Investigation of Colloidal Structure and Biopharmaceutical Properties of New Antibacterial Composition of Gramicidin S

Introduction. Gramicidin S has been conventionally manufactured as buccal tablets. However, in the past decade, the interest in the development of spray formulations has been growing. Those formulations contain excipients that enhance the solubility of the antibiotic in water solutions. However, the real structure of gramicidin S containing sprays remains unrevealed.Aim. Investigation of colloidal structure and biopharmaceutical properties of new gramicidin S antibacterial composition.Materials and methods. The composition sample was obtained using gramicidin S dihydrochloride, propylene glycol, polysorbate-80, ethanol and purified water. Raman spectroscopy has been performed to determine the composition of the phases. Dynamic light scattering analysis was performed to characterize the composition particles. Release of gramicidin S was performed by dialysis method and the concentration was determined by HPLC. The antimicrobial properties were investigated in accordance with the requirements of the XIV edition of the Russian pharmacopoeia.Results and discussion. Dynamic light scattering analysis results show gramicidin S formulation particles having an average size in solution 5–50 nm and ζ-potential (–1.1: +7.9 mV). Based on the obtained data on the composition properties and formulation parameters it was classified as colloidal solution. The kinetic stability evaluation was performed. We compared the solubility in water and release parameters of the active pharmaceutical ingredient in the native state and in the micelles. The enhancement of the antimicrobial activity of the peptide in the colloidal solution was confirmed and ascribed to the synergic effect gramicidin S – surfactant.Conclusion. We reported the colloidal type of the composition, that aggregate gramicidin S at a concentration of 8 mg/mL. We found that gramicidin S inclusion into the colloidal solution led to significant efficiency increase, which reveals the potential to reduce the drug dose and side effects level.

Reversible and spatiotemporal control of colloidal structure formation

Tuning colloidal structure formation is a powerful approach to building functional materials, as a wide range of optical and viscoelastic properties can be accessed by the choice of individual building blocks and their interactions. Precise control is achieved by DNA specificity, depletion forces, or geometric constraints and results in a variety of complex structures. Due to the lack of control and reversibility of the interactions, an autonomous oscillating system on a mesoscale without external driving was not feasible until now. Here, we show that tunable DNA reaction circuits controlling linker strand concentrations can drive the dynamic and fully reversible assembly of DNA-functionalized micron-sized particles. The versatility of this approach is demonstrated by programming colloidal interactions in sequential and spatial order to obtain an oscillatory structure formation process on a mesoscopic scale. The experimental results represent an approach for the development of active materials by using DNA reaction networks to scale up the dynamic control of colloidal self-organization.

DETERGENT PRODUCTION TECHNOLOGY

Работа предназначена для комплексного решения задач синтетического моющего производства: Обеспечение качества мойки, очистки. Каждая из этих проблем требует соблюдения соответствующих физико-химических параметров раствора, подходящих, с одной стороны, для образования мицеллы (при промывке), с другой - для разрушения коллоидной структуры раствора и выделения поверхностно-активных веществ (ПАВ) и загрязняющих веществ при очистке сточных вод. В работе изучены условия электрохимической обработки моющих растворов для повышения качества мойки и эффективной очистки. Полученные результаты позволили представить технологическую технологию, основанную на замкнутом круговороте воды. В качестве регулирующего агента рекомендуется использовать электролиты, которые обеспечивают дезинфекцию моющих растворов без значительной минерализации. The work is intended for a comprehensive solution of the problems of synthetic detergent production: Ensuring the quality of washing and cleaning. Each of these problems requires compliance with the appropriate physical and chemical parameters of the solution, suitable, on the one hand, for the formation of micelles (during washing), on the other - for the destruction of the colloidal structure of the solution and the release of surfactants (surfactants) and pollutants during wastewater treatment. The paper studies the conditions of electrochemical treatment of cleaning solutions to improve the quality of washing and effective cleaning. The results obtained allowed us to present a technological technology based on a closed water cycle. As a regulating agent, it is recommended to use electrolytes that provide disinfection of cleaning solutions without significant mineralization

Polyelectrolyte Multilayered Nanoparticles as Nanocontainers for Enzyme Breakers During Hydraulic Fracturing Process

In this study, Layer-by-Layer (LbL) assembled polyelectrolyte multilayered nanoparticles were developed as a technique for targeted and controlled release of enzyme breakers. Polyelectrolyte multilayers (PEMs) were assembled by means of alternate electrostatic adsorption of polyanions and polycations using colloidal structure of polyelectrolyte complexes (PECs) as LbL building blocks. High enzyme concentrations were introduced into polyethyleneimine (PEI), a positively charged polyelectrolyte solution, to form an electrostatic PECs with dextran sulfate (DS), a negatively charged polyelectrolyte solution. Under the right concentrations and pH conditions, PEMs were assembled by alternating deposition of PEI with DS solutions at the colloidal structure of PEI-DS complexes. Stability and reproducibility of PEMs were tested over time. This work demonstrates the significance of PEMs as a technique for the targeted and controlled release of enzymes based on their high loading capacity, high capsulation efficiency, and extreme control over enzyme concentration. Entrapment efficiency (EE%) of polyelectrolyte multilayered nanoparticles were evaluated using concentration measurement methods as enzyme viscometric assays. Controlled release of enzyme entrapped within PEMs was sustained over longer time periods (> 18 hours) through reduction in viscosity, and elastic modulus of borate-crosslinked hydroxypropyl guar (HPG). Long-term fracture conductivity tests at 40℃ under closure stresses of 1,000, 2,000, and 4,000 psi revealed high fracture clean-up efficiency for fracturing fluid mixed with enzyme-loaded PEMs nanoparticles. The retained fracture conductivity improvement from 25% to 60% indicates the impact of controlled distribution of nanoparticles in the filter cake and along the entire fracture face as opposed to the randomly dispersed unentrapped enzyme. Retained fracture conductivity was found to be 34% for fluid systems containing conventional enzyme-loaded PECs. Additionally, enzyme-loaded PEMs demonstrated enhanced nanoparticle distribution, high loading and entrapment efficiency, and sustained release of the enzyme. This allows for the addition of higher enzyme concentrations without compromising the fluid properties during a treatment, thereby effectively degrading the concentrated residual gel to a greater extent. Fluid loss properties of polyelectrolyte multilayered nanoparticles were also studied under static conditions using a high-pressure fluid loss cell. A borate-crosslinked HPG mixed with nanoparticles was filtered against core plugs with similar permeabilities. The addition of multilayered nanoparticles into the fracturing fluid was observed to significantly improve the fluid- loss prevention effect. The spurt-loss coefficient values were also determined to cause lower filtrate volume than those with crosslinked base solutions. The PEI-DS complex bridging effects revealed a denser, colored filter cake indicating a relatively homogenous dispersion and properly sized particles in the filter cake.

Evaluation of the Composite Mechanism of Nano-Fe2O3/Asphalt Based on Molecular Simulation and Experiments

Asphalt, as an indispensable binder in road paving, plays an important role in transportation development. However, the mechanism of action between the modifier and asphalt cannot be fully explained by the existing test methods. This paper combines molecular simulations with experiments to provide a research and analysis tool to evaluate the “structure−performance” relationship of asphalt. From the trend of experimental results, the optimal content of Nano-Fe2O3 is 1% to 3%. The AFM micrograph of the asphalt material shows that at 3%, the Nano-Fe2O3 can be effectively dispersed in the asphalt and the unique “ bee structures “ of the asphalt can be adsorbed around the modifier. Molecular dynamics studies and results show that when Nano-Fe2O3 are incorporated into the asphalt and have a strong adsorption force on the colloidal structure of asphalt, the “ bee structures “ can be adsorbed around the Nano-Fe2O3. In the range of 208–543 K, the sol-gel structure of asphalt in the Nano-Fe2O3/asphalt composite system is gradually disrupted.