Negatively-charged polymers activate plasma contact systems, causing kinin release and factor V reduction. This surface activation is transient, with polymers becoming inert after initial plasma contact.
Area of Science:
Biomaterials Science
Hematology
Polymer Chemistry
Background:
Artificial devices often utilize negatively-charged polymers.
Understanding polymer interactions with biological systems like plasma is crucial for device safety and efficacy.
Plasma contains complex clotting and kinin systems sensitive to surface interactions.
Purpose of the Study:
To investigate the in vitro effects of negatively-charged polymers on plasma clotting and kinin systems.
To characterize the activation and subsequent inactivation of plasma components upon contact with polyelectrolyte complexes.
To determine the mechanisms behind factor V activity reduction in the presence of these polymers.
Main Methods:
In vitro study using polyelectrolyte complexes and human plasma.
Assay of contact activation, factor XII activity, prekallikrein activity, kinin release, and factor V activity.
Immunological detection of key plasma factors.
Incubation of plasma with polymers, followed by analysis and secondary incubation with fresh plasma.
Main Results:
Contact activation was observed as an immediate, transient, and surface-dependent phenomenon.
Plasma incubation with polymers led to decreased factor XII and prekallikrein activity, with significant kinin release.
Factor V activity decreased in a surface- and time-dependent manner, potentially due to adsorption onto sulfonated polymer groups.
Purified factor V showed immediate inactivation, suggesting direct adsorption, and further factor V loss occurred upon secondary plasma incubation.
Conclusions:
Negatively-charged polymers can initiate contact activation of plasma, leading to kinin release and factor V inactivation.
The observed effects are transient, with the polymer surface becoming inert after initial contact.
Factor V inactivation appears to be a direct adsorption process related to the polymer's sulfonated groups, independent of contact factor activation.