Poly(dimethyl siloxane) surface modification by low pressure plasma to improve its characteristics towards biomedical applications

Poly(dimethyl siloxane) elastomer, (PDMS) is widely used as a biomaterial. However, PDMS is very hydrophobic and easily colonized by several bacteria and yeasts. Consequently, surface modification has been used to improve its wettability and reduce bacterial adhesion. The aim of this work was to mod...

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Published in:	Colloids and surfaces, B, Biointerfaces Vol. 81; no. 1; pp. 20 - 26
Main Authors:	Pinto, S., Alves, P., Matos, C.M., Santos, A.C., Rodrigues, L.R., Teixeira, J.A., Gil, M.H.
Format:	Journal Article
Language:	English
Published:	Netherlands Elsevier B.V 01-11-2010
Subjects:	Animals Atomic force microscopy Bacteria Biocompatible Materials - chemistry Biocompatible Materials - pharmacology Biomaterials Biomedical Technology - methods Cell Survival - drug effects Cells, Cultured Contact angle Dimethylpolysiloxanes - chemistry Dimethylpolysiloxanes - pharmacology Elastomers - chemistry Elastomers - pharmacology Hemolysis - drug effects Hydrophobic and Hydrophilic Interactions Macrophages, Peritoneal - cytology Macrophages, Peritoneal - drug effects Materials Testing - methods Methacrylates - chemistry Mice Mice, Inbred BALB C Microscopy, Atomic Force Photoelectron Spectroscopy Plasma Pluronic ® F-68 Poloxamer - chemistry Poly(dimethyl siloxane) Poly(ethylene glycol) methyl methacrylate Polyethylene Glycols - chemistry Rabbits Silicone resins Siloxanes Surface chemistry Surface modification Surface Properties Surgical implants X-ray photoelectron spectroscopy Plasma Surface modification Pluronic ® F-68 Poly(ethylene glycol) methyl methacrylate Poly(dimethyl siloxane) Biomaterials
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Abstract	Poly(dimethyl siloxane) elastomer, (PDMS) is widely used as a biomaterial. However, PDMS is very hydrophobic and easily colonized by several bacteria and yeasts. Consequently, surface modification has been used to improve its wettability and reduce bacterial adhesion. The aim of this work was to modify the PDMS surface in order to improve its hydrophilicity and bacterial cell repulsion to be used as a biomaterial. Plasma was used to activate the PDMS surface and sequentially promote the attachment of a synthetic surfactant, Pluronic ® F-68, or a polymer, Poly(ethylene glycol) methyl methacrylate, PEGMA. Bare PDMS, PDMS argon plasma activated, PDMS coated with Pluronic ® F-68 and PEGMA-grafted PDMS were characterized by contact angle measurements, X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). The influence of the surface modifications on blood compatibility of the materials was evaluated by thrombosis and haemolysis assays. The cytotoxicity of these materials was tested for mouse macrophages. After modification, AFM results suggest the presence of a distinct layer at the surface and by the contact angle measures it was observed an increase of hydrophilicity. XPS analysis indicates an increase of the oxygen content at the surface as a result of the modification. All the studied materials revealed no toxicity and were found to be non-haemolytic or in some cases slightly haemolytic. Therefore, plasma was found to be an effective technique for the PDMS surface modification.
AbstractList	Poly(dimethyl siloxane) elastomer, (PDMS) is widely used as a biomaterial. However, PDMS is very hydrophobic and easily colonized by several bacteria and yeasts. Consequently, surface modification has been used to improve its wettability and reduce bacterial adhesion. The aim of this work was to modify the PDMS surface in order to improve its hydrophilicity and bacterial cell repulsion to be used as a biomaterial. Plasma was used to activate the PDMS surface and sequentially promote the attachment of a synthetic surfactant, PluronicA+ F-68, or a polymer, Poly(ethylene glycol) methyl methacrylate, PEGMA. Bare PDMS, PDMS argon plasma activated, PDMS coated with PluronicA+ F-68 and PEGMA-grafted PDMS were characterized by contact angle measurements, X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). The influence of the surface modifications on blood compatibility of the materials was evaluated by thrombosis and haemolysis assays. The cytotoxicity of these materials was tested for mouse macrophages. After modification, AFM results suggest the presence of a distinct layer at the surface and by the contact angle measures it was observed an increase of hydrophilicity. XPS analysis indicates an increase of the oxygen content at the surface as a result of the modification. All the studied materials revealed no toxicity and were found to be non-haemolytic or in some cases slightly haemolytic. Therefore, plasma was found to be an effective technique for the PDMS surface modification. Poly(dimethyl siloxane) elastomer, (PDMS) is widely used as a biomaterial. However, PDMS is very hydrophobic and easily colonized by several bacteria and yeasts. Consequently, surface modification has been used to improve its wettability and reduce bacterial adhesion. The aim of this work was to modify the PDMS surface in order to improve its hydrophilicity and bacterial cell repulsion to be used as a biomaterial. Plasma was used to activate the PDMS surface and sequentially promote the attachment of a synthetic surfactant, Pluronic F-68, or a polymer, Poly(ethylene glycol) methyl methacrylate, PEGMA. Bare PDMS, PDMS argon plasma activated, PDMS coated with Pluronic F-68 and PEGMA-grafted PDMS were characterized by contact angle measurements, X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). The influence of the surface modifications on blood compatibility of the materials was evaluated by thrombosis and haemolysis assays. The cytotoxicity of these materials was tested for mouse macrophages. After modification, AFM results suggest the presence of a distinct layer at the surface and by the contact angle measures it was observed an increase of hydrophilicity. XPS analysis indicates an increase of the oxygen content at the surface as a result of the modification. All the studied materials revealed no toxicity and were found to be non-haemolytic or in some cases slightly haemolytic. Therefore, plasma was found to be an effective technique for the PDMS surface modification. Poly(dimethyl siloxane) elastomer, (PDMS) is widely used as a biomaterial. However, PDMS is very hydrophobic and easily colonized by several bacteria and yeasts. Consequently, surface modification has been used to improve its wettability and reduce bacterial adhesion. The aim of this work was to modify the PDMS surface in order to improve its hydrophilicity and bacterial cell repulsion to be used as a biomaterial. Plasma was used to activate the PDMS surface and sequentially promote the attachment of a synthetic surfactant, Pluronic ® F-68, or a polymer, Poly(ethylene glycol) methyl methacrylate, PEGMA. Bare PDMS, PDMS argon plasma activated, PDMS coated with Pluronic ® F-68 and PEGMA-grafted PDMS were characterized by contact angle measurements, X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). The influence of the surface modifications on blood compatibility of the materials was evaluated by thrombosis and haemolysis assays. The cytotoxicity of these materials was tested for mouse macrophages. After modification, AFM results suggest the presence of a distinct layer at the surface and by the contact angle measures it was observed an increase of hydrophilicity. XPS analysis indicates an increase of the oxygen content at the surface as a result of the modification. All the studied materials revealed no toxicity and were found to be non-haemolytic or in some cases slightly haemolytic. Therefore, plasma was found to be an effective technique for the PDMS surface modification.
Author	Pinto, S. Matos, C.M. Santos, A.C. Gil, M.H. Rodrigues, L.R. Teixeira, J.A. Alves, P.
Author_xml	– sequence: 1 givenname: S. surname: Pinto fullname: Pinto, S. email: susanacspinto@gmail.com organization: Department of Chemical Engineering, University of Coimbra, Polo II, Pinhal de Marrocos, Rua Sílvio Lima, 3030-790 Coimbra, Portugal – sequence: 2 givenname: P. surname: Alves fullname: Alves, P. organization: Department of Chemical Engineering, University of Coimbra, Polo II, Pinhal de Marrocos, Rua Sílvio Lima, 3030-790 Coimbra, Portugal – sequence: 3 givenname: C.M. surname: Matos fullname: Matos, C.M. organization: Biophysics/Biomathematics Institute, Medical School of University of Coimbra, Biomedical Institute of Research in Light and Image, Azinhaga de Santa Comba, Celas, 3000-548 Coimbra, Portugal – sequence: 4 givenname: A.C. surname: Santos fullname: Santos, A.C. organization: Biophysics/Biomathematics Institute, Medical School of University of Coimbra, Biomedical Institute of Research in Light and Image, Azinhaga de Santa Comba, Celas, 3000-548 Coimbra, Portugal – sequence: 5 givenname: L.R. surname: Rodrigues fullname: Rodrigues, L.R. organization: IBB – Institute for Biotechnology and Bioengineering, Centre of Biological Engineering, Universidade do Minho, 4710-057 Braga, Portugal – sequence: 6 givenname: J.A. surname: Teixeira fullname: Teixeira, J.A. organization: IBB – Institute for Biotechnology and Bioengineering, Centre of Biological Engineering, Universidade do Minho, 4710-057 Braga, Portugal – sequence: 7 givenname: M.H. surname: Gil fullname: Gil, M.H. organization: Department of Chemical Engineering, University of Coimbra, Polo II, Pinhal de Marrocos, Rua Sílvio Lima, 3030-790 Coimbra, Portugal
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Copyright	2010 Elsevier B.V. Copyright (c) 2010 Elsevier B.V. All rights reserved.
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Snippet	Poly(dimethyl siloxane) elastomer, (PDMS) is widely used as a biomaterial. However, PDMS is very hydrophobic and easily colonized by several bacteria and...
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SubjectTerms	Animals Atomic force microscopy Bacteria Biocompatible Materials - chemistry Biocompatible Materials - pharmacology Biomaterials Biomedical Technology - methods Cell Survival - drug effects Cells, Cultured Contact angle Dimethylpolysiloxanes - chemistry Dimethylpolysiloxanes - pharmacology Elastomers - chemistry Elastomers - pharmacology Hemolysis - drug effects Hydrophobic and Hydrophilic Interactions Macrophages, Peritoneal - cytology Macrophages, Peritoneal - drug effects Materials Testing - methods Methacrylates - chemistry Mice Mice, Inbred BALB C Microscopy, Atomic Force Photoelectron Spectroscopy Plasma Pluronic ® F-68 Poloxamer - chemistry Poly(dimethyl siloxane) Poly(ethylene glycol) methyl methacrylate Polyethylene Glycols - chemistry Rabbits Silicone resins Siloxanes Surface chemistry Surface modification Surface Properties Surgical implants X-ray photoelectron spectroscopy
Title	Poly(dimethyl siloxane) surface modification by low pressure plasma to improve its characteristics towards biomedical applications
URI	https://dx.doi.org/10.1016/j.colsurfb.2010.06.014 https://www.ncbi.nlm.nih.gov/pubmed/20638249 https://search.proquest.com/docview/1770283146 https://search.proquest.com/docview/787171851
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