Simple Surface Modification of Poly(dimethylsiloxane) via Surface Segregating Smart Polymers for Biomicrofluidics

Aslıhan Gökaltun, Tufts University
Young Bok Abraham Kang, George Fox University
Martin L. Yarmush, Rutgers University
O. Berk Usta, Harvard Medical School
Ayse Asatekin, Tufts University

Originally published in Scientific Reports volume 9, Article number: 7377 (2019).

https://www.nature.com/articles/s41598-019-43625-5#rightslink

Abstract

Poly(dimethylsiloxane) (PDMS) is likely the most popular material for microfuidic devices in lab-on-achip and other biomedical applications. However, the hydrophobicity of PDMS leads to non-specifc adsorption of proteins and other molecules such as therapeutic drugs, limiting its broader use. Here, we introduce a simple method for preparing PDMS materials to improve hydrophilicity and decrease nonspecifc protein adsorption while retaining cellular biocompatibility, transparency, and good mechanical properties without the need for any post-cure surface treatment. This approach utilizes smart copolymers comprised of poly(ethylene glycol) (PEG) and PDMS segments (PDMS-PEG) that, when blended with PDMS during device manufacture, spontaneously segregate to surfaces in contact with aqueous solutions and reduce the hydrophobicity without any added manufacturing steps. PDMS-PEGmodifed PDMS samples showed contact angles as low as 23.6°±1° and retained this hydrophilicity for at least twenty months. Their improved wettability was confrmed using capillary fow experiments. Modifed devices exhibited considerably reduced non-specifc adsorption of albumin, lysozyme, and immunoglobulin G. The modifed PDMS was biocompatible, displaying no adverse efects when used in a simple liver-on-a-chip model using primary rat hepatocytes. This PDMS modifcation method can be further applied in analytical separations, biosensing, cell studies, and drug-related studies.