CN113069674B - Medical drug stent - Google Patents

Medical drug stent Download PDF

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Publication number
CN113069674B
CN113069674B CN202110306286.6A CN202110306286A CN113069674B CN 113069674 B CN113069674 B CN 113069674B CN 202110306286 A CN202110306286 A CN 202110306286A CN 113069674 B CN113069674 B CN 113069674B
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Prior art keywords
stent
film
independent
medical drug
coating film
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CN202110306286.6A
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CN113069674A (en
Inventor
陆剑锋
唐烈
高成
张珊
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Polyrey Medical Tech Suzhou Co ltd
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Polyrey Medical Tech Suzhou Co ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M31/00Devices for introducing or retaining media, e.g. remedies, in cavities of the body
    • A61M31/002Devices for releasing a drug at a continuous and controlled rate for a prolonged period of time
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2/06Blood vessels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2/06Blood vessels
    • A61F2/07Stent-grafts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/89Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M29/00Dilators with or without means for introducing media, e.g. remedies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2/06Blood vessels
    • A61F2/07Stent-grafts
    • A61F2002/072Encapsulated stents, e.g. wire or whole stent embedded in lining

Abstract

The invention relates to a medical drug stent, comprising: the independent stents are sequentially arranged at intervals along the axial direction of the medical drug stent, each independent stent comprises a closed annular stent body, an inner wrapping film and an outer wrapping film, the inner wrapping film and the outer wrapping film are respectively arranged on the inner side and the outer side of the stent body, two shaft ends of the inner wrapping film are respectively closed with two shaft ends of the outer wrapping film to form the wrapping films, a gap is formed between each wrapping film and the stent body, and the gap is filled with drugs; and the independent brackets are connected only through the fixed film. The medical drug stent can well coat the drug in the coating film, thereby avoiding the problem that the drug falls off from the medical drug stent when the medical drug stent is not implanted in vivo or in the implantation process; through the arrangement of the spaced independent stents, different drugs can be coated in the types of the drugs coated in the independent stents according to actual needs, so that the drug release maneuverability of the lesion is higher and more targeted.

Description

Medical drug stent
Technical Field
The invention belongs to the technical field of medical instruments, and particularly relates to a medical drug stent for treating lesion occlusion.
Background
In the existing pathological change dilatation, a layer of degradable medicine protective film is coated on the surface of an integrally woven stent, medicines are distributed on a high polymer film through a spraying technology, the medicine exerting time is concentrated, and the medicine supplying time is short; and because of the integrity of the film, only one medicine can be sprayed, and different pathologies cannot be treated; in addition, before the operation enters a human body, the sprayed medicine easily falls off to cause medicine loss and influence the operation effect.
Therefore, in view of the above technical problems, there is a need for a medical drug stent.
Disclosure of Invention
The invention aims to solve the technical problem of providing a medical drug bracket which is not easy to cause drug loss due to the fact that drugs fall off from the medical drug bracket before entering a human body.
In order to achieve the purpose, the invention adopts the technical scheme that:
a medical drug stent having an expanded state and a contracted state, the medical drug stent having an inner diameter in the expanded state that is larger than an inner diameter in the contracted state; the medical drug stent comprises:
the independent stents are sequentially arranged at intervals along the axial direction of the medical drug stent, each independent stent comprises a closed annular stent body, an inner wrapping film and an outer wrapping film, the inner wrapping film and the outer wrapping film are respectively arranged on the inner side and the outer side of the stent body, two shaft ends of the inner wrapping film are respectively sealed with two shaft ends of the outer wrapping film to form the wrapping films, a gap is formed between each wrapping film and the stent body, and the gap is filled with drugs;
and the independent brackets are connected only through the fixing film.
According to the medical drug stent, through the integral improvement of the medical drug stent, on one hand, a plurality of independent stents which are mutually spaced are arranged, and each independent stent adopts a coating film to coat the stent body and the drug in the coating film, so that the support of the independent stent on a lumen is ensured, and the drug can be well prevented from falling off from the coating film; on the other hand, connect into whole with a plurality of independent supports through the fixed film for medical drug stent's bending property is good, also can further avoid the medicine to drop from medical drug stent.
According to some specific and preferred embodiments, the drugs filled in the gaps of the plurality of independent stents are the same or different. The medical drug stent can coat different drugs to perform targeted treatment on different patients and different pathologies.
According to some specific and preferred embodiments, in each independent stent, the drugs are circumferentially arranged on the stent body in a surrounding manner, so that when the stent body is supported on the inner wall of a lumen, the drugs can be better contacted with the inner wall of the lumen, and the time and the distance for the drugs to reach a treatment site are shortened.
According to some specific and preferred embodiments, the stent body has a wavy annular structure, so that the stent body can be well contracted and expanded and can provide a good lumen supporting force.
According to some specific and preferred embodiments, the cross-section of the stent body is circular.
According to some specific and preferred embodiments, the fixed membrane comprises an outer fixed membrane coated outside the independent supports, the outer fixed membrane is made of degradable materials, so that after the outer fixed membrane is degraded, the independent supports can be exposed, and the medicine can be released from the coated membrane conveniently.
Furthermore, the coating film and the stent body are made of degradable materials, and the degradation speed of the external fixing film is greater than that of the coating film and that of the stent body. The materials of the external fixed film, the coating film and the bracket body are selected according to the required degradation time, and the high polymer materials with different degradation times are the existing materials.
According to some specific and preferred embodiments, the stent body is made of a polylactic acid-based polymer or a bioabsorbable magnesium alloy material.
According to some specific and preferred embodiments, the fixing films comprise an inner fixing film positioned in a plurality of the independent stents and an outer fixing film positioned outside the plurality of the independent stents, the inner fixing film is fixedly connected with the inner covering film, and the outer fixing film is fixedly connected with the outer covering film; through setting up internal fixation membrane and external fixation membrane simultaneously, can be better with the medicine cladding in medical drug stent, the influence of the medical drug stent that the internal fixation membrane can avoid implanting moreover to the blood flow, the damage of stake body to the vascular wall can be avoided to the external fixation membrane.
Furthermore, the inner fixing film and the outer fixing film are both made of degradable materials, and the degradation time of the inner fixing film and the degradation time of the outer fixing film can be the same or different.
Further, both axial ends of the inner fixed film are respectively closed with both axial ends of the outer fixed film.
According to some specific and preferred embodiments, micropores for releasing the drug are formed on the covering film and the fixing film, respectively, so that a part of the drug can be slowly released from the micropores before the fixing film and the covering film are not degraded, thereby achieving the effect of slow release.
According to some specific and preferred embodiments, the inner and outer cover films are of equal width.
According to the optimal implementation mode of the invention, after a plurality of independent stents are expanded and fixed, the degraded external fixed membrane exposes out of the independent stents, the coating membrane is matched with different high polymer materials, so that the degradation speed and the degradation sequence are controllable, meanwhile, the release time and the release amount are manually arranged, the coated medicine can be released regularly and quantitatively in the blood vessel of a patient according to the actual requirements, the medicine can be released for a long time, the continuous treatment effect is achieved on the lesion part, meanwhile, different medicines can be coated, the targeted treatment can be carried out on different patients and different pathologies, the medicine release on the lesion part has the controllability, the purpose of accurately treating the lesion is achieved through targeted and different lesion differentiation treatments, the risk of treatment failure is reduced, and the probability of curing the patient is improved.
Due to the application of the technical scheme, compared with the prior art, the invention has the following advantages:
the medical drug stent can well coat the drug in the coating film, thereby avoiding the problem that the drug falls off from the medical drug stent when the medical drug stent is not implanted into the body or in the implantation process; moreover, by arranging the independent brackets at intervals, the types of the medicines coated in the independent brackets can be coated with different medicines according to actual needs, so that the medicine release maneuverability of the pathological changes is higher and more targeted.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present application, the drawings required to be used in the description of the embodiments are briefly introduced below, and it is obvious that the drawings in the description below are only some embodiments of the present application, and it is obvious for those skilled in the art to obtain other drawings without creative efforts.
FIG. 1 is a partial perspective view of a preferred embodiment of a drug stent of the present invention secured in a blood vessel by balloon expansion and showing the structure of the stent body;
FIG. 2 is an exploded view of the preferred embodiment of the present invention;
FIG. 3 is an enlarged view of A in FIG. 2;
FIG. 4 is a schematic structural view of a free-standing stent with a part of an outer coating film removed according to a preferred embodiment of the present invention;
in the figure: 1. the stent comprises a drug stent 10, an inner fixing membrane 101, a channel 12, an independent stent 121, a covering membrane 122, a stent body 124, a drug 1211, an inner covering membrane 1212, an outer covering membrane 14 and an outer fixing membrane.
Detailed Description
In the following, only certain exemplary embodiments are briefly described. As those skilled in the art will recognize, the described embodiments may be modified in various different ways, all without departing from the spirit or scope of the embodiments of the invention. Accordingly, the drawings and description are to be regarded as illustrative in nature, and not as restrictive.
In the description of the embodiments of the present invention, it should be understood that the terms "length", "inside", "upper", and the like indicate orientations or positional relationships based on those shown in fig. 1, and are only used for convenience in describing the embodiments of the present invention and simplifying the description, but do not indicate or imply that the devices or elements referred to must have a specific orientation, be constructed in a specific orientation, and be operated, and thus, should not be construed as limiting the embodiments of the present invention.
Furthermore, the terms "first", "second" and "first" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance or to implicitly indicate the number of technical features indicated. Thus, a feature defined as "first" or "second" may explicitly or implicitly include one or more of that feature. In the description of the embodiments of the present invention, "a plurality" means two or more unless specifically limited otherwise.
In the embodiments of the present invention, unless otherwise explicitly specified or limited, the terms "mounted," "connected," "fixed," and the like are to be construed broadly, e.g., as being fixedly connected, detachably connected, or integrated; the connection can be mechanical connection, electrical connection or communication; they may be directly connected or indirectly connected through intervening media, or may be connected through the use of two elements or the interaction of two elements. Specific meanings of the above terms in the embodiments of the present invention can be understood by those of ordinary skill in the art according to specific situations.
In embodiments of the present invention, unless expressly stated or limited otherwise, the recitation of a first feature "on" or "under" a second feature may include the recitation of the first and second features being in direct contact, and may also include the recitation of the first and second features not being in direct contact, but being in contact with another feature between them. Also, the first feature "on," "above" and "over" the second feature may include the first feature being directly above and obliquely above the second feature, or simply indicating that the first feature is at a higher level than the second feature. A first feature being "under," "below," and "beneath" a second feature includes the first feature being directly above and obliquely above the second feature, or simply meaning that the first feature is at a lesser level than the second feature.
The following disclosure provides many different embodiments or examples for implementing different configurations of embodiments of the invention. To simplify the disclosure of embodiments of the invention, specific example components and arrangements are described below. Of course, they are merely examples and are not intended to limit embodiments of the invention. Moreover, embodiments of the present invention may repeat reference numerals and/or reference letters in the various examples for purposes of simplicity and clarity and do not in themselves dictate a relationship between the various embodiments and/or configurations discussed.
Embodiments of the present invention will be described in detail below with reference to the accompanying drawings.
As shown in fig. 1 and fig. 2, the present embodiment provides a medical drug stent 1, which includes an inner fixing membrane 10, a plurality of independent stents 12 and an outer fixing membrane 14.
The internal fixation film 10 is cylindrical, a channel 101 is formed inside the internal fixation film, the balloon can be conveniently installed in the channel 101, and after the medical drug stent 1 is unfolded, the blood flow can conveniently pass through the channel, and the influence on the flow of the blood flow is not easily caused.
As shown in fig. 2 to 4, a plurality of independent brackets 12 are axially sleeved outside the inner fixing film 10, and the plurality of independent brackets 12 are arranged at intervals; each independent bracket 12 comprises a coating film 121 and a bracket body 122 arranged in the coating film 121; a gap is formed between the coating film 121 and the annular bracket body 122 and is used for filling the medicine 124; each coating film 121 comprises an inner coating film 1211 and an outer coating film 1212 sleeved on the outer side of the inner coating film 1211, the inner coating film 1211 is sleeved on the outer side of the inner fixing film 10 and is fixedly connected with the inner fixing film 10, and the annular support body 122 is sleeved on the outer side of the inner coating film 1211.
The outer fixing film 14 is cylindrical, covers the plurality of outer covering films 1212, and is fixedly connected to the outer covering films 1212.
The coating film 121 of each independent stent 12 can adopt materials with different properties to achieve different degradation times according to requirements, so that the degradation speed and the degradation sequence become controllable, the medicine 124 in the coating film 121 is released in a timed and quantitative manner, the purpose of accurately treating pathological changes is achieved, and a continuous treatment effect is achieved for the pathological change parts. The annular stent body 122 has a high ability to withstand radial pressure. The medicine 123 is arranged in the gap formed by the inner coating 1211 and the outer coating 1212, so that the medicine 124 is prevented from falling off, and the treatment effect is improved. The cooperation through interior fixed film 10 and external fixation membrane 14 plays spacing and combinatorial action to independent support 12 to when implanting, a plurality of independent supports 12 can be in the same place as required, avoids independent support 12's removal simultaneously, realizes that a plurality of independent supports 12 accurately reach the pathological change position, and carries out the connection of a plurality of independent supports 12 through adopting the membrane, more does benefit to medical drug support 1's bending. The inner fixing film 10, the outer fixing film 14 and the annular stent body 122 can be expanded and degraded at a designated time, and the time before the inner fixing film 10 and the outer fixing film 14 are degraded can provide the drug stent 1 with a long time to be fixed in the blood vessel, and the drug stent 1 is not affected when the blood vessel is moved and bent.
According to the invention, the medicine 124 is preferably arranged on the annular bracket body 122 in a circumferential direction in a surrounding manner, so that the medicine 124 is uniformly distributed, and the treatment efficiency and effect are improved.
In order to enhance the expansion of the annular stent body 122 to the blood vessel and to stabilize the annular stent body 122 in the blood vessel, the annular stent body 122 preferably has a wavy annular structure.
In the present invention, it is preferable that the cross-section of the ring-shaped stent body 122 is circular, so as to avoid damage to the blood vessel.
According to the invention, preferably, two axial ends of the inner fixed film 10 are respectively sealed with two axial ends of the outer fixed film 14, so that the plurality of independent brackets 12 are further limited.
The width of the inner wrapping film 1211 is preferably equal to that of the outer wrapping film 1212, the structure is simple, and the stability of the medicine 123 between the inner wrapping film 1211 and the outer wrapping film 1212 is improved.
In order to further prevent the falling of the medicine 123, it is preferable that both axial ends of the inner wrap 1211 are respectively sealed with both axial ends of the outer wrap 1212.
In the present application, the inner covering film 1211 and the outer covering film 1212, the inner covering film 1211 and the inner fixing film 10, and the outer covering film 1212 and the outer fixing film 14 may be fixedly connected by sewing, sealing with glue, or hot pressing.
In the present application, the inner fixing film 10, the inner covering film 1211, the stent body 122, the outer covering film 1212 and the outer fixing film 14 are all made of degradable materials, and the degradation speed of the fixing film is greater than that of the covering film and is greater than that of the stent body 122, wherein the control of different degradation speeds is realized by selecting polymer materials with different degradation speeds; the specific degradation rate can be determined according to the actual needs of the patient during treatment.
In the present invention, the annular stent body 122 is preferably made of a polylactic acid polymer material, and can be degraded by itself when reaching the designed life without being taken out of the blood vessel, but is not limited to the polylactic acid polymer material, and may also be made of a bioabsorbable magnesium alloy material.
When the medical stent is used, the medical stent 1 is in a contraction state in an initial state, a saccule (not shown in the figure) is arranged in the channel 101 of the internal fixing film 10, and the saccule is provided with an inflatable and air-extracting connecting port; the drug stent 1 enters a blood vessel with pathological changes of a human body through a guide wire (not shown in the figure), the saccule is inflated, and the drug stent 1 is then stretched to the unfolding state so that the inner diameter of the drug stent 1 is larger than that of the medical drug stent 1 in the contraction state; after the balloon is pumped out, the drug stent 1 is fixed at the lesion part; after the drug stent 1 is expanded, a plurality of independent stents 12 are embedded into the vessel wall for fixation after a period of time, the stents will not fall off even if the vessel moves and contracts, and the inner fixed membrane 10 and the outer fixed membrane 14 are degraded at the design time; the plurality of independent brackets 12 are exposed after the outer fixed film 12 is degraded, and due to the independent arrangement of the plurality of independent brackets 12, the degradation speed and the degradation sequence are controllable by adopting the collocation of different high polymer materials through the plurality of coating films 121, so that different degradation times are achieved; under the action of different degradation times of the plurality of coating films 121, the drugs can be released according to different sequences, different times and different dosages, and different drugs can be matched in each section; the vessel recovers the blocked lumen by the expansion of the plurality of annular stent bodies 122 and the release of the drug 124, and the plurality of annular stent bodies 122 reach the design life and start to degrade by themselves without being taken out.
It will be evident to those skilled in the art that the invention is not limited to the details of the foregoing illustrative embodiments, and that the present invention may be embodied in other specific forms without departing from the spirit or essential attributes thereof. The present embodiments are therefore to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein. Any reference sign in a claim should not be construed as limiting the claim concerned.

Claims (7)

1. A medical drug stent having an expanded state and a contracted state, the medical drug stent having an inner diameter in the expanded state that is larger than an inner diameter in the contracted state; characterized in that, the medical drug stent comprises:
the medical drug stent comprises a plurality of independent stents, wherein the independent stents are sequentially arranged at intervals along the axial direction of the medical drug stent, each independent stent comprises a closed annular stent body, an inner coating film and an outer coating film, the inner coating film and the outer coating film are respectively arranged on the inner side and the outer side of the stent body, two shaft ends of the inner coating film are respectively sealed with two shaft ends of the outer coating film to form the coating films, a gap is formed between each coating film and the stent body, and drugs are filled in the gap; the medicines filled in the gaps of the independent brackets are the same or different; in each independent bracket, the medicines are circumferentially arranged on the bracket body in a surrounding manner;
the independent brackets are connected only through the fixed film, the fixed film comprises an external fixed film coated outside the independent brackets, the external fixed film is made of degradable materials, the independent brackets are exposed after the external fixed film is degraded, and due to the independent arrangement of the independent brackets, the degradation speed and the degradation sequence are controllable by matching the coating films with different high polymer materials, so that different degradation times are achieved; under the action of different degradation times of the coating films, the medicaments can be released according to different sequences, different times and different dosage.
2. The medical drug stent of claim 1, wherein: the coating film and the stent body are made of degradable materials, and the degradation speed of the external fixing film is larger than that of the coating film and that of the stent body.
3. The medical drug stent of claim 1, wherein: the stent body is made of polylactic acid polymer or bioabsorbable magnesium alloy material.
4. The medical drug stent of claim 1, wherein: the fixed membrane comprises a plurality of internal fixed membranes positioned in the independent supports and a plurality of external fixed membranes positioned outside the independent supports, the internal fixed membranes are fixedly connected with the internal coated membranes, and the external fixed membranes are fixedly connected with the external coated membranes.
5. The medical drug stent of claim 4, wherein: the two shaft ends of the inner fixed film are respectively sealed with the two shaft ends of the outer fixed film.
6. The medical drug stent of claim 1, wherein: micropores for releasing the medicine are respectively formed on the coating film and the fixed film.
7. The medical drug stent of claim 1, wherein: the width of the inner coating film is equal to that of the outer coating film.
CN202110306286.6A 2020-09-30 2021-03-23 Medical drug stent Active CN113069674B (en)

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CN113876465A (en) * 2021-09-26 2022-01-04 刘建强 Combined type tectorial intestinal tract stent and operation method thereof

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CN113069673B (en) 2023-02-28

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