Needle cannula-catheter bonding method and apparatus
A cannula-catheter bonding method and apparatus can include a needle having a specifically configured connector end to reduce the risk of the connector end disengaging with an adapter (e.g., a catheter, a cannula, or a connector of a Huber needle assembly, etc.). The specifically configured needle connector end can be a formation, such as a barb, a bead, an annular structure, a rib, etc. The formation can be formed on the connector end, and may be elongated with a conical shaped nose leading to a base with a bottom. The formation can be used to prevent movement of the needle relative to the adapter. A method for producing the formation can include forming a mold for the formation in a plate, where the connector end can then be placed within the mold so that curable material can be disposed within the mold. Upon hardening of the curable material, the formation can take the shape of at least a portion of the mold.
1. An assembly, comprising:
a needle comprising a needle connector end, a needle tip, a needle shaft extending between the needle connector end and the needle tip, and an aperture extending through the needle from the needle tip to the needle connector end;
at least one formation formed from a first curable material deposited and cured on at least a portion of the needle connector end; and,
an adapter having a lumen,
wherein the needle connector end and the at least one formation are accommodated within the adapter lumen;
wherein the adapter is bonded to at least one of the needle connector end and the at least one formation by a second curable material disposed on at least a portion of at least one of the needle connector end and the at least one formation;
wherein the bond prevents movement of the needle relative to the adapter in at least a forward longitudinal direction; and
wherein the at least one formation prevents disengagement of the adapter from the needle connector end when fluid is introduced through the adapter lumen into the needle aperture.
2. The assembly of claim 1 , wherein the formation prevents disengagement of the adapter from the needle connector end when fluid is introduced through the adapter lumen into the needle aperture at a pressure of at least 400 psi.
3. The assembly of claim 1 , wherein the formation prevents disengagement of the adapter from the needle connector end when fluid is introduced through the adapter lumen into the needle aperture at a pressure ranging from 400 psi to 600 psi.
4. The assembly of claim 1 , wherein the first curable material and the second curable material are the same.
5. The assembly of claim 1 , wherein the first curable material and the second curable material are different.
6. The assembly of claim 1 , wherein the adapter is at least one of a catheter, a cannula, a tubing, and a connector of a Huber needle assembly.
7. The assembly of claim 1 , wherein the at least one formation has an elongated shape with a conical shaped nose portion leading to a base portion.
8. The assembly of claim 7 , wherein the at least one formation is a single formation disposed around an entire circumference of an outer surface of a portion of the needle connector end.
9. The assembly of claim 7 , wherein the second curable material is disposed at a bottom of the base portion.
10. The assembly of claim 1 , wherein each of the first curable material and the second curable material is a thermosetting polymer, or resin that hardens and/or adheres upon exposure to electromagnetic radiation.
11. The assembly of claim 10 , wherein the electromagnetic radiation is UV radiation.
12. The assembly of claim 10 , wherein the first curable material and the second curable material are each selected from the group consisting of polyester, polyurethane, epoxy resin, polyimides, and acrylic adhesives.
13. The assembly of claim 12 , wherein the first curable material and the second curable material are each an acrylic adhesive.