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
3859195
Reference Type
Journal Article
Title
Fluorinated ionic liquids for protein drug delivery systems: Investigating their impact on the structure and function of lysozyme
Author(s)
Alves, M; Vieira, NSM; Rebelo, LPN; Araújo, JMM; Pereiro, AB; Archer, M
Year
2017
Is Peer Reviewed?
Yes
Journal
International Journal of Pharmaceutics
ISSN:
0378-5173
EISSN:
1873-3476
Volume
526
Issue
1-2
Page Numbers
309-320
Language
English
PMID
28478279
DOI
10.1016/j.ijpharm.2017.05.002
Web of Science Id
WOS:000404491400030
Abstract
Since the approval of recombinant human insulin by FDA in 1982, more than 200 proteins are currently available for pharmaceutical use to treat a wide range of diseases. However, innovation is still required to develop effective approaches for drug delivery. Our aim is to investigate the potential use of fluorinated ionic liquids (FILs) as drug delivery systems (DDS) for therapeutic proteins. Some initial parameters need to be assessed before further studies can proceed. This work evaluates the impact of FILs on the stability, function, structure and aggregation state of lysozyme. Different techniques were used for this purpose, which included differential scanning fluorimetry (DSF), spectrophotometric assays, circular dichroism (CD), dynamic light scattering (DLS), and scanning and transmission electron microscopy (SEM/TEM). Ionic liquids composed of cholinium-, imidazolium- or pyridinium- derivatives were combined with different anions and analysed at different concentrations in aqueous solutions (below and above the critical aggregation concentration, CAC). The results herein presented show that the addition of ionic liquids had no significant effect on the stability and hydrolytic activity of lysozyme. Moreover, a distinct behaviour was observed in DLS experiments for non-surfactant and surfactant ionic liquids, with the latter encapsulating the protein at concentrations above the CAC. These results encourage us to further study ionic liquids as promising tools for DDS of protein drugs.
Keywords
Ionic liquids; Therapeutic proteins; Lysozyme; Drug delivery systems; Fluorinated surfactants
Tags
PFAS
•
Additional PFAS (formerly XAgency)
•
^Per- and Polyfluoroalkyl Substances (PFAS)
PFBS (375-73-5)
Literature Search
WOS
•
PFAS 150
Literature Search Update December 2020
WOS
Literature Search August 2019
Web of Science
Not prioritized for screening
Perfluorobutanesulfonate
•
PFBA
Protocol References
•
PFBS
WOS
Excluded/Not on Topic
Search
WOS
Excluded
WOS
•
Yale PFAS Liver study
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity