Single procedure indicators
Disclosed herein are single use indicators and methods for employing the same. Such indicators and their uses are directed towards identifying the discharge status of single procedure devices, which are typically, but not limited to, medical devices.
1. A single procedure device indicator, comprising:
(a) a biocompatible composition comprising a superabsorbent polymer matrix, one or more binders, and one or more additives that are present in the biocompatible composition at predefined ratios by weight percentage in a mixture; and
(b) a surgical device at least partially enveloped by the biocompatible composition thereby forming at least one indicator region on the surgical device;
wherein the at least one indicator region is configured to elicit a volumetric and morphological modification in response to an exposure to water after a medical procedure; and
wherein the at least one indicator region is positioned on the surgical device to not come into contact with bodily fluids of a patient during the medical procedure.
2. The device indicator of claim 1 , wherein the surgical device comprises a proximal end and a distal end, wherein the distal end has a functional region which contacts a patient and wherein the at least one indicator region is located at or about the proximal end of the surgical device.
3. The device indicator of claim 1 , wherein the superabsorbent polymer matrix is a hydrogel polymer possessing swelling capacity range of about 30-500 fold the volume of the superabsorbent polymer matrix prior to being subjected to an exposure.
4. The device indicator of claim 3 , wherein the hydrogel polymer is selected from the group consisting of polyacrylates, polyacrylamides, polyacrylamide copolymers, polyacrylic acid, sodium polyacrylate, potassium polyacrylate, lithium polyacrylate, ammonium polyacrylate, ethylene maleic anhydride copolymer, carboxymethyl cellulose, polyvinyl alcohol copolymers, polyethylene oxide, and copolymers of polyacrylonitrile, and combinations thereof.
5. The device indicator of claim 1 , wherein the one or more binders are selected from the group consisting of alkyds, acrylics, vinyl-acrylics, polyurethanes, polyesters, melamine, epoxies, silanes, siloxanes, and oils, and combinations thereof.
6. The device indicator of claim 1 , wherein the mixture further comprises a solvent selected from the group consisting of xylene, toluene, alcohols, and ketones, and combinations thereof.
7. The device indicator of claim 1 , wherein the one or more additives are selected from the group consisting of clays, kaolin, limestone, silicate compounds, and quartz, and combinations thereof.
8. The device indicator of claim 1 , wherein the at least one indicator region is composed of the biocompatible composition present as a surface layer on the surgical device, wherein the thickness of the surface layer is about 100 μm to 3 mm.
9. A single procedure device indicator, comprising:
at least one indicator region,
the at least one indicator region disposed on a single-use surgical device, wherein the single-use surgical device is configured to be used in a single medical procedure;
the at least one indicator region configured to transition from an unmodified state to a modified state in response to an exposure after the single medical procedure;
the at least one indicator region comprises a biocompatible composition including one or more superabsorbent polymers possessing a swelling capacity range of about 30 - 500 fold the volume of the one or more superabsorbent polymers prior to being subject to the exposure;
wherein, when the at least one indicator region transitions from the unmodified state to the modified state in response to the exposure after the single medical procedure, the at least one indicator region irreversibly identifies that the single-use surgical device has been subjected to the exposure by swelling of the one or more superabsorbent polymers; and
wherein the at least one indicator region is positioned on the single-use surgical device to not come into contact with bodily fluids of a patient during the single medical procedure.
10. The device indicator of claim 9 , wherein the biocompatible composition further comprises one or more binders and/or one or more additives.
11. The device indicator of claim 10 , wherein the one or more binders are selected from the group consisting of alkyds, acrylics, vinyl-acrylics, polyurethanes, polyesters, melamine, epoxies, silanes, siloxanes, and oils, and combinations thereof.
12. The device indicator of claim 10 , wherein the one or more additives are selected from the group consisting of clays, kaolin, limestone, silicate compounds, and quartz, and combinations thereof.
13. The device indicator of claim 10 , wherein the one or more superabsorbent polymers is a matrix of a mixture including the one or more binders and the one or more additives, which are present in the biocompatible composition at predefined ratios by weight percentage in the mixture.
14. The device indicator of claim 13 , wherein the mixture further comprises a solvent selected from the group consisting of xylene, toluene, alcohols, and ketones, and combinations thereof.
15. The device indicator of claim 9 , wherein the surgical device comprises a proximal end and a distal end, wherein the distal end has a functional region which contacts a patient and wherein the at least one indicator region is located at or about the proximal end of the surgical device.
16. The device indicator of claim 9 , wherein the one or more superabsorbent polymers is a hydrogel polymer.
17. The device indicator of claim 16 , wherein the hydrogel polymer is selected from the group consisting of polyacrylates, polyacrylamides, polyacrylamide copolymers, polyacrylic acid, sodium polyacrylate, potassium polyacrylate, lithium polyacrylate, ammonium polyacrylate, ethylene maleic anhydride copolymer, carboxymethyl cellulose, polyvinyl alcohol copolymers, polyethylene oxide, and copolymers of polyacrylonitrile, and combinations thereof.
18. The device indicator of claim 9 , wherein the at least one indicator region is composed of the biocompatible composition present as a surface layer on the surgical device, wherein the thickness of the surface layer is about 100 μm to 3 mm.