The study of the pseudo-polyrotaxane architecture as a route for mild surface functionalization by click chemistry of poly(ε-caprolactone)-based electrospun fibers

被引:10
|
作者
Oster, M. [1 ]
Schlatter, G. [1 ]
Gallet, S. [1 ]
Baati, R. [1 ]
Pollet, E. [1 ]
Gaillard, C. [2 ]
Averous, L. [1 ]
Fajolles, C. [3 ]
Hebraud, A. [1 ]
机构
[1] Univ Strasbourg, ICPEES, UMR 7515, ECPM,CNRS, 25 Rue Becquerel, F-67087 Strasbourg, France
[2] UR 1268 Biopolymeres Interact Assemblages INRA BP, 627 Rue Geraudiere, F-44316 Nantes 3, France
[3] CEA Saclay, UMR3299 SIS2M, IRAMIS, LIONS, Batiment 125,PC 9, F-91191 Gif Sur Yvette, France
关键词
RING-OPENING POLYMERIZATION; NANOFIBERS; CYCLODEXTRIN;
D O I
10.1039/c6tb03089k
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Polycaprolactone (PCL) electrospun fibers are widely developed for biomedical applications. However, their hydrophobicity and passivity towards cell growth is an important limitation. An original method to functionalize PCL nanofibers, making them reactive for bioconjugation of proteins or other molecules of interest in water under mild conditions, is reported here. This method involves the preparation of pseudo-polyrotaxanes (pPRs) of cyclodextrin (CD) and PCL. Core: shell PCL: pPR fibers were then prepared by coaxial electrospinning in order to bring available reactive hydroxyl groups from the CD to the fiber surface. Different pPR architectures (star, miktoarm and block-copolymer-like) were synthesized to study the effect of the pPR structure on fiber morphology and surface reactivity by grafting fluorescein isothiocyanate (FITC). Finally, bicyclononyne groups were grafted onto the star-pPR based fibers allowing the conjugation of a fluorescent dye by click chemistry in water without any copper catalyst proving the potential of the method for the biofunctionalization of PCL-based fibers.
引用
收藏
页码:2181 / 2189
页数:9
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