RESUMO
Olive mill wastewater, also known as olive wastewater, contains biologically active components with various beneficial effects on health. The development of novel adsorbent materials for the recovery of these biologically active substances is important area of research. In this study, copolymeric hydrogels based on N-vinylimidazole (VIm), a new material that has never been used as an adsorbent in the separation of phenolic components, were synthesized. The hydrogels synthesized in this study is copolymer structures based on N-vinylimidazole (VIm) containing [2- (methacryloxy) ethyl] dimethylpentylammonium bromide (QDMAC5) in different moles. QDMAC5 was obtained by quaternization of 2- (dimethylamino) ethyl methacrylate (DMA) with 1-bromopentane (C5). The production of copolymer hydrogels was carried out by free radical solution polymerization. The syntheses were carried out only by changing the monomer composition so that the crosslinker ratio remained constant (1.2 mol%). The QDMAC5 content in the copolymers was 5, 10, 20, 30, and 50 mol%. So, the resulting structures were named PVQ-5%, PVQ-10%, PVQ-20%, PVQ-30%, and PVQ-50%, respectively. Functional group characterizations of hydrogels were made by Fourier Transform Infrared Spectrometry (FTIR). The surface of the hydrogels was analyzed by Scanning Electron Microscopy (SEM). Finally, thermogravimetric analyzes (TGA) were performed to investigate the thermal degradation behavior. The recovery of the rutin present in olive mill wastewater has been investigated as a model study. Kinetic data has been represented by the selected models (pseudo-first order, pseudo-second order, and intraparticle diffusion) convincingly (R2 > 0.76), while the equilibrium findings have fitted well to Langmuir, Freundlich, and Temkin equations (R2 > 0.77). Rutin adsorption process on N-vinylimidazole (VIm) based copolymeric hydrogels has been found as exothermic and spontaneous chemisorption process depending on the thermodynamic analysis.
Assuntos
Olea , Poluentes Químicos da Água , Adsorção , Hidrogéis/química , Concentração de Íons de Hidrogênio , Imidazóis , Cinética , Rutina/análise , Espectroscopia de Infravermelho com Transformada de Fourier , Termodinâmica , Águas Residuárias/química , Poluentes Químicos da Água/análiseRESUMO
Methotrexate (MTX), an analog of folic acid (FA), is a drug widely used in cancer treatment. To prevent its potential toxicity and enhance therapeutic efficacy, targeted drug delivery systems, especially nanotechnology-folate platforms, are a central strategy. Gold nanoparticles (AuNPs) are promising candidates to be used as drug delivery systems because of their small particle sizes and their inertness for the body. In this study, glutathione (GSH)-coated FA-modified spherical AuNPs (5.6 nm) were successfully synthesized, and the anticancer activity of novel MTX-loaded (MTX/Au-GSH-FA) NPs (11 nm) was examined. Dynamic light scattering (DLS) and transmission electron microscopy (TEM) results showed that MTX/AuNPs possess spherical morphology, nanoscaled particle size, narrow size distribution, and good stability. In vitro studies showed that cytotoxicity of MTX/Au-GSH-FA to folate receptor-positive (FR+) human brain (U-87 MG) and cervical (HeLa) cancer cells enhanced significantly (â¼3 and â¼10 fold, respectively) compared to free MTX while there was no significant effect in FR-negative human cell lines A549 (lung carcinoma), PC3 (prostate carcinoma), HEK-293 (healthy embryonic kidney). Moreover, the receptor specificity of the conjugate was shown by fluorescent microscopic imaging. In conclusion, these results indicate that the synthesized novel MTX/Au-GSH-FA NP complex seems to be a good candidate for effective and targeted delivery in FR+ cancer therapy.
Assuntos
Antineoplásicos/farmacologia , Ácido Fólico/farmacologia , Glutationa/química , Ouro/química , Metotrexato/farmacologia , Células A549 , Antineoplásicos/química , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Sinergismo Farmacológico , Ácido Fólico/química , Células HEK293 , Células HeLa , Humanos , Nanopartículas Metálicas , Metotrexato/química , Células PC-3 , Tamanho da PartículaRESUMO
Globally, there are increased threats to available freshwater resources due to pollution, climate change, and increased demand from population growth. Phosphorus is one of the essential nutrients required for animal and plant growth. However, when it is released into freshwater resources in excess amounts, it can become a pollutant through eutrophication. This study aimed to enhance the removal of phosphate from water using modified coal. The coal was magnetised by in-situ synthesis using a precipitation technique. To obtain functional groups and mechanical stability, magnetised coal particles were coated with polyaniline, via the polymerisation of aniline to form Magnetised Unburnt Coal Polyaniline (MUC-PANI). The properties of MUC-PANI were investigated using TGA, BET, XRD, Raman spectroscopy, SEM, and FTIR. TGA reviewed MUC-PANI as 58% magnetised coal and 42% polyaniline, while the specific surface area increased from 30.0 to 42.2â¯m2/g after modification. SEM indicated a cauliflower structure on the surface of MUC-PANI due to the successful polymerisation of polyaniline. The FTIR spectrum showed successful adsorption of phosphate due to the formation of incipient peak at1008 cm-1. The adsorption kinetic data are better fitted to the Elovich model. The Langmuir adsorption capacity of MUC-PANI is 147.1â¯mg PO43-/g at 25⯰C and pH 5.0 (initial concentration 10-200â¯mg/L, dose 0.8â¯g/L). MUC-PANI is a cost-efficient compound for removal of phosphate because it is made from readily available coal.
Assuntos
Carvão Mineral , Fosfatos , Adsorção , Cinética , PolimerizaçãoRESUMO
Novel semi-transparent organic solar cells (ST-OSC) can be designed with high average visible transmittance (AVT) while at the same time exhibiting superior photovoltaic performance. This reach requires their design to be based not only on conventional window applications but also on functional industrial applications that require exceptional optical performance. In ST-OSC, high AVT can be achieved by photonic-based dielectric/metal/dielectric (DMD) transparent contact engineering. Functional optical modification can also be made with a fine-tuned design of DMD that includes a light management engineering-based approach. Thus, ST-OSCs can be suitable for aesthetic, colourful and decorative industrial windows that provide natural lighting. In this study, we determined optimal ST-OSCs based on a novel PTB7:PC71BM polymer blend with MoO3/Ag/WO3 asymmetric DMD top contact by examining extraordinary optical properties such as AVT, colour rendering index, correlated colour temperature and colour perception over 10 thousand designs. In addition to determining the optimality and extraordinary optical limits for PTB7, we also evaluated the photon-harvesting and photovoltaic performance of ST-OSCs from external quantum efficiency and quantum utilization efficiency. In optimal situations, ST-OSCs offering 48.75% AVT, 99.08 CRI, and sky-blue colours were designed and determined to generate short-circuit current densities of 9.88 mA·cm-2, 13.64 mA·cm-2, and 13.06 mA·cm-2, respectively.
RESUMO
Cross-linking agents are incorporated into denture base materials to improve their mechanical properties. This study investigated the effects of various cross-linking agents, with different cross-linking chain lengths and flexibilities, on the flexural strength, impact strength, and surface hardness of polymethyl methacrylate (PMMA). The cross-linking agents used were ethylene glycol dimethacrylate (EGDMA), tetraethylene glycol dimethacrylate (TEGDMA), tetraethylene glycol diacrylate (TEGDA), and polyethylene glycol dimethacrylate (PEGDMA). These agents were added to the methyl methacrylate (MMA) monomer component in concentrations of 5%, 10%, 15%, and 20% by volume and 10% by molecular weight. A total of 630 specimens, comprising 21 groups, were fabricated. Flexural strength and elastic modulus were assessed using a 3-point bending test, impact strength was measured via the Charpy type test, and surface Vickers hardness was determined. Statistical analyses were performed using the Kolmogorov-Smirnov Test, Kruskal-Wallis Test, Mann-Whitney U Test, and ANOVA with post hoc Tamhane test (p ≤ 0.05). No significant increase in flexural strength, elastic modulus, or impact strength was observed in the cross-linking groups compared to conventional PMMA. However, surface hardness values notably decreased with the addition of 5% to 20% PEGDMA. The incorporation of cross-linking agents in concentrations ranging from 5% to 15% led to an improvement in the mechanical properties of PMMA.
RESUMO
Pentylenetetrazole (PTZ)-induced kindling is an animal model for studying human temporal lobe epilepsy (TLE), which is characterized by alterations of hippocampal neurons and memory. Although the intranasal (IN) administration of oxytocin (OT) has limited efficiency, nanoparticles (NPs) are a promising candidate to deliver OT to the brain. However, there are very limited data on epilepsy research about oxytocin-loaded nanoparticles (NP-OTs). The aim of this study is to investigate the effects of IN administration of chronic NP-OTs on the hippocampus of PTZ-induced male epileptic rats in terms of seizure severity, memory, neurogenesis, and neuronal damage. Saline/OT/NP-OTs were administrated to both control (Ctrl) and PTZ groups intranasally. Consequently, saline and PTZ were injected, respectively, 25 times every 48 h. Then, seizure severity (score and latency) was calculated for the PTZ groups. A spatial working memory evaluation test (SWMET) was performed after the last injection. Hippocampus histopathology, neurogenesis, and apoptosis were demonstrated. Serum total antioxidant status (TAS) and total oxidant status (TOS) levels and the oxidative stress index (OSI) were measured. We showed that OTs and NP-OTs prevented the kindling development and had positive effects on seizure severity. SWMET-related behaviors were also recovered in the PTZ + NP-OT group. A significant increase of neurogenesis and decrease of apoptosis in the hippocampus of the PTZ + NP-OT group were observed, while OTs and NP-OTs had protective effects against PTZ-induced damage to hippocampal neurons. Our results indicate that the chronic administration of NP-OTs may have positive effects on hippocampal damage via increasing neurogenesis and decreasing apoptosis and seizure severity.
Assuntos
Epilepsia , Nanopartículas , Ocitocina , Pentilenotetrazol , Animais , Modelos Animais de Doenças , Epilepsia/induzido quimicamente , Epilepsia/tratamento farmacológico , Epilepsia/patologia , Hipocampo/efeitos dos fármacos , Hipocampo/patologia , Masculino , Nanopartículas/administração & dosagem , Neurogênese/efeitos dos fármacos , Neurônios/efeitos dos fármacos , Neurônios/patologia , Ocitocina/administração & dosagem , Pentilenotetrazol/administração & dosagem , Ratos , Convulsões/induzido quimicamente , Convulsões/tratamento farmacológicoRESUMO
Semi-transparent organic solar cells' (ST-OSCs) photovoltaic and high optical performance parameters are evaluated in innovative applications such as power-generating windows for buildings, automobiles, and aesthetic designs in architectural and industrial products. These parameters require the precision design of structures that optimize optical properties in the visible region and aim to achieve the required photon harvest in UV and IR. These designs can be realized by integrating wavelength-selective photonics-based systems into ST-OSC to increase localized absorption in wavelengths greater than 600 nm and NIR and provide modifiable optical properties. In this study, methodologically, we followed highly detailed light management engineering and transfer matrix method-based theoretical and experimental approaches. We discussed the optimal structures by evaluating color, color rendering index, correlated color temperature, and photovoltaic performances for ST-OSCs, including one-dimensional photonic crystal (1D-PC) designed at different resonance wavelengths (λB) and periods. Finally, by integrating fine-tuned (MgF2/MoO3)N 1D-PC, we report the inherently dark purple-red color of the P3HT:PCBM bulk-heterojunction-based ST-OSC neutralizes with the optimal state was 0.3248 and 0.3733 by adjusting close to the Planckian locus. We also enhanced short current density from 5.77 mA/cm2 to 6.12 mA/cm2 and PCE were increased by 7.34% from 1.77% to 1.90% designed for the N = 4 period and λB = 700 nm.
RESUMO
OBJECTIVE: Most currently available antiepileptics are not fully effective in the prevention of seizures in absence epilepsy owing to the presence of blood-brain barrier (BBB). We aimed to test whether binding an antiepileptic drug, lacosamide (LCM), to glucose-coated gold nanoparticles (GNPs) enables efficient brain drug delivery to suppress the epileptic activity in WAG/Rij rats with absence epilepsy. METHODS: In these animals, intracranial-EEG recording, behavioral test, in vivo imaging of LCM and LCM-GNP conjugate distribution in the brain, inductively coupled plasma mass spectrometry analysis, immunofluorescence staining of glucose transporter (Glut)- 1, glial fibrillary acidic protein (GFAP), and p-glycoprotein (P-gp) and electron microscopy were performed. RESULTS: Lacosamide-GNP conjugates decreased the amplitude and frequency of spike-wave-like discharges (SWDs) and alleviated the anxiety-like behavior as assessed by EEG and elevated plus-maze test, respectively (p < 0.01). The in vivo imaging system results showed higher levels of fluorescein dye tagged to LCM-GNP in the brain during the 5-day injection period (p < 0.01). Immunofluorescence staining displayed decreased P-gp, Glut-1, and GFAP expression by LCM-GNP conjugate treatment predominantly in the cerebral cortex suggesting a potential functionality of this brain region in the modulation of neuronal activity in our experimental setting (p < 0.01). SIGNIFICANCE: We suggest that the conjugation of LCM to GNPs may provide a novel approach for efficient brain drug delivery in light of the effectiveness of our strategy not only in suppressing the seizure activity but also in decreasing the need to use high dosages of the antiepileptics to reduce the frequently encountered side effects in drug-resistant epilepsy.
Assuntos
Epilepsia Tipo Ausência , Nanopartículas Metálicas , Animais , Anticonvulsivantes/uso terapêutico , Barreira Hematoencefálica , Modelos Animais de Doenças , Eletroencefalografia/métodos , Epilepsia Tipo Ausência/tratamento farmacológico , Ouro/uso terapêutico , Lacosamida/uso terapêutico , Ratos , Convulsões/tratamento farmacológicoRESUMO
We conducted the present study to design and manufacture a semi-transparent organic solar cell (ST-OSC). First, we formed a transparent top contact as MoO3/Ag/MoO3 in a dielectric/metal/dielectric (DMD) structure. We performed the production of an FTO/ZnO/P3HT:PCBM/MoO3/Ag/MoO3 ST-OSC by integrating MoO3/Ag/MoO3 (10/[Formula: see text]/[Formula: see text] nm) instead of an Ag electrode in an opaque FTO/ZnO/P3HT:PCBM/MoO3/Ag (-/40/130/10/100 nm) OSC, after theoretically achieving optimal values of optical and electrical parameters depending on Ag layer thickness. The transparency decreased with the increase of [Formula: see text] values for current DMD. Meanwhile, maximum transmittance and average visible transmittance (AVT) indicated the maximum values of over 92% for [Formula: see text] = 4 and 8 nm, respectively. For ST-OSCs, the absorption and reflectance increased in the visible region by a wavelength of longer than 560 nm and in the whole near-infrared region by increasing [Formula: see text] up to 16 nm. Moreover, in the CIE chromaticity diagram, we reported a shift towards the D65 Planckian locus for colour coordinates of current ST-OSCs. Electrical analysis indicated the photogenerated current density and AVT values for [Formula: see text] nm as 63.30 mA/cm2 and 38.52%, respectively. Thus, the theoretical and experimental comparison of optical and electrical characteristics confirmed that the manufactured structure is potentially conducive for a high-performance ST-OSC.
RESUMO
An amphiphilic core/shell-type polymer-based drug carrier system (HPAE- PCL-b -MPEG), composed of hyperbranched poly(aminoester)-based polymer (HPAE) as the core building block and poly(ethylene glycol)-b - poly(ε-caprolactone) diblock polymers (MPEG-b -PCL) as the shell building block, was designed. The synthesized polymers were characterized with FTIR, 1 H NMR, 13 C NMR, and GPC analysis. Monodisperse HPAE-PCL-b - MPEG nanoparticles with dimensions of < 200 nm and polydispersity index of < 0.5 were prepared by nanoprecipitation method and characterized with SEM, particle size, and zeta potential analysis. 5-Fluorouracil was encapsulated within HPAE-PCL-b -MPEG nanoparticles. In vitro drug release profiles and cytotoxicity of blank and 5-fluorouracil-loaded nanoparticles were examined against the human colon cancer HCT116 cell line. All results suggest that HPAE-PCL-b - MPEG nanoparticles offer an alternative and effective drug nanocarrier system for drug delivery applications.
RESUMO
Temporal lobe epilepsy (TLE) is the most common form of epilepsy with focal seizures, and currently available drugs may fail to provide a thorough treatment of the patients. The present study demonstrates the utility of glucose-coated gold nanoparticles (GNPs) as selective carriers of an antiepileptic drug, lacosamide (LCM), in developing a strategy to cross the blood-brain barrier to overcome drug resistance. Intravenous administration of LCM-loaded GNPs to epileptic animals yielded significantly higher nanoparticle levels in the hippocampus compared to the nanoparticle administration to intact animals. The amplitude and frequency of EEG-waves in both ictal and interictal stages decreased significantly after LCM-GNP administration to animals with TLE, while a decrease in the number of seizures was also observed though statistically insignificant. In these animals, malondialdehyde was unaffected, and glutathione levels were lower in the hippocampus compared to sham. Ultrastructurally, LCM-GNPs were observed in the brain parenchyma after intravenous injection to animals with TLE. We conclude that glucose-coated GNPs can be efficient in transferring effective doses of LCM into the brain enabling elimination of the need to administer high doses of the drug, and hence, may represent a new approach in the treatment of drug-resistant TLE.