Protein resistance efficacy of PEO-silane amphiphiles: Dependence on PEO-segment length and concentration. (1st September 2016)
- Record Type:
- Journal Article
- Title:
- Protein resistance efficacy of PEO-silane amphiphiles: Dependence on PEO-segment length and concentration. (1st September 2016)
- Main Title:
- Protein resistance efficacy of PEO-silane amphiphiles: Dependence on PEO-segment length and concentration
- Authors:
- Rufin, Marc A.
Barry, Mikayla E.
Adair, Paige A.
Hawkins, Melissa L.
Raymond, Jeffery E.
Grunlan, Melissa A. - Abstract:
- Graphical abstract: Abstract: In contrast to modification with conventional PEO-silanes (i.e. no siloxane tether), silicones with dramatically enhanced protein resistance have been previously achieved via bulk-modification with poly(ethylene oxide) (PEO)-silane amphiphiles α-(EtO)3 Si(CH2 )2 -oligodimethylsiloxane13 - block -PEO n -OCH3 when n = 8 and 16 but not when n = 3. In this work, their efficacy was evaluated in terms of optimal PEO-segment length and minimum concentration required in silicone. For each PEO-silane amphiphile ( n = 3, 8, and 16), five concentrations (5, 10, 25, 50, and 100 μmol per 1 g silicone) were evaluated. Efficacy was quantified in terms of the modified silicones' abilities to undergo rapid, water-driven surface restructuring to form hydrophilic surfaces as well as resistance to fibrinogen adsorption. Only n = 8 and 16 were effective, with a lower minimum concentration in silicone required for n = 8 (10 μmol per 1 g silicone) versus n = 16 (25 μmol per 1 g silicone). Statement of Significance: Silicone is commonly used for implantable medical devices, but its hydrophobic surface promotes protein adsorption which leads to thrombosis and infection. Typical methods to incorporate poly(ethylene oxide) (PEO) into silicones have not been effective due to the poor migration of PEO to the surface-biological interface. In this work, PEO-silane amphiphiles – comprised of a siloxane tether ( m = 13) and variable PEO segment lengths ( n = 3, 8, 16) –Graphical abstract: Abstract: In contrast to modification with conventional PEO-silanes (i.e. no siloxane tether), silicones with dramatically enhanced protein resistance have been previously achieved via bulk-modification with poly(ethylene oxide) (PEO)-silane amphiphiles α-(EtO)3 Si(CH2 )2 -oligodimethylsiloxane13 - block -PEO n -OCH3 when n = 8 and 16 but not when n = 3. In this work, their efficacy was evaluated in terms of optimal PEO-segment length and minimum concentration required in silicone. For each PEO-silane amphiphile ( n = 3, 8, and 16), five concentrations (5, 10, 25, 50, and 100 μmol per 1 g silicone) were evaluated. Efficacy was quantified in terms of the modified silicones' abilities to undergo rapid, water-driven surface restructuring to form hydrophilic surfaces as well as resistance to fibrinogen adsorption. Only n = 8 and 16 were effective, with a lower minimum concentration in silicone required for n = 8 (10 μmol per 1 g silicone) versus n = 16 (25 μmol per 1 g silicone). Statement of Significance: Silicone is commonly used for implantable medical devices, but its hydrophobic surface promotes protein adsorption which leads to thrombosis and infection. Typical methods to incorporate poly(ethylene oxide) (PEO) into silicones have not been effective due to the poor migration of PEO to the surface-biological interface. In this work, PEO-silane amphiphiles – comprised of a siloxane tether ( m = 13) and variable PEO segment lengths ( n = 3, 8, 16) – were blended into silicone to improve its protein resistance. The efficacy of the amphiphiles was determined to be dependent on PEO length. With the intermediate PEO length ( n = 8), water-driven surface restructuring and resulting protein resistance was achieved with a concentration of only 1.7 wt%. … (more)
- Is Part Of:
- Acta biomaterialia. Volume 41(2016)
- Journal:
- Acta biomaterialia
- Issue:
- Volume 41(2016)
- Issue Display:
- Volume 41, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 41
- Issue:
- 2016
- Issue Sort Value:
- 2016-0041-2016-0000
- Page Start:
- 247
- Page End:
- 252
- Publication Date:
- 2016-09-01
- Subjects:
- Poly(ethylene oxide) -- Surface-modifying additive -- Surface restructuring -- Silicone -- Protein-resistant
Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/17427061 ↗
http://www.elsevier.com/wps/find/journaldescription.cws%5Fhome/702994/description ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.actbio.2016.04.020 ↗
- Languages:
- English
- ISSNs:
- 1742-7061
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0602.900500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26162.xml