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A durable and biocompatible ascorbic acid-based covalent coating method of polydimethylsiloxane for dynamic cell
Joni Leivo1, Sanni Virjula2,3, Sari Vanhatupa2,3
1Micro- and Nanosystems Research Group, BioMediTech Institute and Faculty of Biomedical Sciences and Engineering, Tampere University of Technology, Tampere, Finland.
Researchers developed a new, non-cytotoxic method for coating polydimethylsiloxane (PDMS) with collagen. Ascorbic acid (AA) cross-linking improves human adipose stem cell (hASC) attachment and proliferation in microfluidic devices.
Area of Science:
- Biomaterials Science
- Cell Biology
- Microfluidics
Background:
- Polydimethylsiloxane (PDMS) is crucial for microfluidic devices but its hydrophobicity hinders cell attachment.
- Existing covalent coating methods using glutaraldehyde (GA) are cytotoxic, limiting biological applications.
- Improved PDMS surface modification is needed for effective cell culture in dynamic microfluidic systems.
Purpose of the Study:
- To introduce a novel, non-cytotoxic covalent collagen type I coating method for PDMS using ascorbic acid (AA) as a cross-linker.
- To compare the efficacy of AA-based covalent coating against physisorption and GA-based covalent coating.
- To evaluate the biocompatibility and durability of the AA-coated PDMS for human adipose stem cell (hASC) culture under static and dynamic conditions.
Main Methods:
- Covalent binding of collagen type I to PDMS using ascorbic acid (AA) as a cross-linker.
- Characterization of PDMS coatings using immunostaining, contact angle measurements, atomic force microscopy, and infrared spectroscopy.
- Assessment of human adipose stem cell (hASC) attachment, proliferation, and viability on coated PDMS under static and dynamic (stretching) conditions for up to 13 days.
Main Results:
- Ascorbic acid (AA) effectively replaces glutaraldehyde (GA) as a cross-linker for covalent collagen I coating on PDMS.
- The AA-based covalent coating demonstrates durability, withstanding sonication and 6 days of mechanical stretching.
- Human adipose stem cells (hASCs) exhibit significantly improved attachment and proliferation on AA-cross-linked PDMS compared to physisorbed or GA-based coatings.
Conclusions:
- Ascorbic acid provides a safe and effective alternative to glutaraldehyde for covalently immobilizing collagen I on PDMS.
- The developed AA-based coating method enhances cellular adhesion and proliferation, making PDMS suitable for dynamic cell culture.
- This novel coating technique is a significant advancement for PDMS-based microfluidic devices in cell engineering and tissue engineering applications.
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