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Sliding walls: a new paradigm for fluidic actuation and protocol implementation in microfluidics

Microsystems & Nanoengineering 2020年第1期6卷 1093-1102页

作者： Bastien Venzac Yang Liu Ivan Ferrante Pablo Vargas Ayako Yamada Remi Courson Marine Verhulsel laurent malaquin Jean-Louis Viovy Stephanie Descroix Laboratoire Physico Chimie Curie Institut CuriePSL Research UniversityCNRS UMR16875005 ParisFrance Sorbonne Universites UPMC Univ Paris 0675005 ParisFrance Institut Pierre-Gilles de Gennes PSL Research University75005 ParisFrance Institut Curie PSL Research UniversityCNRS UMR 14475005 ParisFrance LAAS-CNRS Universitéde ToulouseCNRS31400 ToulouseFrance

Currently,fluidic control in microdevices is mainly achieved either by external pumps and valves,which are expensive and bulky,or by valves integrated in the *** types of internal valves or actuation methods have been proposed,but they generally impose difficult compromises between performance and fabrication *** propose here a new paradigm for actuation in microfluidic devices based on rigid or semi-rigid walls with transversal dimensions of hundreds of micrometres that are able to slide within a microfluidic chip and to intersect microchannels with hand-driven or translation stage-based *** this new concept for reconfigurable microfluidics,the implementation of a wide range of functionalities was facilitated and allowed for no or limited dead volume,low cost and low *** demonstrate here several fluidic operations,including on/off or switch valving,where channels are blocked or reconfigured depending on the sliding wall *** valves sustain pressures up to *** and reversible compartmentalisation of large microfluidic chambers were also *** last possibility was applied to a“4D”migration assay of dendritic cells in a collagen ***,sliding walls containing a hydrogel-based membrane were developed and used to concentrate,purify and transport biomolecules from one channel to another,such functionality involving complex fluidic transport patterns not possible in earlier microfluidic ***,this toolbox is compatible with“soft lithography”technology,allowing easy implementation within usual fabrication workflows for polydimethylsiloxane *** new technology opens the route to a variety of microfluidic applications,with a focus on simple,hand-driven devices for point-of-care or biological laboratories with low or limited equipment and resources.

关键词： walls hundreds operations

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Rapid prototyping of a polymer MEMS dropletdispenser by laser-assisted 3D printing

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Microsystems & Nanoengineering 2023年第4期9卷 211-221页

作者： Rémi Courson Oleksii Bratash Ali Maziz CloéDesmet Ricardo Alvarado Meza Loïc Leroy Elodie Engel Arnaud Buhot laurent malaquin Thierry Leïchlé LAAS-CNRS Universitéde ToulouseCNRS31400 ToulouseFrance UniversitéGrenoble Alpes CNRSCEAIRIGSyMMES38000 GrenobleFrance Georgia Tech−CNRS International Research Laboratory AtlantaGA 30332USA

In this work, we introduce a polymer version of a previously developed silicon MEMS drop deposition tool for surfacefunctionalization that consists of a microcantilever integrating an open fluidic channel and a reservoir. The device isfabricated by laser stereolithography, which offers the advantages of low-cost and fast prototyping. Additionally,thanks to the ability to process multiple materials, a magnetic base is incorporated into the cantilever for convenienthandling and attachment to the holder of a robotized stage used for spotting. Droplets with diameters ranging from∼50 μm to ∼300 μm are printed upon direct contact of the cantilever tip with the surface to pattern. Liquid loading isachieved by fully immersing the cantilever into a reservoir drop, where a single load results in the deposition of morethan 200 droplets. The influences of the size and shape of the cantilever tip and the reservoir on the printing outcomeare studied. As a proof-of-concept of the biofunctionalization capability of this 3D printed droplet dispenser,microarrays of oligonucleotides and antibodies displaying high specificity and no cross-contamination are fabricated,and droplets are deposited at the tip of an optical fiber bundle.

关键词： cantilever reservoir printing

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High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples

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Microsystems & Nanoengineering 2023年第5期9卷 101-112页

作者： Lucile Alexandre Monica Araya-Farias Manh-Louis Nguyen Nikoletta Naoumi Giacomo Gropplero Electra Gizeli laurent malaquin Stéphanie Descroix Laboratoire Physico-Chimie Curie CNRS UMR 168Institut CuriePSL Research UniversityParisFrance Institut Pierre-Gilles de Gennes(IPGG) Sorbonne UniversityParisFrance Department of Biology University of CreteHeraklionGreece Institute of Molecular Biology and Biotechnology(IMBB)-FORTH HeraklionGreece Laboratoire d’analyse et d’architecture des systèmes(LAAS)CNRS Elia GroupToulouseFrance Present address:Frédéric Joliot Institute for Life Sciences Pharmacology and Immunoanalysis UnitImmunoanalysis Studies and Research LaboratoryAlternative Energies and Atomic Energy Commission(CEA)Gif-sur-YvetteFrance

Liquid biopsy,in particular circulating tumor DNA(ctDNA)analysis,has paved the way for a new noninvasive approach to cancer diagnosis,treatment selection and *** a crucial step in the analysis,the extraction of the genetic material from a complex matrix needs to meet specific requirements such as high specificity and low loss of ***,we developed a new generation of microfluidic fluidized beds(FBs)that enable the efficient extraction and preconcentration of specific ctDNA sequences from human serum with flow rates up to 15µL/*** first demonstrated that implementation of a vibration system inducing flow rate fluctuations combined with a mixture of different bead sizes significantly enhanced bead homogeneity,thereby increasing capture *** advantage of this new generation of high-throughput magnetic FBs,we then developed a new method to selectively capture a double-stranded(dsDNA)BRAF mutated DNA sequence in complex matrices such as patient ***,as proof of concept,ligation chain reaction(LCR)assays were performed to specifically amplify a mutated BRAF sequence,allowing the detection of concentrations as low as 6×104 copies/µL of the mutated DNA sequence in serum.

关键词： diagnosis specificity thereby

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