Cd(II) heavy metal is an extremely dangerous hazardous material for both humans and the environment. Its high toxicity is the reason behind the examination of new techniques for detecting very small concentrations of Cd(II). Recently, Quartz Crystal Microbalance (QCM) has been one of the techniques that have been widely used to detect trace heavy metal ions in solutions. It is a simple, inexpensive, portable, and sensitive gravimetric sensor due to its quality sensitivity lowest to nanograms. In this work, Cuprospinel nanoparticles were synthesized through the green synthesis approach using Psidium guajava L. leaf extract as a reducing agent, which is the first scientific description to report the preparation of these nanoparticles by this method. Subsequently, the synthesized nanoparticles were subjected to the characterization of their crystallinity, structure, and morphology by the XRD, N₂ adsorption–desorption, zeta potential, DLS, AFM, SEM, and TEM analyzers. The prepared Cuprospinel nanoparticles were evaluated as a nanosensor for the detection of the very low concentration of Cd(II) ions in aqueous solutions using the QCM technique. The results of the characterization proved that the Cuprospinel nanoparticles have formed in the nanoscale with sub-spherical shapes and particles size ranging from 20 to 80 nm. The BET surface area and pore size analysis revealed that the synthesized Cuprospinel nanoparticles possess a surface area of 47.3 m²/g, an average pore size of 1.5 nm, and a micropore volume of 0.064 cc/g. The QCM results demonstrated the success of the Cuprospinel nanoparticles sensor in detecting the tiny amounts of Cd(II) ions in the aqueous solutions with concentrations reaching about 3.6 ng/L.

In this study, rosemary leaf extract was effectively used to synthesize cobalt oxide nanoparticles (Co₃O₄ NPs) using a rapid, low-cost, and environmentally friendly approach. The prepared Co₃O₄ NPs were examined using various analytical techniques. However, UV spectrum analysis displayed two sharp absorption peaks at ~350 and 745 nm. The dynamic light scattering and zeta potential measurements were used to evaluate the particle size and the effective stabilization of the synthetic nanoparticles in the suspensions. A semi-triangular pyramidal shape of the Co₃O₄ NPs with a wide particle-size distribution could be observed in the scanning electron microscopy images. The energy-dispersive X-ray spectrum confirmed their successful synthesis, as the experimental atomic percentages agreed with the theoretical values. Moreover, X-ray diffraction analysis revealed that the synthesized Co₃O₄ NPs had a cubic crystalline structure corroborating that of theoretical Co₃O₄. Additionally, the Co₃O₄ NPs were not toxic at ≤62.5 µg/mL for Hep G2 and at ≤31.25 µg/mL for Mcf7. Therefore, these unique environmentally friendly Co₃O₄ NPs at this safe concentration could be studied in the future for their therapeutic activity.

Pb(II) is a significant contaminant that is known to have negative effects on both humans and animals. Recent industrial operations have exacerbated these consequences, and their release of several contaminants, including lead ions, has drawn attention to the potential effects on human health. Therefore, there is a lot of interest in the rapid, accurate, and selective detection of lead ions in various environmental samples. Sensors-based nanomaterials are a significant class among the many tools and methods developed and applied for such purposes. Therefore, a novel green synthesized cobalt ferrite (CoFe₂O₄) nanoparticles and functionalized CoFe₂O₄/Ca-alginate nanocomposite was designed and successfully synthesized for the fabrication of nanoparticles and nanocomposite-coated quartz crystal microbalance (QCM) nanosensors to detect the low concentrations of Pb(II) ions in the aqueous solutions at different temperatures. The structural and morphological properties of synthesized nanoparticles and nanocomposite were characterized using different tools such as X-ray diffraction (XRD), N₂ adsorption–desorption isotherm, dynamic light scattering (DLS), zeta potential analyzer (ζ-potential), atomic force microscopy (AFM), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX). The QCM results revealed that the green synthesized CoFe₂O₄ nanoparticles and functionalized CoFe₂O₄/Ca-alginate nanocomposite-coated QCM nanosensors exhibited high sensitivity, stability, and rapid detection of Pb(II) ions in the aqueous solutions at different temperature. The lowest detection limit for Pb(II) ions in the aqueous solutions could reach 125 ng, which resulted in a frequency shift of 27.49 ± 0.81, 23.63 ± 0.90, and 19.57 ± 0.86 Hz (Δf) for the QCM detector coated with green synthesized CoFe₂O₄ nanoparticles thin films, and 25.85 ± 0.85, 33.87 ± 0.73, and 6.87 ± 0.08 Hz (Δf) for the QCM detector coated with CoFe₂O₄/Ca-Alg nanocomposite thin films in a real-time of about 11, 13, and 13 min at 25 °C, 35 °C, and 45 °C, respectively. In addition, the resonance frequency change results showed the superiority of functionalized CoFe₂O₄/Ca-alginate nanocomposite coated QCM nanosensor over CoFe₂O₄ nanoparticles towards Pb(II) ions detecting, which attributed to the beneficial properties of alginate biopolymer.

In the current study, copper oxide nanoparticles (CuO NPs) were synthesized using chia seed extract in a simple, rapid, and eco-friendly manner for the first time. The synthesized CuO NPs were characterized using different analytical techniques. The images of field emission scanning electron microscopy revealed that the CuO NPs were triangular and pyramid in structure, with a mean particle size of 61.5 nm. The absorption peak of the synthesized CuO NPs was measured using ultraviolet-visible spectroscopy and was recorded at a wavelength of 291 nm. The results of energy-dispersive X-ray analysis confirmed that the CuO NPs synthesized using chia seed extract yielded high-purity CuO NPs. Moreover, the X-ray diffraction analysis indicated the highly crystalline nature of the CuO NPs, and the X-ray photoelectron spectroscopy results indicated that the CuO NPs were prepared successfully. Additionally, electrochemical impedance spectroscopy measurements revealed excellent electrocatalytic conductivity and fast electron transfer at the electrode/electrolyte interface of the synthesized CuO NP-modified glassy carbon electrode.

Magnetite Fe₃O₄ and spinel (2:1) and (4:1) NiFe₂O₄ magnetic nanoparticles (MNPs) were prepared by simple and affordable co-precipitation methods using an extract of star anise (Illicium verum) as a green reducing agent. The morphology and chemical composition of these MNPs were confirmed by field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, UV–visible spectroscopy, and X-ray diffraction (XRD). The synthesized magnetite Fe₃O₄ and spinel (2:1) and (4:1) NiFe₂O₄ MNPs were in the size range of 0.1–1 µm. The MNPs had irregular clustered platelets (magnetite Fe₃O₄) and pyramidal structures (spinel (2:1) and (4:1) NiFe₂O₄ NPs). The average sizes of the synthesized magnetite Fe₃O₄, and spinel (2:1) and (4:1) NiFe₂O₄ MNPs calculated using XRD analysis were 66.8, 72.5, and 72.9 nm, respectively. In addition to the characteristic absorption peaks of magnetite Fe₃O₄, those of spinel (2:1) and (4:1) NiFe₂O₄ MNPs were detected at ~300–350 nm and ~700 nm, respectively. Overall, the results of this study indicate that the synthesized magnetite Fe₃O₄, and spinel (2:1) and (4:1) NiFe₂O₄ MNPs showed high biomedical activities against liver carcinoma cells and non-small lung adenocarcinoma cells.

The main aim of this study was to prepare antimicrobial nanocomposites consisting of alginate, chitosan, and camptothecin (CPT). CPT-loaded calcium alginate (Ca-Alg₂) and calcium alginate/chitosan (Ca-Alg₂-CH) nanomaterials were synthesized and characterized using infrared (IR) spectroscopy, X-ray diffraction (XRD), UV-Vis spectroscopy, and scanning electron microscopy (SEM). The antimicrobial activity and the genetic effects of Ca-Alg₂/CPT and Ca-Alg₂-CH/CPT nanomaterials on Staphylococcus aureus, Escherichia coli, and Klebsiella pneumonia were studied. The repetitive element polymerase chain reaction analysis technique was used to assess the changes in the bacterial genetic material due to the processing of the nanomaterials. The results showed the presence of a strong chemical interaction between alginate and chitosan, and CPT was loaded successfully in both Ca-Alg₂/CPT and Ca-Alg₂-CH/CPT nanomaterials. Furthermore, the antimicrobial test showed that the Ca-Alg₂/CPT nanocomposite was susceptible to S. aureus, E. coli, and K. pneumonia; on the other hand, Ca-Alg₂-CH/CPT nanocomposite was more susceptible to E. coli and K. pneumonia and was resistant to S. aureus. The results showed that the Ca-Alg₂/CPT nanocomposite was less efficient than Ca-Alg₂-CH/CPT nanocomposite in killing Gram-negative treated bacteria. Moreover, results revealed that the PCR analysis revealed a polymorphic banding pattern. This observation provides an excellent guide to the ability of some polymers to induce point mutations in DNA.