Relevant bibliographies by topics / Implantable biosensors

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Implantable biosensors'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Implantable biosensors"

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Rodrigues, Daniela, Ana I. Barbosa, Rita Rebelo, Il Keun Kwon, Rui L. Reis, and Vitor M. Correlo. "Skin-Integrated Wearable Systems and Implantable Biosensors: A Comprehensive Review." Biosensors 10, no. 7 (July 21, 2020): 79. http://dx.doi.org/10.3390/bios10070079.

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Biosensors devices have attracted the attention of many researchers across the world. They have the capability to solve a large number of analytical problems and challenges. They are future ubiquitous devices for disease diagnosis, monitoring, treatment and health management. This review presents an overview of the biosensors field, highlighting the current research and development of bio-integrated and implanted biosensors. These devices are micro- and nano-fabricated, according to numerous techniques that are adapted in order to offer a suitable mechanical match of the biosensor to the surrounding tissue, and therefore decrease the body’s biological response. For this, most of the skin-integrated and implanted biosensors use a polymer layer as a versatile and flexible structural support, combined with a functional/active material, to generate, transmit and process the obtained signal. A few challenging issues of implantable biosensor devices, as well as strategies to overcome them, are also discussed in this review, including biological response, power supply, and data communication.
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Xu, Jian, and Hyowon Lee. "Anti-Biofouling Strategies for Long-Term Continuous Use of Implantable Biosensors." Chemosensors 8, no. 3 (August 7, 2020): 66. http://dx.doi.org/10.3390/chemosensors8030066.

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The growing trend for personalized medicine calls for more reliable implantable biosensors that are capable of continuously monitoring target analytes for extended periods (i.e., >30 d). While promising biosensors for various applications are constantly being developed in the laboratories across the world, many struggle to maintain reliable functionality in complex in vivo environments over time. In this review, we explore the impact of various biotic and abiotic failure modes on the reliability of implantable biosensors. We discuss various design considerations for the development of chronically reliable implantable biosensors with a specific focus on strategies to combat biofouling, which is a fundamental challenge for many implantable devices. Briefly, we introduce the process of the foreign body response and compare the in vitro and the in vivo performances of state-of-the-art implantable biosensors. We then discuss the latest development in material science to minimize and delay biofouling including the usage of various hydrophilic, biomimetic, drug-eluting, zwitterionic, and other smart polymer materials. We also explore a number of active anti-biofouling approaches including stimuli-responsive materials and mechanical actuation. Finally, we conclude this topical review with a discussion on future research opportunities towards more reliable implantable biosensors.
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Ziegler, Kirk J. "Developing implantable optical biosensors." Trends in Biotechnology 23, no. 9 (September 2005): 440–44. http://dx.doi.org/10.1016/j.tibtech.2005.07.006.

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Kotanen, Christian N., Francis Gabriel Moussy, Sandro Carrara, and Anthony Guiseppi-Elie. "Implantable enzyme amperometric biosensors." Biosensors and Bioelectronics 35, no. 1 (May 2012): 14–26. http://dx.doi.org/10.1016/j.bios.2012.03.016.

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Do Thi Hong, Diep, Duong Le Phuoc, Hoai Nguyen Thi, Serra Pier Andrea, and Rocchitta Gaia. "THE ROLE OF POLYETHYLENIMINE IN ENHANCING PERFORMANCE OF GLUTAMATE BIOSENSORS." Volume 8 Issue 3 8, no. 3 (June 2018): 36–41. http://dx.doi.org/10.34071/jmp.2018.3.6.

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Background: The first biosensor was constructed more than fifty years ago. It was composed of the biorecognition element and transducer. The first-generation enzyme biosensors play important role in monitoring neurotransmitter and determine small quantities of substances in complex matrices of the samples Glutamate is important biochemicals involved in energetic metabolism and neurotransmission. Therefore, biosensors requires the development a new approach exhibiting high sensibility, good reproducibility and longterm stability. The first-generation enzyme biosensors play important role in monitoring neurotransmitter and determine small quantities of substances in complex matrices of the samples. The aims of this work: To find out which concentration of polyethylenimine (PEI) exhibiting the most high sensibility, good reproducibility and long-term stability. Methods: We designed and developed glutamate biosensor using different concentration of PEI ranging from 0% to 5% at Day 1 and Day 8. Results: After Glutamate biosensors in-vitro characterization, several PEI concentrations, ranging from 0.5% to 1% seem to be the best in terms of VMAX, the KM; while PEI content ranging from 0.5% to 1% resulted stable, PEI 1% displayed an excellent stability. Conclusions: In the result, PEI 1% perfomed high sensibility, good stability and blocking interference. Furthermore, we expect to develop and characterize an implantable biosensor capable of detecting glutamate, glucose in vivo. Key words: Glutamate biosensors, PEi (Polyethylenimine) enhances glutamate oxidase, glutamate oxidase biosensors
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Zhang, Mingkuan, Xiaohong Wang, Zhiping Huang, and Wei Rao. "Liquid Metal Based Flexible and Implantable Biosensors." Biosensors 10, no. 11 (November 10, 2020): 170. http://dx.doi.org/10.3390/bios10110170.

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Biosensors are the core elements for obtaining significant physiological information from living organisms. To better sense life information, flexible biosensors and implantable sensors that are highly compatible with organisms are favored by researchers. Moreover, materials for preparing a new generation of flexible sensors have also received attention. Liquid metal is a liquid-state metallic material with a low melting point at or around room temperature. Owing to its high electrical conductivity, low toxicity, and superior fluidity, liquid metal is emerging as a highly desirable candidate in biosensors. This paper is dedicated to reviewing state-of-the-art applications in biosensors that are expounded from seven aspects, including pressure sensor, strain sensor, gas sensor, temperature sensor, electrical sensor, optical sensor, and multifunctional sensor, respectively. The fundamental scientific and technological challenges lying behind these recommendations are outlined. Finally, the perspective of liquid metal-based biosensors is present, which stimulates the upcoming design of biosensors.
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Acquaroli, Leandro N., Tim Kuchel, and Nicolas H. Voelcker. "Towards implantable porous silicon biosensors." RSC Adv. 4, no. 66 (2014): 34768–73. http://dx.doi.org/10.1039/c4ra04184d.

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Bobrowski, Tim, and Wolfgang Schuhmann. "Long-term implantable glucose biosensors." Current Opinion in Electrochemistry 10 (August 2018): 112–19. http://dx.doi.org/10.1016/j.coelec.2018.05.004.

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Puggioni, Giulia, Giammario Calia, Paola Arrigo, Andrea Bacciu, Gianfranco Bazzu, Rossana Migheli, Silvia Fancello, Pier Serra, and Gaia Rocchitta. "Low-Temperature Storage Improves the Over-Time Stability of Implantable Glucose and Lactate Biosensors." Sensors 19, no. 2 (January 21, 2019): 422. http://dx.doi.org/10.3390/s19020422.

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Molecular biomarkers are very important in biology, biotechnology and even in medicine, but it is quite hard to convert biology-related signals into measurable data. For this purpose, amperometric biosensors have proven to be particularly suitable because of their specificity and sensitivity. The operation and shelf stability of the biosensor are quite important features, and storage procedures therefore play an important role in preserving the performance of the biosensors. In the present study two different designs for both glucose and lactate biosensor, differing only in regards to the containment net, represented by polyurethane or glutharaldehyde, were studied under different storage conditions (+4, −20 and −80 °C) and monitored over a period of 120 days, in order to evaluate the variations of kinetic parameters, as VMAX and KM, and LRS as the analytical parameter. Surprisingly, the storage at −80 °C yielded the best results because of an unexpected and, most of all, long-lasting increase of VMAX and LRS, denoting an interesting improvement in enzyme performances and stability over time. The present study aimed to also evaluate the impact of a short-period storage in dry ice on biosensor performances, in order to simulate a hypothetical preparation-conservation-shipment condition.
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Edelberg, Jay M., Jason T. Jacobson, David S. Gidseg, Lilong Tang, and David J. Christini. "Enhanced myocyte-based biosensing of the blood-borne signals regulating chronotropy." Journal of Applied Physiology 92, no. 2 (February 1, 2002): 581–85. http://dx.doi.org/10.1152/japplphysiol.00672.2001.

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Biosensors play a critical role in the real-time determination of relevant functional physiological needs. However, typical in vivo biosensors only approximate endogenous function via the measurement of surrogate signals and, therefore, may often lack a high degree of dynamic fidelity with physiological requirements. To overcome this limitation, we have developed an excitable tissue-based implantable biosensor approach, which exploits the inherent electropotential input-output relationship of cardiac myocytes to measure the physiological regulatory inputs of chronotropic demand via the detection of blood-borne signals. In this study, we report the improvement of this application through the modulation of host-biosensor communication via the enhancement of vascularization of chronotropic complexes in mice. Moreover, in an effort to further improve translational applicability as well as molecular plasticity, we have advanced this approach by employing stem cell-derived cardiac myocyte aggregates in place of whole cardiac tissue. Overall, these studies demonstrate the potential of biologically based biosensors to predict endogenous physiological dynamics and may facilitate the translation of this approach for in vivo monitoring.
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Dissertations / Theses on the topic "Implantable biosensors"

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Wang, Ning. "Electrospun membranes for implantable glucose biosensors." Thesis, Brunel University, 2012. http://bura.brunel.ac.uk/handle/2438/8718.

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The goal for this thesis was to apply electrospun biomimetic coatings on implantable glucose biosensors and test their efficacy as mass-transport limiting and tissue engineering membranes, with special focus on achieving reliable and long sensing life-time for biosensors when implanted in the body. The 3D structure of electrospun membranes provides the unique combination of extensively interconnected pores, large pore volumes and mechanical strength, which are anticipated to improving sensor sensitivity. Their structure also mimics the 3D architecture of natural extracellular matrix (ECM), which is exploited to engineer tissue responses to implants. A versatile vertical electrospinning setup was built in our workshop and used to electrospin single polymer - Selectophore™ polyurethane (PU) and two polymer (coaxial) – PU and gelatin (Ge) fibre membranes. Extensive studies involving optimization of electrospinning parameters (namely solvents, polymer solution concentration, applied electric potential, polymer solution feed flow rate, distance between spinneret and collector) were carried out to obtain electrospun membranes having tailorable fibre diameters, pore sizes and thickness. The morphology (scanning electron microscopy (SEM) and optical microscopy), fibre diameter (SEM), porosity (bubble point and gravimetry methods), hydrophilicity (contact angle), solute diffusion (biodialyzer) and uniaxial mechanical properties (tensile tester) were used to characterize certain shortlisted electrospun membranes. Static and dynamic collector configurations for electrospinning fibres directly on sensor surface were optimized of which the dynamic collections system helped achieve snugly fit membranes of uniform thickness on the entire surface of the sensor. The biocompatibility and the in vivo functional efficacy of electrospun membranes off and on glucose biosensors were evaluated in rat subcutaneous implantation model. Linear increase in thickness of electrospun membranes with increasing electrospinning time was observed. Further, the smaller the fibre diameter, smaller was the pore size and higher was the fibre density (predicted), the hydrophilicity and the mechanical strength. Very thin membranes showed zero-order (Fickian diffusion exponent ‘n’ ~ 1) permeability for glucose transport. Increasing membrane thickness lowered ‘n’ value through non-Fickian towards Fickian (‘n’ = 0.5) diffusion. Thin electrospun PU membranes (~10 μm thick) did not affect, while thicknesses between 20 and 140 μm all decreased sensitivity of glucose biosensor by about 20%. PU core - Ge shell coaxial fibre membranes caused decrease in ex vivo sensitivity by up to 40%. The membranes with sub-micron to micron sized pore sizes functioned as mass-transport limiting membranes; but were not permeable to host cells when implanted in the body. However, PU-Ge coaxial fibre membranes, having <2 μm pore sizes, were infiltrated with fibroblasts and deposition of collagen in their pores. Such tissue response prevented the formation of dense fibrous capsule around the implants, which helped improve the in vivo sensor sensitivity. To conclude, this study demonstrated that electrospun membrane having tailorable fibre diameters, porosity and thickness, while having mechanical strength similar to the natural soft tissues can be spun directly on sensor surfaces. The membranes can function as mass-transport limiting membranes, while causing minimal or no effect on sensor sensitivity. With the added bioactive Ge surfaces, evidence from this study indicates that reliable long-term in vivo sensor function can be achieved.
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Katic, Janko. "Efficient Energy Harvesting Interface for Implantable Biosensors." Licentiate thesis, KTH, Integrerade komponenter och kretsar, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-163562.

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Energy harvesting is identified as a promising alternative solution for powering implantable biosensors. It can completely replace the batteries, which are introducing many limitations, and it enables the development of self-powered implantable biosensors. An interface circuit is necessary to correct for differences in the voltage and power levels provided by an energy harvesting device from one side, and required by biosensor circuits from another. This thesis investigates the available energy harvesting sources within the human body, selects the most suitable one and proposes the power management unit (PMU), which serves as an interface between a harvester and biosensor circuits. The PMU targets the efficient power transfer from the selected source to the implantable biosensor circuits. Based on the investigation of potential energy harvesting sources, a thermoelectric energy harvester is selected. It can provide relatively high power density of 100 μW/cm2 at very low temperature difference available in the human body. Additionally, a thermoelectric energy harvester is miniature, biocompatible, and it has an unlimited lifetime. A power management system architecture for thermoelectric energy harvesters is proposed. The input converter, which is the critical block of the PMU, is implemented as a boost converter with an external inductor. A detailed analysis of all potential losses within the boost converter is conducted to estimate their influence on the conversion efficiency. The analysis showed that the inevitable conduction and switching losses can be reduced by the proper sizing of the converter’s switches and that the synchronization losses can be almost completely eliminated by an efficient control circuit. Additionally, usually neglected dead time losses are proved to have a significant impact in implantable applications, in which they can reduce the efficiency with more than 2%. An ultra low power control circuit for the boost converter is proposed. The control is utilizing zero-current switching (ZCS) and zero-voltage switching (ZVS) techniques to eliminate the synchronization losses and enhance the efficiency of the boost converter. The control circuit consumes an average power of only 620 nW. The boost converter driven by the proposed control achieves the peak efficiency higher than 80% and can operate with harvested power below 5 μW. For high voltage conversion ratios, the proposed boost converter/control combination demonstrates significant efficiency improvement compared to state-of-the-art solutions.

QC 20150413

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Katic, Janko. "Highly-Efficient Energy Harvesting Interfaces for Implantable Biosensors." Doctoral thesis, KTH, Integrerade komponenter och kretsar, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-206588.

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Energy harvesting is identified as an alternative solution for powering implantable biosensors. It can potentially enable the development of self-powered implants if the harvested energy is properly handled. This development implies that batteries, which impose many limitations, are replaced by miniature harvesting devices. Customized interface circuits are necessary to correct for differences in the voltage and power levels provided by harvesting devices from one side, and required by biosensor circuits from another. This thesis investigates the available harvesting sources within the human body, proposes various methods and techniques for designing power-efficient interfaces, and presents two CMOS implementations of such interfaces. Based on the investigation of suitable sources, this thesis focuses on glucose biofuel cells and thermoelectric harvesters, which provide appropriate performance in terms of power density and lifetime. In order to maximize the efficiency of the power transfer, this thesis undertakes the following steps. First, it performs a detailed analysis of all potential losses within the converter. Second, in relation to the performed analysis, it proposes a design methodology that aims to minimize the sum of losses and the power consumption of the control circuit. Finally, it presents multiple design techniques to further improve the overall efficiency. The combination of the proposed methods and techniques are validated by two highly efficient energy harvesting interfaces. The first implementation, a thermoelectric energy harvesting interface, is based on a single-inductor dual-output boost converter. The measurement results show that it achieves a peak efficiency of 86.6% at 30 μW. The second implementation combines the energy from two sources, glucose biofuel cell and thermoelectric harvester, to accomplish reliable multi-source harvesting. The measurements show that it achieves a peak efficiency of 89.5% when the combined input power is 66 μW.
Energiskörd har identifierats som en alternativ lösning för att driva inplanterbara biosensorer. Det kan potentiellt möjliggöra utveckling av själv-drivna inplanterbara biosensorer. Denna utveckling innebär att batterier, som sätter många begränsningar, ersätts av miniatyriserade energiskördsenheter. Anpassade gränssnittskretsar är nödvändiga för att korrigera för de skillnader i spänning och effektnivå som produceras av de energialstrande enheterna, och de som krävs av biosensorkretsarna. Denna avhandling undersöker de tillgängliga källorna för energiskörd i den mänskliga kroppen, föreslår olika metoder och tekniker för att utforma effektsnåla gränssnitt och presenterar två CMOS-implementeringar av sådana gränssnitt. Baserat på undersökningen av lämpliga energiskördskällor, fokuserar denna avhandling på glukosbiobränsleceller och termoelektriska energiskördare, som har lämpliga prestanda i termer av effektdensitet och livstid. För att maximera effektiviteten hos effektöverföringen innehåller denna avhandling följande steg. Först görs en detaljerad analys av alla potentiella förluster inom boost-omvandlare. Sedan föreslår denna avhandling en designmetodik som syftar till att maximera den totala effektiviteten och effektförbrukningen. Slutligen presenterar den flera designtekniker för att ytterligare förbättra den totala effektiviteten. Kombinationen av de föreslagna metoderna och teknikerna är varierade genom två högeffektiva lågeffekts energigränssnittskretsar. Den första inplementeringen är ett termoelektriskt energiskördsgränssnitt baserat på en induktor, med dubbla utgångsomvandlare. Mätresultaten visar att omvandlaren uppnår en maximal effektivitet av 86.6% vid 30 μW. Det andra genomförandet kombinerar energin från två källor, en glukosbiobränslecell och en termoskördare, för att åstadkomma en tillförlitlig multi-källas energiskördslösning. Mätresultaten visar att omvandlaren uppnår en maximal effektivitet av 89.5% när den kombinerade ineffekten är 66 μW.

QC 20170508


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Vasylieva, Natalia. "Implantable microelectrode biosensors for neurochemical monitoring of brain functioning." Phd thesis, INSA de Lyon, 2012. http://tel.archives-ouvertes.fr/tel-00861119.

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Identification, monitoring and quantification of biomolecules in the CNS is a field of growing interest for identifying biomarkers of neurological diseases. In this thesis, silicon needle-shaped multi-molecules sensing microprobes were developed. Our microelectrode array design comprises a needle length of 6mm with 100x50 µm2 cross-section bearing three platinum electrodes with a size of 40x200 µm and 200µm spacing between them. We have used these microprobes for simultaneous glucose and lactate monitoring, using the third electrode for control of non-specific current variations. Local microdroplet protein deposition on the electrode surface was achieved using a pneumatic picopump injection system. Enzyme immobilization on the electrode surface is a key step in microelectrode biosensor fabrication. We have developed a simple, low cost, non-toxic enzyme immobilization method employing poly(ethyleneglycol) diglycidyl ether (PEGDE). Successful biosensor fabrication was demonstrated with glucose oxidase, D-amino acid oxidase, and glutamate oxidase. We found that these biosensors exhibited high sensitivity and short response time sufficient for observing biological events in vivo on a second-by-second timescale. PEGDE-based biosensors demonstrated an excellent long-term stability and reliably monitored changes in brain glucose levels induced by sequential administration of insulin and glucose solution. We then carried out a comparative study of five enzyme immobilization procedures commonly used in Neuroscience: covalent immobilization by cross-linking using glutaraldehyde, PEGDE, or a hydrogel matrix and enzyme entrapment in a sol-gel or polypyrrole-derived matrices. Enzymatic microelectrodes prepared using these different procedures were compared in terms of sensitivity, response time, linear range, apparent Michaelis-Menten constant, stability and selectivity. We conclude that PEGDE and sol-gel techniques are potentially promising procedures for in vivo laboratory studies. The comparative study also revealed that glutaraldehyde significantly decreased enzyme selectivity while PEGDE preserved it. The effects that immobilization can have on enzyme substrate specificity, produce dramatic consequences on glutamate detection in complex biological samples and in the CNS. Our biosensor's results were systematically controlled by HPLC or capillary electrophoresis. The highly selective PEGDE-based biosensors allowed accurate measurements glutamate concentrations in the anesthetized and awaked rats at physiological conditions and under pharmacological and electrical stimulations. The microfabricated multielectrodes based on silicon needles coupled to the simple, non-toxic and mild immobilization method based on PEGDE, open new possibilities for specific neurotransmitter detection in the central nervous system and the study of cell-cell communication in vivo.
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Pierce, Mary E. "Engineering a fiber-optic implantable cardiovascular biosensor /." free to MU campus, to others for purchase, 2004. http://wwwlib.umi.com/cr/mo/fullcit?p1422954.

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Moore, Charles Bruce. "The development of in vivo sensors." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296869.

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Meenakshisundaram, Guruguhan. "Development of novel implantable sensors for biomedical oximetry." Columbus, Ohio : Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1217427728.

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Rey, Jose. "Guiding Electric Fields for Electroporation Applications." Scholar Commons, 2011. http://scholarcommons.usf.edu/etd/3308.

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Electroporation is the critical step in an electric field mediated drug or gene delivery protocol. Electroporation based protocols have been successfully demonstrated in cancer clinical trials, however, its impact in other applications is still under investigation. A significant roadblock to long term functioning of implantable biosensors in vivo is the tissue reaction in the form of fibrous encapsulation that results in reduced transport to the sensing element of the biosensor. In vivo gene electroporation has a great potential as a means to modify the transport properties of tissues in the proximity of the sensing element of implantable biosensors. This dissertation examines two postulated electroporation based strategies to modify tissue for enhanced performance of an implantable biosensor. In the first, the implantation protocol is modified to accommodate in vivo electroporation. In the second strategy, the the modification is applied post implantation. This post-implantation in vivo electroporation application requires that electric energy be delivered at the site of electroporation close to the biosensor while minimizing effects far from such site. A novel method, focusing electric fields, developed for this purpose is presented. A theoretical framework as well as in vitro and in vivo experiments are provided as the introduction to the method and in support of its potential as the basis of a viable technology.
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Steinberg, Matthew David. "An implantable glucose biosensor." Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.625092.

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Jaffari, Samarah A. "A potentially implantable amperometric glucose biosensor." Thesis, Cranfield University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.282439.

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Books on the topic "Implantable biosensors"

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Crespilho, Frank N. Nanobioelectrochemistry: From Implantable Biosensors to Green Power Generation. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013.

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Nawito, Moustafa. CMOS Readout Chips for Implantable Multimodal Smart Biosensors. Wiesbaden: Springer Fachmedien Wiesbaden, 2018. http://dx.doi.org/10.1007/978-3-658-20347-4.

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International, Workshop on Wearable and Implantable Body Sensor Networks (6th 2009 Berkeley CA). Proceedings: Sixth International Workshop on Wearable and Implantable Body Sensor Networks : Berkeley, CA 3-5 June 2009. Los Alamitos, Calif: IEEE Computer Society Press, 2009.

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International, Workshop on Wearable and Implantable Body Sensor Networks (4th 2007 Aachen Germany). 4th International Workshop on Wearable and Implantable Body Sensor Networks (BSN 2007): March 26 - March 28, 2007, RWTH Aachen University, Germany. Berlin: Springer, 2007.

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International Workshop on Wearable and Implantable Body Sensor Networks (4th 2007 Aachen, Germany). 4th International Workshop on Wearable and Implantable Body Sensor Networks (BSN 2007): March 26 - March 28, 2007, RWTH Aachen University, Germany. Berlin: Springer, 2007.

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CMOS Readout Chips for Implantable Multimodal Smart Biosensors. Springer Vieweg, 2017.

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Nanobioelectrochemistry From Implantable Biosensors To Green Power Generation. Springer, 2012.

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1923-, Ko Wen H., Mugica Jacques, Ripart Alain, Implantable Sensors Symposium (1984 : Monaco, Monaco), and Cardiostim Conference (1984 : Monaco, Monaco), eds. Implantable sensors for closed-loop prosthetic systems. Mount Kisco, N.Y: Futura Pub. Co., 1985.

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(Editor), Steffen Leonhardt, Thomas Falck (Editor), and Petri Mähönen (Editor), eds. 4th International Workshop on Wearable and Implantable Body Sensor Networks (BSN 2007): March 26-28, 2007 RWTH Aachen University, Germany (IFMBE Proceedings). Springer, 2007.

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Friedrich, Pfeiffer Ernst, and Kerner W, eds. Implantable glucose sensors: The state of the art : international symposium, Reisensburg, 1987. Stuttgart: Thieme, 1988.

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Book chapters on the topic "Implantable biosensors"

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Córcoles, Emma P., and Martyn G. Boutelle. "Implantable Biosensors." In Biosensors and Invasive Monitoring in Clinical Applications, 21–41. Heidelberg: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-00360-3_5.

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Kotanen, Christian N., Francis Gabriel Moussy, Sandro Carrara, and Anthony Guiseppi-Elie. "Implantable Amperometric Biosensors." In Encyclopedia of Biophysics, 1033–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_822.

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Luz, Roberto A. S., Rodrigo M. Iost, and Frank N. Crespilho. "Nanomaterials for Biosensors and Implantable Biodevices." In Nanobioelectrochemistry, 27–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29250-7_2.

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Gotovtsev, Pavel M., Yulia M. Parunova, Christina G. Antipova, Gulfia U. Badranova, Timofei E. Grigoriev, Daniil S. Boljshin, Maria V. Vishnevskaya, et al. "Self-Powered Implantable Biosensors: A Review of Recent Advancements and Future Perspectives." In Macro, Micro, and Nano-Biosensors, 399–410. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-55490-3_20.

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Ohta, Jun, Kiyotaka Sasagawa, and Makito Haruta. "Optical Biosensors: Implantable Multimodal Devices in Freely Moving Rodents." In Handbook of Biochips, 1–15. New York, NY: Springer New York, 2020. http://dx.doi.org/10.1007/978-1-4614-6623-9_45-1.

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Nawito, Moustafa. "Introduction." In CMOS Readout Chips for Implantable Multimodal Smart Biosensors, 1–6. Wiesbaden: Springer Fachmedien Wiesbaden, 2017. http://dx.doi.org/10.1007/978-3-658-20347-4_1.

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Nawito, Moustafa. "The SMARTImplant Project." In CMOS Readout Chips for Implantable Multimodal Smart Biosensors, 7–18. Wiesbaden: Springer Fachmedien Wiesbaden, 2017. http://dx.doi.org/10.1007/978-3-658-20347-4_2.

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Nawito, Moustafa. "ASIC Version 1." In CMOS Readout Chips for Implantable Multimodal Smart Biosensors, 19–40. Wiesbaden: Springer Fachmedien Wiesbaden, 2017. http://dx.doi.org/10.1007/978-3-658-20347-4_3.

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Nawito, Moustafa. "ASIC Version 2." In CMOS Readout Chips for Implantable Multimodal Smart Biosensors, 41–84. Wiesbaden: Springer Fachmedien Wiesbaden, 2017. http://dx.doi.org/10.1007/978-3-658-20347-4_4.

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Nawito, Moustafa. "ASIC Version 3." In CMOS Readout Chips for Implantable Multimodal Smart Biosensors, 85–96. Wiesbaden: Springer Fachmedien Wiesbaden, 2017. http://dx.doi.org/10.1007/978-3-658-20347-4_5.

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Conference papers on the topic "Implantable biosensors"

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Green, Ryan B., and Erdem Topsakal. "Telemetry for Implantable Biosensors." In 2019 IEEE 69th Electronic Components and Technology Conference (ECTC). IEEE, 2019. http://dx.doi.org/10.1109/ectc.2019.00275.

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Ghoreishizadeh, Sara S., Tolga Yalcin, Antonio Pullini, Giovanni De Micheli, Wayne Burleson, and Sandro Carrara. "A lightweight cryptographic system for implantable biosensors." In 2014 IEEE Biomedical Circuits and Systems Conference (BioCAS). IEEE, 2014. http://dx.doi.org/10.1109/biocas.2014.6981765.

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Farahi, R. H., T. L. Ferrell, A. Guiseppi-Elie, and P. Hansen. "Integrated electronics platforms for wireless implantable biosensors." In 2007 IEEE/NIH Life Science Systems and Applications Workshop. IEEE, 2007. http://dx.doi.org/10.1109/lssa.2007.4400876.

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Kovac, M., G. Nagy, V. Stopjakova, and D. Arbet. "Design of CMOS integrated UWB antenna for implantable biosensors." In 2014 22nd Telecommunications Forum Telfor (TELFOR). IEEE, 2014. http://dx.doi.org/10.1109/telfor.2014.7034424.

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Mouris, Boules A., Ahmed M. Soliman, Tamer A. Ali, Islam A. Eshrah, and A. Badawi. "Efficient dual-band energy harvesting system for implantable biosensors." In 2016 17th International Symposium on Antenna Technology and Applied Electromagnetics (ANTEM). IEEE, 2016. http://dx.doi.org/10.1109/antem.2016.7550242.

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O'Neal, D. P., Michael J. McShane, Michael V. Pishko, and Gerard L. Cote. "Implantable biosensors: analysis of fluorescent light propagation through skin." In BiOS 2001 The International Symposium on Biomedical Optics, edited by Alexander V. Priezzhev and Gerard L. Cote. SPIE, 2001. http://dx.doi.org/10.1117/12.429340.

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Razzaghpour, Milad, Saul Rodriguez, Eduard Alarcon, and Ana Rusu. "A highly-accurate low-power CMOS potentiostat for implantable biosensors." In 2011 IEEE Biomedical Circuits and Systems Conference (BioCAS). IEEE, 2011. http://dx.doi.org/10.1109/biocas.2011.6107713.

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Ashraf, Mohammadreza, and Nasser Masoumi. "A fully-integrated power supply design for wireless implantable biosensors." In 2014 22nd Iranian Conference on Electrical Engineering (ICEE). IEEE, 2014. http://dx.doi.org/10.1109/iraniancee.2014.6999530.

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Siontorou, C. G., and F. A. Batzias. "Investigating implantable glucose biosensors pitfalls: a fault tree analysis approach." In BIOMED 2013. Southampton, UK: WIT Press, 2013. http://dx.doi.org/10.2495/bio130091.

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Olivo, Jacopo, Sandro Carrara, and Giovanni De Micheli. "Modeling of printed spiral inductors for remote powering of implantable biosensors." In 2011 5th International Symposium on Medical Information and Communication Technology (ISMICT). IEEE, 2011. http://dx.doi.org/10.1109/ismict.2011.5759790.

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