Adeline
Perro
*a,
Gwenaelle
Lebourdon
a,
Sarah
Henry
b,
Sophie
Lecomte
b,
Laurent
Servant
a and
Samuel
Marre
*c
aInstitut des Sciences Moléculaires, Université de Bordeaux—CNRS, 351 cours de la libération, 33405, Talence, France. E-mail: adeline.perro@enscbp.fr
bChimie et Biologie des Membranes et des Nanoobjets, Université de Bordeaux —CNRS, 2 rue Robert Escarpit, 33607, Pessac, France
cICMCB, CNRS, Univ. Bordeaux, F-33600, Pessac, France. E-mail: samuel.marre@icmcb.cnrs.fr
First published on 10th October 2016
Correction for ‘Combining microfluidics and FT-IR spectroscopy: towards spatially resolved information on chemical processes' by Adeline Perro et al., React. Chem. Eng., 2016, DOI: 10.1039/c6re00127k.
Fig. 5 (I) Schematic view of the procedure of seeding live cells on an ATR device. FTIR images generated using the 1535 cm−1 band (adapted from ref. 54. Copyright 2013 RSC publications). (II) Left: Schematic view of the microfluidic open channel device. The living cells are maintained in a thin film of fluid and nutrients are supplied from the media channel below the membrane. Right: Stability of the IR measurements of cells over a week (adapted with permission from ref. 57 (K. Loutherback, L. Chen and H.-Y. N. Holman, Anal. Chem., 2015, 87, 4601). Copyright 2015 American Chemical Society).
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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