Dietmar M. Wagenknecht
DuPont
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Publication
Featured researches published by Dietmar M. Wagenknecht.
Pharmaceutical Research | 1988
Leonard S. Rosenberg; Cheryl K. Hostetler; Dietmar M. Wagenknecht; Diane A. Aunet
Esmolol hydrochloride degrades in aqueous solutions by the hydrolysis of a labile aliphatic carboxy-ester group. The products are methanol and ASL-8123. The resulting aliphatic carboxylic acid moiety (ASL-8123) has a pK of 4.80, which is within 1 pH unit of the pH of the formulation. ASL-8123 therefore acts as a “secondary buffer” and minimizes the change in pH due to degradation. Equations are presented to calculate the change in the pH when the primary degradation product acts as a secondary buffer. This information can be used in the development of a parenteral product to predict, a priori, the concentration of buffer necessary for optimal pH maintenance. This knowledge can reduce the number of formulation screens required to determine the necessary buffer capacity for optimal drug stability.
Archive | 1989
Leonard S. Rosenberg; Cheryl K. Black; Earl R. Speicher; Dietmar M. Wagenknecht
Archive | 1985
Agustin Escobar; Dietmar M. Wagenknecht; Ahmad Waseem Malick
Archive | 1984
Agustin Escobar; Dietmar M. Wagenknecht; Abu S. Alam
Archive | 1983
Dietmar M. Wagenknecht; Anton H. Amann; Daphne R. Gallagher
Archive | 1989
Earl R. Speicher; Cheryl K. Black; Dietmar M. Wagenknecht; Leonard S. Rosenberg
Archive | 1989
Leonard S. Rosenberg; Cheryl K. Black; Earl R. Speicher; Dietmar M. Wagenknecht
Archive | 1989
Leonard S. Rosenberg; Cheryl K. Black; Earl R. Speicher; Dietmar M. Wagenknecht
Archive | 1989
Leonard S. Rosenberg; Cheryl K. Black; Earl R. Speicher; Dietmar M. Wagenknecht
Archive | 1985
Agustin Escobar; Dietmar M. Wagenknecht; Ahmad Waseem Malick