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P H Wiersema

Publications and source records attributed to P H Wiersema.

6 recordsLinked to original sources

Exchange and aggregation in dispersions of dimyristoyl phosphatidylcholine vesicles containing myristic acid.

Processes occurring in dispersions of dimyristoyl phosphatidylcholine containing myristic acid have been studied by light scattering of dilute dispersions (concn. less than or equal to 1 mg/ml) at temperatures above and below the phase transition temperatures of these dispersions. The transition temperatures increase with increasing mol fraction of myristic acid. Above these temperatures, vesicles with different mol fractions of myristic acid exchange lipid molecules. The exchange process leads to vesicles having phase transition temperatures and radii, which ar both intermediate between the initial transitions and radii, respectively. In contrast with the observations above the phase transitions, it was found that when dimyristoyl phosphatidylcholine/myristic acid vesicles were cooled to a few degrees below the phase transition, larger particles were formed. These observations are consistent with a mechanism consisting of vesicle aggregation followed by fustion of the aggregated vesicles. The aggregation process is of second order in the vesicle concentration, and its rate increases with increasing mol fraction of myristic acid.

Kinetics↗

Phase diagrams and the kinetics of phospholipid exchange for vesicles of different composition and radius.

Interactions between dimyristoyl- and dipalmitoyl phosphatidylcholine vesicles have been studied by light scattering of dilute dispersions (concn less than or equal to 1 mg/ml). It was found that at 50 degrees C, the two types of vesicles exchange lipid molecules, irrespective of the initial radii of the pure vesicles. When the initial radii are different, the process leads eventually to vesicles of intermediate size. The reaction follows second order kinetics. At room temperature no reaction was observed. The phase diagrams for several lipid systems are discussed.

Kinetics↗

Dynamics of phospholipid aggregation in ethanol--water solutions.

The kinetics of liposome and vesicle formation of a synthetic lecithin has been studied by light scattering techniques. It is shown, that by evaporation of alcohol from a lipid--alcohol--water mixture, the aggregates formed undergo several changes in shape. A hypothesis is presented, visualising the formation of liposomes or vesicles from monomers, which is consistent with the experimental observations.

Binding Sites↗

Determination of antibody concentration using a stopped-flow turbidimetric technique.

The aggregation of albumin and anti-albumin is studied during the first seconds of the reaction by measuring the rate of change of the optical density of the mixture. When this rate is plotted against the antigen concentration of a constant serum dilution, bell-shaped curves are obtained. The maxima of these rate curves parallel the maxima of precipitation curves. Thus, the maximum rate establishes the antigen concentration for maximum precipitate. On the basis of these experiments a method for relative quantitation of antibody in sera is proposed. The absolute concentration of precipitating antibody can be obtained by means of an additional one-tube precipitation experiment.

Animals↗