Syringe-based fluid diversion mechanism for bodily fluid sampling

• US 9,999,383 B2
• Filed: 04/29/2014
• Issued: 06/19/2018
• Est. Priority Date: 11/30/2012
• Status: Active Grant

• Current Assignee: Magnolia Medical Technologies Limited
• Original Assignee: Magnolia Medical Technologies Limited
• Inventors: Bullington, Gregory J., Patton, Richard G., Gaw, Shan E.
• Primary Examiner(s): Mehta, Bhisma
• Assistant Examiner(s): LEE, BRANDY SCOTT
• Application Number:
  US14/264,481
• Publication Number:
  US 20150073348A1
• Time in Patent Office: 1,512 Days
• Field of Search: 604187, 604191
• CPC Class Codes: A61B 10/0045 Devices for taking samples of body liquids devices for taking blood samples A61B5/15
• CPC Class Codes: A61B 5/1405 Devices for taking blood samples devices for taking samples of other body liquids A61B10/0045
• CPC Class Codes: A61B 5/1416 by syringes containing more than one piston medical syringes in general A61M5/178
• CPC Class Codes: A61B 5/1427 Multiple blood sampling, e.g. at periodic or pre-established intervals
• CPC Class Codes: A61B 5/1438 using pre-evacuated means
• CPC Class Codes: A61B 5/15003 for venous or arterial blood
• CPC Class Codes: A61B 5/150099 by negative pressure, other than vacuum extraction into a syringe by pulling on the piston rod or into pre-evacuated tubes
• CPC Class Codes: A61B 5/150221 Valves
• CPC Class Codes: A61B 5/150236 Pistons, i.e. cylindrical bodies that sit inside the syringe barrel, typically with an air tight seal, and slide in the barrel to create a vacuum or to expel blood
• CPC Class Codes: A61B 5/150244 Rods for actuating or driving the piston, i.e. the cylindrical body that sits inside the syringe barrel, typically with an air tight seal, and slides in the barrel to create a vacuum or to expel blood
• CPC Class Codes: A61B 5/150251 Collection chamber divided into at least two compartments, e.g. for division of samples injection syringes having more than one chamber A61M5/19; syringes for injection of two or more media A61M5/2448, A61M5/284; sample preparation for further analysis A61B5/150755
• CPC Class Codes: A61B 5/150343 Collection vessels for collecting blood samples from the skin surface, e.g. test tubes, cuvettes sampling from within body cavities A61B5/150015, A61B5/150045
• CPC Class Codes: A61B 5/150389 Hollow piercing elements, e.g. canulas, needles, for piercing the skin
• CPC Class Codes: A61B 5/150633 Protective sleeves which are axially extensible, e.g. sleeves connected to, or integrated in, the piercing or driving device; pivotable protective sleeves
• CPC Class Codes: A61B 5/150732 Needle holders, for instance for holding the needle by the hub, used for example with double-ended needle and pre-evacuated tube,
• CPC Class Codes: A61B 5/153 Devices specially adapted for taking samples of venous or arterial blood, e.g. with syringes
• CPC Class Codes: A61B 5/154 Devices using pre-evacuated means
• CPC Class Codes: A61B 5/155 Devices specially adapted for continuous or multiple sampling, e.g. at predetermined intervals devices loaded with multiple lancets simultaneously A61B5/15146
• CPC Class Codes: B01L 3/0231 having several coaxial pistons

Abstract

A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the scaling member and the housing.

Claims

1. A syringe-based device for parenterally-procuring bodily fluid samples with reduced contamination from a patient, the device comprising:

a housing including a proximal end portion and a distal end portion and defining an inner volume therebetween, the proximal end portion being substantially open and the distal end portion having a port configured to be coupled to a lumen-defining device for receiving bodily fluid from the patient;

a pre-sample reservoir fluidically coupleable to the port and configured to receive and isolate a first volume of bodily fluid withdrawn from the patient; and

an actuator mechanism at least partially disposed in the inner volume of the housing, the actuator mechanism having a proximal end portion and a distal end portion, the distal end portion including a sealing member and the proximal end portion including a first protrusion and a second protrusion configured to selectively engage with the first protrusion to substantially limit a proximal movement of the second protrusion relative to the first protrusion, and configured to move through the substantially open proximal end portion of the housing when receiving the bodily fluid from the patient into a sample reservoir, the sealing member defining a channel extending from a distal end to a proximal end of the sealing member, the actuator mechanism configured to move between a first configuration in which the bodily fluid can flow from the port to the pre-sample reservoir through the channel in the sealing member, and a second configuration in which the bodily fluid can flow from the port to the sample reservoir, the sample reservoir defined at least in part by the sealing member and the housing.

2. The device of claim 1, wherein the actuator mechanism defines an inner volume between the proximal end portion and the distal end portion of the actuator mechanism.

3. The device of claim 2, wherein the pre-sample reservoir is disposed in the inner volume of the actuator mechanism.

4. The device of claim 2, further comprising:

a flow control mechanism operable to selectively control fluid flow between the port and the pre-sample reservoir, the flow control mechanism being configured to be moved between a first configuration in which the bodily fluid can flow through a first flow path to the pre-sample reservoir, and a second configuration in which the bodily fluid can flow through a second flow path to the sample reservoir.

5. The device of claim 1, further comprising:

a valve disposed in the channel.

6. The device of claim 5, wherein the valve is a check valve.

7. The device of claim 1, further comprising:

a second sealing member having a diameter and disposed within the actuator mechanism, wherein the diameter of the second sealing member is less than a diameter of the sealing member at the distal end portion of the actuator mechanism.

8. A syringe-based device for parenterally-procuring bodily fluid samples with reduced contamination from a patient, the device comprising:

a housing including a proximal end portion and a distal end portion and defining an inner volume therebetween, the proximal end portion being substantially open and the distal end portion having a port configured to be coupled to a lumen-defining device for receiving bodily fluids from the patient;

an actuator mechanism movably disposed in the inner volume, the actuator mechanism including a first member having a proximal end portion and a distal end portion and defining an inner volume therebetween, and a second member movably disposed in the inner volume of the first member, the proximal end portion of the first member configured to move through the substantially open proximal end portion of the housing when receiving the bodily fluid samples within the inner volume of the housing,

the first member including a first plunger disposed at the distal end portion of the first member and a first protrusion disposed at a proximal end portion of the first member, the first plunger including a flow channel configured to allow selective fluid communication between the inner volume defined by the housing and the inner volume defined by the first member, and

the second member including a second plunger disposed at a distal end portion of the second member and a second protrusion disposed at a proximal end portion of the second member and configured to selectively engage with the first protrusion of the first member to substantially limit a proximal movement of the second member relative to the first member, and configured to move through the substantially open proximal end portion of the housing when receiving the bodily fluid from the patient into a sample reservoir; and

mechanical stops configured to prevent removal of the actuator mechanism from the housing.

9. The device of claim 8, further comprising:

a valve disposed in the flow channel.

10. The device of claim 9, wherein the valve is a check valve.

11. The device of claim 8, wherein the actuator mechanism is configured to be moved from a first configuration to a second configuration by application of a first force on the actuator mechanism in a proximal direction, the first plunger, the second plunger, and the first member of the actuator mechanism collectively defining a first fluid reservoir in the second configuration.

12. The device of claim 11, wherein the actuator mechanism is configured to be moved from the second configuration to a third configuration by application of a second force on the actuator mechanism in the proximal direction, the first plunger and the housing defining a second fluid reservoir in the third configuration.

13. The device of claim 12, wherein the first fluid reservoir is fluidically isolated from the second fluid reservoir in the third configuration.

14. The device of claim 12, wherein the first force is substantially the same as the second force.

15. The device of claim 12, wherein the second force is greater than the first force.

16. The device of claim 8, wherein the first plunger has a first diameter and the second plunger has a second diameter, the first diameter being greater than the second diameter.

17. The device of claim 8, wherein the first member and the second member are configured to move independently within the housing.

18. The device of claim 8, wherein the first member and the second member are substantially cylindrical.

19. A device for procuring bodily fluid from a patient, the device comprising:

a housing including a proximal end portion and a distal end portion, the proximal end portion being substantially open and the distal end portion having a port configured to receive the bodily fluid from the patient;

a first member movably disposed within the housing and including a first plunger disposed at a distal end portion of the first member and a first protrusion disposed at a proximal end portion of the first member, the first plunger including a flow channel to allow the body fluid to flow therethrough; and

a second member movably disposed within the first member and including a second plunger disposed at a distal end portion of the second member, the second member including a second protrusion disposed at a proximal end portion of the second member and configured to selectively engage with the first protrusion of the first member to substantially limit a proximal movement of the second member relative to the first member and configured to move through the substantially open proximal end portion of the housing when receiving the bodily fluid from the patient into a sample reservoir.

20. The device of claim 19, further comprising:

a mechanical stop to prevent removal of the first member from the housing.

21. The device of claim 19, further comprising:

a pre-sample reservoir collectively defined by the second plunger, the first plunger, and the first member.

22. The device of claim 21, wherein the second plunger moves away from the first plunger by application of a force by a user on the second member to convey the bodily fluid into the pre-sample reservoir.

23. The device of claim 21, further comprising:

a sample reservoir collectively defined by the first plunger, the distal end portion of the housing, and the housing.

24. The device of claim 23, wherein the first plunger moves away from the port by the second protrusion of the second member engaging with the first protrusion of the first member to convey the bodily fluid into the sample reservoir.

25. The device of claim 23, wherein the sample reservoir is fluidically isolated from the pre-ample reservoir.

26. The device of claim 25, further comprising:

a check valve disposed in the flow channel.

27. The device of claim 19, wherein the flow channel is aligned with the port forming a substantially linear flow path.

28. The device of claim 19, wherein the first plunger has a first diameter and the second plunger has a second diameter, the first diameter being greater than the second diameter.

29. The device of claim 19, wherein the first member and the second member are configured to move independently within the housing.

30. The device of claim 19, wherein the first member and the second member are substantially cylindrical.