IP Library Granted Patent US 10,022,696
Granted Patent B2
US 10,022,696 · App. 14/479,284 · Granted Jul 17, 2018

Microfluidic assay systems employing micro-particles and methods of manufacture

Inventors: Martin A. Putnam (Cheshire, CT); Jeffrey T. Branciforte (Hartford, CT); Charles O. Stanwood (Hartford, CT)
Assignee: Cyvek, Inc.
B01J19/0046B01L3/502707B01L3/502715B01L3/502738G01N21/05G01N21/645G01N33/54366B01J2219/005B01J2219/00468B01J2219/00511B01J2219/00522B01J2219/00587B01J2219/00689B01J2219/00691B01L2200/027B01L2200/0689B01L2200/16B01L2300/0636B01L2300/087B01L2300/0819B01L2300/0838B01L2300/0864B01L2300/0874B01L2300/0887B01L2300/123B01L2300/168B01L2400/0481B01L2400/0638B01L2400/0655B01L2400/086G01N2021/0346G01N2021/058G01N2035/00158Y10T29/494
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,022,696
App. No.
14/479,284
Granted
Jul 17, 2018
Kind
B2
Abstract

A method of making an assay device comprising providing micro-elements in the form of micro-particles or micro-length tube detection elements and thereafter with an automated tool, picking and placing the micro-elements into open-sided microfluidic channels in a body.

Claims (23)

1. A method of making an assay device comprising providing micro-elements in the form of micro-particles or micro-length tube detection elements and thereafter with an automated placement tool, picking and placing the micro-elements into open-sided microfluidic channels in a body.

2. The method of claim 1 further comprising bonding a membrane layer to the body thereby closing the open sides of the channels, enclosing the micro-elements and completing the respective portions of the microfluidic channels.

3. The method of claim 2 in which the membrane layer comprises a PDMS membrane which is surface-activated, the body defines an opposing surface that is bondable by covalent bondings to the membrane layer, and the act of closing is performed by the covalent bonding of the membrane and the body.

4. The method of claim 3 in which the body has an opposed surface defined by PDMS that is surface-activated.

5. The method of claim 4 wherein the picking and placing is performed by an automated vision-based picking-placing control system.

6. The method of claim 4 in which the open microfluidic channels have widths greater than the micro-elements and the automated placement tool is caused to move laterally after entry of the elements into the respective channels, to enable the micro-elements to lodge against predetermined side-walls of the channels.

7. The method of claim 4 in which the open microfluidic channels have widths greater than the micro-elements and the placing into the channels includes use of electrostatic attraction to disengage the micro-elements from the automated placement tool and attract them to side walls of the channels.

8. The method of claim 1 in which the microfluidic channels are defined in an elastomeric channel-defining member, including immobilizing the micro-elements within the microfluidic-channels by applying a force to the micro-elements, wherein the force causes the elastomeric channel-defining member to resiliently deform and exert an immobilizing force on the micro-elements.

9. The method of claim 8 in which the micro-elements are force-fit into microfluidic channels of narrower width.

10. The method of claim 4 further comprising, with Drill the automated placement tool, picking up the elements from grooves or pockets in a surface, and placing the elements into the microfluidic channels.

11. The method of claim 4 in which the predetermined channels are located on a platform, wherein the position of the platform is computer-controlled in the X and Y directions and the placement tool does not move in those directions.

12. The method of claim 11 in which the placement tool comprises grippers, wherein the movement of the grippers is computer-controlled.

13. The method of claim 11 in which the placement tool comprises a vacuum pickup head and the movement of the pickup head is computer-controlled.

14. The method of claim 1 further comprising picking up the micro-elements from a smooth surface; placing the micro-elements into the predetermined channel, wherein the predetermined channel comprises an elastomeric channel-defining layer; immobilizing the micro-elements within the micro-channel by applying a force to the micro-elements, wherein the force causes the elastomeric channel-defining layer to resiliently deform and exert an immobilizing force on the micro-elements.

15. The method of claim 4 further comprising picking up the micro-elements from a smooth surface; placing the micro-elements into the predetermined channel, wherein the predetermined channel comprises an elastomeric channel-defining layer; and in conjunction with electrostatic attraction, immobilizing the micro-elements within the micro-channel against a side-wall of the predetermined channel by moving laterally within the channel to a point at which the micro-elements are drawn to and attach to the sidewall.

16. The method of claim 1 further comprising picking up the micro-elements from a smooth surface; placing the micro-elements into the predetermined channel, in which the predetermined channels are located on a platform, wherein the position of the platform is computer-controlled in the X, Y directions and the placement tool moves in a theta direction about a vertical axis to align with the orientation of an automated, visually identified micro-particle.

17. The method of claim 4 wherein forming the micro-particles or micro-detection elements for an assay includes the step of coating the detection elements in bulk with capture agent before picking and placing the elements into microfluidic channels.

18. The method of claim 17 including batch coating the micro-detection elements with capture agent by mixing in solution and then drying before picking and placing the detection elements into the microfluidic channels.

19. The method of claim 4 wherein the micro-elements for an assay comprise micro-length hollow flow elements.

20. The method of claim 19 wherein the micro-length hollow flow elements comprise glass nano reactors.

21. The method of claim 12 in which the grippers comprises automated tweezer fingers engaging oppositely directed portions of the element.

22. A method of making an assay device, comprising: providing micro-elements in the form of glass micro-length tubular detection elements and thereafter with an automated placement tool, picking and placing the micro-elements from a pick-up plate into open-sided microfluidic channels, wherein the pick-up plate defines a flat element-receiving surface and has grooves or pockets in the surface in which the elements become discretely lodged in alignment and wherein the elements are pre-coated with a capture agent prior to being disposed on the pick-up plate.

23. A method of making an assay device having microfluidic channels, comprising: providing micro-elements in the form of micro-length tubular detection elements and thereafter with an automated placement tool, picking up the micro-elements from a pick-up plate and placing the elements into the microfluidic channels, the pick-up plate having a series of pockets formed along grooves, in which the elements are aligned and discretely lodge, and the microfluidic channels having at least one side wall formed of an elastomeric material.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2016
From: PUTNAM, MARTIN A.; BRANCIFORTE, JEFFREY T.; STANWOOD, CHARLES O.
To: CYVEK, INC.
Reel/Frame 038286/0598 →
Continuity (23)
Continuation In Part PCTUS2013000062 · Mar 8, 2013
Continuation 13427857 · Mar 22, 2012
Continuation In Part PCTUS2010057860 · Nov 23, 2010
Continuation In Part PCTUS2011029736 · Mar 24, 2011
Continuation In Part PCTUS2010057860 · Nov 23, 2010
Continuation In Part 14479284
Continuation In Part PCTUS2013033610 · Mar 22, 2013
Continuation 13427857 · Mar 22, 2012
Continuation In Part PCTUS2010057860 · Nov 23, 2010
Continuation In Part PCTUS2011029736 · Mar 24, 2011
Continuation In Part PCTUS2010057860 · Nov 23, 2010
Continuation In Part 14479284
Continuation In Part 13427857 · Mar 22, 2012
Continuation In Part PCTUS2010057860 · Nov 23, 2010
Continuation In Part PCTUS2011029736 · Mar 24, 2011
Continuation In Part PCTUS2010057860 · Nov 23, 2010
Continuation In Part 14479284
Continuation In Part 13511593
Provisional Application 61608570 · Mar 8, 2012
Provisional Application 61754377 · Jan 18, 2013
Provisional Application 61465688 · Mar 22, 2011
Provisional Application 61263572 · Nov 23, 2009
Related Publication 20150087558A1 · Mar 26, 2015
Cited By (1)
US 12,205,325