We have developed a solid-phase immunoadsorbent based on encapsulated
goat anti-apolipoprotein B polyclonal antibodies previously crosslinke
d with a 0.25% glutaraldehyde solution, and designed to remove by immu
noaffinity the excess of apolipoproteins B from the plasma of patients
affected by familial hypercholesterolemia. Compared to a classical im
munoadsorbent prepared by activation of Sepharose CL-4B with cyanogen
bromide, the resulting immunoadsorbent exhibits both optimal adsorptio
n capacity and stability over the entire range of chemical and biochem
ical conditions during its practical handling. This approach will serv
e as a model system to demonstrate the applicability of microparticles
as immunoadsorbents, which can be achieved for other encapsulated cro
sslinked proteins. (C) 1998 John Wiley & Sons, Inc.