Bappa
Maiti
ab,
Mohini
Kamra
a,
Anjali A.
Karande
c and
Santanu
Bhattacharya
*ab
aDepartment of Organic Chemistry, Indian Institute of Science, Bangalore 560012, India. E-mail: sb23in@yahoo.com
bDirector's Research Unit, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India
cDepartment of Biochemistry, Indian Institute of Science, Bangalore 560012, India
First published on 5th February 2019
Correction for ‘Transfection efficiencies of α-tocopherylated cationic gemini lipids with hydroxyethyl bearing headgroups under high serum conditions’ by Bappa Maiti et al., Org. Biomol. Chem., 2018, 16, 1983–1993.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
Footnote |
† Electronic supplementary information (ESI) available: Synthetic procedures and characterization details of gemini lipids, 1H NMR spectra of gemini lipids, TE of neat tocopheryl lipids, optimization of the DOPE content in the co-liposomal formulations, hydrodynamic diameters of the lipoplexes, small angle X-ray diffraction of the optimized co-liposomes and lipoplexes, gel electrophoresis data and cellular internalization of lipoplexes with fluorescein labeled pGL3. See DOI: 10.1039/c7ob02835k |
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