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Lab on a Chip CORRECTION Cite this: Lab Chip, 2022, 22, 652 DOI: 10.1039/d1lc90127c rsc.li/loc Correction: Quantifying nanotherapeutic penetration using a hydrogel-based microsystem as a new 3D in vitro platform Saba Goodarzi, a Audrey Prunet, a Fabien Rossetti, a Guillaume Bort, a Olivier Tillement, a Erika Porcel, b Sandrine Lacombe, b Ting-Di Wu, cd Jean-Luc Guerquin-Kern, cd Hélène Delanoë-Ayari, a François Lux ae and Charlotte Rivière * ae Correction for Quantifying nanotherapeutic penetration using a hydrogel-based microsystem as a new 3D in vitro platformby Saba Goodarzi et al., Lab Chip, 2021, 21, 24952510, DOI: 10.1039/D1LC00192B. In Fig. 2E the legend of the graph should be inversed. The corrected legend is: white bars#2D, black bars#3D. The corrected figure is shown below. 652 | Lab Chip, 2022, 22, 652653 This journal is © The Royal Society of Chemistry 2022 a University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière, F-69622, Villeurbanne, France. E-mail: [email protected] b Université Paris-Saclay, CNRS, Institut des Sciences Moléculaires d'Orsay, 91405, Orsay, France c Institut Curie, Université PSL, Paris, France d Université Paris-Saclay, CNRS, Inserm, Centre d'Imagerie Multimodale, 91401, Orsay, France e Institut Universitaire de France (IUF), France Open Access Article. Published on 17 December 2021. Downloaded on 7/23/2022 2:37:46 PM. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. View Article Online View Journal | View Issue

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Page 1: View Article Online

Lab on a Chip

CORRECTION

Cite this: Lab Chip, 2022, 22, 652

DOI: 10.1039/d1lc90127c

rsc.li/loc

Correction: Quantifying nanotherapeuticpenetration using a hydrogel-based microsystemas a new 3D in vitro platform

Saba Goodarzi,a Audrey Prunet,a Fabien Rossetti,a Guillaume Bort,a

Olivier Tillement,a Erika Porcel,b Sandrine Lacombe,b Ting-Di Wu,cd

Jean-Luc Guerquin-Kern,cd Hélène Delanoë-Ayari,a

François Luxae and Charlotte Rivière*ae

Correction for ‘Quantifying nanotherapeutic penetration using a hydrogel-based microsystem as a new 3D

in vitro platform’ by Saba Goodarzi et al., Lab Chip, 2021, 21, 2495–2510, DOI: 10.1039/D1LC00192B.

In Fig. 2E the legend of the graph should be inversed. The corrected legend is: white bars#2D, black bars#3D. The correctedfigure is shown below.

652 | Lab Chip, 2022, 22, 652–653 This journal is © The Royal Society of Chemistry 2022

a University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière, F-69622, Villeurbanne, France. E-mail: [email protected] Université Paris-Saclay, CNRS, Institut des Sciences Moléculaires d'Orsay, 91405, Orsay, Francec Institut Curie, Université PSL, Paris, FrancedUniversité Paris-Saclay, CNRS, Inserm, Centre d'Imagerie Multimodale, 91401, Orsay, Francee Institut Universitaire de France (IUF), France

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Page 2: View Article Online

Lab Chip, 2022, 22, 652–653 | 653This journal is © The Royal Society of Chemistry 2022

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.

Fig. 2 Quantification of penetration and cellular uptake of AGuIX®-Cy5.5 nanoparticles in HCT-116 tumour spheroids and monolayer cell culture.(A) Representative confocal fluorescence images of HCT-116 spheroids incubated with 0.8, 1.5 and 2 mM concentration of AGuIX®-Cy5.5 for 24 hfor four different depths (0, 30, 60 and 90 μm). (B) Mean intensity along with standard deviation (light colors) of AGuIX®-Cy5.5 as a function of thedistance from the spheroid periphery (see the orthogonal view in the inset, green = nuclei, red = AGuIX®-Cy5.5) for 0.8 mM (yellow, N = 73), 1.5mM (green, N = 68) and 2 mM (red, N = 121); three independent experiments. (C) Representative confocal fluorescence images of monolayerHCT-116 cells exposed to AGuIX®-Cy5.5 nanoparticles with 0.8, 1.5 and 2 mM concentration. (D) Quantification of the mean intensity of AGuIX®-Cy5.5 nanoparticles in maximal projection of confocal fluorescence images of monolayer cells after 24 h of incubation with different AGuIX®-Cy5.5 concentrations: 0.8 mM (yellow, N = 40), 1.5 mM (green, N = 40) and 2 mM (red, N = 40); three independent experiments. Error bars repre-sent the standard deviations. (E) Mean and standard deviation of the concentration of Gd (ppb μm−3) uptaken by the cells after incubation with 0.8,1.5 and 2 mM concentration of AGuIX® for 24 h in HCT-116 cell spheroids and monolayer cell culture measured with ICP-MS (N = 6, two indepen-dent experiments).

Lab on a Chip Correction

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