Publications

1991

1. A coupled enzyme assay for measurement of sialidase activity

   Alon R., Bayer E. A. & Wilchek M. (1991) Journal of Biochemical and Biophysical Methods. 22, 1, p. 23-33  Abstract

   A multi-coupled enzyme assay system for determining sialidase activity is described. Enzymes, substrates and chromogens are reacted in situ and determined spectrophotometrically in ELISA microtiter plates. Sialidase is assayed by the extent of desialylated galactose on an appropriate sialoglyco-conjugate (fetuin), which is otherwise unavailable for oxidation by galactose oxidase. The oxidation is monitored by the coupling of H₂O₂ released to a third enzyme, peroxidase. The rate of change of absorbance at 405 nm, resulting from the oxidized chromogen is a measure of the reation rate of the coupled enzyme system. A similar can be used for determining galactose oxidase in solution, or on blots using galactose as substrate. Due to the small-scale single-step measurement, the described assay is a sensitive, convenient, and inexpensive alternative to the classic colorimetric determination.
2. Liposomal drug delivery: thermodynamic and chemical kinetic considerations

   Margalit R., Alon R., Linenberg M., Rubin I., Roseman T. J. & Wood R. W. (1991) Journal of Controlled Release. 17, 3, p. 285-296  Abstract

   The thermodynamics of encapsulation and the kinetics of efflux were studied for a series of small molecular-weight drugs in multilamellar and unilamellar liposomes. Liposome concentration and drug partition coefficient are proposed to be the dominant factors in drug encapsulation. The theoretical basis for this conclusion is presented together with supportive experimental data for progesterone, vinblastine, pilocarpine, serotonin, leu-enkephalin and a model tripeptide. The kinetics and mechanism of drug efflux were evaluated according to Eyring's absolute rate theory. For all systems studied, the data supported a mechanism of two parallel, first-order processes for the efflux of the encapsulated and the unencapsulated drug, respectively. An inverse dependence, which is proposed to be an expression of deviations from ideality, was found between the rate constant for the efflux of the encapsulated drug and liposome concentration. At liposome concentrations of 100 to 150 (mM lipid), the rate constants for efflux of encapsulated progesterone, vinblastine, serotonin and pilocarpine from MLV are 6 × 10^-4, 3 × 10^-3, 1.3 × 10^-2 and 7 × 10^-2 (h^-1), respectively. Under similar experimental conditions, the corresponding data for unilamellar liposomes are 7 × 10^-4, 0.3 and 0.4 (h^-1) for progesterone, serotonin and pilocarpine, respectively. The application of kinetic studies of this type for the optimization of shelf-life conditions of liposome/drug systems with respect to drug retention is presented and discussed.