Coalesced Poly(ε-caprolactone) Fibers Are Stronger

被引:23
作者
Gurarslan, Alper [1 ,2 ]
Caydamli, Yavuz [1 ]
Shen, Jialong [1 ]
Tse, Shiaomeng [3 ]
Yetukuri, Mahijeeth [4 ]
Tonelli, Alan E. [1 ]
机构
[1] N Carolina State Univ, Coll Text, Fiber & Polymer Sci Program, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
[3] North Carolina Sch Sci & Math, Durham, NC 27705 USA
[4] William G Enloe Magnet & GT High Sch, Raleigh, NC 27610 USA
关键词
INCLUSION-COMPOUNDS; POLYMERS; BONE; UREA; COMPOSITES; SCAFFOLDS; COMPOUND;
D O I
10.1021/bm501799y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Melt-spun fibers were made from poly(epsilon-caprolactone) (PCL) coalesced from stoichiometric inclusion complex crystals formed with host urea. Melting and crystallization behaviors, mechanical properties, and the birefringence of undrawn and cold-drawn fibers were investigated. Undrawn coalesced PCL fibers were observed to have 500-600% higher moduli than undrawn as-received (asr) PCL fibers and a modulus comparable to drawn asr PCL fibers. Drawn coalesced PCL fibers have the highest crystallinity, orientation, and 65% higher moduli than drawn asr PCL fibers. Drawn coalesced PCL fibers have only a 5% higher crystallinity than drawn asr PCL fibers, yet they have 65% higher moduli and lower elongation at break values. Clearly, the intrinsic alignment of the coalesced polymers is the reason for their higher moduli and lower elongation, as confirmed by the birefringence observed in drawn coalesced and asr-PCL fibers. The improved mechanical properties of coalesced PCL fibers make them a better candidate for use in tissue engineering as scaffolds.
引用
收藏
页码:890 / 893
页数:4
相关论文
共 19 条
[1]   Factors influencing the small-scale melt spinning of poly(ε-caprolactone) monofilament fibres [J].
Charuchinda, A ;
Molloy, R ;
Siripitayananon, J ;
Molloy, N ;
Sriyai, M .
POLYMER INTERNATIONAL, 2003, 52 (07) :1175-1181
[2]   INCLUSION COMPOUND FORMED BETWEEN POLY(EPSILON-CAPROLACTONE) AND UREA [J].
CHOI, C ;
DAVIS, DD ;
TONELLI, AE .
MACROMOLECULES, 1993, 26 (06) :1468-1470
[3]   REPRESENTING AND UNDERSTANDING GEOMETRIC FEATURES OF ONE-DIMENSIONAL TUNNEL STRUCTURES IN SOLID INCLUSION-COMPOUNDS [J].
GEORGE, AR ;
HARRIS, KDM .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 1995, 13 (03) :138-141
[4]   Single-Component Polymer Composites [J].
Gurarslan, A. ;
Tonelli, A. E. .
MACROMOLECULES, 2011, 44 (10) :3856-3861
[5]   Single-component poly(ε-caprolactone) composites [J].
Gurarslan, Alper ;
Shen, Jialong ;
Tonelli, Alan E. .
POLYMER, 2013, 54 (21) :5747-5753
[6]   Polymers coalesced from their cyclodextrin inclusion complexes: What can they tell us about the morphology of melt-crystallized polymers? [J].
Gurarslan, Alper ;
Joijode, Abhay S. ;
Tonelli, Alan E. .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2012, 50 (12) :813-823
[7]   Behavior of Poly(ε-caprolactone)s (PCLs) Coalesced from Their Stoichiometric Urea Inclusion Compounds and Their Use as Nucleants for Crystallizing PCL Melts: Dependence on PCL Molecular Weights [J].
Gurarslan, Alper ;
Shen, Jialong ;
Tonelli, Alan E. .
MACROMOLECULES, 2012, 45 (06) :2835-2840
[8]  
Houck MM., 2010, FUNDAMENTALS FORENSI
[9]   Scaffolds in tissue engineering bone and cartilage [J].
Hutmacher, DW .
BIOMATERIALS, 2000, 21 (24) :2529-2543
[10]   Structural Properties of Carboxylic Acid Dimers Confined within the Urea Tunnel Structure: An MD Simulation Study [J].
Ilott, Andrew J. ;
Palucha, Sebastian ;
Batsanov, Andrei S. ;
Harris, Kenneth D. M. ;
Hodgkinson, Paul ;
Wilson, Mark R. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2011, 115 (12) :2791-2800