A blood compatible, lubricious article and composition and method therefor.
8 claims: 6 independent, 2 dependent
- 1A composition being non-leachable for an aqueous vehicle as blood for coating a polymeric surface comprising a mixture of a quanternary ammonium complex of heparin and 2 to 75% by weight of a lubricating silicone, said complex having the formula wherein R₁, R₂, R₃ and R₄ are independently selected from the group consisting of an alkyl group of 1 to 18 carbon atoms and an aralkyl group of 7 to 18 carbon atoms and H⁻ is a negative ion of heparin, said silicone being water insoluble and noncuring and having a viscosity of 20 to 1,000,000 mm²·s⁻¹ (centistokes).
- 2The composition of Claim 1 wherein said silicone is a polydialkyl siloxane.
- 3The composition of Claim 1 wherein R₁, R₂ and R₃ are independently alkyl groups selected from the group having from 8 to 18 carbon atoms.
- 4A medical device for contact with a blood stream comprising an article having a polymeric surface being coated with a composition being non-leachable for an aqueous vehicle as blood, and comprising a mixture of a quaternary ammonium complex of heparin and 2 to 75% by weight of a lubricating silicone, said complex having the formula wherein R₁, R₂, R₃ and R₄ are independently selected from the group consisting of an alkyl group of 1 to 18 carbon atoms and an aralkyl group of 7 to 18 carbon atoms and H⁻ is a negative ion of heparin, said silicone being water insoluble and noncuring, and having a viscosity of 20 to 1,000,000 mm²·s⁻¹ (centistokes).
- 5A medical device for contact with a blood stream comprising a shaped article having a polymeric surface being coated with a composition being non-leachable for an aqueous vehicle as blood, and comprising a mixture of a quanternary ammonium complex of heparin and 20 to 50% by weight of a lubricating polydimethylsiloxane, said complex having the formula wherein R₁, R₂ and R₃ are independently selected from the group consisting of a straight chain alkyl group of 8 to 18 carbon atoms, R₄ is selected from the group consisting of a lower alkyl group of 1 to 4 carbon atoms and H⁻ is a negative ion of heparin, said polydimethylsiloxane being water insoluble and noncuring, and having a viscosity of 1,000 to 60,000 mm²·s⁻¹ (centistokes).
- 6A method for rendering a polymeric surface of a medical article both antithrombogenic and lubricious comprising preparing a composition being non-leachable for an aqueous vehicle as blood by mixing a quanternary ammonium complex of heparin and a lubricating silicone, said complex having the formula wherein R₁, R₂, R₃ and R₄ are independently selected from the group consisting of an alkyl group of 1 to 18 carbon atoms and an aralkyl group of 7 to 18 carbon atoms and H⁻ is a negative ion of heparin, said silicone being water insoluble and noncuring, and having a viscosity of 20 to 1,000,000 mm²·s⁻¹ (centistokes), and applying said composition to said surface of said medical article.
- 7The method in accordance with Claim 6 wherein said mixing is performed by dissolving said complex and silicone in a solvent to provide a solution.
- 8The method in accordance with Claim 7 wherein said applying is performed by immersing said article in said solution, withdrawing said article from said solution and evaporating said solvent from the surface of said article.
Independent claims8
50 paragraphs in 10 sections, as filed
BACKGROUND OF THE INVENTION
00011. <u style="single">Field of the Invention</u>. This invention relates to medical articles, and more particularly relates to a lubricious and antithrombogenic composition and method for its application to a medical article.
00022. <u style="single">Background of the Invention</u>. Extensive investigations have been undertaken over many years to find material that will be biologically and chemically stable toward body fluids. This area of research has become increasingly important with the development of various objects and articles which may come into contact with blood, such as artificial organs, vascular grafts, probes, cannulas, catheters and the like.
0003Synthetic plastics have come to the fore as preferred materials for such articles. However, such materials have the major drawback of being thrombogenic. Even such plastics as polytetrafluoroetheylene and the silicone rubbers, which are more compatible with blood than most plastics, still show thrombogenic characteristics.
0004Often, use of such articles, as for example, probes, cannulas, catheters and the like, include puncture and passage of the article through the skin. Friction between the patient's skin and the plastic surface of the article may cause substantial discomfort to the patient. Further, catheters are often used in conjunction with an introducer device which typically contains a soft rubber one-way check valve through which the catheter must be threaded. When one surface of an article must slide across another surface, friction may develop which can cause damage to the article. In particular, fragile catheter balloons may be damaged by friction during passage through the valve of the introducer. Thus, both antithrombogenicity and lubricity are highly desirable properties for article surfaces to come into contact with blood.
0005Surfaces may be rendered lubricious by simple application of any common lubricant. Silicone oils are generally recognized to be among the best lubricants available. Application of a silicone lubricant to a surface is known to result in significant reduction in the surface drag upon catheter insertion, facilitate catheter placement, and reduce the force required for catheter retraction.
0006Thrombogenicity has conventionally been counteracted by the use of anticoagulants such as heparin. A variety of heparinization procedures have been reported. For example, Solomon et al., in U.S. Patent No. 4,521,564, discloses a method to convalently bond heparin to a polyurethane substrate. Eriksson et al., in U.S. Patent No. 4,118,485, coats a plastic surface with a complex of heparin and either an alkylamine salt or a quaternary amine salt and subsequently stabilizes the heparin by crosslinking with a dialdehyde.
0007Williams et al., in U.S. Patent No. 4,613,517, reveals a process for ionically bonding heparin to a polymeric surface including the steps of plasma-treating the surface, absorbing a surface active agent onto the plasma-treated surface, reacting the surface active agent with heparin, and crosslinking the heparin with glutaraldehyde.
0008Substrates rendered blood compatible by coating with a layer of silicone have been disclosed. Durst et al. in <u style="single">Am. J. of Roent., Radium Ther. and Nuclear Med.</u>, <u style="single">120</u>, 904 (1974) reported that, <u style="single">in vitro</u>, siliconized stainless steel guidewires, polytetrafluoroethylene coated guidewires and polyethylene catheters were hypothrombogenic compared to untreated substrates, but, <u style="single">in vivo</u> in dogs, no antithrombogenic effect was observed except with heparin coated substrates.
0009McGary et al., in U.S. Patent No. 4,678,660, discloses dipping a polyurethane substrate into a solution of a complex of heparin and tridodecylmethyl ammonium chloride (TDMAC) in polyurethane to form a layer of the complex in polyurethane on the substrate. A lower leach rate of heparin is claimed for the patented product having heparin distributed throughout the polyurethane layer as compared to heparin ionically bonded to TDMAC on the surface of the polyurethane substrate.
0010U.S. Patent No. 4,529,614 to Burns discloses coatings of an anticoagulant and a water soluble copolymeric silicone applied to plastic surfaces. The coatings render the surfaces hydrophobic and dissolve in the blood to impart anticoagulant properties to a sample to be analyzed.
0011Thus, while the prior art has recognized for many years the desirability of rendering substrate surfaces antithrombogenic or lubricious, there are no reports known to the authors of the simultaneous achievement of both effects. The present invention addresses this need.
SUMMARY OF THE INVENTION
0012One aspect of the invention is a composition being non-leachable for an aqueous vehicle as blood for coating a polymeric surface comprising a mixture of a quanternary ammonium complex of heparin and 2 to 75% by weight of a lubricating silicone, said complex having the formula <chemistry id="chem0001" num="0001"><img file="EP0338418B1_D0001.tif" /></chemistry> wherein R₁ R₂, R₃ and R₄ are independently selected from the group consisting of an alkyl group of 1 to 18 carbon atoms and an aralkyl group of 7 to 18 carbon atoms and H⁻ is a negative ion of heparin, said silicone being water insoluble and noncuring, and having a viscosity of 20 to 1,000,000 mm²·s⁻¹ (centistokes).
0013In particularly preferred compositions, the complex has three long chain alkyl groups on the nitrogen and the lubricant is a polydimethylsiloxane of viscosity 1,000 to 60,000 mm²·s⁻¹ (centistokes).
0014Another aspect of the invention is a medical device adapted for contact with blood. The device includes a medical article, preferably a shaped medical article having a coating of the composition of the invention on its surface. Preferred medical articles are polymeric, most preferably polyolefin or polyurethane. The most preferred article of the invention is a catheter or catheter introducer having a coating of the composition on its surface.
0015In another aspect of the invention, a method is provided to coat the surface of the article with the composition so that the surface is both antithrombogenic and lubricious. In the preferred method, the article is coated by dipping into a solvent solution of the composition.
0016Thus, the invention solves two problems simultaneously which the prior art has addressed only individually. For example, general intravascular catheters coated with the composition of the invention may be inserted easily into the body consequent to the lubricating silicone and, once inserted, exhibit enhanced hemocompatibility consequent to the heparin. If used as a coating on balloon intravascular catheters, the composition, in addition to the above advantages, provides easier insertion of the balloon segment of the catheter thereby decreasing the potential for damage to the balloon during insertion. Further, large gauge and/or multilumen catheters coated with the composition of the invention may be inserted through a rubber introducer valve with minimal damage to the balloon and reduced abrasive removal of a heparin coating.
0017A particular advantage to coating a medical article with the composition of the invention is that the admixture of heparin and silicone provides lubricity due to the silicone with no compromise of the antithrombogenic activity of the heparin. The water insolubility of the silicone renders the composition resistant to leaching by blood so that antithrombogenicity is retained for periods of up to seven days, and even longer, during medical procedures such as long term catheterization.
DETAILED DESCRIPTION OF THE INVENTION
0018While this invention is satisfied by embodiments in many different forms, there will herein be described in detail preferred embodiments of the invention, with the understanding that the present disclosure is to be considered as exemplary of the principles of the invention and is not intended to limit the invention to the embodiments described. The scope of the invention will be measured by the appended claims and their equivalents.
0019In one aspect of the present invention, there is provided a medical device having a surface which is both antithrombogenic and lubricious. The device includes a shaped medical article and a leach-resistant composition on the surface thereof, and, in another aspect of the invention, there is provided an antithrombogenic and lubricious composition. In still another aspect of the invention, a method for rendering a substrate surface both antithrombogenic and lubricious is provided.
0020The invention will be described in terms of a tubing, such as a catheter; however, it will be apparent to one ordinarily skilled in the art that the substrate may equally be any of a variety of other shaped medical articles. Exemplary, but not limitative, of suitable articles are peripheral and central catheters of all types, including large gauge and multilumen types, introducers and check valves therefor, sheaths, guide wires and stylets. The invention also contemplates applying the composition to either or both of an exterior or interior surface of an article.
0021The lubricated, antithrombogenic tubing of the invention is preferably made of a polymeric material, though it is appreciated by one skilled in the art that other materials, such as glass, metal or ceramic may be used. Suitable polymers are, for example, polyolefins, such as polyethylene or polypropylene, polyvinyl resins such as polyvinylchloride, polyvinylacetate, polyvinylidene fluoride and copolymers thereof, fluorinated polymers such as polytetrafluoroethylene (PTFE), fluorinated ethylene-propylene polymer (FEP) and polytrifluorochloroethylene, polyurethanes, polyamides, silicone elastomers, polystyrenes, styrene-butadiene copolymers, polysiloxane modified polystyrenes and polystyrene-polyolefin copolymers, and thermoplastic interpenetrating network polymers. In addition, the tubing may have an additional coating, such as a hydrogel, on its surface, and the composition of the invention may be applied over the hydrogel coating.
0022The composition of the invention includes an antithrombogenic agent and a lubricant. The antithrombogenic agent is heparin, which froms a complex with an alkylammonium salt of general structure I: <chemistry id="chem0002" num="0002"><img file="EP0338418B1_D0002.tif" /></chemistry> wherein R₁ may be selected from the group consisting of an alkyl group of 7 to 18 carbon atoms and R₂,R₃ and R₄ may independently be selected from the group consisting of hydrogen, an alkyl group of 1 to 18 carbon atoms and an aralkyl group of 7 to 18 carbon atoms and X⁻ may be a halide ion, such as chloride or bromide.
0023The preferred salt to be complexed with heparin is a quaternary ammonium salt of formula I in which R₁,R₂,R₃ and R₄ may independently be an alkyl group, straight chain or branched, of from 1 to 18 carbon atoms, or an aralkyl group of 7 to 18 carbon atoms and X may be a negative monovalent ion, such as a halide ion. For example, the commercially available quaternary salt benzalkonium chloride wherein R₁ is C₈H₁₇, R₂ is C₆H₅CH₂ and R₃ and R₄ are methyl may be used. In particularly preferred quaternary salts for complexation with heparin, R₁,R₂ and R₃ may independently be straight chain alkyl groups of from 8 to 18 carbon atoms and R₄ may be lower alkyl group of from 1-4 carbon atoms. In the most preferred salt, R₁,R₂ and R₃ are dodecyl groups, R₄ is methyl and X⁻ is chloride. This quaternary salt is commonly referred to as TDMAC. Thus, the most preferred complex has the formula I wherein X⁻ is an anion of heparin. Such complexes of heparin are well-known in the art, and are described in McGary et al. and Eriksson et al., supra.
0024The complex as previously described and silicone are mixed to form the composition of the invention. If the complex has sufficient solubility in the silicone, the mixing may be done merely by dissolving the complex in the silicone at the desired concentration. Preferably, the complex and silicone may be mixed merely by dissolving in an appropriate solvent or solvent system. Use of a solvent is particularly advantageous when a silicone oil of high viscosity is included in the composition. Exemplary of suitable solvents are toluene, petroleum ether, methylene chloride or any one of the fluorinated hydrocarbons conventionally termed Freon™. In some cases, it may be desirable to use a more polar solvent such as ethanol or isopropanol in the solvent system to aid in dissolution of the complex. The concentration of the complex in the solvent system is not critical, and may advantageously be from 0.1 to 5% by weight. Higher concentration may be used but generally do not provide any advantage. The preferred concentration is from 1-2%. Determination of a suitable solvent and concentration for the complex is well within the purview of one ordinarily skilled in the art.
0025A lubricating oil is added to the solvent solution of the complex. Any water insoluble lubricating oil may be used, as, for example, refined white oil. Preferred lubricants are stable, noncuring high purity medical grade silicones such as the polydialkylsiloxanes of formula II: <chemistry id="chem0003" num="0003"><img file="EP0338418B1_D0003.tif" /></chemistry> In formula II, R₁ and R₂ may be independently an alkyl group of from 1 to 20 carbon atoms or taken together may form a ring of from 4 to 8 carbon atoms. The number of repeating units, n, is sufficient to provide a viscosity of from 20 to 1,000,000 mm²·s⁻¹ (centistokes). In particularly preferred polydialkylsiloxanes of formula II, R₁ is methyl and the viscosity is from 1,000 to 60,000 mm²·s⁻¹ (centistokes). The most preferred silicones are polydimethylsidoxanes having a viscosity of from 5,000 to 20,000 mm²·s⁻¹ as exemplified by the commercially available product DC-360™ available from Dow Corning, Midland, MI.
0026The quantity of silicone to be added to the solvent solution of the complex may be varied over a wide range. It has been found that a composition having as little as 2% by weight of the silicone, based on the complex, yields a significant improvement in lubricity when applied to the substrate, as described below. On the other hand, as much as 75% by weight of silicone may be advantageous for certain compositions and substrates. A preferred concentration range of silicone may be from 20-50% by weight of the complex.
0027Application of the composition of complex and silicone to the substrate may be carried out by any conventional technique. For example, the composition, preferably in the solvent, may be brushed or sprayed onto the substrate. The preferred method of application is merely to immerse the substrate into the solvent containing the composition. If the substrate is a tubing, such as a catheter, and it is desired to ensure that the composition coats the lumen wall, it may be advantageous to draw the composition into the lumen by the application of reduced pressure.
0028Immersion of the substrate in the solvent solution of the composition may be carried out at any suitable temperature up to the boiling point of the solvent and may be maintained for any convenient length of time. The time and temperature of contact are not critical, but preferably are about 1 second to 1 hour and ambient temperature.
0029After withdrawing the substrate from the solution, the solvent may be removed by evaporation. If desired, the rate of evaporation may be accelerated by application of reduced pressure or mild heat. The coating of the composition applied to the substrate may be of any convenient thickness, and in practice, the thickness will be determined by such factors as the viscosity of the silicone, the temperature of the application and the rate of withdrawal. For most substrates, the film preferably is applied as thinly as practical, since no significant advantage is gained by thicker films.
0030In another embodiment of the invention, the substrate may be treated with a plasma prior to application of the composition. This embodiment of the invention is particularly advantageous for substrates of very low surface energy, such as the fluorinated polymers as exemplified by PTFE and FEP. Suitable conditions for plasma treatment of fluorinated surfaces are described in copending application of common assignee, serial number 081,200, filed August 3, 1987.
0031When a substrate is coated with the composition of the invention, the surface of the substrate is rendered both antithrombogenic and lubricious, as tested by conventional methods described in the examples. A 1.6 mm (1/16 inch) thick natural rubber membrane may be used as a close approximation of human skin for studies simulating the friction or drag which develops when a catheter, introducer, stylet or guide wire is inserted or withdrawn through the skin of a patient.
0032Antithrombogenicity for the substrates coated with the composition of the invention may be determined by measuring clotting times by the standard partial (PTT) and activated partial thromboplastin time (APTT) tests (B.A. Brown, <u style="single">Hematology Principles and Procedures</u>, Third Edition, Lea and Febiger Co., 1980). These tests are qualitative procedures for determining the efficacy of TDMAC-heparin, as a raw material or as a coating. As a measure of the total anti-clotting activity, the APTT can detect the presence of anticoagulants by giving prolonged clotting times. Non-coated control substrates generally give clotting times of between 25 to 40 seconds. The heparinized tubings of the invention give clotting times greater than 1800 seconds.
0033The stability of the coatings on the substrates may be determined by performing leach rate studies using normal saline as leachant, as described in Example V.
0034<u style="single">In vivo</u> thrombus formation on catheters coated with the composition of the invention may be determined by the method of Solomon et al., <u style="single">J. of Biomedical Materials Research</u>, 21,43 (1987), as described in Example VI.
0035This invention will be further described by the following examples, which are illustrative only and not to be considered as limitative. In the examples, the percentages of the complex are given as weight percentages based on the solvent, and the percentages of silicone are weight percentages based on the weight of the complex.
EXAMPLE I
0036To a 1.25% solution of the heparin-TDMAC complex (McGary et al. <u style="single">supra</u>) in 90:10 Freon™ TF/petroleum ether (v/v), various percentages by weight of 12,500 mm²·s⁻¹ (centistoke) silicone oil were added. The solutions were drawn by application of a slight vacuum into the lumens of thermoplastic polyurethane (TPU) catheters of 0.04 and 0.8 mm (0.017 and 0.35 in) inside diameter and 23 mm (0.92 in) outside diameter. The solutions were removed and the lumens were dried at 60°C for 24 hours. Stylet wires were inserted into the lumens of the catheters and then withdrawn at a constant rate of 50mm/min. The forces required for withdrawal were measured using the Instron Universal Testing Instrument. The results of this experiment are tabulated below in Table I. <tables id="tabl0001" num="0001"><table frame="all"><title>TABLE I</title><tgroup cols="7" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col7" align="center">WITHDRAWAL FORCE<sup>a</sup> FOR STYLET WIRE</entry></row><row><entry namest="col1" nameend="col1" align="center">control</entry><entry namest="col2" nameend="col2" align="center">silicone only</entry><entry namest="col3" nameend="col3" align="center">silicone only 90 day aging</entry><entry namest="col4" nameend="col4" align="center">complex only</entry><entry namest="col5" nameend="col5" align="center">complex and 2% silicone</entry><entry namest="col6" nameend="col6" align="center">complex and 10% silicone</entry><entry namest="col7" nameend="col7" align="center">complex and 30% silicone</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="char" char=".">4.85</entry><entry namest="col2" nameend="col2" align="char" char=".">0.31</entry><entry namest="col3" nameend="col3" align="char" char=".">0.35</entry><entry namest="col4" nameend="col4" align="char" char=".">5.20</entry><entry namest="col5" nameend="col5" align="char" char=".">11.80</entry><entry namest="col6" nameend="col6" align="char" char=".">0.30</entry><entry namest="col7" nameend="col7" align="char" char=".">0.20</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">5.25</entry><entry namest="col2" nameend="col2" align="char" char=".">0.34</entry><entry namest="col3" nameend="col3" align="char" char=".">0.31</entry><entry namest="col4" nameend="col4" align="char" char=".">5.30</entry><entry namest="col5" nameend="col5" align="char" char=".">11.50</entry><entry namest="col6" nameend="col6" align="char" char=".">1.50</entry><entry namest="col7" nameend="col7" align="char" char=".">0.12</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">6.30</entry><entry namest="col2" nameend="col2" align="char" char=".">0.36</entry><entry namest="col3" nameend="col3" align="char" char=".">0.39</entry><entry namest="col4" nameend="col4" align="char" char=".">7.00</entry><entry namest="col5" nameend="col5" align="char" char=".">11.00</entry><entry namest="col6" nameend="col6" align="char" char=".">0.75</entry><entry namest="col7" nameend="col7" align="char" char=".">0.15</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">8.30</entry><entry namest="col2" nameend="col2" align="char" char=".">0.32</entry><entry namest="col3" nameend="col3" align="char" char=".">0.37</entry><entry namest="col4" nameend="col4" align="char" char=".">7.90</entry><entry namest="col5" nameend="col5" align="char" char=".">7.50</entry><entry namest="col6" nameend="col6" align="char" char=".">1.10</entry><entry namest="col7" nameend="col7" align="char" char=".">0.13</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">4.90</entry><entry namest="col2" nameend="col2" align="char" char=".">0.39</entry><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" align="char" char=".">9.10</entry><entry namest="col5" nameend="col5" align="char" char=".">7.50</entry><entry namest="col6" nameend="col6" align="char" char=".">0.90</entry><entry namest="col7" nameend="col7" align="char" char=".">0.32</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">6.70</entry><entry namest="col2" nameend="col2" align="char" char=".">0.35</entry><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" align="char" char=".">8.50</entry><entry namest="col5" nameend="col5" align="char" char=".">7.75</entry><entry namest="col6" nameend="col6" align="char" char=".">1.00</entry><entry namest="col7" nameend="col7" align="char" char=".">0.33</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="char" char=".">0.28</entry><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" /><entry namest="col6" nameend="col6" /><entry namest="col7" nameend="col7" /></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="char" char=".">0.36</entry><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" /><entry namest="col6" nameend="col6" /><entry namest="col7" nameend="col7" /></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="char" char=".">0.13</entry><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" /><entry namest="col6" nameend="col6" /><entry namest="col7" nameend="col7" /></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="char" char=".">0.34</entry><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" /><entry namest="col6" nameend="col6" /><entry namest="col7" nameend="col7" /></row><row rowsep="1"><entry namest="col1" nameend="col1" align="char" char=".">6.05<sup>b</sup></entry><entry namest="col2" nameend="col2" align="char" char=".">0.32</entry><entry namest="col3" nameend="col3" align="char" char=".">0.36</entry><entry namest="col4" nameend="col4" align="char" char=".">7.17</entry><entry namest="col5" nameend="col5" align="char" char=".">9.51</entry><entry namest="col6" nameend="col6" align="char" char=".">0.92</entry><entry namest="col7" nameend="col7" align="char" char=".">0.21</entry></row></tbody></tgroup><tgroup cols="7" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><tbody valign="top"><row><entry namest="col1" nameend="col7" align="justify">a) all values are in newtons</entry></row><row><entry namest="col1" nameend="col7" align="justify">b) mean</entry></row></tbody></tgroup></table></tables>
0037It is seen that a coating of silicone only greatly reduces the withdrawal force (column 2) and that this effect remains substantially unchanged after 90 days (column 3). Withdrawal forces are somewhat greater when the catheter is coated with the complex only (column 4), and still greater with 2% silicone (column 5). Columns 6 and 7, however, show that very effective lubrication is achieved when higher concentrations of silicone are used, establishing that the complex does not interfere with lubrication by silicone.
EXAMPLE II
0038Solutions were prepared containing 12.5 g of the TDMAC-heparin complex and DC 360™ silicone oil of 12,500 mm²·s⁻¹ (centistokes) viscosity in 1 liter of 90:10 Freon™ TF/petroleum ether (v/v). Fifteen cm sections of TPU catheters were coated with the composition of the invention by briefly dipping into the solution, quickly withdrawing in less than one second, and drying at 60°C for 24 hours. The catheter sections were pulled at a constant speed of 50 mm/min through the rubber check valve of a catheter introducer and the drag forces measured on an Instron Universal Testing Instrument. The results of this experiment are shown in Table II. <tables id="tabl0002" num="0002"><img file="EP0338418B1_D0004.tif" /></tables><tables id="tabl0003" num="0003"><img file="EP0338418B1_D0005.tif" /></tables>
0039It is seen from Table II that as little as 2.98% of silicone oil in the composition reduces the drag force from an average of 513 grams to 341 grams, and that when the silicone percentage is raised to 75% by weight of the complex, the drag force is reduced to 120 grams, or 20% of the control. As observed in Example I, the presence of the complex does not interfere with the lubricating property of the silicone.
EXAMPLE III
0040Pieces of TPU catheter tubing 15 cm long were coated with TDMAC-heparin complex and benzalkonium-heparin complex by the procedure of Example II using the solvents and silicones indicated in Table III. The coefficients of friction of these tubings were determined by a Friction Drag Test Accessory to the Instron Universal Testing Instrument. The results of this experiment are tabulated in Table III. <tables id="tabl0004" num="0004"><table frame="all"><title>TABLE III</title><tgroup cols="7" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col7" align="center">TUBING FRICTION</entry></row><row><entry namest="col1" nameend="col1" align="center">Test No.</entry><entry namest="col2" nameend="col2" align="center">Control</entry><entry namest="col3" nameend="col4" align="center">TDMAC-heparin</entry><entry namest="col5" nameend="col5" align="center">Benzalk.-heparin</entry><entry namest="col6" nameend="col6" align="center">TDMAC-heparin; 1,000<sup>d</sup></entry><entry namest="col7" nameend="col7" align="center">silicone (2%) 12,500<sup>d</sup></entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" align="center">a</entry><entry namest="col4" nameend="col4" align="center">b</entry><entry namest="col5" nameend="col5" align="center">c</entry><entry namest="col6" nameend="col6" /><entry namest="col7" nameend="col7" /></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="right">1</entry><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" align="char" char=".">1.73</entry><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" align="char" char=".">2.32</entry><entry namest="col6" nameend="col6" /><entry namest="col7" nameend="col7" /></row><row><entry namest="col1" nameend="col1" align="right">2</entry><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" align="char" char=".">1.57</entry><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" align="char" char=".">2.42</entry><entry namest="col6" nameend="col6" /><entry namest="col7" nameend="col7" /></row><row><entry namest="col1" nameend="col1" align="right">3</entry><entry namest="col2" nameend="col2" align="char" char=".">1.32</entry><entry namest="col3" nameend="col3" align="char" char=".">1.58</entry><entry namest="col4" nameend="col4" align="char" char=".">1.43</entry><entry namest="col5" nameend="col5" align="char" char=".">2.06</entry><entry namest="col6" nameend="col6" align="char" char=".">0.96</entry><entry namest="col7" nameend="col7" align="char" char=".">0.68</entry></row><row><entry namest="col1" nameend="col1" align="right">4</entry><entry namest="col2" nameend="col2" align="char" char=".">1.46</entry><entry namest="col3" nameend="col3" align="char" char=".">1.73</entry><entry namest="col4" nameend="col4" align="char" char=".">1.46</entry><entry namest="col5" nameend="col5" align="char" char=".">1.96</entry><entry namest="col6" nameend="col6" align="char" char=".">0.48</entry><entry namest="col7" nameend="col7" align="char" char=".">0.56</entry></row><row><entry namest="col1" nameend="col1" align="right">5</entry><entry namest="col2" nameend="col2" align="char" char=".">1.45</entry><entry namest="col3" nameend="col3" align="char" char=".">1.89</entry><entry namest="col4" nameend="col4" align="char" char=".">1.79</entry><entry namest="col5" nameend="col5" align="char" char=".">1.84</entry><entry namest="col6" nameend="col6" align="char" char=".">0.69</entry><entry namest="col7" nameend="col7" align="char" char=".">0.70</entry></row><row><entry namest="col1" nameend="col1" align="right">6</entry><entry namest="col2" nameend="col2" align="char" char=".">1.00</entry><entry namest="col3" nameend="col3" align="char" char=".">1.68</entry><entry namest="col4" nameend="col4" align="char" char=".">1.43</entry><entry namest="col5" nameend="col5" align="char" char=".">1.86</entry><entry namest="col6" nameend="col6" align="char" char=".">0.86</entry><entry namest="col7" nameend="col7" align="char" char=".">0.59</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="right">7</entry><entry namest="col2" nameend="col2" align="char" char=".">1.31</entry><entry namest="col3" nameend="col3" align="char" char=".">1.69</entry><entry namest="col4" nameend="col4" align="char" char=".">1.53</entry><entry namest="col5" nameend="col5" align="char" char=".">2.07</entry><entry namest="col6" nameend="col6" align="char" char=".">0.75</entry><entry namest="col7" nameend="col7" align="char" char=".">0.63</entry></row></tbody></tgroup><tgroup cols="7" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><tbody valign="top"><row><entry namest="col1" nameend="col7" align="justify">a) toluene-petroleum ether</entry></row><row><entry namest="col1" nameend="col7" align="justify">b) Freon™ TF-petroleum ether</entry></row><row><entry namest="col1" nameend="col7" align="justify">c) isopropanol</entry></row><row><entry namest="col1" nameend="col7" align="justify">d) viscosity in mm²·s⁻¹ (centistokes)</entry></row></tbody></tgroup></table></tables>
0041It is seen from Table III that a coating of heparin complex increases friction over control value, but that a coating of the compositions having the complex admixed with silicone reduces friction.
EXAMPLE IV
0042Pieces of TPU catheter tubing 15 cm long were coated with the TDMAC-heparin complex (30 »g/cm²) admixed with silicone of 12,500 mm²·s⁻¹ (centistoke) viscosity by dipping into Freon™ TF solutions and drying for 24 hours at 60°C. A 78 gram weight was applied to a natural rubber membrane, and the membrane was dragged across the catheters. Coefficients of friction were determined with the Instron Universal Testing Instrument.
0043Clotting times for these coated catheter sections were determined by the standard APTT. The results of this experiment are shown in Table IV. <tables id="tabl0005" num="0005"><table frame="all"><title>TABLE IV</title><tgroup cols="3" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="52.50mm" /><colspec colnum="2" colname="col2" colwidth="52.50mm" /><colspec colnum="3" colname="col3" colwidth="52.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">% silicone</entry><entry namest="col2" nameend="col2" align="center">coefficient of friction</entry><entry namest="col3" nameend="col3" align="center">APTT (s)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="right">0</entry><entry namest="col2" nameend="col2" align="char" char=".">1.35</entry><entry namest="col3" nameend="col3" align="right">1800</entry></row><row><entry namest="col1" nameend="col1" align="right">2</entry><entry namest="col2" nameend="col2" align="char" char=".">0.63</entry><entry namest="col3" nameend="col3" align="right">1800</entry></row><row><entry namest="col1" nameend="col1" align="right">5</entry><entry namest="col2" nameend="col2" align="char" char=".">0.25</entry><entry namest="col3" nameend="col3" align="right">1800</entry></row><row><entry namest="col1" nameend="col1" align="right">10</entry><entry namest="col2" nameend="col2" align="char" char=".">0.28</entry><entry namest="col3" nameend="col3" align="right">1800</entry></row><row><entry namest="col1" nameend="col1" align="right">20</entry><entry namest="col2" nameend="col2" align="char" char=".">0.16</entry><entry namest="col3" nameend="col3" align="right">1800</entry></row><row><entry namest="col1" nameend="col1" align="right">30</entry><entry namest="col2" nameend="col2" align="char" char=".">0.19</entry><entry namest="col3" nameend="col3" align="right">1800</entry></row><row><entry namest="col1" nameend="col1" align="right">50</entry><entry namest="col2" nameend="col2" align="char" char=".">0.13</entry><entry namest="col3" nameend="col3" align="right">1800</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="right">100</entry><entry namest="col2" nameend="col2" align="char" char=".">0.077</entry><entry namest="col3" nameend="col3" align="right">33</entry></row></tbody></tgroup></table></tables>
0044Table IV shows that the coefficient of friction decreases with increasing percentage of silicone, but no decrease is seen in clotting time up to 50% silicone percentage, showing that the anticoagulant effect of the heparin is not compromised by the silicone.
EXAMPLE V
LEACH RATE STUDY
0045Sections of TPU catheters 15 cm long were coated with the TDMAC-heparin complex containing tritiated heparin, with and without admixed silicone oil, by dipping into 2.0 or 1.25 weight percent solutions of the TDMAC complex in the solvents indicated in Tables V and VI. The sections were dried for 24 hours at 60°C, and the quantity of heparin on the catheter surfaces was determined (by liquid scintillation counting and comparison with a standard curve) and expressed as »g heparin/cm². The coated sections were dynamically leached in 1 l of normal saline using an incubator shaker at 37°C and 150 rpm for up to seven days. Saline was changed daily, and samples were removed every 24 hours and tested for heparin remaining. PTT and APTT times were also determined.
0046The results of this experiment are given in Tables V (APTT times) and Table VI (leach rate study). All PTT times for all catheter sections were greater than 1800 s. APTT times are tabulated in Table V and heparin remaining is shown in Table VI. <tables id="tabl0006" num="0006"><img file="EP0338418B1_D0006.tif" /></tables><tables id="tabl0007" num="0007"><img file="EP0338418B1_D0007.tif" /></tables>
0047The results of Example V show that even when the heparin remaining on the catheter sections has been reduced to as low as 2-3 »g/cm² by a seven day saline leach, the PTT and APTT times are still more than 1800 seconds.
EXAMPLE VI
0048TPU catheters (16 gauge) were coated with the heparin-silicone composition of the invention and studied by the <u style="single">in vivo</u> method for evaluation of catheter thrombogenicity of Solomon et al. (supra). Uncoated TPU catheters and polyvinyl chloride catheters (PVC, 16 gauge) served as controls in this experiment. Counts were plotted against time and the curve slopes were determined. <tables id="tabl0008" num="0008"><table frame="all"><title>TABLE VII</title><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Catheter Material</entry><entry namest="col2" nameend="col2" align="center">Slope</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">PVC</entry><entry namest="col2" nameend="col2" align="char" char=".">0.118 ± 0.077</entry></row><row><entry namest="col1" nameend="col1" align="left">TPU</entry><entry namest="col2" nameend="col2" align="char" char=".">0.077 ± 0.042</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">heparinized TPU</entry><entry namest="col2" nameend="col2" align="char" char=".">0.012 ± 0.010</entry></row></tbody></tgroup></table></tables>
0049The significant decreases in the number of counts (deposited platelets) with time is readily apparent from the lower slope of the curve with the heparinized TPU of the invention.
0050Thus, in accordance with the invention, the surfaces of medical articles adapted for contact with blood and friction-generating movement across another surface or a patient's skin may be coated with a composition of anticoagulant, preferably heparin, and silicone. The heparin provides blood compatibility and the silicone provides lubricity without in any way compromising the anticoagulant activity of the heparin. Because the silicone is water insoluble, the composition is resistant to leaching by the blood and remains on the surface of the device for prolonged periods. This is a particular advantage for medical procedures, such as long term catheterizations, and provides both safety and comfort to the patient.
Contents10
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| Document | Relation | Office | Cited during |
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| US10589063B2 | Cited by | United States of America | Applicant |
| US11357962B2 | Cited by | United States of America | Applicant |
| US9956379B2 | Cited by | United States of America | Applicant |
| EP0080908A | Cites | European Patent Office (EPO) | – |
| EP0184465A | Cites | European Patent Office (EPO) | – |
| US3453194A | Cites | United States of America | – |
| US3585647A | Cites | United States of America | – |
| US4082727A | Cites | United States of America | – |
| US4349467A | Cites | United States of America | – |
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| US4678468A | Cites | United States of America | – |
| Hawley's Condensed Chemical Dictionary, 11th Edition, 1987, pp. 1039-1040 | Non-patent | – | – |
| Hawley's Condensed Chemical Dictionary, 11th Edition, 1987, pp. 1039-1040 | Non-patent | – | Examiner |
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| 182694 | – | – | – |
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| Document | Office | Kind | |
|---|---|---|---|
| EP0338418A1 | European Patent Office (EPO) | A1 | |
| JPH02147694A | Japan | A | |
| US5013717A | United States of America | A | |
| US5061738A | United States of America | A | |
| JPH0587120B2 | Japan | B2 | |
| EP0338418B1This record | European Patent Office (EPO) | B1 | |
| AT110285T | Austria | T | |
| ATE110285T1 | Austria | T1 | |
| DE68917631D1 | Germany | D1 | |
| ES2056999T3 | Spain | T3 | |
| DE68917631T2 | Germany | T2 | |
| CA1339091C | Canada | C |
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Numbers
- Publication
- 0338418
- Publication, DOCDB
- 0338418
- Publication, EPODOC
- EP0338418
- Application
- 89106582
- Application, DOCDB
- 89106582
- Application, EPODOC
- EP19890106582
Titles3
- German
- Blutverträglicher, gleitfähiger Artikel sowie Zusammensetzung und Verfahren zu seiner Herstellung
- English
- A blood compatible, lubricious article and composition and method therefor
- French
- Composition et procédé d'obtention d'un article lubrifié compatible avec le sang
Classification
- CPC, 7
- C08L83/04
- A61L29/085
- A61L33/0017
- A61L33/0029
- A61L33/0047
- C08G77/04
- A61L2400/10
- IPC, 11
- A61L29 00
- A61L29 08
- A61L33 00
- C08K5 19
- C08L83 04
- C09D183 04
- C10M169 04
- C10N20 02
- C10N30 00
- C10N30 06
- C10N50 02
Designated states1
- Contracting states, 1
- Sweden
