Chemical Groups Research Articles

Synthesis and characterization of Ketotifen Fumarate Intercalated Zn–Al Layered Double Hydroxides as sustained-release carriers

The present study seeks to synthesize, characterize, and sustain the release of properties of Ketotifen Fumarate Intercalated Zn–Al Layered Double Hydroxides (Zn-Al-KF-LDHs) by the chemical co-precipitation method. A variety of techniques were used to analyze the synthesized products, including Elemental Analysis, X-ray diffraction (XRD), Scanning electron microscope (SEM), Fourier Transform Infrared Spectroscopy (FT-IR), and Thermogravimetry Differential Thermal Analysis (TG-DTA). The XRD patterns successfully highlighted the remarkable crystallinity of the typical hydrotalcite-like materials, Zn-Al-KF-LDHs. While the FT-IR analysis indicates the chemical functional groups and interlayer anions of Zn-Al-KF-LDHs, the elemental analysis determines the content of Zn, Al, S, C, H, and N. The TG-DTA results show that Zn-Al-KF-LDHs possess improved thermal stability. These findings provide an empirical understanding of the supramolecular structure of Zn-Al-KF-LDHs, enabling its comprehensive structural analysis. Additionally, the sustained-release properties of simulated gastric juice and intestinal juice, which followed the theoretical models of Higuchi and Riger-Peppas, indicated that the layered double hydroxides have potential applications as sustained-release carriers for ketotifen fumarate.

Effects of nanoactive fluids on water wettability reversal of shale: Implications for CO2 geo-sequestration

CO2 geo-sequestration (CGS) is crucial in tackling global climate change, and the safety of CO2 storage within the reservoir is intricately linked to wettability. The utilization of nanofluids-surfactants for adjusting reservoirs’ wettability has emerged as a promising approach to enhance the security of CGS. However, the mechanism underlying their impact on reservoir wettability and carbon sequestration remains elusive. Regarding nanoactive fluid (ASNF) compounded with nano-SiO2 and AOS, to explore its potential for wettability reversal of CO2-exposed shale under in situ conditions, comparative experiments were conducted with Longmaxi Formation shale as the subject. The chemical structures and microstructures of shale before and after the experiments were comprehensively characterized. The results showed that a maximum of 67.93 % enhanced the water wettability of samples co-treated with ASNF and ScCO2. The primary reason for shale wettability reversal was increased hydrophilic chemical groups and enhanced interaction energy between organic matter and water molecules, stemming from nanoactive particle retention on the shale surface. The alteration in wettability decreased the mobility of CO2 and increased the distribution of surface water films, enhancing the carbon sequestration capabilities of the trapping mechanism. These findings provided an important foundation for improving the effectiveness and safety of CGS in shale reservoirs.

Laser-based functionalization for superhydrophobic silicon carbide with mechanical durability, anti-icing and anti-fouling properties

The further applications of silicon carbide (SiC) are limited due to the ease of being contaminated and tendency for icing at low temperature caused by its intrinsically hydrophilicity. In recent years, superhydrophobic surface has been widely employed due to the potential value in anti-fouling and passive anti-icing. In this work, a novel laser ablation-silicone oil heat treatment (LASH) composite process is proposed to fabricate superhydrophobic SiC surface. Many microscale “fence” structures and nanoscale “broccoli” fragmental structures are successfully obtained, which can be adjusted by using different laser processing parameters. Besides, the X-ray photoelectron spectroscopy analysis demonstrates that the effective deposition of low surface energy chemical functional groups is the key to realize the superhydrophobic properties of SiC surface. The coupling effect between the micro/nano structures and low surface energy is confirmed to be important for the stability of Cassie-Baxter state at low temperature. In addition, the freezing process of water droplets on the LASH surface at low temperature and the mechanism of the rapid transition from Wenzel state to Cassie-Baxter state are analyzed. The experimental results indicate that the LASH surface possesses a longer static icing time and keeps good hydrophobicity at −5 °C. The icing temperature of the LASH surface decreases to −17.6 °C while the temperature of the untreated surface is −3.7 °C. Moreover, the LASH surface possesses a lower ice adhesion strength which means it is easier for the ice droplets to break away from the surface. After 20 cycles of icing-deicing experiments, the WCA of the LASH surface is still higher than 150° and its ice adhesion strength slightly increases to 240 kPa. Finally, the mechanical robustness of the LASH surface is studied through the abrasive belt and tape stripping tests, and the anti-fouling property is also evaluated. The change of ice adhesion strength on the LASH surface under cyclic icing experiment is analyzed. The experimental results show that the LASH surface has great mechanical durability and anti-fouling property, which is expected to further expand the application prospects of SiC in different fields.

Chitosan-Tricarbocyanine-Based Nanogels Were Able to Cross the Blood-Brain Barrier Showing Its Potential as a Targeted Site Delivery Agent.

Targeting drugs to the central nervous system (CNS) is challenging due to the presence of the blood-brain barrier (BBB). The cutting edge in nanotechnology generates optimism to overcome the growing challenges in biomedical sciences through the effective engineering of nanogels. The primary objective of the present report was to develop and characterize a biocompatible natural chitosan (CS)-based NG that can be tracked thanks to the tricarbocyanine (CNN) fluorescent probe addition on the biopolymer backbone. FTIR shed light on the chemical groups involved in the CS and CNN interactions and between CNN-CS and tripolyphosphate, the cross-linking agent. Both in vitro and in vivo experiments were carried out to determine if CS-NGs can be utilized as therapeutic delivery vehicles directed towards the brain. An ionic gelation method was chosen to generate cationic CNN-CS-NG. DLS and TEM confirmed that these entities' sizes fell into the nanoscale. CNN-CS-NG was found to be non-cytotoxic, as determined in the SH-SY5Y neuroblastoma cell line through biocompatibility assays. After cellular internalization, the occurrence of an endo-lysosomal escape (a crucial event for an efficient drug delivery) of CNN-CS-NG was detected. Furthermore, CNN-CS-NG administered intraperitoneally to female CF-1 mice were detected in different brain regions after 2 h of administration, using fluorescence microscopy. To conclude, the obtained findings in the present report can be useful in the field of neuro-nanomedicine when designing drug vehicles with the purpose of delivering drugs to the CNS.

Risks associated with the presence of PFAS in FCM: An investigation of the Belgian market

Per- and polyfluoroalkyl substances (PFAS) are a group of chemicals that have been widely used by various industries, including the food contact material industry. These substances are favoured for their ability to repel oil and resist moisture. However, exposure to PFAS has been linked to several health problems, including effects on the immune system. According to the European Food Safety Authority (EFSA), food contact materials (FCM) are likely to contribute to human exposure to PFAS. Therefore, this study investigated the exposure to PFAS from FCM. One hundred and ten FCM made of paper and board (e.g. straws, cups, bowls, boxes etc.), sugar cane or wheat pulp-based FCM, called paper analogues (e.g., cup, bowls, plates, hamburger boxes etc.) were carefully selected on the Belgian market and investigated using liquid chromatography coupled with high-resolution mass spectrometery. Out of the 25 PFAS targeted, 11 were detected in the samples, mainly perfluoroalkyl carboxylic acids (PFBA, PFPeA, PFHxA, PFHpA, PFOA, PFNA, PFDA, PFUnDA, PFDoDA, PFTrDA) and PFOS. It was found that all of the paper analogue samples contained PFAS, while 43% of the paper and board samples showed the presence of these chemicals. Except for one sample, most detections suggest contamination rather than intentional use. Finally, a risk assessment was conducted, which revealed potential risks for consumers related to a coffee cup made of paper and board and a food tray made of sugar cane.

Enhancing 3DSPs estimation: The dispersive solubility parameter adjusted by means of molar refraction, coordination number and molar volume using the DiPEVa model

This study comprehensively analyzes the empirical relationships between polarizability measurements, such as refractivity index and molar refraction, or the length of the homologous chain (HCL), and the dispersive solubility parameter (δD). The authors investigated the correlation between these parameters by utilizing a database encompassing various chemical groups across a range of aliphatic and aromatic molecules. An innovative approache enhaces the well known relationship between the the dispersive solubility parameter (δD) and the Lorentz-Lorenz function, adjusting the dispersive solubility parameters by the ratio of coordination numbers and molar volumes as correction factors. Notably, the adjusted δD demonstrated a strong linear correlation with MR, suggesting that MR can be a reliable predictor for δD. This was further substantiated by the strong correlation coefficients obtained (such as an adjusted R-Square of 0.866), indicating the robustness of our empirical models. In conclusion, our research provides new insights into the solubility behaviour of molecules with the derived empirical relationships offering a valuable tool for predicting solubility parameters. These findings have practical implications for solvent selection, understanding liquid behaviours, and the design of chemical processes and materials.

Insights into Cis-Amide-Modified Carbon Nanotubes for Selective Purification of CH4 and H2 from Gas Mixtures: A Comparative DFT Study.

Among a plethora of mixtures, the methane (CH4) and hydrogen (H2) mixture has garnered considerable attention for multiple reasons, especially in the framework of energy production and industrial processes as well as ecological considerations. Despite the fact that the CH4/H2 mixture performs many critical tasks, the presence of other gases, such as carbon dioxide, sulfur compounds like H2S, and water vapor, leads to many undesirable consequences. Thus purification of this mixture from these gases assumes considerable relevance. In the current research, first-principle calculations in the frame of density functional theory are carried out to propose a new functional group for vertically aligned carbon nanotubes (VA-CNTs) interacting preferentially with polar molecules rather than CH4 and H2 in order to obtain a more efficient methane and hydrogen separations The binding energies associated with the interactions between several chemical groups and target gases were calculated first, and then a functional group formed by a modified ethylene glycol and acetyl amide was selected. This functional group was attached to the CNT edge with an appropriate diameter, and hence the binding energies with the target gases and steric hindrance were evaluated. The binding energy of the most polar molecule (H2O) was found to be more than six times higher than that of H2, indicating a significant enhancement of the nanotube tip's affinity toward polar gases. Thus, this functionalization is beneficial for enhancing the capability of highly packed functionalized VA-CNT membranes to purify CH4/H2 gas mixtures.

Examining the impact of polyfluoroalkyl substance exposure on erythrocyte profiles and its related nutrients: Insights from a prospective study on young Taiwanese

Per- and polyfluoroalkyl substances (PFAS) constitute a group of synthetic chemicals extensively utilized across various commonplace products. PFAS are known to have various toxic effects on human health. The relationship between PFAS exposure and erythrocytes has been a subject of interest in epidemiological research, but so far, only limited cross-sectional studies have investigated. Additionally, the role of erythrocyte related nutrition indicators on PFAS-induced changes in erythrograms has not been explored. To fill these knowledge gaps, we launched a longitudinal study over a decade, tracking 502 adolescents and young adults aged 12 to 30 from the YOung TAiwanese Cohort (YOTA). Our analysis encompassed 11 types of plasma PFAS, as well as erythrograms and serum levels of ferritin, transferrin saturation, vitamin B12, and folate. Our examination unveiled positive associations between specific average levels of PFAS compounds, including linear perfluorooctanoic acid (PFOA), branched perfluorooctane sulfonic acid (PFOS), perfluorononanoic acid (PFNA), and perfluorohexane sulfonic acid (PFHxS), and transferrin saturation. Furthermore, linear PFOA and both linear and branched PFOS were negatively correlated with vitamin B12 levels. Specifically, we observed that the average linear PFOA demonstrated positive correlations with mean corpuscular volume (MCV) and mean corpuscular hemoglobin (MCH), while average PFNA also exhibited positive associations with hemoglobin (Hb) and hematocrit (Hct) in a multiple linear regression model. Subsequent analysis revealed noteworthy interactions between vitamin B12 and PFNA, as well as folate and PFNA, in the context of their impact on Hb, Hct, and PFNA relationships. Additionally, an interaction with transferrin saturation was identified in the correlation between Hct and PFNA. These findings suggest a plausible link between PFAS exposure and erythrograms among young populations, underscoring the potential involvement of iron status, vitamin B12, and folate in this association. Further studies are imperative to elucidate the precise effects of PFAS on erythrocyte in human subjects.

Chemical composition of Ecstasy tablets seized in Poland between 2005 and 2020.

The most commonly associated substance found in Ecstasy tablets is MDMA (3,4-methylenedioxymethamphetamine). In our study, we showed how the composition of psychoactive ingredients in Ecstasy tablets seized on the drug market in Poland has changed in the years 2005-2020. The study material consisted of nearly 20,000 single Ecstasy tablets seized by representatives of law enforcement (the police, prosecutors) from 2005 to 2020 and analysed by the Institute of Forensic Research, Krakow, Poland. The analysis of the tablets was carried out by gas chromatography-mass spectrometry (GC-MS), high-performance liquid chromatography with diode array detection (HPLC-DAD) and ultra-high-performance liquid chromatography with photodiode array detection (UHPLC-PDA). Currently, new types of MDMA tablets are introduced onto the market, available in various colours and shapes. Our study showed that tablets sold on the street as Ecstasy have variable purity and sometimes contain little or no MDMA. The mean content of MDMA in one tablet seized in 2005-2011 decreased from 90 to 50mg. In 2013, Ecstasy tablets with a very high MDMA content (average 195mg per tablet) appeared on the market, but in the next 2years, the MDMA content decreased again. From 2016, the average MDMA content began to rise again, ranging from 60 to 280mg. Tablets sold as Ecstasy also contained completely different psychoactive substances, including new psychoactive substances (NPS) (found in almost 20% of all examined tablets sold as Ecstasy) belonging to different chemical groups or their dangerous combinations (i.e. phenylethylamines, piperazines, tryptamines, cathinones, arylalkylamines, arylcyclohexylamines and piperidines). Such a large variety of psychoactive substances in Ecstasy tablets is associated with a high risk for users unaware of their composition.

Lipids from the purple and white açaí (Euterpe oleracea Mart) varieties: nutritional, functional, and physicochemical properties.

The Brazilian superfruit called Açaí or Assaí has gained interested from researcher and consumers worldwide, due to its health-related properties. In this context, this pioneering study aimed to compare the physicochemical, nutritional, and thermal properties of vegetable oils obtained from two varieties of açaí (Euterpe oleracea), purple and white. Both açaí oils from white (WAO) and purple (PAO) varieties were obtained by using the conventional solid-liquid extraction, which resulted in oil yields ranging from 52 to 61%. WAO and PAO were analyzed by their edibility quality parameters given the recommendations from Codex Alimentarius; their nutritional functionality indices and their composition of fatty acids and triglycerides content were estimated. Both oils showed low levels of acidity and peroxides, <1.8 mg KOH g-1 and < 1.7 mEq kg-1, respectively, which are good indicators of their preservation status, agreeing with the food regulations. PAO and WAO showed differences among the composition of fatty acids, mainly related to the content of monounsaturated fatty acids (MUFAs), which were 62.5 and 39.5%, respectively, mainly oleic acid. Regarding the polyunsaturated fatty acids (PUFAs), the WAO showed up to 23% of linoleic acid, whereas the PAO exhibited up to 11% of it. These differences reflect on the values of the nutritional functionality indices, atherogenic (AI), thrombogenic (IT), and hypocholesterolemic/hypercholesterolemic ratio (H/H). Both PAO and WAO showed low levels of AI and TI and superior values of H/H than other oilseeds from the literature. These results indicate the nutritional properties of açaí oils regarding a potential cardioprotective effect when included in a regular dietary intake. The thermogravimetric behavior and the evaluation of oxidation status by infrared spectroscopy (FTIR) were also studied. Both açaí oils demonstrated higher thermal stability (with an onset temperature ranging from 344 to 350 °C) and low indications of oxidation status, as no chemical groups related to it were noted in the FTIR spectrum, which agrees with the determined acidity and peroxide content. Moreover, the FTIR analysis unveiled characteristic chemical groups related to fatty acids and triglycerides, agreeing with the literature reports. These findings collectively contribute to a deeper comprehension of the nutritional and functional properties between white and purple açaí oils, offering valuable insights into their potential health, food, and industrial applications.

Plant-Based Shape Memory Cryogel for Hemorrhage Control.

The escalating global demand for sustainable manufacturing, motivated by concerns over energy conservation and carbon footprints, encounters challenges due to insufficient renewable materials and arduous fabrication procedures to fulfill specific requirements in medical and healthcare systems. Here, biosafe pollen cryogel is engineered as effective hemostats without additional harmful crosslinkers to treat deep noncompressible wounds. A straightforward and low-energy approach is involved in forming stable macroporous cryogel, benefiting from the unique micro-hierarchical structures and chemical components of non-allergenic plant pollen. It is demonstrated that the pollen cryogel exhibits rapid water/blood-triggered shape-memory properties within 2 s. Owing to their inherent nano/micro hierarchical structure and abundant chemical functional groups on the pollen surface, the pollen cryogel shows effective hemostatic performance in a mouse liver penetration model, which is easily removed after usage. Overall, the self-crosslinking pollen cryogel in this work pioneers a framework of potential clinical applications for the first-hand treatment on deep noncompressible wounds.

Dissecting the interaction between Graphene Oxide and Human Transferrin via biophysical, biochemical and in-silico approaches: Implications for nanomaterial anti-fibrillation properties and protein structure

Human Transferrin (HTF) plays a pivotal role in numerous neurological therapies by carrying drugs and nanomaterials through the challenging blood-brain barrier. Nonetheless, the binding of HTF with highly relevant nanomaterials is not fully comprehended. Here, the nanomaterial graphene oxide (GO) has been obtained and their interaction with HTF in the native and fibrillar form has been investigated, by employing multi-spectroscopic, modeling, and microscopic techniques. The fluorescence results reveal that GO quenches the HTF intrinsic fluorescence by following a mix of static and dynamic mechanisms, and the GO-HTF complex formation has been confirmed by UV-Vis spectroscopy. Additionally, HTF attaches firmly to GO (KS≈ 106M−1) through mainly by hydrophobic and hydrogen bonds (according to determined ΔH=-23.77±1.03 kJ.mol−1 and ΔS= +39.53 ± 1.69 J.mol−1.K−1). Further, the in-silico investigation has evidenced the residues and chemical groups involved in HTF-GO interaction. Furthermore, SEM images reveal the formation and inhibition of HTF aggregates by GO, and spectroscopic methods reveal the related protein structural modification involved in the fibrillation process. In summary, all the results open questions concerning GO use for many neurological therapies.

Amino-modified nanoplastics at predicted environmental concentrations cause transgenerational toxicity through activating germline EGF signal in Caenorhabditis elegans

In the real environment, some chemical functional groups are unavoidably combined on the nanoplastic surface. Reportedly, amino-modified polystyrene nanoparticles (PS-A NPs) exposure in parents can induce severe transgenerational toxicity, but the underlying molecular mechanisms remain largely unclear. Using Caenorhabditis elegans as the animal model, this study was performed to investigate the role of germline epidermal growth factor (EGF) signal on modulating PS-A NPs' transgenerational toxicity. As a result, 1–10 μg/L PS-A NPs exposure transgenerationally enhanced germline EGF ligand/LIN-3 and NSH-1 levels. Germline RNAi of lin-3 and nsh-1 was resistant against PS-A NPs' transgenerational toxicity, implying the involvement of EGF ligand activation in inducing PS-A NPs' transgenerational toxicity. Furthermore, LIN-3 overexpression transgenerationally enhanced EGF receptor/LET-23 expression in the progeny, and let-23 RNAi in F1-generation notably suppressed PS-A NPs' transgenerational toxicity in the exposed worms overexpressing germline LIN-3 at P0 generation. Finally, LET-23 functioned in neurons and intestine for regulating PS-A NPs' transgenerational toxicity. LET-23 acted at the upstream DAF-16/FOXO within the intestine in response to PS-A NPs' transgenerational toxicity. In neurons, LET-23 functioned at the upstream of DAF-7/DBL-1, ligands of TGF-β signals, to mediate PS-A NPs' transgenerational toxicity. Briefly, this work revealed the exposure risk of PS-A NPs' transgenerational toxicity, which was regulated through activating germline EGF signal in organisms.

Obtention and Characterization of Microcrystalline Cellulose from Industrial Melon Residues Following a Biorefinery Approach.

Residual melon by-products were explored for the first time as a bioresource of microcrystalline cellulose (MCC) obtention. Two alkaline extraction methods were employed, the traditional (4.5% NaOH, 2 h, 80 °C) and a thermo-alkaline in the autoclave (2% NaOH, 1 h, 100 °C), obtaining a yield of MCC ranging from 4.76 to 9.15% and 2.32 to 3.29%, respectively. The final MCCs were characterized for their chemical groups by Fourier-transform infrared spectroscopy (FTIR), crystallinity with X-ray diffraction, and morphology analyzed by scanning electron microscope (SEM). FTIR spectra showed that the traditional protocol allows for a more effective hemicellulose and lignin removal from the melon residues than the thermo-alkaline process. The degree of crystallinity of MCC ranged from 51.51 to 61.94% and 54.80 to 55.07% for the thermo-alkaline and traditional processes, respectively. The peaks detected in X-ray diffraction patterns indicated the presence of Type I cellulose. SEM analysis revealed microcrystals with rough surfaces and great porosity, which could remark their high-water absorption capacity and drug-carrier capacities. Thus, these findings could respond to the need to valorize industrial melon by-products as raw materials for MCC obtention with potential applications as biodegradable materials.

Melt electrowriting of poly(ϵ-caprolactone)—poly(ethylene glycol) backbone polymer blend scaffolds with improved hydrophilicity and functionality

Melt electrowriting (MEW) is an additive manufacturing technique that harnesses electro-hydrodynamic phenomena to produce 3D-printed fibres with diameters on the scale of 10s of microns. The ability to print at this small scale provides opportunities to create structures with incredibly fine resolution and highly defined morphology. The current gold standard material for MEW is poly(ϵ-caprolactone) (PCL), a polymer with excellent biocompatibility but lacking in chemical groups that can allow intrinsic additional functionality. To provide this functionality while maintaining PCL’s positive attributes, blending was performed with a Poly(Ethylene Glycol) (PEG)-based Acrylate endcapped Urethane-based Precursor (AUP). AUPs are a group of polymers, built on a backbone of existing polymers, which introduce additional functionality by the addition of one or more acrylate groups that terminate the polymer chain of a backbone polymer. By blending with a 20kDa AUP-PEG in small amounts, it is shown that MEW attributes are preserved, producing high-quality meshes. Blends were produced in various PCL:AUP weight ratios (100:0, 90:10 and 0:100) and processed into both solvent-cast films and MEW meshes that were used to characterise the properties of the blends. It was found that the addition of AUP-PEG to PCL significantly increases the hydrophilicity of structures produced with these polymers, and adds swelling capability compared to the non-swelling PCL. The developed blend (90:10) is shown to be processable using MEW, and the quality of manufactured scaffolds is evaluated against pure PCL scaffolds by performing scanning electron microscopy image analysis, with the quality of the novel MEW blend scaffolds showing comparable quality to that of pure PCL. The presence of the functionalisable AUP material on the surface of the developed scaffolds is also confirmed using fluorescence labelling of the acrylate groups. Biocompatibility of the MEW-processable blend was confirmed through a cell viability study, which found a high degree of cytocompatibility.

Towards chemical source tracking and characterization using physics-informed neural networks

This paper presents a new algorithm using physics-informed neural networks (PINNs) to track and characterize spatio-temporally varying chemical sources based on time-resolved measurements of chemical concentration, fluid velocity, and pressure. Chemical source emission functions, chemical concentration, fluid velocity and fluid pressure fields are modeled as multi-layer perceptrons (MLPs). During the training process, sensors readings of chemical concentration, fluid velocity, and fluid pressure are matched to the output of the respective MLPs at the given spatio-temporal locations. Simultaneously, the physics of fluid flow and chemical dispersion at an arbitrary number of spatio-temporal locations in the domain of interest are enforced through regularization. Once trained, the constituent MLPs can be evaluated to generate the time resolved maps of source emissions, chemical concentration, fluid velocity and pressure. Extensive numerical simulation validate the method, including scenarios with both static and dynamic sources in complex flow fields. This innovative approach marks a significant advancement in environmental monitoring technologies.

Carboxymethyl-Cellulose-Based Hydrogels Incorporated with Cellulose Nanocrystals Loaded with Vitamin D for Controlled Drug Delivery

Currently, the development of innovative materials for the treatment of various diseases is highly interesting and effective. Additionally, in recent years, environmental changes, including the search for a sustainable world, have become the main goal behind developing sustainable and suitable materials. In this context, this research produced innovative hydrogels that incorporate cellulose nanocrystals and nanofibres from underutilised fibres from a semiarid region of Brazil; the hydrogels were loaded with vitamin D to evaluate controlled drug release for the treatment of diverse diseases. Spectroscopic (FTIR, Raman, UV–VIS), X-ray diffraction, zeta potential and morphology (SEM, TEM) analyses were used to characterise these hydrogels. In addition, biocompatibility was assessed using a resazurin assay, and the in vitro kinetic accumulative release of vitamin D was measured. The results showed that nanocrystals and nanofibres changed the structure and crystallinity of the hydrogels. In addition, the chemical groups of the hydrogels were red- and blueshifted in the FTIR spectra when the nanocrystals, nanofibres and vitamin D were incorporated. Moreover, the nanocrystals and nanofibres were homogeneously spread into the hydrogel when vitamin D was loaded into the hydrogel matrix. Furthermore, the cytotoxicity was greater than 90%. Additionally, the in vitro accumulative kinetic data of vitamin D release were robust (close to 40 ng·mL−1), with equilibrium being reached in the first 30 min. These results confirm the potential of using these hydrogels as therapeutic biomaterials for diverse diseases and problems in humans, mainly in women, who are the most harmed by vitamin D deficiency.

DNA aptamer-functionalized PDA nanoparticles: from colloidal chemistry to biosensor applications.

Polydopamine nanoparticles (PDA NPs) are widely utilized in the field of biomedical science for surface functionalization because of their unique characteristics, such as simple and low-cost preparation methods, good adhesive properties, and ability to incorporate amine and oxygen-rich chemical groups. However, challenges in the application of PDA NPs as surface coatings on electrode surfaces and in conjugation with biomolecules for electrochemical sensors still exist. In this work, we aimed to develop an electrochemical interface based on PDA NPs conjugated with a DNA aptamer for the detection of glycated albumin (GA) and to study DNA aptamers on the surfaces of PDA NPs to understand the aptamer-PDA surface interactions using molecular dynamics (MD) simulation. PDA NPs were synthesized by the oxidation of dopamine in Tris buffer at pH 10.5, conjugated with DNA aptamers specific to GA at different concentrations (0.05, 0.5, and 5μM), and deposited on screen-printed carbon electrodes (SPCEs). The charge transfer resistance of the PDA NP-coated SPCEs decreased, indicating that the PDA NP composite is a conductive bioorganic material. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) confirmed that the PDA NPs were spherical, and dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FTIR), and Raman spectroscopy data indicated the successful conjugation of the aptamers on the PDA NPs. The as-prepared electrochemical interface was employed for the detection of GA. The detection limit was 0.17μg/mL. For MD simulation, anti-GA aptamer through the 5'terminal end in a single-stranded DNA-aptamer structure and NH2 linker showed a stable structure with its axis perpendicular to the PDA surface. These findings provide insights into improved biosensor design and have demonstrated the potential for employing electrochemical PDA NP interfaces in point-of-care applications.

A systematic study of the impact of aromatic/aliphatic amines and protein corona as coatings of iron oxide magnetic nanoparticles on the interaction with DPPC Langmuir monolayers

The nature of chemical groups exposed by nanoparticles determines their interaction with biological systems, especially with cell membranes. Amino groups are one of the most used to guide nanoparticles within cells. Aromatic and aliphatic amines can establish different types of interactions with lipids, and this may condition the nanoparticles' mode of action as well as their fate. This work is focused on investigating how aromatic and aliphatic amines present at the surface of iron oxide magnetic nanoparticles influence their interaction with Langmuir monolayers as models of cell membranes. For this, we synthesized iron oxide magnetic nanoparticles coated with an arylamine (aromatic) and polyethylenimine (aliphatic). Also, the effect of human serum albumin at the particle surface was evaluated to test how protein corona governs the physicochemical properties of the nanoparticles. The interaction of these nanoparticles with monolayers of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine was systematically studied employing three different experimental approaches. The results signal a notorious influence on the type of amine in the interactions established with the phosphocholine in the model membrane. Managing this knowledge is of ongoing interest for nanomaterials design and improved bioapplications.

A decade of data and hundreds of analytes: Legacy and emerging chemicals in North American herring gull plasma

Between 2010 and 2021, 199 herring gull serum samples were collected from Lake Michigan, Lake Huron, and Lake Erie, including two Areas of Concern: Saginaw Bay and the River Raisin. They were analyzed for 21 polybrominated diphenyl ether congeners, 10 non-PBDE flame retardants, 85 polychlorinated biphenyls, 17 legacy organochlorine pesticides, and 36 per- and polyfluoroalkyl substances. Σ36PFAS, Σ85PCB, Σ21PBDE, and Σ17Pesticide concentrations comprised 41–74%, 17–50%, 3–4%, and 5–9% of the total concentration, respectively. Median concentrations of the chemical groups ranged from 81.5 to 129 ng/g ww for PFAS, 26.3–158 ng/g ww for PCBs, 4.26–8.89 ng/g ww for PBDEs, and 8.08–23.0 ng/g ww for pesticides. The regional concentrations of all four classes of compounds are significantly decreasing when sites are combined with halving times of 11.3 ± 4.8, 8.2 ± 4.3, 5.9 ± 3.1, and 8.3 ± 4.2 years for the Penta-BDE mixture, ΣDDTs, Σ85PCBs and Σ36PFAS, respectively. These results suggest that, while PFAS has emerged as the dominant group of chemicals in the plasma, legacy pollutants continue to represent a threat to herring gulls and wildlife in the Great Lakes basin. PCBs were the largest contributors to the chemical load in plasma of birds whose colonies are located near the River Raisin, and continue to pose a threat to herring gulls within the two Areas of Concern.