Home About us Contact
|
Home About us Contact | ||
|
|
||
Linear Portion (linear + portion)
Selected AbstractsElectrochemical Detection of Trace Concentrations of Cadmium and Lead with a Boron-Doped Diamond Electrode: Effect of KCl and KNO3 Electrolytes, Interferences and Measurement in River WaterELECTROANALYSIS, Issue 3 2004Carol Babyak Abstract Parts-per-billion levels of cadmium and lead were detected using square-wave anodic stripping voltammetry with a boron-doped diamond electrode. Calibration plots (10-minute deposition time) in KCl and KNO3 were non-linear at low concentrations (1,5,ppb) due to the deposition mechanism of these metals. The preferred electrolyte for cadmium was KCl, while lead could be measured in either electrolyte. The lowest concentrations included in the linear portion of the calibration plot (5,minute deposition time) for cadmium were 10,ppb and 50,ppb in KCl and KNO3, respectively, and 10,ppb for lead in KNO3. The presence of either lead or copper suppressed the cadmium stripping peak, but the lead stripping peak was unaffected by cadmium, and enhanced by the addition of copper. A river water sample was analyzed for cadmium and lead, and the cadmium results were confirmed using ICP-AES spectrometry. It was determined electrochemically that a fraction of lead in the river sample was bound by complexing material in the sample. [source] Water sorption kinetics in light-cured poly-HEMA and poly(HEMA- co -TEGDMA); determination of the self-diffusion coefficient by new iterative methodsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007Irini D. Sideridou Abstract The present investigation is concerned with the determination of self-diffusion coefficient (D) of water in methacrylate-based biomaterials following Fickian sorption by two new methods: the Iterative and the Graphical methods. The D value is traditionally determined by means of the initial slope of the corresponding sorption curve and the so-called Stefan's approximation. The proposed methods using equations without approximations and data resulting from the whole sorption range reach to accurate values of D, even when the sorption curve does not present an initial linear portion. In addition to D, the Graphical method allows the extrapolation of the mass of the sorbed water at equilibrium (M,), even when the equilibrium specimen's mass fluctuates around its limited value (m,). The test of the proposed procedures by means of ideal and Monte Carlo simulated data revealed that these methods are fairly applicable. The obtained D values compared with those determined by means of the Stephan's method revealed that the proposed methods provide more accurate results. Finally, the proposed methods were successfully applied to the experimental determination of the diffusion coefficient of water (50°C) in the homopolymer of 2-hydroxyethyl methacrylate (HEMA) and in the copolymer of HEMA with triethylene glycol dimethacrylate (98/2 mol/mol). These polymers were prepared by light curing (, = 470 nm) at room temperature in presence of camphorquinone and N,N -dimethylaminoethyl methacrylate as initiator. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] Measurement of pulmonary surfactant disaturated-phosphatidylcholine synthesis in human infants using deuterium incorporation from body waterJOURNAL OF MASS SPECTROMETRY (INCORP BIOLOGICAL MASS SPECTROMETRY), Issue 7 2005Paola E. Cogo Abstract The aim of the study was to determine surfactant palmitate disaturated-phosphatidylcholine (DSPC-PA) synthesis in vivo in humans by the incorporation of deuterium from total body water into DSPC-PA under steady state condition. We studied three newborns and one infant (body weight (BW) 4.6 ± 2.9 kg, gestational age 37.5 ± 2 weeks, age 9 ± 9 days) and four preterm newborns (BW 1.3 ± 0.6 kg, gestational age 30.3 ± 2.5 weeks, postnatal age 8.8 ± 9.2 h). All infants were mechanically ventilated during the study and the four preterm infants received exogenous surfactant at the start of the study. We administered 0.44 g 2H2O/kg BW as a bolus intravenously, followed by 0.0125 g 2H2O/kg BW every 6 h to maintain deuterium enrichment at plateau over 2 days. Urine samples and tracheal aspirates (TA) were obtained prior to dosing and every 6 h thereafter. Isotopic enrichment curves of DSPC-PA from sequential TA and urine deuterium enrichments were analyzed by Gas Chromatography-Isotope Ratio,Mass Spectrometry (GC-IRMS) and normalized for Vienna Standard Mean Ocean Water. Enrichment data were used to measure DSPC-PA fractional synthesis rate (FSR) from the linear portion of the DSPC-PA enrichment rise over time, relative to plateau enrichment of urine deuterium. Secretion time (ST) was defined as the time lag between the start of the study and the appearance of DSPC-PA deuterium enrichment in TA. Data were given as mean ± SD. All study infants reached deuterium-steady state in urine. DSPC-PA FSR was 6.5 ± 2.8%/day (range 2.6,10.2). FSR for infants who did not receive exogenous surfactant was 5.7 ± 3.5%/day (range 2.6,9.9%/day) and 7.3 ± 2.1%/day (range 5.1,10.2%/day) in the preterms, whereas DSPC-PA ST was 10 ± 10 h and 31 ± 10 h respectively. Surfactant DSPC-PA synthesis can be measured in humans by the incorporation of deuterium from body water. This study is a simpler and less invasive method compared to previously published methods on surfactant kinetics by means of stable isotopes. Copyright © 2005 John Wiley & Sons, Ltd. [source] Defining the linear portion of a sigmoid-shaped curve: bend pointsPHARMACEUTICAL STATISTICS: THE JOURNAL OF APPLIED STATISTICS IN THE PHARMACEUTICAL INDUSTRY, Issue 3 2003J. L. Sebaugh Abstract Formulae are provided that define the ,bend points', the beginning and end of the essentially linear dose,response region, for the four-parameter logistic model. The formulae are expressed in both response and dose units. The derivation of the formulae is shown in order to illustrate the general nature of the methodology. Examples are given that describe how the formulae may be used while planning and conducting bioassays. Copyright © 2003 John Wiley & Sons, Ltd. [source] | ||||||||||