dc.contributor.author
Feng, Jun
dc.contributor.author
Ponomareva, Polina
dc.contributor.author
Liu, Kunpeng
dc.contributor.author
Nie, Chuanxiong
dc.contributor.author
Chen, Rui
dc.contributor.author
Haag, Rainer
dc.date.accessioned
2025-06-30T04:48:25Z
dc.date.available
2025-06-30T04:48:25Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/47712
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-47430
dc.description.abstract
Advancing cancer research depends significantly on developing accurate and reliable models that can replicate the complex tumor microenvironment. Tumor spheroids─three-dimensional clusters of cancer cells─have become crucial tools for this purpose. The overarching goal of tumor spheroid culture is to develop biomaterials that mimic the dynamic mechanical behavior of the native extracellular matrix, enabling high-fidelity culture models. In this study, we developed dynamic hydrogels based on dual-dynamic covalently cross-linked polyglycerol, using boronate bonds and Schiff-base interactions. In addition to good biocompatibility and long-term stability, the hydrogels showed tunable mechanical properties that enabled cells to actively remodel their surrounding microenvironment. This platform was used for successful 3D culture of various cancer cell lines, including HeLa, A549, HT-29, BT-474, and SK-BR-3, which were encapsulated in situ and formed 3D tumor spheroids. These results demonstrate the feasibility and versatility of our dynamic hydrogel system in supporting tumor spheroid culture.
en
dc.format.extent
13 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Cell culture
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften
dc.title
Dual-Dynamic Covalently Cross-Linked Polyglycerol Hydrogels for Tumor Spheroid Culture
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1021/acs.biomac.4c01744
dcterms.bibliographicCitation.journaltitle
Biomacromolecules
dcterms.bibliographicCitation.number
6
dcterms.bibliographicCitation.pagestart
3331
dcterms.bibliographicCitation.pageend
3343
dcterms.bibliographicCitation.volume
26
dcterms.bibliographicCitation.url
https://doi.org/10.1021/acs.biomac.4c01744
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie

refubium.funding
ACS Publications
refubium.note.author
Gefördert aus Open-Access-Mitteln der Freien Universität Berlin.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1526-4602