study investigates the effect of Ga and In on the growth of rice seedlings and examines the accumulation and distribution of those elements in plant tissues. Hydroponic cultures were conducted in phytotron glasshouse with controlled temperature and relative humidity conditions, and the rice seedlings were treated with different levels of Ga and In in the nutrient solutions. The growth index and the concentrations of Ga and In in roots and shoots of rice seedlings were measured after harvesting. A significant increase in growth index with increasing Ga concentrations in culture solutions (<10mgGaL-1) was observed. In addition, the uptake of N, K, Mg, Ca, Mn by rice plants was also enhanced by Ga. However, the growth inhibition were observed while the In concentrations higher than 0.08mgL-1, and the nutrients accumulated in rice plants were also significant decreased after In treatments. Based on the dose-response curve, we observed that the EC10 (effective concentration resulting in 10% growth inhibition) value for In treatment was 0.17mgL-1. The results of plant analysis indicated that the roots were the dominant sink of Ga and In in rice seedlings, and it was also found that the capability of translocation of Ga from roots to shoots were higher than In. In addition, it was also found that the PT10 (threshold concentration of phytotoxicity resulting in 10% growth retardation) values based on shoot height and total biomass for In were 15.4 and 10.6µgplant-1, respectively. The beneficial effects on the plant growth of rice seedlings were found by the addition of Ga in culture solutions. In contrast, the In treatments led to growth inhibition of rice seedlings. There were differences in the phytotoxicity, uptake, and translocation of the two emerging contaminants in rice seedlings.


Asunto(s)
Galio/análisis , Hidroponía , Oryza/efectos de los fármacos , Plantones/efectos de los fármacos , Contaminantes del Suelo/análisis , Biomasa , Galio/toxicidad , Indio/análisis , Indio/toxicidad , Oryza/química , Oryza/crecimiento & desarrollo , Raíces de Plantas/química , Raíces de Plantas/efectos de los fármacos , Raíces de Plantas/crecimiento & desarrollo , Plantones/química , Plantones/crecimiento & desarrollo , Contaminantes del Suelo/toxicidad
18.
Curr Environ Health Rep ; 3(4): 459-467, 2016 12.
Artículo en Inglés | MEDLINE | ID: mdl-27696281

RESUMEN

The rapid growth of new electronics and energy technologies requires the use of rare elements of the periodic table. For many of these elements, little is known about their environmental behavior or human health impacts. This is true for indium and gallium, two technology critical elements. Increased environmental concentrations of both indium and gallium create the potential for increased environmental exposure, though little is known about the extent of this exposure. Evidence is mounting that indium and gallium can have substantial toxicity, including in occupational settings where indium lung disease has been recognized as a potentially fatal disease caused by the inhalation of indium particles. This paper aims to review the basic chemistry, changing environmental concentrations, potential for human exposure, and known health effects of indium and gallium.


Asunto(s)
Electrónica , Galio/toxicidad , Indio/toxicidad , Exposición Profesional/efectos adversos , Exposición a Riesgos Ambientales/análisis , Monitoreo del Ambiente , Humanos , Enfermedades Pulmonares/inducido químicamente , Exposición Profesional/análisis
19.
Mar Pollut Bull ; 112(1-2): 427-435, 2016 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-27423445

RESUMEN

A need exists for appropriate tools to evaluate risk and monitor potential effects of contaminants in tropical marine environments, as currently impact assessments are conducted by non-representative approaches. Here, a novel bioassay is presented that allows for the estimation of the chronic toxicity of contaminants in receiving tropical marine environments. The bioassay is conducted using planktonic larvae of the barnacle Amphibalanus amphitrite and is targeted at generating environmentally relevant, chronic toxicity data for water quality guideline derivation or compliance testing. The developmental endpoint demonstrated a consistently high control performance, validated through the use of copper as a reference toxicant. In addition, the biological effects of aluminium, gallium and molybdenum were assessed. The endpoint expressed high sensitivity to copper and moderate sensitivity to aluminium, whereas gallium and molybdenum exhibited no discernible effects, even at high concentrations, providing valuable information on the toxicity of these elements in tropical marine waters.


Asunto(s)
Aluminio/toxicidad , Bioensayo/métodos , Thoracica/efectos de los fármacos , Animales , Cobre/toxicidad , Galio/toxicidad , Larva/efectos de los fármacos , Molibdeno/toxicidad , Control de Calidad , Reproducibilidad de los Resultados , Calidad del Agua
20.
Biometals ; 29(3): 433-50, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-27003826

RESUMEN

The interplay of manganese and iron homeostasis and oxidative stress in Escherichia coli can give important insights into survival of bacteria in the phagosome and under differing iron or manganese bioavailabilities. Here, we characterized a mutant strain devoid of all know iron/manganese-uptake systems relevant for growth in defined medium. Based on these results an exit strategy enabling the cell to cope with iron depletion and use of manganese as an alternative for iron could be shown. Such a strategy would also explain why E. coli harbors some iron- or manganese-dependent iso-enzymes such as superoxide dismutases or ribonucleotide reductases. The benefits for gaining a means for survival would be bought with the cost of less efficient metabolism as indicated in our experiments by lower cell densities with manganese than with iron. In addition, this strain was extremely sensitive to the metalloid gallium but this gallium toxicity can be alleviated by low concentrations of manganese.


Asunto(s)
Escherichia coli/efectos de los fármacos , Escherichia coli/crecimiento & desarrollo , Hierro/metabolismo , Manganeso/metabolismo , Mutación , Escherichia coli/genética , Escherichia coli/metabolismo , Galio/metabolismo , Galio/toxicidad , Estrés Oxidativo/efectos de los fármacos
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