Claudie BOURGAUX

Dr. Claudie BOURGAUX


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
9 November 2011 in Nucleic Acids Research
Verified
Journal Article
Open access
PDF file
VAVanessa Allain
Vanessa Allain
CBClaudie BOURGAUX
Claudie BOURGAUX
PCPatrick Couvreur
Patrick Couvreur
This short review aims at presenting some recent illustrative examples of spontaneous nucleolipids self-assembly. High-resolution structural investigations reveal the diversity and complexity of assemblies formed by these bioinspired amphiphiles, resulting from the interplay between aggregation of the lipid chains and base–base interactions. Nucleolipids supramolecular assemblies are promising soft drug delivery systems, particularly for nucleic acids. Regarding prodrugs, squalenoylation is an innovative concept for improving efficacy and delivery of nucleosidic drugs.

16 October 2019 in ACS Applied Nano Materials
Verified
Journal Article
Closed access
MSMarlon Nunes da Silva
Marlon Nunes da Silva
JCJosé Miranda de Carvalho
José Miranda de Carvalho
MFMarcia C Carvalho de Abreu FANTINI
Marcia C Carvalho de Abreu FANTINI
LCLeila Chiavacci
Leila Chiavacci
CBClaudie BOURGAUX
Claudie BOURGAUX

11 March 2011 in European Journal of Organic Chemistry
Verified
Journal Article
Closed access
PDF file
JCJoachim Caron
Joachim Caron
ELElise Lepeltier
Elise Lepeltier
LRL. Harivardhan Reddy
L. Harivardhan Reddy
SLSinda Lepêtre‐Mouelhi
Sinda Lepêtre‐Mouelhi
SWSéverine Wack
Séverine Wack
DDDidier Desmaële
Didier Desmaële

28 August 2009 in Journal of Thermal Analysis and Calorimetry
Verified
Journal Article
Closed access
PDF file
BPBarbara Pili
Barbara Pili
CBClaudie BOURGAUX
Claudie BOURGAUX
FMFlorian Meneau
Florian Meneau
PCPatrick Couvreur
Patrick Couvreur
MOMichel Ollivon
Michel Ollivon

30 May 2014 in Langmuir
Verified
Journal Article
Closed access
ELElise Lepeltier
Elise Lepeltier
CBClaudie BOURGAUX
Claudie BOURGAUX
AMAndrey Maksimenko
Andrey Maksimenko
FMFlorian Meneau
Florian Meneau
VRVeronique Rosilio
Veronique Rosilio
PCPatrick Couvreur
Patrick Couvreur

1 April 2015 in European Journal of Nanomedicine
Verified
Journal Article
Closed access
EMEloisa Berbel Manaia
Eloisa Berbel Manaia
RKRenata Cristina Kiatkoski Kaminski
Renata Cristina Kiatkoski Kaminski
BCBruno Leonardo Caetano
Bruno Leonardo Caetano
VBValérie Briois
Valérie Briois
LCLeila Chiavacci
Leila Chiavacci
CBClaudie BOURGAUX
Claudie BOURGAUX
Nanocrystals of ZnO are currently attracting great interest as potential labels for biological applications, such as theranostic devices, due to their luminescent properties and low toxicity in vivo. It has been reported that doping with Mg 2+ ions could enhance the luminescence of ZnO quantum dots (QDs). In the present study Mg-doped ZnO QDs were synthesized by a hydrolysis and condensation reaction. Surface modification of the QDs was performed using oleic acid (OA) to hinder their aggregation and to provide them colloidal stability in non-polar environments. Mg 2+ ions could be incorporated into the ZnO wurtzite lattice owing to the very close values of the Mg 2+ and Zn 2+ ion radii. However, the dopant ions strongly influenced the growth and final size of ZnO nanocrystals, as evidenced by time-resolved synchrotron SAXS measurements. The presence of Mg prevented the aggregation of the primary nanoparticles. Doping with Mg 2+ ions widened the band gap of ZnO QDs and enhanced their visible luminescence. With increasing proportion of Mg 2+ ions, both the absorption and emission spectra experienced a blue shift. The luminescence went through a maximum for a 20 mol% nominal concentration of Mg 2+ ions in the reaction medium. The quantum yield (QY) of 20 mol% Mg-doped ZnO colloidal suspension (64%) was about 6 times higher than that of the ZnO suspension (10%). Mg-doped ZnO QDs capped by OA formed stable colloidal dispersions in chloroforme, with strong visible fluorescence (QY=38%), promising for biological imaging.