Open Access Article
This Open Access Article is licensed under a
Creative Commons Attribution 3.0 Unported Licence

Correction: Toxicity of metal–organic framework nanoparticles: from essential analyses to potential applications

Romy Ettlinger *a, Ulrich Lächelt bc, Ruxandra Gref d, Patricia Horcajada e, Twan Lammers f, Christian Serre g, Patrick Couvreur h, Russell E. Morris a and Stefan Wuttke *ij
aSchool of Chemistry, University of St. Andrews, St. Andrews, UK. E-mail: rle6@st-andrews.ac.uk
bDepartment of Pharmacy and Center for NanoScience (CeNS), Ludwig-Maximilians-Universität München, Munich, Germany
cDivision of Pharmaceutical Technology and Biopharmaceutics, University of Vienna, Vienna, Austria
dInstitut de Sciences Moléculaires d’Orsay, Université Paris Saclay, Paris, France
eMadrid Institute for Advanced Studies, Madrid, Spain
fInstitute for Experimental Molecular Imaging, RWTH Aachen University Clinic, Aachen, Germany
gDépartement de Chimie, Ecole Normale Supérieure de Paris, Paris, France
hInstitut Galien Paris-Sud, Université Paris Saclay, Paris, France
iIkerbasque, Basque Foundation for Science, Bilbao, Spain
jBasque Center for Materials, UPV/EHU Science Park, Leioa, Spain. E-mail: stefan.wuttke@bcmaterials.net

Received 11th January 2023

First published on 19th January 2023


Abstract

Correction for ‘Toxicity of metal–organic framework nanoparticles: from essential analyses to potential applications’ by Romy Ettlinger et al., Chem. Soc. Rev., 2022, 51, 464–484, https://doi.org/10.1039/D1CS00918D.


The authors regret that the information presented in Fig. 12 and discussed in the text on p. 478 may have been unclear, or inconsistent with the information derived from ref. 26. The corrected version of Fig. 12 is presented here. The corresponding sentence on p. 478, beginning, “Herein, endogenous fumaric acid…”, should also be revised as follows:

“Herein, nitro- and tetramethyl-terephthalic acid modifications turned out to be the most biofriendly organic linkers, followed by exogenous trimesic acid, amino-terephthalic acid, and terephthalic acid, and the endogenous fumaric acid had the lowest assessed IC50 value.”


image file: d3cs90014b-f12.tif
Fig. 12 Ranking of different organic linkers, based on their reported IC50 toxicity data.

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


This journal is © The Royal Society of Chemistry 2023
Click here to see how this site uses Cookies. View our privacy policy here.