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Plant-mediated synthesis of nanoparticles is a sustainable approach that has gained widespread scientific acceptance due to its numerous benefits and applications. In this study, a zinc oxide-doped activated carbon (ZAC) derived from palm kernel shells (PKS) was synthesized via a bioreduction route using a water-based extract of Nymphaea lotus leaves as a reducing agent. The synthesized ZAC nanocomposites were characterized using microscopic (TEM, SEM) and spectroscopic (FTIR, EDS, XRD, and UV-Vis) analyses. The adsorptive properties of ZAC and efficiency in scavenging a phenothiazine derivative (methylene blue) from an aqueous solution were investigated. Results reveal that nano-scale ZAC particles were crystalline, exhibited irregular shapes, with an average size of 45 nm, and were highly dispersed. The optimum quantity adsorbed was 248 mg/g at a methylene blue concentration of 140 mg/L for 60 min using 0.02 g/100 mL of ZAC. Adsorption and kinetics data closely aligned with the Freundlich isotherm and the pseudo-second-order model, respectively indicating heterogeneous surface adsorption and chemisorption as the dominant mechanisms. The regeneration study of ZAC shows that over five cycles, thermal regeneration maintained high adsorption capacity with minimal decline and chemical regeneration significantly led to reduction in the adsorption capacity but solvent washing offered a balance between efficacy and structural preservation.

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Photoelectrochemical (PEC) sensing is an emerging technological innovation for monitoring small substances/molecules in biological or non-biological systems. In particular, there has been a surge of interest in developing PEC devices for determining molecules of clinical significance. This is especially the case for molecules that are markers for serious and deadly medical conditions. The increased interest in PEC sensors to monitor such biomarkers can be attributed to the many apparent advantages of the PEC system, including an enhanced measurable signal, high potential for miniaturization, rapid testing, and low cost, amongst others. The growing number of published research reports on the subject calls for a comprehensive review of the various findings. This article is a review of studies on electrochemical (EC) and PEC sensors for ovarian cancer biomarkers in the last seven years (2016-2022). EC sensors were included because PEC is an improved EC; and a comparison of both systems has, expectedly, been carried out in many studies. Specific attention was given to the different markers of ovarian cancer and the EC/PEC sensing platforms developed for their detection/quantification. Relevant articles were sourced from the following databases: Scopus, PubMed Central, Web of Science, Science Direct, Academic Search Complete, EBSCO, CORE, Directory of open Access Journals (DOAJ), Public Library of Science (PLOS), BioMed Central (BMC), Semantic Scholar, Research Gate, SciELO, Wiley Online Library, Elsevier and SpringerLink.

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Mercury is a well-known heavy metal pollutant of global importance, typically found in effluents (lakes, oceans, and sewage) and released into the atmosphere. It is highly toxic to humans, animals and plants. Therefore, the current challenge is to develop efficient materials and techniques that can be used to remediate mercury pollution in water and the atmosphere, even in low concentrations. The paper aims to review the chitosan-based polymer nanocomposite materials that have been used for the environmental remediation of mercury pollution since they possess multifunctional properties, beneficial for the adsorption of various kinds of pollutants from wastewater and the atmosphere. In addition, these chitosan-based polymer nanocomposites are made of non-toxic materials that are environmentally friendly, highly porous, biocompatible, biodegradable, and recyclable; they have a high number of surface active sites, are earth-abundant, have minimal surface defects, and are metal-free. Advances in the modification of the chitosan, mainly with nanomaterials such as multi-walled carbon nanotube and nanoparticles (Ag, TiO2, S, and ZnO), and its use for mercury uptake by batch adsorption and passive sampler methods are discussed.

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To date, in South Africa alone, there are an estimated 4.5 million people receiving antiretroviral (ARV) therapy. This places South Africa as the country with the largest ARV therapy programme in the world. As a result, there are an increasing number of reports on the occurrence of ARVs in South African waters. Achieving efficient and bio-friendly methods for the removal of these pollutants is considered as a concern for environmental researchers. This study aims at studying the efficiency of a moving bed biofilm reactor (MBBR) system for removing ARVs from wastewater. A continuous-flow laboratory scale system was designed, built, installed, and operated at a carrier filling rate of 30%, an organic loading rate of 0.6 kg COD/m3.d-1 OLR, a hydraulic retention time of 18h, and a 27.8 mL/min flow rate. The systems were monitored over time for the elimination of conventional wastewater parameters i.e., Biological Oxygen Demand, Chemical Oxygen Demand, and nutrients. The results showed that the MBBR system as a bio-friendly method has high efficiency in removing Nevirapine, Tenofovir, Efavirenz, Ritonavir and Emtricitabine from the synthetic influent sample with an average removal of 62%, 74%, 94%, 94% and 95%, respectively, after 10 days of operation.

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The disinfection of wastewater using nanoparticles (NPs) has become a focal area of research in water treatment. In this study, zinc oxide (ZnO) NPs were synthesized using the microwave heating crystallization technique and characterized using transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD). Qualitative well diffusion and quantitative minimum inhibitory concentration (MIC) tests were conducted to determine the antimicrobial activity of ZnO NPs against selected waterborne pathogenic microbes. FTIR spectral studies confirmed that the binding of urea with Zn occurs through Zn-O stretching. XRD confirmed the crystallized identity in a hexagonal ZnO wurtzite-type structure. The formation of zones of inhibition and low MIC values in the antimicrobial analysis were indicative of the effective antimicrobial activity of zinc oxide nanoparticles against the test microorganisms. The application of metallic nanoparticles in water treatment could curb the spread of waterborne microbial diseases.

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Nanotechnology can be defined as the field of science and technology that studies material at nanoscale (1-100 nm). These nanomaterials, especially carbon nanostructure-based composites and biopolymer-based nanocomposites, exhibit excellent chemical, physical, mechanical, electrical, and many other properties beneficial for their application in many consumer products (e.g., industrial, food, pharmaceutical, and medical). The current literature reports that the increased exposure of humans to nanomaterials could toxicologically affect their environment. Hence, this paper aims to present a review on the possible nanotoxicology assays that can be used to evaluate the toxicity of engineered nanomaterials. The different ways humans are exposed to nanomaterials are discussed, and the recent toxicity evaluation approaches of these nanomaterials are critically assessed.

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A multifunctional nanobiocomposite polymer was developed in this study through a cross-linking polymerization of cyclodextrin with phosphorylated multi-walled carbon nanotubes followed by sol-gel to incorporate TiO2 and Ag nanoparticles. This work's novelty was to prove that the developed nanobiocomposite polymer is a potential filter nanosponge capable of removing organic, inorganic, and microorganisms' pollutants from wastewater samples. The synthesized multifunctional nanobiocomposite polymer was characterized using a range of spectroscopy and electron microscopy techniques. Fourier-transform infrared (FTIR) confirmed the presence of oxygen-containing groups on the developed nanobiocomposite polymer and carbamate linkage (NH(CO)) distinctive peak at around 1645 cm-1, which is evidence that the polymerization reaction was successful. The scanning electron microscopy (SEM) image shows that the developed nanobiocomposite polymer has a rough surface. The Dubinin-Radushkevich and the pseudo-second-order kinetic models best described the adsorption mechanism of Co2+ and TCE's onto pMWCNT/CD/TiO2-Ag. The efficacy of the developed nanobiocomposite polymer to act as disinfectant material in an environmental media (e.g., sewage wastewater sample) compared to the enriched media (e.g., nutrient Muller Hinton broth) was investigated. From the results obtained, in an environmental media, pMWCNT/CD/TiO2-Ag nanobiocomposite polymer can alter the bacteria's metabolic process by inhibiting the growth and killing the bacteria, whereas, in enriched media, the bacteria's growth was retarded.

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Nowadays, access to clean water sources worldwide and particularly in Southern Africa is inadequate because of its pollution by organic, inorganic, and microorganism contaminants. A range of conventional water treatment techniques has been used to resolve the problem. However, these methods are currently facing the confronts posed by new emerging contaminants. Therefore, there is a need to develop simple and lower cost-effective water purification methods that use recyclable bio-based natural polymers such as chitosan modified with nanomaterials. These novel functional chitosan-based nanomaterials have been proven to effectively eliminate the different environmental pollutants from wastewater to acceptable levels. This paper aims to present a review of the recent development of functional chitosan modified with carbon nanostructured and inorganic nanoparticles. Their application as biosorbents in fixed-bed continuous flow column adsorption for water purification is also discussed.

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A wide variety of biomass materials have been used for the removal of toxic chromium(VI) by biosorption. The current study investigated the efficacy of Macadamia nutshells treated with sodium hydroxide, nitric acid, and the Fenton-like reagent in the removal of Cr(VI). The adsorbents were characterized by FTIR, SEM, TGA, and elemental analysis. Effects of functional parameters influencing the adsorption of Cr(VI), solution pH (pH 1-11), contact time (5-250 min), concentration of adsorbent (1-10 g/L), and adsorbate concentration (10-200 mg/L) were investigated. The optimum conditions for biosorption were pH 1.4, adsorbent dose of 5 g/L, and 160 min of contact time. In all cases, the base-treated adsorbent displayed superior performance compared to others, with highest percent removal of 98%. The adsorbate-adsorbent interactions were better explained by the Freundlich isotherm and the pseudo-first-order rate model. The Macadamia-based adsorbents are potentially useful for Cr(VI) removal from aqueous solutions. PRACTITIONER POINTS: Three different chemical activators were investigated for the modification of Macadamia surface. The base-treated material exhibited the highest specific surface area of 12.1 m2 /g. The Cr(VI) adsorption performance for the base-treated material dwarfed the other materials. Excellent Cr(VI) removal efficiency in the presence of competitors was achieved.

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The application of gold as drug candidate dated back to 2500 BC and its relevance in medicine became more appealing following 1985 FDA approval of ingested Auranofin for the treatment of rheumatoid arthritis. In this study, we have provided a density functional theory (DFT) study of some gold(III)-dithiocarbamate complexes with characteristic anticancer potentials. DFT calculation of the reactivity and selectivity properties of these complexes with an enzyme template of thioredoxin reductase (TrxR) was carried out. The investigation proceeds with theoretical characterization of the selected compounds through spectroscopic analyses. IR and UV-vis analyses were carried out and the calculated values are comparable to experimental results. NMR assignment was determined for the gold compounds and the estimated theoretical chemical shift values agree with available experimental data from literature. The obtained DFT-based chemical parameters proved to be significant in evaluating the selectivity, reactivity and stability of the gold(III) complexes as potential anticancer moieties, specifically against TrxR. Calculated binding free energy gave similar order with the available in vitro inhibition profile of these gold(III)-dithiocarbamate complexes against TrxR. The outcome of this DFT study could serve as a useful guide towards future design of new and potent anticancer drug candidate. The investigated chemical reactivity properties could be considered and applied to a wide range of bioactive compounds and enzyme-inhibitor systems.

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A comparative photocatalytic degradation of 2-chlorophenol (2CP) in aqueous solution was investigated using pristine and Ag-doped semiconductor photocatalysts obtained from TiO2, ZnO and ZnS. Varying percentages (1, 3 and 5%) of Ag nanoparticles were doped on the semiconductor photocatalysts via the sol-gel method. The pristine and Ag-doped photocatalysts were characterized using UV-Vis diffuse reflectance spectroscopy, photo-luminescence spectroscopy, X-Ray diffractometry, Fourier transform infrared spectroscopy and transmission electron microscopy; and these techniques confirmed the successful syntheses of the pristine and Ag-doped species. The photocatalytic activities of all species for the degradation of 2CP were carried in photo-reactor using UV irradiation intensity of 1.4 mW/cm2 for 150 min; and the effects of various operating parameters (such as catalyst loading, pH and 2CP initial concentrations) were studied. The results showed enhanced 2CP degradation in the Ag-doped species in comparison to the pristine species while alkaline pH region was most suitable for 2CP degradation especially at low concentration. Lower loadings of the photocatalysts were usually more effective for the 2CP degradation and the degradation trend in the TiO2 and ZnS species was 5% Ag-doped >3% Ag-doped >1% Ag-doped > Pristine, while it was 1% Ag-doped >3% Ag-doped >5% Ag-doped > Pristine in the ZnO. Thus, although the Ag doping enhanced 2CP by all semiconductor photocatalysts, the Ag-doped TiO2 was more effective than the ZnO and ZnS species.

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Waste from biomass was used to prepare a low-cost biochar-clay hybrid adsorbent. The hybrid adsorbent was synthesised by combining Kaolin with biomass (Vitex doniana), thereafter, modified with Deep Eutectic Solvent (DES). The materials were characterised using scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectrometry (FTIR), Thermal gravimetric analysis (TGA), and Brunauer-Emmett-Teller (BET), also, pHpzc of the materials were studied. The resultant adsorbents were used for both column and batch adsorption of organic pollutants; dye (Acid Blue 74; AB74) and pharmaceuticals (ciprofloxacin; CIP and acetaminophen; ACTE). Column adsorption capacity, effect of pollutant concentration and effect of flow rate were studied, also, the column was modelled using Thomas, Yoon-Nelson and Adams-Bohart model. Furthermore, batch adsorption experiments were performed, effect of change in pH, time, dose and concentration were studied. Batch adsorption data were fitted with isotherm and kinetic models. The experiment showed tremendous increase in adsorption capacity when the hybrid adsorbent (HYD) was modified with DES (HYD-DES). Acid Blue 74 on HYD-DES has the highest column sorption capacity followed by ciprofloxacin and acetaminophen. Adsorption was favoured at pH range of 2-10 for both AB74 and ACTE as there is no significant changes in the % removal performance, while adsorption was best at pH 6 and above for CIP. AB74 and CIP are best described by Langmuir isotherm, whereas ACTE adsorption was best explained by Freundlich isotherm equilibrium. The DES modified HYD has shown it can be effectively utilised as possible adsorbent for adsorbing organic dyes and pharmaceuticals.

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The silver-zinc oxide (Ag-ZnO) polyamide thin film composite (PA-TFC) membrane was prepared by interfacial polymerization. The Ag-ZnO/PA-TFC membrane was characterized by attenuated total reflectance fourier-transform infrared spectroscopy (ATR-FTIR) for polyamide functional groups and contact angle for surface hydrophilicity. The Ag-ZnO/PA-TFC membrane was further characterized by Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM) for morphology and surface roughness, respectively. The performance of the fabricated membrane was investigated using pure water flux, permeability, rejection, flux recovery, and fouling resistance using low molecular weight organic pollutants, 2-chlorophenol (2-CP) and 2,4-dichlorophenol (2,4-DCP). The results were compared to the neat (PA-TFC) membrane. It was observed that incorporation of Ag-ZnO nanocomposites into the PA-TFC membrane improved hydrophilicity, permeation, rejection, and fouling resistance properties of the membrane. The contact angle decreased from 62.8° to 54° for PA-TFC and the Ag-ZnO/PA-TFC membrane, respectively. The presence of Ag-ZnO enhanced permeability of the membrane from 0.9 (Lm-2h-1bar-1) to 1.9 (Lm-2h-1bar-1). Modification of the membrane with Ag-ZnO further showed an enhanced rejection of 2-CP and 2,4-DCP from 43% to 80% and 58% to 85%, respectively. The 2,4-DCP molecules were rejected more than 2-CP due to enhanced repulsive forces from the extra Cl ion. A high flux recovery of about 95% was achieved for the modified membrane compared to 64% for the neat membrane. The improved flux recovery was an indication of enhanced antifouling propensity.

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The importance of improving adsorbent's adsorption efficiency in organic pollutants has been reported by many researchers. Surfactant-based modified adsorbents were a tasteful choice. As a result, the use of surfactants as a modifier for removing organic pollutants has shown to play a very big role in enhancing the adsorption efficiency of different materials. Ionic liquids are receiving extensive interest as green multipurpose compounds, primarily as a replacement for traditional chemicals that are used in many chemical processes. This work gives a brief bibliometric analysis of application of ionic liquid from 1930 to 2017, documents were collected from Scopus database and keywords from the abstracts and titles were analyzed using VOSviewer software. Furthermore, the work presents a review of conventionally known surfactants and the recent likelihood of ionic liquids for modifying adsorbents for adsorption of organic pollutants. Over the period of years between 1930 and 2017, 13,144 documents were published on the application of ionic liquids. VOSviewer software further confirms that adsorption is one of the leading areas in applications of ionic liquids. Review also showed that ionic liquid is a good modifier of adsorbents.

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Macadamia nutshell powder oxidized by hydrogen peroxide solutions (MHP) was functionalized by immobilizing 1,5'-diphenylcarbazide (DPC) on its surface. The effectiveness of grafting was confirmed by the Fourier transform infrared spectrum due to the presence of NH and C=C stretches at 3361, 1591, and 1486 cm-1, respectively, on the grafted material which were absent in the nongrafted material. Thermogravimetric analysis revealed that the presence of DPC on the surface of Macadamia shells lowered the thermal stability from 300°C to about 180°C owing to the volatile nature of DPC. Surface roughness as a result of grafting was appreciated on the scanning electron microscopy images. Parameters influencing the adsorptive removal of Cr(VI) were examined and found to be optimal at pH 2, 120 min, 150 mg/L, and 2.5 g/L. Grafting MHP with DPC leads to an increase in the Langmuir monolayer capacity from 37.74 to 72.12 mg/g. Grafting MHP with DPC produced adsorbent with improved removal efficiency for Cr(VI).

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OBJECTIVE: To evaluate the biological activities of Combretum erythrophyllum (C. erythrophyllum) leaf extracts against infectious diseases' pathogenesis and their cytotoxicity potentials. METHODS: Powdered leaf material (300 g) of C. erythrophyllum was extracted (1:10 w/v) using acetone to obtain the crude extract. Liquid-liquid fractionation was performed on the crude acetone extract (30 g) using solvents of different polarity. The bioautographic method was used to detect the inhibition of bacterial and fungal growth by active compounds present in the crude and fractions. The extracts were then tested on bacterial strains: Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, Pseudomonas aeruginosa; fungal strains: Candida albicans (C. albicans), Cryptococcus neoformans, and Aspergillus fumigatus, by microtitre dilution method for MIC determination. RESULTS: The extracts MIC values ranged between 0.08 and 2.50 mg/mL against the tested pathogens. Water fraction had the highest activity against bacteria strains, while the fungal assay revealed crude acetone extract and ethyl acetate fraction to be active against C. albicans (1.25 mg/mL), dichloromethane extract against C. albicans and A. fumigatus (0.16 mg/mL). Extract fractions showed a good antioxidant activity via DPPH, ABTS and hydroxyl radical scavenging assays, in the order: ethyl acetate > water > acetone > dichloromethane > hexane. The toxicity level of crude extract and fractions evaluated in Vero monkey kidney cells ranged from 34 to 223 µg/mL, while doxorubicin (IC50 = 7.19 µg/mL) served as the positive control. CONCLUSIONS: It can be concluded that the extracts of C. erythrophyllum are safe for medicinal use in folk medicine for treating infectious and stress related diseases.

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The behavior of an amperometric organic-phase biosensor consisting of a gold electrode modified first with a mercaptobenzothiazole self-assembled monolayer, followed by electropolymerization of polyaniline in which acetylcholinesterase as enzyme was immobilized, has been developed and evaluated for organophosphorous pesticide detection. The voltammetric results have shown that the formal potential shifts anodically as the Au/MBT/PANI/AChE/PVAc thick-film biosensor responded to acetylthiocholine substrate addition under anaerobic conditions in selected organic solvent media containing 2% v/v 0.05 M phosphate buffer, 0.1 M KCl (pH 7.2) solution. Detection limits in the order of 0.147 ppb for diazinon and 0.172 ppb for fenthion in acetone-saline phosphate buffer solution, and 0.180 ppb for diazinon and 0.194 ppb for fenthion in ethanol-saline phosphate buffer solution has been achieved.

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