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      Quick removal of metronidazole from aqueous solutions using metal–organic frameworks

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          Abstract

          Two MOFs were assembled, characterized and investigated in detail as efficient adsorbents for removal of the metronidazole antibiotic. Adsorption isotherms and kinetic features were also studied.

          Abstract

          The growing release of antibiotics into the environment has motivated extensive studies on the elimination of these harmful substances and the development of advanced adsorbents. Metronidazole is a major example of antibiotic pollutants due to its extensive usage, high solubility in water and considerable resistance to degradation. The present research focuses on assessing the removal efficiency of metronidazole (MNZ) using two model metal–organic frameworks (MOFs), namely [Fe 33-O)(μ 4-atpa) 3Cl] n (NH 2-MIL-101-Fe; H 2atpa = 2-aminoterephthalic acid) and [Cu 36-tma) 2] n (HKUST-1; H 3tma = trimesic acid), which feature high specific surface areas of 3874 and 569 m 2 g −1, respectively, and minute-scale adsorption rates. The effects of the solution pH, contact time, adsorbent loading and recycling, and initial concentration of MNZ were investigated in detail. In particular, NH 2-MIL-101-Fe exhibited an excellent MNZ adsorption and removal efficiency (above 90%) which can be attributed to its unsaturated metal sites, superior specific surface area, hydrogen bonding, and robust host–guest π–π interactions. The Langmuir and pseudo-second-order models allowed the adsorption isotherms and kinetics to be described, respectively, reflecting a homogenous adsorption surface and the dominance of chemisorption. The adsorption of MNZ by these MOFs can be considered as environmentally benign and the results of this research are expected to further motivate the application of metal–organic frameworks as promising adsorbents for removal of antibiotics from wastewater.

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          Is Open Access

          Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness

          Signaling through the Ror2 receptor tyrosine kinase promotes invadopodia formation for tumor invasion. Here, we identify intraflagellar transport 20 (IFT20) as a new target of this signaling in tumors that lack primary cilia, and find that IFT20 mediates the ability of Ror2 signaling to induce the invasiveness of these tumors. We also find that IFT20 regulates the nucleation of Golgi-derived microtubules by affecting the GM130-AKAP450 complex, which promotes Golgi ribbon formation in achieving polarized secretion for cell migration and invasion. Furthermore, IFT20 promotes the efficiency of transport through the Golgi complex. These findings shed new insights into how Ror2 signaling promotes tumor invasiveness, and also advance the understanding of how Golgi structure and transport can be regulated.
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            Insights into the modeling of adsorption isotherm systems

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              Adsorption — from theory to practice

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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                NJCHE5
                New Journal of Chemistry
                New J. Chem.
                Royal Society of Chemistry (RSC)
                1144-0546
                1369-9261
                May 16 2022
                2022
                : 46
                : 19
                : 9440-9450
                Affiliations
                [1 ]Department of Civil and Environment Engineering, Shahrood University of Technology, Shahrood, Iran
                [2 ]Pharmaceutical Engineering Research Laboratory, Pharmaceutical Process Centers of Excellence, College of Engineering, University of Tehran, P.O. Box 11155-4563, Tehran, Iran
                [3 ]Centro de Química Estrutural, Institute of Molecular Sciences, Departamento de Engenharia Química, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, Portugal
                [4 ]Department of Chemistry, Faculty of Science, University of Maragheh, P.O. Box 55181-83111, Maragheh, Iran
                Article
                10.1039/D1NJ06107K
                5bf8023d-0256-4b8d-a423-8745f0d5bdbd
                © 2022

                http://rsc.li/journals-terms-of-use

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