System and device for high throughput generation of combinatorial droplets and methods of use

Patent metadata

Field	Value
Publication number	US-2016332163-A1
Application number	US-201515112334-A
Country	US
Kind code	A1
Filing date	Jan 26, 2015
Priority date	Jan 24, 2014
Publication date	Nov 17, 2016
Grant date	—

Abstract

The present invention is directed to a microfluidic system comprising a microfluidic chip and a method of performing a chemical assay wherein a sample is processed into multiple daughter droplets and said daughter droplets are incubated with varying reagents. The properties of these droplets can be detected to provide assay data.

First claim

We claim:

1 . A microfluidic system comprising:
a microfluidic chip comprising a chip body defining:
a droplet formation section comprising a sample input channel,
a droplet splitting section fluidly connected to said droplet formation section, and
a reagent injection section fluidly connected said droplet splitting section;
a first sample source selectively connected to said sample input channel; a second sample source selectively connected to said sample input channel; and a rinsing fluid source selectively connected to said sample input channel.

2 . A microfluidic system as in claim 1 , wherein an automated sample loading system is fluidly connected to said microfluidic chip.

3 . A microfluidic system as in claim 1 , wherein an impedance detection system is fluidly connected to said microfluidic chip.

4 . A microfluidic system as in claim 1 , wherein a sample detection system is fluidly connected to said microfluidic chip.

5 . A microfluidic chip comprising a chip body defining:
a droplet formation section comprising:
a main channel,
a sample input channel having a first end fluidly connected to said main channel and a second end configured to receive sample and rinsing fluid,
an input-channel valve in said input channel to selectively allow and block fluid flow from said sample input channel to said main channel,
a rinsing channel fluidly connected to said sample input channel at a position between said input-channel valve and said second end of said sample input channel, and
a rinsing-channel valve in said rinsing channel to selectively allow and block fluid flow from said input channel to said rinsing channel,
wherein said droplet formation section has a first configuration in which said input-channel valve is open and said rinsing-channel valve is closed to provide a sample droplet having a substantially predetermined volume in said main channel suspended in an inert fluid, and wherein said droplet formation section has a second configuration in which said input-channel valve is closed and said rinsing-channel valve is open such that rinsing fluid rinses said sample input channel by a flow of said rinsing fluid through said sample input channel and out said rinsing channel;
a droplet splitting section fluidly connected to said main channel of said droplet formation section to receive said sample droplet from said main channel and split said sample droplet into a plurality of daughter droplets to be output from said droplet splitting section in a respective one of a plurality of secondary channels; and a reagent injection section fluidly connected to each of said plurality of secondary channels and having a corresponding plurality of reagent injection channels arranged such that each reagent of a plurality of reagents is injectable substantially simultaneously into a respective one of said plurality of daughter droplets while said daughter droplets are in said reagent injection section to provide a plurality of sample-reagent droplets output in a corresponding one of a plurality of output channels from said reagent injection section.

6 . A microfluidic chip according to claim 5 , wherein said droplet formation section comprises a pressure relief channel to controllably regulate pressure on said sample droplet while being formed.

7 . A microfluidic chip according to claim 5 , wherein said reagent injection section comprises a pressure relief channel to controllably regulate pressure on said plurality of daughter droplets while each of said plurality of reagents is being injected into a corresponding one of said plurality of daughter droplets.

8 . A microfluidic chip according to claim 5 , wherein said droplet splitting section is a multistage droplet splitter.

9 . A microfluidic chip according to claim 5 , further comprising a sample-reagent droplet splitting section fluidly connected to each of said plurality of output channels from said reagent injection section to receive said plurality of sample-reagent droplets and split each of said sample-reagent droplets into a plurality of daughter sample-reagent droplets to be output from said sample-reagent droplet splitting section in a respective one of a plurality of output channels.

10 . A microfluidic chip according to claim 9 , wherein said sample-reagent droplet splitting section is a multistage droplet splitter.

11 . A microfluidic chip according to claim 5 , further comprising an incubation section fluidly connected to each of said plurality of output channels from said sample-reagent droplet splitting section such that each of said sample-reagent droplets flows into a respective one incubation channel so as to maintain identifiable sample and reagent information thereof.

12 . A microfluidic chip according to claim 11 , wherein said incubation channels are of an equal length.

13 . A microfluidic chip according to claim 5 , further comprising a section with detection channels wherein said detection channels are at least partially transparent for optical measurements.

14 . A microfluidic chip according to claim 5 , wherein said reagent injection section further comprises:
a reagent injection valve in each of said reagent injection channels to selectively allow and block fluid flow from each of said reagent injection channels to said plurality of secondary channels, a rinsing channel fluidly connected to each of said plurality of reagent injection channels, and a rinsing-channel valve in said rinsing channel to selectively allow and block fluid flow from each of said plurality of reagent injection channels to said rinsing channel, wherein said regent injection section has a first configuration in which said reagent injection valve in each of said plurality of reagent injection channels is open and said rinsing-channel valve in each of said plurality of reagent injection channels is closed to provide a reagent in said plurality of secondary channels, and wherein said reagent injection section has a second configuration in which said reagent injection valve in each of said plurality of reagent injection channels is closed and said rinsing-channel valve in each of said plurality of reagent injection channels is open such that rinsing fluid rinses each of said plurality of reagent injection channels by a flow of said rinsing fluid through each of said plurality of reagent injection channels and out said rinsing channel in each of said plurality of reagent injection channels.

15 . A microfluidic chip according to claim 5 , wherein said droplet formation section further comprises:
a second sample input channel having a first end fluidly connected to said main channel and a second end configured to receive sample and rinsing fluid, an input-channel valve in said second sample input channel to selectively allow and block fluid flow from said at second sample input channel to said main channel, a second rinsing channel fluidly connected to said second sample input channel at a position between said input-channel valve and said second end of said second sample input channel, and a rinsing-channel valve in said second rinsing channel to selectively allow and block fluid flow from said second input channel to said second rinsing channel, wherein said droplet formation section has a third configuration in which said input-channel valve of said second sample input channel is open and said rinsing-channel valve of said second sample input channel is closed to provide a sample droplet having a substantially predetermined volume in said main channel suspended in an inert fluid, and wherein said droplet formation section has a

Assignees

• Univ Johns Hopkins

Inventors

• Wang Tza-Huei
• Rane Tushar Dnyandeo
• Zec Helena Claire

Classifications

• C40B50/08

  Liquid phase synthesis, i.e. wherein all library building blocks are in liquid phase or in solution during library creation; Particular methods of cleavage from the liquid support · CPC title

• C40B60/08

  Integrated apparatus specially adapted for both creating and screening libraries · CPC title

• B01J2219/00599

  Solution-phase processes · CPC title

• B01L2300/0867

  Multiple inlets and one sample wells, e.g. mixing, dilution · CPC title

• B01L2200/141

  Preventing contamination, tampering · CPC title