Degradable magnesium alloy drug eluting stent
Technical Field
The invention relates to the technical field of medical instruments, in particular to a degradable magnesium alloy drug eluting stent.
Background
Drug eluting stents, also known as drug releasing stents, carry the drug through a polymer coated on the surface of a metal stent; when the stent is implanted into a diseased part in a blood vessel, the medicine is controllably released from the polymer coating to a blood vessel wall tissue in an elution mode to play a biological effect, so that the formation of atheromatous plaques in the blood vessel is inhibited, and the stenosis degree of the blood vessel is improved; when the drug release in the coating is finished, the stent begins to degrade slowly, and finally the stent is degraded completely, and the blood vessel is recovered to be normal.
The magnesium alloy support structures on the market at present are various, most of the supports are in the expansion process, stress concentration and damage phenomena of different degrees are easily shown on the support rings due to different stress of all parts, and the integral bearing capacity of the support is reduced, even the support loses the supporting force too early.
Disclosure of Invention
Therefore, the technical problem to be solved by the invention is to overcome the defects that the bearing capacity is reduced and even the supporting force is lost too early due to uneven stress of each part of the stent in the expansion process in the prior art, thereby providing the degradable magnesium alloy crown elution stent.
In order to solve the technical problems, the degradable magnesium alloy coronary medicine elution stent provided by the invention comprises:
the support rings are arranged at intervals, and every two adjacent support rings are connected through a plurality of connecting keys;
the support ring is the wave structure that a plurality of support bridge muscle mirror image connection constitutes in proper order, support bridge muscle both ends have respectively towards outside bellied arc section, the width of support bridge muscle is progressively steadilyd decrease from both ends to the centre.
Preferably, the connecting key is located between the minimum spacing of two adjacent support rings.
Preferably, the two adjacent support rings are arranged in a mirror symmetry manner.
Preferably, the connecting key has an S-shaped structure.
Preferably, the connecting bond includes:
a plurality of support rings connected between two ends of the drug eluting stent and the adjacent support rings, wherein the first connecting key is provided with a preformed hole suitable for embedding a developing sheet;
and the second connecting keys are provided with a plurality of S-shaped structures and are connected between two adjacent columns of the support rings between the first connecting keys.
Preferably, the linkages are helically distributed on the drug eluting stent.
Preferably, the width of the two ends of the bridge rib of the bracket is 150-190 μm, and the width of the middle part of the bridge rib of the bracket is 70-100 μm.
The technical scheme of the invention has the following advantages:
1. according to the degradable magnesium alloy drug eluting stent provided by the invention, the bridge ribs of the stent are sequentially connected in a mirror image manner, and the joints are in arc transition, so that the flexibility of the support ring is improved; in the expansion process, the bending degree of the arc transition part of the support ring is maximum, so that the stress concentration degree is maximum, namely the stress concentration degree of the support bridge rib is gradually increased from the middle to the two ends; the width of the bridge rib of the support is gradually decreased from two ends to the middle, so that the strength of the two ends is greater than that of the middle, the condition that the degradation rate is accelerated due to stress concentration damage at the two ends can be balanced, and the defect that the support capacity is prematurely lost due to uneven integral degradation of the support is avoided.
2. According to the degradable magnesium alloy drug eluting stent provided by the invention, the vertical distance of the connecting bond is equal to the minimum distance between two adjacent support rings, so that the radial ductility of the stent is increased, and the stent can be rapidly expanded after reaching a patient position.
3. According to the degradable magnesium alloy drug eluting stent provided by the invention, two adjacent support rings are arranged in a mirror symmetry manner, so that the support rings are uniformly stressed and synchronously degraded.
4. According to the degradable magnesium alloy drug eluting stent provided by the invention, the connecting bond adopts an S-shaped structure, so that the metal surface coverage rate of the whole stent is increased compared with that of a straight line structure; the flexibility of the whole stent is increased, and proper axial retraction supplement can be provided when the stent is expanded.
5. According to the degradable magnesium alloy drug eluting stent provided by the invention, the developing sheet is additionally arranged at the reserved hole of the first connecting key, so that the integral visibility of the stent is improved, and the degradation condition of the stent is convenient to observe.
6. According to the degradable magnesium alloy drug eluting stent provided by the invention, the connecting bonds are spirally distributed on the stent, so that the stress of the whole stent is more balanced and the passing performance is better.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, and it is obvious that the drawings in the following description are some embodiments of the present invention, and other drawings can be obtained by those skilled in the art without creative efforts.
Fig. 1 is a schematic deployment view of a degradable magnesium alloy drug eluting stent provided in the present invention.
Fig. 2 is a schematic structural diagram of a stent bridge rib.
Description of reference numerals:
1. a support ring; 2. a bracket bridge rib; 3. a first connecting key; 4. a second connecting key; 5. wave crest; 6. a trough of a wave; 7. holes are reserved.
Detailed Description
The technical solutions of the present invention will be described clearly and completely with reference to the accompanying drawings, and it should be understood that the described embodiments are some, but not all embodiments of the present invention. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
In the description of the present invention, it should be noted that the terms "center", "upper", "lower", "left", "right", "vertical", "horizontal", "inner", "outer", etc., indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, and are only for convenience of description and simplicity of description, but do not indicate or imply that the device or element being referred to must have a particular orientation, be constructed and operated in a particular orientation, and thus, should not be construed as limiting the present invention.
In the description of the present invention, it should be noted that, unless otherwise explicitly specified or limited, the terms "mounted," "connected," and "connected" are to be construed broadly, e.g., as meaning either a fixed connection, a removable connection, or an integral connection; can be mechanically or electrically connected; they may be connected directly or indirectly through intervening media, or they may be interconnected between two elements. The specific meanings of the above terms in the present invention can be understood in specific cases to those skilled in the art.
In addition, the technical features involved in the different embodiments of the present invention described below may be combined with each other as long as they do not conflict with each other.
The degradable magnesium alloy drug eluting stent provided by the embodiment is formed by laser fusion etching of a magnesium alloy ultrathin tube, and comprises: the drug eluting stent comprises support rings 1 and connecting keys connected among the support rings 1, wherein the drug eluting stent is in a tubular structure formed by encircling the support rings 1.
As shown in fig. 1, which is a development view of a drug eluting stent, the support ring 1 is formed into a wave-shaped structure by connecting a plurality of stent bridge ribs 2 in sequence in a mirror image manner; the support rings 1 are vertically arranged at intervals from left to right, and the adjacent two support rings 1 are arranged in a mirror symmetry manner, so that the support rings 1 are uniformly stressed and synchronously degraded; the support bridge rib 2 is of a centrosymmetric structure, and two ends of the support bridge rib are respectively provided with an arc-shaped section protruding towards the outer side; the arc sections of two adjacent support bridge ribs 2 are in transitional connection, and a plurality of wave crests 5 and wave troughs 6 are sequentially formed on the support ring 1.
As shown in fig. 1, the wave troughs 6 of adjacent support rings 1 are opposite, and the distance between two adjacent wave troughs 6 is the minimum distance between two support rings 1; the connecting key is connected adjacent two between the trough 6 of support ring 1, and adjacent support ring 1 is between the quantity of connecting key is two, is favorable to the radial expansion of support. The connecting keys comprise a first connecting key 3 and a second connecting key 4; the number of the first connecting keys 3 is four, every two of the first connecting keys are divided into a group and are respectively connected between the support rings 1 at two ends of the drug eluting stent and the adjacent support rings 1; first connecting key 3 is circular structure, and center department sets up the preformed hole 7 that is suitable for the scarf joint development piece, the development piece can promote the holistic visuality of support, is convenient for observe the holistic degradation condition of support in real time. The second connecting keys 4 are S-shaped structures and are connected between two adjacent columns of the support rings 1 positioned between the first connecting keys 3; the S-shaped structure of the second connecting bond 4 increases the metal surface coverage rate of the whole stent, and the metal surface coverage rate of the expanded drug eluting stent is not higher than 20%; the S-shaped configuration of the second bonds 4 also increases the overall flexibility of the drug eluting stent, providing for proper axial recoil replenishment during stent expansion.
As shown in fig. 1, the connecting bonds are spirally distributed on the drug eluting stent, and the connecting lines at the positions of the connecting bonds are represented by equally spaced oblique lines on the development view of the drug eluting stent; the connecting keys are distributed on the bracket in a spiral shape, so that the stress of the whole bracket is more balanced, and the passing performance is better.
As shown in fig. 2, the width of the stent bridge rib 2 gradually decreases from the middle to the two ends, so that the strength at the two ends is greater than that at the middle, wherein the width D1 at the two ends is 150-190 μm, and the width D2 at the middle is 70-100 μm; in the expansion process of the support ring 1, the wider design at the two ends of the support bridge rib 2 can balance the condition that the degradation rate is accelerated due to stress concentration damage at the two ends, so that the defect that the support capability is lost too early due to the uneven degradation of the whole support is avoided.
It should be understood that the above examples are only for clarity of illustration and are not intended to limit the embodiments. Other variations and modifications will be apparent to persons skilled in the art in light of the above description. And are neither required nor exhaustive of all embodiments. And obvious variations or modifications therefrom are within the scope of the invention.