Separations
Cavilink polymers are ideal substrates for
separation of biological macromolecules due to the very large, micrometer-size,
cavities contained in every sphere (see section on
Immobilized Enzymes). In
addition, these interconnected cavities allow eluents to flow entirely through
the polymer, thereby accelerating mass transfer and reducing resistance to flow.
Extremely high eluent flow rates can be achieved with these materials.
(See section on The
Polymers for a thorough discussion of the polymers and their properties.)
Bioprocessing
Bioprocessing applications can include semi-preparative, preparative and process-scale chromatography. It is apparent
that Cavilink polymers are ideal substrates for separation
of biological macromolecules due to the very large, micrometer-size cavities
contained in every sphere. In addition, these interconnected cavities allow
eluents to flow entirely through the polymer, thereby accelerating mass
transfer and reducing resistance to flow. Extremely high eluent flow rates can
be achieved with these materials.
Cavilink polymers exhibit properties that are unique and
actually present a new paradigm. Conventional polymers require very large
surface areas in order to improve column efficiencies. However, conventional
polymers do not allow large molecules to interact with interior portions of
media: most interactions occur within the first few angstroms of
particle surfaces. Unlike conventional polymers, Cavilink polymers have
interconnecting pores so that the entire surface area is available for
chromatographic interactions. Taken together, this results in properties
favorable to bioseparations: low flow resistance; improved mass transfer; high
binding capacity, and of course, very large cavities of micrometer dimensions to
allow full access by biopolymers.
Affinity Chromatography
The term, "affinity chromatography", can be applied
to any separation involving attachment of an affinity ligand to
a support matrix. However, it is most often employed in bioseparation problems
involving proteins or nucleic acids. In these cases, a protein or other
substrate with a particular affinity for a target molecule is covalently
attached to an inert matrix. Sample solutions containing target molecules are
passed through these activated columns, and preferential binding is achieved.
Once columns are flushed to remove extraneous components, bound target molecules
are released by employing an appropriate releasing eluent.
(See section on Immobilized Enzymes
for a discussion of purification if IgG.)
Cavilink polymer technology is ideally suited for affinity
applications. The micrometer-size cavities are sufficiently large to permit
groups of macromolecules to interact and bind without steric interferences.
Furthermore, the interconnecting pores permit rapid introduction and egress of
eluents.
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