Literature DB >> 30506173

Plasma processing of PDMS based spinal implants for covalent protein immobilization, cell attachment and spreading.

Daniel V Bax1,2, Yongbai Yin3, Alexey Kondyurin3, Ashish D Diwan4, Divya Bhargav4, Anthony S Weiss5,6,7, Marcela M M Bilek3, David R McKenzie3.   

Abstract

PDMS is widely used for prosthetic device manufacture. Conventional ion implantation is not a suitable treatment to enhance the biocompatibility of poly dimethyl siloxane (PDMS) due to its propensity to generate a brittle silicon oxide surface layer which cracks and delaminates. To overcome this limitation, we have developed new plasma based processes to balance the etching of carbon with implantation of carbon from the plasma source. When this carbon was implanted from the plasma phase it resulted in a surface that was structurally similar and intermixed with the underlying PDMS material and not susceptible to delamination. The enrichment in surface carbon allowed the formation of carbon based radicals that are not present in conventional plasma ion immersion implantation (PIII) treated PDMS. This imparts the PDMS surfaces with covalent protein binding capacity that is not observed on PIII treated PDMS. The change in surface energy preserved the function of bound biomolecules and enhanced the attachment of MG63 osteosarcoma cells compared to the native surface. The attached cells, an osteoblast interaction model, showed increased spreading on the treated over untreated surfaces. The carbon-dependency for these beneficial covalent protein and cell linkage properties was tested by incorporating carbon from a different source. To this end, a second surface was produced where carbon etching was balanced against implantation from a thin carbon-based polymer coating. This had similar protein and cell-binding properties to the surfaces generated with carbon inclusion in the plasma phase, thus highlighting the importance of balancing carbon etching and deposition. Additionally, the two effects of protein linkage and bioactivity could be combined where the cell response was further enhanced by covalently tethering a biomolecule coating, as exemplified here with the cell adhesive protein tropoelastin. Providing a balanced carbon source in the plasma phase is applicable to prosthetic device fabrication as illustrated using a 3-dimensional PDMS balloon prosthesis for spinal implant applications. Consequently, this study lays the groundwork for effective treatments of PDMS to selectively recruit cells to implantable PDMS fabricated biodevices.

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Year:  2018        PMID: 30506173     DOI: 10.1007/s10856-018-6181-y

Source DB:  PubMed          Journal:  J Mater Sci Mater Med        ISSN: 0957-4530            Impact factor:   3.896


  23 in total

1.  Adsorption and inactivation behavior of horseradish peroxidase on various substrates.

Authors:  Sabina Di Risio; Ning Yan
Journal:  Colloids Surf B Biointerfaces       Date:  2010-05-07       Impact factor: 5.268

2.  A lithographically-patterned, elastic multi-electrode array for surface stimulation of the spinal cord.

Authors:  Kathleen W Meacham; Richard J Giuly; Liang Guo; Shawn Hochman; Stephen P DeWeerth
Journal:  Biomed Microdevices       Date:  2008-04       Impact factor: 2.838

3.  A new surface for immobilizing and maintaining the function of enzymes in a freeze-dried state.

Authors:  Neil J Nosworthy; David R McKenzie; Marcela M Bilek
Journal:  Biomacromolecules       Date:  2009-09-14       Impact factor: 6.988

4.  Enhancement of the response of poly(dimethylsiloxane) hollow prisms through air mirrors for absorbance-based sensing.

Authors:  A Llobera; R Wilke; S Büttgenbach
Journal:  Talanta       Date:  2007-11-22       Impact factor: 6.057

5.  The Vroman effect: competitive protein exchange with dynamic multilayer protein aggregates.

Authors:  Stacey L Hirsh; David R McKenzie; Neil J Nosworthy; John A Denman; Osman U Sezerman; Marcela M M Bilek
Journal:  Colloids Surf B Biointerfaces       Date:  2012-11-23       Impact factor: 5.268

6.  Fibroblast stimulation by monocytes cultured on protein adsorbed biomedical polymers. I. Biomer and polydimethylsiloxane.

Authors:  T L Bonfield; E Colton; J M Anderson
Journal:  J Biomed Mater Res       Date:  1991-02

7.  Directed cell attachment by tropoelastin on masked plasma immersion ion implantation treated PTFE.

Authors:  Daniel V Bax; David R McKenzie; Marcela M M Bilek; Anthony S Weiss
Journal:  Biomaterials       Date:  2011-06-12       Impact factor: 12.479

8.  Tropoelastin interacts with cell-surface glycosaminoglycans via its COOH-terminal domain.

Authors:  Thomas J Broekelmann; Beth A Kozel; Hideaki Ishibashi; Claudio C Werneck; Fred W Keeley; Lijuan Zhang; Robert P Mecham
Journal:  J Biol Chem       Date:  2005-09-27       Impact factor: 5.157

9.  A novel cell adhesion region in tropoelastin mediates attachment to integrin αVβ5.

Authors:  Pearl Lee; Daniel V Bax; Marcela M M Bilek; Anthony S Weiss
Journal:  J Biol Chem       Date:  2013-11-29       Impact factor: 5.157

10.  Immobilization of glucose oxidase on a poly(dimethylsiloxane) layer by using poly(L-lysine) as a polymer backbone.

Authors:  Tomoyuki Yasukawa; Eiji Maekawa; Fumio Mizutani
Journal:  Anal Sci       Date:  2009-09       Impact factor: 2.081

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  1 in total

1.  Direct Exposure of Dry Enzymes to Atmospheric Pressure Non-Equilibrium Plasmas: The Case of Tyrosinase.

Authors:  Annamaria Lapenna; Fiorenza Fanelli; Francesco Fracassi; Vincenza Armenise; Valeria Angarano; Gerardo Palazzo; Antonia Mallardi
Journal:  Materials (Basel)       Date:  2020-05-09       Impact factor: 3.623

  1 in total

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