S. Ghoreishizadeh, C. Baj-Rossi, S. Carrara, G. De Micheli
{"title":"Nano-sensor and circuit design for anti-cancer drug detection","authors":"S. Ghoreishizadeh, C. Baj-Rossi, S. Carrara, G. De Micheli","doi":"10.1109/LISSA.2011.5754147","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754147","url":null,"abstract":"The development of new technologies to monitor drugs concentration directly in patient's blood is absolutely required to succeed in personalized drug therapies. In this study, Etoposide - a well-known anti-cancer drug - has been chosen as model for cyclic voltammetry detection of drugs. Carbon nanotubes are chosen as electron-transfer mediators to enhance the system sensitivity. A very low frequency and low slope triangular-wave potential is required to acquire cyclic voltammograms. Cyclic voltammograms are definitely needed for a correct identification and quantification of the drug concentration in the patient serum. The aim of the paper is to investigate the feasibility of VLSI fully-integration of cyclic voltammetry measurements as a tool to develop a low-cost chip for drug monitoring in personalized therapy. A triangular wave generator CMOS circuit is proposed by using Direct Digital Synthesis (DDS) method. The circuit is implemented in 0.18 µm technology and it presents the possibility of changing the slope of the triangular voltage in a wide range of 10 to 100mV/s.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"17 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116988231","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Study of automatic biosounds detection and classification using SVM and GMM","authors":"Bor Jenq. Chua, Xue Li, H. D. Tran","doi":"10.1109/LISSA.2011.5754182","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754182","url":null,"abstract":"Ambulatory devices can be used to detect heart diseases and save lives in critical time. These devices are based on sound classification that usually adopts a suitable data mining algorithm. This paper investigates the performance of Support Vector Machine (SVM) and Gaussian Mixture Model (GMM) classifiers in classifying sound samples. SVM classifier makes use of a linearly separable hyperplane to classify data into different classes, while GMM utilizes a probabilistic model for density estimation through probability density functions. Feature vectors of sound samples were extracted using the Mel-frequency cepstral coefficients (MFCCs) and fed to the classifiers. Our experimental results showed that SVM is more robust than GMM, and SVM achieved >80% classification accuracy in all classes of sound samples collected in this study.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"54 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116303098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A reliable ultra low power merged LNA and Mixer design for medical implant communication services","authors":"Jihoon Jeong, Jeong-Ki Kim, D. Ha, Hyung-Soo Lee","doi":"10.1109/LISSA.2011.5754153","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754153","url":null,"abstract":"This paper presents an ultra low power merged LNA and Mixer design for MICS (Medical Implant Communication Services) applications. A capacitor cross-coupled common gate LNA is implemented for an easy input matching and reasonable noise performance. The mixer operates in weak inversion, which significantly reduces power consumption and relaxes the voltage headroom without sacrificing the LNA performance. The relaxed voltage headroom enables the stacking of the LNA and the mixer with a low supply voltage of 1.2 V. The merged LNA and mixer consumes only 1.83 mW, and achieves 21.6 dB power gain. A NF of the circuit is 3.55 dB at 1 MHz IF, and the IIP3 is −6.08 dBm.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"41 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121540659","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Solid-state nanopores integrated with low-noise preamplifiers for high-bandwidth DNA analysis","authors":"J. Rosenstein, V. Ray, M. Drndić, K. Shepard","doi":"10.1109/LISSA.2011.5754155","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754155","url":null,"abstract":"Nanopore sensing platforms have been limited in bandwidth and noise performance by the use of external measurement electronics with significant parasitic impedances. In this work, we describe progress toward integrating detection electronics with solid-state nanopore sensors. This new platform for high-bandwidth single-molecule electrochemical DNA analysis includes a low-noise 8-channel 0.13µm CMOS preamplifier with integrated Ag/AgCl microelectrodes. We also demonstrate monolithic integration of solid-state nanopores in the amplifier chip. This arrangement provides an opportunity to extend the useful bandwidth of nanopore sensors by a factor of ten or more.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"52 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126254475","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
N. Lei, S. Ramakrishnan, P. Shi, J. Orcutt, L. Kam, R. Yuste, K. Shepard
{"title":"An electrically-stimulate optically-record microsystem based on active CMOS multi-electrode array for dissociated cell cultures","authors":"N. Lei, S. Ramakrishnan, P. Shi, J. Orcutt, L. Kam, R. Yuste, K. Shepard","doi":"10.1109/LISSA.2011.5754184","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754184","url":null,"abstract":"Calcium fluorescence-based optical recording combined with patch-clamp stimulation has become the standard technique for analyzing neural network behavior. At best, stimulation is limited to only a few channels in this case. Passive multielectrode arrays for two-dimensional electrophysiology only offer electrode densities of 60 electrodes per mm2. Here, we report an active multielectrode array, constructed with a standard complementary metal-oxide-semiconductor (CMOS) technology, to perform localized extracellular stimulation of dispersed cell cultures. A 256×256 array integrated with in-pixel stimulators on a 4-by-4 mm2 CMOS chip noninvasively stimulate hippocampal cells cultured on chip at cellular resolution. Combined with calcium imaging using high-affinity indicators, we demonstrate the ability to observe spatiotemporal dynamics of neural activity.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125470483","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yong Mao, K. Cui, W. Lulu, Hong Zhao, F. Nie, Miriam Brandl, D. Beck, Liang Gao, Stephen T C Wong
{"title":"An in-silico approach for drug repositioning to tumour anti-migration using an integrated genomic strategy","authors":"Yong Mao, K. Cui, W. Lulu, Hong Zhao, F. Nie, Miriam Brandl, D. Beck, Liang Gao, Stephen T C Wong","doi":"10.1109/LISSA.2011.5754163","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754163","url":null,"abstract":"Cell migration is a key step for deterioration of many in situ or metastasis malignant tumours. Tumour anti-migration is a promising strategy to treat cancer, but corresponding drugs developed under such a strategy are still in dire poverty, partly due to the lengthly process of drug trials and approval required by the US Food and Drug Administration (FDA). Given there are thousands of FDA approved drugs in the market, we believe that drug repositioning may provide a fast and cost-effective way to identify potential anti-migration drugs. In this paper, an in-silico drug screening method using a genomic strategy is proposed for the goal, in which genomic signature identification combined with support vector machine modelling is adopted to estimate drug efficacy. And a high-throughput, sensitive, 3-dimensional invasion assay by quantitative bioluminescence imaging proved the performance of proposed method on in vitro disease models.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"42 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116290221","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Charge sensing using point-functionalized carbonnanotube transistors for single-molecule detection","authors":"S. Sorgenfrei, C. Chiu, C. Nuckolls, K. Shepard","doi":"10.1109/LISSA.2011.5754156","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754156","url":null,"abstract":"We have demonstrated that carbon-nanotube field-effect transistors act as highly sensitive single-molecule detectors when point functionalized. The hybridization kinetics of two complementary strands of DNA are associated with two-level fluctuations in the conductance of the nanotube to which the DNA is bound. We have studied the temperature dependence of the nanotube conductance and shown that the transport mechanism is consistent with Frenkel Poole emission, in which negatively charged DNA modulates a tunnel barrier at the point functionalized defect site. These transistors represent an important potential sensing platform for label-free single-molecule diagnostics.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"17 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128627167","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"An inexpensive, battery powered and portable instrument for the optical detection of pathogens","authors":"R. Khanna, W. Stanchina, A. Jones, A. Vats","doi":"10.1109/LISSA.2011.5754181","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754181","url":null,"abstract":"In order to satisfy an emergent demand in point of care (POC) diagnostics as well as low resource settings such as in developing countries, we have integrated optical and bio-medical engineering to implement a device, which detects pathogens and displays test results using cell phones. The device employs DNA amplification and off-the-shelf components to obtain the diagnosis.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128671903","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A high-resolution hybrid randomized modulation scheme for switched-mode DC-DC converters","authors":"V. Adrian, J. Chang, Lim Geok Soon","doi":"10.1109/LISSA.2011.5754149","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754149","url":null,"abstract":"Switched-mode dc-dc converters are routinely employed in the power supply section of low-power electronic systems, such as biomedical implants, to convert a supply voltage from one voltage level to another voltage level. The switched-mode dc-dc converter employs a modulator to modulate the output pulses. In Pulse Width Modulation (PWM)-based digital modulators, an N-bit counter is employed to generate 2N possible pulse widths, where the value of N is relatively small (≤10). As a consequence of small N, the output has limited resolution that may cause steady-state limit cycles in closed-loop converters [1]. The limit cycles translate to harmonic distortion in the output power spectrum. The impetus is, therefore, to improve the output resolution without increasing N that would otherwise increase the clock frequency and power dissipation of the counter, and without causing harmonic distortion or limit cycles.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"114 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133433454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Applications of activatable probes in molecular imaging","authors":"Lei Zhu, Xiaoyuan Chen","doi":"10.1109/LISSA.2011.5754174","DOIUrl":"https://doi.org/10.1109/LISSA.2011.5754174","url":null,"abstract":"Most new drug candidates generated during in vitro screenings turn out to be invalid after time-consuming and costly testing in animal models. Therefore, development of noninvasive, real-time, sensitive, and cost-effective tools with higher throughput for monitoring and early detection of drug efficacy in vivo is urgently needed. Of such techniques, optical molecular imaging provides many advantages over other imaging modalities, including the use of non-radioactive materials, high sensitivity, and safe detection using readily available instruments at moderate cost. Performance of in vivo optical imaging is solely dependent on the development of sophisticated imaging probes that exhibit high sensitivity and low background noise. Among diverse applications, peptide-based molecular beacons, so called protease activatable optical probes, have enabled in vivo imaging of proteases activity and demonstrated promising results in the field of protease research and protease-targeted drug development. Matrix metalloproteinases (MMPs) are a family of Zn2+ dependent endopeptidase. It is highly expressed in most cancers, cardiovascular diseases and other diseases. Herein, we are using MMPs as targets to develop an ultra-sensitive activatable probe for throughput drug discovery application.","PeriodicalId":227469,"journal":{"name":"2011 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA)","volume":"186 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2011-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132710064","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}