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Evaporation Method (evaporation + method)
Kinds of Evaporation Method Selected AbstractsOptical properties of 2-aminopyridinium nitrato silverCRYSTAL RESEARCH AND TECHNOLOGY, Issue 3 2010K. P. Bhuvana Abstract Crystals of 2-aminopyridinium nitrato silver have been synthesized by slow evaporation method. Grown crystals have been subjected to FTIR, Single crystal X-Ray diffraction and UV-Visible studies in order to investigate the structural and optical properties of the crystal. The FTIR spectrum reveals the presence of the functional group that corresponds to both 2-aminopyridine and silver nitrate, suggesting the formation of the compound, 2-aminopyridinium nitrato silver. From XRD it is observed that the crystal crystallizes in the structure of monoclinic with the space group of P21/c. The optical transmittance spectrum shows the maximum transparency of about 95% in the visible region is in consistent with the wide band gap, estimated as 4.738 eV. The optical constants n and k has also been determined from the transmittance data. The static dielectric constant is found to be 0.851. The wide band gap and the less dielectric constant suggest the suitability of this compound material for photoconductive applications. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Influence of the substrate temperature on the structural, optical, and electrical properties of tin selenide thin films deposited by thermal evaporation methodCRYSTAL RESEARCH AND TECHNOLOGY, Issue 1 2010N. Kumar Abstract Thin films of tin selenide (SnSe) were deposited on sodalime glass substrates, which were held at different temperatures in the range of 350-550 K, from the pulverized compound material using thermal evaporation method. The effect of substrate temperature (Ts) on the structural, morphological, optical, and electrical properties of the films were investigated using x-ray diffraction analysis (XRD), scanning electron microscopy (SEM), transmission measurements, and Hall-effect characterization techniques. The temperature dependence of the resistance of the films was also studied in the temperature range of 80-330 K. The XRD spectra and the SEM image analyses suggest that the polycrystalline thin films having uniform distribution of grains along the (111) diffraction plane was obtained at all Ts. With the increase of Ts the intensity of the diffraction peaks increased and well-resolved peaks at 550 K, substrate temperature, were obtained. The analysis of the data of the optical transmission spectra suggests that the films had energy band gap in the range of 1.38-1.18 eV. Hall-effect measurements revealed the resistivity of films in the range 112-20 , cm for films deposited at different Ts. The activation energy for films deposited at different Ts was in the range of 0.14 eV-0.28 eV as derived from the analysis of the data of low-temperature resistivity measurements. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Vibrational, optical and microhardness studies of trimethoprim DL -malateCRYSTAL RESEARCH AND TECHNOLOGY, Issue 12 2009S. Franklin Abstract Trimethoprim malate, an organic crystal, has been synthesized using slow evaporation method from its aqueous solution. Structural, optical and the mechanical properties of the grown crystal have been investigated by various characterization techniques which include FTIR spectra, single crystal XRD, UV-Vis spectra and Vickers microhardness testing. The structure of the compound predicted by analysing the recorded FTIR spectrum compliments the structure determined using single crystal X-ray diffraction. Single crystal X-ray diffraction study reveals that the crystals are monoclinic [P21/c, a=12.9850 Å, b=9.3038 Å, c=15.6815 Å and ,=111.065°]. The UV-Vis spectrum exhibits maximum transparency (98%) for a wide range suggesting the suitability of the title compound for optical applications. The optical constants have been calculated and illustrated graphically. Microhardness tests have been performed on the cystal under study and the Vicker hardness number has been calculated. The work hardening coefficient is found to be 2.85 which suggest that the crystal belongs to the family of soft materials. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Effects of annealing on structural, electrical and optical properties of AgGa(Se0.5S0.5)2 thin films deposited by using sintered stoichometric powderCRYSTAL RESEARCH AND TECHNOLOGY, Issue 4 2009H. Karaagac Abstract The structural, electrical and optical properties of AgGa(Se0.5S0.5 )2 thin films deposited by using the thermal evaporation method have been investigated as a function of annealing in the temperature range of 450,600 °C. X-ray diffraction (XRD) analysis showed that the structural transformation from amorphous to polycrystalline structure started at 450 oC with mixed binary phases of Ga2Se3, Ga2S3, ternary phase of AgGaS2 and single phase of S. The compositional analysis with the energy dispersive X-ray analysis (EDXA) revealed that the as-grown film has different elemental composition with the percentage values of Ag, Ga, Se and S being 5.58, 27.76, 13.84 and 52.82 % than the evaporation source powder, and the detailed information about the stoichometry and the segregation mechanisms of the constituent elements in the structure have been obtained. The optical band gap values as a function of annealing temperature were calculated as 2.68, 2.85, 2.82, 2.83, and 2.81 eV for as-grown, annealed at 450, 500, 550, and 600 °C samples, respectively. It was determined that these changes in the band gap are related with the structural changes with annealing. The temperature dependent conductivity measurements were carried out in the temperature range of 250-430 K for all samples. The room temperature resistivity value of as-grown film was found to be 0.7x108 (,-cm) and reduced to 0.9x107 (,-cm) following to the annealing. From the variation of electrical conductivity as a function of the ambient temperature, the activation energies at specific temperature intervals for each sample were evaluated. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Optical and dielectric studies on pure and Ni2+, Co2+ doped single crystals of bis thiourea cadmium chlorideCRYSTAL RESEARCH AND TECHNOLOGY, Issue 4 2008R. Uthrakumar Abstract Good quality single crystals of Ni2+, Co2+ ions doped Bisthiourea Cadmium Chloride (BTCC) are some of the excellent and efficient non-linear optical materials grown from aqueous solution by slow evaporation method. The lattice parameters of the grown crystals are determined by single crystal X-ray analysis. UV spectral analyses on these samples reveal the improved transparency of the doped crystals ascertaining the inclusion of metal ion in the lattice. FTIR spectral analysis carried out on the materials confirm the presence of functional groups. Dielectric measurements reveal that the dielectric constant of pure and doped crystals decreases with increase of frequency. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Growth and characterization of pure and doped nonlinear optical l-arginine acetate single crystalsCRYSTAL RESEARCH AND TECHNOLOGY, Issue 10 2007M. Gulam Mohamed Abstract Single crystals of organic nonlinear optical material of pure, Cu2+ and Mg2+ doped L-arginine acetate (LAA) were successfully grown by slow evaporation method at room temperature. The UV-Vis-NIR spectra of pure and doped LAA indicate that these crystals possess a wide optical transmission window from 240-1600 nm. Non-linear optical studies reveal that the SHG efficiency of LAA is nearly three times that of KDP. The dielectric response of the samples was studied in the frequency region 100 Hz to 2 MHz and the influence of Cu2+ and Mg2+ substitution on the dielectric behaviour had been investigated. Photoconductivity study proves that both pure and Cu2+ and Mg2+ doped LAA crystal exhibit positive photoconductivity. It is evident from the Vickers hardness study that the hardness of the crystal decreases with increasing load both for pure and doped samples. ESR studies confirmed the incorporation of Cu2+ into LAA and the value of g-factor was found to be 2.1654. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Photoconduction and transport mechanisms in polycrystalline zincphthalocyanine thin filmsCRYSTAL RESEARCH AND TECHNOLOGY, Issue 5 2007S. Senthilarasu Abstract Zincphthalocyanine (ZnPc) thin films were prepared by the vacuum evaporation method under a pressure of 10 -6 mbar. The X-ray diffraction analysis of vacuum evaporated ZnPc films reveals that the structure of the films is polycrystalline in nature. The photoconduction properties have been studied in the wavelength range 400 ,800nm using suitable masks. The Photoconductivity of the films as a function of light intensity and applied voltage were studied and results were discussed in detail. The photoconduction was found to increase with higher light illumination and maximum at the band edge of the ZnPc thin film. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Synthesis and characterization of potassium magnesium sulphate hexahydrate crystalsCRYSTAL RESEARCH AND TECHNOLOGY, Issue 4 2006M. Dhandapani Abstract Potassium magnesium sulphate hexahydrate (picromerite) was synthesized and single crystals were obtained from saturated aqueous solution by slow evaporation method at room temperature. The crystals were bright, colourless and transparent having well defined external faces. The grown crystals were characterized through Fourier Transform Infrared (FTIR) spectral studies and thermal analysis. The FTIR data were used to assign the characteristic vibrational frequencies of the various chemical bonds in the compound. The compound crystallizes in monoclinic lattice with the space group P21/c. The thermogravimetry (TG) indicates the removal of only two water molecules around 100 °C. A suitable decomposition pattern was formulated based on the percentage weight losses observed in TG of the compound. The results of differential thermal analysis (DTA) conform to the results of TGA. Differential scanning calorimetry (DSC) analysis carried out at high temperature suggests that the occurrence of two phase transitions in the crystal between 140 and 180 °C. When the crystal was cooled below the room temperature up to ,170 °C, no thermal anomaly was observed. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Growth and characterization of undoped, Sr2+ -, and Mn2+ -doped ammonium tetrachlorozincateCRYSTAL RESEARCH AND TECHNOLOGY, Issue 3 2005M. A. Gaffar Abstract Crystals of ammonium tetrachlorozincate (AZC) undoped and doped with Sr2+ or Mn2+ in different concentrations were grown by the slow evaporation method from an aqueous solution. The crystal morphology changed considerably by doping. The dopant concentration in the crystals was measured by the atomic absorption technique. Slight changes in the unit cell parameters of AZC after doping with Sr2+ - or Mn2+ have been detected. Optical absorption measurements indicated strong influence of Sr2+ and Mn2+ doping. The optical energy gap at room temperature decreased continuously with increasing Sr2+ and Mn2+ concentration but with two different rates. The dc conductivity was also measured as a function of temperature for the undoped and two samples doped with 0.144 Sr2+ and 0.191 Mn2+ and the results were compared. Positions possibly occupied by Sr2+ and Mn2+ cations in AZC lattice have been identified. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Thermal properties of conduction current and carrier behavior in an organic electroluminescent deviceELECTRONICS & COMMUNICATIONS IN JAPAN, Issue 3 2009Masahiro Minagawa Abstract Organic electroluminescent device (OLED) was fabricated using a vacuum evaporation method and thermal properties were investigated. The OLED has an indium tin oxide (ITO)/N,N,-diphenyl- N,N,-bis(3-methylphenyl)-1,1,-biphenyl-4,4,-diamine (TPD)/tris(8-hydroxyquinoline) aluminum (Alq)/lithium fluoride (LiF)/aluminum (Al) structure. An electron-dominant device of Al/Alq/LiF/Al structure, or a hole-dominant device of ITO/TPD/Al structure was also fabricated in order to study the carrier behavior in the OLEDs. The current density versus voltage (J,V) properties with various thickness of organic layers were investigated in both electron- and hole-dominant devices, and the thermal dependence of J,V properties was observed in the devices. At room temperature, conductions in a wide current region were considered to be due to space-charge-limited current for all of the devices. Especially for the Al/Alq/LiF/Al device and the OLED, relationships were observed across a wide current region. At low temperature, tunnel currents were estimated for the ITO/TPD/Al device. For the Al/Alq/LiF/Al device and the OLED, relationships were observed across a wide current region at low temperature. © 2009 Wiley Periodicals, Inc. Electron Comm Jpn, 92(3): 24,31, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/ecj.10048 [source] Tris(8-hydroxyquinoline-5-sulfonate)aluminum Intercalated Mg,Al Layered Double Hydroxide with Blue Luminescence by Hydrothermal SynthesisADVANCED FUNCTIONAL MATERIALS, Issue 17 2010Shuangde Li Abstract Blue luminescent hybrid materials (DDS,AQS(x%)/LDH) are successfully prepared by co-intercalating tris(8-hydroxyquinoline-5-sulfonate)aluminum anions (AQS3,) and dodecyl sulfonate (DDS,) with different molar ratios into Mg,Al layered double hydroxides (LDHs) by the hydrothermal and solution co-precipitation methods. A film of the material on a quartz substrate is obtained by the solvent evaporation method. The results show the blue luminescence is remarkably different from the pristine Na3AQS, which has cyan luminescence (ca. 450,470 nm vs. 495 nm). Furthermore, the hydrothermal product of DDS,AQS(66.67%)/LDH exhibits optimal luminous intensity and a significantly enhanced fluorescence lifetime. Nuclear magnetic resonance and Fourier-transform infrared spectroscopy indicate that the cyan,blue luminescence transition is due to the isomerization of meridianal to facial AQS via ligand flip caused by a host,guest electrostatic interaction, in combination with the dispersion and pre-intercalation effect of DDS. The hydrothermal conditions can promote a more ordered alignment of the intercalated fac -AQS compared with alignment in the solution state, and the rigid LDHs environment can confine the internal mobility of AQS to keep the facial configuration stable. This stability allows a facile preparation of large amounts of blue luminous powder/film, which is a new type of inorganic,organic hybrid photofunctional material. [source] ZnS Branched Architectures as Optoelectronic Devices and Field EmittersADVANCED MATERIALS, Issue 21 2010Zhi-Gang Chen A unique ZnS branched architecture was fabricated by a facile thermal evaporation method. Stable UV emission at 327,nm and superior field emission with a low turn-on field, a high field-enhancement factor, a large current density, and small fluctuation were observed. [source] Microencapsulation of rosmarinic acid using polycaprolactone and various surfactantsINTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Issue 3 2010H.-J. Kim Synopsis Rosmarinic acid (RA) has a number of interesting biological activities, e.g. anti-viral, anti-bacterial, anti-inflammatory and antioxidant. The antioxidant activity of RA is stronger than that of vitamin E. Despite its strong antioxidant activity, it was limited to use in cosmetics because of the low water solubility, discolouration and chemical instability. The purpose of this study was to prepare RA-loaded polycaprolactone (PCL) microspheres using emulsion solvent evaporation method and characterize them with different surfactants used in the formation process. Finally, long-term stability of RA was evaluated in the cosmetic formulation. As a result, PCL microspheres were found to be spherical in shape, with zwitterionic surfactant-PCL particles being the smallest size distribution and highest entrapment efficiency of RA. Emulsions containing RA-loaded PCL microspheres showed a better long-term stability of the RA compared with those containing only RA. These results suggest that RA may be stably and efficiently encapsulated into polycaprolactone microspheres. Résumé Micro encapsulation d'acide rosmarinique utilisant la polycaprolactone et divers surfactants L'acide rosmarinique a un certain nombre d'activités biologiques intéressantes, par exemple antivirales, antibactériennes, anti-inflammatoires et antioxydantes. L'activité antioxydante de l'acide rosmarinique est plus puissante que celle de la vitamine E. Malgré sa forte activité antioxydante, son usage en cosmétique est limité en raison de sa faible solubilité dans l'eau, sa décoloration et son instabilité chimique. Le but de cette étude était de préparer des microsphères de PCL chargées d'acide rosmarinique par la méthode d'émulsification par d'évaporation de solvant et de les caractériser selon les différents surfactants utilisés dans le processus de fabrication. Enfin, la stabilitéà long terme de l'acide rosmarinique a étéévaluée dans la formulation cosmétique. Les microsphères PCL ont été trouvé de forme sphérique, avec les surfactants zwitterioniques, les particules PCL offrent une distribution de petites tailles et une efficacité de piégeage en acide rosmarinique la plus élevée. Les émulsions contenant des microsphères PCL chargées d'acide rosmarinique ont montréà long terme une meilleure stabilité en acide rosmarinique que celles contenant l'acide seul. Ces résultats suggèrent que l'acide rosmarinique peut être encapsulé de façon efficace et stable dans des microsphères de polycaprolactone. [source] Oxidized multiwalled carbon nanotubes as effective reinforcement and thermal stability agents of poly(lactic acid) ligamentsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010K. Chrissafis Abstract In this study, nanocomposites of poly(lactic acid) (PLA) containing 0.5, 1, and 2.5 wt % oxidized multiwalled carbon nanotubes (MWCNT,COOHs) were prepared by the solved evaporation method. From transmission electron microscopy and scanning electron microscopy micrographs, we observed that the MWCNT,COOHs were well dispersed in the PLA matrix and, additionally, there was increased adhesion between PLA and the nanotubes. As a result, all of the studied nanocomposites exhibited higher mechanical properties than neat PLA; this indicated that the MWCNT,COOHs acted as efficient reinforcing agents, whereas in the nonoxidized multiwalled carbon nanotubes, the mechanical properties were reduced. Nanotubes can act as nucleating agents and, thereby, affect the thermal properties of PLA and, especially, the crystallization rate, which is faster than that of neat PLA. From the thermogravimetric data, we observed that the PLA/MWCNT,COOH nanocomposites presented relatively better thermostability than PLA; this was also verified from the calculation of activation energy. On the contrary, the addition of MWCNT,COOH had a negative effect on the enzymatic hydrolysis rate of PLA. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Feasibility study of aerosolized prostaglandin E1 microspheres as a noninvasive therapy for pulmonary arterial hypertensionJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 4 2010Vivek Gupta Abstract This study was designed to test the feasibility of polymeric microspheres as an inhalable carrier for prostaglandin E1 (PGE1) for treatment of pulmonary arterial hypertension. Poly(lactic- co -glycolic acid) (PLGA) microspheres were prepared by a double emulsion,solvent evaporation method. Six different microspheric formulations were prepared using two different blends of PLGA (50:50 and 85:15) and varying concentrations of polyvinyl alcohol (PVA) in the external aqueous phase (EAP). The particles were characterized for morphology, size, aerodynamic diameter, entrapment efficiency, release patterns, and metabolic stability. Pulmonary absorption was studied in a rat model, and safety of the formulations was evaluated by measuring cytotoxicity in Calu-3 cells and assessing injury markers in bronchoalveolar lavage (BAL) fluid. Both actual particle size and aerodynamic diameter of the formulations decreased with increasing PVA concentration. The mass median aerodynamic diameter of the particles was within the respirable range. Entrapment efficiency increased with increasing PVA concentration; PLGA 85:15 showed better entrapment due to hydrophobic interactions with the drug. Compared to intravenously administered PGE1, microspheres prepared with PLGA 85:15 produced a 160-fold increase in the half-life of PGE1 following pulmonary administration. Although plain PGE1 showed rapid degradation in rat lung homogenate, PGE1 entrapped in the particles remained intact for about 8,h. Optimized formulations were demonstrated to be safe, based on analysis of cytotoxicity and lung-injury markers in BAL fluid. Overall, the data suggest that microspheric PGE1 formulations have the potential to be used as a noninvasive and controlled-release alternative to the current medications used for treatment of pulmonary arterial hypertension that are administered by continuous infusion or require multiple inhalations. © 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99: 1774,1789, 2010 [source] Preparation, physiochemical characterization, and oral immunogenicity of A,(1,12), A,(29,40), and A,(1,42) loaded PLG microparticles formulationsJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 6 2009R. Rajkannan Abstract Alzheimer's disease (AD) is caused by the deposition of ,-amyloid (A,) protein in brain. The current AD immunotherapy aims to prevent A, plaque deposition and enhance its degradation in the brain. In this work, the peptides B-cell epitope A,(1,12), T-cell epitope A,(29,40) and full-length A,(1,42) were loaded separately to the poly (D,L -lactide co-glycolide) (PLG) microparticles by using W/O/W double emulsion solvent evaporation method with entrapment efficacy of 70.46%, 60.93%, and 65.98%, respectively. The prepared A, PLG microparticles were smooth, spherical, individual, and nonporous in nature with diameters ranging from 2 to 12 µm. The cumulative in vitro release profiles of A,(1,12), A,(29,40), and A,(1,42) from PLG microparticles sustained for long periods and progressively reached to 73.89%, 69.29%, and 70.08% by week 15. In vitro degradation studies showed that the PLG microparticles maintained the surface integrity up to week 8 and eroded completely by week 16. Oral immunization of A, peptides loaded microparticles in mice elicited stronger immune response by inducing anti-A, antibodies for prolonged time (24 weeks). The physicochemical characterization and immunogenic potency of A, peptides incorporated PLG microparticles suggest that the microparticles formulation of A, can be a potential oral AD vaccine. © 2008 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 98:2027,2039, 2009 [source] Lung-specific delivery of paclitaxel by chitosan-modified PLGA nanoparticles via transient formation of microaggregatesJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 3 2009Rui Yang Abstract Chitosan-modified paclitaxel-loaded poly lactic- co -glycolic acid (PLGA) nanoparticles with a mean diameter of 200,300 nm in distilled water were prepared by a solvent evaporation method. The mean diameter increased dramatically in contact with the mouse (CDF1) plasma, as a function of chitosan concentration in the modification solution (e.g., 2670.5 nm for 0.7% chitosan-modified nanoparticles, NP3), but reverted to almost its original size (i.e., 350.7 nm for NP3) following 5 min of gentle agitation. The zeta potential of PLGA nanoparticles was changed to positive by the chitosan modification. The in vitro uptake into, and cytotoxicity of the nanoparticles against, a lung cancer cell line (A549) were significantly increased by the modification. Most importantly, a lung-specific increase in the distribution index of paclitaxel (i.e., AUClung/AUCplasma) was observed for chitosan-modified nanoparticles (e.g., 99.9 for NP3 vs. 5.4 for TaxolÔ) when nanoparticles were administered to lung-metastasized mice via the tail vein at a paclitaxel dose of 10 mg/kg. Transient formation of aggregates in the blood stream followed by enhanced trapping in the lung capillaries, and electrical interaction-mediated enhanced uptake across the endothelial cells of the lung tumor capillary appear to be responsible for the lung-tumor-specific distribution of the chitosan modified nanoparticles. © 2008 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 98:970,984, 2009 [source] Elastic liposomes mediated transdermal delivery of an anti-hypertensive agent: Propranolol hydrochlorideJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 1 2007Dinesh Mishra Abstract One major problem encountered in transdermal drug delivery is the low permeability of drugs through the skin barrier. In the present investigation ultradeformable lipid vesicles, that is, elastic liposomes were prepared incorporating propranolol hydrochloride for enhanced transdermal delivery. Elastic liposomes bearing propranolol hydrochloride were prepared by conventional rotary evaporation method and characterized for various parameters including vesicles shape and surface morphology, size and size distribution, entrapment efficiency, elasticity, turbidity, and in vitro drug release. In vitro flux, enhancement ratio (ER), and release pattern of propranolol hydrochloride were calculated for transdermal delivery. In vivo study conducted on male albino rats (Sprague Dawley) was also taken as a measure of performance of elastic liposomal, liposomal, and plain drug solution. The better permeation through the skin was confirmed by confocal laser scanning microscopy (CLSM). Results indicate that the elastic liposomal formulation for transdermal delivery of propranolol hydrochloride provides better transdermal flux, higher entrapment efficiency, ability as a self-penetration enhancer and effectiveness for transdermal delivery as compared to liposomes. © 2006 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 96:145,155, 2007 [source] Methotrexate loaded poly(l -lactic acid) microspheres for intra-articular delivery of methotrexate to the jointJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 4 2004Linda S. Liang Abstract A controlled release delivery system that localizes methotrexate (MTX) in the synovial joint is needed to treat inflammation in rheumatoid arthritis (RA). The purpose of this work was to develop and characterize MTX loaded poly(l -lactic acid) (PLLA) microspheres and evaluate in vivo tolerability and MTX plasma concentrations following intra-articular injection into healthy rabbits. MTX loaded PLLA (2 kg/mole) microspheres were prepared using the solvent evaporation method and characterized in terms of size, molecular weight, thermal properties, and release rates into phosphate buffered saline (PBS) (pH 7.4) at 37°C. Biocompatibility was evaluated by observing the swelling of the joints of the rabbits and histological analysis following the injection of the microspheres. MTX concentrations in the plasma and urine samples of rabbits were evaluated by high-performance liquid chromatography (HPLC). MTX loaded microspheres showed a rapid burst phase followed by a slow release phase. MTX loaded and control microspheres were biocompatible and plasma concentrations of MTX were tenfold higher in rabbits injected intra-articularly with free MTX than MTX microspheres. MTX microspheres may retain the drug in the joint by reducing clearance from the joint into the blood. © 2004 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 93: 943,956, 2004 [source] Improvement of dissolution and oral absorption of ER-34122, a poorly water-soluble dual 5-lipoxygenase/cyclooxygenase inhibitor with anti-inflammatory activity by preparing solid dispersionJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 1 2002Ikuo Kushida Abstract Several formulation approaches were attempted to improve the dissolution and the oral absorption of ER-34122, which is a novel dual 5-lipoxygenase/cyclooxygenase inhibitor with potent anti-inflammatory activity. The solid dispersion of ER-34122 with hydroxypropylmethylcellulose (TC-5RW), which is an inert solid carrier, resulted in a significant improvement in the dissolution rate of ER-34122. The solid dispersion was prepared by a solvent evaporation method using ethanol and water. The solid-state characteristics of the solid dispersion, the corresponding physical mixture, and ER-34122 alone were investigated by X-ray powder diffraction, Fourier transform infrared spectroscopy (FTIR), and an automated controlled-atmosphere microbalance. The X-ray powder diffraction patterns suggest that the solid dispersion exists in a totally amorphous state and the others exist in a crystalline state. The FTIR spectra results suggest that ER-34122 can interact with TC-5RW through intermolecular hydrogen bonding in the solid dispersion. This interaction may cause a stabilization of ER-34122 in the higher-energy, faster-dissolving amorphous state. The dissolution rate of ER-34122 from the solid dispersion was significantly greater than that from the physical mixture or the pure drug. Furthermore, when orally administrated to beagle dogs, ER-34122 showed about a 100-fold increase in both maximum concentration (Cmax) and area under the curve of concentration versus time (AUC) compared with the pure drug. Consequently, it was determined that the solid dispersion technique with TC-5RW provides a promising way to increase the dissolution rate and the oral absorption of poorly water-soluble drugs such as ER-34122. © 2002 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 91:258,266, 2002 [source] Preparation and characterization of quercetin-loaded polymethyl methacrylate microcapsules using a polyol-in-oil-in-polyol emulsion solvent evaporation methodJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 12 2007Dong-Hwan Lee Flavonoids and related compounds exhibit a wide range of useful pharmacological properties but present challenges related to their stability and solubility in commonly available solvents. In this study, polymethyl methacrylate (PMMA) microcapsules were prepared using a novel polyol-in-oil-in-polyol (P/O/P) emulsion solvent evaporation method as a means of stabilizing the flavonoids, using quercetin as a model flavonoid drug. The morphology of the microcapsules was evaluated using a scanning electron microscope, revealing a spherical shape with a smooth surface. The cross-section image of the PMMA microcapsules prepared with an amphiphilic polymer in the inner polyol phase showed that the microcapsule was filled with several submicron microspheres. The mean diameter varied from 1.03 ± 0.12 ,m to 2.39 ± 0.42 ,m, and the encapsulation efficiency ranged from 12.7% to 26.9%. When free quercetin was stored at 42°C, the residual quercetin content gradually decreased to 18% over 28 days as a result of oxidation. However, when encapsulated in PMMA microcapsules with an amphiphilic polymer in the inner polyol phase, the residual quercetin content decreased to just 82%. In-vitro release studies indicated a sustained release pattern throughout the 36-h study. The release kinetics of the microcapsules with an amphiphilic polymer followed a diffusion-controlled mechanism and the microcapsule without amphiphilic polymer followed an anomalous diffusion behaviour. This study suggests that the novel P/O/P emulsion solvent evaporation method can be applied to the encapsulation of flavonoids. [source] Nanoparticle formulation enhances the delivery and activity of a vascular endothelial growth factor antisense oligonucleotide in human retinal pigment epithelial cellsJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 9 2003Jithan V. Aukunuru ABSTRACT The objective of this study was to investigate the delivery and activity of a vascular endothelial growth factor (VEGF) antisense oligonucleotide in a human retinal pigment epithelial cell line (ARPE-19) using a biodegradable nanoparticulate delivery system. A 19-mer antisense phosphorothioate oligonucleotide (PS-ODN) complementary to bases 6,24 relative to the translational start site of the VEGF mRNA, a sense PS-ODN and a mismatch PS-ODN were examined for the inhibition of secretion and mRNA expression of VEGF using an enzyme-linked immunosorbent assay and reverse transcription,polymerase chain reaction, respectively. Nanoparticles of the antisense oligonucleotides were formulated using a poly(lactide-co-glycolide) (50:50) copolymer using a double emulsion solvent evaporation method. After preparing nanoparticles, drug loading, encapsulation efficiency and particle size were determined. The cells were exposed to either plain solution of oligonucleotide or nanoparticles of oligonucleotide from Day 3 through Day 6. Alternatively, the cells were incubated with PS-ODNs and lipofectin for 4h on Day 4. In all studies, VEGF secretion and mRNA expression were determined on Day 6. The particle size, drug loading and encapsulation efficiency were 252 nm, 5.5% and 16.5%, respectively. The antisense PS-ODN inhibited VEGF mRNA and protein secretion when delivered using nanoparticles or lipofectin but not in its free form. This was consistent with the ability of nanoparticles and lipofectin to elevate the cellular uptake of the oligonucleotide by 4-fold and 13-fold, respectively. Neither mismatch nor sense oligonucleotides inhibited VEGF secretion. In conclusion, biodegradable nanoparticles enhance cellular delivery of a VEGF antisense oligonucleotide and inhibit VEGF secretion and mRNA expression in a human retinal pigment epithelial cell line. [source] Preparation, characterization and taste-masking properties of polyvinylacetal diethylaminoacetate microspheres containing trimebutineJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 10 2002Yoshimi Hashimoto The objectives of this study were to produce acid soluble, polyvinylacetal diethylaminoacetate (AEA) microspheres containing trimebutine (as maleate), using a water-in-oil-in-water (w/o/w) emulsion solvent evaporation method, to characterize their in-vitro release properties, and to evaluate the taste-masking potential of this formulation in human volunteers. The pH of the external aqueous phase was the critical factor in achieving a high loading efficiency for trimebutine in the microencapsulation process; nearly 90% (w/w) loading efficiency was obtained at above pH 10. Trimebutine was completely released from AEA microspheres within 10 min in a dissolution test at pH 1.2, simulating conditions in the stomach, whereas at pH 6.8, the pH in the mouth, only small quantities of trimebutine were released in the initial 1,2 min. The results of a gustatory sensation test in healthy volunteers confirmed the taste-masking effects of the AEA microspheres. Finally, an attempt was made to encapsulate the salts of other basic drugs (lidocaine, imipramine, desipramine, amitriptyline, promethazine and chlorpheniramine) into AEA microspheres using the w/o/w emulsion evaporation method. The loading efficiencies were ranked in almost inverse proportion with the solubility of the drugs in the external aqueous phase. This study demonstrated the possibility of masking the taste of salts of basic drugs by microencapsulation with AEA using a w/o/w emulsion solvent evaporation method. [source] The evaporation method: Extending the measurement range of soil hydraulic properties using the air-entry pressure of the ceramic cupJOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 4 2010Uwe Schindler Abstract Knowledge of hydraulic functions is required for various hydrological and plant-physiological studies. The evaporation method is frequently used for the simultaneous determination of hydraulic functions of unsaturated soil samples, i.e., the water-retention curve and hydraulic-conductivity function. All methodic variants of the evaporation method suffer from the limitation that the hydraulic functions can only be determined to a mean tension of , 60 kPa. This is caused by the limited measurement range of the tensiometers of typically 80 kPa on the dry end. We present a new, cost- and time-saving approach which overcomes this restriction. Using the air-entry pressure of the tensiometer's porous ceramic cup as additional defined tension value allows the quantification of hydraulic functions up to close to the wilting point. The procedure is described, uncertainties are discussed, and measured as well as simulated test results are presented for soil samples of various origins, different textures (sand, loam, silt, clay, and peat) and variable dry bulk density. The experimental setup followed the system HYPROP which is a commercial device with vertically aligned tensiometers that is optimized to perform evaporation measurements. During the experiment leaked water from the tensiometer interior wets the surrounding soil of the tensiometer cup and can lead to a tension retardation as shown by simulation results. This effect is negligible when the tensiometers are embedded vertically. For coarsely textured soils and horizontal tensiometer alignment, however, the retardation must be considered for data evaluation. [source] Biodegradable Polymeric Microcarriers with Controllable Porous Structure for Tissue EngineeringMACROMOLECULAR BIOSCIENCE, Issue 12 2009Xudong Shi Abstract Porous microspheres fabricated by biodegradable polymers show great potential as microcarriers for cell cultivation in tissue engineering. Herein biodegradable poly(DL -lactide) (PLA) was used to fabricate porous microspheres through a modified double emulsion solvent evaporation method. The influence of fabrication parameters, such as the stirring speed of the primary and secondary emulsion, the polymer concentration of the oil phase, and solvent type, as well as the post-hydrolysis treatment of the porous structure of the PLA microspheres are discussed. Good attachment and an active spread of MG-63 cells on the microspheres is observed, which indicates that the PLA microspheres with controllable porous structure are of great potential as cell delivery carriers for tissue engineering. [source] Interface properties and junction behavior of Pd contact on ZnO thin film grown by vacuum deposition techniquePHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 2 2010Ghusoon M. Ali Abstract In this paper we explain the results of our experimental investigation on interface properties and junction behavior of Pd contact on ZnO thin film based Schottky diode. We used a conventional vacuum evaporation deposition unit for sequential deposition of ZnO film and metallic layer. For the first time a high quality Pd/ZnO Schottky diode is fabricated successfully in our laboratory by vacuum evaporation method. The I-V and C-V characteristics of the devices were studied by using microprobe arrangement. The parameter such as ideality factor, leakage current, resistance-area-product, carrier concentration and barrier height were extracted from the measured data. The surface morphological and the structural properties of thin film were studied by atomic force microscope. The optical band gap of thin film was determined using UV-visible spectrophotometer. The device fabricated by a simple technique exhibited excellent stability for use as an electronic or optoelectronic component. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Thin film electroluminescent cells on the basis of Ce-doped CaGa2S4 and SrGa2S4 prepared by flash evaporation methodPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 8 2006E. Gambarov Abstract Ce-doped CaGa2S4 and SrGa2S4 thin film electroluminescent (TFEL) devices were prepared for the first time on the basis of films deposited by flash evaporation method. Significant crystallization, stoichiometry improvement of the films and increase of photoluminescence intensity were found after annealing in H2S and O2 gas stream. EL spectra of the cells exhibited the characteristic double-band emission similar to that seen for Ce3+ activated CaGa2S4 and SrGa2S4 films under photon excitation. Applied voltage and frequency dependences of the electroluminescence were studied. Low voltage operation as low as 20 V was observed for these cells. Luminance of about 4 cd/m2 at 100 V operating voltage with 2.5 kHz frequency was achieved for the TFEL cell with films annealed in O2 gas stream. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] The analysis on the origin of high resistivity in Cl-doped polycrystalline CdZnTe thick filmsPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 4 2004K. H. Kim Abstract Polycrystalline CdZnTe thick films were grown by thermal evaporation method using CdZnTe and CdZnTe:Cl source. Non-doped CdZnTe thick films have Te-rich stoichiometry having resistivity 3.3 × 109 ,cm. The Cl-doped CdZnTe thick films have 1.2 × 1010 ,cm in resistivity. To evaluate the role of Cl in the increasement of the resistivity, the density of localized states were calculated from the analysis of transient TOF (time of flight)current. From the comparison of Cl-doped CZT thick films with non-doped and O2 annealed CdZnTe thick films, we have found that Cl doping is related to the formation of states at EV + 0.75 eV region and oxygen reduces grain boundary related defects through formation TeO2 or CdTeO3. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Temperature dependence of electrical resistivity in carbon nanofiber/unsaturated polyester nanocompositesPOLYMER ENGINEERING & SCIENCE, Issue 7 2008Toshiaki Natsuki This article described the temperature dependence of electrical resistivity for carbon nanofiber (CNF)/unsaturated polyester resin (UPR) nanocomposites prepared by a solvent evaporation method. It was found that the CNF/UPR nanocomposites had quite low electrical percolation threshold due to CNFs having a large aspect ratio and being well dispersed into the UPR matrix. A sharp decrease in the electrical resistivity was observed at about 1 wt% CNF content. The influence of CNF content on the electrical resistivity was investigated as a function of temperature in detail. The nanocomposites showed a positive temperature coefficient effect for the resistivity, and had a strong temperature dependence near the percolation threshold. When the number of thermal cycles was increased, the electrical resistivity decreased and had a weak temperature dependence, especially in the case of melting temperature. Moreover, the size influences of CNFs on the electrical properties of nanocomposites were analyzed and discussed. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] CdTe solar cell in a novel configurationPROGRESS IN PHOTOVOLTAICS: RESEARCH & APPLICATIONS, Issue 1 2004A. N. Tiwari Abstract Polycrystalline thin-film CdTe/CdS solar cells have been developed in a configuration in which a transparent conducting layer of indium tin oxide (ITO) has been used for the first time as a back electrical contact on p-CdTe. Solar cells of 7·9% efficiency were developed on SnOx:F-coated glass substrates with a low-temperature (<450°C) high-vacuum evaporation method. After the CdCl2 annealing treatment of the CdTe/CdS stack, a bromine methanol solution was used for etching the CdTe surface prior to the ITO deposition. The unique features of this solar cell with both front and back contacts being transparent and conducting are that the cell can be illuminated from either or both sides simultaneously like a ,bi-facial' cell, and it can be used in tandem solar cells. The solar cells with transparent conducting oxide back contact show long-term stable performance under accelerated test conditions. Copyright © 2004 John Wiley & Sons, Ltd. [source] | |||||||||||||||||||||||||