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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

19 0.35 kg) of the circuits make them ideal for lab-on-a-chip applications.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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