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dc.contributor.authorJin, Tiantian
dc.contributor.authorYan, Sheng
dc.contributor.authorZhang, Jun
dc.contributor.authorYuan, Dan
dc.contributor.authorHuang, Xu-Feng
dc.contributor.authorLi, Weihua
dc.date.accessioned2021-09-02T00:06:02Z
dc.date.available2021-09-02T00:06:02Z
dc.date.issued2016
dc.identifier.issn1932-1058
dc.identifier.doi10.1063/1.4949770
dc.identifier.urihttp://hdl.handle.net/10072/407497
dc.description.abstractWhile neurons and glial cells both play significant roles in the development and therapy of schizophrenia, their specific contributions are difficult to differentiate because the methods used to separate neurons and glial cells are ineffective and inefficient. In this study, we reported a high-throughput microfluidic platform based on the inertial microfluidic technique to rapidly and continuously separate neurons and glial cells from dissected brain tissues. The optimal working condition for an inertial biochip was investigated and evaluated by measuring its separation under different flow rates. Purified and enriched neurons in a primary neuron culture were verified by confocal immunofluorescence imaging, and neurons performed neurite growth after separation, indicating the feasibility and biocompatibility of an inertial separation. Phencyclidine disturbed the neuroplasticity and neuron metabolism in the separated and the unseparated neurons, with no significant difference. Apart from isolating the neurons, purified and enriched viable glial cells were collected simultaneously. This work demonstrates that an inertial microchip can provide a label-free, high throughput, and harmless tool to separate neurological primary cells.
dc.description.peerreviewedYes
dc.languageEnglish
dc.publisherAIP Publishing
dc.relation.ispartofissue3
dc.relation.ispartofjournalBiomicrofluidics
dc.relation.ispartofvolume10
dc.subject.fieldofresearchClassical physics
dc.subject.fieldofresearchOther engineering
dc.subject.fieldofresearchNanotechnology
dc.subject.fieldofresearchcode5103
dc.subject.fieldofresearchcode4099
dc.subject.fieldofresearchcode4018
dc.subject.keywordsScience & Technology
dc.subject.keywordsLife Sciences & Biomedicine
dc.subject.keywordsPhysical Sciences
dc.subject.keywordsBiochemical Research Methods
dc.subject.keywordsBiophysics
dc.titleA label-free and high-throughput separation of neuron and glial cells using an inertial microfluidic platform
dc.typeJournal article
dc.type.descriptionC1 - Articles
dcterms.bibliographicCitationJin, T; Yan, S; Zhang, J; Yuan, D; Huang, X-F; Li, W, A label-free and high-throughput separation of neuron and glial cells using an inertial microfluidic platform, Biomicrofluidics, 2016, 10 (3)
dcterms.dateAccepted2016-05-03
dc.date.updated2021-09-02T00:03:24Z
gro.hasfulltextNo Full Text
gro.griffith.authorZhang, Jun


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