Application of automated blind for daylighting in tropical region

This paper reports an experimental and simulation study on application of automated Venetian blind for daylighting in tropical climate. A horizontal blind system operating automatically under programmed control was constructed and integrated onto the glazed windows to form a window system with an automated blind in a room of a laboratory building. A dimming controller was also integrated to the lighting system of the room. Different operation schemes of the window system were devised and tested in the attempt to maximize energy savings while maintaining the quality of the visual environment in the room. Intensive measurement of illuminance of the interior space was undertaken during the experiments. A methodology for calculation of interior daylight illuminance and associated glare corresponding to the configurations of the experiments was adopted. The method was coded into a computer program. Results of calculation from the program agree well with those from experiments for all the schemes of operation conducted. The program was used to simulate the situation when each scheme of operation was implemented for a whole year. It was found that such window system with automated blind enabled energy savings of 80%, but a more sophisticated scheme also helped maintain the interior visual quality at high level.     

Bioconversion of hydrocortisone to prednisolone by immobilized bacterial cells in a two-liquid-phase system

Bioconversion of hydrocortisone to prednisolone by free, immobilized and reused immobilized cells of three bacterial strains (Bacillus sphaericus ATCC 13805, Bacillus sphaericus SRP III and Arthrobacter simplex 6946) in an aqueous and a two-liquid-phase system using different organic solvents was investigated. The experiments were carried out in a 125 cm³ shake flask at 27±2°C, 220 rpm for 96 h. The contents of prednisolone and hydrocortisone in samples taken at 0, 3, 6, 24, 48, 72, 96 and 144 h were determined by HPLC analysis. The immobilized bacterial cells showed higher prednisolone yield than the free form in an aqueous system. In the two-phase systems, the butyl acetate to aqueous media ratio of 1: 30 for all three bacterial strains in immobilized forms gave the highest prednisolone yields, at an incubation time of 144 h, of 87·6, 70·6 and 88·3% respectively. For an n-decane to aqueous ratio of 1: 6, moderate prednisolone yields of 81·8, 47·9 and 71·4% were obtained with shorter incubation times of 72, 96 and 6 h respectively. For cyclohexane and other alcohols, the organisms produced low yields of prednisolone (0–30%). Single reuse of all three immobilized bacterial cells gave a 3–20% lower yield of prednisolone than the non-reused cells. The increase in hydrocortisone concentration decreased the prednisolone production whereas increasing the n-decane to aqueous ratio from 1: 6 to 1: 3 caused no significant change in the productivity. © 1998 Society of Chemical Industry     

Elastic properties investigation of gamma-radiated barium lead borosilicate glass using ultrasonic technique

The ultrasonic velocities were measured in barium lead borosilicate glass samples of different compositions before and after irradiation with γ-rays. Measurements were carried out at room temperature and 4 MHz frequency using ultrasonic technique. The ultrasonic velocities data of glass samples have been used to find the elastic modulus and micro-hardness. Densities of glass samples were measured by Archimedes’s principle using n-hexane as immersion liquid. It was found that ultrasonic velocity, elastic modulus and micro-hardness increase with increasing barium oxide content and increasing γ-radiation dose.     

Bioequivalence Evaluation of Two Formulations of Doxazosin Tablet in Healthy Thai Male Volunteers

ABSTRACT

The bioequivalence of two doxazosin 2 mg tablets was determined in 24 healthy Thai male volunteers after one single dose in a randomized cross-over study with a one week washout period. The study was conducted at Faculty of Pharmaceutical Sciences and Health Sciences Research Institute, Naresuan University, Phitsanulok, Thailand. Reference (Cardura®, Heinrich Mack Nachf. GmbH & Co. GK, Illertissen, Germany) and test (Dozozin-2®, Umeda Co., Ltd., Bangkok Thailand) were administered to volunteers after overnight fasting. Blood samples were collected at specified time intervals and plasma was separated. The validated HPLC method with fluorescence detection was used for quantification of doxazosin in plasma samples. The pharmacokinetic parameters, T_max, C_max, AUC_t, AUC_∞, T_1/2, λ_z, Cl and V_d, were determined from plasma concentration time profile of both formulations by using non-compartment analysis. The calculated pharmacokinetic parameters were compared statistically to evaluate bioequivalence between the two brands. The analysis of variance (ANOVA) using log-transformed C_max, AUC_t, and AUC_∞ did not show any significant difference between two formulations. The point estimates and 90% confidence intervals for C_max, AUC_t and AUC_∞ were within the acceptance range (0.80–1.25), satisfying the bioequivalence criteria of the Thailand Food and Drug Administration Guidelines. These results indicate that Dozozin-2® is bioequivalent to Cardura® and, thus, may be prescribed interchangeably.     

Bioequivalence evaluation of two formulations of doxazosin tablet in healthy thai male volunteers

The bioequivalence of two doxazosin 2 mg tablets was determined in 24 healthy Thai male volunteers after one single dose in a randomized cross-over study with a one week washout period. The study was conducted at Faculty of Pharmaceutical Sciences and Health Sciences Research Institute, Naresuan University, Phitsanulok, Thailand. Reference (Cardura®, Heinrich Mack Nachf. GmbH & Co. GK, Illertissen, Germany) and test (Dozozin-2®, Umeda Co., Ltd., Bangkok Thailand) were administered to volunteers after overnight fasting. Blood samples were collected at specified time intervals and plasma was separated. The validated HPLC method with fluorescence detection was used for quantification of doxazosin in plasma samples. The pharmacokinetic parameters, T_max, C_max, AUC_t, AUC_∞, T_1/2, λ_z, Cl and V_d, were determined from plasma concentration time profile of both formulations by using non-compartment analysis. The calculated pharmacokinetic parameters were compared statistically to evaluate bioequivalence between the two brands. The analysis of variance (ANOVA) using log-transformed C_max, AUC_t, and AUC_∞ did not show any significant difference between two formulations. The point estimates and 90% confidence intervals for C_max, AUC_t and AUC_∞ were within the acceptance range (0.80-1.25), satisfying the bioequivalence criteria of the Thailand Food and Drug Administration Guidelines. These results indicate that Dozozin-2® is bioequivalent to Cardura® and, thus, may be prescribed interchangeably.     

Effects of Coir Fiber and Maleic Anhydride Modification on the Properties of Thermoplastic Starch/PLA Composite Laminates

Coir fiber reinforced composite laminates made of poly(lactic acid) (PLA) with a thermoplastic starch (TPS) were fabricated. Modified thermoplastic starch (MTPS) was prepared by reactive blending of TPS with maleic anhydride (MA). The effect of coir fibers was of our main interest. The tensile properties, water absorption, and morphological properties of the fabricated composite laminates were investigated. The composite laminates between PLA and starch TPS were prepared using coir fiber as reinforcing core, and the physical, mechanical, and morphological properties were studied. The results suggested that the optimum fiber contents for maximum tensile strength for TPS/PLA and MTPS/PLA composites were 20 and 30 wt%, respectively. Using MA for chemical modification of TPS for PLA composites could reduce the PLA content of about 10 wt%, and improve the tensile about 20%. The volume swelling for the MTPS/PLA composites was much lower than that for the TPS/PLA composites, and the swelling reduced with increasing coir fiber content. Based on compressive strength, the pallets produced using MTPS/PLA composites showed a high potential to replace the commercial urea-formaldehyde/PLA composites. It clearly appeared that MA modification to TPS not only improve the mechanical properties of fiber reinforced PLA composites, but also made the PLA composites bio-degrade more quickly.     

Comparative study on the bioequivalence of two formulations of pioglitazone tablet in healthy Thai male volunteers

The bioequivalence study of two 30 mg pioglitazone formulations was determined in healthy Thai male volunteers after a single dose administration in a randomized cross-over study with a 1-week washout period. Due to the high variability of the rate and extent of absorption of pioglitazone, an add-on subject study was required to assess bioequivalence. Reference product (Actos®, Takeda Chemical Industries, Ltd., Osaka, Japan) and test product (Glubosil®, Silom Medical Co. Ltd., Bangkok, Thailand) were given to 35 volunteers after overnight fasting. Blood samples were collected at specified time intervals. Plasma was analyzed for pioglitazone concentration using a validated HPLC method. Pharmacokinetic parameters were compared between test and reference products from plasma concentration-time profile by using non-compartment analysis. The statistical comparison of C_max and AUC_0-t, AUC_t-∞ clearly indicated that no significant difference in two products of pioglitazone tablets in add-on subject study. The 90% confidence intervals for the mean ratio (test/reference) of C_max and AUC_0-t, AUC_t-∞ were within the Thailand Food and Drug Administration acceptance range. Based on the pharmacokinetic and statistical results of this study, we can conclude that Glubosil® is bioequivalent to Actos®, and that two products can be considered interchangeable in medical practice.     

Improvement of the mechanical and thermal properties of silica‐filled polychloroprene vulcanizates prepared from latex system

In this work, well‐dispersed silica suspension having excellent storage stability was prepared by using an ultrasonic probe. The obtained silica suspension and curatives were added into the polychloroprene (CR) latex for preparing silica‐filled CR latex compounds having various silica loadings. Then, the silica‐filled CR vulcanizates were prepared via a dipping process. The thermal and mechanical properties of the dipped CR vulcanizates containing silica dispersed by using an ultrasonic probe were compared with those of the dipped CR vulcanizates containing silica dispersed by using a mechanical stirrer. By using thermogravimetric analysis, it could be seen that thermal resistance of the dipped CR films having silica prepared by ultrasonic probe is greater than that prepared by using the mechanical stirrer. This result corresponds well with their tensile strength after aging in the hot‐air oven. In addition, modulus, tensile strength, and tear strength of the vulcanizates prepared from CR latex compounds containing silica prepared by using the ultrasonic probe are obviously greater than those prepared by using the mechanical stirrer, especially at high silica loading. This is because the silica prepared using the ultrasonic probe is uniformly distributed and dispersed throughout the CR matrix, as can be observed in the scanning electron microscope micrographs. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Comparative Study on the Bioequivalence of Two Formulations of Pioglitazone Tablet in Healthy Thai Male Volunteers

The bioequivalence study of two 30 mg pioglitazone formulations was determined in healthy Thai male volunteers after a single dose administration in a randomized cross-over study with a 1-week washout period. Due to the high variability of the rate and extent of absorption of pioglitazone, an add-on subject study was required to assess bioequivalence. Reference product (Actos®, Takeda Chemical Industries, Ltd., Osaka, Japan) and test product (Glubosil®, Silom Medical Co. Ltd., Bangkok, Thailand) were given to 35 volunteers after overnight fasting. Blood samples were collected at specified time intervals. Plasma was analyzed for pioglitazone concentration using a validated HPLC method. Pharmacokinetic parameters were compared between test and reference products from plasma concentration-time profile by using non-compartment analysis. The statistical comparison of C_max and AUC_0?t, AUC_t?∞ clearly indicated that no significant difference in two products of pioglitazone tablets in add-on subject study. The 90% confidence intervals for the mean ratio (test/reference) of C_max and AUC_0?t, AUC_t?∞ were within the Thailand Food and Drug Administration acceptance range. Based on the pharmacokinetic and statistical results of this study, we can conclude that Glubosil® is bioequivalent to Actos®, and that two products can be considered interchangeable in medical practice.     

Meta-analyses involving cluster randomization trials: a review of published literature in health care

Throughout the 1980s and 1990s cluster randomization trials have been increasingly used to evaluate effectiveness of health care intervention. Such trials have raised several methodologic challenges in analysis. Meta-analyses involving cluster randomization trials are becoming common in the area of health care intervention. However, as yet there has been no empirical evidence of current practice in the meta-analyses. Thus a review was performed to identify and examine synthesis approaches of meta-analyses involving cluster randomization trials in the published literature. Electronic databases were searched for meta-analyses involving cluster randomization trials from the earliest date available to 2000. Once a meta-analysis was identified, papers on the relevant cluster randomization trials included were also requested. Each of the original papers of cluster randomization trials included was examined for its randomized design and unit, and adjustment for clustering effect in analysis. Each of the selected meta-analyses was then evaluated as to its synthesis concerning clustering effect. In total, 25 eligible meta-analyses were reviewed. Of these, 15 meta-analyses reported simple conventional methods of the fixed-effect model as method of analysis, while six did not incorporate the cluster randomization trial results in the synthesis methods but described the trial results individually. Three meta-analyses attempted to account for the clustering effect in the synthesis methods but approaches were in arbitrary. Fifteen meta-analyses included more than one cluster randomization trial, each of which included cluster randomization trials with a mixture of randomized designs and units, and units of analysis. These mixture situations might increase heterogeneity, but have not been considered in any meta-analysis. Some methods dealing with a binary outcome for some specific situations have been discussed. In conclusion, some difficulties in the quantitative synthesis procedures were found in the meta-analyses involving cluster randomization trials. Recommendations in the applications of approaches to some specific situations in a binary outcome variable have also been provided. There are still, however, several methodologic issues of the meta-analyses involving cluster randomization trials that need to be investigated further.