Atmospheric Pressure Plasma Functionalization of Sealed PDMS Microfluidics: Application to Capillary Pumping and Enhanced Cell Growth.

plasma surface chemistry atmospheric plasma microfluidics cell growth

Journal

ChemPlusChem
ISSN: 2192-6506
Titre abrégé: Chempluschem
Pays: Germany
ID NLM: 101580948

Informations de publication

Date de publication:
31 Jul 2024
Historique:
revised: 23 07 2024
received: 23 04 2024
accepted: 26 07 2024
medline: 1 8 2024
pubmed: 1 8 2024
entrez: 31 7 2024
Statut: aheadofprint

Résumé

Microfluidic devices serve as essential tools across diverse fields like medicine, biotechnology, and chemistry, enabling advancements in analytical techniques, point-of-care diagnostics, microfluidic cell cultures, and organ-on-chip models. While polymeric microfluidics are favoured for their cost-effectiveness and ease of fabrication, their inherent hydrophobic properties necessitate surface functionalization, often post-sealing. Here, we introduce a versatile apparatus for functionalizing sealed microfluidic devices using atmospheric plasma processing, with a focus on PDMS (polydimethylsiloxane) microfluidics. Through meticulous analysis of surface properties and capillary velocity, before and after plasma treatment, along with a comparison between vacuum and atmospheric plasma functionalization methods, we demonstrate the efficacy of our approach. Subsequent experimentation within 3D PDMS microfluidic chambers, combining atmospheric pressure plasma treatment with collagen coating to facilitate mesenchymal stem cells (MSCs) growth over five days, reveals enhanced initial cell adhesion and proliferation, highlighting the potential of our method for improving cell-based applications within microfluidic systems.

Identifiants

pubmed: 39085045
doi: 10.1002/cplu.202400290
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202400290

Informations de copyright

© 2024 Wiley‐VCH GmbH.

Auteurs

Angelos Zeniou (A)

NCSR Demokritos, INN, Patr. Gregoriou E & 27 Neapoleos Str, 15341, Agia Paraskevi, GREECE.

Dionysia Kefallinou (D)

NCSR Demokritos, INN, GREECE.

Panagiotis Dimitrakellis (P)

NCSR Demokritos, INN, GREECE.

Evangelia Xenogiannopoulou (E)

NCSR Demokritos, INN, GREECE.

Maria Grigoriou (M)

Biomedical Research Foundation of the Academy of Athens, Laboratory of Inflammation and Autoimmunity, GREECE.

Athanasios Dimoulas (A)

NCSR Demokritos, INN, GREECE.

Dimitrios T Boumpas (DT)

Biomedical Research Foundation of the Academy of Athens, Laboratory of Inflammation and Autoimmunity, GREECE.

Angeliki Tserepi (A)

NCSR Demokritos, INN, GREECE.

Evangelos Gogolides (E)

Ethniko Kentro Ereunas Physikon Epistemon 'Demokritos', Institute of Nanoscience and Nanotechnology, Patriarhou Gregoriou and Neapoleos 27, 15341, Aghia Paraskevi, GREECE.

Classifications MeSH