ライフサイエンスコーパス: microfluidic device

1 ample loop into the fluid flowing within the microfluidic device.

2 number of hepatocyte spheroids cultured in a microfluidic device.

3 program the valve sequences that operate the microfluidic device.

4 retrieved by a water droplet using a digital microfluidic device.

5 easurements of gene expression dynamics in a microfluidic device.

6 achieved in the DAMR system using 3D-printed microfluidic device.

7 recipitate from a single sample-aliquot in a microfluidic device.

8 n spreading of tau in a unique three-chamber microfluidic device.

9 igital LAMP to be performed in a self-driven microfluidic device.

10 nd subjected to chemokine gradients within a microfluidic device.

11 of microwells (7 pL each) in a multilayered microfluidic device.

12 e trapped on-demand in the downstream of the microfluidic device.

13 e period and assessed for CTC burden using a microfluidic device.

14 H2O2 and hydroquinone was injected into the microfluidic device.

15 pended electrodes integrated into a scalable microfluidic device.

16 ble users to build, configure, and operate a microfluidic device.

17 trol the size of microdroplets produced in a microfluidic device.

18 ia the neuromuscular junction (NMJ) within a microfluidic device.

19 rapid in-line separation using an open space microfluidic device.

20 ls), can be robustly recapitulated using the microfluidic device.

21 s for 24+ h at the single-cell level using a microfluidic device.

22 les of each pillar in an array embedded in a microfluidic device.

23 is performed at a disposable paper electrode microfluidic device.

24 owth signals from only tens of bacteria in a microfluidic device.

25 chnique has merits toward the fabrication of microfluidic devices.

26 teractive tool for designing continuous flow microfluidic devices.

27 n applications ranging from photovoltaics to microfluidic devices.

28 mposites, electronic devices, and all-liquid microfluidic devices.

29 nting, have emerged as fabrication tools for microfluidic devices.

30 at significantly expand the functionality of microfluidic devices.

31 ire array, to measure the biointeractions in microfluidic devices.

32 holding geometries, specifically paper-based microfluidic devices.

33 formation at relatively warm temperatures in microfluidic devices.

34 and promoted neurite growth and branching in microfluidic devices.

35 for the operation of macroscale machines and microfluidic devices.

36 ation of isothermal amplification methods in microfluidic devices.

37 Tau propagation from neuron to neuron using microfluidic devices.

38 sympathetic and sensory neurons cultured in microfluidic devices.

39 olutionary technology for the fabrication of microfluidic devices.

40 ation, and tools for the production of paper microfluidic devices.

41 imaging (MRI) incompatible with small-scale microfluidic devices.

42 ompetitive Salmonella typhimurium strains in microfluidic devices.

43 gher than that of conventional, micron-scale microfluidic devices.

44 r to generate simple, versatile and low-cost microfluidic devices.

45 ), and high-shear VWF string formation using microfluidic devices.

46 urther support the rapid prototyping of PDMS microfluidic devices.

47 e analysis of particle manipulation in these microfluidic devices.

48 ies have been adopted for the fabrication of microfluidic devices.

49 brief overview on the integration of MOFs on microfluidic devices.

50 ed by nanoprecipitation in a glass capillary microfluidics device.

51 hia coli cells trapped in a "mother machine" microfluidic device, a scalable platform for long-term s

52 In an open microfluidic device adapted for single-cell electrophore

53 Our microfluidic device allowed the precise and reproducible

54 phase flow will benefit the design of future microfluidic devices, allowing spatiotemporal control of

55 The compartmentalized configuration of the microfluidic device allows the formation of spherical hP

56 culture and minimal processing steps using a microfluidic device and antibody-functionalized magnetic

57 This innovative microfluidic device and its associated instrumentation s

58 The electrode is then integrated with a microfluidic device and used in a standard electrochemic

59 te actuators in various applications such as microfluidic devices and biomimetic microrobots.

60 ect are important for the rational design of microfluidic devices and impedance sensors.

61 l plates and can be integrated with existing microfluidic devices and large-scale screening systems.

62 mic demonstrates rapid cycling of strains in microfluidic devices and leads to an increase in the sta

63 is crucial for accurate flow manipulation in microfluidic devices and maintenance of constant pH in b

64 per determine the performance of paper-based microfluidic devices and permit the design of cellular a

65 e demonstrated the fabrication of wood-based microfluidic devices and their adaptability for single-u

66 ntitative connection between RBC behavior in microfluidic devices and their mechanical properties, wh

67 Cells were focused with a 1D-sheathing microfluidic device, and fluorescence emission generated

68 cal properties of cells in suspension with a microfluidic device, and for relating cell mechanical re

69 ulti-channel in vivo microscopy, analyses in microfluidic devices, and computational modeling, we ide

70 is then confirmed by in vitro experiments in microfluidic devices, and it establishes new insights to

71 r integration into flow-injection analyzers, microfluidic devices, and lab-on-a-chip systems.

72 its potential use in nearly any paper-based microfluidic device application and for creating nearly

73 Paper-based microfluidic devices are gaining large popularity becaus

74 Microtissue spheroids in microfluidic devices are increasingly used to establish

75 Because the design geometries of paper-based microfluidic devices are not standardized, conventional

76 Single-cell microfluidic devices are poised to substantially impact

77 The low-cost and versatile acrylic-tape microfluidic devices are promising tools for application

78 the help of arrays of insulating posts in a microfluidic device around which electric field gradient

79 Here, we adapted our previously developed microfluidic device as a 3D in vitro organotypic model t

80 cell dispersion from collagen spheroids in a microfluidic device as a metric of EMT, the combination

81 Using a glass capillary microfluidic device as the printhead, we dispersed dropl

82 engineering techniques used in the design of microfluidic devices as a part of the standard design wo

83 llows highly accessible rapid prototyping of microfluidic devices, as well as device reconfiguration

84 on combined with a very simple and efficient microfluidic device based on commercial textile threads.

85 cule (EpCAM) and sorted into four zones of a microfluidic device based on EpCAM expression levels.

86 is a commonly used elastomer for fabricating microfluidic devices, but it has previously been shown t

87 ormance of and monitoring experiments within microfluidic devices, but this application suffers from

88 functionalised in situ after assembly of the microfluidic device by electropolymerisation of a copoly

89 We investigated drug absorption into microfluidic devices by treating multiple myeloma (MM) t

90 Using our pipet, complex paper-based microfluidic devices can be fabricated without requiring

91 extending the range of materials from which microfluidic devices can be fabricated; thus, the proble

92 Here, we show that microfluidic devices can be used to sort marker-based he

93 In microfluidic devices CLR01 reduced alpha-synuclein aggre

94 The thermoplastic microfluidic device comprises five tailor-made functiona

95 The applied microfluidic device consisted of a Nafion membrane to in

96 Here, we demonstrate that a biomimetic microfluidic device consisting stenosed and tortuous art

97 The microfluidic device consists of a straight rectangular m

98 The microfluidic device consists of three microchannels, eac

99 Microfluidic devices constructed using low cost material

100 This study presents a microfluidic device containing an array of spheroid trap

101 A microfluidic device containing an integrated porous memb

102 Taken together, our microfluidic device could be a useful tool for the quant

103 Thus, this tortuosity activated microfluidic device could lead to a more quantitative an

104 material encapsulation into alginate using a microfluidic device could substantially increase in vivo

105 d neutrophil migration as determined using a microfluidic device coupled to real-time microscopy and

106 Here, we introduce a microfluidic device delivering crystal laden droplets se

107 Consequently, the microfluidic device described here provides fast and com

108 The 3D cell culturing microfluidic device described in this study, permits on-

109 we addressed these questions by combining a microfluidic device design that mimics multiple tumor mi

110 and the importance of material selection in microfluidic device design, especially in applications i

111 We present a microfluidic device designed to monitor the endothelium

112 hallenges this assumption through the use of microfluidic devices designed to mimic human capillary c

113 d allows the fabrication of various types of microfluidic devices, e.g., Hele-Shaw cells and microflu

114 The microfluidic device employs a droplet flow regime to max

115 The microfluidic device enabled quantitative time-lapse micr

116 A microfluidic device enables clog-free cell retention for

117 A unique platform utilizing a microfluidic device enables the discovery of new exosome

118 Recently, high-pressure microfluidic devices etched into glass and exploiting cr

119 s study, we characterise a 3D cell culturing microfluidic device fabricated from a 3D printed master.

120 e a potential application of the paper-based microfluidic devices fabricated by the proposed method,

121 Currently, reliable valving on integrated microfluidic devices fabricated from rigid materials is

122 s protocol takes ~5 d to complete, including microfluidic device fabrication (2 d), cell seeding (1 d

123 o-electron microscopy (trEM) using a modular microfluidic device, featuring a 3D-mixing unit and vari

124 ave developed a simple capillary force-based microfluidic device for 2D and 3D cell co-cultures.

125 Herein an integrated microfluidic device for AB diagnosis utilizing a new dua

126 Therefore, we report a simple, user-friendly microfluidic device for co-culture of a 3D breast tumour

127 We established a microfluidic device for fully automated, quantitative as

128 d at developing such a device, a paper-based microfluidic device for infection testing by an unskille

129 s a point-of-care electroosmotic flow driven microfluidic device for rapid isolation and detection of

130 experiments using confocal microscopy and a microfluidic device for shear rates up to 20,000 s(-1) a

131 A microfluidic device for simultaneous analysis of total f

132 (RCA) bioassay and an (2) agarose bead-based microfluidic device for the affinity chromatography-base

133 ide detection platforms, there is no compact microfluidic device for the complementary, fast, cheap,

134 t a self-partitioning SlipChip (sp-SlipChip) microfluidic device for the slip-induced generation of d

135 In this study, we report a microfluidic device for the whole-life culture of the ne

136 aking it ideal for integration with existing microfluidic devices for advanced cell and pharmacokinet

137 els for design of more precise and efficient microfluidic devices for applications such as cell sorti

138 evolution is transforming the fabrication of microfluidic devices for artificial cell construction in

139 We also outlined progress on paper microfluidic devices for drug delivery.

140 rdware, which is amenable to deployment with microfluidic devices for point-of-care diagnostics.

141 esults can be further exploited in design of microfluidic devices for rare cells immunocapture.

142 ure, we cover recent advances of single-cell microfluidic devices for studying and diagnosing hematol

143 ted surface enhanced Raman scattering (SERS)-microfluidics device for the detection of immune checkpo

144 crofluidics method, using a so-called H-cell microfluidics device, for the determination of protein d

145 m is the only tool required to manufacture a microfluidic device from transparent glass substrates.

146 unity in using rapid prototyping to engineer microfluidic devices from computer-aided-design (CAD) dr

147 In this study, we report a novel 3D printed microfluidic device functionalized with anti-EpCAM (epit

148 e miniaturization of SPE within a 3D printed microfluidic device further allows for fast and simple e

149 report development of such a system using a microfluidic device, generated from polydimethylsiloxane

150 Microfluidic devices >500 mum, rapid mixing (71% +/- 12%

151 d dielectrophoresis (iDEP) integrated into a microfluidic device has the potential to separate SWNTs

152 Droplet-based microfluidic devices have become widely used to perform

153 Microfluidic devices have historically been prepared usi

154 Paper-based microfluidic devices have many applications in biomedica

155 Several sophisticated microfluidic devices have recently been proposed for fem

156 Microfluidic devices have the potential to automate and

157 Microfluidic devices have the potential to simplify and

158 The customized design of the microfluidic device helped with handling beads with diff

159 bles the manufacturing of a fully-functional microfluidic device in a few hours, without using any pr

160 ow how to immobilize receptors inside closed microfluidic devices in <30 s using bead lane modules in

161 DMS) is likely the most popular material for microfluidic devices in lab-on-a-chip and other biomedic

162 method to fabricate three-dimensional paper microfluidic devices in one step, without the need of st

163 hippocampal neurons (DIV 15-20) cultured in microfluidic devices in order to deliver a localized exc

164 ies particularly suited for developing novel microfluidic devices in these spaces, with insight into

165 Finally, experiments performed in a microfluidic device, in which droplets are formed under

166 arameters important for the operation of the microfluidic device including flow rate, solution exchan

167 on, hepatocyte spheroids were established in microfluidic devices, injured on-chip by exposure to lip

168 rom minute sample volumes using an optimized microfluidic device integrated with pipettes.

169 The PETG-based microfluidic devices integrated with electrochemical sen

170 The 3D microfluidic device is a photoactive polyacrylamide gel

171 The microfluidic device is based on a herringbone channel de

172 In this work, a microfluidic device is developed for in-situ analysis of

173 Conventional manufacturing of glass microfluidic devices is a complex, multi-step process th

174 Fluidic behavior in microfluidic devices is dictated by low Reynolds numbers

175 ehensive understanding of particle motion in microfluidic devices is essential to unlock additional t

176 thods for the fabrication of electrochemical microfluidic devices is urgently needed for transferring

177 The directed transport of microparticles in microfluidic devices is vital for efficient bioassays an

178 BPE and of planar micropores integrated in a microfluidic device lead to the spatial confinement of t

179 .The complexity of fabricating and operating microfluidic devices limits their use.

180 t extrusion direction on fluidic behavior in microfluidic devices made by FDM printing.

181 Here, using an in-house microfluidic device mimicking the pulmonary capillary be

182 In order to engineer in-droplet assays, microfluidic devices must add reagents into droplets, re

183 A combined thread-paper microfluidic device (muTPAD) is presented for the determ

184 Live-cell imaging in microfluidic devices now allows the investigation of cel

185 e studied autochemotaxis quantitatively in a microfluidic device of bifurcating channels: Branch choi

186 cose oxidase (GOx) with an electroanalytical microfluidic device of easy assembly based on cotton thr

187 te outgrowth images with noisy background in microfluidic devices of biomedical engineering fields.

188 The integration in microfluidic devices of the most popular technology for

189 ectrophoretic (DEP) mechanisms integrated in microfluidic devices offer unique advantages for such ap

190 These microfluidic devices often are designed to operate with

191 in an HLF-laden, fibrin-based ECM within our microfluidic device optimally (1) enhances the sprouting

192 Herein we explored the use of microfluidic devices or microchambers as simple and low-

193 may be carried out on a continuous basis in microfluidic devices or split-flow thin channel (SPLITT)

194 ary of strains after time-lapse imaging in a microfluidic device overcomes this problem.

195 this preanalytical challenge, we designed a microfluidic device (PepS) automating and accelerating b

196 This microfluidic device provides a rapid and straightforward

197 We found the microfluidic device provides a simple and efficient plat

198 reliability, and portability, the developed microfluidic device provides a simple method for antimic

199 Thus, the TRIS microfluidics device provides unique insights into the m

200 at human pluripotent stem cells (hPSCs) in a microfluidic device recapitulate, in a highly controllab

201 Cell immunocapture microfluidic devices represent a rapidly developing fiel

202 gration of nucleic acids detection assays in microfluidic devices represents a highly promising appro

203 Collectively, our microfluidic device shows several advantages over tradit

204 l migration through confined spaces within a microfluidic device, subcellular photoactivation of Rac1

205 We use a microfluidic device that allows accurate and rapid manip

206 -based cell assay carried out in a segmental microfluidic device that allows studying the effect of a

207 ch, it is of particular interest to design a microfluidic device that can be tuned and adjusted to se

208 etails of the design and implementation of a microfluidic device that can be used to model human embr

209 ts on the proof of concept for a stretchable microfluidic device that can control the length via a st

210 and increase operation simplicity, a simple microfluidic device that can perform antimicrobial susce

211 In this work, we have developed a microfluidic device that is able to simultaneously chara

212 we developed an integrated double-filtration microfluidic device that isolated and enriched EVs with

213 We describe a microfluidic device that isolates and enumerates periphe

214 Here we present a microfluidic device that triggered liquid-to-liquid phas

215 This study reports an integrated microfluidic device that was capable of executing rapid

216 Microfluidic devices that are being designed to address

217 t step toward designing stretchable inertial microfluidic devices that can be implemented for a wide

218 To overcome the obstacles of pump-based microfluidic devices that need to be precisely controlle

219 Development of paper-based microfluidic devices that perform colorimetric measureme

220 -delivery microparticles, pH sensors, and 3D microfluidic devices that we could not produce using tra

221 form acoustic streaming into an open chamber microfluidic device, the adherent cells within the open

222 crofluidics was conducted using a Y-junction microfluidic device, the design of which was optimized f

223 alytes have been developed using paper-based microfluidic devices, the detection and analysis of bloo

224 As a microfluidic device, this portable novel platform can be

225 on through a permeable membrane in a 2-layer microfluidic device, thus reducing the pH and freeing ca

226 We used a simple microfluidic device to allow eight samples to be process

227 system in combination with a high-throughput microfluidic device to comprehensively study the differe

228 Using a microfluidic device to deliver controlled stimuli to int

229 We developed and optimized a novel Labyrinth microfluidic device to efficiently isolate CTCs from per

230 Using a "Crystal Hotel" microfluidic device to provide well-defined, nanoliter v

231 use an HPLC coupled to a droplet generating microfluidic device to sequentially encapsulate the elut

232 Here, we present a simple microfluidic device to simultaneously follow development

233 ate a non-swelling synthetic hydrogel with a microfluidic device to study chemokine gradient-driven a

234 Here, we used a specially designed microfluidic device to study thermotaxis of Escherichia

235 approach utilizes a photocleavage bead-based microfluidic device to synthesize and deliver stable cDN

236 In addition, it is beneficial for microfluidic devices to be reconfigurable in the field,

237 low-cost fabrication of electrochemical LOC microfluidic devices to be used for enzymatic detection.

238 important to review the recent literature on microfluidic devices to determine how rapidly the techno

239 with gene delivery have been developed using microfluidic devices to increase overall efficiency.

240 They can be integrated into paper microfluidic devices to make circuits that are capable o

241 a a Reservoir-on-a-Chip approach, which uses microfluidic devices to mimic the oil reservoir.

242 Here, we used microfluidic devices to physically isolate these two neu

243 Here, using microfluidic devices to recreate discretely organized ne

244 d compared the performance in our 3D printed microfluidic devices to that in other device materials c

245 fined environments, varying from droplets in microfluidic devices, to cylindrical pores in filtration

246 e for specific DNA hybridization transfer in microfluidic devices under isothermal conditions based o

247 ays increase in relative abundance in planar microfluidic devices under simple flow regimes.

248 To enhance the performance of microfluidic devices, understanding the dynamics of the

249 further development of the vacuum-compatible microfluidic device used in in situ liquid SIMS provides

250 magnetic microbeads were driven through the microfluidic device using both constant forward flow and

251 us manipulation of two particles in a simple microfluidic device using model predictive control.

252 In this study, a new microfluidic device utilized for electrochemical DA dete

253 For this purpose, a microfluidic device was designed for the generation of a

254 The microfluidic device was designed to have a bilaterally c

255 rfacial tension (IFT) and wettability in the microfluidic device was simulated using a phase-field mo

256 The latter microfluidic device was successfully used for the determ

257 A flow focusing microfluidic device was used to form alginate droplets e

258 ture inflammatory responses in mast cells, a microfluidic device was used to precisely control exposu

259 veness of these SPE monoliths and 3D printed microfluidic devices was tested using a panel of nine pr

260 Finally, using a microfluidic device, we found that the effects of ACM we

261 rowth dynamics of D2O ice in liquid H2O in a microfluidic device were investigated between the meltin

262 FU)/reaction was obtained, and all necessary microfluidic devices were actuated by a combination of p

263 To demonstrate their versatility, wood microfluidic devices were adapted for (i) surface plasmo

264 for microchip electrophoresis in 3D printed microfluidic devices were also determined for PTB biomar

265 reservoir pores, the inner channels of glass microfluidic devices were coated with thin layers of cal

266 Using a single and automated print process, microfluidic devices were fabricated containing (i) an o

267 cal vein endothelial cells (HUVECs) grown in microfluidic devices were treated with Angiopoietin 1 an

268 s cells inside the capturing chambers of the microfluidic device, where the hydrodynamic force then i

269 ing effects are expected to be acute in open microfluidic devices, where a single, high-conductivity

270 ion, and operation of a polydimethylsiloxane microfluidic device which enables the generation and dig

271 zing is demonstrated using a custom-designed microfluidic device, which relieves contraction of the m

272 The microfluidic device, which we termed tracking root inter

273 crylate-based monolith, formed in 3D printed microfluidic devices, which can selectively retain pepti

274 ased CTC isolation has also been employed in microfluidic devices, which show higher capture efficien

275 n in giant lipid vesicles as they traverse a microfluidic device while exposed to the drug.

276 Our microfluidic device will allow us to make new discoverie

277 We anticipate this microfluidic device will facilitate drug screening in a

278 nsor concept experimentally, we fabricated a microfluidic device with 10 distributed Coulter sensors

279 ming this limitation, we implement PHIP on a microfluidic device with a 2.5 muL detection volume.

280 We report a low-cost microfluidic device with a conveniently biofunctionalise

281 strated the concept of a low cost disposable microfluidic device with a receptor functionalised on th

282 The immunoassay was performed in a microfluidic device with an integrated antimony/bismuth

283 designed interior structures to fabricate a microfluidic device with high surface area and fluid flo

284 combining size-based microfiltration into a microfluidic device with immunoaffinity for enhanced cap

285 pesticides with algae in a novel glass based microfluidic device with integrated optical pH, oxygen s

286 Here, we report 'Traptasia', a simple microfluidic device with multiple traps designed to isol

287 recover cells embedded in a 3D hydrogel in a microfluidic device with no impact on cell viability.

288 we develop a differential multiconstriction microfluidic device with self-aligned 3D electrodes to s

289 We have developed a microfluidic device with trapping arrays to efficiently

290 have a wide range of applications including microfluidic devices with customizable wettability, sola

291 fied polyethylene terephthalate (PETG)-based microfluidic devices with embedded channels and gold fil

292 entially new approach for the manufacture of microfluidic devices with multiple integrated functional

293 We manufactured microfluidic devices with narrow channels (60-mum(2) rec

294 Here, we generated a microfluidics device with arrays of long monolayer yeast

295 t implications for bubble/drop generation in microfluidic devices, with applications in inkjet printi

296 ing the labor-intensive process of designing microfluidic devices, with very few specialized tools th

297 nt bacteria can be realized on an integrated microfluidic device within 6 h.

298 en nanoliter-sized droplets immobilized in a microfluidic device without loss of tumor cells during t

299 that the spots can be densely arranged on a microfluidic device without significant contamination of

300 d is a primary tool for on-chip detection in microfluidic devices, yet additional expertise, more ela