6 research outputs found

    College of Engineering Drexel E-Repository and Archive (iDEA)

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    www.library.drexel.edu The following item is made available as a courtesy to scholars by the author(s) and Drexel University Library and may contain materials and content, including computer code and tags, artwork, text, graphics, images, and illustrations (Material) which may be protected by copyright law. Unless otherwise noted, the Material is made available for non profit and educational purposes, such as research, teaching and private study. For these limited purposes, you may reproduce (print, download or make copies) the Material without prior permission. All copies must include any copyright notice originally included with the Material. You must seek permission from the authors or copyright owners for all uses that are not allowed by fair use and other provisions of the U.S. Copyright Law. The responsibility for making an independent legal assessment and securing any necessary permission rests with persons desiring to reproduce or use the Material. Please direct questions to [email protected] F M Sasoglu, A J Bohl and B E Layton Microbeam array for nN force measurement Design and microfabrication a high-aspect-ratio PDMS microbeam array for parallel nanonewton force measurement and protein printin

    Towards a method for printing a network of chick forebrain neurons for biosensor applications

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    Paper presented at the 29th Annual International Conference of IEEE-EMBS, Engineering in Medicine and Biology Society, EMBC'07, Lyon, France.The primary goal of this work is to establish a robust, repeatable method for printing arrays of neurons. This work has two endpoints. One is to use a neural array as an experimental testbed for investigating neuronal cell growth hypotheses. The other endpoint is to enable the next generation of cell-based sensors. Herein we compare microcontact printing results previously published by our group with a new method of dip-pen printing. We present preliminary results for neurons growing on these microprinted arrays, assessing contact frequencies and growth characteristics

    Microfabrication procedure of PDMS microbeam array using photolithography for laminin printing and piconewton force transduction on axons

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    Paper presented at 28th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBS), New York, NY: Aug 30 - Sept 3, 2006.The purpose of this paper is to introduce our design for transducing forces on the order of tens of piconewtons by optically measuring deflection of a microfabricated beam tip as it pulls on an array of flexible structures such as axons in an array of lamininprinted neurons. To achieve this we have designed polymeric beams with spring constants on the order of 10pN/μm. We have fabricated circular microbeams with Sylgard® polydimethylsiloxane (PDMS). The elastic modulus of PDMS was determined experimentally using a microscale and a micrometer at different concentrations of curing agent and base agent and found to be on the order of 100kPa. The designed geometry is a 100x100 tapered microcone array with each beam having a length of 100μm, and a base diameter of 10 μm. A SU-8 negative photoresist is etched using photolithography and used as a mold for PDMS soft lithography. PDMS was injected into the mold and the array peeled from the mold

    Design and microfabrication of a high-aspect-ratio PDMS microbeam array for parallel nanonewton force measurement and protein printing

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    Journal of Micromechanics and Microengineering, 17(3): pp. 623-632.Cell and protein mechanics has applications ranging from cellular development to tissue engineering. Techniques such as magnetic tweezers, optic tweezers, and atomic force microscopy have been used to measure cell deformation forces on the order of piconewtons to nanonewtons. In this study, an array of polymeric polydimethylsiloxane (PDMS) microbeams with diameters of 10-40μm and lengths of 118μm was fabricated from Sylgard® with curing agent concentrations ranging from 5% to 20%. Resulting spring constants were 100-300nN/μm. The elastic modulus of PDMS was determined experimentally at different curing agent concentrations and found to be 346kPa to 704kPa in a millimeter-scale array and ~1MPa in a microbeam array. Additionally, the microbeam array was used to print laminin for the purpose of cell adhesion. Linear and non-linear finite element analyses are presented and compared to the closed-from solution. Conclusion: The highly compliant, transparent, biocompatible PDMS may offer a method for more rapid throughput in cell and protein mechanics force measurement experiments with sensitivities necessary for highly compliant structures such as axons
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