Stabilized glucagon formulation for bihormonal pump use

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Abstract

Background: A promising approach to treat diabetes is the development of an automated bihormonal pump administering glucagon and insulin. A physically and chemically stable glucagon formulation does not currently exist. Our goal is to develop a glucagon formulation that is stable as a clear ungelled solution, free of fibrils at a pH of 7 for at least 7 days at 37°C. Methods: Experimental glucagon formulations were studied for stability at 25 and 37°C. Chemical degradation was quantified by reverse phase ultra-performance liquid chromatography. Physical changes were studied using light obscuration and visual observations. Results: Glucagon content of Biodel glucagon and Lilly glucagon at pH 2 and pH 4, as measured by high-performance liquid chromatography at 25°C, was 100% at 7 days compared to 87% and <7%, respectively. Light obscuration measurements indicated Lilly glucagon at pH 4 formed an opaque gel, while Biodel glucagon formulation remained a clear solution beyond 50 days at 37°C. Visual observations confirmed these results. Conclusions: Biodel glucagon is a stabilized formulation at physiological pH and remains chemically and physically stable beyond 7 days at 37°C, suggesting its utility for use in a bihormonal pump. © Diabetes Technology Society.

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APA

Steiner, S. S., Li, M., Hauser, R., & Pohl, R. (2010). Stabilized glucagon formulation for bihormonal pump use. In Journal of Diabetes Science and Technology (Vol. 4, pp. 1332–1337). SAGE Publications Inc. https://doi.org/10.1177/193229681000400606

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