Polymer (PCL) fibers with Zn-doped mesoporous bioactive glass nanoparticles for tissue regeneration

被引:16
|
作者
Nescakova, Zuzana [1 ]
Kankova, Hana [1 ]
Galuskova, Dagmar [1 ]
Galusek, Dusan [1 ,2 ]
Boccaccini, Aldo R. [3 ]
Liverani, Liliana [3 ]
机构
[1] A Dubcek Univ Trencin, Ctr Funct & Surface Functionalized Glass, Trencin, Slovakia
[2] FChPT STU, Joint Glass Ctr IIC SAS, TnUAD, Trencin, Slovakia
[3] Univ Erlangen Nurnberg, Inst Biomat, Dept Mat Sci & Engn, D-91058 Erlangen, Germany
关键词
benign solvents; composite fibers; composites; electrospinning; mesoporous bioactive glass nanoparticles; poly(e-caprolactone); tissue engineering; zinc; SURFACE REACTIVITY; BONE; ZINC; SCAFFOLDS; BEHAVIOR; SOL; POLY(EPSILON-CAPROLACTONE); HEALTH;
D O I
10.1111/ijag.16292
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Composite fibrous membranes based on poly(e-caprolactone) (PCL) and mesoporous bioactive glass nanoparticles (MBGNs) were fabricated by electrospinning. MBGNs and Zn-doped MBGNs prepared by microemulsion sol-gel method were successfully incorporated inside the polymeric fibers of 240 and 385 nm in diameter for undoped and Zn-doped PCL_MBGNs fibers, respectively. Thermal analysis showed that the concentration of MBGNs reached a maximum of around 21 wt% for Zn-doped MBGNs. Both PCL_MBGNs and PCL_MBGNs_Zn composite membrane exhibited bioactivity after immersion in simulated body fluid (SBF). X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) showed the evolution of composite membranes, confirming the formation of hydroxyapatite (HAp). However, the degradation products of membranes did not affect the viability and proliferation of murine stromal cells (ST-2) and thus the new fiber structures represent a suitable environment for cell adhesion. Therefore, the incorporation of mesoporous glass nanoparticles doped with therapeutically active Zn2+ ions inside the PCL fibers offers the possibility to create a multifunctional biomaterial suitable for drug delivery and tissue engineering.
引用
收藏
页码:588 / 600
页数:13
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