TUNED MECHANICAL PROPERTIES ACHIEVED BY VARYING POLYMER STRUCTURE-KNOWLEDGE THAT GENERATES NEW MATERIALS FOR TISSUE ENGINEERING

Anna Finne Wistrand; Ann-Christine Albertsson

Your Location：

Home >

Browse articles >

TUNED MECHANICAL PROPERTIES ACHIEVED BY VARYING POLYMER STRUCTURE-KNOWLEDGE THAT GENERATES NEW MATERIALS FOR TISSUE ENGINEERING

Invited Paper | Updated：2021-06-21

- TUNED MECHANICAL PROPERTIES ACHIEVED BY VARYING POLYMER STRUCTURE-KNOWLEDGE THAT GENERATES NEW MATERIALS FOR TISSUE ENGINEERING
- TUNED MECHANICAL PROPERTIES ACHIEVED BY VARYING POLYMER STRUCTURE-KNOWLEDGE THAT GENERATES NEW MATERIALS FOR TISSUE ENGINEERING
- 高分子科学（英文版） 2007年第2期页码：113-118
- Affiliations：
  
  1.   Department of Fiber and Polymer Technology Royal Institute of Technology
  2.   Stockholm
  3.   Sweden
- Author bio：
- Funds：
  
  This work was supported by the Swedish Foundation for Strategic Research（No. A302:132）.()
- DOI：
  中图分类号： O631.3
- 纸质出版：2007
- Accepted：
Scan QR Code
[1]Anna Finne Wistrand,Ann-Christine Albertsson.TUNED MECHANICAL PROPERTIES ACHIEVED BY VARYING POLYMER STRUCTURE-KNOWLEDGE THAT GENERATES NEW MATERIALS FOR TISSUE ENGINEERING[J].Chinese Journal of Polymer Science,2007(02):113-118.

TUNED MECHANICAL PROPERTIES ACHIEVED BY VARYING POLYMER STRUCTURE-KNOWLEDGE THAT GENERATES NEW MATERIALS FOR TISSUE ENGINEERING[J]. 2007, (2): 113-118.
[1]Anna Finne Wistrand,Ann-Christine Albertsson.TUNED MECHANICAL PROPERTIES ACHIEVED BY VARYING POLYMER STRUCTURE-KNOWLEDGE THAT GENERATES NEW MATERIALS FOR TISSUE ENGINEERING[J].Chinese Journal of Polymer Science,2007(02):113-118. DOI：

TUNED MECHANICAL PROPERTIES ACHIEVED BY VARYING POLYMER STRUCTURE-KNOWLEDGE THAT GENERATES NEW MATERIALS FOR TISSUE ENGINEERING[J]. 2007, (2): 113-118. DOI：

摘要

<正>By changing both the monomer composition and the polymer structure

we have varied the mechanical properties of resorbable polymers. The polymers were synthesized by ring-opening polymerization using L-lactide （LLA）

ε-caprolactone （εCL）

trimethylene carbonate （TMC） and 1

5-dioxepan-2-one （DXO） as monomers. Well-defined triblock copolymers

microblock copolymers and networks have been evaluated

and comparisons between them show that it is possible to tune the mechanical properties. Triblock copolymers with an amorphous middle block of poly（ 1

5-dioxepan-2-one）（PDXO） and semi-crystalline end-blocks of poly（ε-caprolactone）（PCL） were stronger and had a higher strain at break than triblock copolymers with poly（L-lactide）（PLLA） as end-blocks. Polymers with both DXO and TMC in the amorphous middle-block and PLLA as end-blocks showed a lower stress at break

but the material gained elasticity

a property which is very valuable in tissue engineering. Mechanical properties of networks

synthesized by a novel method

containing PDXO and PCL are also presented. Although it is difficult to compare them with the uncross-linked polymers

this is an additional way to modify and widen the properties.

Abstract

By changing both the monomer composition and the polymer structure

we have varied the mechanical properties of resorbable polymers. The polymers were synthesized by ring-opening polymerization using L-lactide （LLA）

ε-caprolactone （εCL）

trimethylene carbonate （TMC） and 1

5-dioxepan-2-one （DXO） as monomers. Well-defined triblock copolymers

microblock copolymers and networks have been evaluated

and comparisons between them show that it is possible to tune the mechanical properties. Triblock copolymers with an amorphous middle block of poly（ 1

but the material gained elasticity

a property which is very valuable in tissue engineering. Mechanical properties of networks

synthesized by a novel method

containing PDXO and PCL are also presented. Although it is difficult to compare them with the uncross-linked polymers

this is an additional way to modify and widen the properties.

关键词

Keywords

references

浏览量

Downloads

CSCD

文章被引用时，请邮件提醒。

Submit

工具集

关联资源

pH-Responsive L-Cysteine-conjugated Polydopamine Nanocarriers for Controlled Release of Emamectin Benzoate against Pieris brassicae

On-demand Peelable UV-curable Adhesives with Superior Bonding Strength: Rational Molecular Engineering of Cohesion-adhesion Synergy

Preparation and Chiral Recognition Ability of Crystalline Cellulose Phenylcarbamate

Highly Regio- and trans-Selective Ring-opening Metathesis Polymerization of Chiral Aza-norbornene with a Simple Phenylimido-Tungsten Catalyst

Improvements of Hydrophobicity and Toughness of Epoxy Coatings Modified with Hydroxyl-terminated Fluororubber