Algeria
Algeria
Echahid Cheikh Larbi-Tebessi University
Abstract: Green biosynthesis of ZnO nanoparticles from Suaeda corniculata extract as a bioactive additive for corrosion-resistant zinc electrodeposition
Corrosion of metallic structures remains a major economic and industrial burden worldwide, causing production interruptions, structural failures, and costly replacement of degraded equipment. Zinc electrodeposition is one of the most widely used methods for protecting mild steel, and coating performance can be substantially improved by incorporating additives into the electrolytic bath. However, most additives used commercially are synthetic organic compounds whose toxicity limits their broader application, motivating a shift toward natural, biodegradable, and environmentally friendly alternatives that can play the same functional role without the associated hazards. This work reports the green biosynthesis of zinc oxide nanoparticles (ZnO NPs) using the aqueous extract of Suaeda corniculata, a salt-tolerant halophyte plant rich in polyphenolic compounds (18.45 ± 0.03 mg GAE/g), which act as natural reducing and stabilizing agents during nanoparticle formation, avoiding the need for hazardous chemical reagents. The biosynthesized ZnO NPs were characterized using four complementary techniques. UV-visible spectroscopy revealed a characteristic absorption band at 370-390 nm, while Fourier-transform infrared spectroscopy confirmed a Zn-O vibration band near 438 cm⁻¹. Scanning electron microscopy showed irregular agglomerates of nanometric grains with spherical and hexagonal morphologies. Energy-dispersive X-ray spectroscopy confirmed Zn and O as the principal elemental constituents, with the Zn:O mass ratio increasing from 41.5:58.5 to 66.6:33.4 after calcination. These biosynthesized nanoparticles were then evaluated as additives in the zinc electrodeposition bath used to coat E24-2 mild steel. Coating parameters, including current density, bath pH, and NPs-ZnO concentration, were systematically optimized, with the best deposit quality obtained at pH 4.5 and 0.09 A. Corrosion resistance of the coated steel was assessed under realistic conditions in natural seawater, using open-circuit potential monitoring, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization. The addition of ZnO NPs markedly improved deposit adhesion, thickness, and brightness compared with the additive-free bath, and shifted corrosion potentials toward more cathodic values. EIS measurements showed a maximum inhibition efficiency of 87.20% at a concentration of 1.2 g/L, closely corroborated by potentiodynamic polarization data, which indicated 86.39% inhibition efficiency at the same concentration, together with a marked reduction in corrosion current density and coating porosity. These findings demonstrate that plant-mediated ZnO nanoparticles, obtained through an inexpensive and eco-friendly biosynthesis route, act as effective multifunctional additives for zinc electroplating baths, simultaneously enhancing coating morphology and corrosion resistance. This approach offers a sustainable, low-cost alternative to toxic synthetic additives, and opens promising perspectives for the metal-coating and marine-protection industries, connecting green nanotechnology with the biochemical valorization of underexploited halophyte flora from arid and saline environments such as those of Algeria.
Nigeria
Nigeria
University of Medical Sciences
ABSTRACT: Fractions of Tetracarpidium conophorum Leaf Migitate 3- Methylcholanthrene Induced Oxidative Stress and Induced selective Apoptosis in Human Cancer-Derived PBMC
Medicinal plants products have been on the uprising in treating many diseases, including cancer, replacing conventional anticancer therapies, due to their safety, availability, potency, and accessibility. This study investigated the anticancer potential of Tetracarpidium conophorum (African walnut) leaf extracts on 3- methylcholanthrene induced oxidative stress in wistar rats, and induced selective apoptosis in human cancer lymphocyte cells.T conophorum leaf was extracted with methanol and n-hexane solvents using soxhlet apparatus, and antioxidant-guided fractionation was identified by column chromatography. 40 male Wistar rats (110g-140g) were divided into 8 groups. The experimental groups include positive control, negative control (3-MC at 150mg/kg), pretreated group and the extracts only group. The pretreated group received graded dosage of T conophorum (100mg/kg and 400mg/kg respectively) extracts for one week and were induced by single interperitoneal dose of 3-MC (150mg/kg) for another one week. Human PBMC samples obtained from healthy individuals and cancer patients were isolated, cultured, and treated with T conophorum leaf fractions at 50 µg/ml and 100 µg/ml respectively.Antioxidant-guided fractionation identified the 70:30 ethyl acetate:methanol (EA:Meth) and ethyl acetate:hexane (EA:Hex) fractions as optimal. Rats induced with 3-MC significantly elevated oxidative stress, inflammation, hepatic and renal injury and also alterations in hepatic and renal function biomarkers compared to the positive control group. Administration of T conophorum leaf extracts mitigates these alterations, with 400 mg/kg EA:Meth fraction exhibiting the most pronounced effect significantly increased (P < 0.05) antioxidant defenses, reduced pro-inflammatory cytokine levels, and maintained organ architecture. In human PBMCs, EA:Meth fraction 100 µg/ml exhibited the most selective cytotoxicity by markedly decreasing viability in cancer-derived lymphocytes while preserving healthy cells. Mechanistically, this selectivity was associated with reduced oxidative stress and inflammation, as well as activation of the intrinsic mitochondrial apoptotic pathway through increased p53/Bax expression and decreased Bcl-2 levels.T. conophorum leaf fractions demonstrate dual anticancer effects by mitigating oxidative stress and inflammation in rats and inducing selective apoptosis in human cancer cells. These results support the plant's ethnomedicinal relevance and underscore its potential as a source of safe and accessible multi-targeted anticancer agents.
