Attenuating Oxidative Stress Via Oxalate Ester‐Containing Ferulic Acid‐Based Poly(anhydride‐esters) that Scavenge Hydrogen Peroxide. Issue 1 (4th December 2015)
- Record Type:
- Journal Article
- Title:
- Attenuating Oxidative Stress Via Oxalate Ester‐Containing Ferulic Acid‐Based Poly(anhydride‐esters) that Scavenge Hydrogen Peroxide. Issue 1 (4th December 2015)
- Main Title:
- Attenuating Oxidative Stress Via Oxalate Ester‐Containing Ferulic Acid‐Based Poly(anhydride‐esters) that Scavenge Hydrogen Peroxide
- Authors:
- Faig, Jonathan J.
Klein, Sarah
Ouimet, Michelle A.
Yu, Weiling
Uhrich, Kathryn E. - Abstract:
- Abstract : Ferulic acid (FA) is a naturally occurring, potent antioxidant commonly utilized in biomedical, food, and cosmetic formulations. While effective, FA's instability decreases its efficacy in formulations. Previous work demonstrates stabilization and controlled release of FA when incorporated into a polymer; however, these polymers lack inherent bioactivity, which can be significant in systems being actively impaired by oxidative stress. To address this limitation, oxalate ester linkages are incorporated into the polymer backbone due to their high reactivity toward hydrogen peroxide, a reactive oxygen species precursor. While polymer thermal properties and weight‐averaged molecular weight are similar to previous FA‐based poly(anhydride‐esters), the relative hydrophobicity, as indicated by contact angle measurements, is significantly higher. In vitro release studies indicate that polymer degradation and corresponding release of free FA are not solely dependent on hydrophobicity; despite higher hydrophobicity, these oxalate‐containing polymers degrade faster than previously published, more hydrophilic FA‐based polymers. Moreover, released FA maintains antioxidant activity, whereas the polymer displays hydrogen peroxide scavenging activity. Cytocompatibility studies demonstrate acceptable in vivo use up to 0.01 mg mL −1 . This polymer system offers a two‐pronged approach to attenuate oxidative stress, as both the release product (i.e., FA) and polymer possess radicalAbstract : Ferulic acid (FA) is a naturally occurring, potent antioxidant commonly utilized in biomedical, food, and cosmetic formulations. While effective, FA's instability decreases its efficacy in formulations. Previous work demonstrates stabilization and controlled release of FA when incorporated into a polymer; however, these polymers lack inherent bioactivity, which can be significant in systems being actively impaired by oxidative stress. To address this limitation, oxalate ester linkages are incorporated into the polymer backbone due to their high reactivity toward hydrogen peroxide, a reactive oxygen species precursor. While polymer thermal properties and weight‐averaged molecular weight are similar to previous FA‐based poly(anhydride‐esters), the relative hydrophobicity, as indicated by contact angle measurements, is significantly higher. In vitro release studies indicate that polymer degradation and corresponding release of free FA are not solely dependent on hydrophobicity; despite higher hydrophobicity, these oxalate‐containing polymers degrade faster than previously published, more hydrophilic FA‐based polymers. Moreover, released FA maintains antioxidant activity, whereas the polymer displays hydrogen peroxide scavenging activity. Cytocompatibility studies demonstrate acceptable in vivo use up to 0.01 mg mL −1 . This polymer system offers a two‐pronged approach to attenuate oxidative stress, as both the release product (i.e., FA) and polymer possess radical scavenging activity, rendering it useful for antioxidant applications. Abstract : Oxalate ester‐containing ferulic acid‐based biodegradable polymers possessing inherent bioactivity are polymerized via solution polymerization from antioxidant‐containing monomers. The polymers exhibit sustained hydrolytic release of ferulic acid over 16 days, maintaining antioxidant potency when compared to free bioactives, whereas the polymer displays hydrogen peroxide scavenging activity. … (more)
- Is Part Of:
- Macromolecular chemistry and physics. Volume 217:Issue 1(2016:Jan.)
- Journal:
- Macromolecular chemistry and physics
- Issue:
- Volume 217:Issue 1(2016:Jan.)
- Issue Display:
- Volume 217, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 217
- Issue:
- 1
- Issue Sort Value:
- 2016-0217-0001-0000
- Page Start:
- 108
- Page End:
- 114
- Publication Date:
- 2015-12-04
- Subjects:
- antioxidant -- ferulic acid -- oxalate ester -- poly(anhydride‐ester) -- radical scavenging
Polymers -- Periodicals
Polymerization -- Periodicals
Synthetic products -- Periodicals
Macromolecules -- Periodicals
547.7 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/macp.201500411 ↗
- Languages:
- English
- ISSNs:
- 1022-1352
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.398000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2528.xml