Pharmacodynamic Comparison of a Nasal Formulation of Verapamil and Intravenous and Oral Dosage Forms

The nasal route has been shown to be effective for the administration of numerous drugs in order to improve drug bioavailability. A nasal gel of verapamil hydrochloride was formulated and evaluated pharmacodynamically in humans, using electrocardiographic results, with comparison to oral and IV routes. Seven volunteers were involved in the study and the pharmacodynamic parameters were evaluated statistically. Experimental nasal gel showed similar pharmacodynamic results with the intravenous route, which is a hint to the reduction in verapamilinduced first-pass metabolism. However, oral route of administration showed a tendency of less efficacy. No reasonable effect of verapamil could be obtained with the placebo group.     

Polymer/bioactive glass nanocomposites for biomedical applications: A review

Nanoscale bioactive glasses have been gaining attention due to their reported superior osteoconductivity when compared to conventional (micron-sized) bioactive glass materials. The combination of bioactive glass nanoparticles or nanofibers with polymeric systems enables the production of nanocomposites with potential to be used in a series of orthopedic applications, including scaffolds for tissue engineering and regenerative medicine. This review presents the state of art of the preparation of nanoscale bioactive glasses and corresponding composites with biocompatible polymers. The recent developments in the preparation methods of nano-sized bioactive glasses are reviewed, covering sol–gel routes, microemulsion techniques, gas phase synthesis method (flame spray synthesis), laser spinning, and electro-spinning. Then, examples of the preparation and properties of nanocomposites based on such inorganic bionanomaterials are presented, obtained using various polymer matrices, including polyesters such as poly(hydroxybutyrate), poly(lactic acid) and poly(caprolactone), and natural-based polymers such as polysaccharides (starch, chitin, chitosan) or proteins (silk fibroin, collagen). The physico-chemical, mechanical, and biological advantages of incorporating nanoscale bioactive glasses in such biodegradable nanocomposites are discussed and the possibilities to expand the use of these materials in other nanotechnology concepts aimed to be used in different biomedical applications are also highlighted.     

Anticonvulsant activity of furanocoumarins and the essential oil obtained from the fruits of Heracleum crenatifolium

The anticonvulsant activity of furanocoumarins, coumarin mixture and the essential oil obtained from the fruits of Heracleum crenatifolium was examined against maximal electroshock (MES)-induced seizures in mice. Bergapten showed significant anticonvulsant activity. The furanocoumarins isolated from the fruits of the plant were identified using thin-layer chromatography, melting points and spectroscopic methods (IR, MS, ¹H NMR) as isobergapten (1), pimpinellin (2), bergapten (3), isopimpinellin (4), sphondin (5) and byak-angelicol (6). The essential oil content of the fruits were found as 5.5%. Twenty-two compounds representing 99.3% of the essential oil obtained from the fruits of H. crenatifolium were determined and the major components were identified as octanol and octyl acetate (3.1% and 88.4% respectively) by GC and GC–MS.     

An Analysis of the Curling Phenomenon in Viscoelastic Bimaterial Strips

A mathematical analysis is performed to obtain relations for the radius of curvature and flexural moments for initially stretched bimaterial strips in which at least one of the materials exhibits viscoelastic behavior. One practical application of this analysis is for pressure sensitive tapes. Consequently, the radius of curvature and flexural moment relations are obtained as functions of backing and adhesive thicknesses and moduli for typical pressure sensitive tapes. The analysis shows that the flexural moment decreases as the backing thickness and/or backing modulus increase. Furthermore, the flexural moment decreases as the adhesive thickness and/or adhesive modulus decreases.     

Structural coloring in large scale core-shell nanowires

We demonstrated two complementary size-dependent structural coloring mechanisms, interference and scattering, in indefinitely long core-shell nanowire arrays. The unusual nanostructures are comprised of an amorphous semiconducting core and a polymer shell layer with disparate refractive indices but with similar thermomechanical properties. Core-shell nanowires are mass produced from a macroscopic semiconductor rod by using a new top-to-bottom fabrication approach based on thermal size reduction. Nanostructures with diameters from 30 to 200 nm result in coloration that spans the whole visible spectrum via resonant Mie scattering. Nanoshell coloration based on thin film interference is proposed as a structural coloration mechanism which becomes dominant for nanowires having 700-1200 nm diameter. Controlled color generation in any part of visible and infrared spectral regions can be achieved by the simple scaling down procedure. Spectral color generation in mass-produced uniform core-shell nanowire arrays paves the way for applications such as spectral authentication at nanoscale, light-scattering ingredients in paints and cosmetics, large-area devices, and infrared shielding.     

Artificial neural network investigation of hardness and fracture toughness of hydroxylapatite

Hardness and fracture toughness of hydroxylapatite were investigated by artificial neural network (ANN). Hardness and fracture toughness of hydroxylapatite were predicted by using its sintering temperature, sintering time, relative density, and grain size with ANN. It was found that prediction results of its hardness and fracture toughness closely matched with the experimental results.     

Viscoelastic and Processing Effects on the Fiber-Matrix Interphase Strength. Part III. The Effects of Postcure

A novel method for tailoring the interphase of carbon fiber-polymer composites by resistive electric heating is presented. The single-fiber fragmentation test is used to investigate the adhesion and fracture properties of the interphase. Electric resistive heating is shown to increase adhesion and toughness at the interphase region. In analyzing the results, the strength and fracture energy of the interphase are related to the thermal postcure conditions created by resistive electric heating. For this purpose, a difference analysis method is used to obtain a numerical solution for the heat conduction problem in the single-fiber test specimen and the temperature distributions are determined. Improvements obtained by using resistive electric heating of the carbon fiber are compared with those obtained by postcuring of the whole sample via convective thermal postcuring. The results obtained using these two different postcure methods seem to be similar.     

Temperature-Dependent Phase Behaviors in Cylinder-Forming Block Copolymers

We demonstrate that the temperature-dependent phase behaviors of parallel and perpendicular cylinder-forming block copolymers are governed by domain-domain segregation forces inherently present in block copolymer material itself. With increasing temperature, a parallel cylinder-forming block copolymer experienced a parallel cylinder straightening process before the order-disorder transition (ODT) and did not show long-range composition fluctuations near the ODT temperature due to the weak segregation forces between the block domains. A perpendicular cylinder-forming block copolymer with a strong segregation force between the block domains displayed cylinder orientation transition from perpendicular to parallel below the ODT temperature. On the other hand, a perpendicular cylinder-forming block copolymer material with an exceptionally strong segregation force between the block domains maintained its initial perpendicular cylinder orientation up to near the ODT temperature. In both cases of perpendicular cylinder-forming block copolymers, submicrometer-scale long-range composition fluctuations were observed well above the ODT temperature due to their intrinsically strong segregation forces between the block domains.     

CHARACTERIZATION OF THE STRUCTURAL FEATURES OF OXIDIZED BEYPAZARI LIGNITE USING DECONVOLUTED SOLID STATE 13C NMR SPECTRA

ABSTRACT

The solid state ¹³C NMR method have been used to investigate the structural changes occurred in Beypazari lignite while oxidizing at 150°C in a dynamic air atmosphere. Least squares curve fitting techniques have been used to resolve the overlapping bands in the 0-220 ppm region of the 13_c NMR spectra. Measurements of the relative intensities of the functional groups observed in the oxidized coals were used to follow the progress of air oxidation. Oxidation reactions seemed to decrease the total intensities of both aliphatics and aromatics, though the reduction in aliphatics was more pronounced. The relative intensities of the total aliphatics decreased from 1.0 to 0.9 and 0.6 in the original and lignites oxidized for 12 and 312 hours, respectively. The relative intensities of Ar-C-C in the 130-148 ppm region for the same set of samples were 1.0, 0.9 and 0.8. The least-squares bands resolved in the carbonyl region were at 175 ppm and 190 ppm in the original lignite; at 180 ppm (carboxylic acids), 195 ppm (meta substituted ketones) 210 ppm (di orto substituted ketones) in the lignite oxidized for 12 hours and at 170 ppm (esters), 180 ppm, 200 ppm (aldehydes) and 210 ppm in the lignite oxidized for 312 hr. Carbonyl intensity increased from 1.0 in the original lignite to 2.3 and 3.3 in the oxidized lignites. The intensity of aromatic ethers increased from 1.0 in the original lignite to 1.9 and 1.6 for the oxidized samples. The mechanism of oxidation ether. Aldehydes are easily oxidized to carboxylic acids in the presence of air by the free radical formation of a peroxy acid. The carboxylic acid formed by disproportionation reactions between the peroxy acid and aldehydes might combine with phenols to produce esters as it was observed in the present work. The presence of high free radical concentration in the oxidation atmosphere probably caused to abstract hydrogen atoms from the aromatic structures thus degrading aromatics to produce hydroperoxides which acted later as it was described above. The gradual degradation of aromatic structures observed in the present study indicated that the oxidation reactions of the aromatic rings should less probable when compared to the oxidation of aliphatic structures.