JPH06192382A - Antithrombotic polyurethane elastomer and medical equipment using the same - Google Patents

Abstract

PURPOSE:To obtain the subject elastomer consisting of a specific polyether diol component, an organic diisocyanate and a specific chain extender, having antithrombotic properties and excellent in mechanical strength. CONSTITUTION:This elastomer consists of 1mol polyether diol of an A-B-A type block copolymer of (A) a polyoxyethylene having preferably 20-60mol content and (B) a polyoxytetramethylene, preferably 2.5-20mol organic diisocyanate component, 1.5-15mol organic diol component and 1.5-15mol organic diamine component.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an antithrombogenic polyurethane elastomer useful as a material for a medical instrument that contacts blood such as artificial blood vessels and artificial organs, and a medical instrument comprising the polyurethane elastomer.

[0002]

2. Description of the Related Art Materials for medical devices that come into contact with blood have good mechanical properties such as flexibility, elasticity, durability and wet strength, and anti-thrombogenicity. It is necessary to have sex. Otherwise, blood will coagulate on the surface of the device to form a thrombus.

Conventionally, silicone and soft polyvinyl chloride have been mainly used as materials for medical devices requiring elasticity. However, when a device made of these materials is brought into direct contact with blood, the blood coagulates on the surface to form a thrombus, and therefore it is necessary to systemically administer an anticoagulant (such as heparin). In this case, if there is bleeding for some reason, there is a risk that hemostasis will not stop.

By the way, it has been proposed to use a polyurethane obtained from polyethylene glycol, an organic diisocyanate and an organic diamine as a medical material. However, this shows good antithrombotic property, but on the other hand, it becomes hydrophilic and therefore wet. Its strength is extremely low and it cannot be put to practical use.

As described above, generally, when the antithrombogenicity and other biocompatibility are improved by making hydrophilic, it is unavoidable that the mechanical strength is lowered. Therefore, it is possible to develop a material having a good balance between the two. It has become an important issue in medical materials.

Under such circumstances, polyoxyethylene (A) and polyoxytetramethylene (B) ABA are used as polyurethanes having both mechanical properties and antithrombotic properties which are sufficiently usable as medical materials. A polyurethane comprising a block copolymer, an organic diisocyanate, and an organic diol chain extender (the molar ratio of these three components is 1: 2: 1) is known [Japan Rubber Association, 62, 242 (1989)]. It has excellent antithrombogenicity and good hydrolysis resistance, but its mechanical strength is still inferior to that of polyurethane using an organic diamine as a chain extender.

Therefore, an object of the present invention is to provide an antithrombogenic polyurethane elastomer which has at least as good antithrombotic properties as conventional ones and is useful as a material for medical devices having further improved mechanical properties. . Another object of the present invention is to provide a medical device having an antithrombotic property at least as good as conventional ones and further improved mechanical properties.

[0008]

Means for Solving the Problems As a result of intensive studies by the present inventors, they have found that the present invention can achieve the above object. That is, the present invention relates to a polyether diol component of an ABA type block copolymer of polyoxyethylene (A) and polyoxytetramethylene (B), an organic diisocyanate, and an organic diol and an organic diol as a chain extender. An antithrombogenic polyurethane elastomer comprising a diamine. The present invention is also a medical device comprising the above antithrombogenic polyurethane elastomer.

In the present invention, the mechanical strength can be improved by using a mixture of an organic diol and an organic diamine as the chain extender in the polyurethane elastomer.

The polyurethane elastomer according to the present invention comprises a polyether diol component of an ABA type block copolymer of polyoxyethylene (A) and polyoxytetramethylene (B), an organic diisocyanate, an organic diol and an organic diamine. Is a polyurethane elastomer.

The polyurethane elastomer of the present invention has, for example, the following formula

[0012]

[Chemical 1]

[Wherein n is an integer of 1 or more, and R ₁ is

[0014]

[Chemical 2]

(A, b and c each represent an integer of 1 or more), the polyether diol residue represented by R is
₂ represents an organic diisocyanate residue, and R ₃ represents an organic diol or organic diamine residue. ] The thing etc. which have a structure represented by these are illustrated.

The polyoxyethylene (A) and polyoxytetramethylene (B) AB- used in the present invention
The A-type block copolymer has the general formula

[0017]

[Chemical 3]

(In the formula, a, b and c each represent an integer of 1 or more.) From the viewpoint of antithrombotic property and mechanical property, the number average molecular weight is usually 300 to 10,000, preferably 500 to. 8000, more preferably 1000-5
It is 000. When the number average molecular weight is less than 300, the antithrombogenicity and elastic properties of the resulting polyurethane elastomer tend to be lowered, and conversely, when it is more than 10,000,
The resulting polyurethane elastomer tends to have reduced mechanical strength and processability.

The polyoxyethylene content in the ABA type block copolymer is 5 to 95 mol%, preferably 10 to 70 mol%, and more preferably 20 to 60 mol%. When the polyoxyethylene content is less than 5 mol%, the resulting polyurethane elastomer tends to be inferior in antithrombogenicity, and when it exceeds 95 mol%, elasticity, flexibility and wet strength tend to be inferior.

The polyurethane elastomer of the present invention preferably has a number average molecular weight of about 1000 to 6000,
More preferably 1500-4500, polyoxyethylene content 10-70 mol%, more preferably 20-60.
Those having a molecular weight of about 20,000 to 60,000, obtained by using a mol% of polyether diol component, are particularly preferable.

The above polyether diol can be produced by anionic or cationic polymerization method using polyoxytetramethylene glycol (PTMG) and ethylene oxide (EO).

As the organic diisocyanate, it suffices to use aliphatic, alicyclic and aromatic diisocyanates conventionally used in the production of polyurethanes, which will be developed in the future as long as the object of the present invention can be achieved. You may use the thing. Specifically, for example, 4,4′-diphenylmethane diisocyanate (MDI), 2,4 (or 2,6) -tolylene diisocyanate (TDI), p
-Xylylene diisocyanate, hexamethylene diisocyanate, 4,4'-dicyclohexyl methane diisocyanate, etc. are mentioned, Preferably 4,4'-diphenyl methane diisocyanate is mentioned. These may be used alone or in combination of two or more.

As the organic diol, it is sufficient to use one which is used as a chain extender in the usual production of polyurethane, and of course, one which will be developed in the future as long as the object of the present invention can be achieved. You may. Specific examples include ethylene glycol, tetramethylene glycol, 1,6-hexanediol, 1,3-propanediol and the like, with ethylene glycol being preferred. These may be used alone or in combination of two or more.

As the organic diamine, it suffices to use one which is used as a chain extender in the usual production of polyurethane, and of course, one which will be developed in the future as long as the object of the present invention can be achieved. You may. Specific examples include alkylenediamines such as ethylenediamine, propylenediamine, and hexamethylenediamine, aromatic diamines such as p-xylylenediamine, p-diphenylmethanediamine, and the like, and ethylenediamine is preferable. These may be used alone or in combination of two or more.

In the polyurethane elastomer of the present invention, an organic diol and an organic diamine are mixed and used as a chain extender, and the molar ratio thereof (organic diol: organic diamine) is 100: 1 to 1: 100, preferably 50 :.
It is 1 to 1:50, more preferably 10: 1 to 1:10.

In the polyurethane elastomer of the present invention, the hard segment means a hydrogen-bonding portion containing urethane and urea bonds, and organic diisocyanate, organic diol, and organic diamine portions correspond to this. The soft segment refers to a rubber-like matrix portion having no hydrogen bonding property, and the polyether diol portion corresponds to this. In the polyurethane elastomer of the present invention, the value of the molar ratio of hard segment / soft segment is 3 to 50 from the viewpoint of mechanical strength and antithrombotic property.
Is preferable, and 3-20 is more preferable.

By varying the mixing ratio of the organic diol and the organic diamine or the value of the molar ratio of the hard segment / soft segment within the above range, the mechanical properties required depending on the site where the medical device is used are optimized. It is also possible to do so.

In the known polyurethane, the mixing ratio of the above-mentioned components is usually about 2 mol of the organic diisocyanate component and about 1 mol of the organic diol (or organic diamine) component per 1 mol of the polyether diol component. In this case, the hard segment / soft segment molar ratio is about 3), but in the present invention, the organic diisocyanate component is 2 to 90 moles, the organic diol component is 1 to 80 moles, and the organic diamine component is per 1 mole of the polyether diol component. It is preferably in the range of 1 to 80 mol, and the organic diisocyanate component 2.5 to 20 mol, the organic diol component 1.5 to 15 mol, and the organic diamine component 1.
It is more preferably 5 to 15 mol.

The polyurethane elastomer may be produced by a method known per se. For example, it is manufactured as follows. ABA of polyoxyethylene (A) and polyoxytetramethylene (B) which are polyether diol components
The required amounts of the mold block copolymer and the organic diisocyanate are added to the reaction solvent and heated to 50 to 100 ° C. for reaction. As the reaction solvent at this time, for example, N, N-dimethylacetamide, dimethylsulfoxide, dibutyl ether, dimethylformamide and the like are used. Also,
If a reaction accelerator such as 1,8-diazabicyclo [5.4.0] undecene-7 or dioctyltin dilaurate is used, the reaction can be carried out near room temperature. Next, the desired amount of organic diol and organic diamine are added to the prepolymer thus obtained, and a chain extension reaction is carried out at around room temperature to obtain the desired polyurethane elastomer.

The medical device of the present invention is preferably one that can be brought into contact with blood. Specifically, for example, a vascular catheter, an AV shunt for an artificial kidney, an artificial heart-lung membrane, an artificial blood vessel, Examples include artificial heart blood pumps, aortic balloon pumps, heart catheters, blood bags, and the like.

[0031]

EXAMPLES Examples will be given below to explain the present invention in detail, but the present invention is not limited to these examples.

Example 1 Commercially available polyoxytetramethylene glycol (PTM
G, number average molecular weight 1830) and metallic potassium in a slight excess over the theoretical amount are reacted at 130 ° C. for 4 hours in a dry air flow, and P
The potassium alcoholate of TMG was produced. The reaction system solidifies when cooled. To this, ethylene oxide (EO) was charged during cooling so that the polyoxyethylene content in the polyether diol after polymerization was 30 mol%,
Using PTMG potassium alcoholate as a polymerization initiator,
EO was polymerized at 45 ° C. for 4 hours. Then, dilute with benzene, add hydrochloric acid isopropanol to stop the polymerization, filter the potassium chloride produced, and use benzene, isopropanol, hydrochloric acid, and hydrochloric acid with a rotary evaporator.
The water was removed. Further extraction with diethyl ether, EO
Was removed and dried under reduced pressure to obtain a polyether diol. 0.02 mol of this polyether diol and 0.04 mol of 4,4'-diphenylmethane diisocyanate were uniformly dissolved in 200 ml of dimethyl sulfoxide, and after reacting for 5 hours while stirring at 80 ° C while introducing dry nitrogen gas. , Cooled. To this reaction liquid, 150 ml of a solution of dimethyl sulfoxide containing 0.018 mol of ethylene glycol and 0.002 mol of ethylenediamine was added dropwise, and the mixture was stirred at room temperature to 30 ° C. for 7 hours for reaction. The reaction solution was poured into water to precipitate the formed polyurethane, which was filtered off. Further, a low molecular weight compound was removed with acetone using a Soxhlet extractor, and the rest was vacuum dried at room temperature to obtain a polyurethane elastomer.

Example 2 0.02 mol of the polyether diol prepared in Example 1, 4,4'-diphenylmethane diisocyanate
A polyurethane elastomer was obtained in the same manner as in Example 1, except that 04 mol, 0.01 mol of ethylene glycol and 0.01 mol of ethylenediamine were used.

Example 3 0.02 mol of the polyether diol prepared in Example 1, 4,4'-diphenylmethane diisocyanate
A polyurethane elastomer was obtained in the same manner as in Example 1, except that 04 mol, 0.002 mol of ethylene glycol and 0.018 mol of ethylenediamine were used.

Example 4 0.02 mol of the polyether diol prepared in Example 1, 4,4'-diphenylmethane diisocyanate
A polyurethane elastomer was obtained in the same manner as in Example 1, except that 06 mol, 0.126 mol of ethylene glycol and 0.014 mol of ethylenediamine were used.

Example 5 0.02 mol of the polyether diol prepared in Example 1, 4,4'-diphenylmethane diisocyanate
A polyurethane elastomer was obtained in the same manner as in Example 1 except that 06 mol, 0.07 mol of ethylene glycol and 0.07 mol of ethylenediamine were used.

Example 6 0.02 mol of the polyether diol prepared in Example 1, 4,4'-diphenylmethane diisocyanate
A polyurethane elastomer was obtained in the same manner as in Example 1, except that 06 mol, 0.014 mol of ethylene glycol and 0.126 mol of ethylenediamine were used.

Comparative Example 1 0.02 mol of the polyether diol prepared in Example 1, 4,4'-diphenylmethane diisocyanate
Using 04 mol and 0.02 mol of ethylene glycol,
A polyurethane elastomer was obtained in the same manner as in Example 1.

Comparative Example 2 0.02 mol of the polyether diol prepared in Example 1, 4,4'-diphenylmethane diisocyanate
A polyurethane elastomer was obtained in the same manner as in Example 1, except that 04 mol and 0.02 mol of ethylenediamine were used.

Experimental Example 1 A 10% dimethylacetamide solution of the polyurethane elastomers obtained in the above Examples and Comparative Examples was poured into a horizontal petri dish placed on a mercury plane, and the solvent was gradually evaporated under reduced pressure to obtain a uniform film. Was prepared. This thickness is about 0.
A 3 mm film was cut into strips and subjected to a tensile test according to the method described in JIS K6301 at 20 ° C. and a pulling speed of 50 mm / min to measure the tensile strength and elongation at break of the film. The results are shown in Table 1.

Experimental Example 2 1 ml of a 10% dimethylacetamide solution of the polyurethane elastomer obtained in the above Examples and Comparative Examples was placed in a test tube with an inner lid of 10 mm and a length of 10 cm, which was equipped with a lapping lid, and was connected to a rotary evaporator to reduce the pressure. The inner wall is evenly coated under rotation. Make 2 tubes for each sample, put 1 ml each of the blood of healthy person immediately after collection into them, and keep them at 37 ° C for 5 minutes. Observe the flow state by inclining the blood sample, perform the same operation for the other one after the blood stops flowing at all, and use the elapsed time from the time when the blood in the test tube stops flowing to the coagulation time of the sample. To do. Further, when two glass test tubes not coated with polyurethane elastomer were evaluated for coagulation time on the glass surface by the same operation as above, it was usually 8 to 14 minutes although there were individual differences. The coagulation time is defined as the average value of the values obtained by testing the glass and each sample five times or more. As an index of antithrombogenicity, the coagulation time on the glass surface was set to 1 and the relative values of the coagulation time of each polyurethane elastomer were compared. The results are shown in Table 1.

[0042]

[Table 1]

Example 7 A polished stainless rod having a diameter of 4 mm was immersed in a 10% dimethylacetamide solution of the polyurethane elastomer of Example 1 and taken out and dried at 60 ° C. to form a polyurethane film on the surface of the rod. After adjusting the thickness to a desired thickness, the stainless steel rod was removed by immersing in ethanol to obtain an antithrombogenic tube (artificial blood vessel).

Example 8 An antithrombogenic tube was obtained in the same manner as in Example 7 except that the polyurethane elastomer of Example 6 was used.

[0045]

INDUSTRIAL APPLICABILITY The antithrombogenic polyurethane elastomer of the present invention and the medical device comprising the polyurethane elastomer are at least equivalent to the conventional antithrombogenicity and several times superior in mechanical strength.

Claims (2)

[Claims] 1. A polyether diol component of an ABA type block copolymer of polyoxyethylene (A) and polyoxytetramethylene (B), an organic diisocyanate, and an organic diol and an organic diamine as a chain extender. An antithrombogenic polyurethane elastomer comprising: 2. A medical device comprising the antithrombogenic polyurethane elastomer according to claim 1.