Enhancement of silicon using micro-patterned surfaces of thin films

Micro-textured biomaterials might enhance cytocompatibility of silicon-based micro-electro-mechanical system (bio-MEMS) dummies. Photolithography-physical vapour deposition was used to produce diamond-like carbon (DLC) or Ti squares and circles on silicon, and also their inverse replicas; then DLC a...

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Main Authors: E Kaivosoja, S Myllymaa, V-P Kouri, K Myllymaa, R Lappalainen, YT Konttinen
Format: Article
Language:English
Published: AO Research Institute Davos 2010-04-01
Series:European Cells & Materials
Subjects:
Online Access:http://www.ecmjournal.org/papers/vol019/pdf/v019a15.pdf
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spelling doaj-e6cc3b5778664434b396bf661fc379e42020-11-25T00:59:35Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622010-04-011914715710.22203/eCM.v019a15Enhancement of silicon using micro-patterned surfaces of thin filmsE KaivosojaS Myllymaa V-P KouriK MyllymaaR LappalainenYT Konttinen0Department of Medicine, Institute of Clinical Medicine, Helsinki University Central Hospital, Haartmaninkatu 8, FI-00029 HUS, FinlandMicro-textured biomaterials might enhance cytocompatibility of silicon-based micro-electro-mechanical system (bio-MEMS) dummies. Photolithography-physical vapour deposition was used to produce diamond-like carbon (DLC) or Ti squares and circles on silicon, and also their inverse replicas; then DLC and Ti were compared for their guiding potential, using a SaOS-2 cell model. Scanning electron microscopy at 48 hours indicated cells were well-spread on large-sized patterns (several cells on one pattern) and assumed the geometrical architecture of underlying features. Medium-sized patterns (slightly smaller than solitary indicator cells) were inhabited by singular cells, which stretched from one island to another, assuming longitudinal or branching morphologies. On small-sized patterns (much smaller than individual cells) cells covered large micro-textured areas, but cellular filopodia bypassed the bare silicon. Immunofluorescence and confocal laser scanning microscopy indicated that the actin cytoskeleton and vinculin-containing adhesion junctions were present on the patterned areas, but not on the bare silicon. Cell density/coverage disclosed a 3.4-3.7-fold preference for the biomaterial patterns over silicon substrate (p < 0.001). Differences in the cellular response between materials were lost at 120 hours when cells were confluent. The working hypothesis was proven; enhancement by micro-patterning depends on the pattern size, shape and material and can be used to improve biocompatibility during the initial integration phase of the device. http://www.ecmjournal.org/papers/vol019/pdf/v019a15.pdfBiocompatibilitysurface modificationmicro-patterningphotolithographyosteoblast
collection DOAJ
language English
format Article
sources DOAJ
author E Kaivosoja
S Myllymaa
V-P Kouri
K Myllymaa
R Lappalainen
YT Konttinen
spellingShingle E Kaivosoja
S Myllymaa
V-P Kouri
K Myllymaa
R Lappalainen
YT Konttinen
Enhancement of silicon using micro-patterned surfaces of thin films
European Cells & Materials
Biocompatibility
surface modification
micro-patterning
photolithography
osteoblast
author_facet E Kaivosoja
S Myllymaa
V-P Kouri
K Myllymaa
R Lappalainen
YT Konttinen
author_sort E Kaivosoja
title Enhancement of silicon using micro-patterned surfaces of thin films
title_short Enhancement of silicon using micro-patterned surfaces of thin films
title_full Enhancement of silicon using micro-patterned surfaces of thin films
title_fullStr Enhancement of silicon using micro-patterned surfaces of thin films
title_full_unstemmed Enhancement of silicon using micro-patterned surfaces of thin films
title_sort enhancement of silicon using micro-patterned surfaces of thin films
publisher AO Research Institute Davos
series European Cells & Materials
issn 1473-2262
publishDate 2010-04-01
description Micro-textured biomaterials might enhance cytocompatibility of silicon-based micro-electro-mechanical system (bio-MEMS) dummies. Photolithography-physical vapour deposition was used to produce diamond-like carbon (DLC) or Ti squares and circles on silicon, and also their inverse replicas; then DLC and Ti were compared for their guiding potential, using a SaOS-2 cell model. Scanning electron microscopy at 48 hours indicated cells were well-spread on large-sized patterns (several cells on one pattern) and assumed the geometrical architecture of underlying features. Medium-sized patterns (slightly smaller than solitary indicator cells) were inhabited by singular cells, which stretched from one island to another, assuming longitudinal or branching morphologies. On small-sized patterns (much smaller than individual cells) cells covered large micro-textured areas, but cellular filopodia bypassed the bare silicon. Immunofluorescence and confocal laser scanning microscopy indicated that the actin cytoskeleton and vinculin-containing adhesion junctions were present on the patterned areas, but not on the bare silicon. Cell density/coverage disclosed a 3.4-3.7-fold preference for the biomaterial patterns over silicon substrate (p < 0.001). Differences in the cellular response between materials were lost at 120 hours when cells were confluent. The working hypothesis was proven; enhancement by micro-patterning depends on the pattern size, shape and material and can be used to improve biocompatibility during the initial integration phase of the device.
topic Biocompatibility
surface modification
micro-patterning
photolithography
osteoblast
url http://www.ecmjournal.org/papers/vol019/pdf/v019a15.pdf
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