IP Library Patent Application 19000073
Patent Application
App. No. 19/000,073

INSULIN INFUSION SET

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Quick Facts
Patent No.
US None
App. No.
19/000,073
Abstract

Embodiments of devices and methods to maintain preservative concentration in a medication delivered using a medical device are provided. A barrier layer can be used to prevent migration of preservatives. A vent can be used to allow release of preservatives prior to delivery to the patient. An absorbent element can be used to maintain preservative concentration at a desired level. A filter can be used to capture particulates from the medication prior to delivery to a patient.

Claims (25)

1 . An insulin delivery system comprising:

a reservoir configured to hold an insulin medication therein;

an infusion hub;

tubing fluidically connecting the insulin reservoir and the infusion hub;

a cannula configured to deliver the insulin medication to a patient; and

an absorbent element positioned within the delivery system and in fluidic contact with the insulin medication, the absorbent element configured to absorb and store preservatives from the insulin medication.

2 . The insulin delivery system of claim 1 , further comprising an impermeable backing layer adjacent to the absorbent element and configured to maintain the preservatives within the absorbent.

3 . The insulin delivery system of claim 1 , wherein the absorbent element comprises EVOH, silicone, a low-density polymer, a PEG block-copolymer (e.g., PETG), PET, nylon, a nylon block-copolymer, a polymeric foam, or a polymeric monolith.

4 . The insulin delivery system of claim 1 , wherein the absorbent element comprises a preservative capacity greater than a maximum concentration of preservative in the insulin medication.

5 . The insulin delivery system of claim 1 , wherein the absorbent element is further configured to release preservatives to the insulin medication after storing the preservatives.

6 . The insulin delivery system of claim 1 , wherein the absorbent element is configured to maintain the preservative concentration at a point of delivery to the patient at a concentration that minimizes local toxicity while maintaining insulin in a stable hexameric state.

7 . The insulin delivery system of claim 6 , wherein the absorbent element is configured to maintain the preservative concentration at a concentration of greater than about 1.25 mg/mL.

8 . The insulin delivery system of claim 6 , wherein the absorbent element is configured to maintain the preservative concentration at a concentration of about 1.15-1.75 mg/mL.

9 . The insulin delivery system of claim 6 , wherein the absorbent element is configured to maintain the preservative concentration at a concentration of about 1.25-1.50 mg/mL.

10 . The insulin delivery system of claim 1 , wherein the absorbent element comprises an interior layer of the tubing.

11 . The insulin delivery system of claim 1 , wherein at least a portion of the insulin delivery system includes a barrier layer configured to prevent migration of preservatives from the insulin medication.

12 . The insulin delivery system of claim 11 , wherein the tubing is a multi-layer tubing, and wherein the barrier layer is at least a portion of a layer of the multi-layer tubing.

13 . The insulin delivery system of claim 11 , wherein the tubing is a multi-layer tubing, and wherein the barrier layer forms an entire layer of the multi-layer tubing.

14 . The insulin delivery system of claim 11 , wherein the tubing comprises the barrier layer.

15 . The insulin delivery system of claim 11 , wherein the barrier layer comprises a coating on the tubing.

16 . The insulin delivery system of claim 11 , wherein the barrier layer comprises an inner layer of the tubing.

17 . The insulin delivery system of claim 11 , wherein the barrier layer comprises polyether block-amide, HDPE, polypropylene, PTFE, chloro- and fluorosilicones, hydrochloro-, hydrofluoro-, and perfluoro-polymers, chlorinated polymers (e.g. viton), metal-coated polymers (e.g., mylar), poly carbonate, organic or inorganic plasma-deposited coatings (e.g. PTFE, PVC, halogenated siloxanes, silicon suboxides), vapor-deposited coatings (such as nitrides, titanium nitride, fluorocarbons, metals), Kapton, or parylene.

18 . The insulin delivery system of claim 11 , further comprising a barrel connected to the cannula, and wherein the barrier layer is positioned on at least a portion of the barrel.

19 . The insulin delivery system of claim 11 , comprising a connector comprising the barrier layer.

20 . The insulin delivery system of claim 11 , wherein the barrier layer extends through an entire fluid path of the system.