Surface molecular property modifications for poly(dimethylsiloxane) (PDMS) based microfluidic devices
Fast advancements of microfabrication processes in past two decades have reached to a fairly matured stage that we can manufacture a wide range of microfluidic devices. At present, the main challenge is the control of nanoscale properties on the surface of lab-on-a-chip to satisfy the need for biomedical applications. For example, poly(dimethylsiloxane) (PDMS) is a commonly used material for microfluidic circuitry, yet the hydrophobic nature of PDMS surface suffers serious nonspecific protein adsorption. Thus the current major efforts are focused on surface molecular property treatments for satisfying specific needs in handling macro functional molecules. Reviewing surface modifications of all types of materials used in microfluidics will be too broad. This review will only summarize recent advances in nonbiofouling PDMS surface modification strategies applicable to microfluidic technology and classify them into two main categories: (1) physical approach including physisorption of charged or amphiphilic polymers and copolymers, as well as (2) chemical approach including self assembled monolayer and thick polymer coating. Pros and cons of a collection of available yet fully exploited surface modification methods are briefly compared among subcategories.
Since the introduction of microelectromechanical system (MEMS) technologies couple decades ago, intensive research efforts have been devoted in the field of microfluidics (Ho and Tai 1998; Stone et al. 2004). At first, silicon and glass based materials were commonly used (Manz et al. 1992; Harrison et al. 1993). Numerous microfluidic components, such as pumps, valves, mixers, and molecules and particles separators and concentrators, have been developed for a broad range of applications including chemistry, biology, physics, and medicine (Auroux et al. 2002; Reyes et al. 2002; Vilkner et al. 2004; Dittrich et al. 2006; West et al. 2008). It is clear that this field has gained enough maturity in the individual component level, as reflected from the number of articles published on this topic in recent years (Abgrall and Gue 2007), and has reached the time to commence an integration of these components into a fully automated system (Whitesides 2006; Haeberle and Zengerle 2007). Technologies already demonstrating multi-components platforms include centrifugal microfluidics (Madou et al. 2006), droplet based microfluidics (Teh et al. 2008) such as electrowetting on dielectric (EWOD, Lee et al. 2002) and two-phase microchannel flow (Song et al. 2006), electrokinetics (Li 2004), and optofluidics (Hunt and Wilkinson 2008).
Yet, silicon and glass based fabrication technologies are fairly time-consuming and require expensive cleanroom usages. On the other hand, poly(dimethylsiloxane) (PDMS) has gained attention for microfluidic applications after two important contributions: soft lithography (McDonald et al. 2000) and microfluidic large scale integration (LSI) (Thorsen et al. 2002). The former was developed for fast fabrication of microchannels while the latter created the possibility for on-chip integration of fluidic elements (valves, mixers, and pumps). The combination of these technologies set a simple pathway to micro total analysis systems (μTAS) technology for a completely integrated and functional system.
Recently, a variety of polymeric materials have been increasingly adopted in producing various microfluidic devices (Quake and Scherer 2000). Commonly used polymers include PDMS (McDonald et al. 2000; Ng et al. 2002; Sia and Whitesides 2003), poly(methyl methacrylate) (PMMA), polycarbonate (PC), poly(ethylene terephthalate) (PET), polyurethane, poly(vinyl chloride) (PVC), and polyester (Shadpour et al. 2006). Techniques commonly used for fabricating polymer microfluidic devices include laser ablation (Roberts et al. 1997), hot embossing (Martynova et al. 1997), injection molding (McCormick et al. 1997), and replica molding (Duffy et al. 1998) and are reviewed by Becker et al. (Becker and Gartner 2000). It is generally agreed that PDMS is among the most popular polymeric materials employed for the fabrication of microfluidic devices owing to a number of advantages: simple fabrication by replica molding, biocompatibility, nontoxicity, excellent optical transparency down to 280 nm, and permeability to gases. In spite of these advantages, the strong hydrophobicity of PDMS surface always impedes PDMS based microfluidic devices from immediate use without any surface processing. The key challenge is the surface fouling problem caused by protein or analyte adsorption on hydrophobic surface enhanced by significant increase in surface to volume ratio in microscale, resulting in low device performance and substantial sample loss. Therefore, it is of key importance to develop efficient surface modification techniques to render PDMS surface protein-resistant.
Extensive amount of works have been performed in developing reliable and reproducible protein-resistant surfaces on various substrate materials. Majority of the works on surface modification of microfluidic device are developed for electrophoresis applications due to the vast exploitation of microchips and demanding stringency on surface properties. Other microfluidic related applications also showed intensive demand on protein resistant surfaces, such as cell culturing and immunoassay (Auroux et al. 2002; Vilkner et al. 2004; Dittrich et al. 2006). Surface modification techniques are basically categorized into physical adsorbed and covalent modifications. Physical adsorbed modification relies on surface bound materials adsorbed via mainly hydrophobic interaction (generally between the hydrophobic PDMS surface and the hydrophobic terminal of, say, amphiphilic molecules or copolymers) or electrostatic interactions while covalent modifications include self assembled monolayer (SAM) and surface grafted polymer chains.
Poly(ethylene glycol) (PEG), also known as poly(ethylene oxide) (PEO), is a well known material for preventing nonspecific adsorption of proteins (Harris 1992; Harris and Zalipsky 1997) as well as its biocompatibility and low toxicity. Besides PEG, many hydrophilic synthetic and natural polymers used for static and dynamic coating in separation science, such as polyacrylamide, poly(vinyl alcohol) (PVA), hydroxylethylcellulose (HEC), poly(N-hydroxyethyl acrylamide) (PHEA), hydroxylpropyl methylcellulse (HPMC), poly(2-hydroxyethyl methacrylate) (pHEMA), poly(vinyl pyrrolidone) (PVP), poly(acrylic acid) (PAA), dextran, hyaluronic acid, and poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC) have been derived for physical or covalent surface modifications of the microchannel wall (Doherty et al. 2003; Dolnik 2004, 2006).
Some excellent reviews have documented on surface modification of microchannel made of various silicon-based and polymeric materials for the prevention of biofouling (Doherty et al. 2003; Makamba et al. 2003; Dolnik 2004; Senaratne et al. 2005; Dolnik 2006; Liu and Lee 2006; Pallandre et al. 2006). Yet there are so far limited number of reviews focused on surface modifications of PDMS (Makamba et al. 2003), despite its role as the most extensively exploited polymeric material in the microfluidic community and a bursting number of works published these few years (Muck and Svatos 2007). This review focuses on recent progress on surface modification methods in preparing nonbiofouling coating for PDMS and silica microfluidic devices and is divided into three main categories: surface activation, physical modification, and chemical modification.
2 Surface activation
Surface activation step is commonly used for cleaning or oxidization of PDMS surfaces to render surface hydrophilic for promoting aqueous solution filling in microchannel and facilitating PDMS microchip bonding. More importantly, surface activation creates reactive silanol functional groups for subsequent surface functionalizations through various surface chemistries including silanization (Ulman 1996), cerium(IV)-catalyzed polymerization (Slentz et al. 2002), UV mediated polymerization (Hu et al. 2002, 2004), plasma induced polymerization (He et al. 2003), and free radical polymerization (Husseman et al. 1999; Edmondson et al. 2004; Tsujii et al. 2006).
Oxygen plasma (Duffy et al. 1998), UV/ozone (Efimenko et al. 2002; Hillborg et al. 2004), and corona discharges (Hillborg and Gedde 1998; Kim et al. 2000) are commonly used for surface activation purpose. Oxygen plasma contains high energy species including electrons, ions, and radicals which strongly oxidize the organic species on the surface. A milder treatment by UV/ozone is through generation of atomic oxygen in a combination of photochemical processes. The 185 nm line produces ozone from molecular oxygen while 254 nm line converts the ozone to atomic oxygen. This reactive species generated by oxygen plasma and UV/ozone attacks the siloxane backbone of PDMS to form oxygen rich SiOx silica-like layer and Si–OH surface structures. The main drawback of these physical modifications is that the oxidized PDMS surface is known to recover its hydrophobicity in just hours after exposure to air (McDonald et al. 2000). A general agreement to this phenomenon is the migration of low molecular weight (LMW) uncrosslinked polymeric chains from the bulk phase to the surface (Hillborg et al. 2004; Chen and Lindner 2007).
Very recently, Eddington et al. (2006) have shown that by removing these LMW species from the bulk phase through thermal aging, hydrophilicity of the oxidized surface can be retained for a much longer time. Another approach to remove the LMW species is through an extraction/oxidation process introduced by Vickers et al. (2006). Cured PDMS was first extracted in a series of solvents to remove unreacted polymer chains from the bulk phase, followed by a plasma oxidation process to generate a layer of hydrophilic SiO2 surface. No noticeable hydrophobic recovery was observed for at least 7 days of storage in air, as evidenced with X-ray photoelectron spectroscopy (XPS) studies.
Apart from oxygen plasma and UV/ozone treatments, hydrophilicity and surface silanol groups of PDMS surface can also be obtained by using a sol–gel method which created an oxide layer on the PDMS channel wall in situ (Roman et al. 2005; Roman and Culbertson 2006). Roman et al. (2005) formed nanometer-sized silica particles uniformly distributed in a cured PDMS piece. The PDMS piece was first soaked and swollen in a solution of sol–gel precursor tetraethyl orthosilicate (TEOS), followed by incubation in an ethylamine catalyzing solution and heated to form nanoparticles inside the PDMS matrix. Besides forming glasslike layer on PDMS surface, the same group also applied similar sol–gel technique with transition metal sol–gel precursors to in situ deposit TiO2, ZrO2, and vanadia coating inside PDMS microchannel (Roman and Culbertson 2006). Contact angle measurements showed a significant reduction of water contact angles of all the modified surfaces indicating that more hydrophilic surfaces were created with this method. Electroosmotic mobility measurements demonstrated that the surfaces were stable for at least 95 days. Moreover, these created inorganic surfaces have the potential to be functionalized with various silane reagents including amine, perfluoro, mercapto, and oligoethylene glycol (OEG) with contact angles of 45°, 120°, 76°, and 23°, respectively, which were stable over a 30-day period.
Recently, a few improvements of this sol–gel method were presented by other groups. To solve the PDMS swelling problem caused by the precursor solution as well as the contraction and cracking problem during the gelation process, Abate et al. (2008) pre-oligomerized sol–gel precursors of TEOS and methyltriethoxysilane (MTES) into higher molecular weight silane oligomers before introducing into oxygen plasma treated PDMS channel. The device was then heated to 100°C to initiate the gelation reaction. The coating efficiently prevents the diffusion of LMW dye (Rhodamine B), suppresses the swelling of PDMS by toluene, and can be functionalized with various silane reagents for specific interfacial applications. On the other hand, it was pointed out that the glasslike layer formed using Roman’s method (Roman et al. 2005) was not covalently bonded to PDMS and was still in the gel form due to relatively low annealing temperature. To further improve the coating for prevention of diffusion and swelling, Orhan et al. (2008) coated the PDMS channel with a borosilicate glass layer using an active solution of alkali-free precursors, TEOS and trimethoxyboroxine (TMB). This active solution was flushed into tetrabutylammonium fluoride (TBAF) oxidized PDMS channel and cured thermally at 160°C. Resulting surface was characterized as a covalently bonded 800 nm-thick crack-free borosilicate glass. Negligible diffusion of Rhodamine B was observed and the swelling of PDMS was effectively prevented during hours of exposure to toluene.
3 Physical adsorption
Surface modification via physical adsorption is vastly used in capillary electrophoresis (CE) for suppression of electroosmotic flow (EOF) and prevention of protein nonspecific binding due to its tremendous simplicity and efficiency compared to other covalent surface modification methods. The most conventional examples are blocking proteins such as bovine serum albumin (BSA) or milk powder due to their easy and simple preparations. One example is the use of avidin protein to achieve reconfigurable surface wetting properties taking advantage of the reversible nonspecific adsorption of avidin on hydrophobic surface (Deval et al. 2004). However, the problems of fast denaturation over time and lack of useful functional groups limit the application of this approach (Nelson et al. 2003; Shadpour et al. 2006). Various coating materials, with a majority of polymers, have been developed and could be physically adsorbed onto the microchannel surface via hydrophobic or electrostatic interactions. Examples of such materials include surfactants, amphiphilic copolymers, and charged polymers such as polyelectrolytes, polysaccharides, and polypeptides (Doherty et al. 2003).
3.1 Nonionic surfactants
Other commonly used nonionic surfactants such as Tween 20 (Boxshall et al. 2006) (Fig. 1b) and n-dodecyl-β-d-maltoside (DDM) (Huang et al. 2005) (Fig. 1c) have been adopted as well for microchannel coating. Tween 20 is a PEO derivative of sorbitan monolaurate with a hydrophilic PEO head group and an alkyl chain of 12 carbons while DDM is an alkyl polyglucoside. Wall coating with these surfactant molecules demonstrated fairly efficient protein resistance on PDMS substrate though long term stability studies have not been fully documented.
Other amphiphilic PEG-copolymers with various block compositions developed for the modification of biomaterial surface properties in various applications (Tessmar and Gopferich 2007) have also been applied for microchannel coating. Pluronic (Fig. 1d) is a series of powerful and widely used surfactants for dynamic coating in CE. This triblock copolymer of poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) (PEO–PPO–PEO) can be directly coupled to a variety of hydrophobic polymeric materials through spontaneous surface adsorption of the hydrophobic PPO (Amiji and Park 1992). Stable cell patterning experiments have been demonstrated by Tan et al. (2004) and Liu et al. (2002) using Pluronic F108 on various surfaces, including glass, PDMS, and polystyrene. Hellmich et al. (2005) also investigated the coating of PDMS with Pluronic. PDMS microbioreactor coated with Pluronic to maintain a steady protein level in the culture system was shown to reduce 85% serum protein adsorption compared to native one (Wu et al. 2006b). Poly(lactic acid)–poly(ethylene glycol) (PLA–PEG) (Fig. 1e) is another well-characterized PEG amphiphilic copolymer commonly used in tissue engineering applications (Lucke et al. 2000) and has been shown to be efficient in protein repellency (Salem et al. 2001). Recently, Sinclair and Salem (2006) have successfully demonstrated using microfluidic networks and PLA–PEG–biotin for cell patterning application.
3.2 Charged polymer
3.3 Polyelectrolyte multilayer
Dubas and Schlenoff (1999) have shown that the adsorption of PEM was not reversible with no spontaneous desorption, yet small extent of desorption by exchange of surface bound polymers with solution took place after a few days, with their PEM model of polystyrene sulfonate (PSS) and poly(diallyldimethyl-ammonium chloride) (PDA) on silicon dioxide surface. Moreover, owing to the fact that PEM surface was strongly dependent on the adsorption conditions and the polyelectrolytes itself and weakly on original substrate surface characteristics, very similar surface properties can be obtained on different substrates treated with the same PEMs (Decher 1997).
The LBL self assembly of polyelectrolytes on a charged surface offers another route of grafting PEG onto substrates. Boulmedais et al. (2004) constructed protein resistant PEM with PEG-derived polypeptides: PLL-g-PEG (Huang et al. 2001; Ruiz-Taylor et al. 2001) and poly(l-glutamic acid)-graft-PEG (PGA-g-PEG). Adhesion of protein was effectively reduced and bacterial adhesion was reduced by 92% with only three bilayers as compared to a glass substrate. PLL-g-PEG was also used as a final topping layer of PEMs on silica surface (Heuberger et al. 2005). Multilayers of poly(allylamine hydrochloride)/poly(styrene sulfonated) (PAH/PSS) were first prepared on oxidized silicon oxide surface. A final layer of PLL-g-PEG is then spontaneously assembled on top. Full serum adsorption on PLL-g-PEG topped PEMs decreased by three orders of magnitude compared to PEMs without the PLL-g-PEG topping layer.
Bovine serum albumin, a well known protein blocking agent, has also been exploited for surface modification with LBL technique. In one example, BSA was applied for PEM preparation with heparin (Tan et al. 2005). Positively charged BSA at pH 3.9 was assembled with heparin on ammonia plasma treated PVC substrate followed with chemical crosslinking with glutaraldehyde for additional stability. The surface showed efficient resistance to platelet adhesion with no thrombus forming. BSA was also applied as a top layer on PEM for PDMS surface modification. Wang et al. (2006a) coated BSA on PEM of chitosan and citrate-stabilized gold nanoparticles to prevent protein adsorption.
4 Covalent modifications
Modifying the surface via physisorption is experimentally simple and quick, however, these surface always suffer from thermal, mechanical, and solvolytic instabilities due to their weak interactions with the bottom substrate. Covalent modifications with SAM or polymer brushes tethering could improve these inherent difficulties for more surface robustness.
Self-assembled monolayers (SAMs) are prepared by spontaneous tethering of molecules with active chemical moieties onto reactive solid surfaces. Due to its ease of preparation, low cost, and versatility (Ulman 1996), the field of SAMs has attracted enormous research interests dedicated to many disciplines (Wink et al. 1997; Fendler 2001; Whitesides et al. 2001; Senaratne et al. 2005). Typical examples of SAM systems are organosilane species on oxidized glass, PDMS, metal oxides, and organosulfur (thiol-derivates) on noble metals, grown in either liquid or vapor phase. Many excellent reviews have been published related to chemistries and preparations of SAMs on various surfaces, as well as countless publications dedicated on patterning of SAMs for various bio and nano applications (Ulman 1996; Whitesides et al. 2001; Gooding et al. 2003; Gates et al. 2005; Love et al. 2005). We will focus this section on recent progresses of applying SAMs for surface passivation purposes in microfluidic devices.
In a common practice, an oxidation/activation step on glass and PDMS surface (e.g. oxygen plasma, UV/ozone, or Piranha) is needed to generate surface silanol (Si–OH) groups before the SAM grafting (Makamba et al. 2003). An in situ approach for performing oxidation step inside assembled PDMS microchannel was introduced by Sui et al. (2006). Acidic H2O2 solution was passed through the PDMS microchannel for oxidation purpose, followed with a sequential silanization process by injecting neat PEG-silane solution into the microchannel. This approach alleviated the use of specialized instruments for surface activation and post-assembly process after silanization.
Besides implementation of SAMs as single functional layer on the surface, it also plays a pivotal role as anchoring sites for further attachments of polymer chains or for initiation of surface confined polymerization (Schreiber 2000). Examples include silane reagents with amino, epoxide, mercapto, vinyl, aldehyde, bromo, and phenyl functional groups for further surface conjugation with corresponding functional polymers (Huang et al. 2006; Janssen et al. 2006).
4.2 Covalent polymer coatings
The advantage of covalent polymer coatings over other surface modification methods, (e.g. SAM and physisorption) is the superior mechanical and chemical robustness, coupled with a high degree of synthetic flexibility towards the introduction of a variety of functional groups (Pallandre et al. 2006). The pioneering work of grafting polymer on surface to reduce protein adsorption for improving CE was introduced by Hjerten (1985), who used surface vinyl groups introduced by vinyl-silane SAMs on silica to graft linear polyacrylamide chains. The covalent polymer coating techniques are commonly classified into two main categories: “grafting-to” and “grafting-from” (Zhao and Brittain 2000).
4.2.1 “Grafting-to” polymer coating
In “grafting-to” method, end-functionalized polymers or block copolymers are covalently tethered onto reactive anchoring layer on the surface (e.g. functional groups introduced by SAM). Several approaches for preparing surface anchoring layers were employed, such as silanization (Hjerten 1985) and Grignard chemistry (Cobb et al. 1990). Early demonstrations of nonfouling surface modifications by “grafting-to” techniques are the works by Effenhauser et al. (1997), who grafted PEG and carbohydrates onto silanized fused silica surface to prevent protein adsorption.
Polysaccharides such as dextran (Osterberg et al. 1995) as a potential alternative to PEG as nonfouling materials was grafted onto aminosilane functionalized glass surface (Martwiset et al. 2006). Different ratios of hydroxyl groups in dextran have been converted by sodium periodate (NaIO4) to aldehyde groups which covalently attach surface amine groups. It was found dextran with ~25% conversion of hydroxyl to aldehyde groups provides the best nonfouling surface with negligible protein adsorption whereas molecular weight of dextran does not play an important role in affecting the nonfouling characteristics. The protein resistant dependence on the relative amount of hydroxyl and aldehyde groups on the molecules implied the importance of interactions between surface and water molecules on protein adsorption.
End-functionalized PEG has also been grafted onto PEMs to passivate PDMS channel. Makamba et al. (2005) covalently topped end-functionalized PEG on PEMs of polyethyleneimine (PEI) and poly(acrylic acid) (PAA) crosslinked via carbodiimide coupling between carboxyl and amine groups of the PEM molecules for enhancing the stability of PEM. The treated PDMS surface presented excellent resistance to protein adsorption and high stability against hydrophobic recovery.
Thermal immobilization of polymers onto surface have been presented in the early work of Gilges et al. (1994), who grafted poly(vinyl alcohol) (PVA) onto fused silica capillary surface at elevated temperature without any precoated surface anchoring layer. This water-insoluble permanent coating was stable over a wide range of pH and effective for preventing protein adsorption. Recently, this technique was applied by Wu et al. (2005) to coat PDMS surface with multilayer of partially hydrolyzed (88%) PVA. This method produced a stable, hydrophilic coating on PDMS surface which substantially prevent both acidic and basic proteins, suppress EOF to a negligible value in the range of pH 3–11. Other PVA immobilization methods such as silanization and Grignard chemistry were also demonstrated elsewhere (Moritani et al. 2003).
Despite the simplicity of this “grafting-to” method, it usually suffers from low grafting density due to kinetic hindrance from the grafted polymer film (brushes) at the surface against new coming polymer chains, thus obstructing further attachment (Mansky et al. 1997). Moreover, film thickness is limited by the molecular weight of the functionalized polymer.
4.2.2 “Grafting-from” polymer coating
A powerful alternative for preparing thicker and denser polymer brush is the “grafting-from” technique [also known as surface initiated polymerization (SIP)], in which polymerization of monomers starts from the surface-anchored initiation sites (e.g. created by SAM) compared to the “grafting-to” case, in which prepolymerized polymers with functional groups are attached on the reactive surface. In this way, monomers added to the growing polymer chains from the surface do not endure considerable molecular hindrance, and thereby a thick and dense layer of polymer brushes can be formed.
22.214.171.124 Free radical polymerization
Early demonstrations of “grafting-from” technique were mostly based on conventional free radical polymerization (Prucker and Ruhe 1998a, b). The free radicals generated mostly photochemically or thermally from the surface immediately attack the double bonds of monomers (such as vinyl groups in methacrylate monomers) and add them to the growing chain. This process at the same time results in the formation of a new radical at the other end of the monomer for successive polymerization until two free radicals meet each other to quench the reactions. Ideally, polymerization is only confined at the surface, not in the solution.
Besides PEG, poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC), a phospholipid polymer comprising a methacrylate monomer and a zwitterionic phosphorylcholine head group in the side chain, has shown excellent resistance against nonspecific protein adsorption (Ishihara et al. 1990, 1998) and has been grafted onto various substrates. Goda et al. (2006) grafted PMPC onto PDMS surface with a similar approach as Hu et al. (2004) by immobilizing benzophenone on PDMS surface followed by UV mediated polymerization of monomers from the surface. Protein adsorption on the grafted PDMS surface decreased 50–70% compared to the unmodified PDMS surface. Comparative friction experiments revealed the presence of a highly hydrated thick water layer around the polymer chains is responsible to the reduction of protein adsorption. A recent example of using the UV mediated polymerization approach developed by Hu et al. (2004) was to create reversible bio-fouling/nonfouling surface using poly(N-isopropylacrylamide) (PNIPAAm) (Ebara et al. 2006). PNIPAAm was demonstrated earlier by Huber et al. (2003) to thermally switch between an antifouling hydrophilic state and a protein-adsorbing hydrophobic state. Ebara et al. further extended the use of this reversible surface to control the capture and rapid-release of PNIPAAm-grafted nanobeads. This chromatography system can find various useful applications in immunoassays and enzyme bioprocesses.
Another fast growing surface modification technique worth discussing is plasma-based polymerization. Advantages of this technique include: (1) modification limited to material surface without altering bulk properties, (2) low amount of waste and byproduct compared to wet chemistry, (3) relatively fast deposition rate, and (4) versatility of the method to use different kinds of monomer for a wide range of surface applications (Barbier et al. 2006). Bodas et al. (Bodas and Khan-Malek 2006; 2007) investigated hydrophilic stability of plasma treated polymerization on PDMS surface using hydrophilic monomer 2-hydroxyethyl methacrylate (HEMA). To graft the polymer onto the surface, HEMA monomer solution was spin coated onto plasma treated PDMS surface, followed by oxygen plasma to crosslink the polymer. Hydrophobic recovery test showed an increase in contact angle from 7° to 49° in 2 weeks. Similar oxygen plasma polymerization process was used to graft copolymer of HEMA and acrylic acid (AA) onto PDMS surface (Karkhaneh et al. 2007). O2 plasma treated PDMS surface was immersed in HEMA/AA monomers to allow the monomer to adsorb on the surface before oxygen plasma polymerization. Hydrophobic recovery test revealed that higher HEMA ratio in the mixture yielded a higher contact angle owing to the replacement of hydroxyl groups in AA by methyl groups in HEMA to minimize surface energy.
Besides grafting hydrophilic polymer layer on the surface using plasma, several works have been demonstrated to generate surface functional groups which can be used for further reactions. He et al. (2003) demonstrated a two-step process to generate cyano (CN) functional groups on PDMS surface with long term surface hydrophilic stability. Mildly activated PDMS by microwave plasma in a mixed gas of Ar and H2 was immersed in acrylonitrile solution to generate the hydrophilic functionalities on the surface. The grafted surface exhibited a low water contact angle and was stable at 35° ± 15° for at least 1 month at room temperature. Nitrile groups were also formed on PDMS by Bae et al. (Bae and Urban 2004), who used microwave plasma to graft imidazole and its alkyl-derivatives onto PDMS surface. Pruden et al. (Pruden and Beaudoin 2005), on the other hand, have attempted to modify PDMS surface with primary amine groups using microwave ammonia plasma treatment. A variety of nitrogen containing groups were formed in the reaction with a higher preference of producing amine groups over oxygen groups at higher plasma power, longer reaction time, and higher temperature. Functionalized dextran was also shown to be successfully attached to the primary amine sites.
Despite the versatility and efficiency of free radical polymerization, the main drawback of free radical polymerization is the lack of control of chain length and chain length distribution of the polymer layer, forming branched and highly polydisperse polymer layer (Lou et al. 2006). Furthermore, the polymerization reaction is limited by the initiator efficiency decrement due to the so called cage effect when the primary free radicals recombines forming macroinitiators with increasing molecular weight (Riess 2003). Moreover, no clear experimental evidence has yet reported confirming structure and properties specific to high-density brushes, suggesting that the achieved graft density may still be in a low grafting density regime (Tsujii et al. 2006).
126.96.36.199 Living radical polymerization
Living radical polymerization (LRP) or controlled radical polymerization (Husseman et al. 1999; Edmondson et al. 2004; Lou et al. 2006; Tsujii et al. 2006), on the other hand, has attracted substantial attention in surface chemistry in recent few years. There are a number of advantages of LRP over conventional free radial polymerization: accurate control on the brush density, composition, and polydispersity, regulated formation of block copolymers on the surface, and allowing polymerizing a wide range of functional monomers. LRP basically relies on a continuous activation/deactivation process of surface-anchored dormant chains immobilized via silane self-assembled on glass surface. Activated polymer chains (capping agents removed), in the presence of monomers, propagates for polymerization until it is randomly deactivated back by the capping agents. Since all chains experience equally frequent activation-deactivation cycles over a long time scale, a slow and nearly simultaneous growing is experienced by all chains, thus producing a low polydispersity polymer brushes. Various capping agents are used for LRP. Examples are halogens with transition metal catalysts for atom transfer radical polymerization (ATRP) (Ejaz et al. 1998; Matyjaszewski et al. 1999), nitroxides for nitroxide mediated radical polymerization (NMP) (Husseman et al. 1999), and dithioester chains for reversible addition-fragmentation chain transfer (RAFT) (Baum and Brittain 2002).
In order to achieve a controlled polymerization process via reversible capping (or deactivation) of the growing chains, the very low overall concentration of halogen capping agents released from surface to solution compared to that of the monomer is insufficient. One approach was by adding extra amount of halogen initiator to the monomer solution to increase the capping agent concentration, as introduced in the work of Ejaz et al. (1998). However, increased amount of nontethered polymer chains formed in the solution then has to be removed in a rinsing step. The other approach reported by Matyjaszewski et al. (1999) was by adding appropriate amount of metal deactivating agents prior to polymerization to increase the frequency of deactivation. This approach eliminated the final rinsing step.
Early demonstrations of ATRP suffered from the slow polymerization rate and limited film thickness (<100 nm), owing to the control nature of the polymerization process. Room temperature ATRP (Jones et al. 2002) in aqueous media employed by Huang et al. (2002) accelerated ATRP by incorporating water in the monomer solution. This aqueous reaction produced 700 nm of poly(2-hydroxyethyl methacrylate) (pHEMA) in just 12 h.
Recently, Xiao et al. performed surface initiated ATRP to graft poly(acrylamide) on PDMS surface (Xiao et al. 2002) for fabrication of PDMS CE microchip (Xiao et al. 2004). ATRP initiator was first immobilized by vapor deposition of (1-trichlorosilyl-2-m-p-chloromethylphenyl) ethane onto UV/ozone oxidized PDMS surface. The silanized channel was then filled with oxygen free polymerizing solutions containing acrylamide monomer, Cu(I)Cl, Cu(II)Cl2, and Tris[2-(dimethylamino)ethyl]amine and polymerization was allowed to proceed. The grafted surface exhibited a 20-fold improvement in resisting irreversible adsorption of lysozyme compared to bare PDMS. The grafted surface maintained the hydrophilicity for at least 1 month.
Poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC) zwitterionic polymer brush was also grafted on silicon surface with ATRP in room temperature (Feng et al. 2005b). The adsorption of fibrinogen and lysozyme on the modified surface was found to decrease with increasing chain length or layer thickness of the PMPC grafts, which was in turn controlled by the ratio of monomer and free initiator concentration in the solution. With a chain length of 200 U, more than 98% of protein adsorption was reduced compared to unmodified silicon surface. The surface was further characterized to show a strong correlation between fibrinogen adsorption and grafting density (Feng et al. 2006). Another example of growing zwitterionic polymer brushes was demonstrated by Zhang et al. (2006), who produced homopolymer brushes of poly(sulfobetaine methacrylate) (pSBMA) and poly(carboxy-betaine methacrylate) (pCBMA) with surface initiated ATRP to create highly nonfouling surface on glass slides. The reduction of fibrinogen and cell adhesion on these surfaces was shown to be comparable to PEG-like films.
The increase of using polymeric materials, especially PDMS, becomes the recent trend of fabricating microfluidic devices due to their unique bulk and surface properties and ease of fabrication. With the substantial increase of surface-to-volume ratio in micro scale, careful surface nano-scale treatment is of vital importance to render devices into practical use. One mostly encountered practical issue is the nonspecific protein adsorption on PDMS surface due to its hydrophobic nature.
This review summarizes surface modification methods published recently in constructing nonbiofouling PDMS surfaces under both physical and chemical means. Physical modification, relying basically on hydrophobic or electrostatic surface interactions, is simple to apply and can be employed in applications where long term chemical or mechanical stability is not a concern. When chemical modification is used, SAM can be applied as final functional layer or as an intermediate anchor layer for subsequent polymer grafting. Polymer grafting can be classified into two categories: grafting-to and grafting-from. “Grafting-to” is a relatively simpler method, supported with a large collection of commercially available chemicals. It can be used in general situation to create nonbiofouling layer coupled with various functional groups where defects in surface homogeneity and uniformity do not significantly matter in practice. “Grafting-from” can be applied where thickness, homogeneity, and chemical and mechanical robustness are highly desired. In additional to the aforementioned approaches where only hydrophilic interfaces were created for the anti-biofouling purpose, another promising approach currently under intensive investigation is the nanostructured superhydrophobic surface (Genzer and Efimenko 2006). These surfaces have been demonstrated to be very effective in suppression of protein adsorption. One possible reason is attributed to a decreased contact area between protein molecules and nanostructures which brings less opportunity for protein molecules to adhere to the surface unless they deform (Sun et al. 2005). Another reason may be due to a greater interfacial slip between the superhydrophobic surface and the liquid, which creates stronger shear stress in flow condition to ease the protein removal (Koc et al. 2008). Besides using surface chemistry approach to tune surface properties of polymeric materials, bulk chemistry approach by modifying composition of polymers to acquire specific surface properties is also progressively receiving attention recently (Muck and Svatos 2007) and may in the future become as handy as surface chemistry.
This work reviews recent progresses of surface chemistry applicable for lab-on-a-chip applications and is intended to serve as a reference for choosing an appropriate and technically feasible method for specific applications. It is obvious that these discussed surface modification concepts are not limited to constructing nonbiofouling surfaces on PDMS material. With an understanding of these surface modification concepts, unique surface properties (e.g. hydrophobicity, surface charge) and functionalities can then be achieved on different substrate material by selecting appropriate methods and reagents for the modification. Realizing proper nanoscale surface molecular property modification is essential to achieve desired microfluidic operations.
This work is supported by Center for Scalable and Integrated Nano Manufacturing (SINAM) Center (NSF DMI-0327077) and Center for Cell Control (CCC) (NIH 5 PN2EY018228).
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