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Douglas N. Fish, Howard D. Beall, S. Diane Goodwin, Janet L. Fox, Stability of sumatriptan succinate in extemporaneously prepared oral liquids, American Journal of Health-System Pharmacy, Volume 54, Issue 14, 15 July 1997, Pages 1619–1622, https://doi.org/10.1093/ajhp/54.14.1619
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Abstract
The stability of sumatriptan succinate in extemporaneously prepared oral liquids was studied.
Suspensions of sumatriptan (as the succinate salt) in Ora-Sweet, Ora-Sweet SF, and Syrpalta syrups (Paddock Laboratories and Humco Laboratory) were extemporaneously compounded to produce a sumatriptan concentration of 5 mg/mL. Each suspension was prepared in triplicate. The suspensions were stored at 4 degrees C in amber glass bottles for 60 days. Two 1-mL samples were removed from each bottle initially and on days 2, 7, 14, 21, 28, 35, and 60. Sumatriptan concentrations were determined by high-performance liquid chromatography. The samples also underwent visual inspection and microbial testing.
The mean concentration of sumatriptan in all suspensions remained above 90% of the initial concentration for up to 21 days. By day 28, the sumatriptan concentration of all suspensions had decreased to less than 90% of the initial concentration. None of the suspensions had microbial growth up to day 28, and there were no visible changes in the suspensions throughout the study period.
Sumatriptan 5 mg/mL (as the succinate salt) in three oral suspensions was stable for up to 21 days when stored without light at 4 degrees C.
Author notes
Supported by a grant from Glaxo Wellcome Inc., Research Triangle Park, NC.
Presented at the ASHP Midyear Clinical Meeting, Las Vegas, NV, December 6, 1995.
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