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Surface chemistry is one of the most crucial aspects for microarray modality biosensor development. As a matter of fact, the immobilization capability of the functionalized surface is one of the limiting factors for the final yield of the binding reaction. In this work, we locally deposited many reactive polymers on a single solid support, allowing for a direct comparison of functionality of probes immobilized on different polymers and demonstrating a new way of multiplexing. Our goal was to investigate the immobilization efficiency of reactive polymers, as well as the resulting affinity of the molecular probes, in a single experiment. This idea was demonstrated by spotting a large number of different reactive polymers on an untreated Si/SiO2 chip, and depositing the same molecular probe on all the spots immediately after. This method proved to be efficient and could be used as an initial qualitative assay to decide which functionalization better suits a certain application. We also showed that the localized functionalization method is applicable to proteins as well as oligonucleotides. Moreover, by means of real-time binding measurements performed with the Interferometric Reflectance Imaging Sensor (IRIS), we demonstrated that this functionalization technique is comparable to the uniformity of classical flat-coating solution. The comparison between the binding curves that were obtained from different polymer spots with the same probe allowed us to decide which polymers would work better to immobilize a model protein, α-Lactalbumin, as well as a peptide extracted from the latter, namely LAC-1. The final outcome is promising, and it highlights the multiplexing power of this method: first, it allows to characterize dozens of polymers at once, within a single 60-minutes experiment. Secondly, it removes the limitation, related to coated surfaces, that only molecules with the same functional groups can be tethered to the same solid support. By applying this innovative protocol, there is no more restriction on the type of molecules that can be studied simultaneously and immobilization for each molecular probe can be individually optimized.

Bioprobes immobilization methods that elevate the probes from the substrate are generally preferred in microarray technology because they prevent steric limitations during the hybridization of the target to probes. A versatile approach to control the thickness of a polymeric coating based on click chemistry to obtain covalently linked layer-by-layer coatings for surface functionalization is presented. By alternating cycles of coating using copolymers bearing click groups, the thickness of the film increases, while remaining functional and stable. Click chemistry reactions provide numerous advantages over standard conjugation procedures typically used in microarrays. They include: quantitative yields and insensitivity of the reaction to pH and hydrolysis. Moreover, click reactions do not interfere with organic groups naturally present in DNA, proteins and peptides such as amino and carboxyl groups allowing orthogonal and chemoselective probe immobilization. In addition to the formation of multilayers, click reactions allow to bind biomolecules to polymer chains generating so-called polymeric probes, which are then immobilized on microarray supports. In a microarray assay of clinical relevance, this methodology provides a miniaturized, tri-dimensional multilayer with higher density of capture probe, improved hybridization efficiency and sensitivity.

Recent advances in biosensing analytical platforms have brought relevant outcomes for novel diagnostic and therapy-oriented applications. In this context, hydrogels have emerged as appealing matrices to locally confine biomolecules onto sensing surfaces under solution mimetic conditions, preserving their structural integrity and function. Here, we describe the application of a self-assembling peptide hydrogel as a suitable matrix for 3D microarray bioassays. The hydrogel is printable and self-adhesive and allows for fast analyte diffusion. As a showcase example, we describe its application in a diagnostic immunoassay for the detection of arbovirus infection.

The interest towards aptamer-based surfaces in the field of bioaffinity assays is constantly growing. A crucial aspect is related to the ability of maintaining the high specificity of these molecules once immobilized on the surface. In this article we compare the immobilization of aptamers on a silanized silicon nitride surface as well as on a soft polymeric layer. An innovative immobilization approach, based on a copolymer, N-dimethylacrylamide-N-acryloyloxysuccinimide-3-(trimethoxysilyl)propylmethacrylate (DMA-NAS-MAPS) coating, able to crosslink itself to the substrate and to bind amino-modified biomolecules is proposed. Comparing this coating with a more classical functionalization process based on silane chemistry, we propose that the better results obtained on the polymeric layer are due to an increased binding efficiency of the aptamers bound to a soft material. The high specificity of immobilized DNA-aptamers is demonstrated using two sequences specific for thrombin detection and a non-sense sequence as negative control. The coating provides higher sensitivity compared to classical self-assembled silane coatings, probably due to a better mobility of bound aptamers. The aptamer immobilization on both surfaces was characterized and optimized using atomic force microscopy, X-ray photoelectron spectroscopy, contact angle and fluorescence microscopy. The comparison between the two different functionalizations highlights the better performances of the copolymer coating in terms of protein recognition, demonstrating thrombin detection down to 0.011 nM in buffer solution and 4.9 nM in complete human serum. Moreover, the localized immobilization of the aptameric sequences, utilized in this work, suggests the possibility of employing this platform also for multianalyte detection.

Biosensing analytical platforms rely on the intimate structure–function relationship of immobilized probes. In this context, hydrogels are appealing semi-wet systems to locally confine biomolecules while preserving their structural integrity and function. Yet, limitations imposed by biomolecule diffusion rates or fabrication difficulties still hamper their broad application. Here, using a self-assembling peptide, a printable and self-adhesive hydrogel was obtained and applied to fabricate arrays of localized bio-functional 3D microenvironments on analytical interfaces. This soft matrix represents a robust and versatile material, allowing fast and selective tuning of analyte diffusion, which is exploited here to run in-gel immunoassays under solution-like conditions in an unprecedented (

In the last years, magnetoresistive biosensors arrays have drawn a great interest due to their high sensitivity and integrability in lab-on-chip platforms. In such devices, the selective functionalization of the sensor active area is a major issue, in order to achieve high sensitivity and quantification capability. Here, we present a straightforward photolithographic procedure to create patterns of bio-reactive polymer regions on the sensor's surface, with micrometric resolution. The effectiveness of the procedure in providing high specificity and improved sensor performance is demonstrated in the case of magnetoresistive biosensors based on magnetic tunneling junctions (MTJs). On-chip biomolecular recognition assays demonstrate an enhanced sensitivity in selectively functionalized sensors with respect to non-patterned sensors, eventually leading to a limit of detection below the pM range, without target pre-concentration or chemical amplification.

The fabrication of high density microarrays requires a precise control of surface physical and chemical properties. In fact, spot morphology has a deep impact on signal level and might affect seriously the reliability and reproducibility of the assay. As a consequence, a proper biomolecule deposition and immobilization increases the accuracy of data analysis. Here we propose a new polymeric coating with intermediate hydrophilic/hydrophobic characteristics able to control the spreading of spots onto the surface as well as their size, thus enabling the reduction of the pitch between spots. The new coating exemplifies the versatility of a copolymer system based on the simultaneous presence of N,N-Dimethylacrylamide (DMA), 3-(trimethoxylsilyl)propyl methacrylate (MAPS) and fluorinated monomers, which impart to the surface a more hydrophobic behavior, reducing the drops spreading and merging. The controlled hydrophobicity allows to control also the size of the spots, thus the possibility of reducing their pitch to 140 μm and to obtain arrays with smaller dimentions, a very useful characteristics in those applications which imply the use of reduced areas, for example in miniaturized biosensors or microfluidic devices. The obtained copolymer is easily adsorbed onto glass or silicon oxide from a diluted aqueous solution of the polymer and the result is a microarray surface with intermediate hydrophobic/hydrophilic properties (average water contact angle is 50° and surface energy values are reduced from 114 mN/m to 50 mN/m), which allows decrease of the spot distance without merging of the droplets. To further improve the spot size and morphology, we have also investigated the use of several detergents added to the spotting buffer: in particular, the use of sucrose monolaurate, together with the hydrophobic surface, permitted the fabrication of surfaces for dense DNA microarray with very high fluorescence signals and low background noise. In fact, as an example of application in DNA microarray, the fluorinated coating has been used for the genotyping of KRAS G12D mutation, a common variant in the KRAS gene implicated in the colorectal cancer.

We report on the modification of a nitrocellulose film with copoly(DMA-NAS-MAPS), a tercopolymer based on N,N-dimethylacrylamide (DMA), N-acryloyloxysuccinimide (NAS), and 3-(trimethoxysilyl)propyl-methacrylate (MAPS). The chains of this polymer, interacting with nitrocellulose fibers, introduce active ester functionalities that promote the covalent binding of short oligonucleotide fragments to the nitrocellulose thin film. Using colorimetric detection, naked eye visible DNA microarrays are developed for easy identification of foodborne pathogens. The fast and robust procedure of nitrocellulose functionalization opens the opportunity to implement this material in disposable analytical microdevices that do not require sophisticated readout systems.

Nanofluidic sensing devices promise high performance by overcoming issues of mass transport of analyte molecules to the sensing surface, whilst micro-porous membranes promise high sensitivity due to a large surface for their capture. Anodic alumina (AAO) filter membranes allow the flow through of samples, and could be used as a convenient and readily available fluidic platform for the targeted delivering of analytes to bioreceptors immobilized on the pore walls. The relatively small pore dimensions, compared to fluidic diffusion lengths, promise highly efficient capture of analytes from the whole sample volume, enabling relatively fast sensing response times and the use of small sample volumes (

In this research, reproducible detection of fluorescently labelled DNA fragments is reported. Separation was carried out on a new microchip device composed of an array of 40 parallel microchannels (length 63 mm, width 300 μm, depth 500 μm). A comparison between coated and uncoated chips is presented, demonstrating the importance of surface coating in microchip devices for DNA separation. After a 6 min run, 10 DNA fragments were clearly observed in the coated chip with excellent reproducibility for intra-channel separation in the array of parallel capillaries. On the other hand, the efficiency of DNA separation in an uncoated microchip was adversely affected by band broadening and irreproducibility band position between channels.

Adsorbed polymers are widely used to suppress electroosmotic flow (EOF) in capillary electrophoresis (CE). Polymeric coatings, physisorbed onto the surface of the capillary wall, are often unstable under harsh conditions. This can be attributed to the reversible nature of the coating which becomes apparent when the adsorbed layer competes with a second species in the electrophoresis buffer solution for attachment/interaction with the capillary surface. In an effort to overcome the problem of coating instability, trimethoxysilane-modified polydimethylacrylamide was synthesized. This copolymer rapidly adsorbs on the wall from ultradilute aqueous solutions. After incubation at a temperature of 60 degrees C silyl groups, which extend from the polymer backbone, form condensation bonds with the silanols on the capillary surface. This enables subsequent formation of strong covalent bonds between the copolymer and the capillary wall. In this research, we establish that physisorption of polymer chains to the surface is essential for close alignment of surface and polymer silane groups which facilitates the formation of covalent bonds.

Here we combine the use of fluorescence-enhancing silicon substrates coated by copoly(DMA-NAS-MAPS), a ter-copolymer based on N,N-dimethylacrylamide (DMA), N-acryloyloxysuccinimide (NAS), and 3-(trimethoxysilyl)propyl-methacrylate (MAPS), with an efficient dynamic incubation to overcome mass transport limitations and obtain femtomolar limits of detection. The high sensitivity was obtained with a conventional microarray scanner without the use of any sophisticated detection strategy or protocol. When the method was applied, an improvement of the analytical sensitivity of approximately three orders of magnitude was achieved for antibody detection when compared with the same assay performed on regular glass slides and static conditions. Moreover, limits of detection of 45 and 54 pg/ml were obtained for hepatitis B superficial antigen and HIV p24 antigen, respectively. (C) 2011 Elsevier Inc. All rights reserved.

To date, photonic biosensing with porous membranes has produced slow responses and long sensing times, due to the narrow (less than 100 nm) closed end pores of the membranes used. Recently, polarimetry was used to demonstrate analyte flow through, and real time biosensing in, free-standing porous alumina membranes. Here, we demonstrate how an improved functionalization technology, has for the first time enabled a real-time immunoassay within a porous membrane with a total assay time below one hour. With the new approach, we show a noise floor for individual biosensing measurements of 3.7 ng/ml (25 pM), and a bulk refractive index detection limit of 5×10-6 RIU, with a standard deviation of less than 5%. The membranes, with their 200 nm pore diameter enabling targeted delivering of analytes to bioreceptors immobilized on the pore walls, therefore provide a route towards rapid and low cost real-time opto-fluidic biosensors for small sample volumes. QC 20150203 Positive

Through the presentation of analytical data from bioassay experiments, measured by polarimetry, we demonstrate for the first time a real time immunoassay within a free standing macroporous alumina membrane. The 200 nm nominal pore diameter of the membrane enables flow-through, thereby providing an ideal fluidic platform for the targeted delivery of analytes to bioreceptors immobilized on the pore walls, enabling fast sensing response times and the use of small sample volumes (

The demand for high sensitivity in microarray technology has stimulated the research of new labeling strategies, new substrates with increased loading capacity and new approaches to amplify the fluorescence signals. Although these methods improve the sensitivity, they are based on non-routine procedures which limit their widespread usage. A simple way to achieve fluorescence enhancement is the optical interference (OI) coating technology based on the use of substrates with films of well-defined thickness that maximize photoabsorption of the dye molecules in the vicinity of the surface and reflect the emitted light toward the detector. Here we introduce a new substrate for fluorescence enhancement composed of a thin aluminum mirror and a single quarter wave silicon oxide as a dielectric layer. The use of such material allows the development of a substrate suited for parallel production in conventional IC (Integrated Circuit's) technology, which produces a 20-fold enhancement of fluorescence compared to glass, which is the most common material used in microarrays. The new substrate was coated with a copolymer of N , N -dimethylacrylamide, N -acryloyloxysuccinimide, and 3-(trimethoxysilyl)propyl methacrylate, copoly(DMA-NAS-MAPS), which forms, by a simple and robust procedure, a functional nanometric film that covalently binds bio-probes on the surface and efficiently suppresses non-specific adsorption. The performance of the new fluorescence-enhancing substrate in microarray technology was demonstrated for the detection of a panel of inflammation biomarkers pushing detection limits into the femtomolar range.

The quality of separation in capillaries electrophoresis is strongly affected by the magnitude of the electroosmotic flow (EOF). The EOF can be efficiently suppressed by coating the capillary wall with hydrophilic polymers. In this paper, experimental data are presented to show the effect of coating thickness and charge on mass transport. Simulations performed with the lattice Boltzmann technique quantitatively reproduce the EOF with and without the coating and with either a neutral or charged coating layer. Experimental, simulation and theoretical analyses converge toward the interpretation that EO suppression arises from the frictional forces acting on the ionic currents and that a detailed representation of the polymeric coating is not needed in order to capture the phenomenon. © 2014 Springer-Verlag Berlin Heidelberg.

A fully automated coating procedure was devised based on adsorption of a new polymer, poly(dimethylacrylamide-co-allyl glycidyl ether) onto the capillary surface. The whole procedure takes less than 30 min and does not require the use of organic solvents, viscous solutions, or elevated temperature. The coating is stable even under harsh conditions such as alkaline pH, elevated temperature, and denaturant conditions that destroy most other presently available adsorbed coatings. This new adsorbed coating is highly stable and easy to produce in quantity, making it quite unique, and further making it possible to operate with any DNA sieving matrix. Finally, the above-mentioned properties facilitate coating regeneration by a simple wash with a strongly alkaline solution, thus extending the lifetime of the capillary, a highly desirable property for any coating used in biopolymer separations.

We report the first demonstration of real-time biosensing in free standing macroporous alumina membranes. The membranes with their 200 nm diameter pores are ideal candidates for biosensing applications where fast response times for small sample volumes are needed as they allow analytes to flow through the pores close to the bioreceptors immobilized on the pores walls. A bulk refractive index sensitivity of 5.2x10 -6 refractive index units was obtained from signal responses to different concentrations of NaCl solutions flowing through the pores. Finally, after functionalizing the alumina pore surfaces with an epoxysilane and then spotting it with β-Lactoglobulin protein, the interactions between the β-lactoglobulin and rabbit anti-β-lactoglobulin, as well as the interaction between the rabbit anti-β-lactoglobulin and a secondary antibody anti-rabbit Immunoglobulin G were monitored in real-time.

In this work, we present a highly sensitive immunoassay for the detection of the Alzheimer's disease (AD) biomarker amyloid-beta 1-42 (Aβ42) based on a label/label-free microarray platform that utilises silicon/silicon oxide (Si/SiO2) substrates. Due to constructive interference, Si/SiO2 layered slides allow enhancement of the fluorescence intensity on the surface with significant improvements in sensitivity of detection. The same substrate allows the label-free multiplexed detection of targets using the Interferometric Reflectance Imaging Sensor (IRIS), a platform amenable to high-throughput detection of mass changes on microarray substrates. Silicon chips are coated with copoly(DMA-NAS-MAPS), a ter-copolymer made from dimethylacrylamide (DMA), 3-(trimethoxysilyl)propyl methacrylate (MAPS) and N-Acryloyloxy succinimide (NAS). Aβ42 aggregation was studied by circular dichroism (CD), and an optimal antibody pair was selected based on specificity of recognition, binding yield and spot morphology of the capture antibody on the coated silicon surface as analysed by IRIS. Finally, incubation conditions were optimised, and an unprecedented Aβ42 detection sensitivity of 73pg/mL was achieved using an artificial cerebrospinal fluid (CSF) sample. Because of their multiplexing capability, low volume sample consumption and efficient sample-to-result time for population-wide screening, microarrays are ideal tools for the identification of individuals with preclinical AD who are still cognitively healthy. The high sensitivity of this assay format, potentially coupled to a pre-concentration step or signal-enhancing modifications, could lead to a non-invasive, inexpensive diagnostic tool for population-wide screening of AD biomarkers in biological fluids other than CSF, such as serum or plasma.

In this work, calculations and preliminary experimental data for determining the optimal condition for the selective bio-functionalization of magnetic tunneling junction (MTJ)-based biosensors are presented. Results on the detection of biomolecular recognition events employing MTJ-based sensor and magnetic beads are presented and interpreted through calculations, taking into account the dependence of the signal on the distribution of the beads with respect to the sensor. Furthermore, it is demonstrated by calculations that a significant increase in the sensor sensitivity and quantification capability can be achieved by selectively bio-functionalizing an area which corresponds to the sensor active area.

Protein and DNA microarrays hold the promise to revolutionize the field of molecular diagnostics. Traditional microarray applications employ labeled detection strategies based on the use of fluorescent and chemiluminescent secondary antibodies. However, the development of high throughput, sensitive, label-free detection techniques is attracting attention as they do not require labeled reactants and provide quantitative information on binding kinetics. In this article, we will provide an overview of the recent author's work in label and label-free sensing platforms employing silicon/silicon oxide (Si/SiO(2)) substrates for interferometric and/or fluorescence detection of microarrays. The review will focus on applications of Si/SiO(2) with controlled oxide layers to (i) enhance the fluorescence intensity by optical interferences, (ii) quantify with sub-nanometer accuracy the axial locations of fluorophore-labeled probes tethered to the surface, and (iii) detect protein-protein interactions label free. Different methods of biofunctionalization of the sensing surface will be discussed. In particular, organosilanization reactions for monodimensional coatings and polymeric coatings will be extensively reviewed. Finally, the importance of calibration of protein microarrays through the dual use of labeled and label-free detection schemes on the same chip will be illustrated.

A new silicon chip for protein microarray development, fabrication and validation is proposed. The chip is made of two areas with oxide layers of different thicknesses: an area with a 500 nm SiO(2) layer dedicated to interferometric label-free detection and quantification of proteins and an area with 100 nm SiO(2) providing enhanced fluorescence. The chip allows, within a single experiment performed on the same surface, label-free imaging of arrayed protein probes coupled with high sensitivity fluorescence detection of the molecular interaction counterparts. Such a combined chip is of high practical utility during assay development process to image arrays, check consistency and quality of the protein array, quantify the amount of immobilized probes and finally detect fluorescence of bioassays. (C) 2011 Elsevier B.V. All rights reserved.

Fluorescence measurements on protein microarrays demand photodetectors with ultra-high sensitivity (down to the single photon level), low noise and parallel readout capability. In the frame of the NANOSPAD FP6 European project, a novel compact instrument capable of ultra-sensitive analysis of multiple proteins in a customized microarray has been designed and implemented. In order to obtain a very compact system, a monolithic 6 X 8 array of single photon avalanche diodes (SPAD) was developed. The SPAD detector technology combines the general advantages of silicon microelectronic devices (miniature size, ruggedness and reliability, low-voltage and low-power operation, insensitivity to magnetic fields, etc.) with very high sensitivity, due to the ability to detect single photons with high efficiency and low detector noise. For performing measurements of chemiluminescent microarrays, around this monolithic detector all the necessary electronic and opto-mechanical set-up and the glass slide coating procedure for protein immobilization were developed. A viable methodology for specific detection of any protein is demonstrated by the NANOSPAD microarray system, suitable for application in the rapidly growing field of proteomic research. (C) 2010 Elsevier B.V. All rights reserved.

The conversion between the detected optical phase and the biological mass accumulated on the surface is determined using a label-free interferometric technique. The results demonstrate a linear phase/mass relationship for DNA and protein microarrays.

In this study, we report on the utilization of layered substrates for increased performance of fluorescentbased detection schemes. Through optimization of layer thicknesses, we demonstrate that enhancement with respect to commonly used microscope slides is achieved for the collected fluorescence signal.

We analyze the electroosmotic flow (EOF) of an electrolytic solution in a polymer coated capillary electrophoresis tube. The polymeric density, charge, thickness, and the capillary tube charge vary as a function of pH and produce a non- trivial modulation of the EOF, including a flow reversal at acid pH conditions. By means of a theoretical argument and numerical simulations, we recover the experimental curve for the EOF, providing a firm approach for predictive analysis of electroosmosis under different polymeric coating conditions. A proposed application of the approach is to determine the near-wall charge of the coating to be used for further quantitative analysis of the electroosmotic flow and mobility. (C) 2015 AIP Publishing LLC.

Modern techniques for DNA and protein analysis and separation rely on measurements of LIF and face a trend toward employing progressively smaller samples. The currently employed detectors that provide the required ultrahigh sensitivity, e.g. photomultiplier tubes (PMTs), are bulky and/or costly and delicate, whereas a key issue for the development of compact and economical instruments is the availability of miniaturized, inexpensive, and ultrasensitive photodetectors. The planar epitaxial silicon single-photon avalanche diodes (SPADs) combine the typical advantages of microelectronics (miniaturization, ruggedness, low voltage, low power, low cost, etc.) with high sensitivity, even better than that of PMTs. The suitability of such SPADs to microchip CE has been here ascertained by developing a new apparatus with dual-wavelength LIF detection. The apparatus has been experimented in studies on the EOF suppression and on the coating stability and tested in rapid sizing of DNA fragments. The experimental results obtained in the separation of Cy5-labeled oligonucleotide demonstrate sensitivity better than 3 pM, which corresponds to less than 100 fluorescent molecules in the 50 pL illuminated volume.

Techniques for DNA and protein analysis and separation rely on laser-induced fluorescence (LIF) and employ ultra-sensitive photo-sensors (photo-multiplier tubes or PMT’s, etc.) that are bulky and costly. A key issue for compact and economical instruments is the availability of miniaturized and economical ultra-sensitive sensors. The planar silicon single-photon avalanche diodes (SPAD’s) join typical microelectronic advantages (miniaturization, ruggedness, low voltage, power, and cost) to sensitivity comparable to PMT’s. A compact system is described with a dual SPAD-based LIF detection system and a glass microchip for capillary electrophoresis (CE). Sensitivity better than 3 pM with injection volume 50 pl is achieved in the separation of CY5 DNA labelled fragments. © 2003 Elsevier B.V. All rights reserved.

Multicompartment electrolyzers (MEs) with isoelectric membranes were introduced in 1989 for purifying proteins in an electric field. At the basis of ME technology there are membranes consisting of cross-linked copolymers of acrylamide and acrylamido monomers bearing protolytic groups. The technology employed for casting the membranes is an extension of the isoelectric focusing in immobilized pH gradient technique for which specific acrylamido monomers, known with the trade name of Immobiline, have been developed. However, the use of continuous membranes presents several disadvantages. Due to the mechanical characteristics of polyacrylamide, the gel must physically adhere onto a rigid support, which prevents it from collapsing. The support must have a highly porous structure in order to be permeable to proteins. The mechanical fragility of the membranes is one of the main problems that hinders the industrial scale application of ME separators. In order to overcome this problem, we propose to substitute the continuous membranes with a bed of gel beads of identical comonomer composition, obtained by an inverse emulsion polymerization process.

The novel polymer matrices reported here are low-viscosity sieving media for DNA capillary electrophoresis. This new family of matrices comprises copolymers of N,N-dimethylacrylamide with different monomers which increase polymer hydrophilicity. All these new copolymers self-coat on fused-silica capillaries. Resolution, peak spacing and peak width were the parameters taken into account to assess the influence of polymer structure on separation selectivity and efficiency. This work demonstrates that the performance of polydimethylacrylamide (PDMA) can be improved through copolymerization with hydrophilic monomers. The improvement is related to the efficiency parameter. The new copolymers, due to their low viscosity high sieving capacity and ability to suppress EOF, represent a better alternative to PDMA and are suitable replaceable matrices for capillary and microchip electrophoresis.

New acrylic polymers bearing oxirane groups were synthesized to be used in the production of coated capillaries. A fully automated coating procedure was devised based on the use of diluted water solutions of these polymers. The whole procedure required less than 30 min. The new polymers rapidly adsorbed from water onto the capillary wall, thus suppressing electroosmotic flow (EOF) to a negligible value. The adsorbed coatings were stable for hundreds of hours at high pH, temperature, and in the presence of 8 M urea. Efficient separations of acidic and basic proteins were achieved in the new phases.

Femtosecond-laser-written optical waveguides are integrated into a commercial capillary electrophoresis chip. A fluorescence detection scheme is implemented, resulting in a compact device. Testing is performed by electrophoresis and detection of a 1-nM oligonucleotide plug.