Auto-assemblage de copolymères à blocs amphiphiles Suming LI
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1 Auto-assemblage de copolymères à blocs amphiphiles Suming LI Institut Européen des Membranes Université de Montpellier Montpellier, France
2 Self-assembly of amphiphilic block copolymers Colloidal systems : - hydrogels, - micelles, - polymersomes... Applications in drug delivery
3 PLA/PEG block copolymers Poly(lactic acid) : PLA Poly(ethylene glycol) : PEG -(--CH-C-) * n - CH 3 -(-CH 2 -CH 2 --) n - - biocompatible - biobased - degradable - Hydrophobic - L- and D-enantiomers - biocompatible - bioresorbable (Mn < 30000) - water soluble
4 Synthesis of ABA and AB-type PLA/PEG copolymers Ring opening polymerization (RP) of lactide with PEG: CH 3 H CH 3 H + H(-CH 2 -CH 2 --) n H H H H-(-C-C-) x -(-CH2 -CH2-) n-(-c-c-) x H CH 3 CH 3 L-Lactide D-lactide DL-lactide PEG Mn=2K - 20K PLLA-PEG-PLLA (L x E y L x ) PDLA-PEG-PDLA (D x E y D x ) PDLLA-PEG-PDLLA (DL x E y DL x ) CH 3 H L-Lactide D-lactide CH 3 H H + H(-CH 2 -CH 2 --) n CH 3 H-(-C-C-) x -(-CH 2 -CH 2 -) n -CH 3 CH 3 mpeg Mn=2K, 5K PLLA-PEG (L x E y ) PDLA-PEG (D x E y )
5 Synthesis of BAB-type PEG-PLA-PEG copolymers by combination of RP and click chemistry n H x Zn(Lac) 2 n H 2x mpeg-plla mpeg L-Lactide H DCC, DMAP mpeg H m 1. MSCl, Et 3 N 2. NaN 3 N 3 m n CuBr, PMDETA 2x n 2x N N N m PEG-PLLA-PEG (E x L y E z )
6 Hydrogels
7 Formation of hydrogels from PLA/PEG aqueous solutions due to stereocomplexation between L-PLA and D-PLA blocks 20% L 12 E 104 L 12 solution after 48h at 25ºC Hydrogel formed by 20% L 12 E 104 L 12 / D 13 E 104 D 13 solution after 48h at 25ºC
8 Stereocomplex of poly(l-lactide) and poly(d-lactide) Both PLLA and PDLA are crystalline polymers with a pseudoorthorhombic crystal of 10 3 helix, ptically active PLLA and PDLA can form a stereocomplex by blending in solution or in melt, with triclinic crystal of 3 1 helix. PLLA Stereocomplex Theta (degree) X-ray diffraction spectra of PLLA and PLLA/PDLA stereocomplex
9 Time-dependent gelation of aqueous solutions of L-PLA/PEG and D-PLA/PEG 250 G' Modulus (Pa) G" Time (hours) Time-dependent changes of storage (G') and loss moduli (G") of a 15% L 12 E 104 L 12 / D 13 E 104 D 13 sample at 37ºC and at 1Hz
10 Release profiles of bovine serum albumin (BSA) 50 15% BSA Released (%) % 25% 30% Time (h) BSA release from L 28 E 113 / D 27 E 113 hydrogels with different concentrations
11 Spherical Micelles
12 Self-assembly micelles prepared by direct dissolution of PLA/PEG in water PLA-PEG diblock PLA-PEG-PLA triblock PEG blocks PLA blocks
13 Size distribution of single and mixed micelles by DLS 100 Lc 21 E 454 L L 21 E 454 L 21 /D 22 E 454 D nm nm Diameter (nm) Diameter (nm)
14 TEM micrographs of L/D mixed micelles L 21 E 454 L 21 + D 22 E 454 D 22
15 Critical micelle concentration determination of PLA/PEG copolymers from surface tension measurements (mn/m) CMC 48 L 12 E lgc (g/l)
16 Determination of the aggregation number (Nagg) of micelles by aqueous GPC L 25 E 114 N agg = M W micelle M W unimer 0.25g/l Mw=7650 Mw= g/l Time (min)
17 Efficient anticancer drug (ovarian cancer, breast cancer, lung cancer ) Poor aqueous solubility (< 0.5 g/ml ) Paclitaxel Taxol : 50:50 (v/v) Cremophor EL and dehydrated alcohol (hypersensitivity, neurotoxicity ) PLA/PEG micelles (great potential as paclitaxel carrier)
18 PTX Paclitaxel release from PLA/PEG micelles in PBS at 37 o C L 12 E 104 L 12 Released TAX (%) L 12 E 104 L 12 /D 13 E 104 D Release time (d)
19 Antitumor efficacy of PTX-loaded micelles as compared to saline and clinical formulation on female mice bearing lung cancer cells 7 Mean relative tumor volume Saline 1-mixed L 12 E 104 Lmicelles 12 /D 13 E 104 D 13 -PTX Clinical Formulation Days after administration
20 Rod-like Micelles
21 TEM micrographs of rod-like micelles obtained from PLA/PEG copolymers with high PEG fraction D 11 E 91 D 11 D 31 E 114
22 Schematic presentation of micelles prepared from high PEG fraction PLA/PEG copolymers (A) micelle with void, (B) rod-like micelle (A) (B)
23 Worm-like Micelles (filomicelles)
24 Morphological changes as a function of E/LA ratio for PEG5000 derived diblock copolymers L 54 E 114 L 63 E nm L 85 E 114 L 63 E nm
25 Morphological changes as a function of E/LA ratio for PEG2000 derived diblock copolymers L 18 E 45 L 22 E 45 1 μm L 41 E 45 L 73 E 45 1μm 1μm 200 nm
26 Polymersomes
27 TEM images of polymersomes obtained from BABtype E 45 L 46 E 113 copolymers a b 200 nm 200 nm c d 100 nm 100 nm
28 Nanotubes
29 TEM images of nanotubes obtained from BAB-type E 12 LA 21 E 45 copolymers a b 200 nm 200 nm c d 200 nm 200 nm
30 TEM images of nanotubes obtained from BAB-type E 12 LA 46 E 113 copolymers a b 200 nm 200 nm c d 200 nm 200 nm
31 AFM images of polymersomes and nanotubes
32 Schematic presentation of polymersomes and nanotubes prepared from PEG-PLA-PEG copolymers N agg f N agg > f Geometry: Thermodynamics: N agg ~ length of the chains
33 Reverse micelles
34 Normal micelles and reverse micelles PLA block PEG block Normal micelle in H 2 Reverse micelle in organic solvents
35 Reverse micelles formation Dissolution of PLA/PEG in toluene-ethanol Addition of water Stirring transparent/translucent (a) (b) (c) (a) D 24 E 182 D 24 (b) D 21 E 91 D 21 (c) E 45 L 6 (a) (b) (c)
36 DLS and TEM of reverse micelles prepared from D21E91D21
37 DLS results of blank reverse micelles Copolymer Water (m<<l) Mean size (nm) E 45 L E 45 L E 113 D E 113 L L 12 E 91 L D 11 E 91 D D 21 E 91 D L 25 E 182 L D 24 E 182 D
38 Conclusion Various colloidals such as hydrogels, spherical and anisotropic micelles, filomicelles, polymersomes and reverse micelles can be obtained by self-assembly of PLA/PEG copolymers, These systems present great potential as injectable drug delivery carriers, in particular proteins, peptides, and hydrophobic anticancer drugs.
39 ACKNWLEDGEMENTS Thi Bich Tran Nguyen, André Deratani Institut Européen des Membranes, Université de Montpellier, France Xiaohan Wu, Vincent Darcos, Abdelslam El Ghzaoui Institut des Biomolécules Max Mousseron, Université de Montpellier, France Liu Yang, Zhongyong Fan Department of Materials Science, Fudan University, Shanghai, China Yourong Duan, Fei Mo Shanghai Cancer Institute, Xietu Road, Shanghai , China Katarzyna Jelonek, Janusz Kasperczyk Canter of Carbon and Polymer Materials, Polish Academy of Sciences, Zabrze, Poland Financial supports : - Ministry of Education of France, - PICS CNRS of France - Chinese Scholarship Council
40 Merci
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