Scaffolds with tuneable hydrophilicity from electrospun microfibers of polylactide and poly(ethylene glycol) mixtures: morphology, drug release behavior, and biocompatibility

被引:20
作者
Llorens, Elena [1 ]
del Valle, Luis J. [1 ]
Ferran, Ricard [1 ]
Rodriguez-Galan, Alfonso [1 ]
Puiggali, Jordi [1 ,2 ]
机构
[1] Univ Politecn Cataluna, ETSEIB, Dept Engn Quim, E-08028 Barcelona, Spain
[2] Univ Politecn Cataluna, CrNE, Ctr Res & Nanoengn, E-08028 Barcelona, Spain
关键词
Scaffolds; Electrospinning; Polylactide; Poly(ethylene glycol); Biocompatibility; TISSUE-ENGINEERING SCAFFOLDS; HYBRID FIBROUS SCAFFOLDS; SOLUBILITY PARAMETER; POLY(L-LACTIC ACID); THERMAL-DEGRADATION; POLYETHYLENE OXIDE; NANOFIBERS; POLYMER; POLYCAPROLACTONE; POLYGLYCOLIDE;
D O I
10.1007/s10965-014-0360-4
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Electrospun mats were obtained from different mixtures of polylactide (PLA) and poly(ethylene glycol) (PEG). Processing conditions were optimized for all compositions and the resulting micro/nanofiber morphologies (i.e., diameter size and surface texture) were characterized by scanning electron microscopy (SEM). NMR and FTIR spectroscopies were employed to verify the final compositions, and thermal properties were evaluated by DSC and TGA. XPS spectroscopy revealed that PEG was mainly deposited on the surfaces of the electrospun micro/nanofibers, leading to smooth textures. Interestingly, PLA/PEG scaffold solubility in ethanol was very different to that in water, since a significant amount of PEG was effectively retained in the PLA matrix after immersion in ethanol whereas only a low level of PEG was retained in the PLA matrix after immersion in water. The hydrophilicities of the scaffolds obtained from PLA/PEG mixtures were consequently higher than that of the PLA, even after exposure to water. As PEG can be used as a sacrificial polymer due to its high solubility in water, it was possible to increase the porosity of PLA/PEG scaffolds. PLA/PEG scaffolds loaded with triclosan (TCS) had very different release profiles in hydrophilic (e. g., PBS) and hydrophobic (e. g., Srensen/ethanol 30: 70v/v) media, while differences were small between scaffolds with different PLA/PEG ratios. TCS-loaded scaffolds exhibited good antibacterial properties for all compositions and allowed the adhesion of epithelial cells (i.e., MDCK and VERO). Significant differences in cell proliferation were found between unloaded and TCS-loaded scaffolds due to the clear improvement in cell colonization observed with increasing PEG content.
引用
收藏
页数:15
相关论文
共 42 条
[21]   Drug release from and hydrolytic degradation of a poly(ethylene glycol) grafted poly (3-hydroxyoctanoate) [J].
Kim, HW ;
Chung, CW ;
Hwang, SJ ;
Rhee, YH .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2005, 36 (1-2) :84-89
[22]   Ibuprofen-Loaded Poly(Lactic Acid) Electrospun Mats: The Morphology, Physicochemical Performance, and In Vitro Drug Release Behavior [J].
Sun, Chenkai ;
Zou, Liming ;
Xu, Yongjing ;
Wang, Yanli .
MACROMOLECULAR MATERIALS AND ENGINEERING, 2020, 305 (12)
[23]   Synthesis of Pentablock and Multibranched Copolymers Bearing Poly(ethylene glycol), Hyperbranched Polyglycidol, and Poly(L-lactide) with Biocompatibility for Controlled Drug Release [J].
Wang, Jing ;
Kim, Min Hee ;
Kang, Dong Eun ;
Suh, Hongsuk ;
Kim, Il .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2012, 50 (13) :2553-2564
[24]   Pulsatile drug release from electrospun poly(ethylene oxide)-sodium alginate blend nanofibres [J].
Kaassis, Abdessamad Y. A. ;
Young, Neil ;
Sano, Naoko ;
Merchant, Hamid A. ;
Yu, Deng-Guang ;
Chatterton, Nicholas P. ;
Williams, Gareth R. .
JOURNAL OF MATERIALS CHEMISTRY B, 2014, 2 (10) :1400-1407
[25]   Preparation and Drug-Release Behavior of Minocycline-Loaded Poly[hydroxyethyl methacrylate-co-poly(ethylene glycol)-methacrylate] Films [J].
Bayramoglu, Guelay ;
Batislam, Ertan ;
Arica, M. Yakup .
JOURNAL OF APPLIED POLYMER SCIENCE, 2009, 112 (02) :1012-1020
[26]   Chitosan-poly(ε-caprolactone)-poly(ethylene glycol) graft copolymers: Synthesis, self-assembly, and drug release behavior [J].
Chen, Chen ;
Cai, Guoqiang ;
Zhang, Haiwen ;
Jiang, Hongliang ;
Wang, Liqun .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2011, 96A (01) :116-124
[27]   Synthesis and in vitro drug release behavior of amphiphilic triblock copolymer nanoparticles based on poly (ethylene glycol) and polycaprolactone [J].
Zhang, Y ;
Zhuo, RX .
BIOMATERIALS, 2005, 26 (33) :6736-6742
[28]   Biocompatibility and drug release behavior of curcumin conjugated gold nanoparticles from aminosilane-functionalized electrospun poly (N-vinyl-2-pyrrolidone) fibers [J].
Kurniawan, Alfin ;
Gunawan, Farrel ;
Nugraha, Adi Tama ;
Ismadji, Suryadi ;
Wang, Meng-Jiy .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 516 (1-2) :158-169
[29]   pH-responsive drug release from functionalized electrospun poly(caprolactone) scaffolds under simulated in vivo environment [J].
Jassal, Manisha ;
Boominathan, Vijay P. ;
Ferreira, Tracie ;
Sengupta, Sukalyan ;
Bhowmick, Sankha .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2016, 27 (13) :1380-1395
[30]   Controlled drug release behavior of metformin hydrogen chloride from biodegradable films based on chitosan/poly(ethylene glycol) methyl ether blend [J].
Sarwar, M. Sohail ;
Ghaffar, Abdul ;
Islam, Atif ;
Yasmin, Farhat ;
Oluz, Zehra ;
Tuncel, Eylul ;
Duran, Hatice ;
Qaiser, Asif Ali .
ARABIAN JOURNAL OF CHEMISTRY, 2020, 13 (01) :393-403