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1-4 of 4
M. N. Rao
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Proceedings Papers
Proc. ASME. SMASIS2018, Volume 1: Development and Characterization of Multifunctional Materials; Modeling, Simulation, and Control of Adaptive Systems; Integrated System Design and Implementation, V001T03A006, September 10–12, 2018
Paper No: SMASIS2018-7978
Abstract
In the present article, we focus on the forced vibration and control analysis of functionally graded (FG) graphene-polymer composites bonded with piezoelectric layers considering strong electric fields. Different non-uniform gradient distributions of graphene platelets (GPLs) are assumed through the thickness direction. The Modified Halpin-Tsai micromechanics model is used to obtain the effective material properties of GPL/polymer composites. Electromechanical coupling of piezoelectric layers is described by two rotationally invariant non-linear constitutive relations. A four-node shell element considering transverse shear effect based on the Reissner-Mindlins hypothesis has been developed for forced vibration and control analysis of smart FG-GPL/composites using the principle of virtual work considering nonlinear material law for the piezoelectric layers. The developed element is verified and compared with the numerical results those available in the literature. Different configurations of FG-GPL composite shells have been analysed and discussed to compare in terms of settling time, first resonance frequency and absolute amplitude corresponding to first resonant frequency by carrying out time and frequency response analysis, and the effects of weight fraction of GPLs on vibration response of such shell structures are also discussed. The influence of electromechanical nonlinear constitutive relations is also presented and discussed by performing active control analysis on different FG-GPL composite shell structures. Moreover, the results show that the GPL distribution and weight-fraction of GPLs have a significant effect on the vibration and damping characteristics of the FG-GPL composite shell structures.
Journal Articles
Article Type: Research Papers
J. Nanotechnol. Eng. Med. May 2011, 2(2): 021007.
Published Online: May 16, 2011
Abstract
Vascular smooth muscle cells (VSMCs) are constantly exposed to cyclic stretch in the body, which makes it beneficial to study the effects of cyclic stretch on VSMCs. In this study, we developed a poly(dimethyl siloxane) (PDMS) compact six-well device that can be used to study the combined effect of cyclic strain and various growth factors on cultured VSMCs. Cell adhesion, alignment, and proliferation under 10% or 20% cyclic strain at 1 Hz were studied using this surface-enhanced PDMS device. The combined effects of cyclic strain with either transforming growth factor- β , vascular endothelial growth factor, fibroblast growth factor, or epidermal growth factor on VSMC proliferation was also examined. Results showed that VSMCs adhered well on the surface-enhanced multiwell device and they aligned perpendicularly to the direction of the cyclic strain. Cell proliferation was inhibited by 10% cyclic strain at 1 Hz compared with static control. The mitogenic effects of the growth factor were less potent under either 10% or 20% cyclic strain. With simple modification to accommodate more wells, this device could potentially be a useful tool for more economical, high throughput screening application.
Proceedings Papers
Proc. ASME. NEMB2010, ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology, 143-144, February 7–10, 2010
Paper No: NEMB2010-13300
Abstract
We have designed and characterized a poly-dimethyl-siloxane (PDMS) based microfluidic device called MiMiC™ that enables time-lapse study of cell migration. Cell migration is a key step of malignant metastasis during cancer progression. The device mimics the narrow confines the cells need to traverse and the microenvironments that are similar to the ones inside human body. Photolithography and soft lithography processes were used to fabricate the microfluidic devices. The device consists of two separate chambers connected by microfluidic channels allowing introduction of cells in one chamber and chemoattractants in the other. The response of lung-metastasized prostate cancer (PC-3-ML) cells and their migration response to chemoattractants were observed and analyzed. The numbers of cells under migration were determined from time-lapse images and compared to control groups. Our microfluidic assays provide advantages over the traditional Boyden chambers such as time-lapse observation, use of smaller amounts of reagents and direct assessment of cells under migration.
Journal Articles
Smitha M. N. Rao, Victor K. Lin, Uday Tata, Ganesh V. Raj, Jer-Tsong Hsieh, Kytai Nguyen, J.-C. Chiao
Article Type: Research Papers
J. Nanotechnol. Eng. Med. May 2010, 1(2): 021003.
Published Online: May 5, 2010
Abstract
Migration of cancer cells from the primary organ site via the bloodstream to distant sites is critical to the development of malignant metastasis and is in part determined by soluble host factors in the serum. Conventional Boyden chamber assays to evaluate cell motility require high volumes of reagents and are impractical for high-throughput analysis. We have designed and evaluated a poly-dimethylsiloxane (PDMS) microfluidic device in order to systematically study cancer cell migration. Photolithography and soft lithography processes were used to fabricate the PDMS devices from a negative photoresist (SU-8) mold. The device provides two separate identical chambers that are interconnected by an array of identical narrow channels, 10 μ m high, 25 μ m wide, and 1000 μ m long. One chamber is seeded with cancer cells whose migration characteristics are to be evaluated, while the other chamber contains media with chemoattractants toward which the cancer cells migrate. In this microfluidic chamber model, the migration of cancer cells within and across the microfluidic channels over a prescribed time was quantified using time-lapse photographs. The microfluidic chamber is a cost-effective platform that uses small volumes of reagents, can maintain stable chemokine gradients, allow real-time quantitative study of cancer cell migration, and provide information about cellular dynamics and biomechanical analysis. This work demonstrated the utility of the microfluidic device as a platform to study cancer cell migration as well as the potential applications in the identification of specific chemokine agents and development of drugs targeting cell migration.