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Merck
  • Compatibility of intravenous fosaprepitant with intravenous 5-HT3 antagonists and corticosteroids.

Compatibility of intravenous fosaprepitant with intravenous 5-HT3 antagonists and corticosteroids.

Cancer chemotherapy and pharmacology (2013-07-19)
Susan Sun, Joseph Schaller, Jiri Placek, Brett Duersch
要旨

Fosaprepitant dimeglumine for injection is the water-soluble phosphorylated prodrug of the neurokinin-1 receptor antagonist aprepitant. Both agents are approved (in combination with a 5-HT3 antagonist and a corticosteroid) for prevention of chemotherapy-induced nausea and vomiting. Because fosaprepitant is likely to be combined and stored in the same intravenous (IV) bag with 5-HT3 antagonists and corticosteroids, the in vitro compatibility of fosaprepitant with these agents and other IV diluents was assessed. Fosaprepitant (1 mg/mL in 0.9 % sodium chloride injection solution) was combined in binary or tertiary fashion with therapeutic-dose preparations of a 5-HT3 antagonist (ondansetron, granisetron, palonosetron, or tropisetron) and/or a corticosteroid (dexamethasone sodium phosphate or methylprednisolone sodium succinate). For diluent compatibility assessment, fosaprepitant was also prepared 1 mg/mL in 0.9 % sodium chloride injection solution, water for injection, or 5 % dextrose injection solution. After 24-h storage under ambient conditions, samples were assayed for degradation. Fosaprepitant demonstrated compatibility when combined in the same IV infusion bag with common 5-HT3 antagonists and corticosteroids for storage and IV coadministration, with the exception of palonosetron (incompatible under all experimental conditions) and tropisetron (incompatible unless combined with a corticosteroid). No incompatibility was observed between fosaprepitant and any of the 3 diluents tested. Use of fosaprepitant in combination with other antiemetics may provide a flexible option for administration of antiemetics to patients receiving moderately or highly emetogenic chemotherapy.

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製品内容

Sigma-Aldrich
デキサメタゾン 21-リン酸 二ナトリウム塩, ≥98%
USP
Methylprednisolone hemisuccinate, United States Pharmacopeia (USP) Reference Standard
デキサメタゾン 21-リン酸 二ナトリウム塩, European Pharmacopoeia (EP) Reference Standard
Methylprednisolone hydrogen succinate, European Pharmacopoeia (EP) Reference Standard
Methylprednisolone hydrogen succinate for performance test, European Pharmacopoeia (EP) Reference Standard