File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

차채녕

Cha, Chaenyung
Integrative Biomaterials Engineering Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 700 -
dc.citation.number 2 -
dc.citation.startPage 691 -
dc.citation.title BIOMACROMOLECULES -
dc.citation.volume 19 -
dc.contributor.author Jang, Jinhyeong -
dc.contributor.author Cha, Chaenyung -
dc.date.accessioned 2023-12-21T21:10:26Z -
dc.date.available 2023-12-21T21:10:26Z -
dc.date.created 2018-02-23 -
dc.date.issued 2018-02 -
dc.description.abstract Hydrogels possess favorable physical properties ideally suited for various biotechnology applications. To tailor to specific needs, a number of modification strategies have been employed to tune their properties. Herein, a multifunctional polymeric cross-linker based on polyaspartamide is developed, which allows for the facile adjustment of the type and number of reactive functional groups to fit different reaction schemes and control the physical properties of the hydrogels. The amine-based nucleophiles containing desired functional groups are reacted with polysuccinimide to synthesize polyaspartamide cross-linkers. The cross-linking density and the concurrent change in mechanical properties of the resulting hydrogels are controlled in a wide range only with the degree of substitution. This multivalency of the polyaspartamide linkers also induced the degradation of hydrogels by the unreacted functional groups on polyaspartamide involved in the hydrolysis. Furthermore, the polyaspartamide cross-linker conjugated with cell-recognition molecules via the same conjugation mechanism (i.e., nucleophilic substitution) render the hydrogels cell-responsive without the need of additional processing steps. This versatility of polyaspartamide-based cross-linker is expected to provide an efficient and versatile route to engineer hydrogels with controllable properties for biomedical applications. -
dc.identifier.bibliographicCitation BIOMACROMOLECULES, v.19, no.2, pp.691 - 700 -
dc.identifier.doi 10.1021/acs.biomac.8b00068 -
dc.identifier.issn 1525-7797 -
dc.identifier.scopusid 2-s2.0-85041905594 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/23693 -
dc.identifier.url https://pubs.acs.org/doi/full/10.1021/acs.biomac.8b00068 -
dc.identifier.wosid 000425193600043 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title Multivalent Polyaspartamide Cross-Linker for Engineering Cell-Responsive Hydrogels with Degradation Behavior and Tunable Physical Properties -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Biochemistry & Molecular Biology; Chemistry, Organic; Polymer Science -
dc.relation.journalResearchArea Biochemistry & Molecular Biology; Chemistry; Polymer Science -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus DRUG-DELIVERY SYSTEMS -
dc.subject.keywordPlus L-ASPARTIC ACID -
dc.subject.keywordPlus SWELLING PROPERTIES -
dc.subject.keywordPlus GLYCOL) HYDROGELS -
dc.subject.keywordPlus LINKING -
dc.subject.keywordPlus ALGINATE -
dc.subject.keywordPlus DERIVATIVES -
dc.subject.keywordPlus DESIGN -
dc.subject.keywordPlus POLY(SUCCINIMIDE) -
dc.subject.keywordPlus POLYCONDENSATION -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.