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Biomedical subjects

Eli Ruckenstein

Publications and source records attributed to Eli Ruckenstein.

56 records · Page 4Linked to original sources

Hydrophobic Core/Hydrophilic Shell Amphiphilic Particles.

Amphiphilic colloidal particles with hydrophobic cores and hydrophilic shells were prepared via a two-step method. First, polystyrene cores were obtained through the concentrated emulsion polymerization. A mixture of styrene, ethyl benzene, divinyl benzene, azobisisobutyronitrile, and cumene hydroperoxide (CHPO) was partially polymerized at 80 degrees C for 40 min and subsequently used as the dispersed phase of a concentrated emulsion in water. The concentrated emulsion was subjected to complete polymerization at 60 degrees C for 12 h; colloidal particles of crosslinked polystyrene were thus obtained. In the second step, the polystyrene particles were dispersed in water, after which acrylamide, N,N'-methylenebisacrylamide, and ferrous sulfate (FS) were added. The system was heated (typically at 30 degrees C) to conduct the polymerization of the hydrophilic monomers. The CHPO present on the surface of the polystyrene particles and the FS present in the aqueous phase (both together constitute a redox initiator) ensured that the initiation occurred mostly on the surface of the particles and that the hydrophilic polymer obtained formed a shell encapsulating the particles. Under proper conditions, a porous outer shell could be generated, making the hydrophobic core accessible to the outside medium. Copyright 2001 Academic Press.

Journal Article↗

Cellulose and glass fiber affinity membranes for the chromatographic separation of biomolecules.

Macroporous cellulose and glass membranes were prepared from filter paper and glass fiber filter, respectively. To enhance their stability, the cellulose membranes were crosslinked with epichlorohydrin, and the glass membranes were crosslinked with glutaraldehyde or organic bifunctional silanes. Several pathways for the modification, activation, and ligand immobilization were used and compared. For cellulose membranes, the diazotization method provided the best results, whereas the glutaraldehyde method provided the best performance for glass membranes, regarding both their stability and ligand immobilization capacity. The characterization of the membranes was made by using a triazine dye, bovine serum albumin, and trypsin as test ligands. The membrane morphologies and the uniformities of ligand distribution across the membrane cartridges were investigated. Numerous affinity ligands were immobilized onto the membranes, and the prepared affinity membranes have been used to separate or purify concanavalin A, peroxidase, protease inhibitors, globulin, fibronectin, and other biomolecules.

Biopolymers↗