Ethylenediaminetetraacetic acid titration by end-point pH measurements for determination of lead

1980 ◽  
Vol 52 (3) ◽  
pp. 591-592 ◽  
Author(s):  
C. H. Culberson ◽  
C. L. Washburne
Keyword(s):  
Ethylenediaminetetraacetic Acid ◽  
Ph Measurements ◽  
End Point ◽  
Acid Titration

THE DETERMINATION OF CALCIUM AND MAGNESIUM IN BLOOD USING ONE INDICATOR

1959 ◽  
Vol 37 (1) ◽  
pp. 225-229 ◽  
Author(s):  
H. M. Czajkowska Robinson ◽  
J. C. Rathbun
Keyword(s):  
Ethylenediaminetetraacetic Acid ◽  
Total Calcium ◽  
Eriochrome Black T ◽  
End Point ◽  
Acid Titration ◽  
Calcium And Magnesium

A rapid ethylenediaminetetraacetic acid titration for calcium and magnesium in serum requiring 0.1 ml of blood is described. Eriochrome black T is used as the sole indicator and the end point is observed photometrically. After determination of total calcium and magnesium, the calcium is removed as oxalate, the magnesium determined separately, and the calcium obtained by difference. The method is highly reproducible and is sensitive to ± 0.1 mg% of either calcium or magnesium.

THE DETERMINATION OF CALCIUM AND MAGNESIUM IN BLOOD USING ONE INDICATOR

1959 ◽  
Vol 37 (2) ◽  
pp. 225-229 ◽  
Author(s):  
H. M. Czajkowska Robinson ◽  
J. C. Rathbun
Keyword(s):  
Ethylenediaminetetraacetic Acid ◽  
Total Calcium ◽  
Eriochrome Black T ◽  
End Point ◽  
Acid Titration ◽  
Calcium And Magnesium

A rapid ethylenediaminetetraacetic acid titration for calcium and magnesium in serum requiring 0.1 ml of blood is described. Eriochrome black T is used as the sole indicator and the end point is observed photometrically. After determination of total calcium and magnesium, the calcium is removed as oxalate, the magnesium determined separately, and the calcium obtained by difference. The method is highly reproducible and is sensitive to ± 0.1 mg% of either calcium or magnesium.

scholarly journals A Simple and Accurate Approach for Determining the VFA Concentration in Anaerobic Digestion Liquors, Relying on Two Titration Points and an External Inorganic Carbon Analysis

2021 ◽  
Vol 5 (2) ◽  
pp. 15
Author(s):  
Paz Nativ ◽  
Yonatan Gräber ◽  
Yaron Aviezer ◽  
Ori Lahav
Keyword(s):  
Partial Pressure ◽  
Volatile Fatty Acids ◽  
Inorganic Carbon ◽  
Strong Acid ◽  
Direct Analysis ◽  
Anaerobic Digesters ◽  
Acid Titration ◽  
Partial Pressure Of Co2 ◽  
Ph Range

A new analytic approach is presented for determining the total volatile fatty acids (VFAT) concentration in anaerobic digesters. The approach relies on external determination of the inorganic carbon concentration (CT) in the analyzed solution, along with two strong-acid titration points. The CT concentration can be determined by either a direct analysis (e.g., by using a TOC device) or by estimating it from the recorded partial pressure of CO2(g) in the biogas (often a routine analysis in anaerobic digesters). The titration is carried out to pH 5.25 and then to pH 4.25. The two titration results are plugged into an alkalinity-mass-based equation and then the two terms are subtracted from each other to yield an equation in which VFAT is the sole unknown (since CT is known and the effect of the total orthophosphate and ammonia concentrations is shown to be small at this pH range). The development of the algorithm and its verification on four anaerobic reactor liquors is presented, on both the raw water and on acetic acid-spiked samples. The results show the method to be both accurate (up to 2.5% of the expected value for VFAT/Alkalinity >0.2) and repetitive when the total orthophosphate and ammonia concentrations are known, and fairly accurate (±5% for VFAT >5 mM) when these are completely neglected. PHREEQC-assisted computation of CT from the knowledge of the partial pressure of CO2(g) in the biogas (and pH, EC and temperature in the liquor) resulted in a very good estimation of the CT value (±3%), indicating that this technique is adequate for the purpose of determining VFAT for alarming operators in case of process deterioration and imminent failure.

scholarly journals KD determination from time-resolved experiments on live cells with LigandTracer and reconciliation with end-point flow cytometry measurements

2021 ◽  
Author(s):  
Diana Spiegelberg ◽  
Jonas Stenberg ◽  
Pascale Richalet ◽  
Marc Vanhove
Keyword(s):  
Flow Cytometry ◽  
Live Cells ◽  
Time Resolved ◽  
Surface Receptors ◽  
Full Characterization ◽  
End Point ◽  
Titration Curves ◽  
Kinetics Of

AbstractDesign of next-generation therapeutics comes with new challenges and emulates technology and methods to meet them. Characterizing the binding of either natural ligands or therapeutic proteins to cell-surface receptors, for which relevant recombinant versions may not exist, represents one of these challenges. Here we report the characterization of the interaction of five different antibody therapeutics (Trastuzumab, Rituximab, Panitumumab, Pertuzumab, and Cetuximab) with their cognate target receptors using LigandTracer. The method offers the advantage of being performed on live cells, alleviating the need for a recombinant source of the receptor. Furthermore, time-resolved measurements, in addition to allowing the determination of the affinity of the studied drug to its target, give access to the binding kinetics thereby providing a full characterization of the system. In this study, we also compared time-resolved LigandTracer data with end-point KD determination from flow cytometry experiments and hypothesize that discrepancies between these two approaches, when they exist, generally come from flow cytometry titration curves being acquired prior to full equilibration of the system. Our data, however, show that knowledge of the kinetics of the interaction allows to reconcile the data obtained by flow cytometry and LigandTracer and demonstrate the complementarity of these two methods.

scholarly journals THE EFFECTS ON BIOLOGICAL MATERIALS OF FREEZING AND DRYING BY VACUUM SUBLIMATION

1954 ◽  
Vol 100 (1) ◽  
pp. 81-88 ◽  
Author(s):  
Donald Greiff ◽  
Henry Pinkerton
Keyword(s):  
Influenza Virus ◽  
Biological Materials ◽  
Continuous Operation ◽  
Virus Suspension ◽  
Vacuum Sublimation ◽  
End Point ◽  
Different Temperatures ◽  
Time Required

A vacuum sublimation apparatus is described which will permit, (a) the removal of water from virus suspensions at temperatures ranging down to –80°C., (b) continuous operation with a minimum of attention from the investigator, (c) sealing off of samples at operating pressures (10–5 mm. Hg), (d) simultaneous lyophilization of aliquot samples at different temperatures, (e) isolation of a portion of the apparatus without disturbing the remainder of the system, and (f) determination of the end-point of sublimation without disturbing the samples. The time required for drying 0.1 ml. of influenza virus suspension was shown to increase markedly with decrease of temperature, 8 days being required for dehydration at –80°C. in contrast to 2 days at –30°C. and 1 day at 0°C.

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