Low pain penetrating member

Patent metadata

Field	Value
Publication number	US-9144401-B2
Application number	US-30242305-A
Country	US
Kind code	B2
Filing date	Dec 12, 2005
Priority date	Jun 11, 2003
Publication date	Sep 29, 2015
Grant date	Sep 29, 2015

Abstract

Reducing the volume or drag on skin or sharpness of the penetrating member entering the wound during the cutting process will reduce the pain associated with lancing, and result in less power desired for retraction of the penetrating member from the skin. A variety of other penetrating member configuration as shown in the application.

First claim

What is claimed is:

1. A device comprising:
a housing;
a penetrating member for piercing tissue and positioned in the housing and configured to be advanced from the housing and retracted back into an interior of the housing, the penetrating member including a rod of a given diameter and geometry, and a piercing distal end with a primary facet and two side facets and a ratio of a primary facet length to a side facet length is less than 2.24:0.63, the penetrating member including a splined cross-section or dimples impressed across a contact area of the penetrating member, the primary facet having an angle cut that is different from angle cuts of the two side facets, the two side facets having the same angle cut;
a drive force generator configured to be coupled to the penetrating member for advancing the penetrating member along a path into a tissue site, create a penetration and a subsequent flow of a blood sample into a receiving channel of the housing; and
a processor with a memory for storage and retrieval of a set of penetrating member profiles utilized with the penetrating member driver, wherein each penetrating member profile from the set of penetrating member profiles includes the given diameter and geometry that correspond with upper and lower limits of attainable blood volume based on predetermined displacement and velocity profiles.

2. The device of claim 1 wherein the primary facet length of the penetrating member is less than about 1.0 mm.

3. The device of claim 1 wherein the primary facet length of the penetrating member is more than about 2.0 mm.

4. The device of claim 1 wherein the ratio of the primary facet length to the side facet length is less than 2:1, and wherein the primary facet length of the penetrating member is less than about 1.0 mm.

5. The device of claim 1 wherein the primary facet length of the penetrating member is more than about 1.60 mm.

6. The device of claim 1 wherein the primary facet length of the penetrating member is more than about 1.70 mm.

7. The device of claim 1 wherein the primary facet length of the penetrating member is more than about 1.80 mm.

8. The device of claim 1 wherein the primary facet length of the penetrating member is more than about 1.90 mm.

9. The device of claim 1 wherein the primary facet length of the penetrating member is more than about 2.00 mm.

10. The device of claim 1 wherein the primary facet length of the penetrating member is more than about 2.10 mm.

11. The device of claim 1 wherein the primary facet length of the penetrating member is more than about 2.20 mm.

12. The device of claim 1 wherein the penetrating member has a primary facet angle less than about 7.0 degrees.

13. The device of claim 1 wherein the penetrating member has a primary facet angle less than about 7.5 degrees.

14. The device of claim 1 wherein the penetrating member has a bevel joint length less than about 0.24 mm.

15. The device of claim 1 wherein the penetrating member has a bevel joint angle less than about 16 degrees.

16. The device of claim 1 wherein the penetrating member has a bevel joint angle less than about 15.5 degrees.

17. The device of claim 1 wherein the penetrating member has a cutting efficiency sufficient to bring at least 1 micro liter of blood to a skin surface after penetrating about 600 to 800 microns into the skin.

18. The device of claim 1 wherein the penetrating member has a cutting efficiency sufficient to bring at least 1 micro liter of blood to a skin surface after penetrating about 0.5 to 1.0 mm into the skin.

19. The device of claim 1 wherein the penetrating member comprises a shaft having a bar stock with a half-round cross section to reduce volume of the penetrating member.

20. The device of claim 1 wherein a portion of the penetrating member has a first cross-sectional volume and a second cross-sectional volume greater than the first for mechanical coupling with a driver to drive the penetrating member.

21. The device of claim 1 wherein a front end portion of the penetrating member has a smashed end configuration to reduce volume of the penetrating member inside the tissue.

Assignees

• Freeman Dominique M
• Alden Don
• Wittig Michael
• Boecker Dirk
• Sanofi Aventis Deutschland

Inventors

• Freeman Dominique M
• Alden Don
• Wittig Michael
• Boecker Dirk

Classifications

• A61B5/15161

  Characterized by propelling the piercing element in a radial direction relative to the disc · CPC title

• A61B5/15151

  Each piercing element being stocked in a separate isolated compartment · CPC title

• A61B5/15123

  comprising magnets or solenoids · CPC title

• A61B5/150511

  Details of construction of shaft · CPC title

• A61B5/150427

  Specific tip design, e.g. for improved penetration characteristics · CPC title