Cell-Based Dose Responses from Open-Well Microchambers
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hamon, Morgan | - |
dc.contributor.author | Jambovane, Sachin | - |
dc.contributor.author | Bradley, Lauren | - |
dc.contributor.author | Khademhosseini, Ali | - |
dc.contributor.author | Hong, Jong Wook | - |
dc.date.accessioned | 2021-06-23T03:23:06Z | - |
dc.date.available | 2021-06-23T03:23:06Z | - |
dc.date.created | 2021-01-21 | - |
dc.date.issued | 2013-05 | - |
dc.identifier.issn | 0003-2700 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/27997 | - |
dc.description.abstract | Cell-based assays play a critical role in discovery of new drugs and facilitating research in cancer, immunology, and stem cells. Conventionally, they are performed in Petri dishes, tubes, or well plates, using milliliters of reagents and thousands of cells to obtain one data point. Here, we are introducing a new platform to realize cell-based assay capable of increased throughput and greater sensitivity with a limited number of cells. We integrated an array of open-well microchambers into a gradient generation system. Consequently, cell-based dose responses were examined with a single device. We measured IC50 values of three cytotoxic chemicals, Triton X-100, H2O2 and cadmium chloride, as model compounds. The present system is highly suitable for the discovery of new drugs and studying the effect of chemicals on cell viability or mortality with limited samples and cells. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | Cell-Based Dose Responses from Open-Well Microchambers | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Hong, Jong Wook | - |
dc.identifier.doi | 10.1021/ac400743w | - |
dc.identifier.scopusid | 2-s2.0-84878313798 | - |
dc.identifier.wosid | 000319651100057 | - |
dc.identifier.bibliographicCitation | ANALYTICAL CHEMISTRY, v.85, no.10, pp.5249 - 5254 | - |
dc.relation.isPartOf | ANALYTICAL CHEMISTRY | - |
dc.citation.title | ANALYTICAL CHEMISTRY | - |
dc.citation.volume | 85 | - |
dc.citation.number | 10 | - |
dc.citation.startPage | 5249 | - |
dc.citation.endPage | 5254 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
dc.subject.keywordPlus | MICROFLUIDIC DEVICE | - |
dc.subject.keywordPlus | DRUG DISCOVERY | - |
dc.subject.keywordPlus | ANTITUMOR-ACTIVITY | - |
dc.subject.keywordPlus | PERFUSION CULTURE | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | GENERATION | - |
dc.subject.keywordPlus | CYTOTOXICITY | - |
dc.subject.keywordPlus | ARRAY | - |
dc.subject.keywordPlus | OPTIMIZATION | - |
dc.subject.keywordPlus | MICROARRAY | - |
dc.identifier.url | https://pubs.acs.org/doi/10.1021/ac400743w | - |
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