Study on phosphate and sulphide capacities of CaO-CaCl2 slags

Experiments were carried out at 1175–1350°C to study the phosphate capacity of CaO-CaCl₂ slags and the sulphide capacity was calculated according to the correlation between the two capacities. At 1200°C the logarithm of the phosphate capacity increased from 24.5 to 26.5 with increasing CaO mole fraction from 0 to 0.22 in the slags and it decreased with increasing temperature. Sulphide capacity increased both with increasing CaO mole fraction and temperature. A good linear correlation was found between slag carbonate capacity and phosphate capacity as well as sulphide capacity. Optical basicity was used to evaluate the property of the CaO-CaCl₂ slag in the present study. The value of optical basicity of CaCl₂ is established as 0.63. The correlations of optical basicity with above mentioned three capacities were found to be linear.     

One world, one hope: the cost of providing antiretroviral therapy to all nations

OBJECTIVE: To estimate the potential direct cost of making triple combination antiretroviral therapy widely available to HIV-positive adults and children living in countries throughout the world. METHODS: For each country, antiretroviral costs were obtained by multiplying the annual cost of triple antiretroviral therapy by the estimated number of HIV-positive persons accessing therapy. Per capita antiretroviral costs were computed by dividing the antiretroviral costs by the country's total population. The potential economic burden was calculated by dividing per capita antiretroviral costs by the gross national product (GNP) per capita. All values are expressed in 1997 US dollars. RESULTS: The potential cost of making triple combination antiretroviral therapy available to HIV-positive individuals throughout the world was estimated to be over US$ 65.8 billion. By far the greatest financial burden was on sub-Saharan Africa. The highest per capita drug cost in this region would be incurred in the subregions of Southern Africa (US$ 149) followed by East Africa (US$ 116), Middle Africa (US$ 44), and West Africa (US$ 42). In the Americas, subregional data indicated the highest per capita drug cost would be in the Latin Caribbean (US$ 22), followed by the Caribbean (US$ 17), Andean Area (US$ 7), the Southern Cone (US$ 6), North America (US$ 6), and Central American Isthmus (US$ 5). In Asia and Europe the percentage of the GNP necessary to finance drug therapy was less than 1% in most countries examined. CONCLUSION: Our results demonstrate that the cost of making combination antiretroviral therapy available worldwide would be exceedingly high, especially in countries with limited financial resources.     

Moisture sorption isotherms and isosteric heat of sorption of leaves and stems of lemon balm (Melissa officinalis L.) established by dynamic vapor sorption

The equilibrium moisture contents (MC) of leaves and stems of lemon balm (Melissa officinalis L.) were determined separately at temperatures of 25, 35 and 45 °C over a stepwise increase of relative humidity (RH) ranging from 3 to 90% by an automatic, gravimetric analyzer (DVS system). Equilibrium was achieved within 6 h for most of the target values of relative humidity. The equilibrium moisture content of leaves was significantly higher than that of stems (p < 0.05). Differences in moisture sorption capacity between the leaves and stems can be attributed to chemical composition and structure of the tissues. Five three-parameter moisture sorption models (modifications of Chung–Pfost, GAB, Halsey, Henderson and Oswin) were tested for their effectiveness to fit the experimental sorption data. The modified Oswin equation was found to be the best model to describe the adsorption isotherms of both leaves and stems of lemon balm. The recommended MC values of leaves and stems for microbial safe storage at 25 °C were 0.124 and 0.113 kg water per kg dry solids, respectively. The net isosteric heat of sorption was computed from the predicted sorption data by applying the integrated form of the Clausius–Clapeyron equation.     

Antimicrobial coatings produced by “tethering” biocides to the coating matrix: A comprehensive review

Covalently attached, non-leaching biocidal-moieties are being explored as an environmentally friendly option for replacing antimicrobial coatings that release biocides. This review highlights studies on antimicrobial surface treatments and coatings in which the antimicrobial agent is covalently bound (i.e. tethered) to the surface or coating matrix. In addition, test methods for measuring antimicrobial surface activity are reviewed, and a discussion of advantages and disadvantages of the various methods is provided.     

Buckling initiation and displacement dependence in compression of vertically aligned carbon nanotube arrays

Carbon nanotube (CNT) arrays have shown the remarkable ability to react as foam-like structures and exhibit localized buckling coordinated within specific regions. Here, we report on the low-cycle compression of bulk vertically aligned CNT arrays to observe initiation and growth of the buckling as a function of compressive strain. A critical strain is found above which the buckling region length increased and below which it remained at or below the applied strain. As previously observed, the buckling region of the CNT array propagates from the surface where growth occurred, which, in the test specimen, is a free surface and later receives compressive contact by a polished silicon substrate. The results are corroborated with nanoindentation on the surfaces, which indicate a stiffening of the near surface with increasing applied strain. Observation and results of the buckling region nature are important for applications of nanotube arrays as energy absorbing cushions, tunable dampers, thermal contacts, or in sliding contact.     

Design,Synthesis, Radiosynthesis and Biological Evaluation of Fenretinide Analogues as Anticancer and Metabolic Syndrome-Preventive Agents

Fenretinide (4-HPR) is a synthetic derivative of all-trans-retinoic acid (ATRA) characterised by improved therapeutic properties and toxicological profile relative to ATRA. 4-HPR has been mostly investigated as an anti-cancer agent, but recent studies showed its promising therapeutic potential for preventing metabolic syndrome. Several biological targets are involved in 4-HPR's activity, leading to the potential use of this molecule for treating different pathologies. However, although 4-HPR displays quite well-understood multitarget promiscuity with regards to pharmacology, interpreting its precise physiological role remains challenging. In addition, despite promising results in vitro, the clinical efficacy of 4-HPR as a chemotherapeutic agent has not been satisfactory so far. Herein, we describe the preparation of a library of 4-HPR analogues, followed by the biological evaluation of their anti-cancer and anti-obesity/diabetic properties. The click-type analogue 3 b showed good capacity to reduce the amount of lipid accumulation in 3T3-L1 adipocytes during differentiation. Furthermore, it showed an IC₅₀ of 0.53±0.8 μM in cell viability tests on breast cancer cell line MCF-7, together with a good selectivity (SI=121) over noncancerous HEK293 cells. Thus, 3 b was selected as a potential PET tracer to study retinoids in vivo, and the radiosynthesis of [¹⁸F] 3b was successfully developed. Unfortunately, the stability of [¹⁸F] 3b turned out to be insufficient to pursue imaging studies.     

NMR analysis of butyl acrylate/methylmethacrylate/α‐methyl styrene terpolymers

Composition analysis for butyl acrylate (BA)/ methyl methacrylate (MMA)/α‐methyl styrene terpolymers was carried out by NMR spectroscopy methods. ¹H‐NMR was used primarily for this analysis, but because the method did not provide independent measurements for the BA and MMA fractions, the terpolymer composition analysis was open to higher than normal levels of uncertainty. Supplementary analyses were made with quantitative ¹³C‐NMR methods to confirm the results from ¹H‐NMR (quantitative ¹³C‐NMR was used to provide corroboration of selected composition analyses). To confirm spectral assignments in the ¹H‐ and ¹³C‐NMR spectra, heteronuclear multiple quantum coherence and J Modulated Spin Echo (JMOD) pulse sequences were used. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2093–2098, 2007     

DNA Comet Giemsa Staining for Conventional Bright-Field Microscopy

This study was undertaken to evaluate the compatibility of Giemsa staining protocol with the comet assay. We showed, for the first time, that DNA comets can be visualized and analyzed using Giemsa staining. We generated DNA damage dose response curves for human peripheral blood lymphocytes exposed to X-ray radiation using the comet assay with either SybrGreen I or Giemsa stain. The dose response curves were fitted by linear regressions (R² > 0.977). The SybrGreen I results showed only ~1.2-fold higher slope coefficient (method sensitivity) compared to the Giemsa results. The unexpectedly high sensitivity of Giemsa staining for the comet assay is due to the Romanowsky-Giemsa effect, the stain photo-stability and the higher resolution of bright-field imaging compared to fluorescence imaging. Our results demonstrate that Giemsa staining can effectively be used for measuring DNA damage by the comet assay. The low cost and availability of Giemsa stain makes this method affordable for any low budget research and will facilitate new applications of the comet assay in biology and medicine.     

Domain Wall Motion Across Various Grain Boundaries in Ferroelectric Thin Films

Domain wall movement at and near engineered 10°, 15°, and 24° tilt and 10° and 30° twist grain boundaries was measured by band excitation piezoresponse force microscopy for Pb(Zr,Ti)O₃ films with Zr/Ti ratio of 45/55 and 52/48. A minimum in nonlinear response was observed at the grain boundary for the highest angle twist and tilt grain boundaries, while a maximum in nonlinear response was observed at the 10° tilt grain boundaries. The observed nonlinear response was correlated with the domain configurations imaged in cross section by transmission electron microscopy.