Jump to main content
US EPA
United States Environmental Protection Agency
Search
Search
Main menu
Environmental Topics
Laws & Regulations
About EPA
Health & Environmental Research Online (HERO)
Contact Us
Print
Feedback
Export to File
Search:
This record has one attached file:
Add More Files
Attach File(s):
Display Name for File*:
Save
Citation
Tags
HERO ID
9415771
Reference Type
Journal Article
Title
Stability of Aprepitant Injectable Emulsion in Alternate Infusion Bags, in Refrigerated Storage, and Admixed with Dexamethasone and Palonosetron
Author(s)
Ottoboni, T; Lerner, L; Santhouse, A
Year
2021
Is Peer Reviewed?
Yes
Journal
Drug Design, Development and Therapy
ISSN:
1177-8881
Publisher
Dove Medical Press Ltd
Location
ALBANY
Volume
15
Page Numbers
2519-2527
Language
English
PMID
34163138
DOI
10.2147/DDDT.S282058
Web of Science Id
WOS:000662316600001
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85108624894&doi=10.2147%2fDDDT.S282058&partnerID=40&md5=29fcf148f3e61dce0d726bac147642c6
Exit
Abstract
Purpose:
The stability of aprepitant injectable emulsion is evaluated in various admixture bags and solutions, under different storage conditions, and when combined with other antiemetics.
Methods:
A volume of 18 mL aprepitant injectable emulsion was added to infusion bags (either non-di-(2-ethylhexyl) phthalate [DEHP], polyvinyl chloride [PVC]-containing bags or non-DEHP, non-PVC bags) containing 100, 130, or 250 mL of 0.9% normal saline solution (NSS) or 5% dextrose in water (D5W). Bags were stored at controlled room temperature (20-25°C) for up to 12 hours or refrigerated (2-8°C) for up to 72 hours. Compatibility/stability was also assessed in admixtures combined with either dexamethasone or palonosetron. At specified time points, bags were tested for appearance, pH, assay for aprepitant (ie, percent label claim of aprepitant) and aprepitant-related substances, Z-average particle size, globule size distribution, particulate matter, and DEHP content (PVC bags). In separate analyses to assess microbial burden, bags containing aprepitant were inoculated with seven different organisms and assessed for microbial growth.
Results:
There was no detectable impact on the physicochemical properties or potential to promote microbial growth of aprepitant when diluted with various amounts of either NSS or D5W and when admixed with either dexamethasone or palonosetron at room temperature for at least 6 hours or during refrigeration for up to 72 hours in either PVC- or non-PVC-containing bags.
Conclusion:
Aprepitant-containing admixtures are stable under these conditions, a finding that may improve patient and provider convenience and reduce medication wastage.
Keywords
Chemotherapy-induced nausea and vomiting; DEHP; Di-(2-ethylhexyl) phthalate; Microbial growth; Physicochemical; Polyvinyl chloride; PVC
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity