Full metadata record
DC FieldValueLanguage
dc.contributor.authorDhawan, Udeshen_US
dc.contributor.authorPan, Hsu-Anen_US
dc.contributor.authorShie, Meng-Jeen_US
dc.contributor.authorChu, Ying Haoen_US
dc.contributor.authorHuang, Guewha S.en_US
dc.contributor.authorChen, Po-Chunen_US
dc.contributor.authorChen, Wen Liangen_US
dc.date.accessioned2019-04-03T06:41:06Z-
dc.date.available2019-04-03T06:41:06Z-
dc.date.issued2017-02-06en_US
dc.identifier.issn1556-276Xen_US
dc.identifier.urihttp://dx.doi.org/10.1186/s11671-016-1810-1en_US
dc.identifier.urihttp://hdl.handle.net/11536/144091-
dc.description.abstractThe successful application of a nanostructured biomaterial as an implant is strongly determined by the nanotopography size triggering the ideal cell response. Here, nanoporous topography on 304L stainless steel substrates was engineered to identify the nanotopography size causing a transition in the cellular characteristics, and accordingly, the design of nanostructured stainless steel surface as orthopedic implants is proposed. A variety of nanopore diameters ranging from 100 to 220 nm were fabricated by one-step electrolysis process and collectively referred to as artificial microenvironments. Control over the nanopore diameter was achieved by varying bias voltage. MG63 osteoblasts were cultured on the nanoporous surfaces for different days. Immunofluorescence (IF) and scanning electron microscopy (SEM) were performed to compare the modulation in cell morphologies and characteristics. Osteoblasts displayed differential growth parameters and distinct transition in cell behavior after nanopore reached a certain diameter. Nanopores with 100-nm diameter promoted cell growth, focal adhesions, cell area, viability, vinculin-stained area, calcium mineralization, and alkaline phosphatase activity. The ability of these nanoporous substrates to differentially modulate the cell behavior and assist in identifying the transition step will be beneficial to biomedical engineers to develop superior implant geometries, triggering an ideal cell response at the cell-nanotopography interface.en_US
dc.language.isoen_USen_US
dc.subjectNanotopographyen_US
dc.subjectOsteoblasten_US
dc.subjectNanoporousen_US
dc.subjectStainless steelen_US
dc.subjectExtracellular matrixen_US
dc.subjectArtificial microenvironmenten_US
dc.titleThe Spatiotemporal Control of Osteoblast Cell Growth, Behavior, and Function Dictated by Nanostructured Stainless Steel Artificial Microenvironmentsen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s11671-016-1810-1en_US
dc.identifier.journalNANOSCALE RESEARCH LETTERSen_US
dc.citation.volume12en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000415582500001en_US
dc.citation.woscount2en_US
Appears in Collections:Articles


Files in This Item:

  1. 2ed370d763faf981ec3b057ce73f4337.pdf

If it is a zip file, please download the file and unzip it, then open index.html in a browser to view the full text content.