Fabrication and application of coaxial polyvinyl alcohol/chitosan nanofiber membranes

被引:32
作者
Kuo, Ting-Yun [1 ]
Jhang, Cuei-Fang [1 ]
Lin, Che-Min [1 ]
Hsien, Tzu-Yang [2 ]
Hsieh, Hsyue-Jen [1 ]
机构
[1] Natl Taiwan Univ, Dept Chem Engn, Taipei 106, Taiwan
[2] China Univ Technol, Gen Educ Ctr, Taipei 116, Taiwan
来源
OPEN PHYSICS | 2017年 / 15卷 / 01期
关键词
electrospinning; core/shell structures; gum arabic; drug release; Korsmeyer-Peppas model; CORE-SHELL NANOFIBERS; CHITOSAN NANOFIBERS; POLYMER NANOFIBERS; CONTROLLED-RELEASE; FIBERS; DEGRADATION;
D O I
10.1515/phys-2017-0125
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
It is difficult to fabricate chitosan-wrapped coaxial nanofibers, because highly viscous chitosan solutions might hinder the manufacturing process. To overcome this difficulty, our newly developed method, which included the addition of a small amount of gum arabic, was utilized to prepare much less viscous chitosan solutions. In this way, coaxial polyvinyl alcohol (PVA)/chitosan (as core/shell) nanofiber membranes were fabricated successfully by coaxial electrospinning. The core/shell structures were confirmed by TEM, and the existence of PVA and chitosan was also verified using FT-IR and TGA. The tensile strength of the nanofiber membranes was increased from 0.6-0.7 MPa to 0.8-0.9 MPa after being crosslinked with glutaraldehyde. The application potential of the PVA/chitosan nanofiber membranes was tested in drug release experiments by loading the core (PVA) with theophylline as a model drug. The use of the coaxial PVA/chitosan nanofiber membranes in drug release extended the release time of theophylline from 5 minutes to 24 hours. Further, the release mechanisms could be described by the Korsmeyer-Peppas model. In summary, by combining the advantages of PVA and chitosan (good mechanical strength and good biocompatibility respectively), the coaxial PVA/chitosan nanofiber membranes are potential biomaterials for various biomedical applications.
引用
收藏
页码:1004 / 1014
页数:11
相关论文
共 31 条
[1]   Theophylline particle design using chitosan by the spray drying [J].
Asada, M ;
Takahashi, H ;
Okamoto, H ;
Tanino, H ;
Danjo, K .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 270 (1-2) :167-174
[2]   Nanowire-in-Microtube Structured Core/Shell Fibers via Multifluidic Coaxial Electrospinning [J].
Chen, Hongyan ;
Wang, Nu ;
Di, Jiancheng ;
Zhao, Yong ;
Song, Yanlin ;
Jiang, Lei .
LANGMUIR, 2010, 26 (13) :11291-11296
[3]   Electrospun collagen-chitosan nanofiber: A biomimetic extracellular matrix for endothelial cell and smooth muscle cell [J].
Chen, Z. G. ;
Wang, P. W. ;
Wei, B. ;
Mo, X. M. ;
Cui, F. Z. .
ACTA BIOMATERIALIA, 2010, 6 (02) :372-382
[4]   Modeling and comparison of dissolution profiles [J].
Costa, P ;
Manuel, J ;
Lobo, S .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 13 (02) :123-133
[5]  
Dash S, 2010, ACTA POL PHARM, V67, P217
[6]   Thermal Stability and Degradation of Chitosan Modified by Acetophenone [J].
Diab, M. A. ;
El-Sonbati, A. Z. ;
Bader, D. M. D. ;
Zoromba, M. Sh. .
JOURNAL OF POLYMERS AND THE ENVIRONMENT, 2012, 20 (01) :29-36
[7]  
DOSHI J, 1995, J ELECTROSTAT, V35, P151, DOI 10.1016/0304-3886(95)00041-8
[8]  
Gilman J.W., 1995, P ACS S FIR POL AM C, P161, DOI DOI 10.1021/BK-1995-0599.CH01
[9]   Refractive index, surface tension, and density of aqueous mixtures of carboxylic acids at 298.15 K [J].
Granados, Karla ;
Gracia-Fadrique, Jesus ;
Amigo, Alfredo ;
Bravo, Ramon .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2006, 51 (04) :1356-1360
[10]  
Haider A., ARAB J CHEM IN PRESS