METHODS OF STERILIZING A HYDROPHILICALLY COATED MEDICAL DEVICE

Abstract

Method for sterilizing a hydrophilically coated medical device.

Claims

1. A method of sterilizing a medical device having a hydrophilic surface, comprising: applying a protective coating over a hydrophilic surface of a medical device; placing the medical device in a hydration environment; and exposing the medical device to sterilizing radiation.

2. The method of claim 1 wherein the hydrophilic surface comprises a hydrophilic coating disposed on the medical device.

3. The method of claim 2 wherein the hydrophilic coating comprises a crosslinked hydrophilic polymer.

4. The method of claim 1 wherein the protective coating comprises a polyol.

5. The method of claim 4 wherein the polyol comprises a carbon chain including between 3 and 24 carbon atoms.

6. The method of claim 1 wherein the protective coating comprises one or more of glycerol, propylene glycol and tetraethylene glycol.

7. The method of claim 1 wherein the hydrophilic surface comprises polyvinylpyrrolidone.

8. The method of claim 1 wherein the sterilizing radiation comprises E-beam or gamma radiation.

9. The method of claim 1 wherein the placing the medial device within a hydration environment comprises placing the catheter in a package containing a hydration fluid.

10. The method of claim 8 wherein the package is sealed prior to exposing the medical device to sterilizing radiation.

11. The method of claim 1 wherein the medical device is a urinary catheter.

12. A method of making a ready to use hydrophilically coated medical device assembly, comprising: applying a protective coating over a hydrophilic coating of a medical device; placing the medical device into a package along with liquid water; sealing the package; and exposing the medical device assembly to sterilizing radiation.

13. The method of claim 12 further including delaying the distribution of the medical device assembly for a time period sufficient to allow hydration of the hydrophilic coating to occur.

14. The method of claim 12 wherein the liquid water is in direct liquid contact with the medical device.

15. The method of claim 12 wherein the liquid water produces a water vapor that hydrates the medical device.

16. The method of claim 15 wherein the liquid water is separated from the medical device.

17. The method of claim 12 wherein the protective coating comprises a polyol.

18. The method of claim 12 wherein the polyol comprises one or more of glycerol, propylene glycol and tetraethylene glycol.

19. (canceled)

20. The method of claim 12 wherein the medical device is a urinary catheter.

21. A hydrophilically coated medical assembly, comprising: a package containing: a medical device having a hydrophilic coating thereon and a protective coating over the hydrophilic coating; and an amount of water.

22.-28. (canceled)

Description

DESCRIPTION

[0010] The embodiments disclosed herein are for the purpose of providing a description of the present subject matter, and it is understood that the subject matter may be embodied in various other forms and combinations not shown in detail. Therefore, specific embodiments and features disclosed herein are not to be interpreted as limiting the subject matter as defined in the accompanying claims.

[0011] The present disclosure relates to methods for sterilizing medical devices having a hydrophilic surface, such as a medical device having a hydrophilic coating on a surface of the medical device. Such methods may include applying a protective coating over the hydrophilic surface of the medical device, placing the medical device into a hydration environment, and then exposing the medical device to a sufficient amount of sterilization radiation, such as gamma or E-Beam radiation. The hydration environment may be an environment wherein the medical device is in direct contact with liquid water and/or wherein the medical device is exposed to water vapor.

[0012] The protective coating may temporarily prevent the hydrophilic surface from being hydrated for a desired period of time or temporarily limit the level of hydration for a desired period of time. In other words, the protective coating may temporarily prevent or limit liquid water and/or water vapor from coming into contact with and being absorbed into the hydrophilic material. In one embodiment, the protective coating limits/prevents hydration of a hydrophilic surface for a time period sufficient to allow the medical device to be radiation sterilized prior to hydration of the hydrophilic material. It is understood, without being held to any particular theory, that the protective coating coats the surface of the hydrophilic material and is absorbed into the interstices of the hydrophilic material's polymer matrix, thereby repelling the absorption of water into the hydrophilic coating, i.e., preventing or limiting the amount of liquid or vapor water from entering the hydrophilic polymer matrix. This causes a delay in the hydration of the hydrophilic material for a desired period of time, during which the medical device is exposed to sterilizing radiation. Eventually, liquid water or water vapor permeates through/past the protective coating and/or displaces at least some of the protective coating, thereby hydrating the hydrophilic material so that it is in a ready-to-use condition for the end user.

[0013] In one embodiment, the protective coating is a liquid that has a viscosity between about 30 cP to about 60 cP at 25 C. The protective coating may be applied in any suitable manner, such as by dip coating, spraying or painting. The amount or level of coating can vary depending on the viscosity of the protective coating, the dwell time, dip time or amount of protective coating applied by spraying or painting. The protective coating may include, for example, one or more polyols. Such polyols may include, but are not limited to, 3-carbon sugar alcohols (Glycerol); 4-carbon sugar alcohols (Erythritol, Threitol); 5-carbon sugar alcohols (Arabitol, Xylitol, Adonitol), 6-carbon sugar alcohols (Mannitol, Sorbitol, Galactitol, Fucitol, Iditol, Inositol), 7-carbon sugar alcohols (Volemitol), 12-carbon sugar alcohols (Isomalt, Maltitol, Lactitol), 18-carbon sugar alcohols (Maltotriitol), and 24-carbon sugar alcohols (Maltotetraitol), propylene glycol, tetraethylene glycol.

[0014] When the hydrophilic surface of the medical device is a hydrophilic coating, the hydrophilic coating may include a hydrophilic polymer, among other components, including but not limited to antioxidants, polyelectrolytes, plasticizers and the like. The hydrophilic polymer may be, for example, polyvinylpyrrolidone (PVP), polyethylene oxide, methyl cellulose, ethyl cellulose, polyethylene glycol, hydroxyl methylcellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, carboxymethyl cellulose, polyvinyl alcohol, or mixtures thereof. Furthermore, when formed on the medical device, the hydrophilic coating may be a crosslinked hydrophilic coating.

[0015] In one method of forming a sterilized ready-to-use hydrophilically coated medical device assembly, a protective coating is applied over the hydrophilic surface, such as a hydrophilic coating, of the medical device by, for example, dipping the medical device into the protective coating. In one embodiment, the hydrophilic coating may be a crosslinked hydrophilic coating that was applied to the medical device in any suitable manner. In one embodiment, a hydrophilically coated urinary catheter may be dip coated with a polyol, such as glycerol. The hydrophilically coated medical device is then placed within a hydration environment. For example, the medical device may be placed into a package along with liquid water and the package may then be sealed. In one embodiment, after the catheter is coated with a polyol, the catheter may be positioned in a sleeve that contains water and the sleeve may be the package or the sleeve may be placed in an outer package. The sleeve may be, for example, a no-touch sleeve wherein the user uses the sleeve to insert the catheter. The liquid water may be in direct contact with the medical device and/or the liquid water may produce a water vapor that is in contact with the medical device. The package may be made from a material that is liquid and gas impermeable. Furthermore, in one embodiment wherein the liquid water produces a water vapor for hydrating the hydrophilic coating, the liquid water is kept separated from the medical device. For instance, the liquid water may be retained by a liquid sequestering element, such as an absorbent member that holds the water or a compartment that is at least partially made from a liquid impermeable, gas permeable material.

[0016] After the medical device is placed in the hydration environment, the medical device is exposed to sterilization radiation. For example, after the medical device is placed in the package along with liquid water and the package is sealed, the package is exposed to sterilizing radiation, such as E-beam or gamma radiation. The distribution of the package may then be delayed for a time sufficient for the hydration environment to hydrate the hydrophilic coating, i.e., sufficient amount of time to allow the liquid and/or vapor water to permeate through the protective coating to hydrate the device. In one embodiment, the packages may be stored for a period of time after radiation and then distributed.

[0017] As can be seen from the above description, the present disclosure has several different aspects, which are not limited to the specific aspects and which do not necessarily need to be used together. Variations of these concepts or structures may be embodied in other structures without departing from the present invention as set forth in the appended claims.