Donald E. Pearson

Removal of Refractory Organics from Water by Aeration. I. Methyl Chloroform

Abstract A mathematical model for the removal of volatile organics from water by aeration and by solvent sublation into an organic phase is presented. The model includes the effect of the finite rate of solute mass transfer from the aqueous into the vapor phase. Results are calculated for the removal of 1,1,1-trichloroethane (TCE) chloroform, and benzene from water with 1-octanol, anisole, or kerosene as the organic phase. Experimental data on the aeration of TCE and on its solvent sublation into I-octanol are in good agreement with the model. Small bubbles and long water columns greatly reduce the inefficiency of the process caused by mass transfer rate limitations.

Advantages of deuterium modification of nitroxide spin labels for biological epr studies

Abstract The spin label, perdeuterio-N-(1-oxy 1-2,2,6,6-tetramenthyl-4-piperidinyl)maleimide (DMSL) was synthesized and its EPR and saturation transfer EPR spectra were compared to those of the hydrogen analogue, HMSL- The labels were studied as freely tumbling entities and also bound to bovine serum albumin (BSA). Significant gains in spectral resolution and detectability were observed for DMSL relative to HMSL.

The synthesis of deuterium-substituted, spin-labeled analogues of AMP and NAD+ and their use in ESR studies of lactate dehydrogenase

Two spin-labeled analogues of AMP and NAD+ were synthesized, in which a perdeuterated nitroxide radical (4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl, TEMPAMINE) was attached to C-6 or C-8 position of the adenine ring. The ESR spectra of these derivatives exhibit a 4-fold increase in sensitivity and a concomitant decrease in line-width as compared to the corresponding protonated analogues. The improved resolution of composite spectra consisting of freely tumbling and immobilized components is demonstrated in ternary complexes of the spin-labeled NAD+ derivatives with lactate dehydrogenase (L-lactate:NAD+ oxidoreductase, EC 1.1.1.27) and oxalate.

High resolution spin labeled fatty acid: synthesis and EPR spectral characteristics

Abstract Stearic acid spin label substituted with deuterium in all positions and 15 N in the paramagnetic group has been synthesized and was found to display a 5.5 fold gain in sensitivity in the EPR spectrum and a 60% decrease in linewidth compared to the unmodified analog.

Effect of some organic acid salts of tris(hydroxymethyl)aminomethane in the incubation step on plasma renin activity

The tris(hydroxymethyl)aminomethane salts of the organic acids acetylsalicylic, phenoxyacetic, salicylic, benzoic, acetic, and maleic were used to buffer the pH of plasma between 7.4 and 7.7 in a 1 h incubation step of the procedure for the determination of plasma renin activity. When compared to the plasma renin activity determined with tris(hydroxymethyl)aminomethane hydrochloride or with no buffer, it was found that all of the tris(hydroxymethyl)aminomethane salts of the organic acids studied produced a statistically significant increase in plasma renin activity except the salt of acetic acid when compared to tris(hydroxymethyl)aminomethane hydrochloride. In comparison to tris(hydroxymethyl)aminomethane hydrochloride and unbuffered plasma the organic acid salts and their mean percent difference in plasma renin activity are as follows: tris(hydroxymethyl)aminomethane phenoxyacetate (101%, 105%); tris(hydroxymethyl)aminomethane acetylsalicylate (79%, 115%); tris(hydroxymethyl)aminomethane benzoate (70%, 107%); tris(hydroxymethyl)aminomethane salicylate (64%, 70%); tris(hydroxymethyl)aminomethane maleate (32%, 60%); and tris(hydroxymethyl)aminomethane acetate (--1.6%, 43%).

Angiotensin I recovery from plasma incubated with organic reagents

(1) In order to explore the possible mechanism that organic reagents used in the incubation step of the plasma renin activity (PRA) analysis act as a angiotensinase inhibitors we did angiotensin I (AI) recovery studies from plasma with such reagents. The organic acids and their mean difference in percent recovery of AI as compared to that for hydrochloric acid (HCI) are respectively as follows for one and a three hour incubation time: maleic (0.7%, 4.5%); and potassium hydrogen phthalate (KHphthalate) (7.2%, 9.6%). The tris(hydroxymethyl)aminomethane (Tris) organic acid salts and their mean difference in percent recovery of AI as compared to that for Tris-HCl are as follows for a one hour incubation: Tris-acetylsalicylate (3.6%), Tris-phenoxyacetate (3.6%), Tris-benzoate (2.6%), and Tris-salicylate (4.9%). (2) Of the reagents studied KHphthalate after a three hour incubation produced a statistically significant difference from the HCl reagent. The recovery data for all the organic reagents suggested that the primary mechanism of action was not that of an angiotensinase inhibitory one.