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Proceedings Paper

Towards optical cell transfection inside a micro flow cell
Author(s): H. G. Breunig; A. Uchugonova; K. König
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Paper Abstract

For optical transfection, cells are shortly subjected to intense, focused laser radiation which leads to a temporary opening in the cell membrane. Although the method is very efficient and ensures high cell viability, the targeting of single cells with laser pulses is a tedious and slow approach. We present first measurements aiming at an experimental setup which is suitable for high throughput and automated optical cell transfection. In our setup, cells flow through a micro flow cell where they are spatially confined. The laser radiation is focused into the cell in a way that an elongated focal region is realized. This makes the time consuming aiming of the laser beam at individual cells unnecessary and opens the possibility to develop a completely automated system. The elongated laser focal region is realized by a quasi-Bessel beam which is generated by an axicon lens setup and continuously scanned from side to side of the cell. We present test measurements of the newly employed setup and discuss its suitability to be fully integrated into a flow cell sequencing system.

Paper Details

Date Published: 4 March 2014
PDF: 5 pages
Proc. SPIE 8947, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XII, 89471J (4 March 2014); doi: 10.1117/12.2038454
Show Author Affiliations
H. G. Breunig, Saarland Univ. (Germany)
JenLab GmbH (Germany)
A. Uchugonova, Saarland Univ. (Germany)
JenLab GmbH (Germany)
K. König, Saarland Univ. (Germany)
JenLab GmbH (Germany)


Published in SPIE Proceedings Vol. 8947:
Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XII
Daniel L. Farkas; Dan V. Nicolau; Robert C. Leif, Editor(s)

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