Investigation of the simulated microgravity impact on heavy metal biosorption by Saccharomyces cerevisiae.

Heavy metals are one of the most dangerous environmental pollutions, and their elimination is one of the health system's priorities. Microorganisms have been introduced as a safe absorber of such pollution and this ability is related to the characteristics of their surface layers. There are reports about some bacteria's increment of cell envelope thickness in space conditions. Therefore, this study investigated SMG effect on heavy metals biosorption using Saccharomyces (S.) cerevisiae. Furthermore, the stability of complex, isotherm, and kinetic absorption models has been investigated. The results showed that the SMG positively affected the biosorption of mercury (Hg) 97% and lead (Pb) 72.5% by S. cerevisiae. In contrast, it did not affect cadmium (Cd) and arsenic (As) biosorption. In gastrointestinal conditions, Hg, Cd, and As-yeast complexes were stable, and their biosorption increased. In the case of the Pb-yeast complex, in simulated gastric exposure, the binding decreased at first but increased again in simulated intestinal exposure in both SMG and normal gravity (NG). The metals' biosorption by yeast followed the pseudo-second-order kinetic and the Langmuir isotherm models for all metals (As) matched with Langmuir and Freundlich. The current research results demonstrate that microgravity provides desirable conditions for heavy metal biosorption by S. cerevisiae. Furthermore, the biosorbent-heavy metal complex remains stable after simulated gastrointestinal conditions. Altogether, the results of this study could be considered in detoxifying food and beverage industries and maintaining astronauts' health.

The Luminescence of Laser-Produced Carbon Nanodots: The Effect of Aggregation in PEI Solution.

Carbon nanodots (CNDs) produced in pure water by the ablation of graphite with a nanosecond laser pulse exhibit weak photoluminescence. A small addition of polyethyleneimine (PEI) to the aqueous suspension of CNDs causes a significant increase in emissions. This paper presents experimental and theoretical studies of the emission properties of CND/PEI systems. The obtained CNDs responded to even trace amounts of PEI in solution (~0.014% v/v), resulting in a significant increase in the initial weak blue emission of CNDs and PEI taken separately. Morphology and size measurements showed that particle aggregation occurred in the presence of the polymer. A decrease in the calculated Stokes shift values was observed with increasing PEI content in the solution. This indicates a reduction in the number of non-radiative transitions, which explains the increase in the emission intensity of the CND/PEI systems. These results therefore confirmed that the increase in the emission of CND/PEI systems is caused by particle aggregation. Kinetic studies proved that the process is controlled mainly by diffusion, the initial stage of which has a dominant influence on determining the optical properties of the system.

Comparative Analysis of Hydrogel Adsorption/Desorption with and without Surfactants.

In this particular study, a hydrogel known as SAP-1 was synthesized through the grafting of acrylic acid-co-acrylamide onto pullulan, resulting in the creation of Pul-g-Poly (acrylic acid-co-acrylamide). Additionally, a sponge hydrogel named SAP-2 was prepared by incorporating the surfactant sodium dodecyl benzene sulfonate (SDBS) into the hydrogel through free radical solution polymerization. To gain further insight into the composition and properties of the hydrogels, various techniques, such as Fourier transform infrared spectroscopy, hydrogen nuclear magnetic resonance (1H NMR), atomic absorption spectroscopy, and field emission scanning electron microscopy (FE-SEM), were employed. Conversely, the absorption kinetics and the equilibrium capacities of the prepared hydrogels were investigated and analyzed. The outcomes of the investigation indicated that each of the synthesized hydrogels exhibited considerable efficacy as adsorbents for cadmium (II), copper (II), and nickel (II) ions. In particular, SAP-2 gel displayed a remarkable cadmium (II) ion absorption ability, with a rate of 190.72 mg/g. Following closely, SAP-1 gel demonstrated the ability to absorb cadmium (II) ions at a rate of 146.9 mg/g and copper (II) ions at a rate of 154 mg/g. Notably, SAP-2 hydrogel demonstrated the ability to repeat the adsorption-desorption cycles three times for cadmium (II) ions, resulting in absorption capacities of 190.72 mg/g, 100.43 mg/g, and 19.64 mg/g for the first, second, and third cycles, respectively. Thus, based on the abovementioned results, it can be concluded that all the synthesized hydrogels possess promising potential as suitable candidates for the adsorption and desorption of cadmium (II), copper (II), and nickel (II) ions.

Synthesis of sustainable mesoporous sulfur-doped biobased carbon with superior performance sodium diclofenac removal: Kinetic, equilibrium, thermodynamic and mechanism.

Over the last years, the strategy of employing inevitable organic waste and residue streams to produce valuable and greener materials for a wide range of applications has been proven an efficient and suitable approach. In this research, sulfur-doped porous biochar was produced through a single-step pyrolysis of birch waste tree in the presence of zinc chloride as chemical activator. The sulfur doping process led to a remarkable impact on the biochar structure. Moreover, it was shown that sulfur doping also had an important impact on sodium diclofenac (S-DCF) removal from aqueous solutions due to the introduction of S-functionalities on biochar surface. The adsorption experiments suggested that General and Liu models offered the best fit for the kinetic and equilibrium studies, respectively. The results showed that the kinetic was faster for the S-doped biochar while the maximum adsorption capacity values at 318 K were 564 mg g-1 (non-doped) and 693 mg g-1 (S-doped); highlighting the better affinity of S-doped biochar for the S-DCF molecule compared to non-doped biochar. The thermodynamic parameters (ΔH0, ΔS0, ΔG0) suggested that the S-DCF removal on both adsorbents was spontaneous, favourable, and endothermic.

Comparative study of synthesis methods and pH-dependent adsorption of methylene blue dye on UiO-66 and NH2-UiO-66.

Metal-organic frameworks (MOFs) are highly promising adsorbents with notable properties such as elevated adsorption capacities and versatile surface design capabilities. This study introduces two distinct synthesis methods, one lasting 1 h and the other 24 h, for UiO-66 and NH2-UiO-66. While both methods yield structures with comparable crystallinity and morphology, the adsorption performance of the cationic methylene blue dye varies at different pH levels. Despite the 24 h synthesis time being optimal for maximum adsorption in both MOFs, the relative difference in NH2-UiO-66 adsorption percentage at different times suggests reduced dependency on synthesis time for this property. Notably, NH2-UiO-66 exhibits consistent and effective performance across three pH levels, warranting further investigation into its adsorption kinetics and isotherm. The achievement of high adsorption efficiency coupled with a significantly reduced synthesis time underscores the importance of developing simplified synthetic methods, essential for enhancing the practical applicability of MOFs in diverse applications.

A novel scalable polycationic melamine sponge-based filtration matrix for continuous ultrafast adsorption of anionic pollutants.

Effective capturing of anionic pollutants from wastewater under industrial operating conditions, which requires high processing flux and fast adsorption rate remains a challenge. Here, a commercially available melamine sponge (MS) with reticulated 3D macroporous structures was covalently modified with positively charged moieties using a single step functionalization under mild conditions. The developed novel polycationic melamine sponge (MS+) was formed by a nucleophilic addition reaction between glycidyltrimethylammonium chloride (GMTA) and MS, followed by a self-propagation of GMTA. The produced MS+ possessed strong electrostatic interactions with different anions such as Rose Bengal (RB) and phosphates (P) under a wide pH range (3-11). The MS+ exhibited promoted static adsorption efficiencies of 400 mg g-1 (P) and 600 mg g-1 (RB), within 5 min and 60 s, respectively. Furthermore, the MS+ showed high stability and recyclability for up to 15 cycles of uses, and the recycling process was environmentally friendly by using 1 M NaCl as a releasing solution. Benefiting from fast flow through the macroporous MS+ and highly positive charged skeleton, the MS+ was applied for rapid dynamic enrichment process of P from real manure wastewater with an enrichment factor of 4.4. Utilization of the MS+ as the substrate brings additional advantages such as low cost, availability, and flexibility to fit into existing filtration devices. The developed MS+ could be expanded for enrichments of other anionic species from various polluted water sources.

Detailed insights in adsorption process of heavy metals on tire wear particles.

Road traffic induced tire wear particles (TWP) attracted widespread attention due to their potential environmental impact. Here, the adsorption process of heavy metals like Pb2+ and Cd2+ on tire wear particles produced by filing (TWP-f) is studied to elucidate the underlying kinetics and thermodynamics. This work includes voltammetric experiments to investigate the concentration and temperature dependency of the adsorption. The adsorption kinetics in buffer solution spiked with heavy metals follows a pseudo-second-order rate equation involving rate-controlling boundary layer adsorption and a side-by-side intraparticle diffusion process. Meanwhile, the adsorption tendencies under the studied conditions for TWP-f were Pb2+ > Cd2+. The equilibrium adsorption data were modulated by the Langmuir, Freundlich, and Dubinin-Radushkevich (DR) isotherms. Both the Freundlich and DR isotherms were found to be feasible for describing the adsorption on TWP-f. The adsorption energy obtained from the DR isotherm is 1.6 kJ mol-1 for Pb2+ and 2 kJ mol-1 for Cd2+, indicating physisorption as the dominating force. According to the Freundlich isotherm, multilayer adsorption is proposed. The thermodynamic parameters show that the adsorption of Pb2+ and Cd2+ is endergonic. Due to small Gibbs enthalpy values near the thermodynamic equilibrium, the adsorption process is mainly dependent on the ambient conditions. So, close-to-nature experiments were conducted to verify the received results. Therefore, tire and road wear particles including road sediments (TRWP+RS) were added to prefiltered freshwater samples of the river Freiberger Mulde (having naturally elevated trace element concentrations). The adsorption kinetics were investigated by ICP-MS/MS emphasizing the pseudo-second-order rate equation. Moreover, it is suggested that the tire wear particles in the TRWP+RS sample are majorly responsible for the adsorption of at least Cd2+.

Synthesis, Properties and Adsorption Kinetic Study of New Cross-Linked Composite Materials Based on Polyethylene Glycol Polyrotaxane and Polyisoprene/Semi-Rotaxane.

New composite materials were prepared via cross-linking of polyethylene glycol/2-hydroxypropyl-ß-cyclodextrins polyrotaxane (PEG/HPßCD) and polyisoprene/HPßCD semi-polyrotaxane (PI/HPßCD SR) with 1,6-hexamethylene diizocyanate (HMDI). Advanced instrumental methods (such WAXS (wide angle X-ray scattering), AFM (atomic force microscopy), SEM (scanning electron microscopy), and thermal and dynamic vapor sorption) were employed for the structural, morphological and thermal characterization of the resulting composite materials. The roughness parameters calculated using AFM indicate a smoother surface for the composite material with 10 wt% of PI/HPßCD SR, denoting that a homogeneous film was obtained. SEM analysis reveals porous morphologies for both composite materials and the pore sizes increase with the increasing concentration of PI/HPßCD SR in the matrix. Dynamic vapor sorption/desorption measurements and type IV isotherms confirmed the hydrophilic and porous materials, which are in agreement with SEM analysis. The composite with a higher PI/HPßCD SR concentration in the matrix showed increased thermal stability than that of the pure cross-linked material. This material was further tested as a sorbent for methylene blue (MB) dye removal from an aqueous solution. The adsorption capacity of the composite film was found to be 2.58 mg g-1 at 25 °C.

Three-Dimensional Mass Transfer Modeling of Hydroquinone Adsorption on Phragmites australis Biochar.

In this work, the overall adsorption kinetic process of hydroquinone on Phragmites australis biochar (PAC) was analyzed in depth. A 3D mass transfer model of pore volume and surface diffusion was established, and the diffusion mechanism was analyzed. The characterization results show PAC has a higher porosity value, which is conducive to the adsorption of hydroquinone. The adsorption process modeling results show that the combined effect of pore volume diffusion and surface diffusion promotes the total diffusion process of hydroquinone in the PAC particles, and the two mechanisms of pore volume and surface diffusion exist simultaneously. Under the different operating concentrations, the range of surface diffusion coefficient Ds is 2.5 × 10-10-1.74 × 10-9 cm2/s, and the contribution rate of surface diffusion SDCP% is close to 100%, which is much larger than pore volume diffusion, revealing that regardless of the contact time and position, surface diffusion occupies the main position in intraparticle diffusion.

Facile synthesis of polyethyleneimine-modified cellulose nanocrystal/silica hybrid aerogel for CO2 adsorption.

Cellulose nanocrystal (CNC)/silica hybrid aerogel (CSA) was synthesized from CNC and sodium silicate hybridization using the one-step sol-gel method under atmospheric drying. At a weight ratio of CNC to silica of 1:1, the obtained CSA-1 had a highly porous network, a high specific area of 479 m2 g-1, and a CO2 adsorption capacity of 0.25 mmol g-1. Then, polyethyleneimine (PEI) was impregnated on CSA-1 to improve CO2 adsorption performance. The parameters governing CO2 adsorption performance on CSA-PEI, such as temperatures (70-120 °C) and PEI concentrations (40-60 wt%), were investigated systematically. The optimum adsorbent (CSA-PEI50) exhibited an excellent CO2 adsorption capacity of 2.35 mmol g-1 at 70 °C and a PEI concentration of 50 wt%. The adsorption mechanism of CSA-PEI50 was elucidated by analyzing many adsorption kinetic models. The CO2 adsorption behaviors of CSA-PEI at various temperatures and PEI concentrations had the goodness of fit with the Avrami kinetic model, which can correspond to the multiple adsorption mechanism. The Avrami model also showed fractional reaction orders in a range of 0.352-0.613, and the root mean square error is negligible. Moreover, the rate-limiting kinetic analysis showed that film diffusion and intraparticle diffusion resistance controlled the adsorption speed and dominated the subsequent adsorption stages, respectively. The CSA-PEI50 also exhibited excellent stability after ten adsorption-desorption cycles. This study illustrated that CSA-PEI was a potential adsorbent for CO2 capture from flue gas.

Hydrothermal Pretreatment of KOH for the Preparation of PAC and Its Adsorption on TC.

The environment has been heavily contaminated with tetracycline (TC) due to its excessive use; however, activated carbon possessing well-developed pores can effectively adsorb TC. This study synthesized pinecone-derived activated carbon (PAC) with high specific surface area (1744.659 cm2/g, 1688.427 cm2/g) and high adsorption properties (840.62 mg/g, 827.33 mg/g) via hydrothermal pretreatment methods utilizing pinecones as precursors. The results showed that PAC treated with 6% KOH solution had excellent adsorption properties. It is found that the adsorption process accords with the PSO model, and a large amount of C=C in PAC provides the carrier for π-πEDA interaction. The results of characterization and the isothermal model show that TC plays a key role in the adsorption process of PAC. It is concluded that the adsorption process of TC on PAC prepared by hydrothermal pretreatment is mainly pore filling and π-πEDA interaction, which makes it a promising adsorbent for TC adsorption.

Adsorption Kinetics of Methyl Orange from Model Polluted Water onto N-Doped Activated Carbons Prepared from N-Containing Polymers.

This study aimed to assess the role of polymeric sources (polypyrrole, polyaniline, and their copolymer) of nitrogen (N)-doped activated carbons (indexed as PAnAC, PPyAC, and PnyAC, respectively) on their adsorption efficiency to remove methyl orange (MO) as a model cationic dye. The adsorbents were characterized using FTIR, SEM, TGA, elemental analysis, and surface area. The kinetic experiments were performed in batches at different MO concentrations (C0) and adsorbent dosages. The adsorption kinetic profiles of pseudo-first-order, pseudo-second-order (PSO), Elovich, intraparticle diffusion, and liquid film diffusion models were compared. The results showed a better fit to the PSO model, suggesting a chemisorption process. The adsorption capacity (qe, mg/g) was found to have increased as MO C0 increased, yet decreased as the adsorbent quantity increased. At the adsorption operating condition, including MO C0 (200 ppm) and adsorbent dose (40 mg), the calculated qe values were in the order of PAnAC (405 mg/g) > PPyAC (204 mg/g) > PnyAC (182 mg/g). This trend proved the carbon precursor's importance in the final properties of the intended carbons; elemental analysis confirmed that the more nitrogen atoms are in the activated carbon, the greater the number of active sites in the adsorbent for accommodating adsorbates. The diffusion mechanism also assumed a rate-limiting step controlled by the film and intraparticle diffusion. Therefore, such an efficient performance may support the target route's usefulness in converting nitrogenous-species waste into valuable materials.

Adsorption-enhanced catalytic oxidation for long-lasting dynamic degradation of organic dyes by porous manganese-based biopolymeric catalyst.

Improving the adsorption kinetics of metal-oxide catalysts is critical for the enhancement of catalytic performance in heterogeneous catalytic oxidation reactions. Herein, based on the biopolymer pomelo peels (PP) and metal-oxide catalyst manganese oxide (MnOx), an adsorption-enhanced catalyst (MnOx-PP) was constructed for catalytic organic dyes oxidative-degradation. MnOx-PP shows excellent methylene blue (MB) and total carbon content (TOC) removal efficiency of 99.5 % and 66.31 % respectively, and keeps the long-lasting stable dynamic degradation efficiency during 72 h based on the self-built continuous single-pass MB purification device. The chemical structure similarity and negative-charge polarity sites of the biopolymer PP improve the adsorption kinetics of organic macromolecule MB, and construct the adsorption-enhanced catalytic oxidation microenvironment. Meanwhile, the adsorption-enhanced catalyst MnOx-PP obtains lower ionization potential and O2 adsorption energy to promote the continuous generation of active substance (O2*, OH*) for the further catalytic oxidation of adsorbed MB molecules. This work explored the adsorption-enhanced catalytic oxidation mechanism for the degradation of organic pollutants, and provided a feasible technical idea for designing adsorption-enhanced catalysts for the long-lasting efficient removal of organic dyes.

Preparation and Characterization of a New Bis-Uracil Chitosan-Based Hydrogel as Efficient Adsorbent for Removal of Anionic Congo Red Dye.

A new hydrogel, based on chitosan crosslinked with 2-chlorophenyl-bis(6-amino-1,3-dimethyluracil-5-yl) methane, (2Clph-BU-Cs), has been successfully created. Various instrumental techniques such as elemental analysis, FTIR, SEM, and XRD were used to prove its structure. Its removal efficiency for anionic Congo red (CR) dye under different conditions for industrial wastewater treatment was studied. For optimizing the conditions to maximize CR dye removal, the impacts of temperature, contact time, pH, and initial concentration of the dye on adsorption capacity were investigated. The removal of the dye was pH-dependent, with a much higher value achieved at pH 4 than at pH 7 and 9. The maximum adsorption capacity of the hydrogel was 93.46 mg g-1. The model of adsorption process was fitted to the pseudo-second-order kinetic model. The intraparticle diffusion demonstrated the multi-step nature of the adsorption process. The thermodynamic results showed that the adsorption process was endothermic because of the positive value of enthalpy (43.70 kJ mol-1). The process of adsorption at high temperatures was spontaneous, according to the values of ∆G0. An increase in randomness was seen in the value of ∆S°. Generally, the investigated hydrogel has the potential to be used as a promising effective reusable adsorbent for industrial wastewater remediation.

Efficient removal of dyes from aqueous solutions using short-length bimodal mesoporous carbon adsorbents.

Ordered mesoporous carbons (OMCs) with controlled mesopore lengths and volumes were synthesized and investigated to remove the model dye methylene blue (MB) from aqueous solutions. The pore size, specific surface area, pore volume, and pore length of OMCs (CMK-3, sCMK-3, and sCMK-5) were analyzed and benchmarked against commercial activated carbon (AC). CMK-3 and sCMK-3 had narrow pore size distributions (PSDs) centered at ∼4.4 nm, whereas the PSD of sCMK-5 was bimodal, derived from the same pores as CMK-3 (∼4.4 nm) and the inner diameter of the carbon nanotubes (∼5.8 nm). The pore length decreased from 743 nm for CMK-3 to 173 nm for sCMK-3 and 169 nm for sCMK-5, facilitating the MB accessibility and efficient utilization of internal mesopores. The MB adsorption on the prepared adsorbents was well described by a pseudo-second-order kinetic model (R2 > 0.999), and the initial adsorption rate (h) on sCMK-5 was 34.07-fold faster than that on commercial AC. The Langmuir model adequately explained the equilibrium adsorption data, and the increase in the Langmuir maximal adsorption capacity (qm) of the OMCs was proportional to the specific surface area. The MB adsorption on sCMK-5 was endothermic and spontaneous, and proceeded primarily through physical adsorption as well as chemisorption reacting with oxygen atoms in hydroxyl groups. The prepared adsorbents were also suitable for polishing textile wastewater containing color-causing substances along with the background organic matter. These OMCs are promising for treating wastewater as efficient adsorbents for large molecular pollutants such as dyes.

Preparation of Copper Ion Adsorbed Modified Montmorillonite/Cellulose Acetate Porous Composite Fiber Membrane by Centrifugal Spinning.

The natural adsorption material montmorillonite (MMT) was selected, and cellulose acetate (CA) was used as the loading substrate to design and prepare a kind of green and environment-friendly recyclable porous composite fiber membrane with good heavy metal ion adsorption performance. Acetic acid modified montmorillonite (HCl-MMT), sodium dodecyl sulfonate modified montmorillonite (SDS-MMT), and chitosan modified montmorillonite (CTS-MMT) were prepared by inorganic modification and organic modification, and the porous MMT/CA composite fiber membrane was constructed by centrifugal spinning equipment. The morphological and structural changes of MMT before and after modification and their effects on porous composite fiber membranes were investigated. The morphology, structure, and adsorption properties of the composite fibers were characterized by scanning electron microscopy (SEM) and atomic absorption spectrometry (ASS). The experimental results showed that the maximum adsorption capacity of Cu2+ on the prepared 5 wt% CTS-MMT composite fiber membrane was 60.272 mg/g after 10 h static adsorption. The adsorption of Cu2+ by a porous composite fiber membrane conforms to the quasi-second-order kinetic model and Langmuir isothermal adsorption model. The main factor of the Cu2+ adsorption rate is chemical adsorption, and the adsorption mechanism is mainly monolayer adsorption.

Novel Graphene oxide-Polyethylene Glycol mono-4-nonylphenyl Ether adsorbent for solid phase extraction of Pb2+ in blood and water samples.

A novel and efficient Graphene Oxide-Polyethylene Glycol mono-4-nonylphenyl Ether (GO-PEGPE) nanocomposite was synthesized and used for solid phase extraction of trace levels of Pb2+ in different water and blood samples. The synthesized adsorbent was then characterized by the Fourier Transform-Infrared spectrophotometry (FT-IR), Field Emission-Scanning Electron Microscopy (FE-SEM), Energy dispersive X-ray spectroscopy (EDX) and X-ray diffraction analysis (XRD). To optimize the critical parameters including pH of samples solution, amounts of adsorbent and extraction time, the response surface methodology based on the central composite design (RSM-CCD) was used and based on the results, pH = 6.0, extraction time = 22 min and amounts of adsorbent = 15 mg were selected as the optimum conditions. The relative standard deviation based on seven replicate analysis of 2 µg L-1 Pb2+ was 5.2% and the limit of detection was 0.023 µg L-1 (n = 8). The results of adsorption isotherm investigation show that the adsorption of Pb2+ onto the GO-PEGPE nanocomposite obeyed by the Langmuir isotherm with the maximum adsorption capacity of 69.44 mg g-1. Also, based on the Temkin and Dubinin-Radushkevich (DR) isotherms, the adsorption of Pb2+ onto the GO-PEGPE nanocomposite is a physisorption phenomenon and the consequences of the kinetic models illustrated that the adsorption of Pb2+ followed by the pseudo second order adsorption kinetic model. Finally, the proposed method was successfully applied for preconcentration of Pb2+ in different water and blood samples of turning industry workers.

One-pot alkanolamines-assisted synthesis of magnetic mesoporous silica for synthetic dye adsorption.

Magnetic mesoporous silica (MMS) was synthesized in a one-pot system using various alkanolamines (triethanolamine, diethanolamine, tris (hydroxymethyl)aminomethane) as a basic catalyst. The characterization of the composites was conducted using scanning electron microscope, transmission electron microscope, X-ray diffractometer, surface area analyzer, and X-ray photoelectros spectroscopy. The MMS synthesized with tris(hydroxymethyl)aminomethane (MMSTRIS) showed the highest specific surface area, pore volume, and average pore diameter. However, when the composites were applied as adsorbents for brilliant green (BG) dye, MMS synthesized with diethanolamine (MMSDEA) showed the highest maximum adsorption capacity of 339.7 mg g-1. The fastest adsorption rate constant of 1.57 × 10-2 g mg-1 min-1 was obtained for MMSTRIS, which has the largest average pore size among all composites. The adsorption kinetic study suggested that the adsorption of BG onto the prepared MMS composites was mainly chemisorption process, which most likely involves electrostatic interaction and hydrogen bonding between BG molecule and the surface of the composites.

Fabrication of a Double Core-Shell Particle-Based Magnetic Nanocomposite for Effective Adsorption-Controlled Release of Drugs.

There has been very limited work on the control loading and release of the drugs aprepitant and sofosbuvir. These drugs need a significant material for the control of their loading and release phenomenon that can supply the drug at its target site. Magnetic nanoparticles have characteristics that enable them to be applied in biomedical fields and, more specifically, as a drug delivery system when they are incorporated with a biocompatible polymer. The coating with magnetic nanoparticles is performed to increase efficiency and reduce side effects. In this regard, attempts are made to search for suitable materials retaining biocompatibility and magnetic behavior. In the present study, silica-coated iron oxide nanoparticles were incorporated with core-shell particles made of poly(2-acrylamido-2-methylpropane sulfonic acid)@butyl methacrylate to produce a magnetic composite material (MCM-PA@B) through the free radical polymerization method. The as-prepared composite materials were characterized through Fourier-transform infrared (FTIR)spectroscopy, scanning electron microscopy (SEM), X-ray diffraction analysis (XRD), energy-dispersive X-Ray Analysis (EDX), and thermogravimetric analysis (TGA), and were further investigated for the loading and release of the drugs aprepitant and sofosbuvir. The maximum loading capacity of 305.76 mg/g for aprepitant and 307 mg/g for sofosbuvir was obtained at pH 4. Various adsorption kinetic models and isotherms were applied on the loading of both drugs. From all of the results obtained, it was found that MCM-PA@B can retain the drug for more than 24 h and release it slowly, due to which it can be applied for the controlled loading and targeted release of the drugs.

Rotating Magnetic Field-Assisted Reactor Enhances Mechanisms of Phage Adsorption on Bacterial Cell Surface.

Growing interest in bacteriophage research and use, especially as an alternative treatment option for multidrug-resistant bacterial infection, requires rapid development of production methods and strengthening of bacteriophage activities. Bacteriophage adsorption to host cells initiates the process of infection. The rotating magnetic field (RMF) is a promising biotechnological method for process intensification, especially for the intensification of micromixing and mass transfer. This study evaluates the use of RMF to enhance the infection process by influencing bacteriophage adsorption rate. The RMF exposition decreased the t50 and t75 of bacteriophages T4 on Escherichia coli cells and vb_SauM_A phages on Staphylococcus aureus cells. The T4 phage adsorption rate increased from 3.13 × 10-9 mL × min-1 to 1.64 × 10-8 mL × min-1. The adsorption rate of vb_SauM_A phages exposed to RMF increased from 4.94 × 10-9 mL × min-1 to 7.34 × 10-9 mL × min-1. Additionally, the phage T4 zeta potential changed under RMF from -11.1 ± 0.49 mV to -7.66 ± 0.29 for unexposed and RMF-exposed bacteriophages, respectively.