Viscoelasticity,mechanical properties,and in vivo biocompatibility of injectable polyvinyl alcohol/bioactive glass composite hydrogels as potential bone tissue scaffolds

Abstract

An injectable composite hydrogel composed of polyvinyl alcohol (PVA) and bioactive glass (BG) particles were synthesized by a physical crosslinking approach. The morphology, mechanical properties, and viscoelasticity of the PVA/BG composite hydrogel were characterized. Scanning electronic microscopy (SEM) showed uniform and homogeneous distribution of BG particles throughout the composite hydrogel. The incorporation of 2.5?wt% of BG particles in the composite hydrogel formulations, enhanced the static compressive strength and static elastic modulus by 325% and 150%, respectively. The storage molds (G′) was greater than the loss modules (G′′) at all the frequency range studied, which revealed a self-standing elastic composite hydrogel with a smooth injectability. The PVA/BG composite hydrogel was also implanted subcutaneously in the dorsal region of adult male rats. After 4?weeks of implantation, no inflammatory cells were seen within and around the implant, which indicated that the composite hydrogel was biocompatible. The properties of the synthesized injectable PVA/BG composite hydrogel demonstrate its capability toward bone regeneration.     

Critical micelle concentrations for alkyltrimethylammonium bromides in water from 25 to 160°C

Critical micelle concentrations were determined by conductance measurements for decyl-, dodecyl-, tetradecyl- and hexadecyltrimethylammonium bromide in water at 25, 60, 95, 130, and 160°C. The results are discussed in terms of the equilibrium model and the nonlinear Poisson-Boltzmann model for micelle formation. The free energies of transferring a methylene group from water to the oil-like interior of the micelle are found to be –781 at 25°C, –796 at 60°C, –819 at 95°C, –815 at 130°C, and –787 at 160°C cal-mol^–1.     

Nonlinear instability of superposed magnetic fluids in the presence of an oblique magnetic field

The nonlinear evolution of interfacial waves separating two magnetic fluids subjected to an oblique magnetic field is studied in two dimensions, with the use of the method of multiple scales. It is shown that the evolution of the envelope is governed by two partial differential equations. These equations can be combined to yield two alternate Schrödinger equations with cubic nonlinearity; one of them leads to the determination of the cutoff wave number separating stable from unstable deformations while the other Schrödinger equation is used to analyze the stability of the system. The stability of the system is discussed both theoretically and computationally, and the stability diagrams are obtained. It is found in the linear theory that the oblique magnetic field has a stabilizing influence if 0 ₁ + ₂ < /2, or 3/2 < ₁ + ₂ 2 and a destabilizing influence if /2 < ₁ + ₂ < 3/2, where 0 _j , (j=1, 2) and , is the angle between the field and the horizontal axis.In the nonlinear theory, the stability analysis reveals that there exist different regions of stability and instability. It is reported that the oblique magnetic field plays a dual role in the stability criterion and the angles ₁ and ₂ play a distinctive role in this analysis besides the effect of the variation of the magnetic permeabilities.     

Radiation grafting from binary monomer mixtures. I. Vinyl ether of monoethanolamine and vinyl ether of ethyleneglycol

Gamma-radiation grafting of vinyl ether of monoethanolamine and vinyl ether of ethyleneglycol (VEEG) on polyethylene films has been studied from binary monomer mixtures. The effect of co-monomer composition and total exposure radiation dose on the grafting process is investigated. A combination of potentiometric and gravimetric techniques is applied to determine the grafting degree of each monomer in the final graft copolymer. The presence of more active monomer VEEG in the mixture was found to enhance the grafting of both monomers because the increasing of copolymerization rate which in turn increases the total grafting degree. The modification of the hydrophilic properties of the graft copolymer is studied by examining the grafted films for water- and copper (II) ions uptake.     

Synthetic analgesics: preparation of racemic 6,7-benzomorphans

A simple preparation of 2-carbomethoxy-2-azabicyclo[3.3.1]nonan-6-one ($\text{7}$ and its conversion to the racemic benzomorphans: $\text{9}$, $\text{10}$, $\text{14}$ are described.     

Enaminones in heterocyclic synthesis: Synthesis and chemical reactivity of 3‐anilino‐1‐substituted‐2‐propene‐1‐ one

The 3‐anilinoenones 3a,b were prepared from the corresponding 3‐dimemyl‐aminopropenones. The reactivity of 3a,b towards a variety of carbon and nitrogen nucleophiles as well as naphthoquinones is reported.     

Carbon‐based Nanosensors for Salicylate Determination in Pharmaceutical Preparations

Thiourea derivative‐based carbon paste electrode (TUD1‐CPE) was constructed as a potentiometric sensor for the determination of salicylate anion in pharmaceutical formulations, Aspocid® and Aspirin®. The optimized CPE contained 45.5 % graphite, 0.5 % reduced graphene oxide (rGO), 46.0 % nitrophenyl octyl ether (NPOE) plasticizer, 5.0 % TUD1 ionophore, and 3.0 % tridodecylmethyl ammonium chloride as additive. The incorporation of NPOE of high dielectric constant, and rGO in electrode caused better performance of the sensor; Nernstian response of 59.0 mV decade^?1 in the concentration range of 10^?1–10^?5 mole L^?1, a detection limit of 1×10^?5 mole L^?1 in a very short response time of 6 seconds. The prepared sensor showed high selectivity against similar anions (i. e. , benzoate, I^?, SCN^?). Selectivity was confirmed by calculating the formation constant (K_β) using sandwich membrane method, where K_β for TUD1‐salicylate is 10^0.43. Theoretical calculations at DFT‐B3LY/6‐31G** level of theory were performed to find interaction mechanism, Energies of HOMO and LUMO orbitals, non‐linear optical (NLO) properties (the electronic dipole moment (μ), first‐order hyperpolarizability (β), the hyper‐Rayleigh scattering (β_HRS) and the depolarization ratio (DR)), and other global properties; these calculations showed lower values of β and DR, higher value of β_HRS, and the shortest lengths of the four N?H bonds between TUD1 and salicylate which confirm their strong complexation and salicylate‐selectivity. Also, all the studied anion‐TUD1 exhibited relatively high NLO properties, and these results were considered as a preliminary study for investigating new types of NLO bearing materials. The sensors were applied successfully for the determination of salicylate anion in Aspocid® and Aspirin®.     

Comparative Studies on the Behavior of 3-Amino-2-phenyl-4(3 H )-quinazolinone Towards Some Organophosphorus Reagents

The reaction of 3-amino-2-phenyl-4(3H)-quinazolinone with oxovinylidenetriphenylphosphorane afforded 5-phenylpyrazolo[1,5-c] quinazoline-2(3H)-one and triphenylphosphine oxide. On the other hand, when quinazolinone reacts with phosphorus ylides, the corresponding phosphorane adducts were obtained. Moreover, quinazolinone reacts with trisdialkylaminophosphines to give the new (dialkylamino)oxophosphonium dipolar products. Possible reaction mechanisms are considered and the structural assignments are based on analytical and spectroscopic results.     

The use of Omega Chrome Fast Blue 2G in the microdetermination of some metals

Summary Omega Chrome Fast Blue 2G has been found to be a suitable indicator for the detection of the equivalence point of calcium, magnesium and manganese in the presence of cadmium, nickel, and aluminium, when they are masked by the addition of cyanide or triethanolamine. It is also a suitable indicator for the back titration of aluminium using calcium or magnesium as a back titrant.This dye has also been found to be a suitable reagent for the colorimetric determination of calcium, magnesium, manganese and thorium.     

Infrared absorption spectra of some lanthanide acetylacetonate complexes

The infrared absorption spectra of 12 lanthanide acetylacetonate complexes were measured in the region 400–2000 cm^?1 and discussed. Assignments of the bands especially those due to metal-oxygen (M—O), C=O and C=C stretching vibration is given. It is found that the band at 530 ± 5 cm^?1 is due mainly to Ln—O stretching vibration. In the carbonyl region, it is confirmed that the band at lower frequency is a C=C stretching vibration while that at higher frequency is due to C=O stretching vibration. Integral intensities for the M—O, C=O and C=C stretching vibrations were calculated in KB₁ and CHCl₃ solutions. The variation of the intensities of the M—O bands witn complexed cation were discussed in terms of crystal field stabilization energy (CFSE).