Method of washing an aspiration probe of an in-vitro diagnostic system, in-vitro diagnostic method, and in-vitro diagnostic system

Patent metadata

Field	Value
Publication number	US-11879904-B2
Application number	US-202117507874-A
Country	US
Kind code	B2
Filing date	Oct 22, 2021
Priority date	Dec 23, 2016
Publication date	Jan 23, 2024
Grant date	Jan 23, 2024

Abstract

A method of washing an aspiration probe of an in-vitro diagnostic system is disclosed. The aspiration probe comprises an outer surface and an inner surface forming an inner space for receiving a fluid. The method comprises dipping the aspiration probe into a first wash fluid so that the outer surface is immersed at least in part into the first wash fluid, aspirating an amount of the first wash fluid into the inner space of the aspiration probe, propagating an ultrasonic vibration to the outer surface of the aspiration probe via the first wash fluid, and rinsing the outer surface and the inner surface of the aspiration probe with a second wash fluid. Further, an in-vitro diagnostic method and an in-vitro diagnostic system are disclosed.

First claim

The invention claimed is:

1. An in-vitro diagnostic method comprising performing a first diagnostic test and a second diagnostic test, the first diagnostic test having a higher susceptibility to carryover than the second diagnostic test, the method comprising:
providing a reusable aspiration probe comprising an outer surface and an inner surface forming an inner space for receiving a fluid,
providing a first probe wash station comprising a first wash chamber holding a first wash fluid and an ultrasonic cleaner comprising an ultrasonic vibrator configured to propagate an ultrasonic vibration to the outer surface of the aspiration probe via the first wash fluid,
sequentially aspirating different respective test fluids with the reusable aspiration probe,
washing the aspiration probe before performing the first diagnostic test and before performing the second diagnostic test, wherein washing the aspiration probe before performing the first diagnostic test comprises:
dipping the aspiration probe into a first wash fluid so that the outer surface is immersed at least in part into the first wash fluid,
aspirating an amount of the first wash fluid into the inner space of the aspiration probe,
propagating an ultrasonic vibration to the outer surface of the aspiration probe via the first wash fluid, while the first wash fluid is within the inner space of the aspiration probe,
expelling the first wash fluid from the inner space, and
rinsing the outer surface and the inner surface of the aspiration probe with a second wash fluid, wherein the first wash fluid is a different fluid from the second wash fluid, and
wherein washing the aspiration probe before performing the second diagnostic test with lower susceptibility to carry over comprises only rinsing the outer surface and the inner surface of the aspiration probe with the second wash fluid.

2. The method according to claim 1 comprising repeating any one or more of the individual steps.

3. The method according to claim 1 wherein the first wash fluid is a chemically aggressive fluid.

4. The method according to claim 3 wherein the first wash fluid is an alkaline solution.

5. The method according to claim 4 wherein the alkaline solution comprises a detergent.

6. The method according to claim 1 wherein the second wash fluid is water.

7. An in-vitro diagnostic method comprising sequentially aspirating different test fluids or different aliquots of a test fluid with a reusable aspiration probe, wherein the method comprises washing the aspiration probe according to claim 1 before and/or after aspirating a test fluid and/or at maintenance intervals.

8. The in-vitro diagnostic method according to claim 7 wherein the method comprises performing at least one of or a combination of any two or more of an immunochemical test, a clinical chemical test, a nucleic acid test, a coagulation test, a hematology test, a mass spectrometric test.

9. The in-vitro diagnostic method according to claim 1 wherein the first diagnostic test is an immunochemical test and the second diagnostic test is a clinical chemistry test.

Assignees

• Roche Diagnostics Operations Inc
• Hitachi High Tech Corp

Inventors

• Nonaka Kouhei
• Mori Takamichi
• Aruga Yoichi
• Horie Yosuke
• Mccaughey Andrew
• Seiler Alexander

Classifications

• G01N35/1004 Primary

  Cleaning sample transfer devices · CPC title

• G01N35/1009

  Characterised by arrangements for controlling the aspiration or dispense of liquids · CPC title

• B01F31/00

  Mixers with shaking, oscillating, or vibrating mechanisms · CPC title

• B01L3/0275

  Interchangeable or disposable dispensing tips · CPC title

• G01N2035/00524

  Mixing by agitating sample carrier · CPC title