Julien Alliot
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Julien Alliot has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Edmond Gravel
Université Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, 91191, Gif-sur-Yvette, France
2 shared publications - Eric Doris
Université Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, 91191, Gif-sur-Yvette, France
2 shared publications - Frédéric Ducongé
CEA, DRF, Institut of biology JACOB, Molecular Imaging Research Center (MIRCen), Université Paris Saclay, CNRS UMR9199, Fontenay aux roses, France
2 shared publications - Ioanna Theodorou
Molecular Imaging Research Center (MIRCen)
2 shared publications - Cynthia Forier
Molecular Imaging Research Center (MIRCen)
1 shared publication - Dinh-Vu Nguyen
Service de Chimie Bioorganique et de Marquage (SCBM), CEA, Université Paris-Saclay, 91191 Gif-sur-Yvette, France
1 shared publication
Latest Publications
- 20 November 2019
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 55 (99) , 14968-14971
Polyamine transport system-targeted nanometric micelles assembled from epipodophyllotoxin-amphiphiles
Micelle-forming amphiphilic drug conjugates were synthesized starting from a biologically active epipodophyllotoxin derivative which was covalently inserted in between a hydrophilic targeting spermine unit, and a hydrophobic stearyl chain. The amphiphilic drug conjugates were further assembled into the corresponding micelles and evaluated in vitro for the active targeting of tumor cells overexpressing the polyamine transport system.
- 20 November 2019
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 55 (99) , 14968-14971
Polyamine transport system-targeted nanometric micelles assembled from epipodophyllotoxin-amphiphiles
Micelle-forming amphiphilic drug conjugates were synthesized starting from a biologically active epipodophyllotoxin derivative which was covalently inserted in between a hydrophilic targeting spermine unit, and a hydrophobic stearyl chain. The amphiphilic drug conjugates were further assembled into the corresponding micelles and evaluated in vitro for the active targeting of tumor cells overexpressing the polyamine transport system.
- 22 April 2019
- Published by Royal Society of Chemistry (RSC) in Nanoscale
- Vol. 11 (19) , 9756-9759
Tumor targeted micellar nanocarriers assembled from epipodophyllotoxin-based amphiphiles
Micelle-forming amphiphilic drug conjugates were synthesized starting from a biologically active epipodophyllotoxin derivative which was covalently inserted in between a hydrophilic PEG unit and a hydrophobic stearyl chain. The epipodophyllotoxin-containing amphiphiles were assembled into the corresponding micelles which were evaluated in vivo for their tumor targeting properties.
- 22 April 2019
- Published by Royal Society of Chemistry (RSC) in Nanoscale
- Vol. 11 (19) , 9756-9759
Tumor targeted micellar nanocarriers assembled from epipodophyllotoxin-based amphiphiles
Micelle-forming amphiphilic drug conjugates were synthesized starting from a biologically active epipodophyllotoxin derivative which was covalently inserted in between a hydrophilic PEG unit and a hydrophobic stearyl chain. The epipodophyllotoxin-containing amphiphiles were assembled into the corresponding micelles which were evaluated in vivo for their tumor targeting properties.