Consequences of Dispersity on the Self-Assembly of ABA-Type Amphiphilic Block Co-Oligomers

被引:58
作者
Das, Anindita
Petkau-Milroy, Katja [1 ]
Klerks, Gilian
van Genabeek, Bas
Lafleur, Rene P. M.
Palmans, Anja R. A. [1 ]
Meijer, E. W. [1 ]
机构
[1] Eindhoven Univ Technol, Inst Complex Mol Syst, POB 513, NL-5600 MB Eindhoven, Netherlands
来源
ACS MACRO LETTERS | 2018年 / 7卷 / 05期
关键词
DRUG-DELIVERY; POLY(ETHYLENE GLYCOL); COPOLYMERS; POLYMERS; CRYSTALLIZATION; FUNCTIONALIZATION; DESIGN; WELL;
D O I
10.1021/acsmacrolett.8b00168
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Intriguingly, little is known about the impact of dispersity on the crystallization driven self-assembly (CDSA) of amphiphilic block copolymers in aqueous media. Here, we investigate the influence of dispersity on the CDSA of ABA-type amphiphilic block co-oligomers (ABCOs). Two pairs of ABCOs are synthesized comprising discrete (D = 1.00) or disperse (D = 1.20) isotactic L-lactic acid 16-mers as the semicrystalline hydrophobic block and either oligo(ethylene glycol) methyl ether (MeOoEG) or oligo (tetraethylene glycol succinate) (oTEGSuc) as the discrete hydrophilic block. Self-assembly studies in water with 10% THE reveal uniform nanofibers/2D sheets for the discrete oligomers, but such structural regularity is largely compromised in the disperse oligomers. The results are corroborated by sharp melting transitions in both solution and bulk for the discrete ABCOs, unlike their disperse analogues that show a lack of crystallization. Interestingly, the discrete MeOoEG-LLA oligomer reveals crystallization driven gelation, illustrating the contrasting differences between the discrete oligomers and their disperse counterparts.
引用
收藏
页码:546 / 550
页数:9
相关论文
共 32 条
[1]   Formation of Well-Defined, Functional Nanotubes via Osmotically Induced Shape Transformation of Biodegradable Polymersomes [J].
Abdelmohsen, Loai K. E. A. ;
Williams, David S. ;
Pille, Jan ;
Ozel, Sema G. ;
Rikken, Roger S. M. ;
Wilson, Daniela A. ;
van Hest, Jan C. M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (30) :9353-9356
[2]   Synthesis of amphiphilic poly(tetraethylene glycol succinate) and the thermosensitivity of its aggregation in water [J].
Chen, Shusen ;
Wang, Yinong ;
Fan, Yunge ;
Ma, Jianbiao .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2009, 88A (03) :769-777
[3]  
Gilroy JB, 2010, NAT CHEM, V2, P566, DOI [10.1038/NCHEM.664, 10.1038/nchem.664]
[4]   The convergence of synthetic organic and polymer chemistries [J].
Hawker, CJ ;
Wooley, KL .
SCIENCE, 2005, 309 (5738) :1200-1205
[5]   Poly(lactic acid)-poly(ethylene oxide) (PLA-PEG) nanoparticles: NMR studies of the central solidlike PLA core and the liquid PEG corona [J].
Heald, CR ;
Stolnik, S ;
Kujawinski, KS ;
De Matteis, C ;
Garnett, MC ;
Illum, L ;
Davis, SS ;
Purkiss, SC ;
Barlow, RJ ;
Gellert, PR .
LANGMUIR, 2002, 18 (09) :3669-3675
[6]   Template-Assisted Selective Radical Addition toward Sequence-Regulated Polymerization: Lariat Capture of Target Monomer by Template Initiator [J].
Ida, Shohei ;
Ouchi, Makoto ;
Sawamoto, Mitsuo .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (42) :14748-14750
[7]   Biodegradable block copolymers as injectable drug-delivery systems [J].
Jeong, B ;
Bae, YH ;
Lee, DS ;
Kim, SW .
NATURE, 1997, 388 (6645) :860-862
[8]  
Jiang Y, 2016, J AM CHEM SOC, V138, P9369, DOI [10.1021/jacs.6b04964, 10.1021/Jacs.6b04964]
[9]   Poly(ethylene glycol) in Drug Delivery: Pros and Cons as Well as Potential Alternatives [J].
Knop, Katrin ;
Hoogenboom, Richard ;
Fischer, Dagmar ;
Schubert, Ulrich S. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (36) :6288-6308
[10]   A Versatile and Scalable Strategy to Discrete Oligomers [J].
Lawrence, Jimmy ;
Lee, Sang-Ho ;
Abdilla, Allison ;
Nothling, Mitchell D. ;
Ren, Jing M. ;
Knight, Abigail S. ;
Fleischmann, Carolin ;
Li, Youli ;
Abrams, Austin S. ;
Schmidt, Bernhard V. K. J. ;
Hawker, Michael C. ;
Connal, Luke A. ;
McGrath, Alaina J. ;
Clark, Paul G. ;
Gutekunst, Will R. ;
Hawker, Craig J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (19) :6306-6310