Mechanical properties and osteocompatibility of novel biodegradable alanine based polyphosphazenes: Side group effects

被引:91
作者
Sethuraman, Swaminathan [2 ]
Nair, Lakshmi S. [1 ,3 ]
El-Amin, Saadiq [4 ]
Nguyen, My-Tien [5 ]
Singh, Anurima [6 ]
Krogman, Nick [6 ]
Greish, Yaser E. [8 ]
Allcock, Harry R. [6 ]
Brown, Paul W. [7 ]
Laurencin, Cato T. [1 ,3 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Orthopaed Surg, Farmington, CT USA
[2] SASTRA Univ, Ctr Nanotechnol &Adv Biomat, Thanjavur, India
[3] Univ Connecticut, Dept Chem Mat & Biomol Engn, Storrs, CT USA
[4] Hosp Special Surg, Dept Orthopaed Surg, New York, NY 10021 USA
[5] Univ Virginia, Dept Biol, Charlottesville, VA USA
[6] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[7] Penn State Univ, Mat Res Inst, University Pk, PA 16802 USA
[8] United Arab Emirates Univ, Dept Chem, Al Ain, U Arab Emirates
关键词
Biodegradable polyphosphazenes; Mechanical properties; Osteocompatibility; Gene expression; GENE-EXPRESSION; MESSENGER-RNA; OSTEOBLAST PHENOTYPE; CONTROLLED-RELEASE; COLLAGEN-SYNTHESIS; MATRIX PROTEINS; BONE; TISSUE; BIOMATERIALS; DEGRADATION;
D O I
10.1016/j.actbio.2009.12.012
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The versatility of polymers for tissue regeneration lies in the feasibility to modulate the physical and biological properties by varying the side groups grafted to the polymers. Biodegradable polyphosphazenes are high-molecular-weight polymers with alternating nitrogen and phosphorus atoms in the backbone. This study is the first of its kind to systematically investigate the effect of side group structure on the compressive strength of novel biodegradable polyphosphazene based polymers as potential materials for tissue regeneration. The alanine polyphosphazene based polymers, poly(bis(ethyl alanato) phosphazene) (PNEA), poly((50% ethyl alanato) (50% methyl phenoxy) phosphazene) (PNEA(50)mPh(50)), poly((50% ethyl alanato) (50% phenyl phenoxy) phosphazene) (PNEA(50)PhPh(50)) were investigated to demonstrate their mechanical properties and osteocompatibility. Results of mechanical testing studies demonstrated that the nature and the ratio of the pendent groups attached to the polymer backbone play a significant role in determining the mechanical properties of the resulting polymer. The compressive strength of PNEA(50)PhPh(50) was significantly higher than poly(lactide-co-glycolide) (85:15 PLAGA) (p <0.05). Additional studies evaluated the cellular response and gene expression of primary rat osteoblast cells on PNEA, PNEA50mPh50 and PNEA50PhPh50 films as candidates for bone tissue engineering applications. Results of the in vitro osteocompatibility evaluation demonstrated that cells adhere, proliferate, and maintain their phenotype when seeded directly on the surface of PNEA, PNEA(50)mPh(50), and PNEA(50)PhPh(50). Moreover, cells on the surface of the polymers expressed type I collagen, alkaline phosphatase, osteocalcin, osteopontin, and bone sialoprotein, which are characteristic genes for osteoblast maturation, differentiation, and mineralization. (C) 2009 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
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页码:1931 / 1937
页数:7
相关论文
共 48 条
[1]  
Allcock H.R.:., 2002, Chemistry and Applications of Polyphosphazenes
[2]   SYNTHESIS OF POLY[(AMINO ACID ALKYL ESTER)PHOSPHAZENES] [J].
ALLCOCK, HR ;
FULLER, TJ ;
MACK, DP ;
MATSUMURA, K ;
SMELTZ, KM .
MACROMOLECULES, 1977, 10 (04) :824-830
[3]   POLY[(AMINO ACID ESTER)PHOSPHAZENES] AS SUBSTRATES FOR THE CONTROLLED-RELEASE OF SMALL MOLECULES [J].
ALLCOCK, HR ;
PUCHER, SR ;
SCOPELIANOS, AG .
BIOMATERIALS, 1994, 15 (08) :563-569
[4]   POLY(ORGANOPHOSPHAZENES) WITH OLIGOPEPTIDES AS SIDE GROUPS - PROSPECTIVE BIOMATERIALS [J].
ALLCOCK, HR ;
CHANG, JY .
MACROMOLECULES, 1991, 24 (05) :993-999
[5]   HYDROLYSIS PATHWAYS FOR AMINOPHOSPHAZENES [J].
ALLCOCK, HR ;
FULLER, TJ ;
MATSUMURA, K .
INORGANIC CHEMISTRY, 1982, 21 (02) :515-521
[6]   POLY[(AMINO-ACID-ESTER)PHOSPHAZENES] - SYNTHESIS, CRYSTALLINITY, AND HYDROLYTIC SENSITIVITY IN SOLUTION AND THE SOLID-STATE [J].
ALLCOCK, HR ;
PUCHER, SR ;
SCOPELIANOS, AG .
MACROMOLECULES, 1994, 27 (05) :1071-1075
[7]   GLYCERYL POLYPHOSPHAZENES - SYNTHESIS, PROPERTIES, AND HYDROLYSIS [J].
ALLCOCK, HR ;
KWON, S .
MACROMOLECULES, 1988, 21 (07) :1980-1985
[8]   Degradable polyphosphazene/poly(α-hydroxyester) blends:: degradation studies [J].
Ambrosio, AMA ;
Allcock, HR ;
Katti, DS ;
Laurencin, CT .
BIOMATERIALS, 2002, 23 (07) :1667-1672
[9]   Protein release from polyphosphazene matrices [J].
Andrianov, AK ;
Payne, LG .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 31 (03) :185-196
[10]  
[Anonymous], 1990, [No title captured], P163