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1.
PLoS One ; 18(9): e0291034, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37683017

RESUMO

BACKGROUND: COVID-19 precipitated a plethora of mental health difficulties, particularly for those with pre-existing mental health concerns such as depression or addictive tendencies. For some, the distress that emanated from the experience of the pandemic prompted excessive engagement in the safety of online interactions on social media. The present study examined whether variation in individuals' sense of control explained the association between depression and addictive social media use. METHOD: A sample of 1322 participants from two Middle Eastern nations provided data collected during the peak of the pandemic from February to May 2021. A combination of convenience and snowball sampling were used to recruit and collect data from college-aged students enrolled at two universities in Egypt and the United Arab Emirates, respectively. This study adopted a cross-sectional design in which participants completed a self-administered survey that consisted of measures that assessed depressive affect, sense of control, and addictive social media use. RESULTS: Depression was significantly and positively associated with addictive SMU. Sense of control was negatively related to both depression and SMU and significantly mediated the association between these two variables (ß = .62, SE = .03, 95%CI .56, .68). CONCLUSION: This study identified a potential protective variable that could be targeted by psychological treatment to ameliorate the potential onset of addictive SMU in individuals with depressive symptoms under conditions of immense psychological distress such as a worldwide pandemic.


Assuntos
COVID-19 , Mídias Sociais , Humanos , Adulto Jovem , COVID-19/epidemiologia , Pandemias , Estudos Transversais , Depressão/epidemiologia , Controle Interno-Externo
2.
Chemistry ; 23(52): 12754-12757, 2017 Sep 18.
Artigo em Inglês | MEDLINE | ID: mdl-28753730

RESUMO

We present a simple microfluidic system for rapid screening of Escherichia coli (E. coli) O157:H7 employing the specificity of immunomagnetic separation (IMS) via immiscible filtration assisted by surface tension (IFAST), and the sensitivity of the subsequent adenosine triphosphate (ATP) assay by the bioluminescence luciferin/luciferase reaction. The developed device was capable of detecting E. coli O157:H7 from just 6 colony forming units (CFU) in 1 mL spiked buffer within 20 min. When tested with wastewater discharged effluent samples, without pre-concentration, the device demonstrated the ability to detect 104  CFU per mL seeded; suggesting great potential for point-of-need microbiological water quality monitoring.


Assuntos
Trifosfato de Adenosina/metabolismo , Escherichia coli O157/isolamento & purificação , Medições Luminescentes/métodos , Águas Residuárias/microbiologia , Escherichia coli O157/metabolismo , Luciferina de Vaga-Lumes/química , Luciferina de Vaga-Lumes/metabolismo , Dispositivos Lab-On-A-Chip , Luz , Luciferases/metabolismo , Medições Luminescentes/instrumentação , Tensão Superficial
3.
Magn Reson Chem ; 42(7): 617-23, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15181632

RESUMO

The syntheses of a novel trishomocubane hydantoin and its mono- and bis-protected t-Boc derivatives are described. The less nucleophilic N-3' nitrogen of the hydantoin ring is protected first when treated with di-tert-butyl dicarbonate (t-Boc anhydride), possibly owing to steric hindrance by the bulky trishomocubane cage skeleton. More basic conditions were required to form the bis-protected t-Boc hydantoin with the same reagent. The structures of these novel compounds were elucidated with 2D NMR techniques. The proton spectrum of the trishomocubane skeleton is complex owing to major overlap of proton signals. A high-level DFT calculation was used to determine some of the crucial interatomic positions, which assisted with the elucidation of the structures. The assignment of proton and carbon signals of the three structures is described and it differs significantly from each other and also from the trishomocubanol precursor. The bis-Boc hydantoin is required for a more facile hydrolysis to the corresponding trishomocubane amino acid at room temperature.


Assuntos
Alcanos/química , Hidantoínas/química , Espectroscopia de Ressonância Magnética/métodos , Modelos Moleculares , Peptídeos/química , Alcanos/análise , Isótopos de Carbono , Hidantoínas/análise , Conformação Molecular , Peptídeos/análise , Prótons
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