Automated clinical diagnostic system and method using parallel liquid chromatography channels and sample preparation workflows

Patent metadata

Field	Value
Publication number	US-10775355-B2
Application number	US-201816009434-A
Country	US
Kind code	B2
Filing date	Jun 15, 2018
Priority date	Dec 18, 2015
Publication date	Sep 15, 2020
Grant date	Sep 15, 2020

Abstract

A clinical diagnostic system is presented and comprises a sample preparation station for automatically preparing samples comprising analytes of interest, a liquid chromatography (LC) separation station comprising a plurality of LC channels and a sample preparation/LC interface for inputting prepared samples into the LC channels. The system further comprises a controller to assign samples to pre-defined sample preparation workflows each comprising a pre-defined sequence of sample preparation steps and requiring a pre-defined time for completion depending on the analytes. The controller further assigns an LC channel for each prepared sample depending on the analytes and plans an LC channel input sequence for inputting the prepared samples that allows analytes from different LC channels to elute in a non-overlapping LC eluate output sequence based on expected elution times. The controller further sets and initiates a start sequence that generates a prepared sample output sequence that matches the LC channel input sequence.

First claim

We claim:

1. A clinical diagnostic system, the clinical diagnostic system comprising:
a sample preparation station for the automated preparation of samples comprising analytes of interest;
a liquid chromatography (LC) separation station comprising a plurality of LC channels (C 1 - n , C′ 1 - n ) arranged in parallel;
a sample preparation/LC interface for inputting prepared samples into any one of the LC channels (C 1 - n , C′ 1 - n ); and
a controller programmed to:
assign samples to pre-defined sample preparation workflows, each comprising a pre-defined sequence of sample preparation steps and requiring a pre-defined time for completion depending on the analytes of interest,
assign an LC channel (C 1 - n , C′ 1 - n ) for each prepared sample depending on the analytes of interest,
plan an LC channel input sequence (I 1 - n ) for inputting the prepared samples that allows analytes of interest from different LC channels (C 1 - n , C′ 1 - n ) to elute in a non-overlapping LC eluate output sequence (E 1 - n ) based on expected elution times,
set and initiate a sample preparation start sequence (S 1 - n ) that generates a prepared sample output sequence (P 1 - n ) out of the sample preparation station that matches the LC channel input sequence (I 1 - n ), so that when preparation of a sample is completed the assigned LC channel (C 1 - n , C′ 1 - n ) is also available and the prepared sample can be inputted into the assigned LC channel (C 1 - n , C′ 1 - n ), before preparation of another sample is completed or before the next prepared sample arrives to the sample preparation/LC interface,
set a reference period and start preparation of at most one sample per reference period with possible one or more reference periods between consecutive samples in the sample preparation start sequence (S 1 - n ) and/or complete preparation of at most one sample per reference period with possible one or more reference periods between consecutive prepared samples of the prepared sample output sequence (P 1 - n ) and/or input one prepared sample per reference period into one of the LC channels (C 1 - n , C′ 1 - n ) with possible one or more reference periods between consecutive LC channel inputs of the LC channel input sequence (I 1 - n ) and/or output one LC eluate per reference period with possible one or more reference periods between consecutive LC eluates of the LC eluate output sequence (E 1 - n ).

2. The clinical diagnostic system according to claim 1 , wherein the LC separation station comprises at least one faster LC channel (C 1 - n ) with a shorter cycle time and at least one slower LC channel (C′ 1 - n ) with a longer cycle time.

3. The clinical diagnostic system according to claim 2 , wherein the controller is programmed to set the reference period to be as long as the shorter cycle time and wherein the at least one slower LC channel (C′ 1 - n ) has an elution time window for the elution of analytes of interest that is as long as or shorter than the reference period.

4. The clinical diagnostic system according to claim 2 , wherein the shorter cycle time is less than 60 seconds and the longer cycle time is more than 60 seconds.

5. The clinical diagnostic system according to claim 2 , wherein the longer cycle time is n times the reference period, wherein n is an integer number equal or greater than 2.

6. The clinical diagnostic system according to claim 2 , wherein the at least one faster LC channel (C 1 - n ) is a capillary flow-injection-analysis channel or a rapid trap and elute online liquid chromatography channel and the at least one slower LC channel (C′ 1 - n ) is an ultra-high-performance liquid chromatography channel.

7. The clinical diagnostic system according to claim 1 , wherein the sample preparation station comprises a magnetic bead handling unit for treating samples with magnetic beads carrying analyte and/or matrix selective groups.

8. The clinical diagnostic system according to claim 1 , further comprising,
a mass spectrometer; and
an LC/MS interface for connecting the LC separation station to the mass spectrometer.

9. The clinical diagnostic system according to claim 8 , wherein the LC/MS interface comprises an ion mobility module between an ionization source and the mass spectrometer.

10. The clinical diagnostic system according to claim 8 , wherein all LC channels (C 1 - n , C′ 1 - n ) are alternately connectable to the LC/MS interface and the controller controls a valve switching according to the LC eluate output sequence (E 1 - n ).

11. A clinical diagnostic method, the clinical diagnostic method comprising:
automatically preparing samples comprising analytes of interest by a sample preparation station and inputting prepared samples via a sample preparation/LC interface into a liquid chromatography (LC) separation station comprising a plurality of LC channels (C 1 - n , C′ 1 - n ) arranged in parallel;
assigning samples to pre-defined sample preparation workflows, each comprising a pre-defined sequence of sample preparation steps and requiring a pre-defined time for completion depending on the analytes of interest;
assigning an LC channel (C 1 - n , C′ 1 - n ) for each prepared sample depending on the analytes of interest;
planning an LC channel input sequence (I 1 - n ) for the prepared samples that allows analytes of interest from different LC channels (C 1 - n , C′ 1 - n ) to elute in a non-overlapping LC eluate output sequence (E 1 - n ) based on expected elution times;
setting and initiating a sample preparation start sequence (S 1 - n ) that generates a prepared sample output sequence (P 1 - n ) out of the sample preparation station that matches the LC channel input sequence (I 1 - n ), so that when preparation of a sample is completed the assigned LC channel (C 1 - n , C′ 1 - n ) is also available and the prepared sample can be inputted into the assigned LC channel (C 1 - n , C′ 1 - n ), before preparation of another sample is completed or before the next prepared sample arrives to the sample preparation/LC interface;
setting a reference period; and
starting preparation of at most one sample per reference period with possible one or more reference periods between consecutive samples in the sample preparation start sequence (S 1 - n ); and/or
completing preparation of at most one sample per reference period with possible one or more reference periods between consecutive prepared samples of the prepared sample output sequence (P 1 - n ); and/or
inputting one prepared sample per reference period into one of the LC channels (C 1 - n , C′ 1 - n ) with possible one or more reference periods between consecutive LC channel inputs of the LC channel input sequence (I 1 - n ); and/or
outputting one LC eluate per reference period with possible one or more reference periods between consecutive LC eluates of the LC eluate output sequence (E 1 - n ).

12. The clinical diagnostic method according to claim 11 further comprising,
alternately connecting the LC channels (C 1 - n , C′ 1 - n ) to an LC/MS interface connecting the LC separation station to a mass spectrometer according to the LC eluate output sequence (E 1 - n ).

13. The clinical diagnostic method according to claim 11 , wherein the plurality of LC channels (C 1 - n , C′ 1 - n ) comprises at least one faster LC channel (C 1 - n ) with a shorter cycle time and at least one slower LC channel (C′ 1 - n ) with a longer cycle time.

14. The clinical diagnostic method according to claim 13 , further comprising,
setting the reference period to be as long as the shorter cycle time, wherein the at least one slower LC channel (C′ 1 - n ) has an elution time window for th

Assignees

• Roche Diagnostics Operations Inc

Inventors

• Franz Tobias
• Kobold Uwe
• Kupser Peter
• Thiele Roland

Classifications

• G01N30/6039

  in series · CPC title

• B01D15/1885

  placed in parallel · CPC title

• G01N1/405

  by adsorption or absorption · CPC title

• G01N30/06

  Preparation · CPC title

• G01N30/466

  with separation columns in parallel · CPC title