Advanced Microfluidic Platform for Tumor Spheroid Formation and Cultivation Fabricated from OSTE+ Polymer
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985858%3A_____%2F24%3A00599469" target="_blank" >RIV/67985858:_____/24:00599469 - isvavai.cz</a>
Alternative codes found
RIV/44555601:13440/24:43898493
Result on the web
<a href="https://link.springer.com/article/10.1007/s13206-024-00167-x" target="_blank" >https://link.springer.com/article/10.1007/s13206-024-00167-x</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s13206-024-00167-x" target="_blank" >10.1007/s13206-024-00167-x</a>
Alternative languages
Result language
angličtina
Original language name
Advanced Microfluidic Platform for Tumor Spheroid Formation and Cultivation Fabricated from OSTE+ Polymer
Original language description
In the evolving landscape of cancer research, 3D cell cultures, particularly tumor cell spheroids, are increasingly preferred in drug screening due to their enhanced mimicry of in vivo tumor environments, especially in drug resistance aspects. However, the consistent formation of uniform spheroids and their precise manipulation remain complex challenges. Among various methodologies, droplet microfluidics emerges as a highly effective approach for tumor spheroid formation. This paper introduces a novel, multifaceted microfluidic system that streamlines the entire spheroid cultivation process: generating tumor spheroids from cell suspensions within individual droplets, merging these droplets into a continuous aqueous phase once spheroid formation is complete, and transferring the spheroids to a specialized cultivation area within the chip, equipped with trapping elements for extended cultivation in perfusion mode. Remarkably, this process requires no hydrogel encapsulation or external handling, as all operations are conducted within the microfluidic chip. Fabricated from the innovative OSTE+ (off-stoichiometry thiol-ene epoxy) polymer, the chip is designed for repeated use. To show its efficacy, we successfully formed spheroids from MCF-7, GAMG, and U87 cell lines in our system and compared them with spheroids prepared by a traditional agarose microwell method. Additionally, our methodology has successfully enabled the in-chip release of spheroids from droplets, followed by their effective trapping for subsequent cultivation, a process we have exemplified with MCF-7 spheroids. To our knowledge, this research represents the first instance of a fully integrated droplet microfluidic platform achieving scaffoldless tumor spheroid formation and handling. Our method holds promise for improving high-throughput, automated procedures in the formation, transfer, and cultivation of tumor cell spheroids.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30402 - Technologies involving the manipulation of cells, tissues, organs or the whole organism (assisted reproduction)
Result continuities
Project
<a href="/en/project/LM2023066" target="_blank" >LM2023066: Nanomaterials and Nanotechnologies for Environment Protection and Sustainable Future</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2024
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
BioChip Journal
ISSN
1976-0280
e-ISSN
2092-7843
Volume of the periodical
18
Issue of the periodical within the volume
3
Country of publishing house
KR - KOREA, REPUBLIC OF
Number of pages
17
Pages from-to
393-409
UT code for WoS article
001280665000001
EID of the result in the Scopus database
2-s2.0-85200037919