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
3038578
Reference Type
Journal Article
Title
Stabilization of eptifibatide by cosolvents
Author(s)
Zhao, LW; Yalkowsky, SH
Year
2001
Is Peer Reviewed?
Yes
Journal
International Journal of Pharmaceutics
ISSN:
0378-5173
EISSN:
1873-3476
Volume
218
Issue
1-2
Page Numbers
43-56
PMID
11337148
DOI
10.1016/S0378-5173(01)00618-4
Web of Science Id
WOS:000168739000004
Abstract
Eptifibatide is a potent and highly specific inhibitor of platelet receptor glycoprotein IIb/IIIa and is indicated in the treatment of acute coronary syndrome. The commercial product Integrilin (R) (eptifibatide) Injection requires a cold/refrigerator storage condition. In an effort to improve the drug stability for room temperature storage and transportation, this study proposed a semi-aqueous formulation that contains: 2 mg/ml eptifibatide, 10%, ethanol, 40% propylene glycol and 50% 0.025 M citrate buffer. The stability study was conducted in the pH range 4.25-6.25 under accelerated temperatures: 48, 60, 72.5 degreesC. The results indicate that the proposed semi-aqueous vehicles substantially increased the drug stability in comparison with aqueous vehicles. The predicted drug shelf-lire T-90 at 25 degreesC shows that an almost twofold increase can be achieved by formulating eptifibatide in the semi-aqueous vehicle, which is 60 months at its maximum stability of pH 5.75. as opposed to the 33 months in the aqueous vehicle at its maximum stability of pH 5.25. (C) 2001 Elsevier Science B.V. All rights reserved.
Keywords
eptifibatide; integrilin; cosolvents; stability
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity