Ibuprofen Research Articles

High-performance novel ZIF-67 and ZIF-67@MWNTs composite adsorbents for efficient removal of pharmaceutical contaminant from water: Exceptional capacity and excellent reusability

The removal of pharmaceutical waste products like ibuprofen (IBP) from water is very important for the environment and the health of human and aquatic organisms. In the present work, the adsorption of IBP from aqueous solution was investigated by synthesizing novel ZIF-67 and ZIF-67@MWNTs hybrid composite material by incorporating ZIF-67 particles with carboxyl functionalized multiwalled carbon nanotubes (COOH-MWNT). The synthesized ZIF-67 and ZIF-67@MWNTs adsorbents were characterized by the XPS, XRD, SEM, TEM, BET, FTIR, and TGA analysis to examine their physio-chemical properties. The synthesized novel ZIF-67 has a 1743 m2/g BET surface and 0.692 cm3/g total pore volume. The IBP adsorption process including isotherm and kinetic studies as well as the effect of different parameters i.e. pH, initial concentration, time, adsorbents, and their dosage were examined. Among all the synthesized composite materials, the ZIF-67@MWNT-50 mg material showed the highest IBP adsorption capacity of 841 ± 5 mg/g, about 467 ± 5 mg/g more than the ZIF-67 following the Langmuir and pseudo-second-order model. The enhancement in the IBP adsorption is because of the incorporation of COOH-MWNT and the presence of a large number of active binding sites which showed the van der Waal interactions, host–guest interactions, π- π interactions, and H-bonding between the adsorbate and adsorbent. For the detailed study of the IBP adsorption mechanism of ZIF-67, molecular dynamic (MD) simulations were performed. Additionally, the reusability of ZIF-67@MWNT-50 mg material via a simple regeneration method up to five cycles while maintaining about 96 % adsorption capacity of the pristine non-used ZIF-67@MWNT-50 mg material revealed its importance as an effective adsorbent for the adsorptive elimination of different pharmaceutical hazardous materials from water.

Enhanced SERS performance of cavity-hosting silver dendrites grown over TiO2 nanotubes

Silver nanostructures, utilized as SERS substrates, consistently exhibit exceptional performance in detecting organic compounds through Raman spectroscopy, primarily due to the electromagnetic enhancement mechanism. This study explores an advanced SERS substrate composed of cavities formed by silver dendrites (Ag-Ds) on TiO2 nanotubes (TiO2-NT), demonstrating exceptional performance in detecting organic compounds through Raman spectroscopy. TiO2-NT acts as a template, guiding the nucleation and growth of Ag-D to create the cavity structures. The deposition time of silver significantly influences substrate performance in detecting Rhodamine 6G (R6G) and Ibuprofen (IB). It has been observed that an extended deposition time diminishes the enhancement factor. In contrast, a shorter deposition time yields notable enhancement due to the combined effects of electromagnetic and chemical enhancement mechanisms. An optimum deposition time limits dendrite growth, forming cavities where the electric field couples with multiple light reflections, further amplifying the SERS enhancement. The cavity-hosted Ag-D/TiO2-NT substrate achieves an impressive analytic SERS enhancement factor of up to 2 × 109, enabling the detection of R6G and IB at a low detection limit of 10-12 M.

Sorption interactions and behavior of bentonite-lignite based composite toward immobilization of dyes, pharmaceuticals and surfactants

The presence of dyes, pharmaceuticals, and surfactants in the environment results from extensive industrial and societal progress, prompting the need to explore efficient and safe techniques for their removal. Common concentrations in wastewater can range from micrograms to milligrams per liter, which is concerning due to their persistence and potential health impacts. The sustainable approach of using a nonconventional, eco-friendly mineral-organic composite might address this environmental issue. This study focuses on utilizing a composite of bentonite (BEN) and lignite (LIG) as a sorbent for dyes: Rhodamine b (RB), Remazol brilliant blue r (RBBR), pharmaceuticals: ibuprofen (IB), sulfamethoxazole (STX), and surfactant: sodium dodecylbenzenesulfonate (SDBS) from both synthetic solutions and real wastewater. BEN was chosen for its high cation exchange capacity, while LIG was selected for its ability to adsorb both anionic and cationic formsdiverse functional groups. The composite with BEN to LIG ratio of 20:80 (BL 20:80) demonstrated superior sorption capacity. The adsorption performance is quantified, showing removal efficiencies of up to 18.9 mg RBBR/g, 22.8 mg RB/g, 1.77 mg IB/g, 1.47 mg STX/g, and 4.7 mg SDBS/g. Sorption efficiency is influenced by factors such as the initial sorbate concentration, the pH of the solution, the form of sorbates, and the adsorbents textural, physicochemical (point of zero charge pHZPC), ion-exchange capacity, hydrophobicity/hydrophilicity) properties. Generally, STX and RB is favored by slightly acidic conditions (pH 4–7), while RBBR and IB are favored by alkaline conditions (pH > 7). The complex physical sorption mechanism includes hydrogen bonding, electrostatic and dispersion forces, as well as π-π interactions. Nuclear magnetic resonance spectroscopy (NMR) suggests that a significant portion of the hydrogen bonding interactions contributes to RB adsorption. The sorption results indicate that the specially-designed mineral composite can effectively remove various chemically distinct organic compounds from real wastewater. Subsequent investigations will focus on the granulated BL 20:80 composite and its applicability in dynamic column systems. This aligns with the ongoing development of purification technologies.

Synthesis of leek-based N,S self-doped CQDs/TiO2 and its application in the photocatalytic degradation of organic pollutants

In this work, N,S self-doped CQDs (N,S-CQDs/TiO2) were synthesized from leeks via a microwave method, and a new leek-based N,S-CQDs/TiO2 composite photocatalytic material was prepared by roasting. The structural characteristics, optical properties, and electrical properties of the N,S-CQDs/TiO2 composites were characterized by Scanning electron microscope (SEM), Transmission electron microscope (TEM), X-ray powder diffraction (XRD), Solid ultraviolet–visible diffuse reflectance (UV–vis-DRS), Fourier transform infrared Spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), transient photocurrent response, and Electrochemical impedance spectroscopy (EIS). In addition, the catalytic degradation effect of N,S-CQDs/TiO2 was evaluated by the photocatalytic degradation of Rhodamine B (RhB) and ibuprofen (IBU). The experimental results showed that the photocatalytic degradation effect of leek-based N,S-CQDs/TiO2 was significantly better than that of TiO2, and N,S-CQDs/TiO2 with 1.86 wt% N,S-CQDs (1.86-N,S-CQDs/TiO2), which demonstrated optimal photocatalytic degradation. The photocatalytic degradation rate of RhB (20 mg/L) was 94.65 % within 120 min of high-voltage mercury lamp irradiation, which was 41.15 % higher than that of TiO2(53.50 %), and the degradation rate was 80.10 % after four cycles. After 180 min, the photocatalytic degradation rate of IBU (10 mg/L) was 96.92 %, which was 26.39 % higher than that of TiO2 (70.53 %), and the degradation rate could still reach 78.94 % after four cycles. In this work, the photocatalytic degradation mechanisms of RhB and IBU by N,S-CQDs/TiO2 were explored by free radical capture and ESR free radical detection experiments. This study may serve as an important reference for enhancing the photocatalytic degradation effect by using biomass self-doped CQDs/TiO2 composite photocatalytic materials, and as a reference for the photocatalytic treatment of organic pollutants in water.

Preparation of CS coated graded ordered porous ZrO2 implantable drug carrier

ZrO2 is bioceramic known for its excellent chemical stability and biocompatibility. Porous ZrO2, with its large surface area, has attracted considerable attention in the field of orthopedic implant drug delivery. However, the shortcomings of poor bioactivity and insufficient drug loading capacity in traditionally prepared porous ZrO2 limit its application. In this paper, graded ordered porous ZrO2 with interconnected open pores was prepared by colloid crystal templating, which exhibited large specific surface area and excellent slow-release properties. Then, it was surface-coated with chitosan (CS) possessing bioactivity and strong adsorption capacity. Factors affecting microscopic morphology, drug loading and slow-release properties of this composite were systematically investigated using ibuprofen (IBU) as a drug model. Results showed that graded ordered porous ZrO2 significantly enhanced drug loading capacity compared to normal ordered porous ZrO2, reaching 125.66 mg/g. Additionally, surface coating modification of the composite by CS significantly affected IBU loading capacity. By regulating process parameters such as CS concentration and coating time, high-efficiency loading of IBU was realized and drug loading capacity reached up to 194.17 mg/g. In vitro drug simulation experiments showed that CS coating effectively controlled the initial burst release of IBU and prolonged the effective release time; maximum cumulative release rate reached 93.7 %. This study provides a new idea for implantable drug sustained-release systems, which may better meet medical needs.

Design of Selective Nanoparticles of Layered Double Hydroxide (Mg/Al-LDH) for the Analysis of Anti-Inflammatory Non-Steroidal Agents in Environmental Samples, Coupled with Solid-Phase Extraction and Capillary Electrophoresis

A simple, fast, and low-cost pre-concentration methodology based on the application of solid-phase extraction coupled to layered double hydroxides (LDHs) and capillary electrophoresis was developed for the determination of naproxen (NPX), diclofenac (DFC), and ibuprofen (IBP) in environmental sample waters. A systematic study of the LDH composition was designed, including the effects of interlayer anions (NO3−, Cl−, CO32−, BenO−, and SDS−) and the effect of molar ratio (Mg:Al). The optimal composition of MgAl/Cl−-LDH (Mg:Al; 1.5:1.0) was coupled to an SPE system: pH (neutral pH), LDH amount (15 mg), and extraction capacity ranged from 79.71 to 83.11% for the three anti-inflammatory non-steroidal agents analyzed. A recovery rate of up to 80.87% was obtained when 0.01 M chloride acid in methanol was used as the eluent and 50 mL of sample was used. Under optimal conditions, the linear range of the calibration curve ranges from 18.02 to 200 μg L−1, with limits of detection ranging from 6.03 to 18.02 μg L−1 for the three NSAIDs. The precision of the methodology was evaluated in terms of inter- and intra-day repeatability, with %RSD < 10% in all cases. The proposed method was applied to analyze environmental water samples (bottle, tap, cistern, well, and river water samples). The developed method is a robust technique capable of combining with other analytical methods to quantitatively determine anti-inflammatory non-steroidal agents.

Construction a flow through catalytic ozonation system with activated sludge based ceramsite for enhanced ibuprofen removal

Emerging contaminants had drawn much attention due to their ubiquitous occurrence in aquatic environment, and their potential negative effects. In this study, a flow catalytic ozonation system with activated sludge based ceramsite was established, and its catalytic performance was evaluated for degradation of ibuprofen (IBU). Firstly, the proportion of activated sludge and fly ash was 1:1 based on Reliy model for successfully preparation of ceramsite which could catalyze ozone to completely remove IBU within 10 min, while degradation ratio was just 19.9 % in ozonation system. The effects of operational conditions including initial concentration of IBU, ozone dosage, hydraulic retention time, and pH were considered to further verify the applicability of the system. The prepared ceramsite could not only enhance ozone dissolution, but also promote the decomposition of ozone to produce more •OH, which was contributed by metal ions active sites and surface hydroxyl groups. And the contribution of •OH for IBU degradation was about 95.3 % indicating that the •OH played an important role in degradation. The inorganic ions except CO32−/HCO3− and phosphates had less effect on catalytic performances. Furthermore, the degradation products and possible pathways were proposed. The catalytic ozonation system could effectively control the toxicity of the treatment solution. This study not only provided new ideas for resource utilization, but also provided advisable practice application of heterogeneous catalysts for dealing with wastewater.

Nitrite sensitized photolysis of ibuprofen in the liquid and ice phases: Roles of reactive species and influences of the main dissolved components

This study evaluated the kinetics, mechanisms, toxicity assessment, and influencing factors of ibuprofen (IBP) photolysis induced by nitrite (NO2–) in the liquid and ice phases. The photon-flux-normalized rate constant for IBP photolysis (kIBP*) increased monotonically with increasing NO2– concentrations in the liquid and ice phases. kIBP* in the ice phase was decreased by 21.5–29.9 %, as compared with those obtained with the same NO2– concentration in the liquid phase. Reactive nitrogen species (RNS) contributed more to NO2–-sensitized photolysis of IBP than hydroxyl radicals (•OH) in the liquid and ice phases, and the contributions of RNS to IBP degradation in the ice phase were higher than those in the liquid phase. The NO2–-sensitized photolysis mechanisms of IBP in the ice phase seemed to be similar to those in the liquid phase, including hydroxylation, nitration, nitrosation, decarboxylation, side-chain cleavage and ketonization. The reactions of IBP with RNS were more favored in the ice phase due to higher photon flux, leading to greater generation of photoproducts with higher toxicity. Bicarbonate (HCO3–) inhibited NO2–-sensitized photolysis of IBP. Although dissolved organic matter (DOM) itself could induce IBP photolysis, it exhibited an inhibitory effect on NO2–-sensitized photolysis of IBP. For the real water and ice samples containing low NO2– concentrations (≤ 3.6 μM) and medium DOM concentrations (2.6–5.1 mg C/L), DOM played a more important role in IBP photolysis than NO2– in the liquid phase and particularly in the ice phase. kIBP* for the real samples in the ice phase were 32.1–136.4 % higher than those in the liquid phase.

Performance evaluation of different nitrogenous biomass pyrolysis chars: Physicochemical properties and ibuprofen adsorption

The preparation of high-performance porous carbons (HPPCs) using biomass as adsorbent is a viable strategy for the treatment of ibuprofen (IB) in water. In the present study, pyrolyzed carbon was prepared from duckweed (DW) and rice straw (SW) at 400, 500, and 600 °C, and subsequently mixed pyrolysis with KOH to prepare the HPPCs. The HPPCs were used for the treatment of ibuprofen (IB) in water to evaluate their absorption performance. The physicochemical properties of biochar and HPPCs were investigated using scanning electron microscopy, X-ray electron microscopy, Raman microscopy, and the Brunauer-Emmett-Taylor method. In IB adsorption experiments, adsorption equilibrium was evaluated using Langmuir and Freundlich isotherm models. The maximum adsorption capacities of DW and SW were 0.952 and 0484 g/g, respectively, at an IB concentration of 0.5 g/L. The adsorption capacity of HPPCs for IB is influenced by a multifactorial combination of the specific surface area, nitrogen content, and nitrogen-containing functional groups on the surface. Generally, the HPPCs showed great potential for the removal of the IB pharmaceutical contaminants from aqueous solutions.

Ibuprofen removal by modified natural zeolite: characterization, modeling, and adsorption mechanisms

AbstractBACKGROUNDDeveloping robust technologies to remove emerging pollutants from water is urgent since conventional treatments are not technically prepared to remove them. This paper investigated the ibuprofen (IBU) adsorption capacity onto natural zeolite (NZ) and hydrothermally modified zeolite in an acidic medium followed by impregnation with the cationic surfactant cetyltrimethylammonium bromide (CTAB) (MZHT‐CTAB). The materials characterization included scanning electron microscopy (SEM), X‐ray diffraction (XRD), atomic absorption spectroscopy (AAS), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA/DTG), N2 adsorption/desorption isotherm (BET), Zeta Potential (ZP), and Point of Zero Charge (pHPZC). The adsorptive capacity studies were carried out by varying the pH solution, a kinetic study at three concentrations (25, 50, and 100 mg L−1), and the contaminant concentration influence (5–100 mg L−1).RESULTSThe results showed that the MZHT‐CTAB obtained both the highest removal efficiency (~ 37%) and the highest adsorption capacity (~ 14 mg g−1) at pH 5.0. The Pseudo Second‐Order (PSO) model, which showed the best fit to the experimental data, is significant as it indicates the reliability of our results. The maximum adsorption capacity for the concentration of 100 mg L−1 was 11.93 mg g−1. According to Giles's classification, the isotherm was classified as S‐3 type, indicating the competition between the adsorbate and water molecules for the active sites on the adsorbent surface.CONCLUSIONThe adsorption studies demonstrate that the novel adsorbent (MZHT‐CTAB) is highly effective in removing IBU, presenting a significant removal capacity and feasibility. This promising result contributes to the ongoing search for alternative materials for water treatment. © 2024 Society of Chemical Industry (SCI).

Preparation of TiO2 nanotube array/black phosphorus hydrogel drug slow release system based on reactive oxygen response

Black phosphorus quantum dots (BPQDs) were prepared by liquid stripping method, combined with a gel with reactive oxygen species (ROS) decomposition property, and wrapped onto TiO2 nanotube arrays loaded with ibuprofen (IBU) to construct a drug delivery system with near-infrared light (NIR) stimulation response. The generated ROS due to the presence of BPQDs can not only break the dynamic covalent bonds in the gel structure, leading to the decomposition of the gel, achieving NIR-responsive release of IBU and accelerating the release rate of IBU, but at the same time, ROS can play an obvious antibacterial role.

Efficient removal of antibiotics from wastewater by chitosan/polyethyleneimine/Ti3C2 MXene composite hydrogels: Synthesis, adsorption, kinetics and mechanisms

A novel chitosan-based composite hydrogel (CS/PEI-MXene) made of polyethyleneimine and Ti3C2 MXene as modifiers and acrolein as crosslinker has been synthesized simply and conveniently, which could be applied in the removal of residual antibiotic pharmaceuticals (chlortetracycline (CTC), ibuprofen (IBU), etc.) from aqueous environments. The CS/PEI-MXene was used as an adsorbent for chlortetracycline and ibuprofen. The removal rates of CTC and IBU could be achieved to 91.1 % and 99.25 %, respectively. In addition, the reusability of CS/PEI-MXene for CTC and IBU appeared good capacity, and the removal rate was maintained at approximately 70 % after five cycles. FT-IR, XPS, and zeta potential were used to show that the hydrogel was successfully synthesized, and its physicochemical characteristics were studied. Systematically examined were conducted on the effects of pH (3−10), contact time (0–120 min), and temperature (30–40 °C) on the adsorption efficiency of CS/PEI-MXene. The adsorption mechanism of CS/PEI-MXene on CTC and IBU mainly included electrostatic interactions and hydrogen bonding. Overall, the development of MXene based hydrogel adsorbent will provide a practical approach to the treatment of wastewater containing antibiotic pharmaceuticals and have great potential for practical applications.

Insight into the performance and mechanism of N,O,S-codoped porous carbon based CO single-atom catalysts in organic oxidation through peroxymonosulfate activation

Single-atom catalysts (SACs) are charming for heterogeneous Fenton-like processes due to their unique and adjustable electron structure. Developing novel SACs and elucidating their mechanisms are critical for the development of water purification techniques. Herein, we present an N,O,S-codoped carbon based Co SAC (CoSA-N-CO,S) synthesized by anchoring isolated Co atoms onto porous carbon derived from low-cost protic salt. This catalyst exhibits significant efficiency in activating peroxymonosulfate (PMS) for rapid ibuprofen (IBU) degradation, achieving approximately 98.2 % within 10 min at a concentration of 0.2 g/L catalyst and 2 mM PMS, under ambient pH and at 30 °C, and demonstrates excellent reusability. Intensive studies reveal that the highly active atomic Co sites are favorable for activating PMS to produce both radical (SO4− and OH) and nonradical 1O2, while the electron-rich O and S sites contribute to PMS reduction to generate SO4− and OH. The CoSA-N-CO,S/PMS system leverages the synergy between radical and nonradical oxidation across multiple active sites, resulting in exceptional resistance to interference and high efficiency in degradation and mineralization of diverse organic pollutants. This study develops a novel single-atom catalyst for wastewater treatment and elucidates the mechanism behind PMS activation by a carbon-based cobalt single atom catalyst.

How Does the Powder Mixture of Ibuprofen and Caffeine Attenuate the Solubility of Ibuprofen? Comparative Study for the Xanthine Derivatives to Recognize Their Intermolecular Interactions Using Fourier-Transform Infrared (FTIR) Spectra, Differential Scanning Calorimetry (DSC), and X-ray Powder Diffractometry (XRPD).

Molecular interactions between active pharmaceutical ingredients (APIs) and xanthine (XAT) derivatives were analyzed using singular value decomposition (SVD). XAT derivatives were mixed with equimolar amounts of ibuprofen (IBP) and diclofenac (DCF), and their dissolution behaviors were measured using high-performance liquid chromatography. The solubility of IBP decreased in mixtures with caffeine (CFN) and theophylline (TPH), whereas that of DCF increased in mixtures with CFN and TPH. No significant differences were observed between the mixtures of theobromine (TBR) or XAT with IBP and DCF. Mixtures with various molar ratios were analyzed using differential scanning calorimetry, X-ray powder diffraction, and Fourier-transform infrared spectroscopy to further explore these interactions. The results were subjected to SVD. This analysis provides valuable insights into the differences in interaction strength and predicted interaction sites between XAT derivatives and APIs based on the combinations that form mixtures. The results also showed the impact of the XAT derivatives on the dissolution behavior of IBP and DCF. Although IBP and DCF were found to form intermolecular interactions with CFN and TPH, these effects resulted in a reduction of the solubility of IBP and an increase in the solubility of DCF. The current approach has the potential to predict various interactions that may occur in different combinations, thereby contributing to a better understanding of the impact of health supplements on pharmaceuticals.

Effects of Non-steroidal Anti-inflammatory Drugs (Ibuprofen and Diclofenac) and Their Mixtures on the Growth of Three Green Algae

Ibuprofen (IBU) and diclofenac (DFN) are the most widely consumed non-steroidal anti-inflammatory (NSAIDs) worldwide. Since they are not completely metabolized in the human body, the unaltered active ingredients can reach aquatic ecosystems through domestic effluents. The aim of this study was to analyse the toxic effects of IBU and DFN, individually and in mixtures, on three freshwater green algae strains, the international standard strain Raphidocelis subcapitata and two native strains, Ankistrodesmus fusiformis and Tetradesmus obliquus. Bioassays were carried out according to the 72-h algal growth inhibition test. The concentration-response curve of the mixture was compared to predicted effects based on both the concentration addition (CA) and the independent action (IA) models. The two drugs tested individually were toxic to all three algal strains, with EC50 values <100 mg L-1. According to these values, the most sensitive strain was R. subcapitata (IBU = 20 mg L-1 and DFN = 8 mg L-1). The most resistant strain was T. obliquus (IBU = 74.1 mg L-1 and DFN = 92.7 mg L-1) and the A. fusiformis strain showed intermediate sensitivity (IBU = 26.7 mg L-1 and DFN = 14.6 mg L-1). The mixtures showed a synergistic effect on R. subcapitata, an additive effect on A. fusiformis, and an antagonistic effect on T. obliquus. Neither the CA nor the IA model was appropriate for predicting the toxicity of the mixtures. In conclusion, IBU and DFN showed toxic effects on the algae growth at the concentrations tested. Individual and mixed toxicity was different according to the species. These differences could be species-specific, showing the importance of including native strains in ecotoxicological studies to evaluate the potential effects of pollutants in regional aquatic environments.

In vitro impacts of polystyrene microplastics and environmental pollutants on ethoxyresorufin-O-deethylase and glutathione S-transferase activity in Mossambica tilapia

Microplastic (MP) pollution is a potential threat to marine organisms. In vitro toxicity of MPs and other pollutants, such as pharmaceutically active compounds (PhACs) and brominated flame retardants (BFRs), has been understudied. This study aimed to investigate the effects of polystyrene microplastics (PS-MPs) with different particle sizes on two biomarkers: ethoxyresorufin-O-deethylase (EROD) and glutathione S-transferase (GST) in tilapia liver homogenates. The study also examined the combined effects of PS-MPs with various environmental contaminants, including three metal ions (Cu2+, Zn2+, Pb2+), three BFRs, and six PhACs. PS-MPs alone had no remarkable effects on the two biomarkers at the selected concentrations. However, PS-MPs combined with other pollutants significantly affected the two biomarkers in most situations. For EROD activity, PS + metal ions (except Zn2+ at 1000 μg/L), PS + BFRs (except decabromodiphenyl oxide (BDE-209)) or PS+ trimethoprim (TMP) significantly inhibited activity values, whereas PS+ 4-acetaminophen (AMP) induced EROD activity. For GST, PS together with most tested pollutants (except PS+ ibuprofen (IBF)) greatly decreased the activities. Accordingly, future research should focus on combined toxicity of mixtures to set more reasonable environmental safety evaluation standards.

Synthesis, Optimization and Molecular Self-Assembly Behavior of Alginate-g-Oleylamine Derivatives Based on Ugi Reaction for Hydrophobic Drug Delivery.

To achieve the optimal alginate-based oral formulation for delivery of hydrophobic drugs, on the basis of previous research, we further optimized the synthesis process parameters of alginate-g-oleylamine derivatives (Ugi-FOlT) and explored the effects of different degrees of substitution (DSs) on the molecular self-assembly properties of Ugi-FOlT, as well as the in vitro cytotoxicity and drug release behavior of Ugi-FOlT. The resultant Ugi-FOlT exhibited good amphiphilic properties with the critical micelle concentration (CMC) ranging from 0.043 mg/mL to 0.091 mg/mL, which decreased with the increase in the DS of Ugi-FOlT. Furthermore, Ugi-FOlT was able to self-assemble into spherical micellar aggregates in aqueous solution, whose sizes and zeta potentials with various DSs measured by dynamic light scattering (DLS) were in the range of 653 ± 25~710 ± 40 nm and -58.2 ± 1.92~-48.9 ± 2.86 mV, respectively. In addition, RAW 264.7 macrophages were used for MTT assay to evaluate the in vitro cytotoxicity of Ugi-FOlT in the range of 100~500 μg/mL, and the results indicated good cytocompatibility for Ugi-FOlT. Ugi-FOlT micellar aggregates with favorable stability also showed a certain sustained and pH-responsive release behavior for the hydrophobic drug ibuprofen (IBU). Meanwhile, it is feasible to control the drug release rate by regulating the DS of Ugi-FOlT. The influence of different DSs on the properties of Ugi-FOlT is helpful to fully understand the relationship between the micromolecular structure of Ugi-FOlT and its macroscopic properties.

Performance of pharmaceutical products removal in a bioelectrochemical system at low temperatures and changes in microbial communities and antibiotic resistance genes.

Biological methods do not effectively remove pharmaceutical products (PPs) and antibiotic resistance genes (ARGs) from wastewater at low temperatures, leading to environmental pollution. Therefore, anaerobic-aerobic-coupled upflow bioelectrochemical reactors (AO-UBERs) were designed to improve the removal of PPs at low temperatures (10 ± 2 °C). The result shows that diclofenac (DIC) and ibuprofen (IBU) removals in the system with aerobic anodic and anaerobic cathodic chambers were 91.7% and 94.7%, higher than that in the control system (12.2 ± 1.5%, 36.5 ± 5.9%), and aerobic zone favors DIC and IBU removal; fluoroquinolone antibiotics (FQs) removals in the system with aerobic cathodic and anaerobic anodic chambers were 17.5-22.4% higher than that in the control system (9.1-22.4%), and anaerobic zone favors FQs removal. Analysis of microbial community structure and ARGs showed that different electrotrophic microbes (Flavobacterium, Acinetobacter, and Delftia) with cold-resistant ability to degrade PPs were enriched in different electrode combinations, and the aerobic cathodic chambers could remove certain ARGs. These results showed that AO-UBERs under intermittent electrical stimulation mode are an alternative method for the effective removal of PPs and ARGs at low temperatures.

Removal of ibuprofen and paracetamol from water using a blend activated carbon from paper waste and avocado seeds

The presence of pharmaceuticals in water is a major problem worldwide. To alleviate this, this study produced carbon blends from avocado seeds and paper waste and activated them with hydrogen peroxide (H2O2), nitric acid (HNO3) and potassium permanganate (KMnO4). The effectiveness of the adsorbents was tested in removing ibuprofen (IBU) and paracetamol (PRC) from water. Characterization of the adsorbents by SEM, BET, FTIR and TGA revealed that the morphology was porous, with a large surface area and several functional groups bound to the surface. The concentration effect experiments showed that the uptake of IBU and PRC increased with an increasing initial concentration and that these data were consistent with the Freundlich model. The contact time effect showed that the uptake of PRC was rapid in the initial phase for all the adsorbents. However, the rate gradually slowed down and equilibrium was reached after 40 min for BCMN, 60 min for BCMH and BCMP and 120 min for BCM. IBU, on the other hand, showed that equilibrium was reached after 30 min for BCMN, BCMH and BCMP and after 120 min for BCM. These data complemented the PSOM. The model is based on chemisorption, where electrons are transferred and shared, and hydrogen bonding and π-π interactions. The △Ho value confirms that the sorption of IBU and PRC was endothermic. The △So was positive, indicating greater freedom at the solution interface during uptake.

Ibuprofen removal from water using the IB-COF covalent organic framework

The rising presence of ibuprofen (IBP) in natural water bodies, restricting from its widespread pharmaceutical usage, necessitates effective remediation strategies. This study introduces IB-COF, a novel covalent organic framework synthesized via a solvothermal method, specifically engineered for IBP extraction from aqueous solutions. IB-COF showcases remarkable adsorption performance, achieving equilibrium within 60 min with a capacity of 512 mg/g, outperforming conventional adsorbents. Its adsorption kinetics align with pseudo-second-order and Langmuir models, indicating efficient monolayer adsorption. Significantly, IB-COF exhibits robust recyclability over five cycles. Among the prevalence of IBP contamination, IB-COF demonstrates promise in selectively extracting IBP even in the presence of competing pharmaceuticals. Overall, our findings underscore the potential of IB-COF as an advanced adsorbent for mitigating IBP pollution in water sources, contributing significantly to environmental purification efforts and water pollution mitigation strategies.