Patterning device

Abstract

A novel miniaturized and highly automated method for the controlled printing of large arrays of nano- to femtoliter droplets is presented by actively transporting mother droplets over hydrophilic-in-hydrophobic micropatches. The proposed technology consists of single plate or double-plate devices where mother droplets can be actuated and hydrophilic-in-hydrophobic micropatches on one or both plates of the device where nano- to femtoliter droplets are printed. Due to the selective wettability of the more wettable hydrophilic micropatches in a hydrophobic matrix, large nano- to femtoliter droplet arrays are created when mother droplets are transported over these arrays. The parent droplets can be moved by different droplet actuation principles, for example, by using the principle of electrowetting-on-dielectric droplet actuation. We propose another method that uses two plates that are placed on top of each other while being separated by a spacer. One plate is dedicated to confirming and guiding of parent droplets by using hydrophilic patches in a hydrophobic matrix, while the other plate contains hydrophilic-in-hydrophobic arrays dedicated to the printing of nano- to femtoliter droplets. When the plate dedicated to parent droplet guiding is rotated over the plate dedicated to printing of nano- to femtoliter droplets, nano- to femtoliter droplets are dispensed inside the hydrophilic-in-hydrophobic array due to their selective wettability. All these proposed methods allow the parent droplets to be moved over the hydrophilic-in-hydrophobic arrays many times, providing unique advantages for performing bio-assays or miniaturized materials synthesis in nano- to femtoliter sized droplets. Upon the controlled evaporation of the dispensed droplets of solution, large arrays of the printed material can be generated on an automated way in seconds of time on a very flexible way. The method disclosed herein provides a distinct nano- to femtoliter droplet printing technique for a wide variety of applications such as protein- or cell-based bio-assays or printing of crystalline structures, suspensions of nanoparticles or components for microelectronics.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a national phase entry under 35 U.S.C. §371 of International Patent Application PCT / BE2013 / 000004, filed Jan. 24, 2013, designating the United States of America and published in English as International Patent Publication WO2013 / 110146 A2 on Aug. 1, 2013, which claims the benefit under Article 8 of the Patent Cooperation Treaty to Great Britain Application Serial No. 1201277.9, filed Jan. 24, 2012, U.S. Provisional Application Ser. No. 61 / 592,399, filed Jan. 30, 2012, Great Britain Application Serial No. 1218994.0, filed Oct. 23, 2012, Great Britain Application Serial No. 1218995.7, filed Oct. 23, 2012, and U.S. Provisional Application Ser. No. 61 / 725,268, filed Nov. 12, 2012, the disclosure of each of which is hereby incorporated herein in its entirety by this reference.BACKGROUND[0002]A. Field of the Disclosure[0003]The disclosure relates generally to a patterning device for printing arrays of nano- to femtoliter dro...

AI Technical Summary

Benefits of technology

The patent describes a new method for selecting and isolating aptamers, which are small molecules that can bind to specific molecules with high affinity. The method is faster and more efficient than previous methods, using a digital microfluidic chip and magnetic particles to accelerate the trapping of magnetic particles. The method also prevents the evaporation of droplets and ensures consistent and reliable results. The apparatus used for the method includes a hydrophilic chip with a matrix of microwells and a magnet for facilitating the movement of magnetic particles. The distance between the hydrophilic elements is designed to prevent pinning of droplets to the surface of the device. Overall, this patent provides a more efficient and reliable method for selecting and isolating aptamers.

Problems solved by technology

Usually, these methods are restricted in minimum amount of volume that they are able to dispense and the throughput that is achieved.

Moreover, inkjet systems are usually expensive and the printing of very large arrays is time-consuming.

The classical selection procedure is still lengthy, with weeks to months needed to generate a new aptamer and requiring multiple rounds of selection.

Furthermore, kinetic biases are known limitations of the system because the single representation of a given aptamer sequence among the billions of available sequences not only requires cyclic enrichment to isolate that particular single copy but also increases the probability that a certain aptamers molecule will never enter in contact with the target molecule.

Moreover, although a synthetic library theoretically contains 1016 random single stranded DNA / RNA sequences, practically they are never all analyzed because of the limited amount of aptamers-target mixture that can be loaded on capillary electrophoresis.

Finally, the amount of target molecule needed to perform all the selection cycles is rather high, rendering difficult the isolation of aptamers against expensive molecules (e.g., human growth factors) or targets that are available in limited amounts (recombinant proteins).

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