Martin C Woodle, Francis J Martin, Annie Yau Young, Carl T Redemann: Liposomes with enhanced circulation time. Liposome Technology, Peter J Dehlinger, May 7, 1991: US05013556 (748 worldwide citation)

A liposome composition which contains between 1-20 mole percent of an amphipathic lipid derivatized with a polyalkylether, as exemplified by phosphatidylethanolamine derivatized with polyethyleneglycol. The derivatized lipid enchances the circulation time of the liposomes severalfold, and this enhan ...

Viola T Kung, Carl T Redemann: Protein-liposome conjugates. Liposome Technology, Ciotti & Murashige Irell & Manella, August 9, 1988: US04762915 (102 worldwide citation)

A lipid coupling reagent for use in coupling amine-containing molecules, such as proteins, to liposomes. The reagent includes phosphatidylethanolamine coupled to a 3-20 atom carbon-containing spacer arm terminating at a carboxyl or thiocarboxyl group. Also disclosed are liposomes prepared to include ...

Luke S S Guo, Carl T Redemann, Ramachandran Radhakrishnan, Annie Yau Young: Liposomes with enhanced retention on mucosal tissue. Liposome Technology, Peter J Dehlinger, June 13, 1989: US04839175 (42 worldwide citation)

A liposome composition designed for enhanced binding to mucosal tissue, The liposomes contain about 10-40 mole percent of an amine-derivatized lipid component in which a charged amine group is spaced from a lipid polar head region by a carbon-containing spacer arm at least 3 atoms in length. The lip ...

Eleanor Canova Davis, Viola T Kung, Carl T Redemann: Homogeneous enzyme immunoassay system and method. Cooper Lipotech, Ciotti & Murashige Irell & Manella, November 8, 1988: US04783400 (19 worldwide citation)

A liposome assay reagent for determination of an analyte in a homogeneous immunoassay. The reagent includes a suspension of oligolamellar lipid vesicles containing encapsulated glucose-6-phosphate dehydrogenase (G6PD), at a specific activity of between about 1-15 units/.mu.mole vesicle lipid, and gl ...

Carl T Redemann: Preparation of 2,3,5-trichloropyridine. The Dow Chemical Company, S Preston Jones, C Kenneth Bjork, September 5, 1978: US04111938 (8 worldwide citation)

2,3,5-Trichloropyridine is prepared by the direct reaction of pentachloropyridine or 2,3,5,6-tetrachloropyridine with metallic zinc in the presence of a strongly alkaline aqueous solution and a water-immiscible reaction medium.