SAMPLE PROCESSING CASSETTE, SYSTEM, AND METHOD

• US 20100291536A1
• Filed: 05/14/2010
• Published: 11/18/2010
• Est. Priority Date: 05/14/2009
• Status: Abandoned Application

• Current Assignee: Streck
• Original Assignee: Streck
• Inventors: Pienaar, Elsje, Whitney, Scott E., Termaat, Joel R., Viljoen, Hendrik J., Freifeld, Alison
• Application Number:
  US12/780,345
• Publication Number:
  US 20100291536A1
• Time in Patent Office: Days
• US Class Current: 435/4
• CPC Class Codes: A61B 10/0051 for taking saliva or sputum samples devices for receiving spittle A61J9/00
• CPC Class Codes: A61B 10/0096 Casings for storing test samples A61B10/0038 and A61B10/0045 take precedence; preservation of living parts of the human or animal body A01N1/02; containers for retaining a material to be analysed B01L3/50; containers for enzymology or microbiology C12M1/16; swab-sampler being part of enzymology or microbiology container C12M1/30
• CPC Class Codes: A61B 90/98 using electromagnetic means, e.g. transponders
• CPC Class Codes: B01L 2200/0689 Sealing
• CPC Class Codes: B01L 2300/021 Identification, e.g. bar codes
• CPC Class Codes: B01L 2300/0864 comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
• CPC Class Codes: B01L 3/505 flexible containers not provided for above
• CPC Class Codes: G01N 2001/005 Packages for mailing or similar transport of samples

Abstract

The present invention provides a method and device for collecting treating and analysis of biological or chemical material by introducing a source material into a specimen container, transferring the source material to a processing device and thermally, chemically and/or mechanically treating the source material to alter at least one constitutive characteristic of the source material and to release or create a target material from the source material.

Claims

1. A method for preparing a source material comprising:

introducing a source material into a specimen container;

transferring the source material from the specimen container into a processing device;

treating the source material thermally, mechanically, chemically or any combination thereof within the processing device to alter at least one constitutive characteristic of the source material and to release or create a target material from the source material.

2. The method of claim 1, wherein the step of treating the source material mechanically includes mixing of the source material along with any chemical processing agents in the processing device to promote increased contact between the source material and chemical processing agents for causing cell lysis therein.

3. The method of claim 1, further including a step of amplifying the target material, detecting a target material, or both.

4. The method of claim 1, wherein the step of treating includes the use of a chemical processing agent and a mechanical device that cyclically impinges upon the source material to alter the at least one constitutive characteristic of the source material.

5. The method of claim 1, wherein the step of treating the source material within the processing device includes a step of maintaining the temperature of the processing device at one or more temperatures above room temperature sufficient for mucolysis and cell lysis.

6. The method of claim 1, further including a step of extracting the target material from the treated source material and a step of transferring extracted target material from a first portion of the processing device to a second portion of the processing device that is spaced apart from the first portion.

7. The method of claim 1, further including a step of extracting the target material from the treated source material and a step of transferring extracted target material from a first portion of the processing device to a second portion of the processing device that is spaced apart from the first portion but in fluid communication therewith using a motor-driven member that operates both as a pump and as a mixer.

8. The method of claim 1, further including a step of amplifying the target material by positioning some or all of the target material along with one or more PCR reagents between at least two opposing spaced apart thermoelectric elements that operate by the Peltier effect, in a polymerase chain reaction thermal cycling instrument, thereafter performing a plurality of successive steps of increasing and decreasing temperature of the target material by way of the thermoelectric elements.

9. The method of claim 8, wherein the step of amplifying the target material further includes a step of real-time detection of an attribute of the target material.

10. The method of claim 9, wherein the attribute of the target material is indicative of tuberculosis presence.

11. The method of claim 1, wherein the method is performed at a single point of care medical facility.

12. The method of claim 1, wherein the step of treating the source material chemically includes contacting the source material with one or more chemical processing agents comprising:

a reducing agent selected from the group consisting of dithiothreitol (DTT), mercaptoethanol, mercaptoethylamine, Tris[2-carboxyethyl]phosphine (TCEP), (N-acetylcysteine), Nacystelyn, dornase alfa, thymosin β

₄, guaifenesin, or any combination thereof;

a nuclease inhibitor selected from the group consisting of diethyl pyrocarbonate, ethanol, aurintricarboxylic acid (ATA), formamide, vanadyl-ribonucleoside complexes, macaloid, ethylenediamine tetraacetic acid (EDTA), proteinase K, heparin, hydroxylamine-oxygen-cupric ion, bentonite, ammonium sulfate, dithiothreitol (DTT), beta-mercaptoethanol, cysteine, dithioerythritol, tris(2-carboxyethyl)phosphene hydrochloride, a divalent cation such as Mg⁺², Mn⁺², Zn⁺², Fe⁺², Ca⁺², Cu⁺² or any combination thereof; and

a lysis buffer selected from the group consisting of tris-HCl, EDTA, tris-EDTA, EGTA, SDS, deoxycholate, TritonX, NaCl, sodium phosphate, NP-40, phosphate buffered saline (PBS), or any combination thereof.

13. The method of claim 1, further including a step transporting some or all of the target material to an external device for amplification.

14. The method of claim 1, wherein the method takes place in less than 30 minutes.

15. The method of claim 1, wherein the target material is transferred through a capturing medium such as a microporus filter, chromatography column, antibody coated packing or beads, magnetic packing, DNA/RNA probe coated packing, or any combination thereof in order to extract the target material while any remaining source material passes through the capturing medium to assist in purification of the target material.

16. A processing device for biological or chemical samples comprising:

a mixing portion into which a source material is introduced and treated to alter at least one constitutive characteristic of the source material and to release or create a target material from the source material through mechanical, thermal, and chemical treatment;

at least one interface for a control device that controls the temperature, mixing operation, or both within the mixing portion during mixing; and

a covering means for enclosing the mixing portion.

17. The processing device of claim 16, further including an amplification portion for subjecting the target material to amplification by thermocycling.

18. The processing device of claim 17, wherein the amplification portion is optionally integrated with the processing device.

19. The processing device of claim 16, wherein the constitutive characteristic is selected from one or any combination of:

rheological (e.g., viscosity), physical (e.g., physically deform or rupture cells), or chemical (e.g. composition, concentration, digestion of suspended solids).

20. The processing device of claim 16, wherein the mixing portion includes a mechanical mixer having a structural member that contacts the source material.

21. The processing device of claim 16, wherein a heater, temperature sensor, and optionally a cooling device are proximate to or included within the mixing portion.

22. The processing device of claim 16, wherein an interface controls or is in communication with one or more heaters, temperature sensors, motors, or any combination thereof.

23. The processing device of claim 16, wherein the mixing portion includes a walled structure defining a cavity that has an opening into which a sample is introduced and an opening into which a motor or impeller shaft passes.

24. The processing device of claim 16, wherein the mixing portion may have one or more ports for the entry and exit of source material, target material, chemical processing agents, or any combination thereof.

25. The processing device of claim 16, wherein the mixing portion has one or more interior wall surfaces adapted to have a sealing fit with a flexible walled bag containing the source material.

26. The processing device of claim 16, wherein multiple processing devices may be used simultaneously under identical mechanical, chemical or thermal treatment conditions, or each may be used simultaneously under different treatment conditions.

27. A processing device for biological or chemical samples comprising:

a device for mixing, pumping, or both;

a body configured to include a processing well adapted to receive the device;

optionally including a fluid transport path optionally including a valve;

at least one heating element and optionally at least one cooling device disposed within the body proximate to or included within the processing well in thermal communication with the device;

a temperature sensing device disposed within the body proximate to or included within the processing well;

a covering for placement over the device so that any contents of the device remain therein.

28. The processing device of claim 27, wherein the processing well or body includes an electric motor with an output shaft that engages an input shaft of the device for mixing and pumping.

29. The processing device of claim 27, wherein the mixing member includes a dual-functional head configured for:

i. homogenization or reducing the viscosity of the contents; and

ii. pumping some or all of the contents from the device to a downstream location.