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1.
Chemosphere ; 275: 129935, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-33667770

RESUMO

Petrographic and mineralogical analyses combined with sequential extractions and leaching experiments as a function of pH were performed on black clayey sediments fulfilling karsts in the Hydrogeological Experimental Site (HES) of Poitiers (France) to investigate the behavior of arsenic and selenium in a fractured limestone aquifer. Sequential extractions showed that arsenic is mainly associated with pyrite (about 35%) and secondary iron oxyhydroxides (around 13%), along with a substantial exchangeable fraction (about 13%). The soluble fraction and the fraction associated to organic matter are âˆ¼2% and ∼5%, respectively. The distribution of selenium is mainly pyritic (around 39%) or associated with organic matter (about 18%). Its association to secondary iron oxyhydroxides minerals is low (around 2%), whereas its soluble fraction is around 5%. SEM analyses revealed the presence of arsenic "hot spots" into euhedral pyrite crystals surrounded by a halo of iron oxyhydroxides resulting from their alteration, and both are enriched with arsenic. Selenium has a similar pyritic origin but after alteration, it is predominantly associated with organic matter. Despite different distributions, the leaching experiment as a function of pH showed that the mobilization of arsenic and selenium overlapped below pH 2 and above pH 8. The main differences were observed between pH 2 and 8 with a plateau at 5% of released selenium, whereas the amount of mobilized arsenic continuously decreased. The pH-dependence of both elements is attributed to the partial dissolution of pyrite in acidic conditions combined with desorption processes at higher pH values.


Assuntos
Arsênio , Água Subterrânea , Selênio , Poluentes Químicos da Água , Arsênio/análise , Carbonatos , França , Sedimentos Geológicos , Selênio/análise , Poluentes Químicos da Água/análise
2.
Osteoarthritis Cartilage ; 21(12): 1924-32, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23978656

RESUMO

OBJECTIVE: To determine the in vitro conditions which promote expression of superficial zone protein (SZP). METHODS: Chondrocytes from 6-month-old calves were expanded in monolayer culture and the expression of SZP in alginate bead and monolayer culture was quantified with quantitative real time-polymerase chain reaction (qRT-PCR) and immunostaining. The effect of oxygen tension on SZP expression was determined by qRT-PRC analysis of cells cultured in two dimension (2D) and three dimension (3D) under hypoxic (1% pO2) or normoxic (21% pO2) conditions. Finally, to examine the effect of cyclic tensile strain on expression of SZP in 2D and 3D cultures, chondrocytes encapsulated in alginate beams or seeded on type I collagen coated polydimethylsiloxane (PDMS) chambers were subjected to 5% strain at 1 Hz, 2 h/day for 4 days or 2 h at the fourth day of culture and mRNA levels were quantified. RESULTS: Bovine chondrocytes in monolayer showed a drastic decrease in SZP expression, similar in trend to the commonly reported downregulation of type II collagen (Col2). Chondrocytes embedded in alginate beads for 4 days re-expressed SZP but not Col2. SZP expression was higher under normoxic conditions whereas Col2 was upregulated only in alginate beads under hypoxic conditions. Cyclic mechanical strain showed a tendency to upregulate mRNA levels of SZP. CONCLUSIONS: A microenvironment encompassing a soft encapsulation material and 21% oxygen is sufficient for fibroblastic chondrocytes to re-express SZP. These results serve as a guideline for the design of stratified engineered articular cartilage and suggest that microenvironmental cues (oxygen tension level) strongly influence the pattern of SZP expression in vivo.


Assuntos
Cartilagem Articular/metabolismo , Microambiente Celular/genética , Condrócitos/metabolismo , Colágeno Tipo II/genética , Hipóxia/genética , Proteoglicanas/genética , RNA Mensageiro/análise , Estresse Mecânico , Animais , Cartilagem Articular/citologia , Bovinos , Técnicas de Cultura de Células , Diferenciação Celular , Células Cultivadas , Microambiente Celular/fisiologia , Colágeno Tipo II/metabolismo , Hipóxia/metabolismo , Imuno-Histoquímica , Proteoglicanas/metabolismo , Reação em Cadeia da Polimerase em Tempo Real , Engenharia Tecidual/métodos
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