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Integrated microfluidic array plate (iMAP) for cellular and molecular analysis
Indexado
WoS WOS:000293173300009
Scopus SCOPUS_ID:79960963700
DOI 10.1039/C1LC20105K
Año 2011
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Just as the Petri dish has been invaluable to the evolution of biomedical science in the last 100 years, microfluidic cell assay platforms have the potential to change significantly the way modern biology and clinical science are performed. However, an evolutionary process of creating an efficient microfluidic array for many different bioassays is necessary. Specifically for a complete view of a cell response it is essential to incorporate cytotoxic, protein and gene analysis on a single system. Here we present a novel cellular and molecular analysis platform, which allows access to gene expression, protein immunoassay, and cytotoxicity information in parallel. It is realized by an integrated microfluidic array plate (iMAP). The iMAP enables sample processing of cells, perfusion based cell culture, effective perturbation of biologic molecules or drugs, and simultaneous, real-time optical analysis for different bioassays. The key features of the iMAP design are the interface of on-board gravity driven flow, the open access input fluid exchange and the highly efficient sedimentation based cell capture mechanism (similar to 100% capture rates). The operation of the device is straightforward (tube and pump free) and capable of handling dilute samples (5-cells per experiment), low reagent volumes (50 nL per reaction), and performing single cell protein and gene expression measurements. We believe that the unique low cell number and triple analysis capabilities of the iMAP platform can enable novel dynamic studies of scarce cells.

Revista



Revista ISSN
Lab On A Chip 1473-0197

Métricas Externas



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Disciplinas de Investigación



WOS
Chemistry, Multidisciplinary
Chemistry, Analytical
Biochemical Research Methods
Instruments & Instrumentation
Nanoscience & Nanotechnology
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Dimov, Ivan K. Hombre Dublin City Univ - Irlanda
Universidad de Valparaíso - Chile
Dublin City University - Irlanda
National Centre for Sensor Research - Irlanda
2 Kijanka, Gregor Hombre Dublin City Univ - Irlanda
Dublin City University - Irlanda
National Centre for Sensor Research - Irlanda
3 Park, Younggeun - UNIV CALIF BERKELEY - Estados Unidos
University of California, Berkeley - Estados Unidos
4 Ducree, Jens Hombre Dublin City Univ - Irlanda
Dublin City University - Irlanda
National Centre for Sensor Research - Irlanda
5 Kang, Taewook - Sogang Univ - Corea del Sur
Sogang University - Corea del Sur
6 Lee, Luke P. Hombre UNIV CALIF BERKELEY - Estados Unidos
University of California, Berkeley - Estados Unidos

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Financiamiento



Fuente
Science Foundation Ireland
Irish Cancer Society
Center for Nanostructured Materials Technology
U. S. National Cancer Institute (NCI)
Ministry of Education, Science and Technology, Korea

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



Agradecimiento
The authors would like to thank Dr Arman Rahman for providing the non-adherent plasma cells U266. This work was supported by the Science Foundation Ireland under Grant No. 05/CE3/B754, Irish Cancer Society Research Fellowship Award CRF10KIJ, U. S. National Cancer Institute (NCI) award CCNE-T U54CA151459 and the Center for Nanostructured Materials Technology (Grant Nos. 2010K000352, 2010K000353, and 2010K000354) under "21st Century Frontier R&D Programs" of the Ministry of Education, Science and Technology, Korea.

Muestra la fuente de financiamiento declarada en la publicación.