Sample processing devices, systems and methods

Patent metadata

Field	Value
Publication number	US-12018248-B2
Application number	US-202117140854-A
Country	US
Kind code	B2
Filing date	Jan 4, 2021
Priority date	Mar 15, 2016
Publication date	Jun 25, 2024
Grant date	Jun 25, 2024

Abstract

This instant disclosure provides methods of processing a sample in an automated sample processing device including devices configured for the automated extraction or isolation of nucleic acids. Also provided are plungers for use in such devices and methods of sample processing. Systems for performing the described methods and employing the described plungers are also provided.

First claim

What is claimed is:

1. A method of eluting nucleic acid from attached magnetic particles, the method comprising:
a) inserting into an elution well comprising an elution buffer a magnetized plunger comprising magnetically attached magnetic particles comprising attached nucleic acid;
b) centering the magnetized plunger in the elution well by driving the magnetized plunger against the bottom of the elution well;
c) retracting a magnet out of the plunger to demagnetize the plunger;
d) reciprocating the demagnetized plunger up and down in the elution buffer at a first vertical speed sufficient to elute the nucleic acid; and
e) removing the plunger from the elution buffer at a second vertical speed, wherein the second vertical speed is slower than the first vertical speed.

2. The method according to claim 1 , wherein the method further comprises two or more steps of driving the demagnetized plunger to the bottom of the elution well to center the demagnetized plunger in the elution well.

3. The method according to claim 1 , wherein the driving the demagnetized plunger to the bottom of the elution well to center the demagnetized plunger in the elution well is performed at a third vertical speed that is faster than both the first and second vertical speeds.

4. The method according to claim 1 , wherein the method further comprises one or more mixing steps comprising reciprocating the plunger sufficient to mix the elution buffer prior to removing the plunger in step e).

5. The method according to claim 4 , wherein at least one of the one or more mixing steps comprises a pause of the plunger in the elution buffer.

6. The method according to claim 5 , wherein during the pause the magnet is inserted into the plunger for a period of time sufficient to allow the magnetic particles to reattach to the remagnetized plunger and then the magnet is removed from the plunger to allow the magnetic particles to disassociate from the plunger into the elution buffer.

7. The method according to claim 1 , wherein following elution of the nucleic acid and removal of the plunger the nucleic acid containing elution buffer is removed.

8. The method according to claim 7 , wherein removal of the nucleic acid containing elution buffer is performed by pipetting.

9. The method according to claim 1 , wherein the volume of elution buffer is between 10 μl and 300 μl.

10. The method according to claim 1 , wherein the plunger comprises an elongated hollow cone structure comprising:
an open top;
a closed tip comprising an end nub, wherein the end nub protrudes beyond the end of the closed tip so that upon complete insertion of the plunger into the elution well, the end nub contacts the bottom of the elution well and leaves a space between the bottom of the elution well and the closed tip, and wherein the elution well is configured to receive and align the plunger to the center of the elution well when the plunger is inserted into the elution well.

11. The method according to claim 10 , wherein the closed tip of the plunger is a closed rounded tip.

12. The method according to claim 10 , wherein the plunger comprises a diameter adjacent to the closed tip equal to the smallest diameter of the elution well and a height that is longer than the depth of the elution well.

13. The method according to claim 10 , wherein the plunger further comprises a plurality of flutes arranged parallel to the long axis of the elongated hollow cone structure extending from the closed tip.

14. The method according to claim 1 , wherein the plunger comprises an elongated hollow cone structure comprising:
an open top,
a closed tip,
a plurality of flutes arranged parallel to the long axis of the elongated hollow cone structure extending from the closed tip, wherein the elution well is configured to receive and align the plunger to the center of the sample processing well when the plunger is inserted into the elution well.

15. The method according to claim 14 , wherein the closed tip of the plunger is a closed rounded tip.

16. The method according to claim 14 , wherein the plunger comprises a diameter adjacent to the closed tip equal to the smallest diameter of the elution well and a height that is longer than the depth of the elution well.

17. The method according to claim 14 , wherein plunger further comprises an end nub that protrudes beyond the end of the closed rounded tip so that upon complete insertion of the plunger into the elution well, the end nub contacts the bottom of the elution well and leaves a space between the bottom of the elution well and the closed rounded tip.

Assignees

• Abbott Molecular Inc

Inventors

• Talmer Mark
• Keck Jody L
• Addison Wesley W

Classifications

• G01N1/12

  Dippers; Dredgers · CPC title

• C12N15/1003

  Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor · CPC title

• G01N35/10

  Devices for transferring samples {or any liquids} to, in, or from, the analysis apparatus, e.g. suction devices, injection devices {(G01N35/0099 takes precedence)} · CPC title

• G01N2035/1053

  for separating part of the liquid, e.g. filters, extraction phase · CPC title

• B01L2400/043

  magnetic forces · CPC title