Home About us Contact
|
Home About us Contact | ||
|
|
||
Time Method (time + method)
Selected AbstractsComparison of Proximal Isovelocity Surface Area Method and Pressure Half Time Method for Evaluation of Mitral Valve Area in Patients Undergoing Balloon Mitral ValvotomyECHOCARDIOGRAPHY, Issue 9 2005Thottuvelil Narayanan Sunil Roy M.D. Background: The pressure half time (PHT) method is unreliable for measurement of mitral valve area (MVA) immediately after valvotomy. The proximal isovelocity surface area (PISA) method has been used to derive mitral valve area in patients with mitral stenosis. The aim of our study was to compare PISA method and PHT method in patients undergoing percutaneous balloon mitral valvotomy (BMV). Methods: The PISA was recorded from the apex and MVA was calculated using continuity equation by the formula 2,r2 Vr/Vm, where 2,r2 is the hemispheric isovelocity area, Vr is the velocity at the radial distance "r" from the orifice, and Vm is the peak velocity. A plain angle correction factor (,)/180 was used to correct the inlet angle subtended by leaflet tunnel as a result of leaflet doming. Results: MVA calculated using PISA method (r = 0.5217, P < 0.0001, SE = 0.016) and PHT (r = 0.6652, P < 0.0001, SE = 0.017) correlated well with 2D method in patients with mitral stenosis before BMV. After BMV, MVA by PISA method correlated well with 2D planimetry (r = 0.5803, P < 0.0001, SE = 0.053) but PHT showed poor correlation (r = 0.1334, P = 0.199, SE = 0.036). The variability of measurement of MVA was most marked with PHT method in the post-BMV period. Conclusion: The PISA method correlates well with 2D planimetry in patients with mitral stenosis before and after BMV and is superior to the PHT method in the post-BMV period where the latter may be unreliable. [source] Development and validation of fixed-time method for the determination of isoxsuprine hydrochloride in commercial dosages formsDRUG TESTING AND ANALYSIS, Issue 9 2010Dr Nafisur Rahman Abstract The main aim of this work was to develop a kinetic spectrophotometric method for the quantitative analysis of isoxsuprine hydrochloride in commercial tablets. The method is based on the reaction of isoxsuprine hydrochloride (ISx) with hydroxylamine hydrochloride and ammonium cerium (IV) nitrate in sulphuric acid medium at room temperature which resulted in the formation of yellow-coloured product peaking at 380 nm. The reaction is followed spectrophotometrically by measuring the absorbance as a function of time. Fixed time method (,A = A4,A2, where A2 and A4 refer to absorbance measurements taken at 2 and 4 min, respectively) was adopted for constructing the calibration curve which was found to be linear over the concentration range of 30,80 µgmL,1 with molar absorptivity of 5.95 × 103 L mol,1 cm,1. The method has been applied successfully to the determination of isoxsuprine hydrochloride in tablets. Statistical comparison (point and interval hypothesis tests) of the results showed that there is no significant difference between the proposed method and reference method. Copyright © 2010 John Wiley & Sons, Ltd. [source] Occurrence, prediction and hydrological effects of water repellency amongst major soil and land-use types in a humid temperate climateEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 5 2006S. H. Doerr Summary Knowledge of soil water repellency distribution, of factors affecting its occurrence and of its hydrological effects stems primarily from regions with a distinct dry season, whereas comparatively little is known about its occurrence in humid temperate regions such as typified by the UK. To address this research gap, we have examined: (i) water repellency persistence (determined by the water drop penetration time method, WDPT) and degree (determined by the critical surface tension method, CST) for soil samples (0,5, 10,15 and 20,25 cm depth) taken from 41 common soil and land-use types in the humid temperate climate of the UK; (ii) the supposed relationship of soil moisture, textural composition and organic matter content with sample repellency; and (iii) the bulk wetting behaviour of undisturbed surface core samples (0,5 cm depth) over a period of up to 1 week. Repellency was found in surface samples of all major soil textural types amongst most permanently vegetated sites, whereas tilled sites were virtually unaffected. Repellency levels reached those of the most severely affected areas elsewhere in the world, decreased in persistence and degree with depth and showed no consistent relationship with soil textural characteristics, organic matter or soil moisture contents, except that above a water content of c. 28% by volume, repellency was absent. Wetting rate assessments of 100 cm3 intact soil cores using continuous water contact (,20 mm pressure head) over a period of up to 7 days showed that across the whole sample range and irrespective of texture, severe to extreme repellency persistence consistently reduced the maximum water content at any given time to well below that of wettable soils. For slightly to moderately repellent soils the results were more variable and thus hydrological effects of such repellency levels are more difficult to predict. The results imply that: (i) repellency is common for many land-use types with permanent vegetation cover in humid temperate climates irrespective of soil texture; (ii) supposedly influential parameters (texture, organic matter, specific water content) are poor general predictors of water repellency, whereas land use and the moisture content below which repellency can occur seem more reliable; and (iii) infiltration and water storage capacity of very repellent soils are considerably less than for comparable wettable soils. [source] Kinetic study of triphenylphosphine addition to para -benzoquinoneINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 9 2004Davood Nori-Shargh Kinetics of the addition reaction of triphenylphosphine to para -benzoquinone in 1,2-dichloroethane as solvent was studied. Initial rate method was used to determine the order of the reaction with respect to the reactants. Pseudo-first-order method was also used to calculate the rate constant. This reaction was monitored by UV-vis spectrophotometry at 520 nm by variable time method. On the basis of the obtained results, the Arrhenius equation of this reaction was obtained: The activation parameters, Ea, ,H#, ,G#, and ,S# at 300 K were 5.701, 6.294, 19.958 kcal mol,1 and ,45.853 cal mol,1 K,1, respectively. This reaction is first and second order with respect to triphenylphosphine and para -benzoquinone, respectively. © 2004 Wiley Periodicals, Inc. Int J Chem Kinet 36:472,479, 2004 [source] Lower critical solution temperature determination of smart, thermosensitive N -isopropylacrylamide- alt -2-hydroxyethyl methacrylate copolymers: Kinetics and physical propertiesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008Mohammad M. Fares Abstract The lower critical solution temperatures (LCSTs) were verified and determined for different molar feed ratios of N -isopropylacrylamide (NIPAAm) and 2-hydroxyethyl methacrylate (HEMA) monomers with ultraviolet spectroscopy and differential scanning calorimetry techniques. Increases in the NIPAAm monomer content played a crucial role in the LCST, which increased up to 36.7°C at 50 mol %. However, a further increase in the NIPAAm monomer content steadily reduced the LCST, which decreased to 33°C at 100 mol % NIPAAm [i.e., pure poly(N -isopropylacrylamide)]. The rate of copolymerization, assessed by the conventional conversion (%),time method, and the apparent activation energies were determined. The reactivity ratios of the monomers, determined by the Kelen,Tudos and Fineman,Ross techniques, together with the results of an equation, showed that the copolymer which formed was an alternating copolymer. The Q,e values for the NIPAAm monomer were determined. The equation showed the linear Arrhenius behavior of ln(r1r2) versus the reciprocal of the temperature (where r1 and r2 are the reactivity ratios of NIPAAm and HEMA, respectively): the activation energy difference [i.e., (E12 + E21) , (E11 + E22), where E12, E21, E11, and E22 are various activation energies] was found to be ,109 kJ/mol. The copolymers were characterized with 1H-NMR, 13C-NMR, Fourier transform infrared, ultraviolet,visible, thermogravimetric analysis, differential scanning calorimetry, X-ray diffraction, and scanning electron microscopy techniques. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Trypsin Inhibitor Activity In Vitro Digestibility and Sensory Quality of Meat-Like Yuba Products as Affected by ProcessingJOURNAL OF FOOD SCIENCE, Issue 3 2002G. Su ABSTRACT: : Soybeans (Glycine max) were soaked and ground to obtain soymilk. The soymilk was cooked in an open tank and held at 85 to 90 deg;C. Yuba films were picked up in 20 min intervals and dried for 20 min. Yuba films were soaked in chicken-flavor solutions (25% and 35%), and baking soda (BS) solutions (0%, 1%, 2%, and 3% BS), and cooked at 100 °C for 30 min, 60 min, and 90 min. TIA decreased (p < 0.05) with the increase of heating time and BS concentration. In vitro protein digestibility (IVPD) decreased with heating time and BS concentration (p < 0.05). Sensory characteristics were affected by flavor concentration. By using 0% BS, 25% of the chicken flavor concentration, and a short heating time method, meat-like products with low TIA, high IVPD, and good sensory characteristics were obtained. [source] Optimization of dispersive liquid,liquid microextraction of Co(II) and Fe(III) as their oxinate chelates and analysis by HPLC: Application for the simultaneous determination of Co(II) and Fe(III) in water samplesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 23-24 2009Mir Ali Farajzadeh Abstract In this study, dispersive liquid,liquid microextraction method was used for the preconcentration and simultaneous determination of Co(II) and Fe(III) in water samples as their oxinate chelates. In dispersive liquid,liquid microextraction process, methanol and chloroform were used as disperser and extracting solvents, respectively, and the ligand 8-hydroxy quinoline was used as a chelating agent for the extraction of Co(II) and Fe(III). HPLC was applied for the quantitation of the analytes after preconcentration. An experimental design, central composite design, coupled with response surface methodology was used for the optimization of the involved experimental parameters. In addition, the effect of various experimental parameters in the extraction was investigated using one variable at a time method. The calibration graphs were linear in the range of 20,4000,,g/L with the LODs of 3,,g/L for both analytes. The RSDs for six replicate measurements of 500,,g/L of Co2+ and Fe3+ were 3.3 and 4.1%, respectively. [source] Prospective Evaluation of Intraoperative Hemodynamics in Liver Transplantation with Whole, Partial and DCD GraftsAMERICAN JOURNAL OF TRANSPLANTATION, Issue 8 2010M. Sainz-Barriga The interaction of systemic hemodynamics with hepatic flows at the time of liver transplantation (LT) has not been studied in a prospective uniform way for different types of grafts. We prospectively evaluated intraoperative hemodynamics of 103 whole and partial LT. Liver graft hemodynamics were measured using the ultrasound transit time method to obtain portal (PVF) and arterial (HAF) hepatic flow. Measurements were recorded on the native liver, the portocaval shunt, following reperfusion and after biliary anastomosis. After LT HAF and PVF do not immediately return to normal values. Increased PVF was observed after graft implantation. Living donor LT showed the highest compliance to portal hyperperfusion. The amount of liver perfusion seemed to be related to the quality of the graft. A positive correlation for HAF, PVF and total hepatic blood flow with cardiac output was found (p = 0.001). Portal hypertension, macrosteatosis >30%, warm ischemia time and cardiac output, independently influence the hepatic flows. These results highlight the role of systemic hemodynamic management in LT to optimize hepatic perfusion, particularly in LDLT and split LT, where the highest flows were registered. [source] | |||||||||||||