Characterization of Polydimethylsiloxane (PDMS) Properties for Biomedical Micro/Nanosystems

Colloids and Surfaces B: Biointerfaces, 2010

Poly(dimethyl siloxane) elastomer, (PDMS) is widely used as a biomaterial. However, PDMS is very hydrophobic and easily colonized by several bacteria and yeasts. Consequently, surface modification has been used to improve its wettability and reduce bacterial adhesion.

Surface and Interface Analysis

Successful realization of various BioMEMS devices demands effective surface modification techniques of PDMS elastomer. This paper presents a detailed report on a simple and cost effective approach for surface modification of PDMS films involving wet chemical treatment in two-step processes: primarily involving piranha solution followed by KOH dip to improve hydrophilicity and stability of PDMS surface. Chemical composition of the solution and surface treatment condition have been varied and optimized to significantly increase the surface energy. The effect of surface modification of the elastomer after wet chemical treatment is analyzed using contact angle measurement and FTIR-ATR study. PDMS surface treated in piranha solution with H2O2 and H2SO4 in the ratio of 2:3 followed by a dip in KOH solution for 15 min duration each, demonstrated a maximum reduction of contact angle to ∼27° as compared to untreated sample having a contact angle of ∼110°. The removal of hydrophobic methyl group from elastomer surface and subsequent hydrophilization of surface by wet chemical process was confirmed from FTIR-ATR spectra. This result is also supported by improved adhesion and electrical continuity of deposited aluminum metal film over the modified PDMS surface. Copyright © 2011 John Wiley & Sons, Ltd.

Tissue Engineering, 2007

This article demonstrates that the micro-topography of the surface with respect to the pattern size and pitch influences cell adhesion and proliferation. Extensive research has shown the dependence of cell proliferation on substrate chemistry, but the influence of substrate topography on cell attachment has only recently been appreciated. To evaluate the effect of substrate physical properties (i.e., periodic microstructures) on cell attachment and morphology, we compared the response of several cell types (fibroblasts, HeLa, and primary hepatocytes) cultured on various polydimethylsiloxane (PDMS) patterns. PDMS has been used as an artificial construct to mimic biological structures. Although PDMS is widely used in biomedical applications, membrane technology, and microlithography, it is difficult to maintain cells on PDMS for long periods, and the polymer has proved to be a relatively inefficient substrate for cell adhesion. To improve adhesion, we built polyelectrolyte multilayers (PEMs) on PDMS surfaces to increase surface wettability, thereby improving attachment and spreading of the cells. Micrographs demonstrate the cellular response to physical parameters, such as pattern size and pitch, and suggest that surface topography, in part, regulates cell adhesion and proliferation. Therefore, varying the surface topography may provide a method to influence cell attachment and proliferation for tissueengineering applications.

Surface and Coatings Technology, 2011

There have been few studies on the effect of the grafting of nitrogen-containing functional groups on polydimethylsiloxane (PDMS) surfaces and, in particular, the CN bond, on cell adhesion to the surfaces. In this study, two different silanes, one containing an amine group [(3-aminopropyl)trimethoxysilane; APTMS] and the other a nitrile group [(3-cyanopropyl)triethoxysilane; CPTES], were adopted to modify PDMS following oxygen plasma treatment. The effects of surface modification on the density of HeLa and MDCK cells were evaluated, in addition to the measurement of the contact angle with the surface and the chemical composition. The results indicated that the CPTES modification allowed the PDMS surface to have better hydrophilicity than the APTMS modification. Nitrogen-containing functionalities were more beneficial for cell spreading, in comparison with the pristine and oxygen plasma-treated PDMS. The present method of APTMS and CPTES grafting provides a simple and efficient method for promoting cell adhesion on PDMS.

Journal of Materials Chemistry B, 2013

This study presents a novel and inexpensive method to prepare a disposable micro-bioreactor for stem cell expansion. The micro-bioreactor was fabricated in the form of a fixed bed bioreactor with a microchannel reactor bed. The micro-bioreactor was constructed from polydimethylsiloxane (PDMS), and the microchannel was functionalized to enable cell adhesion and resistance to bovine serum albumin protein adsorption. The PDMS reactor bed surface was activated by oxygen plasma, then aminized with trimethoxysilylpropyl(polyethyleneimine), followed by grafting with carboxylmethyl cellulose (CMC) and gelatin in sequence. The functionalized PDMS surface demonstrated improved hydrophilicity and antifouling properties. The grafting of gelatin promoted cell adhesion. The functionalized surface was found to be biocompatible with MDA-MB-231 and Oct4b2 cells and was demonstrated to facilitate cell proliferation. The expanded Oct4b2 cells retained their proliferation potential, undifferentiated phenotype and pluripotency.

Colloids and surfaces. B, Biointerfaces, 2014

The effect of physicochemical surface properties and chemical structure on the attachment and viability of bacteria and mammalian cells has been extensively studied for the development of biologically relevant applications. In this study, we report a new approach that uses chlorogenic acid (CA) to modify the surface wettability, anti-bacterial activity and cell adhesion properties of polydimethylsiloxane (PDMS). The chemical structure of the surface was obtained by X-ray photoelectron spectroscopy (XPS), the roughness was measured by atomic force microscopy (AFM), and the water contact angle was evaluated for PDMS substrates both before and after CA modification. Molecular modelling showed that the modification was predominately driven by van der Waals and electrostatic interactions. The exposed quinic-acid moiety improved the hydrophilicity of CA-modified PDMS substrates. The adhesion and viability of E. coli and HeLa cells were investigated using fluorescence and phase contrast microscopy. Few viable bacterial cells were found on CA-coated PDMS surfaces compared with unmodified PDMS surfaces. Moreover, HeLa cells exhibited enhanced adhesion and increased spreading on the modified PDMS surface. Thus, CA-coated PDMS surfaces reduced the ratio of viable bacterial cells and increased the adhesion of HeLa cells. These results contribute to the purposeful design of anti-bacterial surfaces for medical device use.

Biosensors, 2020

Microfluidic lab-on-a-chip cell culture techniques have been gaining popularity by offering the possibility of reducing the amount of samples and reagents and greater control over cellular microenvironment. Polydimethylsiloxane (PDMS) is the commonly used polymer for microfluidic cell culture devices because of the cheap and easy fabrication techniques, non-toxicity, biocompatibility, high gas permeability, and optical transparency. However, the intrinsic hydrophobic nature of PDMS makes cell seeding challenging when applied on PDMS surface. The hydrophobicity of the PDMS surface also allows the non-specific absorption/adsorption of small molecules and biomolecules that might affect the cellular behaviour and functions. Hydrophilic modification of PDMS surface is indispensable for successful cell seeding. This review collates different techniques with their advantages and disadvantages that have been used to improve PDMS hydrophilicity to facilitate endothelial cells seeding in PDMS...

Materials Science and Engineering C

At an implant site, a manmade material meets human tissue, and the manmade material is highly perturbed by the preceeding surgical procedure. The focus of the action, and thus the focus of scientific interest, is the interface between the foreign material and the tissue. The primary interaction occurs on a molecular scale, and involves adsorption and reactions of biomolecules, water and inorganic ions respectively from the bioliquid as well as dissolution of atomic, ionic or molecular fragments from the biomaterial. Successively changing conditions in the tissue, owing to the ongoing healing process and concerted modifications of the surface properties of the biomaterial, make the material-tissue interface a dynamic, non-reversible system in space and time. Secondary processes, induced by the primary processes, may occur far from the interface in the surrounding tissue or as systemic effects.

Soft lithography fabrication procedure for PDMS hydrophobic surface. 1) Silicon wafer 2) Photoresist coating 3) Photolithography 4) Silicon DRIE with photoresist masking 5) PDMS casting over the etched silicon 6) PDMS peelingoff from the silicon mold Fig 2: (A) SEM image of DRIE etched honeycomb pattern silicon. (B) Confocal laser microscopy images of the fabricated PDMS honeycombs.

Plasma-induced grafting of polydimethylsiloxane (PDMS) onto the surface of polyurethane (PU) film. The virgin, plasma treated, and PDMS grafted PU films were characterized by means of attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, water drop contact angle measurements, and scanning electron microscopy (SEM). The ATR-FTIR spectrogram of the grafted film showed the new characteristic peaks of PDMS. These grafted surfaces exhibited higher hydrophobicity and homogenous morphology. In vitro cell culture study showed that modified surfaces as well as virgin film were compatible with fibroblast cells. The formation of graft polymers combines the biostability of silicone with excellent physical and mechanical properties of PU.

RSC Advances, 2011

This paper describes a simple and inexpensive procedure to produce thin-films of poly(dimethylsiloxane). Such films were characterized by a variety of techniques (ellipsometry, nuclear magnetic resonance, atomic force microscopy, and goniometry) and used to investigate the adsorption kinetics of three model proteins (fibrinogen, collagen type-I, and bovine serum albumin) under different conditions. The information collected from the protein adsorption studies was then used to investigate the adhesion of human dermal microvascular endothelial cells. The results of these studies suggest that these films can be used to model the surface properties of microdevices fabricated with commercial PDMS. Moreover, the paper provides guidelines to efficiently attach cells in BioMEMS devices.

Journal of Biomedical Materials Research Part A, 2014

The current study demonstrates the first surface modification for poly(dimethylsiloxane) (PDMS) microfluidic networks that displays a long shelf life as well as extended hemocompatibility. Uncoated PDMS microchannel networks rapidly adsorb high levels of fibrinogen in blood contacting applications. Fibrinogen adsorption initiates platelet activation, and causes a rapid increase in pressure across microchannel networks, rendering them useless for long term applications. Here, we describe the modification of sealed PDMS microchannels using an oxygen plasma pre-treatment and poly(ethylene glycol) grafting approach. We present results regarding the testing of the coated microchannels after extended periods of aging and blood exposure. Our PEG-grafted channels showed significantly reduced fibrinogen adsorption and platelet adhesion up to 28 days after application, highlighting the stability and functionality of the coating over time. Our coated microchannel networks also displayed a significant reduction in the coagulation response under whole blood flow. Further, pressure across coated microchannel networks took over 16 times longer to double than the uncoated controls. Collectively, our data implies the potential for a coating platform for microfluidic devices in many blood-contacting applications.

Stable surface modifications of polydimethylsiloxane (PDMS) are of crucial importance for the exploitation of the versatile physical properties of silicone in many biological applications. Surface hydrophobic recovery in fact poses severe time limitations to the observation of biological events and, in particular, to cell culturing. A novel method of stable modification of PDMS surface chemistry was therefore elaborated, relying on the use of genipin as a natural low-toxicity cross-linker, and involving free amine moieties. Its effectiveness to long-term cultures was studied by preparation of thin PDMS films with different stiffness. After assessment of surface chemistry and substrate stiffness, H9c2 muscle cells were cultured on the modified films, and differentiating myoblasts were observed for a period of four weeks since differentiation induction. A lower PDMS stiffness increased myotube width and supported a higher actin and myosin colocalization within myotubes, suggesting the achievement of myotube functional maturity. These results provide evidence of the effectiveness of the proposed procedures to PDMS surface chemistry modification. Furthermore, modified PDMS membranes prove to be suitable to several long-term studies of cell behaviour in vitro, including muscle cell contractility investigations.

Analytical Chemistry, 2002

Poly(dimethylsiloxane) (PDMS)-based microfluidic devices are increasing in popularity due to their ease of fabrication and low costs. Despite this, there is a tremendous need for strategies to rapidly and easily tailor the surface properties of these devices. We demonstrate a one-step procedure to covalently link polymers to the surface of PDMS microchannels by ultraviolet graft polymerization. Acrylic acid, acrylamide, dimethylacrylamide, 2-hydroxylethyl acrylate, and poly(ethylene glycol)monomethoxyl acrylate were grafted onto PDMS to yield hydrophilic surfaces. Water droplets possessed contact angles as low as 45°on the grafted surfaces. Microchannels constructed from the grafted PDMS were readily filled with aqueous solutions in contrast to devices composed of native PDMS. The grafted surfaces also displayed a substantially reduced adsorption of two test peptides compared to that of oxidized PDMS. Microchannels with grafted surfaces exhibited electroosmotic mobilities intermediate to those displayed by native and oxidized PDMS. Unlike the electroosmotic mobility of oxidized PDMS, the electroosmotic mobility of the grafted surfaces remained stable upon exposure to air. The electrophoretic resolution of two test peptides in the grafted microchannels was considerably improved compared to that in microchannels composed of oxidized PDMS. By using the appropriate monomer, it should be possible to use UV grafting to impart a variety of surface properties to PDMS microfluidics devices. Polymer-based microfluidic devices are rapidly gaining in popularity primarily due to their ease of fabrication, inexpensive costs, and increasing versatility. 1-3 These devices have been fabricated from a variety of different polymers including poly-(methyl methacrylate) (PMMA), polycarbonate, polystyrene, and poly(dimethylsiloxane) (PDMS). In particular, PDMS-based devices can easily and inexpensively be fabricated by casting the polymer against a mold prior to cross-linking. Since the casting step does not require access to a cleanroom, this methodology is accessible to a large number of investigators. The low Young's modulus and durability of PDMS make it an excellent choice for fabrication of pumps and valves. Additionally, PDMS readily seals with itself as well as many other materials such as glass and PMMA. PDMS has also been utilized in the "rapid prototyping" of devices designed for electrophoretic separations. 9 Despite these advantages, systems fabricated from PDMS exhibit a number of weaknesses that must be overcome before PDMS can be considered the material of choice for microsystems employing electrophoresis. These disadvantages are as follows: (1) the extreme hydrophobicity of PDMS making the devices difficult to fill with aqueous solutions, (2) the strong tendency to adsorb other molecules onto the surface with some molecules actually migrating into the polymer matrix itself, and (3) the unstable and poorly controlled electroosmotic flow. A variety of solutions, primarily surface modifications, have been proposed, for example, oxygen plasma treatment, silanization, adsorbed coatings (Polybrene/ dextran sulfate), and protein or lipid coatings. . However, surface modifications such as oxygen plasma treatment and

The application of synthetic polymers in the growing field of materials for medical applications is illustrated by examples from recent work at the Materials Institute of the Swiss Federal Institute of Technology in Lausanne. The review highlights the need for functionalization and chemical control of material surfaces at a molecular/functional level. After a brief introduction into the surface chemical analysis tools, i.e., X-ray Photoelectron Spectroscopy (XPS) and Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) combined with contact angle measurements, phosphorylcholine biomimicking polymers as well as immobilization of carbohydrates on polystyrene are presented.