Transcutaneous analyte sensor
US-9668682-B2 · Jun 6, 2017 · US
US12414713B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12414713-B2 |
| Application number | US-202418423162-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 25, 2024 |
| Priority date | Dec 5, 2017 |
| Publication date | Sep 16, 2025 |
| Grant date | Sep 16, 2025 |
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Medical devices configured for in vivo assays of one or more analytes can sometimes be problematic if left inserted in a tissue, such as skin, for an extended time. Certain medical device surface profiles may aid in alleviating this issue. Accordingly, medical devices may comprise a base surface having a tissue-facing surface profile defined thereon, and a sensor extending through the base surface and at least a portion of the tissue-facing surface profile. The tissue-facing surface profile deviates from the base surface, and the tissue-facing surface profile is also configured to undergo a change in shape, hardness, or a combination thereof after contacting a tissue for a length of time. A dynamic material may be present in at least a portion of the tissue-facing surface profile.
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What is claimed is the following: 1. A medical device for monitoring an analyte in a biological fluid, the medical device comprising: a sensor housing comprising: a core extending from a base surface of the sensor housing, wherein the core comprises a core material, and a protrusion disposed on a tip of the core and having a convex surface, wherein the protrusion comprises a dynamic material that is different than the core material; and an analyte sensor at least partially arranged within the sensor housing, wherein a portion of the analyte sensor extends through the base surface, the core, and the protrusion, wherein the portion of the analyte sensor is configured to be positioned under a skin surface of a user and in contact with the biological fluid, wherein the protrusion is configured to be placed against the skin surface of the user and comprises a surface profile that is symmetric about a centerline of the protrusion, wherein the analyte sensor extends along the centerline, and wherein the dynamic material degrades over a period of time in which the medical device is in use. 2. The medical device of claim 1 , wherein the protrusion is at least partially enclosed within a shell material. 3. The medical device of claim 1 , wherein the dynamic material comprises a material that is degradable by air, water, or light. 4. The medical device of claim 1 , wherein the dynamic material comprises one of cellulose, polyglycolides, or thermoplastic polymers. 5. The medical device of claim 1 , further comprising a drug substance or biologically active material disposed upon or within a tissue-facing surface profile of the sensor housing, the drug substance or biologically active material being releasable from the protrusion upon the protrusion undergoing degradation. 6. The medical device of claim 1 , wherein the analyte sensor is a dermal sensor. 7. The medical device of claim 1 , wherein the protrusion comprises a hemispherical shape. 8. The medical device of claim 1 , wherein the protrusion comprises a planar face, and wherein the analyte sensor extends through the planar face of the protrusion. 9. The medical device of claim 1 , wherein the protrusion is one of a plurality of protrusions of a tissue-facing surface profile of the sensor housing. 10. The medical device of claim 1 , wherein the dynamic material comprises a material that is thermally degradable above physiological temperatures. 11. The medical device of claim 10 , wherein the dynamic material degrades between 37° C. and 50° C., inclusive. 12. The medical device of claim 1 , wherein the analyte sensor is a glucose sensor. 13. The medical device of claim 1 , wherein at least a portion of the surface profile comprises an adhesive configured to promote adhesion to the skin surface. 14. A method, comprising: monitoring analyte levels in a bodily fluid by a medical device, wherein the medical device comprises: a base surface, a core extending from the base surface, wherein the core comprises a core material, a protrusion disposed on a tip of the core and having a convex surface, wherein the protrusion comprises a dynamic material different than the core material, and an analyte sensor extending through the base surface, the core, and the protrusion; positioning the base surface against a skin surface of a user; positioning a portion of the analyte sensor under the skin surface and in contact with the bodily fluid; and degrading the dynamic material over a period of time in which the medical device is in use. 15. The method of claim 14 , wherein monitoring analyte levels comprises monitoring glucose levels, and wherein the analyte sensor is a glucose sensor. 16. The method of claim 15 , wherein the analyte sensor is inserted at a depth below the skin surface, wherein degrading the dynamic material causes the depth at which the analyte sensor is arranged below the skin surface to increase. 17. A medical device for monitoring an analyte, the medical device comprising: a sensor housing comprising: a base surface, a core extending from the base surface, a protrusion disposed on a tip of the core and having a convex surface, wherein the protrusion comprises a dynamic material and comprises a surface profile that is symmetric about a centerline of the protrusion; and an analyte sensor at least partially arranged within the sensor housing, wherein a portion of the analyte sensor extends through the base surface and the protrusion, wherein the portion of the analyte sensor is configured to be positioned under a skin surface of a user and in contact with a biological fluid of the user, wherein the analyte sensor extends along the centerline and through a channel formed in the core and the protrusion, and wherein the dynamic material dissolves over a period of time in which the medical device is in use. 18. The medical device of claim 17 , wherein a rate of dissolution of the dynamic material changes when the dynamic material is exposed to an aqueous environment. 19. The medical device of claim 17 , wherein the dynamic material comprises at least one of organic salts, inorganic salts, compressed powder, dehydrated borates, and polyhydroxylated compounds. 20. The medical device of claim 17 , wherein the analyte sensor is a glucose sensor.
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