W. Mehnert and K. Mäder, Solid lipid nanoparticles Production, characterization and applications, Advanced Drug Delivery Reviews, vol.47, issue.2-3, pp.165-196, 2001.
DOI : 10.1016/S0169-409X(01)00105-3

A. J. Almeida and E. Souto, Solid lipid nanoparticles as a drug delivery system for peptides and proteins???, Advanced Drug Delivery Reviews, vol.59, issue.6, pp.478-490, 2007.
DOI : 10.1016/j.addr.2007.04.007

P. Blasi, S. Glovagnoli, A. Schoubben, M. Ricci, and C. Rossi, Solid lipid nanoparticles for targeted brain drug delivery???, Advanced Drug Delivery Reviews, vol.59, issue.6, pp.454-477, 2007.
DOI : 10.1016/j.addr.2007.04.011

H. Huang, S. Barua, G. Sharma, S. K. Dey, and K. Rege, Inorganic nanoparticles for cancer imaging and therapy, Journal of Controlled Release, vol.155, issue.3, pp.344-357, 2011.
DOI : 10.1016/j.jconrel.2011.06.004

S. Bhattacharyya, R. A. Kudgus, R. Bhattacharya, and P. Mukherjee, Inorganic Nanoparticles in Cancer Therapy, Pharmaceutical Research, vol.107, issue.276, pp.237-259, 2011.
DOI : 10.1073/pnas.1006507107

S. J. Son, X. Bai, and S. B. Lee, Inorganic hollow nanoparticles and nanotubes in nanomedicine: Part 1. Drug/gene delivery applications. Drug Discovery Today, pp.650-656, 2007.

B. G. Trewyn, I. I. Slowing, S. Giri, H. Chen, and V. S. Lin, Synthesis and Functionalization of a Mesoporous Silica Nanoparticle Based on the Sol???Gel Process and Applications in Controlled Release, Accounts of Chemical Research, vol.40, issue.9, pp.846-853, 2007.
DOI : 10.1021/ar600032u

C. K. Kim, P. Ghosh, C. Pagliuca, Z. Zhu, S. Menichetti et al., Entrapment of Hydrophobic Drugs in Nanoparticle Monolayers with Efficient Release into Cancer Cells, Journal of the American Chemical Society, vol.131, issue.4, pp.1360-1361, 2009.
DOI : 10.1021/ja808137c

C. S. Kim, G. Y. Tonga, D. Solfiell, and V. M. Rotello, Inorganic nanosystems for therapeutic delivery: Status and prospects, Advanced Drug Delivery Reviews, vol.65, issue.1, pp.93-99, 2013.
DOI : 10.1016/j.addr.2012.08.011

M. A. Mintzer and M. W. Grinstaff, Biomedical applications of dendrimers: a tutorial, Chem. Soc. Rev., vol.229, issue.1, pp.173-190, 2010.
DOI : 10.1148/radiol.2291021033

C. Hawker and J. Frechet, A new convergent approach to monodisperse dendritic macromolecules, J. Chem. Soc., Chem. Commun., vol.102, issue.15, pp.1010-1013, 1990.
DOI : 10.1002/cber.19691020902

E. Buhleier, W. Wehner, and F. Vögtle, "Cascade"- and "Nonskid-Chain-like" Syntheses of Molecular Cavity Topologies, Synthesis, vol.1978, issue.02, pp.155-158, 1978.
DOI : 10.1055/s-1978-24702

H. Arima and K. Motoyama, Recent Findings Concerning PAMAM Dendrimer Conjugates with Cyclodextrins as Carriers of DNA and RNA, Sensors, vol.19, issue.Pt 3, pp.6346-6361, 2009.
DOI : 10.1021/bc800125u

J. Six and Y. Gnanou, From star-shaped to dendritic poly(ethylene oxide)s: Toward increasingly branched architectures by anionic polymerization, Macromolecular Symposia, vol.17, issue.1, pp.137-150, 1995.
DOI : 10.1063/1.1747157

X. Feng, D. Taton, E. L. Chaikof, and Y. Gnanou, Toward an Easy Access to Dendrimer-like Poly(ethylene oxide)s, Journal of the American Chemical Society, vol.127, issue.31, pp.10956-10966, 2005.
DOI : 10.1021/ja0509432

URL : https://hal.archives-ouvertes.fr/hal-00393673

M. E. Fox, F. C. Szoka, and J. M. Frechet, Soluble Polymer Carriers for the Treatment of Cancer: The Importance of Molecular Architecture, Accounts of Chemical Research, vol.42, issue.8, pp.1141-1151, 2009.
DOI : 10.1021/ar900035f

S. Svenson and D. A. Tomalia, Dendrimers in biomedical applications???reflections on the field, Advanced Drug Delivery Reviews, vol.57, issue.15, pp.2106-2129, 2005.
DOI : 10.1016/j.addr.2005.09.018

S. Perrier, C. Barner-kowollik, J. F. Quinn, P. Vana, and T. P. Davis, Origin of Inhibition Effects in the Reversible Addition Fragmentation Chain Transfer (RAFT) Polymerization of Methyl Acrylate, Macromolecules, vol.35, issue.22, pp.8300-8306, 2002.
DOI : 10.1021/ma0203445

J. Wang, K. Matyjaszewski, and . Controlled, Controlled/"living" radical polymerization. atom transfer radical polymerization in the presence of transition-metal complexes, Journal of the American Chemical Society, vol.117, issue.20, pp.5614-5615, 1995.
DOI : 10.1021/ja00125a035

J. Wang, K. Matyjaszewski, and . Controlled, Controlled/"Living" Radical Polymerization. Halogen Atom Transfer Radical Polymerization Promoted by a Cu(I)/Cu(II) Redox Process, Macromolecules, vol.28, issue.23, pp.7901-7910, 1995.
DOI : 10.1021/ma00127a042

K. Matyjaszewski, T. E. Patten, J. Xia, and . Controlled, Controlled/???Living??? Radical Polymerization. Kinetics of the Homogeneous Atom Transfer Radical Polymerization of Styrene, Journal of the American Chemical Society, vol.119, issue.4, pp.674-680, 1997.
DOI : 10.1021/ja963361g

W. Tang and K. Matyjaszewski, , Reverse ATRP and SR&NI ATRP, Macromolecular Theory and Simulations, vol.34, issue.7-8, pp.359-375, 2008.
DOI : 10.1002/aic.690481118

W. Jakubowski and K. Matyjaszewski, Activator Generated by Electron Transfer for Atom Transfer Radical Polymerization, Macromolecules, vol.38, issue.10, pp.4139-4146, 2005.
DOI : 10.1021/ma047389l

K. Min, H. Gao, and K. Matyjaszewski, Preparation of Homopolymers and Block Copolymers in Miniemulsion by ATRP Using Activators Generated by Electron Transfer (AGET), Journal of the American Chemical Society, vol.127, issue.11, pp.3825-3830, 2005.
DOI : 10.1021/ja0429364

W. Jakubowski, K. Min, and K. Matyjaszewski, Activators Regenerated by Electron Transfer for Atom Transfer Radical Polymerization of Styrene, Macromolecules, vol.39, issue.1, pp.39-45, 2006.
DOI : 10.1021/ma0522716

K. Min, H. Gao, and K. Matyjaszewski, Use of Ascorbic Acid as Reducing Agent for Synthesis of Well-Defined Polymers by ARGET ATRP, Macromolecules, vol.40, issue.6, pp.1789-1791, 2007.
DOI : 10.1021/ma0702041

K. Matyjaszewski, H. Dong, W. Jakubowski, J. Pietrasik, and A. Kusumo, Grafting from Surfaces for ???Everyone???:?? ARGET ATRP in the Presence of Air, Langmuir, vol.23, issue.8, pp.4528-4531, 2007.
DOI : 10.1021/la063402e

L. Mueller, W. Jakubowski, W. Tang, and K. Matyjaszewski, Successful Chain Extension of Polyacrylate and Polystyrene Macroinitiators with Methacrylates in an ARGET and ICAR ATRP, Macromolecules, vol.40, issue.18, pp.6464-6472, 2007.
DOI : 10.1021/ma071130w

B. M. Rosen and V. Percec, Single-Electron Transfer and Single-Electron Transfer Degenerative Chain Transfer Living Radical Polymerization, Chemical Reviews, vol.109, issue.11, pp.5069-5119, 2009.
DOI : 10.1021/cr900024j

A. Gennaro and K. Matyjaszewski, Reversible-Deactivation Radical Polymerization in the Presence of Metallic Copper. Comproportionation?Disproportionation Equilibria and Kinetics, Macromolecules, vol.46, pp.3793-3802, 2013.

I. Partie, S. R. Samanta, M. E. Levere, and V. Percec, Synthèse et homopolymérisation de l'ADEGChol par ATRP . (42) SET-LRP of hydrophobic and hydrophilic acrylates in trifluoroethanol, Polymer Chemistry, vol.4, pp.3212-3224, 2013.

H. Fischer, The Persistent Radical Effect In ???Living??? Radical Polymerization, Macromolecules, vol.30, issue.19, pp.5666-5672, 1997.
DOI : 10.1021/ma970535l

H. Fischer, The persistent radical effect in controlled radical polymerizations, Journal of Polymer Science Part A: Polymer Chemistry, vol.28, issue.13, pp.1885-1901, 1999.
DOI : 10.1071/CH9901215

H. Fischer, The Persistent Radical Effect:?? A Principle for Selective Radical Reactions and Living Radical Polymerizations, Chemical Reviews, vol.101, issue.12, pp.3581-3610, 2001.
DOI : 10.1021/cr990124y

H. Zhang, B. Klumperman, W. Ming, H. Fischer, and R. Van-der-linde, Effect of Cu(II) on the Kinetics of the Homogeneous Atom Transfer Radical Polymerization of Methyl Methacrylate, Macromolecules, vol.34, issue.18, pp.6169-6173, 2001.
DOI : 10.1021/ma0104736

Y. A. Kabachii, S. Y. Kochev, L. M. Bronstein, I. B. Blagodatskikh, and P. M. Valetsky, Atom transfer radical polymerization with Ti(III) halides and alkoxides, Polymer Bulletin, vol.50, pp.271-278, 2003.

E. Le-grognec, R. Claverie, and R. Poli, Radical Polymerization of Styrene Controlled by Half-Sandwich Mo(III)/Mo(IV) Couples:?? All Basic Mechanisms Are Possible, Journal of the American Chemical Society, vol.123, issue.39, pp.9513-9524, 2001.
DOI : 10.1021/ja010998d

S. H. Chan, L. S. Lam, C. W. Tse, K. Y. Man, W. T. Wong et al., Photosensitivity of Functional Polystyrene and Poly(methyl methacrylate) Synthesized by Controlled Radical Polymerization, Macromolecules, vol.36, issue.15, pp.5482-5490, 2003.
DOI : 10.1021/ma030161y

H. Yu, Z. Zhang, Z. Cheng, J. Zhu, N. Zhou et al., ATRP of styrene catalyzed by elemental Fe(0) and Br2: An easy and economical ATRP process, Journal of Polymer Science Part A: Polymer Chemistry, vol.90, issue.11, pp.2182-2187, 2012.
DOI : 10.1002/app.12738

D. He, S. K. Noh, and W. S. Lyoo, In situ-generated Ru(III)-mediated ATRP from the polymeric Ru(III) complex in the absence of activator generation agents, Journal of Polymer Science Part A: Polymer Chemistry, vol.101, issue.21, pp.4594-4602, 2011.
DOI : 10.1021/cr940534g

W. Zhang, M. Shiotsuki, and T. Masuda, Synthesis of Substituted Polyacetylenes Grafted with Polystyrene Chains by the Macromonomer Method and Their Characterization, Macromolecular Chemistry and Physics, vol.30, issue.11, pp.933-940, 2006.
DOI : 10.1007/3-540-12793-3_6

E. Duquesne, J. Habimana, P. Degee, and P. Dubois, Nickel-Catalyzed Supported ATRP of Methyl Methacrylate Using Cross-Linked Polystyrene Triphenylphosphine as Ligand, Macromolecules, vol.38, issue.24, pp.9999-10006, 2005.
DOI : 10.1021/ma051413t

P. Lecomte, I. Drapier, P. Dubois, P. Teyssié, and R. Jérôme, Controlled Radical Polymerization of Methyl Methacrylate in the Presence of Palladium Acetate, Triphenylphosphine, and Carbon Tetrachloride, Macromolecules, vol.30, issue.24, pp.7631-7633, 1997.
DOI : 10.1021/ma970890b

T. Pintauer and K. Matyjaszewski, Atom transfer radical addition and polymerization reactions catalyzed by ppm amounts of copper complexes, Chemical Society Reviews, vol.46, issue.6, pp.1087-1097, 2008.
DOI : 10.1039/b714578k

W. Tang, Y. Kwak, W. Braunecker, N. V. Tsarevsky, M. L. Coote et al., Understanding Atom Transfer Radical Polymerization: Effect of Ligand and Initiator Structures on the Equilibrium Constants, Journal of the American Chemical Society, vol.130, issue.32, pp.10702-10713, 2008.
DOI : 10.1021/ja802290a

C. Peng, J. Kong, F. Seeliger, and K. Matyjaszewski, Mechanism of Halogen Exchange in ATRP, Macromolecules, vol.44, issue.19, pp.7546-7557, 2011.
DOI : 10.1021/ma201035u

K. Matyjaszewski, D. A. Shipp, J. Wang, T. Grimaud, and T. Patten, Utilizing Halide Exchange To Improve Control of Atom Transfer Radical Polymerization, Macromolecules, vol.31, issue.20, pp.6836-6840, 1998.
DOI : 10.1021/ma980476r

K. Matyjaszewski and T. P. Davis, Handbook of Radical Polymerization, 2003.
DOI : 10.1002/0471220450

H. Bergenudd, G. Coullerez, and M. Jonsson, Solvent Effects on ATRP of Oligo(ethylene glycol) Methacrylate. Exploring the Limits of Control, Macromolecules, vol.42, issue.9, pp.3302-3308, 2009.
DOI : 10.1021/ma8028425

D. A. Shipp, J. Wang, and K. Matyjaszewski, Synthesis of Acrylate and Methacrylate Block Copolymers Using Atom Transfer Radical Polymerization, Macromolecules, vol.31, issue.23, pp.8005-8008, 1998.
DOI : 10.1021/ma981033q

K. A. Davis and K. Matyjaszewski, -Butyl Acrylate and Preparation of Block Copolymers, Macromolecules, vol.33, issue.11, pp.4039-4047, 2000.
DOI : 10.1021/ma991826s

I. Partie, S. H. Qin, J. Saget, J. R. Pyun, S. J. Jia et al., Synthèse et homopolymérisation de l'ADEGChol par ATRP Synthesis of block, statistical, and gradient copolymers from octadecyl(meth)acrylates using atom transfer radical polymerization, Macromolecules, vol.36, issue.63, pp.8969-8977, 2003.

E. Vargun and A. Usanmaz, Polymerization of 2-hydroxyethyl acrylate in bulk and solution by chemical initiator and by ATRP method, Journal of Polymer Science Part A: Polymer Chemistry, vol.74, issue.17, pp.3957-3965, 2005.
DOI : 10.1248/cpb.48.850

K. Ibrahim, B. Löfgren, and J. Seppälä, Synthesis of tertiary-butyl acrylate polymers and preparation of diblock copolymers using atom transfer radical polymerization, European Polymer Journal, vol.39, issue.10, 2003.
DOI : 10.1016/S0014-3057(03)00128-9

T. E. Patten and K. Matyjaszewski, Atom Transfer Radical Polymerization and the Synthesis of Polymeric Materials, Advanced Materials, vol.10, issue.12, pp.901-915, 1998.
DOI : 10.1002/(SICI)1521-4095(199808)10:12<901::AID-ADMA901>3.0.CO;2-B

W. Van-camp, F. E. Du-prez, and S. Bon, Atom Transfer Radical Polymerization of 1-Ethoxyethyl (Meth)acrylate:?? Facile Route toward Near-Monodisperse Poly((meth)acrylic acid), Macromolecules, vol.37, issue.18, pp.6673-6675, 2004.
DOI : 10.1021/ma0491208

J. Schumers, C. Fustin, A. Can, R. Hoogenboom, U. S. Schubert et al., Are o- Nitrobenzyl (Meth)acrylate Monomers Polymerizable by Controlled-Radical Polymerization? Journal of Polymer Science Part A: Polymer Chemistry, pp.6504-6513, 2009.

K. A. Davis, H. J. Paik, and K. Matyjaszewski, Kinetic Investigation of the Atom Transfer Radical Polymerization of Methyl Acrylate, Macromolecules, vol.32, issue.6, pp.1767-1776, 1999.
DOI : 10.1021/ma9815051

J. Lejnieks, A. Mourran, W. Tillmann, H. Keul, and M. Möller, Thin film of Poly(acrylic acid-co-allyl acrylate) as a Sacrificial Protective Layer for Hydrophilic Self Cleaning Glass, Materials, vol.199, issue.5, pp.3369-3384, 2010.
DOI : 10.1016/S1010-6030(03)00205-3

M. Bednarek and K. Jankova, Novel polymers based on atom transfer radical polymerization of 2-methoxyethyl acrylate, Journal of Polymer Science Part A: Polymer Chemistry, vol.37, issue.3, pp.333-340, 2007.
DOI : 10.1002/pola.21784

K. Matyjaszewski, S. Coca, and C. B. Jasieczek, Polymerization of acrylates by atom transfer radical polymerization. Homopolymerization of glycidyl acrylate, Macromolecular Chemistry and Physics, vol.198, issue.12, pp.4011-4017, 1997.
DOI : 10.1002/macp.1997.021981219

M. Reyes, X. Yu, D. A. Shipp, /. Br, N. et al., Kinetic Analysis of the Atom Transfer Radical Polymerization of Butyl Acrylate Mediated by Cu(I)Br/N,N,N?????,N?????,N?????-Pentamethyldiethylenetriamine, Macromolecular Chemistry and Physics, vol.202, issue.17, pp.3268-3272, 2001.
DOI : 10.1002/1521-3935(20011101)202:17<3268::AID-MACP3268>3.0.CO;2-H

D. J. Haloi, S. Roy, and N. K. Singha, Copper catalyzed atom transfer radical copolymerization of glycidyl methacrylate and 2-ethylhexyl acrylate, Journal of Polymer Science Part A: Polymer Chemistry, vol.20, issue.23, pp.6526-6533, 2009.
DOI : 10.1002/mrc.1260321315

A. A. Kavitha and N. K. Singha, High temperature resistant tailor-made poly(meth)acrylates bearing adamantyl group via atom transfer radical polymerization, Journal of Polymer Science Part A: Polymer Chemistry, vol.203, issue.21, pp.7101-7113, 2008.
DOI : 10.1021/bk-1996-0624.ch011

H. Datta and N. K. Singha, Atom transfer radical polymerization of hexyl acrylate and preparation of its ???all-acrylate??? block copolymers, Journal of Polymer Science Part A: Polymer Chemistry, vol.32, issue.11, pp.3499-3511, 2008.
DOI : 10.1081/MA-100101565

K. L. Beers and K. Matyjaszewski, THE ATOM TRANSFER RADICAL POLYMERIZATION OF LAURYL ACRYLATE, Journal of Macromolecular Science, Part A, vol.38, issue.7, pp.731-739, 2001.
DOI : 10.1081/MA-100103876

L. Liénafa, S. Monge, and J. Robin, A versatile synthesis of poly(lauryl acrylate) using N-(n-octyl)-2-pyridylmethanimine in copper mediated living radical polymerization, European Polymer Journal, vol.45, issue.6, pp.1845-1850, 2009.
DOI : 10.1016/j.eurpolymj.2009.03.014

F. Dutertre, P. Pennarun, O. Colombani, and E. Nicol, Straightforward synthesis of poly(lauryl acrylate)-b-poly(stearyl acrylate) diblock copolymers by ATRP, European Polymer Journal, vol.47, issue.3, pp.343-351, 2011.
DOI : 10.1016/j.eurpolymj.2010.12.003

G. Street, D. Illsley, and S. J. Holder, Optimization of the synthesis of poly(octadecyl acrylate) by atom transfer radical polymerization and the preparation of all comblike amphiphilic diblock copolymers, Journal of Polymer Science Part A: Polymer Chemistry, vol.53, issue.5, pp.1129-1143, 2005.
DOI : 10.1021/bk-2000-0768

S. G. Roos and A. H. Müller, Evidence for chain transfer in the atom transfer radical polymerization of butyl acrylate, Macromolecular Rapid Communications, vol.21, issue.12, pp.864-867, 2000.
DOI : 10.1002/1521-3927(20000801)21:12<864::AID-MARC864>3.0.CO;2-E

I. Partie and I. , Synthèse et homopolymérisation de l'ADEGChol par ATRP . (82) Cai

D. M. Haddleton, M. C. Crossman, B. H. Dana, D. J. Duncalf, A. M. Heming et al., Atom Transfer Polymerization of Methyl Methacrylate Mediated by Alkylpyridylmethanimine Type Ligands, Copper(I) Bromide, and Alkyl Halides in Hydrocarbon Solution, Macromolecules, vol.32, issue.7, pp.2110-2119, 1999.
DOI : 10.1021/ma981670g

H. Zhang and R. Van-der-linde, Atom transfer radical polymerization ofn-butyl acrylate catalyzed by CuBr/N-(n-hexyl)-2-pyridylmethanimine, Journal of Polymer Science Part A: Polymer Chemistry, vol.35, issue.21, pp.3549-3561, 2002.
DOI : 10.1021/ma011575z

H. V. Penfold, S. J. Holder, and B. Mckenzie, Octadecyl acrylate ??? Methyl methacrylate block and gradient copolymers from ATRP: Comb-like stabilizers for the preparation of micro- and nano-particles of poly(methyl methacrylate) and poly(acrylonitrile) by non-aqueous dispersion polymerization, Polymer, vol.51, issue.9, pp.1904-1913, 2010.
DOI : 10.1016/j.polymer.2010.02.029

W. Tang, A. K. Nanda, and K. Matyjaszewski, Effect of [Pyridylmethanimine]/[CuI] Ratio, Ligand, Solvent and Temperature on the Activation Rate Constants in Atom Transfer Radical Polymerization, Macromolecular Chemistry and Physics, vol.34, issue.12, pp.1171-1177, 2005.
DOI : 10.1080/10601329708010308

A. K. Nanda and K. Matyjaszewski, Effect of [PMDETA]/[Cu(I)] Ratio, Monomer, Solvent, Counterion, Ligand, and Alkyl Bromide on the Activation Rate Constants in Atom Transfer Radical Polymerization, Macromolecules, vol.36, issue.5, pp.1487-1493, 2003.
DOI : 10.1021/ma0340107

I. Partie and I. Chapitre, Synthèse de glycopolymère Dex-g-PADEGChol

I. ?. Partie, Chapitre-III : propriétés physico-chimiques et auto-assemblage des Dex-g-PADEGChol

L. Jia, A. Cao, D. Lévy, B. Xu, P. Albouy et al., Smectic polymer vesicles, Smectic polymer vesicles, pp.3446-3451, 2009.
DOI : 10.1039/b907485f

URL : http://arxiv.org/pdf/0904.2749

B. Cabane and S. Hénon, Liquides: Solutions, dispersions, émulsions, gels; édition revue et augmentée.; Belin, pp.147-164, 2007.

C. Nouvel, C. Frochot, V. Sadtler, P. Dubois, E. Dellacherie et al., Polylactide-Grafted Dextrans: Synthesis and Properties at Interfaces and in Solution, Macromolecules, vol.37, issue.13, pp.4981-4988, 2004.
DOI : 10.1021/ma049857x

URL : https://hal.archives-ouvertes.fr/hal-00079353

E. Rotureau, M. Leonard, E. Dellacherie, and A. Durand, Amphiphilic derivatives of dextran: Adsorption at air/water and oil/water interfaces, Journal of Colloid and Interface Science, vol.279, issue.1, pp.68-77, 2004.
DOI : 10.1016/j.jcis.2004.06.040

URL : https://hal.archives-ouvertes.fr/hal-00079357

R. Pinol, L. Jia, F. Gubellini, D. Levy, P. Albouy et al., -Liquid Crystal Polymer:?? The Role of Smectic Order in the Formation of Nanofibers, Macromolecules, vol.40, issue.16, pp.5625-5627, 2007.
DOI : 10.1021/ma071064y

S. Oissé, J. Rieger, A. Di-cicco, P. Albouy, C. Bui et al., Synthesis via RAFT of Amphiphilic Block Copolymers with Liquid-Crystalline Hydrophobic Block and Their Self- Assembly in Water, Polymer vesicles formed by amphiphilic diblock copolymers containing a thermotropic liquid crystalline polymer block, pp.8688-8696, 2005.

J. Yang, R. Piñol, F. Gubellini, D. Lévy, P. Albouy et al., Formation of Polymer Vesicles by Liquid Crystal Amphiphilic Block Copolymers, Langmuir, vol.22, issue.18, pp.7907-7911, 2006.
DOI : 10.1021/la061436g

D. E. Discher and A. Eisenberg, Polymer Vesicles, Science, vol.297, issue.5583, pp.967-973, 2002.
DOI : 10.1126/science.1074972

L. Jia, P. Albouy, A. Cicco, A. Cao, and M. Li, Self-assembly of amphiphilic liquid crystal block copolymers containing a cholesteryl mesogen: Effects of block ratio and solvent, Polymer, vol.52, issue.12, pp.2565-2575, 2011.
DOI : 10.1016/j.polymer.2011.04.001

C. Houga, J. Giermanska, S. Lecommandoux, R. Borsali, D. Taton et al., Micelles and Polymersomes Obtained by Self-Assembly of Dextran and Polystyrene Based Block Copolymers, Biomacromolecules, vol.10, issue.1, pp.32-40, 2009.
DOI : 10.1021/bm800778n

URL : https://hal.archives-ouvertes.fr/hal-00357611

C. Houga, J. L. Meins, R. Borsali, D. Taton, and Y. Gnanou, Synthesis of ATRP-induced dextran-bpolystyrene diblock copolymers and preliminary investigation of their self-assembly in water, Chemical Communications, issue.12, pp.3063-3065, 2007.

J. Babin, D. Taton, M. Brinkmann, and S. Lecommandoux, Synthesis and Self-Assembly in Bulk of Linear and Mikto-Arm Star Block Copolymers Based on Polystyrene and Poly(glutamic acid), Macromolecules, vol.41, issue.4, pp.1384-1392, 2008.
DOI : 10.1021/ma702071y

URL : https://hal.archives-ouvertes.fr/hal-00338966

C. Schatz, S. Louguet, J. Le-meins, and S. Lecommandoux, -polypeptide Copolymer Vesicles: Towards Synthetic Viral Capsids, Angewandte Chemie International Edition, vol.67, issue.14, pp.2572-2575, 2009.
DOI : 10.1002/anie.200805895

D. Wang, J. Tan, H. Kang, L. Ma, X. Jin et al., Synthesis, self-assembly and drug release behaviors of pH-responsive copolymers ethyl cellulose-graft-PDEAEMA through ATRP. Carbohydrate Polymers, pp.195-202, 2011.

W. Yuan, X. Li, S. Gu, A. Cao, and J. Ren, Amphiphilic chitosan graft copolymer via combination of ROP, ATRP and click chemistry: Synthesis, self-assembly, thermosensitivity, fluorescence, and controlled drug release, Polymer, vol.52, issue.3, pp.658-666, 2011.
DOI : 10.1016/j.polymer.2010.12.052

W. Yuan, Z. Zhao, S. Gu, and J. Ren, Synthesis, characterization, and properties of amphiphilic chitosan copolymers with mixed side chains by click chemistry, Journal of Polymer Science Part A: Polymer Chemistry, vol.43, issue.15, pp.3476-3486, 2010.
DOI : 10.1002/pola.24136

X. Wang, Y. Zhai, D. Tang, G. Liu, and Y. Wang, Self-assembly, drug-delivery behavior, and cytotoxicity evaluation of amphiphilic chitosan-graft-poly(1,4-dioxan-2-one) copolymers, Journal of Polymer Research, vol.44, issue.9, pp.1-9, 2012.
DOI : 10.1016/S0032-3861(03)00676-1

W. Liu, Y. Liu, X. Hao, G. Zeng, W. Wang et al., Backbone-collapsed intra- and inter-molecular self-assembly of cellulose-based dense graft copolymer, Carbohydrate Polymers, vol.88, issue.1, pp.290-298, 2012.
DOI : 10.1016/j.carbpol.2011.12.001

.. Synthèse-des-monomères-adegchol-et-achol, i I.1.2 ATRP de l'

-. Ère-Étape-synthèse-du-chol and .. Du-degchol, ii I.2.1.2 2 ème étape : synthèse

). Ère-Étape, vii I.5.2 Fixation des groupements amorceurs sur un DexAc 71 (2 ème étape), Acétylation des fonctions hydroxyle du dextrane

.. Phase-organique, I. Xi, I. Xii, and T. , XIII II, PROPRIETES MESOMORPHES, vol.5, issue.51

I. Schéma, a) dextrane-bpolystyrène , (b) dextrane-b-poly(éthylène glycol), (c) dextrane-b-poly(L-glutamate de ?benzyle, Synthèse de quelques glycopolymères à base de dextrane, p.57

I. Schéma, Croissance de greffons de poly(?-caprolacotone) par ROP à partir d'une surface cellulose, p.60

I. Schéma, Synthèse de glycopolymères CS-g-P(MMA-co-AN) et CS-g-PSS par NMP à partir de chitosane en un milieu hétérogène, p.60

I. Schéma, M. Des-monomères, H. , and A. , (b) Greffage de chaînes de poly(MMA-co-HMA) sur la surface du coton par « chimie click ». PPMI :N-(npropyl )-2-pyridylméthanimine, p.61

I. Schéma, Fonctionnalisation de la cellulose par la poly(?-caprolactone) via une chimie click thiol-ène en milieu hétérogène, p.62

I. Schéma, Schéma de synthèse multi-étapes des glycopolymères (a) Dextrane-g-PLA et (b) dextrane-g-PMMA dans un milieu homogène selon la stratégie « grafting from », p.64

I. Schéma, Schéma de synthèse du glycopolymère Dextrane-g-PHBHV selon la stratégie « grafting onto » par (A) estérification et (B) chimie click, p.67

I. Schéma, Réaction de substitution secondaire du groupement OTs par les ions chlorure, p.83

I. Schéma, Réaction d'élimination du groupement OTs à haute température, p.83

I. Schéma, Hydrolyse de la fonction carbonate de l'AChol dans des conditions basiques, p.89

I. Schéma, Réaction d'équilibre d'une NMP. Cas particulier du nitroxyde TEMPO. k d , k rec sont respectivement les constantes cinétiques de dissociation et de recombinaison, p.93

I. Schéma and .. Et-de-terminaison, Mécanisme général de la polymérisation radicalaire par transfert d'atome (ATRP) K act , k désact , k p, k t , sont respectivement les constantes cinétiques d'activation, désactivation, propagation, p.97

I. Schéma, Comparaison de la croissance des chaînes de polymère en utilisant (a) l'ATRP conventionnelle, (b) l'ATRP avec échange d'halogène. (schéma inspiré de la référence 57 ), p.102

I. Schéma, Equilibre de formation des complexes de Cu I en présence du ligand OPMI dans les solvants polaires et apolaires, p.115

I. Schéma, Mécanisme d'hydrolyse d'un DexAc dans un milieu non anhydre, p.150