ライフサイエンスコーパス: microfluidic device

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

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

3 both attractive and repulsive gradients in a microfluidic device.

4 utrophils in a CXCL1 gradient generated by a microfluidic device.

5 oxygen gradient produced by a three-channel microfluidic device.

6 ind that embryos develop normally within the microfluidic device.

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

8 ting microparticles and cells in an inertial microfluidic device.

9 in an integrated, benchtop, millilitre-scale microfluidic device.

10 s encapsulated in a hydrogel scaffold into a microfluidic device.

11 (3-methylcholanthrene) induction agents in a microfluidic device.

12 ulobacter crescentus to a glass surface in a microfluidic device.

13 ss with an acoustically-driven, bubble-based microfluidic device.

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

15 tool, within a span of 5 min using an ac-EHD microfluidic device.

16 ue SERS-active substrate incorporated into a microfluidic device.

17 ory enables to define geometrical sizes of a microfluidic device.

18 le and perfusing it with culture medium in a microfluidic device.

19 of gel-shell beads (GSBs) with the help of a microfluidic device.

20 ed with enzyme and protein measurements in a microfluidic device.

21 ed cellulose paper was used as a paper-based microfluidic device.

22 nd subjected to chemokine gradients within a microfluidic device.

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

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

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

26 H2O2 and hydroquinone was injected into the microfluidic device.

27 pended electrodes integrated into a scalable microfluidic device.

28 formation at relatively warm temperatures in microfluidic devices.

29 , artificial hearing systems, biomedical and microfluidic devices.

30 the fabrication of stretchable implants and microfluidic devices.

31 lenges in the development and application of microfluidic devices.

32 nvironments and chemotactic gradients within microfluidic devices.

33 ter in other instrument platforms or modular microfluidic devices.

34 esting, self-cleaning, oil spill removal and microfluidic devices.

35 >100x larger than are typically processed on microfluidic devices.

36 een taken to implement optical tunability in microfluidic devices.

37 d materials that appeal to the developers of microfluidic devices.

38 and promoted neurite growth and branching in microfluidic devices.

39 ics and integrated photonic, electronic, and microfluidic devices.

40 as a design methodology in conjunction with microfluidic devices.

41 asurement of cell mechanical properties with microfluidic devices.

42 amer formation can lead to rapid clogging of microfluidic devices.

43 for the operation of macroscale machines and microfluidic devices.

44 with embryonic stem cell-derived neurons in microfluidic devices.

45 ation of isothermal amplification methods in microfluidic devices.

46 meet the needs for detection in small-scale microfluidic devices.

47 ted with human hepatic stellate cells inside microfluidic devices.

48 alysis of trace amounts of proteins, e.g. in microfluidic devices.

49 holding geometries, specifically paper-based microfluidic devices.

50 sympathetic and sensory neurons cultured in microfluidic devices.

51 olutionary technology for the fabrication of microfluidic devices.

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

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

54 ompetitive Salmonella typhimurium strains in microfluidic devices.

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

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

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

58 ed by nanoprecipitation in a glass capillary microfluidics device.

59 calculated during buffer diffusion using the microfluidic device (14.9 +/- 3.2 nm) was not different

60 Our magnetic structure embedded microfluidic device achieved over 90% capture efficiency

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

62 LOC) biosensor approach utilizing well mixed microfluidic device and a microsphere-based assay capabl

63 e the capability of our method in vitro in a microfluidic device and also in cells, via the determina

64 generated by a bipolar electrode (BPE) in a microfluidic device and elucidates the impact of faradai

65 , we trapped multiple worms in parallel in a microfluidic device and illuminated for photoactivation

66 glucose stimulation across the islet using a microfluidic device and measured how these perturbations

67 e performed in parallel, were developed in a microfluidic device and tested for the detection of free

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

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

70 starving single Escherichia coli bacteria in microfluidic devices and measured their activity by moni

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

72 These cells were infused into the microfluidic devices and stimulated to commence cytokine

73 We first used a combination of microfluidic devices and time-lapse fluorescence microsc

74 ng approach, electrodes were integrated into microfluidic devices and used to dynamically monitor cyt

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

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

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

78 Paper-based microfluidic devices are gaining large popularity becaus

79 Microtissue spheroids in microfluidic devices are increasingly used to establish

80 Single-cell microfluidic devices are poised to substantially impact

81 Paper based microfluidic devices are robust and relatively simple to

82 n the hanging-drop network concept: The open microfluidic devices are seamlessly combined with fluore

83 However, the vast majority of PDMS microfluidic devices are still made with extensive manua

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

85 The sensor is composed of the embedded in a microfluidic device array of microwells filled with ion-

86 ector with on-board heater integrated with a microfluidic device as NMR sample holder.

87 ganisms, while suggesting future oscillating microfluidic devices, as well as novel ways for micro an

88 xities of NA isolation with miniaturized and microfluidic devices, as well as the considerations when

89 nd cost-effective nature of the process make microfluidic devices available to those who might benefi

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

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

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

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

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

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

96 The described spiral microfluidic devices can be produced at an extremely low

97 upled to a hybrid polydimethylsiloxane-glass microfluidic device capable of selectively extracting th

98 Here, to test this model, we developed a microfluidic device (chip) that emulates a mucosal surfa

99 SERS nanoparticle clusters as labels, with a microfluidic device comprising multiple channels, a robu

100 drug-loaded hydrogel embolic beads within a microfluidic device consisting of a network of interconn

101 cal properties of cells in suspension with a microfluidic device consisting of a parallel array of mi

102 The microfluidic device consists of a straight rectangular m

103 Microfluidic devices constructed using low cost material

104 A microfluidic device containing an integrated porous memb

105 infusing anti-TGF-beta1 antibodies into the microfluidic devices containing activated stellate cells

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

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

108 eviously, we have demonstrated an integrated microfluidic device coupling CE with electrospray ioniza

109 l modeling and subsequently implemented in a microfluidic device demonstrating at least 2 orders of m

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

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

112 We present a microfluidic device designed to monitor the endothelium

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

114 method for the surface modification of glass microfluidic devices designed to perform electrophoretic

115 d with the same nanoyeast-scFv reagents in a microfluidic device employing surface-enhanced Raman sca

116 The microfluidic device enabled quantitative time-lapse micr

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

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

119 ber of advances compared to more traditional microfluidic devices fabricated with polydimethylsiloxan

120 resistance to high temperatures required for microfluidic device fabrication.

121 We developed a microfluidic device featuring facile cell loading, simpl

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

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

124 We present a microfluidic device for coupled phase I/phase II metabol

125 Herein, we report a multiplexed microfluidic device for highly specific capture and dete

126 The introduction of paper into the microfluidic device for LAMP reactions enables stable te

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

128 rk we report on the production of a low cost microfluidic device for the multiplexed electrochemical

129 late) (PMMA) micropillars populated within a microfluidic device for the on-chip digestion of double-

130 We demonstrate a simple microfluidic device for the rapid, electrically-based de

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

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

133 deal candidate for the future integration in microfluidic devices for drug discovery.

134 ration when designing relevant scaffolds and microfluidic devices for osteogenic induction in the fut

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

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

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

138 g samples within polydimethylsiloxane (PDMS) microfluidic devices has facilitated the study of hard-t

139 l emulsion droplets created in droplet-based microfluidic devices have been tested and used recently

140 Paper-based microfluidic devices have many applications in biomedica

141 Several sophisticated microfluidic devices have recently been proposed for fem

142 Microfluidic devices have the potential to automate and

143 re of bacterial floc mediated streamers in a microfluidic device in a creeping flow regime using both

144 -based amplification of mRNA within a simple microfluidic device in relevant analytical volumes.

145 the light source and the positioning of the microfluidic device in the picture.

146 Using microfluidic devices in combination with fluorescence ti

147 The application of microfluidic devices in diagnostic systems is well-estab

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

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

150 lications such as welding, drug delivery and microfluidics devices in controlling small droplets and

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

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

153 The microfluidic device incorporates removable needle type i

154 e generation of portable, multiplexed and/or microfluidic devices incorporating sensitive nanoparticl

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

156 The microfluidic device is based on a herringbone channel de

157 A microfluidic device is being developed by University of

158 The capillary microfluidic device is capable of autonomous and sequent

159 The microfluidic device is composed of glass etched with rea

160 Although the microfluidic device is demonstrated on filamentous fungi

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

162 This paper-based microfluidic device is extremely simple in terms of mani

163 The microfluidic device is fabricated using multilayer soft

164 Here, a microfluidic device is presented that is easy to use and

165 n in combination with a low-cost paper-based microfluidic device is presented.

166 Because the microfluidic device is readily assembled from standard p

167 A microfluidic device is reported that employs an out-of-p

168 amic focusing with embedded capillaries in a microfluidic device is shown to enable both surface enha

169 e electrochemical activity of the fabricated microfluidic device is validated and demonstrated repeat

170 Culture of cells using various microfluidic devices is becoming more common within expe

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

172 g of intact three-dimensional tissues within microfluidic devices is fundamentally hindered by intrat

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

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

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

176 er, replica molding, and plasma bonding like microfluidic devices made of poly(dimethylsiloxane) (PDM

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

178 This paper presents a thread-based microfluidic device (muTAD) that includes ionophore extr

179 ing unprocessed human serum and a disposable microfluidic device; no optics are involved in the imple

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

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

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

183 Microfluidic devices offer automation and high-throughpu

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

185 detection of heavy metals using paper-based microfluidic devices on the basis of various detection m

186 n be precisely and dynamically controlled in microfluidic devices, optical sensors capable of unique

187 Here, we present a microfluidic device optimized for the analysis of single

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

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

190 ning of naked DNA molecules presented within microfluidic devices, or localized within live bacterial

191 des on strong cation exchange resin within a microfluidic device, peptides react to contain fixed, pe

192 rnessed for "on demand" pumping in nano- and microfluidic devices powered by an intrinsic energy sour

193 ematology analyzers, microscopy, and bedside microfluidic devices provide clinically feasible, high-t

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

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

196 pico- to nanoliter water-in-oil droplets in microfluidic devices provides a solution for massive vol

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

198 n of these immuno-functionalized surfaces on microfluidic devices remains a significant challenge to

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

200 This platform includes an optimized microfluidic device specifically for live embryos and al

201 In this article, we report a microfluidic device that addresses this analytical chall

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

203 A "crystal hotel" microfluidic device that allows crystal growth in confin

204 Using a microfluidic device that allows spatio-temporal variatio

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

206 Thus, we designed a microfluidic device that allows the addition of chemical

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

208 his study, we have designed and fabricated a microfluidic device that combines hydrodynamic trapping

209 To provide such a sample, we developed a microfluidic device that facilitates dielectrophoretic s

210 atani et al. describe employing an ingenious microfluidic device that gently cages individual cells.

211 In this report, we demonstrate a simple microfluidic device that integrates sonication and immun

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

213 nstrate the development of an acoustic-based microfluidic device that is capable of high-throughput s

214 tion in artificial cells, we develop a novel microfluidic device that is capable of trapping double e

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

216 We describe a microfluidic device that isolates and enumerates periphe

217 Here we describe a microfluidic device that mimics a network of stenosed ar

218 We designed a microfluidic device that trapped swimming bacteria withi

219 We describe a microfluidic device that utilizes this principle to dete

220 ll fluorescence imaging-based approaches and microfluidic devices that enable measurements of signali

221 we have developed and implemented a class of microfluidic devices that mix two components to completi

222 ations, here we have designed and fabricated microfluidic devices that offer continuous and automated

223 s the possibility of creating very sensitive microfluidic devices that respond readily to small physi

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

225 nitial steps or require a highly specialized microfluidics device that is not readily available.

226 ous conformation-reporter binding assay in a microfluidic device, that a substantial fraction of beta

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

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

229 coating can be dissolved from the surface of microfluidic devices through biologically compatible tem

230 he production and use of a label-free spiral microfluidic device to allow size-based isolation of via

231 The extrusion system is then coupled to a microfluidic device to control the bioink arrangement de

232 present the design of a noncontact scanning microfluidic device to efficiently present reagents on s

233 We used a three-channel microfluidic device to establish a high degree of contro

234 this end, we designed an "endothelial-ized" microfluidic device to introduce controlled FeCl3 concen

235 The development of a microfluidic device to mechanically activate artificial

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

237 We utilized a microfluidic device to recapitulate both shear stress an

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

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

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

241 t study is carried out with 5- and 7-channel microfluidic devices to acquire one-shot binding curves

242 on" module that can be integrated with other microfluidic devices to allow analysis of dilute cellula

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

244 We used microfluidic devices to characterize the engineered lysi

245 ve study of mammalian sperm rheotaxis, using microfluidic devices to investigate systematically swimm

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

247 n many fields to now apply the advantages of microfluidic devices to particle separation, even for ap

248 from human embryonic stem cells, cultured in microfluidic devices, to enable direct biochemical measu

249 perosmotic shocks, combined with custom made microfluidic devices, to show that cells fully recover t

250 cle transport in a nonlinear post array in a microfluidic device under the periodic action of electro

251 accurate prediction of analytes transport in microfluidic devices under EOF.

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

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

254 The functionality of microfluidic devices using the presented method is evalu

255 We report a microfluidic device, using segmented flow in a two-phase

256 The microfluidic device was characterized using finite eleme

257 As a proof-of-concept study, our microfluidic device was coupled to lab-built wireless po

258 The microfluidic device was designed to have a bilaterally c

259 In this study, a laminated microfluidic device was fabricated to mimic the drug ADM

260 asily scalable poly(dimethylsiloxane) (PDMS) microfluidic device was fabricated using soft lithograph

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

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

263 Here, by using a microfluidic device, we show that microtubule stiffness

264 ng time-lapse luminescence microscopy with a microfluidic device, we tracked the dynamics of cell cyc

265 aging of rat hippocampal neurons cultured in microfluidic devices, we show that the activity-dependen

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

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

268 Here, using microfluidic devices where both geometry and oxygen leve

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

270 , we report the development of an integrated microfluidic device which enables the analytical charact

271 of cellular interrogation using programmable microfluidic devices which exploits the additional infor

272 The microfluidic device, which we termed tracking root inter

273 ively simple to operate, compared to channel microfluidic devices, which is perhaps their greatest ad

274 The integration of microfluidic devices-which efficiently handle small liqu

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

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

277 of two glass nanopores into a segmented flow microfluidic device with a view on enhancing the functio

278 We describe a microfluidic device with an integrated nanochannel array

279 infection of neurons derived from hESCs in a microfluidic device with cell-free parental Oka (POka) V

280 In this study, we present a novel microfluidic device with embedded electrodes that enable

281 re we present a high-throughput, transparent microfluidic device with embedded microwell arrays sandw

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

283 of detection achieved without the use of the microfluidic device with the exception that coefficients

284 phere-based assay into well-mixed yet simple microfluidic device with turbulent flow profiles in the

285 A microfluidic device with two nanoporous membranes was de

286 A completely customized microfluidic device with wavy patterns can be created wi

287 CorelDRAW or AutoCAD, the protocol produces microfluidic devices with a design-to-device time of app

288 We integrated the preserved microfluidic devices with a lensless complementary metal

289 inexpensive polyester-toner, rotation-driven microfluidic devices with a smartphone as a potential al

290 a new generation of inexpensive and portable microfluidic devices with commercial immunoassay reagent

291 We describe a technique for fabricating microfluidic devices with complex multilayer architectur

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

293 rse double-emulsion droplets in two steps in microfluidic devices with different surface characterist

294 on conductivity-induced DEP using affordable microfluidic devices with easy operation.

295 ce-area structures, including fabrication of microfluidic devices with high-surface-area channels and

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

297 Microfluidic devices with pure wavy and wavy-herringbone

298 Interfacing microfluidic devices with the external world can be diff

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

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