Institution
Zayed University
Education•Abu Dhabi, United Arab Emirates•
About: Zayed University is a education organization based out in Abu Dhabi, United Arab Emirates. It is known for research contribution in the topics: Web service & Computer science. The organization has 1030 authors who have published 3346 publications receiving 42546 citations.
Papers published on a yearly basis
Papers
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TL;DR: A comprehensive survey of multimodal medical signals fusion schemes that have been proposed for smart healthcare applications is presented in this paper, focusing on recent developments, thus only works published between 2014-2020 are considered.
73 citations
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TL;DR: This paper used Bayesian Model Averaging techniques and an updated cross-country data set for long-term growth in the period 1970-2014, including 91 countries and 54 potential growth determinants.
73 citations
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08 Aug 2020
TL;DR: The aims of the current review are to highlight the important chemical, microbiological, and pharmacological properties of polymyxins, to discuss their mechanistic effects on bacterial membranes, and to revise the current knowledge about Gram-negative acquired resistance to these agents.
Abstract: Following their initial discovery in the 1940s, polymyxin antibiotics fell into disfavor due to their potential clinical toxicity, especially nephrotoxicity. However, the dry antibiotic development pipeline, together with the rising global prevalence of infections caused by multidrug-resistant (MDR) Gram-negative bacteria have both rejuvenated clinical interest in these polypeptide antibiotics. Parallel to the revival of their use, investigations into the mechanisms of action and resistance to polymyxins have intensified. With an initial known effect on biological membranes, research has uncovered the detailed molecular and chemical interactions that polymyxins have with Gram-negative outer membranes and lipopolysaccharide structure. In addition, genetic and epidemiological studies have revealed the basis of resistance to these agents. Nowadays, resistance to polymyxins in MDR Gram-negative pathogens is well elucidated, with chromosomal as well as plasmid-encoded, transferrable pathways. The aims of the current review are to highlight the important chemical, microbiological, and pharmacological properties of polymyxins, to discuss their mechanistic effects on bacterial membranes, and to revise the current knowledge about Gram-negative acquired resistance to these agents. Finally, recent research, directed towards new perspectives for improving these old agents utilized in the 21st century, to combat drug-resistant pathogens, is summarized.
72 citations
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TL;DR: This study showed the potent and rapid antibacterial activity of CAMPs on both laboratory and clinical isolates of S. aureus and P. aeruginosa either susceptible or resistant to antibiotics.
Abstract: Methicillin-resistant Staphylococcus aureus and multidrug-resistant Pseudomonas aeruginosa are becoming difficult to treat with antibiotics whereas Cationic Antimicrobial Peptides (CAMPs) represent promising alternatives. The effects of four CAMPs (LL-37: human cathelicidin, CAMA: cecropin(1–7)-melittin A(2–9) amide, magainin-II and nisin) were investigated against clinical and laboratory S. aureus (n = 10) and P. aeruginosa (n = 11) isolates either susceptible or resistant to antibiotics. Minimal Inhibitory Concentrations (MICs), Minimal Bactericidal Concentrations (MBCs), and bacterial survival rates (2 h post-treatment) were determined by microbroth dilution. The antipseudomonal effects of the antibiotics colistin or imipenem combined to LL-37 or CAMA were also studied. The toxicity of CAMPs used alone and in combination with antibiotics was evaluated on two human lung epithelial cell lines by determining the quantity of released cytoplasmic lactate dehydrogenase (LDH). Attempts to induce bacterial resistance to gentamicin, LL-37 or CAMA were also performed. The results revealed the rapid antibacterial effect of LL-37 and CAMA against both antibiotic susceptible and resistant strains with almost a total reduction in bacterial count 2 h post-treatment. Magainin-II and nisin were less active against tested strains. When antibiotics were combined with LL-37 or CAMA, MICs of colistin decreased up to eight-fold and MICs of imipenem decreased up to four-fold. Cytotoxicity assays revealed non-significant LDH-release suggesting no cell damage in all experiments. Induction of bacterial resistance to LL-37 was transient, tardive and much lower than that to gentamicin and induction of resistance to CAMA was not observed. This study showed the potent and rapid antibacterial activity of CAMPs on both laboratory and clinical isolates of S. aureus and P. aeruginosa either susceptible or resistant to antibiotics. Most importantly, CAMPs synergized the efficacy of antibiotics, had non toxic effects on human cells and were associated with transient and low levels of induced resistance.
72 citations
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TL;DR: In this paper, the use of a deep eutectic solvent (DES) for promoting the yield and stability of ceria nanoparticles used for the degradation of flumequine (FLU) under UV-C irradiation was investigated.
Abstract: This study investigated the use of a deep eutectic solvent (DES) for promoting the yield and stability of ceria nanoparticles used for the degradation of flumequine (FLU) under UV-C irradiation. The characterization by Fourier transform infrared spectroscopy, X-ray diffraction spectroscopy, Raman spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, high resolution transmission electron microscopy, thermogravimetric analysis, and BET surface area analysis revealed the synthesis of highly stable, highly crystalline, and mesoporous ceria nanoparticles using DES which led to the high removal, i.e., 50 % and 94 % of FLU using DES-Ceria and UV-C/DES-Ceria, respectively. Removal of FLU by the UV-C mediated ceria nanoparticles was due to OH and thus factors that influenced the reactivity and yield of OH retarded the removal efficiency of FLU. The pH of aqueous solution affected the removal of FLU by the photocatalysts and removal of FLU was inhibited at highly alkaline and acidic pH. The degradation pathways of FLU were established from the pattern of its degradation and nature of the degradation products. Acute and chronic toxicities of FLU as well as its products were measured. The photocatalyst synthesized in DES was found to be environmentally benign and showed significant potential in the remediation of FLU.
72 citations
Authors
Showing all 1070 results
Name | H-index | Papers | Citations |
---|---|---|---|
John P. Rice | 99 | 450 | 46587 |
Muhammad Imran | 94 | 3053 | 51728 |
Richard P. Bentall | 94 | 431 | 30580 |
Md. Rabiul Awual | 91 | 133 | 15622 |
Mary A. Carskadon | 88 | 245 | 35740 |
Ling Shao | 78 | 782 | 26293 |
Hussein T. Mouftah | 55 | 962 | 14710 |
Fahad Shahbaz Khan | 51 | 196 | 19641 |
Dong-Hee Shin | 49 | 260 | 8730 |
Emilia Mendes | 45 | 238 | 6699 |
Zakaria Maamar | 38 | 408 | 5313 |
Fakhri Karray | 38 | 354 | 7018 |
Mohammad Shahid | 36 | 309 | 5866 |
Karthik Nandakumar | 36 | 75 | 10623 |
Rik Crutzen | 35 | 229 | 5099 |