TY - JOUR
T1 - Cell screening using disposable photonic lab on a chip systems
AU - Ibarlucea, Bergoi
AU - Fernandez-Rosas, Elisabet
AU - Vila-Planas, Jordi
AU - Demming, Stefanie
AU - Nogues, Carme
AU - Plaza, Jose A.
AU - Büttgenbach, Stephanus
AU - Llobera, Andreu
PY - 2010/5/15
Y1 - 2010/5/15
N2 - A low-cost photonic lab on a chip with three different working regimes for cell screening is presented. The proposed system is able to perform scattering, scattering + absorption, and absorption measurements without any modification. Opposite to the standard flow cytometers, in this proposed configuration, a single 30 ms scan allows to obtain information regarding the cell optical properties. An additional novelty is that the whole spectrum is obtained and analyzed, being then possible to determine for each regime which is the optimal working wavelength that would provide the best performance in terms of sensitivity and limit of detection (LOD). Experimental results have provided with an LOD of 54.9 ± 0.7 cells (in the scattering regime using unlabeled cells), 53 ± 1 cells (in the scattering + absorption regime using labeled cells), and 105 ± 4 cells (in the absorption regime using labeled cells). Finally, the system has also been used for measuring the dead/live cell ratio, obtaining LODs between 7.6 ± 0.4% and 6.7 ± 0.3%, depending on the working regime used. © 2010 American Chemical Society.
AB - A low-cost photonic lab on a chip with three different working regimes for cell screening is presented. The proposed system is able to perform scattering, scattering + absorption, and absorption measurements without any modification. Opposite to the standard flow cytometers, in this proposed configuration, a single 30 ms scan allows to obtain information regarding the cell optical properties. An additional novelty is that the whole spectrum is obtained and analyzed, being then possible to determine for each regime which is the optimal working wavelength that would provide the best performance in terms of sensitivity and limit of detection (LOD). Experimental results have provided with an LOD of 54.9 ± 0.7 cells (in the scattering regime using unlabeled cells), 53 ± 1 cells (in the scattering + absorption regime using labeled cells), and 105 ± 4 cells (in the absorption regime using labeled cells). Finally, the system has also been used for measuring the dead/live cell ratio, obtaining LODs between 7.6 ± 0.4% and 6.7 ± 0.3%, depending on the working regime used. © 2010 American Chemical Society.
U2 - https://doi.org/10.1021/ac100590z
DO - https://doi.org/10.1021/ac100590z
M3 - Article
VL - 82
SP - 4246
EP - 4251
JO - Analytical Chemistry
JF - Analytical Chemistry
SN - 0003-2700
ER -