Antimicrobial peptides, such as GL13K, have a high binding selectivity toward bacterial membranes, while not affecting healthy mammalian cells at therapeutic concentrations. However, delivery of these peptides is challenging since they are susceptible to proteolytic hydrolysis and exhibit poor cellular uptake. A protective nanocarrier is thus proposed to overcome these obstacles. We investigate the potential to employ biodegradable phytoglycogen nanoparticles as carriers for GL13K using a simple loading protocol based on electrostatic association rather than chemical conjugation, eliminating the need for control of chemical cleavage for release of the peptide in situ. Both the native (quasineutral) and carboxymethylated (anionic) phytoglycogen were evaluated for their colloidal stability, loading capacity, and release characteristics. We show that the anionic nanophytoglycogen carries a greater cationic GL13K load and exhibits slower release kinetics than native nanophytoglycogen. Isotope exchange measurements demonstrate that the antimicrobial peptide is entrapped in the pores of the dendritic-like macromolecule, which should provide the necessary protection for delivery. Importantly, the nanoformulations are active against a Pseudomonas aeruginosa clinical isolate at concentrations comparable to those of the free peptide and representative, small molecule antibiotics. The colloidal nanocarrier preserves peptide stability and antimicrobial activity, even after long periods of storage (at least 8 months).

Water is the most important resource for life, but it has been greatly exhausted over the past century as a result of the human population and environmentally harmful activities. The excessive quantity of dyes exists in the wastewater produced from the textile industries which is the main reason for serious human health and environmental problems. There are many dye removal techniques, and the most promising one is the adsorption technique. The novelty of this research is using unmodified synthesized hydroxyapatite (HAp) as an adsorbent for the removal of gentian violet (GV) dye from aqueous solutions as there are no sufficient data in the literature about using it in the adsorption of GV dye from aqueous solutions. Unmodified HAp was synthesized by a combined precipitation microwave method. The prepared adsorbent was characterized by scanning electron microscopy (SEM), energy dispersive X-ray (EDX), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and zeta potential analyses. The kinetic study showed that the pseudo-second-order (PSO) model was the best fitted model with the experimental data. Analysis of adsorption isotherms using different models showed that this adsorption system was better described by the Halsey isotherm with a maximum adsorption capacity (qmax)  of 1.035 mg/g. The effects of experimental factors such as initial solution pH, initial dye concentration, adsorbent dose, and contact time were studied during the investigation of GV dye removal efficiency. The experimental results indicated that the maximum adsorption efficiency (99.32%) of the GV dye using HAp adsorbent was achieved at the following conditions: contact time = 90 min, pH = 12, initial GV dye concentration = 3 mg/L, and adsorbent dose = 1 g/L. The adsorption mechanism of the GV dye using HAp might be explained by the electrostatic interaction between the negatively charged surface of the HAp and the positively charged group of the GV dye. Thermodynamics study was performed on the adsorption process of GV dye from aqueous solutions using the synthesized HAp which revealed that this process was endothermic and spontaneous due to positive values of ΔH and ΔS and negative values of ΔG.