ライフサイエンスコーパス: lab-on-a-chip

1 ced rapidly toward the goal of a 'sequencing lab-on-a-chip'.

2 lity for the readout of DNA microarrays in a lab-on-a-chip.

3 ther charged species as part of a microscale lab-on-a-chip.

4 storage, and autonomous decision making for lab-on-a-chips.

5 luidic chip-based technologies can bring the Lab-on-a-Chip a step closer to fully automated analytica

6 ical biosensing technologies integrated in a lab-on-a-chip allows for continuous, label-free, and non

7 On the other hand, the microfluidic lab-on-a-chip (also called a micro-total analysis system

8 fundamental discoveries are being applied to lab-on-a-chip analyses.

9 This highly sensitive and rapid lab-on-a-chip analysis method establishes the feasibilit

10 idics leads to the highly promising photonic lab-on-a-chip analytical systems (PhLoCs).

11 gives potential for future integration into lab-on-a-chip analytical systems for characterizing ioni

12 r various applications, such as microfluidic lab-on-a-chip and adaptive materials.

13 microfluidics are growing with the trend of Lab-on-a-Chip and distributed healthcare, the fully inkj

14 n technology that could be integrated within lab-on-a-chip and microfluidic separation devices.

15 ld promise for radically new applications in lab-on-a-chip and microfluidic technology, diagnostics a

16 of liquids in microfluidic systems (such as lab-on-a-chip and organ-on-a-chip devices) or structurin

17 popular material for microfluidic devices in lab-on-a-chip and other biomedical applications.

18 ion are therefore ideal candidates for novel lab-on-a-chip and remote manipulation applications in bi

19 , and potentially offer enhanced control of 'lab-on-a-chip' and optically driven microstructures.

20 applications in biosensing, mechanobiology, lab-on-a-chip, and cell-cell communication research.

21 ications, including DNA microarrays, digital lab-on-a-chip, anti-fogging and fog-harvesting, inkjet p

22 ng, photonics, microfluidic, optofluidic and lab-on-a-chip applications as they do not require extern

23 is often moved about microetched channels in lab-on-a-chip applications using electrokinetic flows (e

24 eceived much interest in the past decade for lab-on-a-chip applications, primarily preconcentration o

25 fective designs for various telemedicine and lab-on-a-chip applications.

26 platforms holds promise for high-throughput lab-on-a-chip applications.

27 pe distortion for assays and separations for lab-on-a-chip applications.

28 rocedures making it an attractive module for lab-on-a-chip applications.

29 0.35 kg) of the circuits make them ideal for lab-on-a-chip applications.

30 ance microfluidic channel designs of various lab-on-a-chip applications.

31 nanofluidic systems with logic circuits for lab-on-a-chip applications.

32 nal processing, sensing and increasingly for lab-on-a-chip applications.

33 ces with detection, sample, and reagents for lab-on-a-chip applications.

34 ocesses to programmable particle delivery in lab-on-a-chip applications.

35 achment are also addressable by our magnetic lab-on-a-chip approach.

36 ical system, nanomedicine, microfluidics and lab-on-a-chip architectures.

37 signs are often fairly advanced, whereas the lab-on-a-chip aspect is still rather simplistic in many

38 TRAP has application in lab-on-a-chip bioanalytical devices as well as in the fa

39 characterization of a multiplexed label-free lab-on-a-chip biosensor using silicon nitride (SiN) micr

40 or is, thus, a promising component in future lab-on-a-chip biosensors for detection of clinically rel

41 this technological gap, we have developed a lab-on-a-chip capable of mechanically inducing circular

42 and inexpensive technology can be used as a lab-on-a-chip component for initial whole blood sample p

43 ow cell designed within the framework of the lab-on-a-chip concept, using only the analyte and readil

44 nd reaction devices, bringing to reality the lab-on-a-chip concept.

45 in the field of biosensors, microarrays, and lab-on-a-chip development.

46 ity of coupling the muPAD technique with the lab on a chip device to detect and identify 1 mug of exp

47 n analyzed with the Agilent 2100 Bioanalyzer lab on a chip device with minimum detectable amounts of

48 Using the TipChip, a microfluidic lab-on-a-chip device developed for tip-growing cells, we

49 n be tailored to broad applications spanning lab-on-a-chip device engineering to analysis of bioelect

50 We report a novel lab-on-a-chip device integrating a multigate electrolyte

51 ic the sample preparation procedure within a lab-on-a-chip device or cartridge, but these systems req

52 Thus, in conjunction with a microfluidic lab-on-a-chip device our electrochemical immunosensing a

53 This lab-on-a-chip device thoroughly exploits the power of mi

54 In this study, we use a lab-on-a-chip device to understand, observe, and quantif

55 The devised lab-on-a-chip device was demonstrated to have 24 pg/ml l

56 this research, a new design of channels in a lab-on-a-chip device with flat electromembrane extractio

57 e, analytic component for a portable, robust lab-on-a-chip device.

58 can apply a linear temperature gradient to a lab-on-a-chip device.

59 iter-scale samples of [1-(13)C]fumarate in a lab-on-a-chip device.

60 orm multistep chemical processes on a single lab-on-a-chip device.

61 a life-like gut mucosal layer using in vitro lab-on-a-chip devices (to wit, the gut-on-a-chip) and sh

62 Electrochemical biosensors and associated lab-on-a-chip devices are the analytical system of choic

63 sical systems and open a path to stand-alone lab-on-a-chip devices capable of highly complex function

64 Microfabricated lab-on-a-chip devices employing a fully integrated elect

65 e bonding process enables the fabrication of lab-on-a-chip devices incorporating biomolecules, as is

66 which offer promise for incorporation within lab-on-a-chip devices or as dynamic substrates for cellu

67 Micro-particle operations in many lab-on-a-chip devices require active-type techniques tha

68 mass production of economical, miniaturized lab-on-a-chip devices that will have applications in a w

69 nd applied in electrochemical biosensors and lab-on-a-chip devices to assist in this endeavor.

70 chanism, one that may enable new designs for lab-on-a-chip devices used in DNA analysis.

71 ng the sensitivity of coulter based flexible lab-on-a-chip devices which have a wide range of applica

72 d patterns, controlled drug release systems, lab-on-a-chip devices, and biosensors.

73 automated analysis, pharmaceutical sensing, lab-on-a-chip devices, and quality control applications.

74 ans of implementing new functionalities into lab-on-a-chip devices, e.g., dynamic control over multip

75 Microfluidic devices, including lab-on-a-chip devices, have many advantages over convent

76 Microfabricated fluidics technology, e.g., lab-on-a-chip devices, offers many attractive features f

77 emented into electrochemical biosensor-based lab-on-a-chip devices, seminal studies discussing import

78 lative technologies including microfluidics, lab-on-a-chip devices, soft robotics, biochemical assays

79 ion, such as disposable paper-based devices, lab-on-a-chip devices, wearable sensors, and artificial

80 have a profound impact on the advancement of lab-on-a-chip devices.

81 f facilitating and improving portability for Lab-on-a-chip devices.

82 esolution NMR spectroscopy with microfluidic lab-on-a-chip devices.

83 rategy for inducing fluid flow and mixing in lab-on-a-chip devices.

84 imaging, in miniaturized microscopes and in lab-on-a-chip devices.

85 in microseparation techniques like HPLC and lab-on-a-chip devices.

86 accelerate the development of polymer-based lab-on-a-chip devices.

87 for the successful development of disposable lab-on-a-chip devices.

88 iology with easily manufactured microfluidic lab-on-a-chip devices.

89 he successful development and application of lab-on-a-chip devices.

90 plications such as self-cleaning surfaces or lab-on-a-chip devices.

91 miautomated extraction methodologies used in lab-on-a-chip devices.

92 cal process advances towards real and useful lab-on-a-chip devices.

93 ices and accelerate the commercialization of lab-on-a-chip devices.

94 lasmonic tweezers for further development in lab-on-a-chip devices.

95 on the chip and promotes the versatility of lab-on-a-chip devices.

96 targeted drug delivery, bioengineering, and lab-on-a-chip devices.

97 lectrical manipulation of microstructures in lab-on-a-chip devices.

98 ization of on-chip optical communication and lab-on-a-chip devices.

99 The development of small, portable "lab-on-a-chip" devices has the potential to provide indi

100 A class of "lab-on-a-chip" devices use external air pressure for pum

101 ited to miniaturization and integration into lab-on-a-chip-devices.

102 ple preparation or purification step in many lab-on-a-chip diagnostic devices.

103 roducts such as inkjet printer cartridges to lab-on-a-chip diagnostic systems.

104 A dual lab on a chip (DLOC) approach that enables simultaneous

105 monstrate the advantageous qualities of this lab-on-a-chip electrochemical sensor for clinical applic

106 ments: (i) enzyme-linked immunosorbent assay-lab-on-a-chip (ELISA-LOC) with fluidics, (ii) a charge-c

107 station has been designed to implement quick lab-on-a-chip experiments instead of wire bonding.

108 rates a new rationale for using microfluidic Lab-on-a-Chip flow cytometry (muFCM) with a simple 2D hy

109 To use a lab-on-a-chip for diagnostic applications, the optimizat

110 ces of Chlamydia trachomatis in a bead-based lab-on-a-chip format, incorporating a solid-phase sample

111 f the photothermal biosensing principle in a lab-on-a-chip format.

112 applied in portable analytical devices in a lab-on-a-chip format.

113 time frame, e.g. for pathogen detection in a lab-on-a-chip format.

114 es with the sample preparation process in a 'Lab-on-a-Chip' format is also covered.

115 Adaptation of these approaches to lab-on-a-chip formats is providing a new class of resear

116 reports the development of a graphene-based lab-on-a-chip (G-LOC) for the digital testing of renal f

117 Microchannels in lab-on-a-chip geometries are often not rectangular in cr

118 mediated isothermal amplification (LAMP) and lab-on-a-chip have proven to be ideal.

119 We report a lab-on-a-chip immunosesnor for quantification of the inf

120 To fully realize the enormous potential of lab-on-a-chip in proteomics, a major advance in interfac

121 omated chemical and biochemical analysis and lab-on-a-chip integration.

122 Lab-on-a-chip-level integration enables complete Sanger

123 tic fields has potential for use in portable lab-on-a-chip (LOAC) and analytical devices.

124 Amperometric detection at microelectrodes in lab-on-a-chip (LOAC) devices lose advantages in signal-t

125 s is a fundamental prerequisite in designing Lab on a Chip (LOC) devices for applications in biosensi

126 In this work, a new, highly sensitive lab on a chip (LOC) immunoassay has been designed, devel

127 The design of microfluidic Lab on a Chip (LoC) systems is an onerous task requiring

128 Lab on a chip (LOC) systems provide interesting and low-

129 is is the last step for the fabrication of a Lab on a Chip (LOC), a biodevice integrating DNA sensor

130 tector allows the hyphenation with versatile lab-on-a chip (LOC) technology.

131 or low-cost, point-of-care (POC) devices and lab-on-a-chip (LOC) applications.

132 Lab-on-a-Chip (LOC) biomicrofluidic technologies are rap

133 In this study we describe a simple lab-on-a-chip (LOC) biosensor approach utilizing well mi

134 nduced polarization (PHIP) in a microfluidic lab-on-a-chip (LoC) device and achieve 8.5% (13)C polari

135 Herein, a simple lab-on-a-chip (LOC) device based on biocompatible and bi

136 Herein, a novel lab-on-a-chip (LoC) device fabricated by 3D printing bas

137 We present a novel lab-on-a-chip (LOC) device for the simultaneous detectio

138 A closed droplet based lab-on-a-chip (LOC) device has been developed for the di

139 Lab-on-a-chip (LOC) devices for electrochemical analysis

140 h resource, the use of autonomous disposable lab-on-a-chip (LOC) devices-conceived as only accessorie

141 en a few attempts to incorporate SP-PCR into lab-on-a-chip (LOC) devices.

142 m in enhancing the performance of analytical lab-on-a-chip (LOC) devices.

143 Lab-on-a-chip (LOC) is one of the most recent techniques

144 polydimethylsiloxane/polyester amperometric lab-on-a-chip (LOC) microsystem with an integrated SPE.

145 We have developed a lab-on-a-chip (LOC) platform for electrochemical detecti

146 gene, mcr-9, using a portable and affordable lab-on-a-chip (LoC) platform, offering a promising alter

147 d an ultra-low-cost, rapid, and miniaturized lab-on-a-chip (LOC) platform.

148 sed technologies, paper-based assays (PBAs), lab-on-a-chip (LOC) platforms, novel assay formats, and

149 Over the last decade, lab-on-a-chip (LOC) systems have come to serve for micro

150 covering capillary electrophoresis (CE) and lab-on-a-chip (LOC) technologies in their analytical che

151 Here, we demonstrate the use of lab-on-a-chip (LoC) technologies to expose Latinx life s

152 ine the use of host gene signatures with our Lab-on-a-Chip (LoC) technology enabling low-cost POC exp

153 Lab-on-a-Chip (LoC) technology has the potential to revo

154 urable smartphone-interfaced electrochemical Lab-on-a-Chip (LoC) with two working electrodes for dual

155 ors have capability of being integrated into lab-on-a-chip (LOC), microfluidics, and micro total anal

156 tion have enabled the creation of disposable lab-on-a-chips (LOCs) as the new tools for neuroscience

157 use in mass spectrometry, electrowetting and lab-on-a-chip manipulations.

158 DMF is a "lab on a chip" method allowing for the movement, mixing,

159 Unlike other lab-on-a-chip methods, where the sample moves through ch

160 1D silicon surfaces has many applications in lab-on-a-chip, micro/nano-fluidic devices, roll-to-roll

161 ns that include cell biology, microfluidics, lab-on-a-chip, microelectromechanical systems and flexib

162 This analytical concept is integrated into a lab-on-a-chip microfluidic cell that allows for a high s

163 We have used a lab-on-a-chip microfluidic device and fluorescence micro

164 By taking advantage of a lab-on-a-chip microfluidic device developed in our labor

165 stals and their ability for integration into lab-on-a-chip microfluidic systems can both be harnessed

166 stigation of protein-protein interactions in lab-on-a-chip microfluidic systems.

167 orting and fractionation within integrated ('lab-on-a-chip') microfluidic systems, and can be applied

168 Here we analyse the progress made by lab-on-a-chip microtechnologies in recent years, and dis

169 incorporation of this new electrode array to lab-on-a-chip or MEMs (micro-electro mechanic systems) t

170 ade to design miniaturized platforms-such as lab-on-a-chip or microarrays-to run sensitive and reliab

171 sed in various virus sensing platforms (e.g. lab-on-a-chip, paper, and smartphone-based point-of-care

172 In this work, we proposed a novel lab on a chip platform capable of real-time and continuo

173 Herein, we describe a lab-on-a-chip platform based on dielectrophoresis (DEP).

174 We developed a lab-on-a-chip platform consisting of: (i) tandem-repeat

175 lation system (MEIS-chip) was developed as a lab-on-a-chip platform for human epidermal growth factor

176 s is the first report describing a DEP-based lab-on-a-chip platform for the quick, arrayed, software-

177 chnology can also be easily transferred to a lab-on-a-chip platform for use in resource limited setti

178 aration on a commercially available and open lab-on-a-chip platform, which provides an alternative au

179 wnstream analytical technologies in a single lab-on-a-chip platform.

180 gradients of dissolved oxygen (DO) within a lab-on-a-chip platform.

181 ption and dissipation in electronic devices, lab-on-a-chip platforms and energy harvest/conversion sy

182 w how that real-time fluorescent imaging and Lab-on-a-Chip platforms have the potential to be used fo

183 the complexity of an organism's physiology, lab-on-a-chip platforms provide a suitable primary model

184 exibly control micro-particles in integrated lab-on-a-chip platforms with minimal external equipment.

185 e liquids and single suspended particles for lab-on-a-chip platforms.

186 cs technology to develop a multiplexed rapid lab-on-a-chip point of care (POC) assay for the serologi

187 ing it suitable for further integration into lab-on-a-chip point-of-care devices.

188 The new "lab-on-a-chip" protocol integrates precolumn reactions o

189 This report describes a new "lab-on-a-chip" protocol integrating on-line precolumn bi

190 n this work, we present a photonic enzymatic lab-on-a-chip reactor based on cross-linked enzyme cryst

191 out analytical tools remain the goal of much lab on a chip research, but miniaturized methods capable

192 position modeling (FDM) in a (bio)analytical/lab-on-a-chip research laboratory is described.

193 ential applications in microfluidic devices, lab-on-a-chip, sensor, microreactor and self-cleaning ar

194 door to novel high-throughput CE devices and lab-on-a-chip sensors in the future.

195 n (LOQ), and the linear dynamic range of the lab-on-a-chip SERS (LoC-SERS) method for NTX detection i

196 present the development and application of a lab-on-a-chip spray approach that combines rapid sample

197 The lab-on-a-chip studies with live-cell multiparametric ima

198 fluidic control systems with a wide range of lab-on-a-chip substrates.

199 n microfluidics have enabled the design of a lab-on-a-chip system capable of measuring cellular membr

200 a future platform for the integration into a Lab-on-a-chip system for online monitoring of foodborne

201 se transcription LAMP (ddRT-LAMP) assay as a lab-on-a-chip system for rapid virus detection in the en

202 Here, we present a lab-on-a-chip system for real-time monitoring of magneti

203 y obtained with the microfluidic device, the lab-on-a-chip system should be widely applicable in high

204 ument is attractive for miniaturization on a lab-on-a-chip system to deliver point-of-care medical di

205 chamber can be developed into a microfluidic lab-on-a-chip system use at the point of care.

206 Employing our magnetic lab-on-a-chip system, we present magnetoresistive-based

207 man scattering (SERS) spectroscopy (532 nm) "lab-on-a-chip" system to rapidly detect and differentiat

208 larity as a means of fluidic manipulation in lab-on-a-chip systems can potentially reduce the complex

209 nt examples, showing a staggering variety of lab-on-a-chip systems for biosensing applications, are p

210 This review is mostly focused on describing Lab-on-a-chip systems for cardiac tissue engineering.

211 lytical performances of various microfluidic Lab-on-a-chip systems for PDT efficacy analysis on 3D cu

212 y effective strategy toward fully integrated lab-on-a-chip systems for various biomedical application

213 Lab-on-a-chip systems may be the solution which could al

214 The success of lab-on-a-chip systems may depend on a low-cost device th

215 Miniaturized lab-on-a-chip systems offer properties - e.g. low sample

216 handling and fluidic manipulation offered by lab-on-a-chip systems promises to yield powerful tools f

217 Microfabricated lab-on-a-chip systems provide cost- and time-efficient o

218 ate the feasibility of using microfabricated lab-on-a-chip systems to analyze extraterrestrial sample

219 The device has great potential for enabling lab-on-a-chip systems to be used with real-world samples

220 tential for integration with smartphones and lab-on-a-chip systems to develop applications for in sit

221 we review developments in the application of lab-on-a-chip systems to the bioenergy sciences.

222 otential as a tool to map velocity fields in lab-on-a-chip systems was discussed.

223 The use of Lab-on-a-chip systems with appropriate microstructure ge

224 islets and, in combination with appropriate Lab-on-a-chip systems, can be used as a Micro Total Anal

225 tus of PDT investigations using microfluidic Lab-on-a-Chip systems, including recent developments of

226 e also been devised based on nanobiosensors, lab-on-a-chip systems, or nanopore technology.

227 in miniaturized analytical devices, such as lab-on-a-chip systems, showcases their compatibility wit

228 formance and footprint near those viable for lab-on-a-chip systems, smartphones, and other consumer t

229 jection analyzers, microfluidic devices, and lab-on-a-chip systems.

230 mputation time) and scalable to more complex lab-on-a-chip systems.

231 grated as generic components in a variety of lab-on-a-chip systems.

232 eening systems and demonstrates the power of lab-on-a-chip systems.

233 nanorobotics, three-dimensional imaging, and lab-on-a-chip systems.

234 rocessing, and tunable particle transport in lab-on-a-chip systems.

235 e for the development of simple and portable lab-on-a-chip systems.

236 luding the construction of fully integrated 'lab-on-a-chip' systems.

237 Recent advances in lab-on-a-chip techniques have allowed single-cell captur

238 ment of miniaturized medical diagnostics and lab on a chip technologies.

239 Lab-on-a-chip technologies have the potential to deliver

240 The McMOA exploits lab-on-a-chip technologies to fully integrate complex au

241 We imagine a future where lab-on-a-chip technologies utilize novel predictive mark

242 ng sophisticated fluid manipulation tools in lab-on-a-chip technologies.

243 ons such as sensing, medical diagnostics and lab-on-a-chip technologies.

244 implemented on-chip, using microfluidic and lab-on-a-chip technologies.

245 ble point-of-care diagnostics by integrating lab-on-a-chip technology and electrochemical analysis.

246 the design and validation of a microfluidic Lab-on-a-Chip technology for automation of the zebrafish

247 es a novel handheld analyzer with disposable lab-on-a-chip technology for the electrical detection of

248 In this context, microfluidics and lab-on-a-chip technology have emerged as the most promis

249 Microfluidics or lab-on-a-chip technology offer clear advantages over con

250 li-responsive materials and the microfluidic lab-on-a-chip technology, we also present the stimuli-re

251 components on the same chip to produce true lab-on-a-chip technology.

252 development and application of a 3D-printed lab-on-a-chip that concurrently detects, via multiplexed

253 ion medicine, we propose a novel paper-based lab-on-a-chip to deliver a cost-effective and easy to us

254 d an approach and an electrochemical-optical lab-on-a-chip to observe cellular responses in localized

255 meter scale, offer applications ranging from lab-on-a-chip to optofluidics.

256 and can form a frugal, versatile, bona fide lab-on-a-chip with wide-ranging applications in liquid h

257 esented, suited for the development of novel lab-on-a-chips with an integrated DNA microarray.

258 Summarized, the proposed automated lab-on-a-chip workflow for customizable library preparat