Biocompatible and Biodegradable Poly(trimethylene carbonate)-b-Poly (L-glutamic acid) Polymersomes: Size Control and Stability

被引:151
作者
Sanson, Charles [1 ,2 ]
Schatz, Christophe [1 ,2 ]
Le Meins, Jean-Francois [1 ,2 ]
Brulet, Annie [3 ]
Soum, Alain [1 ,2 ]
Lecommandoux, Sebastien [1 ,2 ]
机构
[1] Univ Bordeaux, ENSCPB, F-33607 Pessac, France
[2] CNRS, Lab Chim Polymeres Organ, UMR5629, Pessac, France
[3] CEA Saclay, CNRS, LLB, UMR12, F-91191 Gif Sur Yvette, France
关键词
EPSILON-CAPROLACTONE POLYMER; BLOCK-COPOLYMER VESICLES; TRIMETHYLENE CARBONATE; NANOPARTICLE FORMATION; CIRCULAR-DICHROISM; DIBLOCK COPOLYMER; IN-VIVO; MICELLES; POLYPEPTIDE; SOLUBILIZATION;
D O I
10.1021/la902786t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Poly(trimethylene carbonate)-b-poly(L-glutamic acid) (PTMC-b-PGA) diblock copolymers have been synthesized by ring-opening polymerization (ROP) of gamma-benzyl-L-glutamate N-carboxyanhydride (BLG) initiated by amino functionalized PTMC and subsequent hydrogenation. Self-assembly in water gave well-defined vesicles which have been Studied combining light and neutron scattering techniques with electron microscopy imaging. The size and dispersity of vesicles have been tuned by varying preparation conditions, direct dissolution, or nanoprecipitation. In addition, PGA conformation could be reversibly manipulated as a function of environmental changes such as pH and ionic strength. Vesicles showed high tolerance and stability toward nonionic surfactant and pH due to a thick membrane and were revealed to be nonpermeable to water. Nevertheless, they can be rapidly degraded by enzymatic hydrolysis of the polycarbonate block. The ability to tune their size through the formation process, their stimuli responsiveness, their high stability, and their biodegradability make them suitable for biomedical applications.
引用
收藏
页码:2751 / 2760
页数:10
相关论文
共 60 条
[21]   Mechanism for rapid self-assembly of block copolymer nanoparticles [J].
Johnson, BK ;
Prud'homme, RK .
PHYSICAL REVIEW LETTERS, 2003, 91 (11)
[22]   CIRCULAR-DICHROISM OF POLYPEPTIDE SOLUTIONS IN VACUUM ULTRAVIOLET [J].
JOHNSON, WC ;
TINOCO, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (12) :4389-&
[23]   EFFECT OF THE CHOLESTEROL CONTENT OF SMALL UNILAMELLAR LIPOSOMES ON THEIR STABILITY INVIVO AND INVITRO [J].
KIRBY, C ;
CLARKE, J ;
GREGORIADIS, G .
BIOCHEMICAL JOURNAL, 1980, 186 (02) :591-598
[24]   Block copolymer vesicles - using concepts from polymer chemistry to mimic biomembranes [J].
Kita-Tokarczyk, K ;
Grumelard, J ;
Haefele, T ;
Meier, W .
POLYMER, 2005, 46 (11) :3540-3563
[25]   Polypeptides and 100 years of chemistry of α-amino acid N-carboxyanhydrides [J].
Kricheldorf, Hans R. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (35) :5752-5784
[26]  
KUMAR M, 2007, P NATL ACAD SCI US
[27]   Biodegradable polycarbonate-b-polypeptide and polyester-b-polypeptide block copolymers:: Synthesis and nanoparticle formation towards biomaterials [J].
Le Hellaye, Maude ;
Fortin, Nicolas ;
Guilloteau, Julien ;
Soum, Alain ;
Lecommandoux, Sebastien ;
Guillaume, Sophie M. .
BIOMACROMOLECULES, 2008, 9 (07) :1924-1933
[28]   On the physics of block copolymers [J].
Lecommandoux, S. ;
Borsali, R. .
POLYMER INTERNATIONAL, 2006, 55 (10) :1161-1168
[29]   Tumor pH-responsive flower-like micelles of poly(L-lactic acid)-b-poly (ethylene glycol)-b-poly(L-histidine) [J].
Lee, Eun Seong ;
Oh, Kyung Taek ;
Kim, Dongin ;
Youn, Yu Seok ;
Bae, You Han .
JOURNAL OF CONTROLLED RELEASE, 2007, 123 (01) :19-26
[30]   A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures: micelles, nanospheres, nanocapsules and polymersomes [J].
Letchford, Kevin ;
Burt, Helen .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2007, 65 (03) :259-269