5 research outputs found

    Dissolution and sorption mechanisms at the aluminosilicate and carbonate mineral-AMD (Acid Mine Drainage) interface

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    Aluminosilicate/silicate and carbonate materials (pure and industrial) interacted with natural Acid Mine Drainage (AMD) under ambient conditions for different time periods in order to elucidate the chemical processes at the aluminosilicate and carbonate mineral-AMD interface. More precisely, powdered materials were subjected to macroscopic neutralization experiments (using on-line pH-measurements, Inductively Coupled Plasma Optical Emission Spectroscopy, Powder X-ray Diffraction and Scanning Electron Microscopy with Energy Dispersive Spectroscopy), whereas interacted mm-sized single crystals were examined by means of nanoscale microscopic (in-situ Atomic Force Microscopy) and surface & bulk spectroscopic techniques (X-ray Photoelectron Spectroscopy, 12C-Rutherford Backscattering Spectroscopy, Solid-State 29Si and 27Al Magic-Angle-Spinning Nuclear Magnetic Resonance). The carbonates were proven to be more effective for neutralization of AMD, related to adequate removal of metals from the contaminated aqueous medium, but they are readily dissolved. The application of aluminosilicate/silicates showed that the removal of metals is considerably lower, and the pH stabilized at lower values, but they are more resistant. The investigation of interacted zeolite and calcite crystals revealed changes to the macrotopography, microtopography and nanotopography of surfaces. It was indicated that coupled dissolution and sorption (surface precipitation/co-precipitation, nucleation/crystal growth, adsorption or even absorption-including solid-state diffusion) phenomena occur simultaneously. Based on the experimental results, two generalized models -in nano(molecular)-scale- can be suggested regarding interaction of AMD with aluminosilicate and carbonate mineral surfaces

    Hypertension study in anesthetized rabbits: Protocol proposal for AT1 antagonist screening

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    Introduction: The aim of this study was to establish an optimized fast and safe protocol for the pharmacological screening of AT1 antagonists. Materials and methods: The pharmaceutical prototype AT1 antagonist losartan, its active metabolite EXP3174 and the synthetic compound MMK1 were analysed in order to validate the protocol. Ang II was continuously infused while the animals received the drugs in two procedures. Results: In the post-treatment procedure drugs were administered either in a single bolus dose or in a sequential manner. When losartan was administered in a single bolus dose, efficacy was evident until the 7th min (p=0.012) whilst EXP3174 infusion extended the efficiency up to the end of the study (p=0.006). In addition, the sequential injections of losartan prolonged the inhibitory time interval until the end of the study (p=0.045). In the pre-treatment procedure, results suggested a dosedependent inhibitory effect for both antagonists. The pressor response to Ang II was unchanged after MMK1 administration either in the post- or in the pre-treatment mode. Conclusions: The proposed protocol appears to be safe, simple and fast for the pharmacological screening of AT1 antagonists and enables the evaluation of new antagonists using lower doses than any other reported in the literature
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