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Structure-Property Relationships of 3D-Printable Chain-Extended Block Copolymers with Tunable Elasticity and Biodegradability

Authors
Kim, Ryung IlLee, GeonchangLee, Jung-HyunPark, Ji JongLee, Albert S.Hwang, Seung Sang
Issue Date
9-Sep-2021
Publisher
AMER CHEMICAL SOC
Keywords
3D printing; biodegradable polymers; bioelastomer; block copolymer; polyurethane
Citation
ACS APPLIED POLYMER MATERIALS, v.3, no.9, pp.4708 - 4716
Indexed
SCIE
SCOPUS
Journal Title
ACS APPLIED POLYMER MATERIALS
Volume
3
Number
9
Start Page
4708
End Page
4716
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/136373
DOI
10.1021/acsapm.1c00860
ISSN
2637-6105
Abstract
Elastomeric bioscaffolds with tunable elasticity and biodegradability were synthesized via ring opening polymerization of polycaprolactone (PCL) and polylactide (PLA) with a bifunctional polyethylene glycol macroinitiator, followed by chain extension with diisocyanate to form urethane linkages. Through fine tuning of the macroinitiator and PCL/PLA weight fraction and molecular weight, a data set of elastomeric bioscaffolds gives structure-property insights into their thermal, mechanical, and biodegradability properties as they relate to triblock copolymer composition and mechanical weight. These materials were targeted to be 3D-printed by commercial devices, and their unique rheological properties enable impeccable multiscale microstructure formation. Simplicity in synthesis and fabrication as well as tunable biodegradability (1 day to 2 months) and elasticity (modulus 32-94 MPa) suggest the vast wide-ranging utility and prospective application in bioscaffolds for future therapeutic treatments.
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