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차채녕

Cha, Chaenyung
Integrative Biomaterials Engineering Lab.
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dc.citation.endPage 472 -
dc.citation.number 3 -
dc.citation.startPage 465 -
dc.citation.title BIOMEDICAL MICRODEVICES -
dc.citation.volume 15 -
dc.contributor.author Oh, Jonghyun -
dc.contributor.author Kim, Keekyoung -
dc.contributor.author Won, Sung Wook -
dc.contributor.author Cha, Chaenyung -
dc.contributor.author Gaharwar, Akhilesh K. -
dc.contributor.author Selimovic, Seila -
dc.contributor.author Bae, Hojae -
dc.contributor.author Lee, Kwang Ho -
dc.contributor.author Lee, Dong Hwan -
dc.contributor.author Lee, Sang-Hoon -
dc.contributor.author Khademhosseini, Ali -
dc.date.accessioned 2023-12-22T03:45:26Z -
dc.date.available 2023-12-22T03:45:26Z -
dc.date.created 2014-10-27 -
dc.date.issued 2013-06 -
dc.description.abstract Chitosan has been used as a scaffolding material in tissue engineering due to its mechanical properties and biocompatibility. With increased appreciation of the effect of micro- and nanoscale environments on cellular behavior, there is increased emphasis on generating microfabricated chitosan structures. Here we employed a microfluidic coaxial flow-focusing system to generate cell adhesive chitosan microtubes of controlled sizes by modifying the flow rates of a chitosan pre-polymer solution and phosphate buffered saline (PBS). The microtubes were extruded from a glass capillary with a 300 μm inner diameter. After ionic crosslinking with sodium tripolyphosphate (TPP), fabricated microtubes had inner and outer diameter ranges of 70-150 μm and 120-185 μm. Computational simulation validated the controlled size of microtubes and cell attachment. To enhance cell adhesiveness on the microtubes, we mixed gelatin with the chitosan pre-polymer solution. During the fabrication of microtubes, fibroblasts suspended in core PBS flow adhered to the inner surface of chitosan-gelatin microtubes. To achieve physiological pH values, we adjusted pH values of chiotsan pre-polymer solution and TPP. In particular, we were able to improve cell viability to 92 % with pH values of 5.8 and 7.4 for chitosan and TPP solution respectively. Cell culturing for three days showed that the addition of the gelatin enhanced cell spreading and proliferation inside the chitosan-gelatin microtubes. The microfluidic fabrication method for ionically crosslinked chitosan microtubes at physiological pH can be compatible with a variety of cells and used as a versatile platform for microengineered tissue engineering. -
dc.identifier.bibliographicCitation BIOMEDICAL MICRODEVICES, v.15, no.3, pp.465 - 472 -
dc.identifier.doi 10.1007/s10544-013-9746-z -
dc.identifier.issn 1387-2176 -
dc.identifier.scopusid 2-s2.0-84877728399 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/7864 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84877728399 -
dc.identifier.wosid 000318812900009 -
dc.language 영어 -
dc.publisher SPRINGER -
dc.title Microfluidic fabrication of cell adhesive chitosan microtubes -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Chitosan-gelatin hydrogel -
dc.subject.keywordAuthor Microfluidic flow-focusing -
dc.subject.keywordAuthor Microtube -
dc.subject.keywordAuthor Cell
viability
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dc.subject.keywordPlus TISSUE ENGINEERING APPLICATIONS -
dc.subject.keywordPlus REGENERATIVE MEDICINE -
dc.subject.keywordPlus HYDROGELS -
dc.subject.keywordPlus ENCAPSULATION -
dc.subject.keywordPlus MICROSPHERES -
dc.subject.keywordPlus SCAFFOLDS -
dc.subject.keywordPlus MICROFIBERS -
dc.subject.keywordPlus DELIVERY -
dc.subject.keywordPlus SYSTEMS -
dc.subject.keywordPlus MATRIX -

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