Green synthesis of Ag nanoparticles from Argemone mexicana L. leaf extract coated with MOF-5 for the removal of metronidazole antibiotics from aqueous solution.

There are growing concerns about the toxicity of metronidazole (MNZ) antibiotics in wastewater, which must be removed. This study used AgN/MOF-5 (1:3) to investigate the adsorptive removal of MNZ antibiotics from wastewater. Green synthesis of Ag-nanoparticles was from Argemone mexicana leaf aqueous extract blended with the synthesized MOF-5 in 1:3 by proportion. The adsorption materials were characterized by scanning electron microscope (SEM), N2 adsorption-desorption analysis, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The surface area increased due to the appearance of micropores. Besides, the efficiency of AgN/MOF-5 (1:3) for MNZ removal was evaluated by adsorption properties, including key influential parameters (adsorbent dosage, pH, contact time, etc.) and adsorption mechanism, kinetics/isotherms. The results from the adsorption process conformed to pseudo-second-order kinetics (R2 = 0.998) and well fitted with the Langmuir isotherm having 191.1 mg/g maximum adsorption capacity. The adsorption mechanism of AgN/MOF-5 (1:3) was due to the interactions of π-π stacking, Ag-N-MOF covalent bonding and hydrogen bonding. Thus, AgN/MOF-5 (1:3) is a potential adsorbent for the removal of aqueous MNZ. The adsorption process is endothermic, spontaneous, and feasible based on the obtained thermodynamic parameter of ΔHO and ΔSO having 14.72 and 0.129 kJ/mol respectively.

Biochemical Studies on the Colorectal Tissues of Wistar Rats Treated with Methanol Leaf and Stem Bark Extracts of Annona muricata (Soursop).

Annona muricata (AMC), is a tropical plant species of the Annonaceae family known for its medicinal uses in ameliorating and/or protecting several organs and tissues in the body. In this study we elucidated the influence of the methanol extracts of AMC leaf and stem bark on the biochemical and histological integrity of the colorectum. Different doses (100, 200, 400, 600, and 800mg of extract/kg body weight) of methanol extracts of the leaves and stembark were orally administered to adult male Wistar rats of average weight (100 - 150 g) for 28 days. At the end of the experimental period, the rats were sacrificed and colorectal tissues harvested for analyses. Adenosine triphosphatase (ATPases), lactate dehydrogenase (LDH), glucose-6-phosphate dehydrogenase (G6PD) activities, and tissue protein (TP) concentration, were evaluated by colorimetric method using appropriate test kits. The results in the colorectal tissue analysed showed that total ATPase, LDH and G6PD (energy markers) activities increased significantly in the groups which received methanol leaf and stem bark extracts of AMC when compared with control. However, a general decrease was observed in TP and Na+/K+-ATPase activity but there was a twist in Na+/K+-ATPase activity in stem bark doses of 200mg/kg and 400mg/kg which showed significant increases in dose dependent manner when compared with the control. Even though G6PD activity showed fluctuating patterns for both extracts, the highest dose (800mg/kg) reflected the most significant increase when compared with the control. The histology confirmed the toxicological results by the biochemical parameters. Under the condition of this study, we inferred that the methanol leaf and stem-bark extracts of AMC may significantly influence the enzymes by reducing and increasing total ATPase and Na+/K+-ATPase activities depending on the doses and administration should therefore depend on the desired outcome.

Biochemical investigation of the upstream anti-sickling mechanisms of soursop (Annona muricata): 15-acetyl guanacone as an inhibitor of deoxyhaemoglobin polymerisation.

Current sickle cell disease (SCD) therapies are limited and inefficient. The ethnomedicinal values of Annona muricata in the treatment of SCD, leading to this present research. Leaves and fruits of Annona muricata were processed using solvent extraction and partitioning; aqueous, chloroform and ethyl acetate fractions. In vitro (anti-oxidant and anti-sickling), in silico, quantitative (amino acids) and kinetic simulation experiments were done. 15-acetyl guanacone, was used, in silico against 2,3-bisphosphoglycerate (2, 3-BPG) mutase and deoxyhaemoglobin. The ethyl acetate and chloroform fractions better NO● scavengers, iron-chelators and ferric reducing. In vitro unsickling (UT50) had ethyl acetate = 5 h and methanol = 7 h. Chloroform fraction had EC50 1.00 mg/mL (EC50 = 546 mg/mL) to 10.00 mg/mL (EC50 = 99 mg/mL). EC50 and IC50 of ethyl acetate fraction had steady-decrease. At higher concentration, chloroform fraction had higher Bmax (1.48 × 1021 U/mL) and higher Kd (3.66 × 1019 mg/mL), whereas, at a lower concentration, the ethyl acetate fraction demonstrated higher Bmax (7.23 × 1012 U/mL) and lower Kd (2.12 × 1011 mg/mL); The relative affinity (BP) of chloroform fraction increased progressively with concentration. The amino acid profile revealed rich concentrations glycine, valine, leucine, lysine, phenylalanine, histidine, arginine, and tryptophan. From the in silico experiments, 15-acetyl guanacone specifically targeted the A and B chains, with greater affinity for the beta subunit. This suggested that 15-acetyl guanacone might be able to prevent the polymerisation of deoxyHbSS, induce an allosteric conformational change that increases the oxygen affinity, and decrease the cellular 2, 3-BPG concentration.Communicated by Ramaswamy H. Sarma.