Effect of Aluminum Incorporation into Mesoporous Aluminosilicate Framework on Drug Release Kinetics

Mesoporous silica materials are promising nanocarriers for the development of drug delivery systems. In this study, the influence of pore size, volume, surface area, and doping the silica framework on the release kinetics of a model drug, metoprolol, has been studied. 20% or 50% wt. therapeutic agent was loaded into the carrier mesopores through incipient wetness impregnation. The carriers and drug-loaded samples have been characterized by small- and wide-angle X-ray diffraction, FT-IR spectroscopy, scanning electron microscopy, and nitrogen adsorption-desorption isotherms. The in vitro release profiles have been fitted using a three-parameter kinetic model and they have been explained in terms of the release rate during the burst and sustained release stages and the fraction of drug molecules released during the burst stage. The silica framework doping with aluminum was found to decrease the amount of drug released in the burst stage, without affecting the other kinetic parameters. The therapeutic agent release rates depend mainly on the pore size and volume of the mesoporous carriers and drug-loaded samples

Thermal behaviour of the TiO2-based gels obtained by microwave-assisted sol-gel method

In order to establish the influence of the preparation method on thermal behaviour of gels obtained by the sol-gel and microwave-assisted sol-gel methods, a comparative thermal analysis study was conducted by the thermogravimetric and differential thermal analysis (TG/DTG/DTA) and evolved gas analysis (EGA) on TiO2 and V2O5-doped TiO2 gels, where TiO2:V2O5 molar ratio was set to 99.95:0.05 and 98.0:2.0. In contrast to TiO2 gels, for which the thermal behaviour was not significantly influenced by the preparation method, the microwave-irradiated binary samples showed a more complex and prolonged decomposition compared to their non-irradiated counterparts. This observation was correlated with influence of microwaves in enhancing the reaction rate between the Ti and V reagents leading to formation of more complex compositions of gels. Based on TG/DTG/DTA results, the temperatures of 300 and 450 A degrees C were chosen for the processing of powders in air. All samples thermally treated at 300 and 450 A degrees C crystallized in a single anatase phase except the TiO2:V2O5 with a molar ratio 99.95:0.05, obtained by microwave-assisted sol-gel method that contains also small amount of rutile phase. At 550 A degrees C all samples contain mixture of anatase and rutile phases

Aqueous Dispersions of Silica Stabilized with Oleic Acid Obtained by Green Chemistry

The present study describes for the first time the synthesis of silica nanoparticles starting from sodium silicate and oleic acid (OLA). The interactions between OLA and sodium silicate require an optimal OLA/OLANa molar ratio able to generate vesicles that can stabilize silica particles obtained by the sol-gel process of sodium silicate. The optimal molar ratio of OLA/OLANa can be ensured by a proper selection of OLA and respectively of sodium silicate concentration. The titration of sodium silicate with OLA revealed a stabilization phenomenon of silica/OLA vesicles and the dependence between their average size and reagent’s molar ratio. Dynamic light scattering (DLS) and scanning electron microscopy (SEM) measurements emphasized the successful synthesis of silica nanoparticles starting from renewable materials, in mild condition of green chemistry. By grafting octadecyltrimethoxysilane on the initial silica particles, an increased interaction between silica particles and the OLA/OLANa complex was achieved. This interaction between the oleyl and octadecyl chains resulted in the formation of stable gel-like aqueous systems. Subsequently, olive oil and an oleophylic red dye were solubilized in these stable aqueous systems. This great dispersing capacity of oleosoluble compounds opens new perspectives for future green chemistry applications. After the removal of water and of the organic chains by thermal treatment, mesoporous silica was obtained

Green Synthesis of Hydrogel-Based Adsorbent Material for the Effective Removal of Diclofenac Sodium from Wastewater

The removal of pharmaceutical contaminants from wastewater has gained considerable attention in recent years, particularly in the advancements of hydrogel-based adsorbents as a green solution for their ease of use, ease of modification, biodegradability, non-toxicity, environmental friendliness, and cost-effectiveness. This study focuses on the design of an efficient adsorbent hydrogel based on 1% chitosan, 40% polyethylene glycol 4000 (PEG4000), and 4% xanthan gum (referred to as CPX) for the removal of diclofenac sodium (DCF) from water. The interaction between positively charged chitosan and negatively charged xanthan gum and PEG4000 leads to strengthening of the hydrogel structure. The obtained CPX hydrogel, prepared by a green, simple, easy, low-cost, and ecological method, has a higher viscosity due to the three-dimensional polymer network and mechanical stability. The physical, chemical, rheological, and pharmacotechnical parameters of the synthesized hydrogel were determined. Swelling analysis demonstrated that the new synthetized hydrogel is not pH-dependent. The obtained adsorbent hydrogel reached the adsorption capacity (172.41 mg/g) at the highest adsorbent amount (200 mg) after 350 min. In addition, the adsorption kinetics were calculated using a pseudo first-order model and Langmuir and Freundlich isotherm parameters. The results demonstrate that CPX hydrogel can be used as an efficient option to remove DCF as a pharmaceutical contaminant from wastewater

Preparation and Biocompatibility of Poly Methyl Methacrylate (PMMA)-Mesoporous Bioactive Glass (MBG) Composite Scaffolds

In recent years, the rising number of bone diseases which affect millions of people worldwide has led to an increased demand for materials with restoring and augmentation properties that can be used in therapies for bone pathologies. In this work, PMMA- MBG composite scaffolds containing ceria (0, 1, 3 mol%) were obtained by the phase separation method. The obtained composite scaffolds were characterized by X-ray diffraction, infrared spectroscopy, and scanning electron microscopy. UV–Vis measurement and EDX analysis confirmed the presence of cerium ions in the composite scaffolds. Evaluation of the in-vitro biocompatibility using MTT assay showed that composite scaffold containing 1 mol% of ceria presented higher viability than control cells (100%) for concentrations ranging between 5 and 50% after 96 h of incubation

Development of Immediate Release Tablets Containing Calcium Lactate Synthetized from Black Sea Mussel Shells

Nowadays, the use of marine by-products as precursor materials has gained great interest in the extraction and production of chemical compounds with suitable properties and possible pharmaceutical applications. The present paper presents the development of a new immediate release tablet containing calcium lactate obtained from Black Sea mussel shells. Compared with other calcium salts, calcium lactate has good solubility and bioavailability. In the pharmaceutical preparations, calcium lactate was extensively utilized as a calcium source for preventing and treating calcium deficiencies. The physical and chemical characteristics of synthesized calcium lactate were evaluated using Fourier Transform Infrared Spectroscopy, X-ray diffraction analysis and thermal analysis. Further, the various pharmacotechnical properties of the calcium lactate obtained from mussel shells were determined in comparison with an industrial used direct compressible Calcium lactate DC (PURACAL®). The obtained results suggest that mussel shell by-products are suitable for the development of chemical compounds with potential applications in the pharmaceutical domain

Band-Gap Engineering of Layered Perovskites by Cu Spacer Insertion as Photocatalysts for Depollution Reaction

A multi-step ion-exchange methodology was developed for the fabrication of Cu(LaTa2O7)2 lamellar architectures capable of wastewater depollution. The (001) diffraction line of RbLaTa2O7 depended on the guest species hosted by the starting material. SEM and TEM images confirmed the well-preserved lamellar structure for all intercalated layered perovskites. The UV–Vis, XPS, and photocurrent spectroscopies proved that Cu intercalation induces a red-shift band gap compared to the perovskite host. Moreover, the UV–Vis spectroscopy elucidated the copper ions environment in the Cu-modified layered perovskites. H2-TPR results confirmed that Cu species located on the surface are reduced at a lower temperature while those from the interlayer occur at higher temperature ranges. The photocatalytic degradation of phenol under simulated solar irradiation was used as a model reaction to assess the performances of the studied catalysts. Increased photocatalytic activity was observed for Cu-modified layered perovskites compared to RbLaTa2O7 pristine. This behavior resulted from the efficient separation of photogenerated charge carriers and light absorption induced by copper spacer insertion

Thermal behaviour of the TiO2-based gels obtained by microwave-assisted sol–gel method

In order to establish the influence of the preparation method on thermal behaviour of gels obtained by the sol-gel and microwave-assisted sol-gel methods, a comparative thermal analysis study was conducted by the thermogravimetric and differential thermal analysis (TG/DTG/DTA) and evolved gas analysis (EGA) on TiO2 and V2O5-doped TiO2 gels, where TiO2:V2O5 molar ratio was set to 99.95:0.05 and 98.0:2.0. In contrast to TiO2 gels, for which the thermal behaviour was not significantly influenced by the preparation method, the microwave-irradiated binary samples showed a more complex and prolonged decomposition compared to their non-irradiated counterparts. This observation was correlated with influence of microwaves in enhancing the reaction rate between the Ti and V reagents leading to formation of more complex compositions of gels. Based on TG/DTG/DTA results, the temperatures of 300 and 450 A degrees C were chosen for the processing of powders in air. All samples thermally treated at 300 and 450 A degrees C crystallized in a single anatase phase except the TiO2:V2O5 with a molar ratio 99.95:0.05, obtained by microwave-assisted sol-gel method that contains also small amount of rutile phase. At 550 A degrees C all samples contain mixture of anatase and rutile phases