Increasing the Risk of Stroke by Opium Addiction

IntroductionStroke is among the leading causes of mortality and morbidity in the world. Besides the identified risk factor, Ischemic stroke evidence show drug use develops or exacerbates the atherosclerotic process. The current study aimed at comparing cerebrovascular ultrasounds’ changes in addicted and nonaddicted people who developed ischemic stroke.MethodsIn the current cross-sectional study, a total of 133 patients with ischemic stroke who were admitted to Vali-Asr hospital from June 2016 to April 2017 were enrolled. For obtaining the quantitative data, t test or Mann-Whitney test was employed to compare the addict or no-addict groups, as well as, categorical data testing was performed using chi-square test. Also, the multiple logistic regression was used for identifying the factors and the significance level was set at 5%.ResultsThe current study was performed on 133 patients, among them 41 patients (30.8%) were opium addicted, and 92 patients (69.2%) were nonaddict. The mean [IQR] number of atherosclerotic plaques were significantly higher in opium addicted group in comparison with the nonaddicted group (3.0 [1.0-4.0] versus 1.5 [0.0-3.0], P = .008). The possibility of increasing the number of plaques in addicted patients was 1.42 times higher than the nonaddicted patients (odds ratio (95% confidence interval): 1.42 (1.11-1.81), P = .005).ConclusionThe findings demonstrated a significant difference in the vessel stenosis pattern between the addict and nonaddict ischemic stroke groups. To investigate the possible effects of opium use and its associated parameters, ie, dosage, duration of use, and the way of opium use on ischemic stroke, further studies are required.     

Robust,highly active,and stable supported Co(ii) nanoparticles on magnetic cellulose nanofiber-functionalized for the multi-component reactions of piperidines and alcohol oxidation

The new recyclable cobalt three-core magnetic catalyst obtained by anchoring a Schiff base ligand sector and cellulose nanofiber slings on MNP (Fe₃O₄) was prepared and named as MNP@CNF@ATSM–Co(ii). Separately, MNPs and CNF have adsorbent properties of great interest. In this way, this catalyst was designed to synthesize piperidine derivatives under solvent-free conditions and alcohol oxidation reactions in EtOH as the solvent. It should be noted that this catalyst is environmentally safe and does not need an external base. This MNPs@CNF@ATSM–Co(ii) separable catalyst has been evaluated using various characterization techniques such as FT-IR, XRD, FE-SEM, EDX, EDS, ICP, TGA, DLS, HRTEM, and VSM. The catalyst was compatible with a variety of benzyl alcohols, benzaldehydes, and amines derivatives, and gave complimentary coupling products with sufficient interest for all of them. The synergistic performance of Co (trinuclear) in the catalyst was demonstrated and its different homologs such as MNPs, MNPs@CNF, MNPs@CNF@ATS–Co(ii), and MNPs@CNF@ATSM–Co(ii) were separately synthesized and applied to a model reaction, and then their catalytic activity was investigated. Also, the performance of these components for the oxidation reaction of alcohols was evaluated. The advantages of the current protocol include the use of a sustainable and safe low temperature, eco-friendly solvent no additive, and long-term stability and magnetic recyclability of the catalyst for at least five successive runs, thus following green chemistry principles. This protocol is a benign and environment-friendly method for oxidation and heterocycle synthesis. This powerful super-magnetic catalyst can use its three arms to advance the reactions, displaying its power for multi-component reactions and oxidation.

The new recyclable cobalt three-core magnetic catalyst obtained by anchoring a Schiff base ligand sector and cellulose nanofiber slings on MNP (Fe₃O₄) was prepared and named as MNP@CNF@ATSM–Co(ii).     

Design and synthesis of magnetic Fe3O4@NFC-ImSalophCu nanocatalyst based on cellulose nanofibers as a new and highly efficient,reusable, stable and green catalyst for the synthesis of 1,2,3-triazoles

The Fe₃O₄@NFC-ImSalophCu catalyst was used as a highly stable, reusable, active, green catalyst for the synthesis of 1,2,3-triazoles via one-pot three-component reaction of phenacyl bromides, sodium azide and alkynes. A Cu(ii)–Schiff base complex containing an imidazolium ionic phase was prepared and decorated on core shell Fe₃O₄@NFC magnetic nanoparticles (Fe₃O₄@NFC-ImSalophCu) and was used as an efficient catalyst. The heterogeneous catalyst was characterized by FT-IR spectroscopy, FE-SEM, TEM, XRD spectroscopy, EDX spectroscopy, VSM, and ICP spectroscopy. This catalyst shows the dual function of the metal sites and imidazolium moieties. The catalytic system mentioned above also showed excellent activity in the synthesis of bis 1,4-disubstituted 1,2,3-triazoles. Moreover, the catalyst could be recycled and reused for four cycles without any decrease in its catalytic activity.

A new and efficient method has been developed for click chemistry reactions using a bifunctional Fe₃O₄@NFC-ImSalophCu catalyst with part imidazolium under moderate conditions.