Method and apparatus for penetrating tissue
View Patent ↗These and other objects of the present invention are achieved in a body fluid sampling system for use on a tissue site that includes a drive force generator and a penetrating member operatively coupled to the force generator. The force generator moves the member along a path out of a housing with a penetrating member exit, into the tissue site, stops in the tissue site, and withdraws out of the tissue site. The drive force generator is configured to be controlled to follow a predetermined velocity trajectory into the tissue and out of the tissue. A tissue stabilizing member is associated with the device and at least partially surrounds an impact location of the penetrating member on the tissue site.
1. A body fluid sampling system for use on a tissue site, the system comprising:
a housing;
an electrically powered drive force generator;
a penetrating member operatively coupled to the electrically powered drive force generator, the electrically powered drive force generator moving the penetrating member along a path out of the housing having a penetrating member exit, into the tissue site, stopping in the tissue site, and withdrawing out of the tissue site following a predetermined velocity vs. position profile;
a penetrating member sensor configured to monitor depth of penetration and velocity of the penetrating member;
a processor coupled to the electrically powered drive force generator with program instructions that provide an input to the electrically powered drive force generator to control depth of penetration and velocity of the penetrating member to match the predetermined velocity vs. position profile via a feedback loop of the depth of penetration and velocity of the penetrating member from the penetrating member sensor; and
a tissue stabilizing member associated with said housing and positioned to at least partially surround an impact location of the penetrating member on the tissue site wherein the tissue stabilizer member is configured to apply a force to a target tissue and cause the target tissue to press in an inward direction relative to the housing member.
2. The system of claim 1 , wherein the penetrating member sensor includes an interference encoder.
3. The system of claim 1 , further comprising an analyte detecting member.
4. The system of claim 1 , further comprising a plurality of analyte detecting members positioned to receive body fluid.
5. The system of claim 1 , further comprising:
a sample chamber with an opening for transport of a body fluid into the sample chamber, the sample chamber being sized to receive no more than 1.0 μL of the body fluid.
6. The system of claim 1 , further comprising:
a sample chamber with an opening for transport of a body fluid into the sample chamber, the sample chamber being sized to receive no more than 0.75 μL of the body fluid.
7. The system of claim 1 , further comprising:
a sample chamber with an opening for transport of a body fluid into the sample chamber, the sample chamber being sized to receive no more than 0.5 μL of the body fluid.
8. The system of claim 1 , further comprising:
a sample chamber with an opening for transport of a body fluid into the sample chamber, the sample chamber being sized to receive no more than 0.25 μL of the body fluid.
9. The system of claim 1 , further comprising:
a sample chamber with an opening for transport of a body fluid into the sample chamber, the sample chamber being sized to receive no more than 0.1 μL of the body fluid.
10. The system of claim 1 , further comprising:
an analyte detecting member coupled to a sample chamber, the analyte detecting member being configured to determine a concentration of an analyte in a body fluid using a sample that does not exceed a volume of 1 μL of a body fluid disposed in the sample chamber.
11. The system of claim 1 , further comprising:
an analyte detecting member coupled to a sample chamber, the analyte detecting member being configured to determine a concentration of an analyte in a body fluid using a sample that does not exceed a volume of 0.75 μL of a body fluid disposed in the sample chamber.
12. The system of claim 1 , further comprising:
an analyte detecting member coupled to a sample chamber, the analyte detecting member being configured to determine a concentration of an analyte in a body fluid using a sample that does not exceed a volume of 0.5 μL of a body fluid disposed in the sample chamber.
13. The system of claim 1 , further comprising:
an analyte detecting member coupled to a sample chamber, the analyte detecting member being configured to determine a concentration of an analyte in a body fluid using a sample that does not exceed a volume of 0.25 μL of a body fluid disposed in the sample chamber.
14. The system of claim 1 , further comprising:
an analyte detecting member coupled to a sample chamber, the analyte detecting member being configured to determine a concentration of an analyte in a body fluid using a sample that does not exceed a volume of 0.1 μL of a body fluid disposed in the sample chamber.
15. The system of claim 1 , wherein the penetrating member has a packing density of no more than 1.0 cm3/penetrating member.
16. The system of claim 1 , wherein the penetrating member has a packing density of no more than 0.75 cm3/penetrating member.
17. The system of claim 1 , wherein the the penetrating member has a packing density of no more than 0.5 cm3/penetrating member.
18. The system of claim 1 , wherein the penetrating member has a packing density of no more than 0.25 cm3/penetrating member.
19. The system of claim 1 , wherein the penetrating member has a packing density of no more than 0.1 cm3/penetrating member.
20. The system of claim 1 , wherein the penetrating member and an associated sample chamber have a combined packing density of no more than 1.0 cm3.
21. The system of claim 1 , wherein the penetrating member and an associated sample chamber have a combined packing density of no more than 0.75 cm3.
22. The system of claim 1 , wherein the penetrating member and an associated sample chamber have a combined packing density of no more than 0.5 cm3.
23. The system of claim 1 , wherein the penetrating member and an associated sample chamber have a combined packing density of no more than 0.25 cm3.
24. The system of claim 1 , wherein the penetrating member and an associated sample chamber have a combined packing density of no more than 0.1 cm3.
25. The system of claim 1 , wherein the tissue stabilizing member is configured to enhance fluid flow from a target tissue.
26. The system of claim 1 , wherein the tissue stabilizing member creates a stretching of a skin surface.
27. The system of claim 1 , wherein the tissue stabilizing member includes a plurality of protrusions.
28. The system of claim 1 , wherein the tissue stabilizing member applies a vacuum to a target tissue.
29. The system of claim 1 , wherein the tissue stabilizing member applies a stimulation to a target tissue.
30. The system of claim 1 , further comprising:
a seal formed by a fracturable material between the penetrating member and a cartridge, the seal being positioned at least one of a distal port or a proximal port of the cartridge.
31. The system of claim 30 , further comprising
a second fracturable seal located at least one of the distal port or proximal port of the cartridge.
32. The system of claim 1 , wherein the penetrating member is an elongate member without molded attachments.
33. The system of claim 1 , further comprising:
a penetrating member transport device for moving the penetrating member into a position aligned with the driver.
34. The system of claim 1 , further comprising,
a belt for holding the penetrating member in an array configuration.
35. The system of claim 1 , further comprising:
a tape device configured to hold the penetrating member in an array configuration.
36. The system of claim 1 , further comprising:
a support channel configured to hold the penetrating member in an array configuration.
37. The system of claim 1 , further comprising:
a cog configured to hold the penetrating member in an array configuration.
38. The system of claim 1 , further comprising:
a plurality of connectors between a plurality of penetrating members for holding the penetrating members in an array configuration.
39. The system of claim 1 , further comprising:
a support structure for receiving the penetrating member.
40. The system of claim 39 , wherein the support structure is a bandolier.
41. The system of claim 39 , wherein the support structure is a drum.
42. A body fluid sampling system for use on a tissue site, the system comprising:
an electrically powered drive force generator;
a penetrating member operatively coupled to said electrically powered drive force generator, said electrically powered drive force generator moving said penetrating member along a path out of a housing having a penetrating member exit, into said tissue site, stopping in said tissue site, and withdrawing out of said tissue site following a predetermined velocity vs. position profile;
a penetrating member sensor configured to monitor depth of penetration and velocity of the penetrating member;
a processor coupled to the electrically powered drive force generator with program instructions that provide an input to the electrically powered drive force generator to control depth of penetration and velocity of the penetrating member to match the predetermined velocity vs. position profile via a feedback loop of the depth of penetration and velocity of the penetrating member from the penetrating member sensor; and
a vacuum source associated with said system for creating a lower atmosphere environment to draw fluid from a wound created by said penetrating member.