Your browser doesn't support javascript.
loading
Streamlined digital bioassays with a 3D printed sample changer.
Menezes, Roberta; Dramé-Maigné, Adèle; Taly, Valérie; Rondelez, Yannick; Gines, Guillaume.
Afiliación
  • Menezes R; Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, USPC, Université Paris Descartes, Université Paris Diderot, MEPPOT/Equipe labellisée Ligue Nationale contre le cancer, INSERM UMR-S1147, CNRS SNC5014, F-75006 Paris, France.
  • Dramé-Maigné A; Laboratoire Gulliver, UMR7083 CNRS, ESPCI Paris, PSL Research University, 10 rue Vauquelin, 75005 Paris, France. guillaume.gines@espci.fr.
  • Taly V; Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, USPC, Université Paris Descartes, Université Paris Diderot, MEPPOT/Equipe labellisée Ligue Nationale contre le cancer, INSERM UMR-S1147, CNRS SNC5014, F-75006 Paris, France.
  • Rondelez Y; Laboratoire Gulliver, UMR7083 CNRS, ESPCI Paris, PSL Research University, 10 rue Vauquelin, 75005 Paris, France. guillaume.gines@espci.fr.
  • Gines G; Laboratoire Gulliver, UMR7083 CNRS, ESPCI Paris, PSL Research University, 10 rue Vauquelin, 75005 Paris, France. guillaume.gines@espci.fr.
Analyst ; 145(2): 572-581, 2020 Jan 21.
Article en En | MEDLINE | ID: mdl-31769452
Droplet-based microfluidics has permeated many areas of life sciences including biochemistry, biology and medicine. Water-in-oil droplets act as independent femto- to nano-liter reservoirs, enabling the parallelization of (bio)chemical reactions with a minimum sample input. Among the range of applications spanned by droplet microfluidics, digital detection of biomolecules, using Poissonian isolation of single molecules in compartments, has gained considerable attention due to the high accuracy, sensitivity and robustness of these methods. However, while the droplet throughput can be very high, the sample throughput of these methods is poor in comparison to well plate-based assays. This limitation comes from the necessity to convert independently each sample into a monodisperse emulsion. In this paper, we report a versatile device that performs the quick sequential partitioning of up to 15 samples using a single microfluidic chip. A 3D printed sample rotor is loaded with all samples and connected to a pressure source. Simple magnetic actuation is then used to inject the samples in the microfluidic chip without pressure disruption. This procedure generates monodisperse droplets with high sample-to-sample consistency. We also describe a fluorescent barcoding strategy that allows all samples to be collected, incubated, imaged and analyzed simultaneously, thus decreasing significantly the time of the assay. As an example of application, we perform a droplet digital PCR assay for the quantification of a DNA amplicon from 8 samples in less than 2 hours. We further validate our approach demonstrating the parallel quantification of 11 microRNAs from a human sample using an isothermal nucleic acid amplification chemistry. As an off-chip device, the sample changer can be connected to a variety of microfluidic geometries and therefore, used for a wide range of applications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Técnicas Analíticas Microfluídicas / Impresión Tridimensional Límite: Humans Idioma: En Revista: Analyst Año: 2020 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Técnicas Analíticas Microfluídicas / Impresión Tridimensional Límite: Humans Idioma: En Revista: Analyst Año: 2020 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido