Apparatus for diagnostic testing and method

• US 20060030049A1
• Filed: 08/01/2005
• Published: 02/09/2006
• Est. Priority Date: 08/04/2004
• Status: Abandoned Application

• Current Assignee: IMI Vision Ltd. (IMI PLC)
• Original Assignee: IMI Vision Ltd. (IMI PLC)
• Inventors: Hunter, John, Bhimani, Alan, Rathbone, David
• Application Number:
  US11/194,856
• Publication Number:
  US 20060030049A1
• Time in Patent Office: Days
• US Class Current: 436/43
• CPC Class Codes: B01L 2200/147 Employing temperature sensors
• CPC Class Codes: B01L 2200/16 Reagents, handling or storing thereof
• CPC Class Codes: B01L 2300/022 Transponder chips
• CPC Class Codes: B01L 2400/0605 check valves
• CPC Class Codes: B01L 3/0206 of the plunger pump type
• CPC Class Codes: G01K 3/005 Circuits arrangements for indicating a predetermined temperature fire detection G08B17/00
• CPC Class Codes: G01K 3/04 in respect of time
• CPC Class Codes: G01N 2035/00673 of reagents
• CPC Class Codes: G01N 2035/00683 of detectors
• CPC Class Codes: G01N 2035/00782 reprogrammmable code
• CPC Class Codes: G01N 35/00663 of consumables
• CPC Class Codes: G01N 35/00732 Identification of carriers, materials or components in automatic analysers
• CPC Class Codes: G01N 35/1002 Reagent dispensers
• CPC Class Codes: Y10T 436/11 Automated chemical analysis
• CPC Class Codes: Y10T 436/2575 Volumetric liquid transfer

Abstract

Controlled dispense of a flowable reagent in a diagnostic system is characterized by placing in the diagnostic system at least one cartridge containing a reservoir of reagent and carrying an identifier device that has information pertinent to the reagent in the reservoir. The diagnostic system automatically reads the information contained in the identifier device and uses the information to control the diagnostic system in dispensing the reagent. The information contained in the identifier device may consist of one or more of an identification of the reagent in the reservoir; the expiration date of the reagent the active shelf life of the reagent; the volume of the reagent in the reservoir; an identification of the origin of the reagent; and the maximum storage temperature of the reagent.

Claims

1. A method of controlling dispensing of a flowable reagent in an in vitro diagnostic system, comprising the steps of:

placing in the diagnostic system a cartridge having a reservoir of reagent, a temperature sensor for sensing the temperature of the reagent and an identifier that contains information pertinent to the reagent including the sensed temperature of the reagent;

reading with the diagnostic system the information contained in the identifier; and

using the information read by the diagnostic system to control the diagnostic system in dispensing reagent from the cartridge.

2. A method according to claim 1, wherein the cartridge has a disposable sanitary pump for dispensing reagent from the reservoir, and including the steps of:

driving the pump with the diagnostic system to dispense reagent; and

controlling the diagnostic system in performing said driving step in accordance with information contained in the identifier.

3. A method according to claim 1, wherein information contained in the identifier consists of one or more of:

an identification of the reagent in the reservoir;

the expiration date of the reagent;

the active shelf life of the reagent;

the volume of the reagent in the reservoir;

an identification of the origin of the reagent; and

the maximum storage temperature of the reagent.

4. A method according to claim 1, said placing step comprising placing a plurality of cartridges in the diagnostic system, the identifier of each cartridge containing information relating to the identity of the reagent in the reservoir of the cartridge, said reading step comprising reading with the diagnostic system the identity of the reagent in the reservoir of each cartridge, and said using step comprising using the identity of the reagent in the reservoir of each cartridge to control the diagnostic system in dispensing reagent from a selected one or more of the cartridges.

5. A method according to claim 1, wherein the cartridge identifier contains information concerning the expiration date of the reagent in the reservoir, and said using step includes the step of preventing the diagnostic system from dispensing reagent that has expired.

6. A method according to claim 1, wherein the cartridge identifier contains information concerning the active shelf life of the reagent in the reservoir, and said using step includes the step of preventing the diagnostic system from dispensing the reagent if the active shelf life of the reagent has expired.

7. A method according to claim 1, wherein the cartridge identifier contains information concerning the active shelf life of the reagent in the reservoir, and said using step controls the diagnostic system to generate a signal upon expiration of the active shelf life of the reagent.

8. A method according to claim 1, wherein the identifier of the cartridge is permanently associated with the cartridge and the information contained in it is for being read by the diagnostic system.

9. A method according to claim 8, wherein the cartridge identifier includes a radio frequency identification (RFID) tag and said reading step includes reading the RFID tag with a reader of the diagnostic system.

10. A method according to claim 9, wherein said placing step comprises placing a plurality of cartridges in the diagnostic system, and said reading step comprises providing the diagnostic system with an RFID tag reader at each position where a cartridge is placed for reading only the information contained in the identifier of the cartridge placed in that position.

11. A method according to claim 10, wherein each diagnostic system RFID reader includes a short range reader circuit.

12. A method according to claim 11, wherein the short range reader circuit of each diagnostic system RFID reader has a limited operating range, such that the RFID reader cannot read the information contained in the REID tag of a cartridge until the cartridge is substantially inserted into the diagnostic system.

13. A method according to claim 12, wherein the short range reader circuit of each diagnostic system RFID reader has a single operating frequency.

14. A method according to claim 13, wherein the single frequency of the short range reader circuit of each diagnostic system RFID reader is above 13 MHz.

15. A method according to claim 8, wherein said reading step includes providing the diagnostic system with an identifier reader/writer so that the diagnostic system can read information from the cartridge identifier, write information to the identifier and overwrite information contained by the identifier.

16. A method according to claim 15, wherein the cartridge identifier is a universal data tag comprising at least one of memory circuitry and processor circuitry and is attached to the cartridge.

17. A method according to claim 16, wherein the universal data tag consists of a printed circuit board on which the at least one of memory circuitry and processor circuitry is provided, and including the step of providing the printed circuit board with a transceiver for communicating with the diagnostic system reader/writer.

18. A method according to claim 17, including the step of providing the printed circuit board with a printed 1000 μ

H inductor for inductive non-contact communication between the at least one of memory circuitry and processor circuitry and the diagnostic system reader/writer, thereby enabling the use of radio frequency identification (RFID) type devices ranging from 125 kHz to 13.56 kHz operating frequency.

19. A method according to claim 18, wherein the printed circuit board is a double sided board having the inductor mounted on one side and the at least one of memory circuitry and processor circuitry mounted on the other side.

20. A method according to claim 17, including the steps of providing the printed circuit board with a plurality of contact pads and the diagnostic system with physical spring contacts, and establishing contact between the contact pads and spring contacts to enable the diagnostic system to read and write information from and to the cartridge universal data tag.

21. A method according to claim 16, wherein the at least one of memory circuitry and processor circuitry comprises an Electro-Erasable-Programmable-Read Only Memory (EEPROM) chip.

22. A method according to claim 21, including the step of providing the EEPROM chip with four contacts comprising a ground contact, a positive voltage in contact and two signal contacts.

23. A method according to claim 22, including the step of reading information from and programming information to the EEPROM in a serial addressed manner.

24. A method according to claim 21, including the steps of providing a power supply for the EEPROM by charging an internal capacitor of the EEPROM from a positive voltage sing from data sent to the EEPROM by the diagnostic system.

25. A method according to claim 16, including the step of using the universal identification tag in an active role by providing it with a central processor and a battery power source.

26. A method according to claim 25, wherein said step of providing a battery power source provides the battery power source as a separate component located on the cartridge, and including the step of providing the circuit board with contacts to connect to the battery.

27. A method according to claim 8, wherein the identifier stores information in magnetic form.

28. A method according to claim 8, wherein the identifier stores information on a read/write magnetic strip.

29. A method according to claim 1, wherein the identifier contains information relating to the volume of reagent in the cartridge reservoir, said reading step including reading with the diagnostic system the volume of reagent in the reservoir upon the cartridge being placed in the diagnostic system and then, as the reagent is used, performing with the diagnostic system the additional steps of calculating the volume of reagent remaining in the cartridge reservoir, and writing to the cartridge identifier information relating to the volume of reagent remaining.

30. A method according to claim 29, wherein said step of writing information to the cartridge identifier relating to the volume of reagent remaining in the cartridge reservoir is performed every time reagent is used from the reservoir.

31. A method according to claim 29, wherein said step of writing information to the cartridge identifier relating to the volume of reagent remaining in the cartridge reservoir is performed prior to the cartridge being removed from the diagnostic system.

33. A method according to claims 15, wherein the cartridge identifier includes information relating to the active shelf life of the reagent in the cartridge reservoir, and said reading step comprises reading with the diagnostic system the active shelf life of the reagent when the cartridge is first inserted into the diagnostic system, and including the steps, performed by the diagnostic system, of using the date of insertion of the cartridge into the diagnostic system to calculate the expiration date of the active shelf life of the reagent, and writing the active shelf life expiration date of the reagent to the cartridge identifier.

34. A method according to claim 33, including the step of inhibiting the diagnostic system from dispensing further reagent from a cartridge once the active shelf life expiration date of the reagent has passed.

35. A method according to claim 8, wherein the information contained by the cartridge identifier is stored on a bar code.

36. A method according to claim 1, including the steps of detecting the temperature of the reagent in the cartridge, and recording in the cartridge identifier an occurrence of the reagent temperature changing past at least one predetermined temperature, said reading step reading from the cartridge identifier the occurrence of the reagent temperature changing past the at least one predetermined temperature when the cartridge is place in the diagnostic system.

37. A method according to claim 36, wherein said detecting and recording steps are performed by providing the cartridge with a dedicated circuit containing a thermal fuse associated with the identifier.

38. A method according to claim 36, wherein said detecting and recording steps are performed by providing the cartridge with an electronic temperature monitor associated with the identifier.

39. A method according to claims 36, including the step of measuring the time for which the temperature of the reagent remains changed past the at least one predetermined temperature.

40. A method according to claim 36, wherein the cartridge identifier is a magnetic device that loses a portion of its magnetic coding while the temperature of the reagent remains changed past the at least one predetermined temperature.

41. A cartridge for containing reagent for use in an in vitro diagnostic system, said cartridge comprising:

a reservoir for holding reagent;

means for sensing the temperature of the reagent;

means for dispensing reagent from said reservoir;

and data means containing information pertinent to reagent contained in said reservoir, including the sensed temperature of the reagent.

42. A cartridge as in claim 41, said temperature sensing means sensing the storage temperature of the reagent and providing the storage temperature to said data means.

43. A cartridge as in claim 41, wherein said means for dispensing reagent from said cartridge includes a disposable sanitary pump.

44. A cartridge as in claim 41, said data means containing information pertinent to one or more of:

an identification of the reagent in said reservoir;

the expiration date of the reagent;

the active shelf life of the reagent;

the volume of reagent in said reservoir;

the origin of the reagent; and

the maximum storage temperature of the reagent.

45. A cartridge as in claim 41, wherein said data means comprises a radio frequency identification (RFID) tag.

46. A cartridge as in claim 41, wherein said data means is for having information both read from and written to said data means.

47. A cartridge as in claim 41, wherein said data means comprises a printed circuit board having at least one of memory circuitry and processor circuitry, said data means also having a transceiver for use in reading information from and writing information to said at least one of said memory circuitry and said processor circuitry.

48. A cartridge as in claim 47, wherein said cartridge further includes electrical contact means electrically coupled to said data means for reading data from and writing data to said data means.

49. A cartridge as in claim 47, wherein said at least one of said memory circuitry and said processor circuitry comprises an Electro-Erasable-Programmable-Read Only Memory (EEPROM) chip.

50. A cartridge as in claim 49, said cartridge further including a power supply for said EEPROM comprising a capacitor charged by a positive voltage sing from data sent to said EEPROM.

51. A cartridge as in claim 47, further including battery means for powering said data means.

52. A cartridge as in claim 41, wherein said data means comprises a read/write magnetic strip.

53. A cartridge as in claim 41, wherein said data means comprises read/write data means.

54. An in vitro diagnostic system that uses a flowable reagent in the performance of diagnostic testing, said system comprising:

a cartridge including a reservoir for holding reagent, means for dispensing reagent from said reservoir, means for sensing the temperature of reagent in said reservoir, and data means containing information pertinent to reagent in said reservoir, including the sensed temperature of the reagent; and

an apparatus for receiving said cartridge and for using reagent in said cartridge reservoir to diagnostically test a fluid, said apparatus including reader means for reading information contained by said cartridge data means, means for operating said cartridge dispensing means to dispense reagent from said cartridge reservoir, and control circuit means for controlling said operating means to dispense reagent from said cartridge reservoir in accordance with information read by said reader means from said cartridge data means.

55. A system according to claim 54, wherein the cartridge dispensing means includes a disposable sanitary pump for dispensing reagent from said reservoir, said apparatus operating means operating said pump under control of said control circuit means to dispense reagent in accordance with information read by said reader means from said cartridge data means.

56. A system according to claim 54, wherein information contained in said cartridge data means consists of one or more of:

an identification of reagent in said reservoir;

the expiration date of the reagent;

the active shelf life of the reagent;

the volume of the reagent in said reservoir;

an identification of the origin of the reagent; and

the maximum storage temperature of the reagent.

57. A system according to claim 56, wherein said apparatus control circuit means prevents operation of said operating means to dispense reagent from said cartridge reservoir in response to said reader means reading from said cartridge data means an expiration date of the reagent that has passed.

58. A system according to claim 56, wherein said apparatus control circuit means prevents operation of said operating means to dispense reagent from said cartridge reservoir in response to said reader means reading from said cartridge data means an active shelf life of the reagent that has passed.

59. A system according to claim 54, wherein said cartridge data means includes a radio frequency identification (RFID) tag and said apparatus reader means reads information contained by said RFID tag.

60. A system according to claim 54, wherein said cartridge data means is a read/write data means and said apparatus reader means is a read/write means for both reading information from and writing information to said cartridge read/write data means.

61. A system according to claim 60, wherein said cartridge data means comprises at least one of memory circuitry and processor circuitry.

62. A system according to claim 61, wherein said cartridge data means comprises a printed circuit board having said at least one of said memory circuitry and said processor circuitry and including a transceiver, and said apparatus reader means including read/write means for reading information from and writing information to said at least one of said memory circuitry and said processor circuitry via said transceiver.

63. A system according to claim 62, wherein said at least one of said memory circuitry and said processor circuitry comprises an Electro-Erasable-Programmable-Read Only Memory (EEPROM) chip.

64. A system according to claim 63, including a power supply for said EEPROM chip comprising a capacitor charged by a positive voltage sing from data sent to the EEPROM by said apparatus read/write means.

65. A system according to claim 54, said cartridge data means including central processor means and battery means.

66. A system according to claim 54, said cartridge data means including magnetic data storage means.

67. A system according to claim 66, wherein said magnetic data storage means comprises a read/write magnetic strip.

68. A system according to claim 54, wherein said cartridge data means includes a bar code.

69. A system according to claim 54, wherein said cartridge temperature sensing means comprises a thermal fuse.

70. A system according to claim 54, wherein said cartridge temperature sensing means comprises an electronic temperature monitor.

71. A system according to claim 54, wherein said cartridge temperature sensing means comprises magnetic temperature sensing means that loses a portion of its magnetic coding while the temperature of the reagent remains changed past at least one predetermined temperature.