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1.
J Int Med Res ; 50(10): 3000605221130039, 2022 Oct.
Article in English | MEDLINE | ID: mdl-36284451

ABSTRACT

OBJECTIVE: This cross-sectional study aimed to assess the prevalence and awareness of drug and substance abuse among undergraduates in four southwestern universities in Nigeria. METHODS: The sample of 400 students included 100 male and female students in the 15- to 29-year age range from each of the four selected universities in southwest Nigeria between December 2019 and June 2020. Descriptive statistics and Pearson chi-square tests were used for data analysis using the statistical package for social sciences (SPSS). RESULTS: Four hundred students satisfied the inclusion criteria and suitably completed the questionnaire. Most respondents were in the 15- to 19-year and 20- to 24-year age groups and were female (68%). Drug and substance abuse prevalence was 45.7%; one in every four students abused substances despite an aggregate risk awareness level of 94.6%. Alcohol and cigarettes-legally and socially accepted substances-were the most abused (61.5% and 54.5%, respectively). Codeine-containing syrup and tramadol topped the list of drugs, ranking higher than cannabis. The major motive was to 'get high' and numb emotional problems caused by predominantly socioeconomic and societal factors. CONCLUSION: The study showed a notable prevalence of drug and substance abuse across the selected universities in southwest Nigeria.


Subject(s)
Substance-Related Disorders , Tramadol , Male , Female , Humans , Universities , Cross-Sectional Studies , Nigeria/epidemiology , Students/psychology , Substance-Related Disorders/epidemiology , Prevalence , Surveys and Questionnaires , Codeine
2.
Molecules ; 25(5)2020 Feb 26.
Article in English | MEDLINE | ID: mdl-32110916

ABSTRACT

This article reviews the excited-state quenching, pro-vitamin A activity and anticarcinogenicity of carotenes and xanthophylls in relation to their chemical structures. Excited-state quenching improved with the length of the conjugated chain structure. Pro-vitamin A activity was dependent on the presence of at least one beta-ionyl ring structure. The effectiveness of carotenoids as antioxidants depended on their ability to trap peroxyl radicals with production of resonance-stabilized carotenyl radicals. The products identified from oxidations of carotenes and xanthophylls with molecular oxygen and other oxidizing agents are presented. The free radical-mediated mechanisms that have been proposed to account for the different classes of products are reviewed.


Subject(s)
Carotenoids/chemistry , Free Radicals/chemistry , Xanthophylls/chemistry , Animals , Antioxidants/chemistry , Carcinogenesis/pathology , Humans , Oxidation-Reduction
3.
Arch Pharm (Weinheim) ; 349(7): 475-506, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27213292

ABSTRACT

Benzimidazole derivatives are crucial structural scaffolds found in diverse libraries of biologically active compounds which are therapeutically useful agents in drug discovery and medicinal research. They are structural isosteres of naturally occurring nucleotides, which allows them to interact with the biopolymers of living systems. Hence, there is a need to couple the latest information with the earlier documentations to understand the current status of the benzimidazole nucleus in medicinal chemistry research. This present work unveils the benzimidazole core as a multifunctional nucleus that serves as a resourceful tool of information for synthetic modifications of old existing candidates in order to tackle drug resistance bottlenecks in therapeutic medicine. This manuscript deals with the recent advances in the synthesis of benzimidazole derivatives, the widespread biological activities as well as pharmacokinetic reports. These present them as a toolbox for fighting infectious diseases and also make them excellent candidates for future drug design.


Subject(s)
Benzimidazoles/chemistry , Benzimidazoles/chemical synthesis , Drug Design , Animals , Benzimidazoles/pharmacology , Drug Resistance/drug effects , Humans , Molecular Docking Simulation , Molecular Structure , Structure-Activity Relationship
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