Transfection in perfused microfluidic cell culture devices: A case study.

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Title: Transfection in perfused microfluidic cell culture devices: A case study.
Authors: Raimes, William1, Rubi, Mathieu1, Super, Alexandre1, Marques, Marco P.C.1, Veraitch, Farlan1, Szita, Nicolas1 n.szita@ucl.ac.uk
Source: Process Biochemistry. Aug2017 Part B, Vol. 59, p297-302. 6p.
Subjects: Cell culture, Gene transfection, Microfluidics, Cellular therapy, Pluripotent stem cells, Fluorescein
Abstract: Automated microfluidic devices are a promising route towards a point-of-care autologous cell therapy. The initial steps of induced pluripotent stem cell (iPSC) derivation involve transfection and long term cell culture. Integration of these steps would help reduce the cost and footprint of micro-scale devices with applications in cell reprogramming or gene correction. Current examples of transfection integration focus on maximising efficiency rather than viable long-term culture. Here we look for whole process compatibility by integrating automated transfection with a perfused microfluidic device designed for homogeneous culture conditions. The injection process was characterised using fluorescein to establish a LabVIEW-based routine for user-defined automation. Proof-of-concept is demonstrated by chemically transfecting a GFP plasmid into mouse embryonic stem cells (mESCs). Cells transfected in the device showed an improvement in efficiency (34%, n = 3) compared with standard protocols (17.2%, n = 3). This represents a first step towards microfluidic processing systems for cell reprogramming or gene therapy. [ABSTRACT FROM AUTHOR]
Copyright of Process Biochemistry is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Engineering Source
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DbLabel: Engineering Source
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  Data: <searchLink fieldCode="DE" term="%22Cell+culture%22">Cell culture</searchLink><br /><searchLink fieldCode="DE" term="%22Gene+transfection%22">Gene transfection</searchLink><br /><searchLink fieldCode="DE" term="%22Microfluidics%22">Microfluidics</searchLink><br /><searchLink fieldCode="DE" term="%22Cellular+therapy%22">Cellular therapy</searchLink><br /><searchLink fieldCode="DE" term="%22Pluripotent+stem+cells%22">Pluripotent stem cells</searchLink><br /><searchLink fieldCode="DE" term="%22Fluorescein%22">Fluorescein</searchLink>
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  Data: Automated microfluidic devices are a promising route towards a point-of-care autologous cell therapy. The initial steps of induced pluripotent stem cell (iPSC) derivation involve transfection and long term cell culture. Integration of these steps would help reduce the cost and footprint of micro-scale devices with applications in cell reprogramming or gene correction. Current examples of transfection integration focus on maximising efficiency rather than viable long-term culture. Here we look for whole process compatibility by integrating automated transfection with a perfused microfluidic device designed for homogeneous culture conditions. The injection process was characterised using fluorescein to establish a LabVIEW-based routine for user-defined automation. Proof-of-concept is demonstrated by chemically transfecting a GFP plasmid into mouse embryonic stem cells (mESCs). Cells transfected in the device showed an improvement in efficiency (34%, n = 3) compared with standard protocols (17.2%, n = 3). This represents a first step towards microfluidic processing systems for cell reprogramming or gene therapy. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of Process Biochemistry is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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      – Type: doi
        Value: 10.1016/j.procbio.2016.09.006
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      – Code: eng
        Text: English
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        StartPage: 297
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        Type: general
      – SubjectFull: Gene transfection
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      – SubjectFull: Microfluidics
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      – SubjectFull: Cellular therapy
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      – SubjectFull: Pluripotent stem cells
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      – SubjectFull: Fluorescein
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      – TitleFull: Transfection in perfused microfluidic cell culture devices: A case study.
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            NameFull: Raimes, William
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            NameFull: Marques, Marco P.C.
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              Text: Aug2017 Part B
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              Y: 2017
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