HYDROPHILIC COATINGS FOR MEDICAL DEVICES

Abstract

Lubricious hydrophilic coatings and methods of making the same.

Claims

1. A lubricious hydrophilic coating with a hydration indicator, comprising: a hydrophilic coating that becomes lubricious when hydrated with an amount of hydration fluid; and the hydrophilic coating having a first visual appearance when in a non-hydrated state and transitioning to a second visual appearance when in a hydrated state.

2. The lubricious hydrophilic coating of claim 1, wherein the transition from the first visual appearance to the second visual appearance is a gradual transition that depends on the amount of hydration fluid absorbed into the hydrophilic coating.

3. The lubricious hydrophilic coating of claim 1, wherein the transparency of the coating varies between the first visual appearance and the second visual appearance.

4. The lubricious hydrophilic coating of claim 3, wherein the first visual appearance is transparent and the second visual appearance is opaque or translucent.

5. The lubricious hydrophilic coating of claim 1, wherein the color of the coating varies between the first visual appearance and the second visual appearance.

6. The lubricious hydrophilic coating of claim 5, wherein the first visual appearance is a first color and the second visual appearance is a second color that is different from the first color.

7. The lubricious hydrophilic coating of claim 1, wherein the hydrophilic coating includes a hydrochromism agent.

8. The lubricious hydrophilic coating of claim 1, wherein the hydrochromism agent comprises a non-polar liquid.

9. The lubricious hydrophilic coating of claim 8, wherein the non-polar liquid comprises oil or an oil-like substance.

10. The lubricious hydrophilic coating of claim 7, wherein the hydrochromism agent comprises tocopherol.

11. The lubricious hydrophilic coating of claim 7, wherein the hydrochromism agent is an amount between about 0.02 grams and 0.15 grams.

12. The lubricious hydrophilic coating of claim 7, wherein the hydrochromism agent is in an amount between about 3.5 weight percent and about 80 weight percent of the hydrophilic coating.

13. A medical device, including: a hydrophilic coating disposed on a surface of the medical device, wherein the hydrophilic coating includes a non-polar liquid in an amount between about 0.35 weight percent and about 80 weight percent.

14. The medical device of claim 13, wherein the non-polar liquid comprises oil or an oil-like substance.

15. The medical device of claim 13, wherein the non-polar liquid comprises tocopherol.

16. The medical device of claim 13, wherein the non-polar liquid is an amount of about 0.02 grams and 0.15 grams.

17. The medical device of claim 13, wherein the non-polar liquid comprises an essential oil.

18. The medical device of claim 17, wherein the essential oil comprises menthol, carvacrol, thymol or combinations thereof.

19. The medical device of claim 13, wherein the non-polar liquid provides an antimicrobial effect.

20.-22. (canceled)

23. A method of making a medical device having a hydrophilic coating, comprising: applying a solution of a non-polar liquid and an alcohol to a hydrophilic coating wherein the hydrophilic coating is disposed on the surface of the medical device, and wherein the non-polar liquid is between about 0.1 weight percent to about 20 weight percent of the solution.

24.-33. (canceled)

Description

BRIEF DESCRIPTION OF THE FIGURES

[0009] FIG. 1 is a picture of a hydrophilic catheter that includes a hydrophilic coating in a dry state, the hydrophilic coating will change in visual appearance when hydrated; and

[0010] FIG. 2 is a picture of the hydrophilic catheter of FIG. 1 shown with the hydrophilic coating in a hydrated state and wherein the visual appearance of the coating has become more opaque or translucent as compared to the coatings visual appearance in FIG. 1.

DETAILED DESCRIPTION

[0011] The present disclosure relates to lubricious hydrophilic coatings and devices having such coatings thereon. The hydrophilic coatings may be disposed on the surfaces of medical devices. Such medical devices may include shafts or tubes that may be inserted into and advanced within a lumen of a body, such as a urethra, esophagus, or fallopian tube. Such medical devices include urinary catheters, endovascular catheters, endoscopes, exploratory and biopsy devices, etc. While some of the embodiments set forth below may be described in the context of urinary catheters, the disclosure is not limited to such and the features disclosed herein may be applicable to any medical tubing that is inserted into a body lumen.

[0012] The hydrophilic coating on the surface of the medical device, such as a urinary catheter, may be any suitable hydrophilic coatings. For example, the hydrophilic coating may be formed from any suitable hydrophilic polymer. Such hydrophilic polymers may include but are not limited to polyvinylpyrrolidone (PVP), polyethylene oxide, polyurethanes, hyaluronic acid, homo- and copolymers of acrylic and methacrylic acid, polyvinyl alcohol, polyvinyl ethers, maleic anhydride based copolymers, polyesters, vinyl amines, polyethylenimines, poly(carboxylic acids), polyamides, polyanhydrides, polyphosphazenes, cellulosics, for example methyl cellulose, carboxymethyl cellulose, hydroxymethyl cellulose, and hydroxypropyl cellulose, other polysaccharides.

[0013] The hydrophilic coating may also include or be infused with a non-polar liquid, such as a hydrophobic liquid. The non-polar liquid may be an oil or oil-like substance. The oil or oil-like substance may be synthesized oil, a plant or a vegetable oil, or it may be derived from a plant or a vegetable oil. In one embodiment, the non-polar liquid is a tocopherol. The non-polar liquid also may be an essential oil, including but not limited to menthol, carvacrol, thymol, etc. and mixtures thereof, or a mixture of an essential oil with tocopherol. The non-polar liquid may provide any number of characteristics to the hydrophilic coating including but not limited to inducing chromism, antimicrobial effects, fragrances, providing lubricity (including providing supplemental and/or enhanced lubricity), and/or increasing dry-out times. The amount of non-polar liquid incorporated into the hydrophilic coating may vary depending on the application. For example, if a non-polar liquid, such as an essential oil, is incorporated into the coating to provide a pleasant fragrance, the non-polar liquid may be in an amount that is greater than about 0.35 weight percent of the coating. In other embodiments wherein the non-polar liquid provides other characteristics, the amount of non-polar liquid may be greater than about 3.5 weight percent or greater than about 5.0 weight percent. The non-polar liquid may be between about 3.5 weight percent and about 80 weight percent of the hydrophilic coating.

[0014] In one embodiment, the non-polar liquid may induce chromism wherein the hydrophilic coating changes in visual appearance depending on its environment. For example, the non-polar liquid may produce hydrochromic, thermochromic, photochromic, and/or solvatochromic responses. In one embodiment, the hydrophilic coating having a non-polar liquid may be hydrochromic in that the coating will change in visual appearance in response to being hydrated. In one embodiment, the hydrophilic coating may be transparent in the dry state and may be opaque or translucent in a hydrated state. For example, a hydrophilic coating may include between 3.5 weight percent and 80 weight percent of a non-polar liquid, such as a tocopherol, which may be alpha-tocopherol. As shown in FIG. 1, the dry hydrophilic coating of the catheter may have a transparent or colorless visual appearance. As shown in FIG. 2, when hydrated, the visual appearance of the hydrophilic coating changes to a more opaque or white appearance. Furthermore, the level of opaqueness may depend on the hydration amount of the hydrophilic coating and the change in appearance may take place gradually. Also, the change of the visual appearance may be reversible in that the visual appearance of the hydrophilic coating may change back upon drying.

[0015] One of the issues of incorporating a non-polar liquid into a hydrophilic material or coating is that the non-polar substances and hydrophilic material of the coating, in general, do not mix well. Because the substances do not mix well, it has been difficult to incorporate non-polar substances into hydrophilic coatings. When the hydrophilic coating formulations include water, it can be very difficult to incorporate an effective amount of oil into the coating. The hydrophilic coatings of the present disclosure include about 0.35 weight percent to about 80 weight percent non-polar liquid of the hydrophilic coating. In another embodiment, the non-polar liquid may be in an amount greater than about 3.5 weight percent or greater than about 5.0 weight percent. In one embodiment, a urinary catheter having a hydrophilic coating may include between about 0.02 grams and 0.15 grams of a non-polar liquid, such as a tocopherol.

[0016] One embodiment of making a medical device having a hydrophilic coating includes infusing a non-polar liquid into the coating. The method may include applying a solution of a non-polar liquid and an alcohol to the hydrophilic coating of the medical device. The non-polar liquid of the solution may be in amount between about 1 weight percent to about 20 weight percent of the solution. For example, the non-polar liquid may be in an amount of about 5 weight percent, 10 weight percent or 20 weight percent. The solution may be applied to the hydrophilic coating by dipping (immersion), spraying, bushing or any other means. The application or infusion period may be any suitable period. For example, when applied by dipping, the application or infusion period may be seconds or tens of seconds. After the solution is applied and infused into the coating, the alcohol is then evaporated or dried off from the coating, and optionally, the hydrophilic coating may be washed. The drying may take place under ambient conditions or may take place in an oven.

[0017] In one embodiment, a urinary catheter having a hydrophilic coating is dipped (immersed) into a solution of tocopherol and ethanol. The tocopherol may be alpha-tocopherol, and the tocopherol may be in an amount of between about 0.1 weight percent and about 20 weight percent of the solution. After the solution has been infused into the coating, the ethanol is then dried off from the hydrophilic coating and, optionally, the hydrophilic coating may be washed with water. The resulting hydrophilic catheter may include a hydrophilic coating that includes about 0.35 weight percent to about 80 weight percent of the infused non-polar liquid. In one embodiment, the hydrophilic coating may include between about 0.02 grams and 0.15 grams of a non-polar liquid, such as a tocopherol.

EXAMPLES

Example I

[0018] Samples of hydrophilically coated intermittent urinary catheters (sized 14 CH) were immersed in a 100% ethanol or alpha-tocopherol/ethanol solutions of varying concentrations of alpha tocopherol. The hydrophilic coatings of the catheters were formed from polyvinylpyrrolidone. Each of the samples was immersed in one of the solutions for a period of 10 to 60 seconds. The coating infused with the solution was washed by quickly dipping the catheter into a vessel containing pure ethanol to remove traces of infused alpha-tocopherol that may reside on the coatings surface. The treated catheters were then placed on mandrels to dry under gentle airflow at ambient temperature to remove the ethanol.

[0019] After ethanol removal, the catheters were immersed in water for four minutes to hydrate the hydrophilic coating. Initial coefficient of friction (CoF), abraded CoF and ten minute dry-out CoF were measured for each of the samples. The CoFs were measured using a Harland Friction Tester Model FTS6000. During the CoF measurement, the proximal end portion of the catheter is cut (40 mm from the tip end of the catheter) and a mandrel was inserted into the remaining section of the coated catheter tube. The tube was then clamped between two pieces of silicone rubber at 100 g applied load wherein the silicone rubber had a Shore hardness of 60 A. The clamp force being 200 g (two times the 100 g applied load). The tube with the mandrel inserted therein was pulled through the two pieces of silicone rubber at a speed of 10 mm/s. The force required to pull about 80 mm of the tube through the two pieces of silicone rubber was measured and recorded using a universal tensile tester equipped with a 200 N load cell. The CoF value was calculated from the ratio of recorded to applied loads (i.e., the recorded load divided by 2 times the applied load or 200 g) when steady state was reached.

[00001]$CoF=\frac{\mathrm{Average}\mathrm{State}\mathrm{Stage}\mathrm{Force}\mathrm{Recorded}\mathrm{load}}{\mathrm{Clamp}\mathrm{Force}}$

[0020] The initial CoF was measured immediately after the hydrophilic coating was hydrated. For the abraded CoF measurements, the hydrated catheters were placed in a water bath and abraded 50 times by passing the catheter tubes back and forth 25 times through 4.14 mm diameter hole in a 1 mm thick silicone pad with Shore hardness of 60 A. The abrading took place while the catheter was immersed in the water bath. This test is designed to remove any portions of the coating that are not well adhered to the catheter. After abrading, the CoF of the abraded catheters were measured in the above-described manner.

[0021] The CoF was also measured after a time minute dry out. For the dry-out CoF measurement, after the hydrophilic coating of the catheter was hydrated, it was placed in a controlled atmosphere with a constant relative humidity of 50% RH and a constant temperature of 23° C. for 10 minutes prior to measuring the CoF.

[0022] The CoF of the samples are listed below in Table 1.

TABLE-US-00001 TABLE 1 Concentration (% w/v) A-Tocopherol CoF CoF CoF 10 min in Ethanol Initial Abraded Dry Out 0 0.013 0.009 0.016 0 0.013 0.012 0.018 0 0.013 0.008 0.016 0 0.014 0.009 0.019 0 0.013 0.008 0.014 0 0.010 0.008 0.017 1 0.013 0.008 0.019 1 0.013 0.011 0.017 1 0.014 0.007 0.022 1 0.017 0.011 0.018 1 0.017 0.008 0.021 1 0.016 0.010 0.022 5 0.025 0.014 0.024 5 0.022 0.013 0.031 5 0.017 0.011 0.025 5 0.043 0.012 0.059 5 0.018 0.010 0.024 5 0.018 0.011 0.024

[0023] The mean for CoF for the above samples is listed in Table 2.

TABLE-US-00002 TABLE 2 Concentration (% w/v) Mean Mean Mean CoF A-Tocopherol CoF CoF 10 min in Ethanol Initial Abraded Dry Out 0% 0.012 0.009 0.017 1% 0.015 0.009 0.020 5% 0.024 0.012 0.031

Example II

[0024] In this Example, samples of hydrophilically coated intermittent urinary catheters (sized 14 CH/40 cm) were immersed in a 100% ethanol or alpha-tocopherol/ethanol solutions of varying concentrations of alpha-tocopherol. The hydrophilic coatings of the catheters were formed from polyvinylpyrrolidone. Each of the samples was immersed in one of the solutions for a period of 60 seconds. The treated catheters were then placed on mandrels to dry under gentle airflow at ambient temperature to remove the ethanol. After ethanol removal, the weight of each catheter was then measured and recorded. The catheter was then immersed in water for four minutes to hydrate the hydrophilic coating. The catheter was then weighed and the difference in weight between the dry catheter and hydrated catheter was calculated to determine the amount of water retained in the hydrated catheter. Table 3 shows the results.

TABLE-US-00003 TABLE 3 Concentration (% w/v) A- Weight (g) Weight (g) Water Tocopherol in Hydrated Dried Capacity Ethanol Catheter Catheter (g) 0 3.90 3.33 0.58 0 3.95 3.37 0.59 0 3.92 3.36 0.56 0 4.02 3.35 0.67 0 3.92 3.35 0.57 0 3.94 3.31 0.63 1 3.88 3.39 0.50 1 4.00 3.42 0.58 1 4.02 3.43 0.60 1 3.93 3.37 0.55 1 3.97 3.35 0.62 1 4.03 3.41 0.62 5 3.81 3.36 0.45 5 3.80 3.38 0.42 5 3.77 3.34 0.43 5 3.80 3.36 0.44 5 3.85 3.35 0.50 5 3.76 3.38 0.38

[0025] The mean amount of water retained for the above samples is listed in Table 4.

TABLE-US-00004 TABLE 4 Concentration (% w/v) A- Tocopherol in Mean Water Ethanol Capacity (g) 0% A-T 0.60 1% A-T 0.58 5% A-T 0.43

Example III

[0026] In this Example, samples of hydrophilically coated intermittent urinary catheters (sized 14 CH/40 cm) were weighed and the weight was recorded. The hydrophilic coatings of the catheters were formed from polyvinylpyrrolidone. The hydrophilic coatings of the catheters were immersed for one minute in alpha-tocopherol/ethanol solutions of varying concentrations of alpha-tocopherol. The thus treated catheters were then placed on mandrels to dry under gentle airflow at ambient temperature to remove the ethanol. After ethanol removal, the weight of each catheter was then measured and the difference in weight between the catheter prior to immersion in the solution and after the immersion and drying was calculated to determine the amount of alpha-tocopherol retained in the catheter. The results are shown in Tables 5-8 below.

TABLE-US-00005 TABLE 5 W1 W2 Solution Before After concentration Difference Sample Dipping Dipping % w/w in Amount # (g) (g) Ethanol (g) 1 5.6756 5.7096 1% 0.0340 2 5.6548 5.687  1% 0.0322 3 5.6728 5.7053 1% 0.0325 4 5.6483 5.6688 1% 0.0205 5 5.6730 5.7052 1% 0.0322 6 5.6755 5.7083 1% 0.0328 7 5.6584 5.7029 1% 0.0445 8 5.6578 5.6938 1% 0.0360 9 5.6593 5.6946 1% 0.0353 10 5.6977 5.7291 1% 0.0314 11 5.6707 5.7026 1% 0.0319 12 5.6630 5.7037 1% 0.0407 Mean 0.0337 point

TABLE-US-00006 TABLE 6 W1 W2 Solution Before After concentration Difference Sample Dipping Dipping % w/w in Amount # (g) (g) Ethanol (g) 1 5.6656 5.6976 5% 0.0320 2 5.6335 5.689 5% 0.0555 3 5.6216 5.6707 5% 0.0491 4 5.6537 5.7152 5% 0.0615 5 5.6023 5.6497 5% 0.0474 6 5.6351 5.681 5% 0.0459 7 5.6747 5.7223 5% 0.0476 8 5.6543 5.7048 5% 0.0505 9 5.6892 5.7416 5% 0.0524 10 5.6503 5.7015 5% 0.0512 11 5.6634 5.7148 5% 0.0514 Mean 0.0495 Difference

TABLE-US-00007 TABLE 7 W1 W2 Solution Before After concentration Difference Sample Dipping Dipping % w/w in Amount # (g) (g) Ethanol (g) 1 5.6620 5.7146 10% 0.0526 2 5.7117 5.7637 10% 0.0520 3 5.6729 5.7388 10% 0.0659 4 5.6891 5.7400 10% 0.0509 5 5.7007 5.7683 10% 0.0676 6 5.7418 5.7964 10% 0.0546 7 5.7260 5.7936 10% 0.0676 8 5.6821 5.7548 10% 0.0727 9 5.6898 5.7652 10% 0.0754 10 5.6496 5.7226 10% 0.0730 11 5.7052 5.7916 10% 0.0864 12 5.7464 5.8299 10% 0.0835 Mean 0.0669 Difference

TABLE-US-00008 TABLE 8 W1 W2 Solution Before After concentration Difference Sample Dipping Dipping % w/w in Amount # (g) (g) Ethanol (g) 1 5.6930 5.8046 20% 0.1116 2 5.7222 5.8332 20% 0.1110 3 5.7087 5.8371 20% 0.1284 4 5.7236 5.8473 20% 0.1237 5 5.7486 5.8739 20% 0.1253 6 5.7124 5.8486 20% 0.1362 7 5.7061 5.8226 20% 0.1165 8 5.7488 5.851 20% 0.1022 9 5.6767 5.7965 20% 0.1198 10 5.6784 5.8108 20% 0.1324 11 5.7028 5.8447 20% 0.1419 12 5.6763 5.8186 20% 0.1423 Mean 0.1243 Difference

[0027] It will be understood that the embodiments described above are illustrative of some of the applications of the principles of the present subject matter. Numerous modifications may be made by those skilled in the art without departing from the spirit and scope of the claimed subject matter, including those combinations of features that are individually disclosed or claimed herein. For these reasons, the scope hereof is not limited to the above description but is as set forth in the following claims, and it is understood that claims may be directed to the features hereof, including as combinations of features that are individually disclosed or claimed herein.