| 38 | Hoyin Lai and Albert Folch, "Design and characterization of "single-stroke" peristaltic PDMS micropumps", Lab Chip 11, 336 (2011). | ![]() |
| We demonstrate a new design of PDMS peristaltic pumps operated with a single control line. | ||
| 37 | Anna Boardman, Tim Chang, Albert Folch, and Norman J. Dovichi, "Indium-Tin Oxide Coated Microfabricated Device for the Injection of a Single Cell into a Fused Silica Capillary for Chemical Cytometry", Analytical Chemistry 82, 9959 (2010). | ![]() |
| We describe a microfabricated device for the capture and injection of a single mammalian cell into a fused silica capillary for subsequent analysis by chemical cytometry. | ||
| 36 | Nirveek Bhattacharjee, Nianzhen Li, Thomas M. Keenan, and Albert Folch, "A neuron-benign microfluidic gradient generator for studying the response of mammalian neurons towards axon guidance factors", Integrative Biology 2, 669 (2010). | ![]() |
| We record axonal growth of mouse embryonic cortical neurons in response to netrin gradients generated with a low-shear, open-bath microfluidic device. | ||
| 35 | David M. Cate, Christopher Sip, and Albert Folch, "A microfluidic platform for generation of sharp gradients in open-access culture", Biomicrofluidics 4, 044105 (2010). | ![]() |
| We demonstrate a membrane-based gradient generator that is compatible with open cell cultures. | ||
| 34 | John M. Hoffman, Mitsuhiro Ebara, James J. Lai, Allan S. Hoffman, Albert Folch, and Patrick Stayton, "A helical flow, circular microreactor for separating and enriching "smart: polymer-antibody capture reagents", Lab Chip 10, 3130 (2010). |
![]() |
| We report a mechanistic study of how flow and recirculation in a microreactor can be used to optimize the capture and release of stimuli-responsive polymerprotein reagents on stimuli-responsive polymer-grafted channel surfaces. | ||
| 33 | Ellen Tenstad, Anna Tourovskaia, Albert Folch, Ola Myklebost, and Edith Rian, "Extensive adipogenic and osteogenic differentiation of patterned human mesenchymal stem cells in a microfluidic device", Lab Chip 10, 1401 (2010).--> Inside cover article |
![]() |
| Adipogenic and osteogenic differentiation of patterned human mesenchymal stem cells is demonstrated using long-term microfluidic perfusion. | ||
| 32 | Figueroa, X.A., Cooksey, G.A., Votaw, S.V., Horowitz, L.F., and Folch, A., "Large-scale investigation of the olfactory receptor space using a microfluidic microwell array", Lab Chip 10, 1120 (2010). --> Cover article & Cited in Chemical Technology Highlights section. |
![]() |
| We show simultaneous calcium recordings of mouse dissociated olfactory sensory neurons in large microarrays so that the whole repertoire of mouse olfactory receptors is probed in one experiment. | ||
| 31 | Keenan, T.M., Frevert, C.W., Wu, A., Wong, V., and Folch, A., "A New Method for Studying Gradient-Induced Neutrophil Desensitization Based on an Open Microfluidic Chamber", Lab Chip 10, 116 (2010). |
![]() |
| This paper demonstrates neutrophil chemotaxis measurements in an open microfluidic chamber. | ||
| 30 | Sidorova, J.M. Li, N., Schwartz, D.C., Folch, A., and Monnat Jr., R.J. "Microfluidic-assisted analysis of replicating DNA molecules", Nature Protocols 4, 849 (2009). |
![]() |
| This paper presents detailed protocols on how to stretch DNA on glass surfaces using microfluidic channels. | ||
| 29 | Cooksey, G.A., Sip, C.G., and Folch, A., "A multi-purpose microfluidic perfusion system with combinatorial choice of inputs, mixtures, gradient patterns, and flow rates", Lab on a Chip 9, 417 (2009). |
![]() |
| We demonstrate a microfluidic perfusion system where the user can choose one of 64 combinations of 2,4, 8 or 16 inlets, stepwise or smoothened gradients, homogeneized mixtures, and 16 levels of flow rates going into a chamber designed for cell culture applications. | ||
| 28 | Tourovskaia, A., Li, N., and Folch, A., "Localized acetylcholine receptor clustering dynamics in response to microfluidic focal stimulation with agrin", Biophys. J. 95, 3009 (2008) --> Cited in Lab on a Chip Research Highlights section. |
![]() |
| In this paper we show that the synaptogenic factor agrin can have an important role in stabilizing agrin-predating acetylcholine receptor clusters. | ||
| 27 | Sidorova, J.M., Li, N., Folch, A., and Monnat Jr., R. "The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest", Cell Cycle 7, 796 (2008). |
![]() |
| We use flow in microchannels to stretch DNA on the surface for fundamental studies of genomic stability and prediction of DNA-targeting chemotherapy outcomes. | ||
| 26 | Keenan, T.M. and Folch, A. "Biomolecular gradients in cell culture systems", Lab on a Chip 8, 35 (2008) --> Cited in the cover. |
![]() |
| In this paper we review the major biological phenomena in which biomolecule gradients are employed, traditional in vitro gradient-generating methods developed over the past 50 years, and new microfluidic devices for generating gradients. | ||
| 25 | Chen, H.-H., Purtteman, J.J.P., Heimfeld, S., Folch, A., and Gao, D. "Development of a Microfluidic Device for Determination of Cell Osmotic Behavior and Membrane Transport Properties", Cryobiol. 55, 200 (2007). |
![]() |
| We demonstrate the measurement of volumetric changes of single cells trapped in microchannels in response to osmolarity changes for cryobiology applications. | ||
| 24 | Seng, K.-Y., Figueroa-Masot, X., Folch, A., and Vicini, P. "Objective Quantification of Acetylcholine Receptor Aggregation Using Fast Fourier Transforms", Comp. Meth. Prog. Biomed. 85, 220 (2007). |
![]() |
| We were able to automate the measurement of acetylcholine receptor clustering in myotube cultures. | ||
| 23 | Lam, E.W., Cooksey, G.A., Finlayson, B.A., and Folch, A., "Microfluidic Circuits with Tunable Flow Resistances", Applied Physics Letters 89, 164105 (2006) --> featured in the Virtual Journal of Nanoscale Science & Technology (Vol. 14, Iss. 18). |
![]() |
| In this paper we present the concept and implementation of a microfluidic "resistor" (a segment of a microchannel with user-controlled flow resistance). | ||
| 22 | Hsu, C.-H. and Folch, A., "Spatiotemporally- Complex Concentration Profiles Using a Tunable Chaotic Micromixer", Applied Physics Letters 89, 144102 (2006) --> featured in the Virtual Journal of Nanoscale Science & Technology (Vol. 14, Iss. 16). |
|
| We demonstrate the generation of temporal sequences of complex concentration profiles using a single device containing tunable microtopographies. | ||
| 21 |
Chen, C. and Folch, A., "A High-Performance Elastomeric Patch Clamp Chip", Lab on a Chip 6, 1338 (2006). |
![]() |
| We report a microfluidic patch clamp chip that allows for performing whole-cell recordings with unprecedented yields and exchanges of the extracellular and intracellular solutions. | ||
| 20 | Tourovskaia, A., Figueroa-Masot, X. and Folch, A., "Long-term Microfluidic Cultures of Myotube Microarrays for High-Throughput Focal Stimulation ", Nature Protocols 1, 1092 (2006). |
![]() |
| In this paper we report the precise protocols for culturing and focally stimulating single-myotube microarrays in a microfluidic device. | ||
| 19 | Keenan, T.M., Hsu, C.-H., and Folch, A. "Microfluidic "Jets" for Generating Steady-State Gradients of Soluble Molecules on Open Surfaces", Applied Physics Letters 89, 114103 (2006) --> featured in the Virtual Journal of Nanoscale Science & Technology (Vol. 14, Iss. 13) and in the Virtual Journal of Biological Physics Research (Vol. 12, Iss. 6). |
|
| In this paper we demonstrate the use of microfluidic "jets" to create dynamic gradients of soluble molecules on open surfaces. | ||
| 18 | Frevert, C.W., Boggy, G., Keenan, T.M., and Folch, A. "Measurement of Cell Migration in Response to an Evolving Radial Chemokine Gradient Triggered by a Microvalve", Lab on a Chip 6, 849 (2006) --> cited in the cover. |
![]() |
| In this paper we use a microfluidic valve to create chemotactic gradients and obtain neutrophil migration measurements correlated with spatiotemporal gradient values. | ||
| 17 | Tourovskaia, A., T.F. Kosar, and Folch, A. "Local Induction of Acetylcholine Receptor Clustering in Myotube Cultures Using Microfluidic Application of Agrin", Biophysical Journal 90, 2192 (2006). |
![]() |
| This paper shows the local clustering of acetylcholine receptors on selected areas of cultured myotubes using microfluidic focal application of agrin. | ||
| 16 | T.F. Kosar, Tourovskaia, A., Figueroa-Masot, X., Adams, M., and Folch, A. "A Nanofabricated Planar Aperture as a Mimic of the Nerve-Muscle Contact During Synaptogenesis", Lab Chip 6, 632 (2006). --> featured in Chemical Biology (top-viewed article in May 2006) and in the Faculty of 1000 Biology. |
![]() |
| This article demonstrates that nanofluidic delivery of soluble agrin to myotubes induces local clustering of acetylcholine receptors. | ||
| 15 | Li, N. and Folch, A. "Integration of topographical and biochemical cues by axons during growth on microfabricated 3-D substrates", Experimental Cell Research 311, 307 (2005). |
![]() |
| This paper reports effects of the microscale substrate composition and topography on axon growth in cultured embryonic cortical neurons. | ||
| 14 | Li, N., Hsu, C.-H., and Folch, A. "Parallel mixing of Photolithographically-Defined Nanoliter Volumes Using Elastomeric Microvalve Arrays", Electrophoresis 26, 3758 (2005). |
|
| This article demonstrates the use of microvalve arrays to create multiple titrations simultaneously (demonstration of a calcium-sensitive dye calibration). | ||
| 13 | Stucky, N.L., Chen, C., Kosar, T.F., and Folch, A. "Fabrication of Microfluidically-Accessible Planar Nanoholes on Elastomeric Substrates", Journal of Biomedical Nanotechnology 1, 384 (2005). | ![]() |
| This paper reports the fabrication of nanoholes on silicon nitride membranes to stimulate cells from underneath the cell culture surface. | ||
| 12 | Kosar, T.F., Chen, C., Stucky, N.L., and Folch, A. "Arrays of Microfluidically-Addressable Nanoholes", Journal of Biomedical Nanotechnology 1, 161 (2005). |
|
| This paper reports the fabrication of nanoholes on silicon nitride membranes to stimulate cells from underneath the cell culture surface. | ||
| 11 | Rettig, J.R. and Folch, A. "Large-Scale Single-Cell Trapping and Imaging Using Microwell Arrays", Analytical Chemistry 77, 5628 (2005). |
![]() |
| This article demonstrates the use of microwells to trap single cells in large arrays. | ||
| 10 | Keenan, T.M., Hooker, A., Spilker, M. E., Boggy, G. J., Li, N., Vicini, P., and Folch, A. "Automated Identification of Axonal Growth Cones in Time-Lapse Image Sequences", J. Neurosci. Methods 151, 232 (2005). |
![]() |
| This paper reports an image recognition software to track and quantitate the growth of axons from sequences of time-lapse phase-contrast micrographs of neurons growing on a flat substrate. | ||
| 9 | Hsu, C.-H., Chen, C., and Folch, A. "Microfluidic Devices with Tunable Microtopographies", Applied Physics Letters 86, 023508 (2005) --> featured in the Virtual Journal of Nanoscale Science & Technology (Vol. 11, Iss. 2) and in the Virtual Journal of Biological Physics Research (Vol. 9, Iss. 2). |
![]() |
| This paper implements our tunable-microtopography technique inside a microfluidic channel to demonstrate novel micromixers and fluid traps. | ||
| 8 | Tourovskaia, A., Figueroa-Masot, X. and Folch, A., "Differentiation-on-a-chip: A Microfluidic Platform for Long-Term Cell Culture Studies", Lab on a Chip 5, 14 (2005) --> cited in the cover and featured in Sample Content (thus available free of charge). |
![]() |
| This paper demonstrates the first 2-week-long cell culture in a (optionally, heterogeneous) microfluidic environment. | ||
| 7 | Hoffman, J., Shao, J., Hsu, C.-H., and Folch, A. "Elastomeric Molds with Tunable Microtopographies", Advanced Materials 16, 2201 (2004). |
![]() |
| This paper reports a micromolding method based on molds whose microtopography can be tuned by the user, thereby producing features that are difficult or impossible to obtain by traditional photolithography. | ||
| 6 | Hsu, C.-H., Chen, C., and Folch, A. "'Microcanals' for Micropipette Access to Single Cells in Microfluidic Environments", Lab on a Chip 4, 420 (2004) --> featured in the RSC's Chemical Biology Virtual Journal (2004, Iss. 19). |
![]() |
| This paper reports the first implementation of open-air microfluidic channels and their use to probe single cells with micropipettes within a microfluidic environment. | ||
| 5 | Neils, C. M., Tyree, Z., Finlayson, B., and Folch, A. "Combinatorial Mixing of Microfluidic Streams", Lab on a Chip 4, 342 (2004)--> featured in The Washington Post. |
![]() |
| In this paper we describe a microfluidic mixer that outputs all the sixteen combinations of four titrations of two dyes in continuous flow. | ||
| 4 | Li, N., Tourovskaia, A., and Folch, A. "Biology on a Chip: Microfabrication in Cell Culture Studies", Critical Reviews in Biomedical Engineering 31, 68 (2003). | |
| This paper reviews work on cell culture studies that incorporate microfabrication in order to modulate the microenvironment of cells. | ||
| 3 | Chen, C., Hirdes, D., and Folch, A. "Gray-Scale Photolithography Using Microfluidic Photomasks", Proceedings of National Academy of Sciences 100, 1499 (2003) --> see feature in the New York Times, Materials Today, Science News, Physics World, Photonics Spectra, Biophotonics International, and Physics Web. |
![]() |
| This paper reports the development of photolithographic masks that contain fluidic features of tunable opacity, yielding unique 3D microstructures. | ||
| 2 | Tourovskaia, A., Barber, T., Wickes, B., Hirdes, D., Grin, B., Castner, D. G., Healy, K. E., and Folch, A. "Micropatterns of Chemisorbed Cell Adhesion-Repellent Films Using Oxygen Plasma Etching and Elastomeric Masks", Langmuir 19, 4754 (2002). |
![]() |
|
This paper reports a method to confine cells for many days to micropatterns of proteins adsorbed on glass. |
||
| 1 |
Folch, A. and Toner, M. "Microengineering of Cellular Interactions", Annual Rev. of Biomedical Engineering 2, 227 (2000). |
|
|
This paper is a review that covers microfabrication techniques used to modulate cell-substrate, cell-cell, and cell-medium interactions. |
||