This is application claims priority to JP 2022-141908 filed Sep. 7, 2022. The disclosure of the prior application is hereby incorporated by reference herein in its entirety.
The technology disclosed herein relates to a catheter.
A catheter is an elongated medical device to be inserted for use into a biological lumen such as a blood vessel to diagnose or treat the biological lumen.
A catheter having two or more lumens is known for the purposes such as for improving the vascular selectivity of a guide wire. For example, a catheter of this type has a configuration in which a plurality of inner tubes each having a lumen are inserted into an outer tube and welded to the outer tube (for example, see Patent Document 1). When the tubes of the catheter are welded together, the wall thickness of the tubes may become thinner and the strength of the tubes may be decreased. Reduced strength of the tubes each having a lumen may, for example, cause a guide wire to unintentionally protrude out of a lumen.
Conventionally, a catheter having a protective film placed between an inner tube and an outer tube or between a plurality of inner tubes has been proposed to prevent decreased wall thickness due to inter-tube welding.
In the aforementioned configurations of the conventional catheters, there is room for improving the strength of a tube having a lumen.
Disclosed herein is a technology which can solve the above problem.
The technology disclosed herein can be implemented, for example, according to the following aspects.
(1) A catheter disclosed herein comprises a first tube having a first lumen, and a second tube having a second lumen. The first tube has an inner layer corresponding to the innermost layer of the first tube, an outer layer surrounding the inner layer, and a reinforcing layer sandwiched between the inner and the outer layer.
According to the present catheter, the strength of the first tube having the first lumen can be improved by means of the reinforcing layer sandwiched between the inner layer and the outer layer. This can, for example, prevent a guide wire from unintentionally protruding out of the first lumen, or can prevent a guide wire from being stuck due to a collapse of the first lumen.
(2) The above catheter may further comprise a connecting layer covering at least a portion of outer peripheral surfaces of the first tube and the second tube to connect the first tube and the second tube, and having a melting point lower than those of the inner layer and the outer layer. This configuration can prevent the inner layer and the outer layer for the first tube from becoming thinner due to welding, effectively increasing the strength of the first tube, and can also prevent the reinforcing layer sandwiched between the inner layer and the outer layer from being exposed.
(3) In the above catheter, an outer periphery of the catheter may be elliptical in a transverse section. This configuration can improve the passability through a lesion site and the operability of a concomitantly-used device as compared to a configuration in which an outer periphery is circular in a transverse section.
(4) In the above catheter, the reinforcing layer may be a coil. This configuration enables the coil as a reinforcing layer to improve the strength of the first tube while ensuring the flexibility required for the catheter.
(5) In the above catheter, the reinforcing layer may be a first reinforcing layer, and the inner layer may be a first inner layer, and the outer layer may be a first outer layer, and the second tube may have a second inner layer corresponding to the innermost layer of the second tube, a second outer layer surrounding the second inner layer, and a second reinforcing layer sandwiched between the second inner layer and the second outer layer. This configuration can improve the strength of the second tube having the second lumen by means of the second reinforcing layer sandwiched between the second inner layer and the second outer layer. This can, for example, prevent a guide wire from unintentionally protruding out of the second lumen, or can prevent a guide wire from being stuck due to a collapse of the second lumen.
The technology disclosed herein can be implemented according to various aspects, for example, according to the aspects of catheters, medical devices including catheters, methods of manufacturing them or methods of using them, and the like.
The catheter 10 is an elongated medical device to be inserted for use into a biological lumen such as a blood vessel to diagnose or treat the biological lumen. As shown in
The shaft 20 is an elongated tubular member. As shown in
Two lumens (a first lumen L1 and a second lumen L2) extending along the longitudinal direction of the shaft 20 are formed in the shaft 20. The first lumen L1 is a lumen for a guide wire. The second lumen L2 is a lumen for a guide wire. An opening 116 at the distal end side of the first lumen L1 is arranged at the distal end of the shaft 20 and connected to the distal tip 30, while an opening 117 at the proximal end side of the first lumen L1 is arranged on the peripheral wall at the middle portion of the shaft 20 and is open to the outside of the catheter 10. That is, the first lumen L1 is a lumen of the rapid exchange (RX) type formed in a region from the distal end portion to the middle portion of the shaft 20. Meanwhile, an opening 126 at the distal end side of the second lumen L2 is arranged at the distal end portion of the shaft 20, and an opening 127 at the proximal end side of the second lumen L2 is arranged at the proximal end of the shaft 20, and connected to the connector 40. That is, the second lumen L2 is a lumen of the over-the-wire (OTW) type formed throughout substantially the entire length (a region from the distal end portion to the proximal end portion) of the shaft 20. The configuration of the shaft 20 will be described in detail below.
The distal tip 30 is a tubular (hollow) member, and joined to the distal end of the shaft 20. A method of joining the distal tip 30 to the shaft 20 may be, for example, welding, adhesion by adhesives, or the like. An inner cavity extending in the longitudinal direction of the catheter 10 is formed in the distal tip 30, and the inner cavity is in communication with the first lumen L1 formed in the shaft 20. The distal tip 30, for example, is tapered with the outer diameter decreasing progressively toward the distal end side.
As a material for the distal tip 30, resin materials may be used, for example, polyurethane, polyurethane elastomer, polyamide, and polyamide elastomer, and the like. Powders of radiopaque materials (e.g., tungsten, gold, platinum, and the like) may be mixed with these resin materials to make the resins visible under exposure of X-rays. Alternatively, a marker formed of a radiopaque material may be provided in the distal tip 30.
The connector 40 is a member to be held by an operator such as a medical practitioner, and connected to the proximal end of the shaft 20. An inner cavity extending in the longitudinal direction of the catheter 10 is formed in the connector 40, and the inner cavity is in communication with the second lumen L2 formed in the shaft 20.
Next, the configuration of the shaft 20 will be described in more detail. The shaft 20 has a first tube 110, a second tube 120, and a connection layer 130.
The first tube 110 is a tubular member having the first lumen L1. The first tube 110 is arranged in a region from the distal end portion to the middle portion of the shaft 20. Consequently, the first lumen L1 is formed in the region from the distal end portion to the middle portion of the shaft 20, as described above.
As shown in
The second tube 120 is a tubular member having the second lumen L2. The second tube 120 is arranged throughout substantially the entire length (a region from the distal end portion to the proximal end portion) of the shaft 20. Consequently, the second lumen L2 is formed throughout substantially the entire length of the shaft 20, as described above.
As shown in
As shown in
As materials for the first inner layer 111 and the first outer layer 112 of the first tube 110, and the second inner layer 121 and the second outer layer 122 of the second tube 120, resin materials may be used, for example, polyimide, polyamide, polyamide elastomer, polyolefin, polyester, polyester elastomer, nylon, polytetrafluoroethylene, and the like. The materials of the above layers may be the same or different from each other. As materials for the first reinforcing layer 113 and the second reinforcing layer 123, for example, metal materials such as stainless steel and Ni—Ti alloys, and resin materials such as PEEK may be used.
The connection layer 130 is a layer covering at least a portion of the outer peripheral surfaces of the first tube 110 and the second tube 120 to connect the first tube 110 and the second tube 120. As shown in
As a material for the connection layer 130, resin materials may be used, for example, polyamide, polyamide elastomer, polyolefin, polyester, polyester elastomer, nylon, and the like. It is noted that the melting point of the connection layer 130 is preferably lower than a melting point of each of the first inner layer 111 and the first outer layer 112 of the first tube 110 and the second inner layer 121 and the second outer layer 122 of the second tube 120. As a material for the core wire 50, metal materials may be used, for example, stainless steel, Ni—Ti alloys, cobalt-chromium alloys, and the like.
The shaft 20 having such a configuration can be, for example, manufactured as follows. First, a cored bar is coated with the first inner layer 111 for the first tube 110, and a coil as the first reinforcing layer 113 is wound around the outer peripheral surface of the first inner layer 111. Then, the first inner layer 111 and the first reinforcing layer 113 are coated and covered with the first outer layer 112, and the first outer layer 112 welded under compression with a contraction tube. Thereby, the first tube 110 is formed having a configuration in which the first reinforcing layer 113 is sandwiched between the first inner layer 111 and the first outer layer 112. The second tube 120 is prepared by an analogous method.
Next, the first tube 110, the second tube 120, and the core wire 50 are coated and integrally covered with a material for forming the connection layer 130, and the material welded under compression with a contraction tube. Thereby, the connection layer 130 is formed covering at least a portion of the outer peripheral surfaces of the first tube 110 and the second tube 120 to connect the first tube 110 and the second tube 120. The welding temperature at this time is set to, for example, a temperature higher than the melting point of the connection layer 130, but lower than the melting points of the first inner layer 111 and the first outer layer 112 for first tube 110 and the second inner layer 121 and the second outer layer 122 for second tube 120. When the welding temperature is set in this manner, the first inner layer 111 and the first outer layer 112 for the first tube 110 and the second inner layer 121 and the second outer layer 122 for the second tube 120 can maintain their shapes (outer diameter and wall thickness) during welding without melting. On the other hand, the connection layer 130 melts, and flows out from the both ends in a direction where the first tube 110 and the second tube 120 are aligned side by side (the Y-axis direction) as shown in
As described above, the catheter 10 according to the present embodiment comprises the first tube 110 having the first lumen L1, and the second tube 120 having the second lumen L2. The first tube 110 has the first inner layer 111 corresponding to the innermost layer of the first tube 110, the first outer layer 112 surrounding the first inner layer 111, and the first reinforcing layer 113 sandwiched between the first inner layer 111 and the first outer layer 112.
In the catheter 10 according to the present embodiment, the first reinforcing layer 113 sandwiched between the first inner layer 111 and the first outer layer 112 can improve the strength of the first tube 110 having the first lumen L1 as described above. This can, for example, prevent a guide wire from unintentionally protruding out of the first lumen L1, or can prevent a guide wire from being stuck due to a collapse of the first lumen.
The catheter 10 according to the present embodiment further comprises the connection layer 130. The connection layer 130 covers at least a portion of the outer peripheral surfaces of the first tube 110 and the second tube 120 to connect the first tube 110 and the second tube 120. The melting point of the connection layer 130 is lower than those of the first inner layer 111 and the first outer layer 112 for first tube 110. Therefore, the catheter 10 according to the present embodiment can prevent the first inner layer 111 and the first outer layer 112 for the first tube 110 from becoming thinner due to welding, effectively increasing the strength of the first tube 110, and can also prevent the first reinforcing layer 113 sandwiched between the first inner layer 111 and the first outer layer 112 from being exposed.
Moreover, in the catheter 10 according to the present embodiment, the outer periphery of the catheter 10 is elliptical in a transverse section. In the catheter 10 according to the present embodiment, this can improve the passability through a lesion site and the operability of a concomitantly-used device as compared to a configuration in which an outer periphery is circular in a transverse section.
Furthermore, in the catheter 10 according to the present embodiment, the first reinforcing layer 113 is a coil. Therefore, in the catheter 10 according to the present embodiment, the coil as the first reinforcing layer 113 can improve the strength of the first tube 110 while ensuring the flexibility required for the catheter 10.
In the catheter 10 according to the present embodiment, the second tube 120 has the second inner layer 121 corresponding to the innermost layer of the second tube 120, the second outer layer 122 surrounding the second inner layer 121, and the second reinforcing layer 123 sandwiched between the second inner layer 121 and the second outer layer 122. Therefore, in the catheter 10 according to the present embodiment, the second reinforcing layer 123 sandwiched between the second inner layer 121 and the second outer layer 122 can improve the strength of the second tube 120 having the second lumen L2. This can, for example, prevent a guide wire from unintentionally protruding out of the second lumen L2, or can prevent a guide wire from being stuck due to a collapse of the second lumen L2.
The technology disclosed herein is not limited to those embodiments as described above, and can be modified to various forms without departing the spirit of the present disclosure. For example, the following modifications are possible.
The configurations of the catheter 10 in the above embodiments are merely illustrative, and can be modified in various ways. For example, in the above embodiments, the first reinforcing layer 113 for the first tube 110 and the second reinforcing layer 123 for the second tube 120 are sparsely wound coils, but the first reinforcing layers 113 and the second reinforcing layer 123 may be tightly wound coils or may be in the forms other than coils (such as braids or tubes).
In the above embodiments, the outer periphery of the catheter 10 in a transverse section is elliptical, but the outer periphery may have a different shape (for example, a circular shape). In the above embodiments, the outer and inner diameters of the first tube 110 and the second tube 120 are substantially the same to each other, but they may be different from each other.
In the above embodiments, both the first tube 110 and the second tube 120 are configured each to have a reinforcing layer sandwiched between an inner layer and an outer layer, but only one of the first tube 110 and the second tube 120 may have such a configuration.
In the above embodiments, the catheter 10 has two lumens, but the catheter 10 may have three or more lumens. In such a case, the strength of the resulting tube can be improved when at least one of the three or more lumens is configured to have a reinforcing layer sandwiched between an inner layer and an outer layer. At least any one of the lumens may not be for a guide wire. For example, a certain lumen may serve as a flow path of a fluid (for example, a drug liquid).
According to the above embodiments, the core wire 50 is embedded in the connection layer 130, but the core wire 50 may be omitted.
In the above embodiments, the technology disclosed herein is described with reference to the catheter 10 to be inserted into a blood vessel as an example, but the technology disclosed herein can equally be applicable to catheters in general to be inserted into a biological lumen (digestive organs such as bile duct, gallbladder, pancreas, esophagus, duodenum, small intestine, and large intestine; blood vessel; urinary tract; trachea; and the like).
Number | Date | Country | Kind |
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2022-141908 | Sep 2022 | JP | national |