Many industries use various dyes to beautify their products and discharge the waste into the water without proper treatment. Such wastewater is not only dangerous for aquatic life but it is also toxic to human life and can cause numerous problems, such as skin diseases, and some dyes are carcinogenic or even mutagenic as well. Rhodamine-B (RhB) is one of those synthetic organic dyes which is widely used in textile, paper making, leather manufacturing, stained glass work, cosmetics, and many other industries owing to its high tinting strength, high stability, and bright colour. Therefore, it is essential to either remove or reduce its concentration before releasing it into aquatic streams, as well as to minimize or control the cause of several diseases. Several physical and chemical methods have been used for the removal of different dyes from wastewater; nevertheless, adsorption is one of the best techniques used for the removal of dyes due to its high efficiency and low cost. In this regard, we used Chamaecyparis lawsoniana (C. lawsoniana) fruit as a bio-adsorbent for the removal of RhB from an aqueous solution. An 85.42% dye adsorption was achieved at optimized conditions (pH 2, 40 ppm initial dye concentration, 105 min, and 50 mg adsorbent). Adsorption occurs by pseudo-second-order kinetics, according to kinetic studies. Several samples from various sources, including tap water, distilled water, river water, and filtered river water, were tested for RhB removal, and the study revealed good results even in river water. Thus, C. lawsoniana fruit can be used for its real-world application.

Photodynamic antimicrobial chemotherapy is an attractive and novel therapeutic approach to treat microbial infections. Antimicrobial peptides (AMPs) have the potential to specifically target and kill the microorganism while showing no effect toward mammalian cells. In the current study, antimicrobial peptide (GGG(RW)3), an analogue of MP-196, was conjugated to a zinc phthalocyanine (ZnPc) photosensitizer (PS) for photoinactivation assay to enhance the bacterial killing efficacy of the peptide. The AMPs showed selectivity toward the Gram-positive strain of bacteria. We observed that the conjugate ZnPc-GGG(RW)3 also displayed a photoinactivation effect against the Gram-positive strains of S. aureus. The results showed that ZnPc-GGG(RW)3 induced a 6-log reduction (i.e., 99.999% cell killing) in Gram-positive S. aureus at a light dose of 22 J/cm² upon illumination under red light, while the peptide did not exhibit such a significant effect when tested alone at the same concentration. The conjugate also showed 50% inhibition of the bacterial strain in the dark at a higher concentration. Furthermore, the addition of potassium iodide salt to the PS at lower concentrations also significantly killed the Gram-negative E. coli strain and killed the E. coli strain with up to a 5-log reduction at a light dose of 22 J/cm² under red light illumination. We demonstrated the efficacy of antimicrobial peptide (GGG(RW)3 enhanced by conjugation to a ZnPc photosensitizer.

In the present study, we determined the levels of chlorinated pesticide residues in surface water samples collected from the Charsadda district (KPK, Pakistan). SPME-GC-ECD with COMBI PAL CTC autosampler was used for extraction and analysis of 20 organochlorine pesticides in the collected water samples. For maximum efficiency of the SPME procedure, several parameters were studied, including the extraction and desorption time of the fiber, solution pH, agitation of samples, and stirring speed, etc. This method showed good liner response, with R² values in the range of 0.9887 to 0.9999 for all pesticides. This method also provided good percent recoveries at 1 µg L⁻¹ (87.5 to 106.0%) and at 2 µg L⁻¹ (88.5 to 109.2%). Lower limits of detection for all 20 chlorinated pesticides were found to be lower than their maximum permissible contamination levels. Approximately 50% of the surface water samples collected from the Charsadda district were found to be contaminated with the pesticides γ-BHC, heptachlor, aldrin and dieldrin, with maximum concentrations of 0.023, 0.108, 0.014 and 0.013 µg L⁻¹, respectively. For adults and children, the cancer risk from water due to contamination by various pesticides ranged from 0 to 33.29 × 10⁻⁶. The non-carcinogenic risk from each pollutant in the water samples of the Charsadda district was found to be in the order of heptachlor > aldrin > dieldrin > γ-BHC. However, the pesticides α-BHC, β-BHC, heptachlor epoxide, chlordane, endrin, 4,4′-DDD, endrin ketone, 4,4′-DDT, endosulfan sulfate and methoxychlor were not detected in any of the surface water samples of investigated in the present study.

Ferene is the most commonly used chromogenic agent for the determination of serum iron in blood. In this work we have successfully synthesized Ferene-S-conjugated silver nanoparticles (Ferene-S-AgNPs) for the first time characterized by UV-visible, Fourier-Transform Infrared Spectroscopy (FTIR), and Matrix-Assisted Laser Desorption/Ionization-Time Of Flight (MALDI-TOF) mass spectrometry techniques. Particle size of the synthesized nanoparticles was determined by atomic-force microscopy and scanning electron microscopy techniques with size ranges from 10–90 nm in diameter. Ferene-S-AgNPs were explored for their chemosensing potential with various metal ions such as Sb³⁺, Pb²⁺, Ca²⁺, Fe²⁺, K⁺, Co²⁺, Ba²⁺, V⁵⁺, Cu⁺, Cd²⁺, Hg²⁺, Ni²⁺, Cu²⁺, Fe³⁺, Mg²⁺, Mn²⁺, Al³⁺, and Cr³⁺. Ferene-S-AgNPs were found to show selective quenching effects and slight bathochromic shifts to the surface plasmon resonance absorption band after treatment with Fe²⁺. Furthermore, the developed chemosensor also exhibited substantial selectivity towards Fe²⁺ in the presence of other competitive ions. We observed that Ferene-S-AgNPs mimic the selectivity of the parent compound of Ferene towards Fe²⁺. The system obeyed Beer’s law over concentration ranges of 110–190 nM. The detection limit was found to be 110 nM.

The silver nanoparticles were synthesized, functionalized with afzelechin and characterized using UV-Visible spectroscopy. A difference of 20 nm was observed in surface plasmon resonance of bare and functionalized silver nanoparticles which indicates afzelechin conjugation with silver nanoparticles. The atomic force microscopy (AFM) technique was used for the determination of the size and morphology of synthesized silver nanoparticles. The afzelechin conjugated silver nanoparticles were spherical and their sizes ranged from 3 to 10 nm with an average size of 8 nm while the bare silver nanoparticles were also spherical and their sizes ranged from 3 to 10 nm with an average size of 6 nm. The average sizes were also calculated by fitting their UV-Visible absorption spectra. Fitting is based on the Mie and Mie Gans models, which deduced that afzelechin conjugated silver nanoparticles were 96.5% spherical and 3.5% spheroidal with an average size of 5 nm while bare silver nanoparticles were 100% spherical with an average size of 4 nm. Both the fitting model as well as the AFM results showed a difference of 3 nm between the sizes of afzelechin conjugated silver nanoparticles while 2 nm differences was observed for bare silver nanoparticles. The band gap energy of afzelechin conjugated silver nanoparticles and bare silver nanoparticles were calculated via Tauc’s equation and were found to be 5.1 eV and 5.4 eV, respectively. A difference of 0.3 eV was observed in band gap energies of afzelechin conjugated silver nanoparticles and bare silver nanoparticles.