CATHETER AND CHOKE CATHETER
20240001090 ยท 2024-01-04
Inventors
Cpc classification
A61M2025/1079
HUMAN NECESSITIES
A61M25/005
HUMAN NECESSITIES
International classification
Abstract
A catheter includes a tubular component (100) and a functional component. The tubular component (100) includes an outer tube (101) and an inner tube (102). The outer tube (101) is sleeved over the inner tube (102), and a first lumen is formed between the outer tube (101) and the inner tube (102). The outer tube (101) includes an outer tube main segment (1011) and a first recess (1012). The first recess (1012) is located at a distal end of the outer tube main segment (1011). The functional component is disposed on the tubular component (100) and is at least partially connected to the first recess (1012). This arrangement imparts increased compatibility and higher accessibility to the catheter with the functional component.
Claims
1. A catheter, comprising a tubular component and a functional component, wherein the tubular component comprises an outer tube and an inner tube, wherein the outer tube is sleeved over the inner tube, and a first lumen is formed between the outer and inner tubes, wherein the outer tube comprises an outer tube main segment and a first recess, and wherein the first recess is located at a distal end of the outer tube main segment, and wherein the functional component is disposed on the tubular component and is at least partially connected to the first recess.
2. The catheter of claim 1, wherein the functional component is at least one of an occlusion component, a radiopaque component, an electronic element and a thrombus removal element.
3. The catheter of claim 1, wherein the first recess is formed by an inward recess in an outer surface of the outer tube, and wherein an inner diameter of the first recess is smaller than or equal to an inner diameter of the outer tube main segment; or wherein the first recess is formed by an outward recess in an inner surface of the outer tube, and wherein an outer diameter of the first recess is smaller than or equal to an outer diameter of the outer tube main segment; and/or wherein the first recess has an axial length of 2-30 mm.
4. (canceled)
5. (canceled)
6. (canceled)
7. (canceled)
8. The catheter of claim 1, wherein the first recess comprises a first transition section and a first straight section from a proximal end to a distal end thereof, and wherein the first transition section is a diameter-varying section where at least one of an inner diameter and an outer diameter of the outer tube increases or decreases.
9. The catheter of claim 8, wherein the first transition section has an axial length of 0 mm to 10 mm; and/or wherein an inner surface and/or an outer surface of the first transition section is/are each inclined at an angle of 0-90 with respect to an axis of the outer tube main segment, and wherein the inner and outer surfaces of the first transition section are inclined at a same angle with respect to the axis of the outer tube main segment; and/or wherein a ratio of an outer diameter of the first straight section to an outer diameter of the outer tube main segment is 0.7-1.0, and wherein the outer diameter of the outer tube main segment is 1.0 mm to 3.7 mm, and wherein the outer diameter of the first straight section is 0.7 mm to 3.5 mm.
10. (canceled)
11. (canceled)
12. (canceled)
13. (canceled)
14. The catheter of claim 1, wherein the outer tube further comprises an outer-tube distal section located at a distal end of the first recess, wherein an outer diameter of the outer-tube distal section at a proximal end thereof is greater than an outer diameter of the first recess at the distal end thereof, and wherein the outer-tube distal section is fixedly connected to the inner tube at a distal location, wherein the outer-tube distal section comprises a second transition section and a second straight section from a proximal end to a distal end thereof, and wherein the second transition section is a diameter-varying section where at least one of an inner diameter and an outer diameter of the outer tube increases or decreases.
15. (canceled)
16. The catheter of claim 1, wherein the inner tube comprises an inner tube main segment and a second recess, wherein the second recess is located at a distal end of the inner tube main segment, and wherein the second recess is formed by an inward recess in an outer surface of the inner tube.
17. The catheter of claim 16, wherein the second recess comprises a third transition section and a third straight section from a proximal end to a distal end thereof, and wherein the third transition section is a diameter-varying section where an outer diameter of the inner tube decreases; and/or wherein the second recess has an axial length of 2-60 mm.
18. (canceled)
19. The catheter of claim 17, wherein an outer surface of the third transition section is inclined at an angle of 0-90 with respect to an axis of the inner tube main segment, and wherein the third transition section has an axial length of 0-10 mm; and/or wherein a ratio of an outer diameter of the third straight section to an outer diameter of the inner tube main segment is greater than or equal to 0.6 and is smaller than 1.0, wherein the outer diameter of the inner tube main segment is 0.5 mm to 3.2 mm, and wherein the outer diameter of the third straight section is greater than or equal to 0.3 mm and is smaller than 3.2 mm; and/or wherein a most distal end of the outer tube main segment forms a first transition location, and wherein a most distal end of the inner tube main segment forms a second transition location, and wherein a projection of the first transition location on the axis of the tubular component is distal with respect to a projection of the second transition location on the axis of the tubular component; wherein the first recess comprises a first transition section and a first straight section from a proximal end to a distal thereof; and wherein an outer surface of the third transition section is inclined at a first angle with respect to the axis of the tubular component, wherein an inner surface of the first transition section is inclined at a second angle with respect to the axis of the tubular component, and wherein the first angle is greater than or equal to the second angle.
20. (canceled)
21. (canceled)
22. (canceled)
23. The catheter of claim 16, wherein the inner tube further comprises an inner-tube distal section located at a distal end of the second recess.
24. The catheter of claim 23, wherein the inner-tube distal section has an axial length of 1-500 mm; and/or wherein an outer diameter of the inner-tube distal section is smaller than an outer diameter of the second recess, and wherein the inner-tube distal section is disposed at a head portion of the catheter; and/or wherein the inner-tube distal section comprises a fourth transition section and a fourth straight section from a proximal end to a distal end thereof, wherein the fourth transition section is a diameter-varying section where an outer diameter of the inner tube decreases, and wherein the fourth straight section has an outer diameter of 0.2 mm to 3.1 mm.
25. (canceled)
26. (canceled)
27. (canceled)
28. The catheter of claim 2, wherein the functional component is an occlusion component, and wherein a proximal end of the occlusion component is secured to the first recess.
29. The catheter of claim 28, wherein the occlusion component is a polymer film, wherein the occlusion component is in an expanded configuration when the first lumen is filled with a liquid, and wherein the occlusion component is in a collapsed configuration when the first lumen is in a vacuum; and/or wherein a distal end of the occlusion component is fixedly connected to the inner tube, or wherein the occlusion component is disposed on the first recess and each of a proximal end and the distal end of the occlusion component is fixedly connected to the outer tube, wherein a distal end of the outer tube is connected to the inner tube, and wherein the first recess is provided with liquid passage apertures for dilation of the occlusion component with a liquid.
30. (canceled)
31. (canceled)
32. The catheter of claim 1, wherein the inner tube comprises an inner tube main segment and a second recess, wherein the second recess is disposed at a distal end of the inner tube main segment, and wherein the second recess has an outer diameter smaller than an outer diameter of the inner tube main segment, wherein the functional component is an occlusion component, and wherein a proximal end of the occlusion component is fixedly connected to the first recess and a distal end of the occlusion component is fixedly connected the second recess.
33. The catheter of claim 1, wherein each of the inner and outer tubes comprises at least one polymer layer made of one or more of polyether block amide, nylon, polyurethane, polytrafluoroethylene, polyethylene and polyolefin elastomer, wherein the outer tube and/or the inner tube further comprise(s) reinforcing layer(s), wherein the reinforcing layer is a structure braided from filaments, a structure consisting of spirally wound filaments, a cut tube or a combination thereof, wherein the reinforcing layer is made of stainless steel, a nickel-titanium alloy, a cobalt-chromium alloy or a polymer, and wherein the outer tube and/or the inner tube is/are triple-layered structure(s) each consisting of an innermost first polymer layer, an intermediate reinforcing layer and an outermost second polymer layer.
34. (canceled)
35. (canceled)
36. The catheter of claim 1, further comprising: a first radiopaque ring disposed at a head portion of the catheter; and/or a second radiopaque ring disposed at a location on the inner tube, wherein the second radiopaque ring is adapted to a location of the functional component.
37. The catheter of claim 1, wherein the inner tube is provided with a second lumen having a constant inner diameter across an entire length thereof, wherein a ratio of the inner diameter of the second lumen to an outer diameter of the outer tube main segment is 0.2-0.9, wherein the inner diameter of the second lumen is 0.1 mm to 3.0 mm, and wherein the outer diameter of the outer tube main segment is 0.5 mm to 3.7 mm.
38. (canceled)
39. (canceled)
40. The catheter of claim 1, wherein the first recess has a tapered outer surface with a gradually decreasing outer diameter, wherein a proximal end of the functional component is secured to the tapered surface of the first recess, wherein a distal end face of the outer tube is a first beveled surface forming the outer surface of the first recess, and wherein the functional component forms at a proximal end thereof a second beveled surface mating with and fixedly connected to the first beveled surface.
41. (canceled)
42. An occlusion catheter, comprising a tubular component and an occlusion component, wherein the tubular component comprises an outer tube and an inner tube, wherein the outer tube is sleeved over the inner tube, and a first lumen is formed between the outer and inner tubes, wherein the outer tube comprises an outer tube main segment and a first recess, and wherein the first recess is located at a distal end of the outer tube main segment, and wherein the occlusion component is disposed on the tubular component and is at least partially connected to the first recess.
43. The occlusion catheter of claim 42, wherein the occlusion component is a polymer film, wherein the occlusion component is in an expanded configuration when the first lumen is filled with a liquid, and wherein the occlusion component is in a collapsed configuration when the first lumen is in a vacuum.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0063] Those of ordinary skill in the art would appreciate that the following drawings are presented merely to enable a better understanding of the present invention rather than limit the scope thereof in any sense. In the drawings,
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[0076] In these figures, [0077] 100, a tubular component; 200, an occlusion component; 101, an outer tube; 102, an inner tube; 1011, an outer tube main segment; 1012, a first recess; 1012-1, a first transition section; 1012-2, a first straight section; 1013, an outer-tube distal section; 1013-1, a second transition section; 1013-2, a second straight section; 1014, liquid passage apertures; 1021, an inner tube main segment; 1022, a second recess; 1022-1, a third transition section; 1022-2, a third straight section; 1023, an inner-tube distal section; 1023-1, a fourth transition section; 1023-2, a fourth straight section; 300, a first transition location; and 400, a second transition location.
DETAILED DESCRIPTION
[0078] Objects, advantages and features of the present invention will become more apparent from the following more detailed description of particular embodiments made in conjunction with the accompanying drawings. Note that the figures are provided in a very simplified form not necessarily drawn to exact scale for the only purpose of helping to explain the disclosed embodiments in a more convenient and clearer way. In addition, structures shown in the figures are usually a part of actual structures. In particular, as the figures tend to have distinct emphases, they are often drawn to different scales.
[0079] As used herein and in the appended claims, the singular forms a, an and the include plural referents unless the context clearly dictates otherwise. As used herein and in the appended claims, the term or is employed in the sense including and/or unless the context clearly dictates otherwise. Additionally, the terms proximal and distal are generally used to refer to an end closer to an operator and an end closer to a lesion site in a patient, respectively.
[0080] In principle, the present invention is intended to provide a catheter, including a tubular component and a functional component, the tubular component including an outer tube and an inner tube, the outer tube sleeved over the inner tube, and a first lumen formed between the outer and inner tubes, the outer tube including an outer tube main segment and a first recess located at a distal end of the outer tube main segment, the functional component disposed on the tubular component and at least partially connected to the first recess. The functional component may be any component disposed on the catheter to perform a medical function, such as an occlusion, radiopaque, electronic, thrombus removal or other component. The functional component may be connected to the catheter at one end and free at the other end. Alternatively, it may be connected to the catheter at both ends. Still alternatively, it may be overall secured to the catheter. Structural details of the catheter of the present invention will be described in detail below with reference to the following embodiments, in which an occlusion component is described as a representative example of the functional component. Other types of the functional component may have similar relationships with the catheter to that of the occlusion component.
[0081] A more detailed description is set forth with reference to the accompanying drawings.
Embodiment 1
[0082] In a first embodiment of the present invention, there is provided a catheter.
[0083] In Embodiment 1, the first recess 1012 is formed by an inward recess in an outer surface of the outer tube 101. In some other embodiments, it may be formed by an outward recess in an inner surface of the outer tube 101.
[0084] In Embodiment 1, an outer diameter of the first recess 1012 is smaller than an outer diameter of the outer tube main segment 1011, and an inner diameter of the first recess 1012 is smaller than an inner diameter of the outer tube main segment 1011. A proximal end of the occlusion component 200 is secured to an outer surface of the first recess 1012. In some other embodiments, the outer diameter of the first recess 1012 may be smaller than the outer diameter of the outer tube main segment 1011, and the inner diameter of the first recess 1012 may be equal to the inner diameter of the outer tube main segment 1011, with a proximal end of the occlusion component 200 being secured to the outer surface of the first recess 1012. In some other embodiments, the outer diameter of the first recess 1012 may be equal to the outer diameter of the outer tube main segment 1011, and the inner diameter of the first recess 1012 may be greater than the inner diameter of the outer tube main segment 1011, with a proximal end of the occlusion component 200 being secured to an inner surface of the first recess 1012. In some other embodiments, the outer diameter of the first recess 1012 may be smaller than the outer diameter of the outer tube main segment 1011, and the inner diameter of the first recess 1012 may be greater than the inner diameter of the outer tube main segment 1011, with a proximal end of the occlusion component 200 being secured to the inner or outer surface of the first recess 1012.
[0085] In each case, the first recess 1012 has an axial length of 2-20 mm. In Embodiment 1, the axial length of the first recess 1012 is 12 mm. In some other embodiments, the axial length of the first recess 1012 may be 2 mm. In some other embodiments, the axial length of the first recess 1012 may be 5 mm. In some other embodiments, the axial length of the first recess 1012 may be 10 mm. In some other embodiments, the axial length of the first recess 1012 may be 15 mm. In some other embodiments, the axial length of the first recess 1012 may be 20 mm. The recess provided in the outer tube 101 of the catheter can accommodate at least a part of the occlusion component 200, allowing a reduced joint thickness which can partially or completely eliminate the influence of the occlusion component on the catheter's hardness. In this way, it can be ensured that the catheter has sufficient flexibility that allows its smooth advancement through a blood vessel. Moreover, the catheter is allowed to have a reduced overall thickness, which enables the catheter to have a sufficiently large inner cavity but not an excessive outer diameter. Thus, relatively large medical devices can be delivered through the catheter's inner cavity, and the catheter itself can be smoothly advanced within a tortuous blood vessel while less stimulating the wall thereof to access a relatively distal location in the blood vessel.
[0086] As shown in
[0087] As shown in
[0088] In each case, the outer diameter of the outer tube main segment 1011 is 1.0 mm to 3.7 mm, the outer diameter of the first straight section 1012-2 is 0.7 mm to 3.5 mm, and a ratio of the outer diameter of the first straight section 1012-2 to the outer diameter of the outer tube main segment 1011 is 0.7-1.0. In Embodiment 1, the outer diameter of the outer tube main segment 1011 is 2.8 mm, the outer diameter of the first straight section 1012-2 is 2.6 mm, and the ratio of the outer diameter of the first straight section 1012-2 to the outer diameter of the outer tube main segment 1011 is 0.928. In some other embodiments, the outer diameter of the outer tube main segment 1011 may be 3.7 mm, the outer diameter of the first straight section 1012-2 may be 2.8 mm, and the ratio of the outer diameter of the first straight section 1012-2 to the outer diameter of the outer tube main segment 1011 may be 0.757. In some other embodiments, the outer diameter of the outer tube main segment 1011 may be 3.5 mm, the outer diameter of the first straight section may be 3.5 mm, and the ratio of the outer diameter of the first straight section 1012-2 to the outer diameter of the outer tube main segment 1011 may be 1.0. In some other embodiments, the outer diameter of the outer tube main segment 1011 may be 1.0 mm, the outer diameter of the first straight section 1012-2 may be 0.7 mm, and the ratio of the outer diameter of the first straight section 1012-2 to the outer diameter of the outer tube main segment 1011 may be 0.7.
[0089] In each case, the catheter has an overall length of 80-160 cm. In Embodiment 1, the overall length of the catheter is 130 cm. In some other embodiments, the overall length of the catheter may be 80 cm. In some other embodiments, the overall length of the catheter may be 160 cm. In some other embodiments, the overall length of the catheter may be 115 cm. In some other embodiments, the overall length of the catheter may be 110 cm. In some other embodiments, the overall length of the catheter may be 140 cm. In some other embodiments, the overall length of the catheter may be 150 cm.
[0090] In Embodiment 1, the occlusion component 200 is a polymer film. The first lumen is configured for passage or suction of a liquid therethrough, which can cause a switch of the occlusion component 200 between the expanded and collapsed configurations. The liquid that can be passed or sucked through the first lumen may be, for example, a contrast fluid, a physiological saline solution or the like. Filling the first lumen with the liquid can bring the occlusion component 200 into the expanded configuration. Emptying the first lumen can bring the occlusion component 200 into the collapsed configuration. In Embodiment 1, the polymer film has a thickness of 0.10 mm. In some other embodiments, the thickness of the polymer film may be 0.05 mm to 0.15 mm, such as 0.05 mm, 0.08 mm, 0.12 mm or 0.15 mm. In Embodiment 1, the polymer film is made of silicone. In some other embodiments, the polymer film may be made of polyurethane (PU). In some other embodiments, the polymer film may be made of latex. In some other embodiments, the polymer film may be made of polyethylene (PE). In some other embodiments, the polymer film may be made of polytrafluoroethylene (PTFE). In some other embodiments, the polymer film may be made of expanded PTFE (ePTFE). In some other embodiments, the polymer film may be made of PU and PE mixed at a ratio of 2:1. In some other embodiments, the polymer film may be made of PTFE and ePTFE mixed at a ratio of 1:1. In some other embodiments, the polymer film may be made of silicone, PU and PE mixed at a ratio of 1:1:1. In Embodiment 1, a proximal end of the occlusion component 200 is connected to the first straight section 1012-2, for example, by gluing, bonding or fusion. In some other embodiments, a proximal end of the occlusion component 200 may be connected to the first transition section 1012-1, for example, by gluing, bonding or fusion.
[0091] In Embodiment 1, the inner tube 102 is a triple-layered structure consisting of an innermost first polymer layer, an intermediate reinforcing layer and an outermost second polymer layer. The first polymer layer is made of PTFE, and the reinforcing layer is a structure braided from stainless steel filaments. The second polymer layer is composed of axially spliced polyether block amide (PEBA), nylon, PU, PE and polyolefin elastomer (POE). The outer tube 101 consists of a single polymer layer made of PEBA. In some other embodiments, both the inner tube 102 and the outer tube 101 may be triple-layered structures each consisting of an innermost first polymer layer, an intermediate reinforcing layer and an outermost second polymer layer. In some other embodiments, the inner tube 102 may be a single-layered polymer structure, and the outer tube 101 may be a triple-layered structure. In some other embodiments, the inner tube 102 may be a triple-layered structure, and the outer tube 101 may be a double-layered polymer structure. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each be a structure consisting of spirally wound filaments. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each be a cut tube. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each consist of both a structure braided from filament and a structure consisting of spirally wound filaments. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each consisting of a structure braided from filament and a cut tube. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each consist of a cut tube and a structure consisting of spirally wound filaments. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each be made of a material including a nickel-titanium (NiTi) alloy. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may be each made of a material including a cobalt-chromium (CoCr) alloy. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each be made of a material including a polymer. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each be made of both a NiTi alloy and stainless steel. In some other embodiments, the reinforcing layer(s) in the inner tube 102 and/or the outer tube 101 may each be made of both a NiTi alloy and a polymer.
[0092] In Embodiment 1, the catheter includes a first radiopaque ring disposed at a head portion of the catheter and a second radiopaque ring disposed at a location of the inner tube 102 that is adapted to the location of the occlusion component 200.
[0093] In Embodiment 1, the inner tube 102 of the catheter forms a second lumen therein, which has a constant inner diameter across its entire length. In each case, the second lumen has an inner diameter of 0.1 mm to 3.0 mm, and the outer diameter of the outer tube main segment 1011 is 0.5 mm to 3.7 mm. In Embodiment 1, the inner diameter of the second lumen is 2.3 mm, the outer diameter of the outer tube main segment 1011 is 2.8 mm, and a ratio of the inner diameter of the second lumen to the outer diameter of the outer tube main segment 1011 is 0.821. In some other embodiments, the inner diameter of the second lumen may be 0.1 mm, the outer diameter of the outer tube main segment 1011 may be 0.5 mm, and the ratio of the inner diameter of the second lumen to the outer diameter of the outer tube main segment 1011 may be 0.2. In some other embodiments, the inner diameter of the second lumen may be 3.0 mm, the outer diameter of the outer tube main segment 1011 may be 3.6 mm, and the ratio of the inner diameter of the second lumen to the outer diameter of the outer tube main segment 1011 may be 0.833. In some other embodiments, the inner diameter of the second lumen may be 2.7 mm, the outer diameter of the outer tube main segment 1011 may be 3.0 mm, and the ratio of the inner diameter of the second lumen to the outer diameter of the outer tube main segment 1011 may be 0.9. In some other embodiments, the inner diameter of the second lumen may be 2.5 mm, the outer diameter of the outer tube main segment 1011 may be 3.7 mm, and the ratio of the inner diameter of the second lumen to the outer diameter of the outer tube main segment 1011 may be 0.676, In Embodiment 1, the second lumen is configured for passage of a medical device therethrough.
[0094] In Embodiment 1, there are angled transitions between the outer tube main segment 1011 and the first recess 1012, and between the first transition section 1012-1 and the first straight section 1012-2. In some other embodiments, there may be smooth curved transition(s) between the outer tube main segment 1011 and first recess 1012, and/or between the first transition section 1012-1 and the first straight section 1012-2. In Embodiment 1, the first straight section 1012-2 has a flat, smooth surface. In some other embodiments, the first straight section 1012-2 may provide on its surface with convexities and concavities, grooves or curved portions, while having constant inner and outer diameters across its entire length.
Embodiment 2
[0095] In a second embodiment of the present invention, there is provided a catheter.
[0096] In each case, the second recess 1022 has an axial length of 2-60 mm. In Embodiment 2, the axial length of the second recess 1022 is 30 mm. In some other embodiments, the axial length of the second recess 1022 may be 2 mm. In some other embodiments, the axial length of the second recess 1022 may be 10 mm. In some other embodiments, the axial length of the second recess 1022 may be 25 mm. In some other embodiments, the axial length of the second recess 1022 may be 45 mm. In some other embodiments, the axial length of the second recess 1022 may be 60 mm.
[0097] As shown in
[0098] In some embodiments, the outer diameter of the inner tube main segment 1021 is 0.5 mm to 3.2 mm, the outer diameter of the third straight section 1022-2 is 0.3 mm to 3.2 mm, and a ratio of the outer diameter of the third straight section 1022-2 to the outer diameter of an outer tube main segment 1011 is 0.6-1.0. In Embodiment 2, the outer diameter of the inner tube main segment 1021 is 2.8 mm, the outer diameter of the third straight section 1022-2 is 2.4 mm, and the ratio of the outer diameter of the third straight section 1022-2 to the outer diameter of the outer tube main segment 1011 is 0.857. In some other embodiments, the outer diameter of the inner tube main segment 1021 may be 3.2 mm, the outer diameter of the third straight section 1022-2 may be 3.2 mm, and a ratio of the outer diameter of the third straight section 1022-2 to the outer diameter of the inner tube main segment 1021 may be 1.0. In some other embodiments, the outer diameter of the inner tube main segment 1021 may be 0.5 mm, the outer diameter of the third straight section 1022-2 may be 0.3 mm, and the ratio of the outer diameter of the third straight section 1022-2 to the outer diameter of the inner tube main segment 1021 may be 0.6. In some other embodiments, the outer diameter of the inner tube main segment 1021 may be 1.0 mm, the outer diameter of the third straight section 1022-2 may be 0.8 mm, and the ratio of the outer diameter of the third straight section 1022-2 to the outer diameter of the inner tube main segment 1021 may be 0.8. In some other embodiments, the outer diameter of the inner tube main segment 1021 may be 2.0 mm, the outer diameter of the third straight section 1022-2 may be 1.8 mm, and the ratio of the outer diameter of the third straight section 1022-2 to the outer diameter of the inner tube main segment 1021 may be 0.9.
[0099] As shown in
[0100] In Embodiment 2, both the inner tube 102 and the outer tube 101 are triple-layered structures each consisting of an innermost first polymer layer, an intermediate reinforcing layer and an outermost second polymer layer. The first polymer layer in the inner tube 102 is made of PTFE and POE. The reinforcing layer in the inner tube 102 is a structure consisting of spirally wound NiTi alloy filaments. The second polymer layer in the inner tube 102 is a structure consisting of axially spliced PEBA, nylon, PU, PTFE, PE, PEBA mixed with an additive resulting in a lower friction coefficient and POE. The first polymer in the outer tube 101 is made of PTFE. The reinforcing layer in the outer tube 101 is a structure braided from polymer filaments. The second polymer layer in the outer tube 101 is a structure consisting of axially spliced PEBA, nylon, PU, PE and POE.
[0101] In Embodiment 2, the catheter includes a first radiopaque ring disposed at an end of the catheter.
[0102] In Embodiment 2, there are angled transitions between the inner tube main segment 1021 and the second recess 1022, and between the third transition section 1022-1 and the third straight section 1022-2. In some other embodiments, there may be smooth curved transition(s) between the inner tube main segment 1021 and the second recess 1022, and/or between the third transition section 1022-1 and the third straight section 1022-2. In Embodiment 2, the third straight section 1022-2 has a flat, smooth surface. In some other embodiments, the third straight section 1022-2 may provide on its surface with convexities and concavities, grooves or curved portions, while having constant inner and outer diameters across its entire length.
Embodiment 3
[0103] In a third embodiment of the present invention, there is provided a catheter.
[0104] As shown in
[0105] In some other embodiments, the inner-tube distal section 1023 may include 2-10 transition sections and straight sections. The transition sections may alternate with the straight sections, resulting in a gradually decreasing outer diameter profile of the inner-tube distal section 1023. The outer diameter of the inner-tube distal section 1023 may gradually decrease from 3 mm at the proximal end to 0.6 mm at the distal end. In some other embodiments, the inner-tube distal section 1023 may include 5 alternating transition and straight sections, and the outer diameter of the inner-tube distal section 1023 may decrease from 2.7 mm at the proximal end to 0.9 mm at the distal end. In some other embodiments, the inner-tube distal section 1023 may include 10 alternating transition and straight sections, and the outer diameter of the inner-tube distal section 1023 may decrease from 3.0 mm at the proximal end to 0.6 mm at the distal end. In some other embodiments, the inner-tube distal section 1023 may include 2 alternating transition and straight sections, and the outer diameter of the inner-tube distal section 1023 may decrease from 2.4 mm at the proximal end to 1.65 mm at the distal end. In some other embodiments, the inner-tube distal section 1023 may be a taped tubular structure with a gradually decreasing outer diameter. In some embodiments, the outer diameter of the inner-tube distal section 1023 may decrease from 3 mm at the proximal end to 0.6 mm at the distal end. In some embodiments, the outer diameter of the inner-tube distal section 1023 may decrease from 2.5 mm at the proximal end to 0.6 mm at the distal end. In some embodiments, the outer diameter of the inner-tube distal section 1023 may decrease from 2 mm at the proximal end to 0.9 mm at the distal end.
[0106] In Embodiment 3, a projection of a first transition location 300 on an axis of a tubular component 100 is distal with respect to a projection of a second transition location 400 on the axis of the tubular component 100.
[0107] In Embodiment 3, the inner tube 102 is a triple-layered structure consisting of an innermost first polymer layer, an immediate reinforcing layer and an outermost second polymer layer. The outer tube 101 is a double-layered structure consisting of an outer polymer layer and an inner reinforcing layer. The reinforcing layer of the outer tube 101 is provided by a cut tube.
[0108] In Embodiment 3, the catheter includes a second radiopaque ring disposed at a location of the inner tube 102 that is adapted to the location of the occlusion component 200.
[0109] In Embodiment 3, there are angled transitions between the second recess 1022 and the inner-tube distal section 1023, and between the fourth transition section 1023-1 and the fourth straight section 1023-2. In some other embodiments, there may be smooth curved transition(s) between the second recess 1022 and the inner-tube distal section 1023, and/or between the fourth transition section 1023-1 and the fourth straight section 1023-2. In Embodiment 3, the fourth straight section 1023-2 has a flat, smooth surface. In some other embodiments, the fourth straight section 1023-2 may provide on its surface with convexities and concavities, grooves or curved portions, while having constant inner and outer diameters across its entire length.
Embodiment 4
[0110] In a fourth embodiment of the present invention, there is provided a catheter.
[0111] In Embodiment 4, a projection of a first transition location 300 on the axis of the tubular component 100 is distal with respect to a projection of a second transition location 400 on the axis of the tubular component 100.
[0112] In Embodiment 4, the inner tube 102 is a triple-layered structure consisting of an innermost first polymer layer, an immediate reinforcing layer and an outermost second polymer layer. The outer tube 101 is a double-layered structure consisting of an outer polymer layer and an inner reinforcing layer. The reinforcing layer of the outer tube 101 is provided by a cut tube.
[0113] In Embodiment 4, the catheter includes a first radiopaque ring disposed at a head portion of the catheter and second and third radiopaque rings disposed at locations of the inner tube 102 that are adapted to the location of the occlusion component 200. Specifically, the second radiopaque ring may be disposed at a distal end of the occlusion component 200, and the third radiopaque ring may be disposed at a proximal end of the occlusion component 200.
Embodiment 5
[0114] In a fifth embodiment of the present invention, there is provided a catheter.
[0115] In Embodiment 5, a projection of a first transition location 300 on the axis of the tubular component 100 is distal with respect to a projection of a second transition location 400 on the axis of the tubular component 100.
[0116] In Embodiment 5, the inner tube 102 is a double-layered structure consisting of an inner first polymer layer and an outer second polymer layer. The outer tube 101 is a single-layered polymer structure.
[0117] In Embodiment 5, the catheter includes second and third radiopaque rings disposed at locations of the inner tube 102 that are adapted to the location of the occlusion component 200. Specifically, the second radiopaque ring may be disposed at a distal end of the occlusion component 200, and the third radiopaque ring may be disposed at a proximal end of the occlusion component 200.
[0118] As shown in
Embodiment 6
[0119] In a sixth embodiment of the present invention, there is provided a catheter.
[0120] As shown in
[0121] In Embodiment 6, inner and outer surfaces of the second transition section 1013-1 are inclined both at the same angle of 60 with respect to an axis of the tubular component 100. In some other embodiments, the inner and outer surfaces of the second transition section 1013-1 may be inclined both at the same or different angles with respect to the axis of the tubular component 100, which may each be any value in the range of 0-90, such as 5, 15, 30, 40, 45, 60, 75 or 85. In some other embodiments, the inner and outer surfaces of the second transition section 1013-1 may be both perpendicular to the axis of the tubular component 100. In some other embodiments, the inner surface of the second transition section 1013-1 may be parallel to the axis of the tubular component 100, and the outer surface of the second transition section 1013-1 may be included at an angle with respect to the axis of the tubular component 100, which may be any value in the range of 0-90, such as 5, 30, 40, 45, 60, 75 or 85. In some other embodiments, the inner surface of the second transition section 1013-1 may be parallel to the axis of the tubular component 100, and the outer surface of the second transition section 1013-1 may be perpendicular to the axis of the tubular component 100. In each case, an axial length of the second transition section 1013-1 is 0-10 mm. In Embodiment 6, the axial length of the second transition section 1013-1 is 5 mm. In some other embodiments, the axial length of the second transition section 1013-1 may be 0 mm. In some other embodiments, the axial length of the second transition section 1013-1 may be 3 mm. In some other embodiments, the axial length of the second transition section 1013-1 may be 8 mm. In some other embodiments, the axial length of the second transition section 1013-1 may be 10 mm. In each case, an axial length of the outer-tube distal section 1013 is 1-15 mm. In Embodiment 6, the axial length of the outer-tube distal section 1013 is 10 mm. In some other embodiments, the axial length of the outer-tube distal section 1013 may be 1 mm. In some other embodiments, the axial length of the outer-tube distal section 1013 may be 8 mm. In some other embodiments, the axial length of the outer-tube distal section 1013 may be 12 mm. In some other embodiments, the axial length of the outer-tube distal section 1013 may be 15 mm.
[0122] In each case, the outer diameter of the second straight section 1013-2 is 1.0-3.7 mm. In Embodiment 6, the outer diameter of the second straight section 1013-2 is 2.8 mm. In some other embodiments, the outer diameter of the second straight section 1013-2 may be 1.0 mm. In some other embodiments, the outer diameter of the second straight section 1013-2 may be 2.0 mm. In some other embodiments, the outer diameter of the second straight section 1013-2 may be 3.0 mm. In some other embodiments, the outer diameter of the second straight section 1013-2 may be 3.7 mm.
[0123] In Embodiment 6, the outer-tube distal section 1013 is connected to the inner tube 102 (not shown) so that a distal end of the first lumen is closed. As a result, when a liquid is flowing through the first lumen, it will not leak from the distal end of the catheter, thereby enabling expansion and collapse of the occlusion component 200. To this end, there may be a diameter-varying section (not shown) at the distal end of the outer-tube distal section 1013, which may have outer diameter gradually decreasing from its proximal to distal end and can be connected to the inner tube 102. The outer-tube distal section 1013 may be connected to the inner tube 102 either at the most distal end of the inner tube 102, or at another location thereof.
[0124] As shown in
[0125] In Embodiment 6, a projection of a first transition location 300 on the axis of the tubular component 100 is distal with respect to a projection of a second transition location 400 on the axis of the tubular component 100.
[0126] In Embodiment 6, the inner tube 102 is a triple-layered structure consisting of an innermost first polymer layer, an immediate reinforcing layer and an outermost second polymer layer. The outer tube 101 is a double-layered structure consisting of an outer layer that is a polymer layer and an inner layer that is a polymer layer.
[0127] In Embodiment 6, the catheter includes a first radiopaque ring sleeved over the inner tube and located at a head portion of the catheter. The catheter also includes a second radiopaque ring sleeved over the inner tube 102 at a location that is adapted to the location of the occlusion component 200.
[0128] As shown in
[0129] In Embodiment 6, there are angled transitions between the first recess 1012 and the outer-tube distal section 1013, and between the second transition section 1013-1 and the second straight section 1013-2. In some other embodiments, there may be smooth curved transition(s) between the first recess 1012 and the outer-tube distal section 1013, and/or between the second transition section 1013-1 and the second straight section 1013-2. In Embodiment 6, the second straight section 1013-2 has a flat, smooth surface. In some other embodiments, the second straight section 1013-2 may provide on its surface with convexities and concavities, grooves or curved portions, while having constant inner and outer diameters across its entire length.
Embodiment 7
[0130] In a seventh embodiment of the present invention, there is provided a catheter including: a first recess 1012 having a taped outer surface with a gradually decreasing outer diameter; and a proximal end of an occlusion component 200 secured to the tapered surface of the first recess 1012. That is, the first recess 1012 includes only a first transition section 1012-1 but not a first straight section 1012-2.
[0131] In some other embodiments, a distal end of an outer tube may have a first beveled surface, which forms an outer surface of the first recess 1012. Moreover, a proximal end of an occlusion component 200 may have a second surface, which mates with, and is fixedly connected to, the first beveled surface. That is, the first recess 1012 includes only a first transition section 1012-1 but not a first straight section 1012-2. Further, the beveled surface of the occlusion component 200 located at the proximal end may be sloped at the same angle as the beveled surface of the outer tube at the distal end so that they can mate with and be fixedly connected to each other.
[0132] The foregoing description presents some preferred embodiments of the present invention and is not intended to limit the scope of the present invention in any way. Any and all changes and modifications made by those of ordinary skill in the art in light of the above teachings without departing from the spirit of the present invention are intended to be embraced in the scope as defined by the appended claims.