Abstract: The present invention relates to a multi-hole stent for digestive organs, the multi-hole stent including: a body configured to form a plurality of cells through the intersection of wires and to be provided in a hollow cylindrical shape; and a film configured to be installed in contact with the inner surface of the body; wherein one or more discharge holes are formed in the film. The multi-hole stent for digestive organs is placed in a stenotic region in a biliary track, and can thus secure a discharge path by restoring a narrowed diameter. Furthermore, the film is installed on the inner surface of the body, and can thus prevent the entry of a lesion into the stent and re-stenosis attributable to the growth of the lesion and can thus provide discharge paths for body fluids generated from side branches through the discharge holes formed in the film.

Abstract: The present invention relates to a stent and a method for manufacturing the same. The stent includes: a first hollow cylindrical body portion formed by weaving a metal wire; a second hollow cylindrical body portion formed by weaving a metal wire, and configured to surround the first body portion; an expanded portion configured to form two adjacent ends of the first body portion and the second body portion integrally; and a membrane inserted between the first body portion and the second body portion, and configured to surround the outside of the first body portion. According to the present invention, there is no risk of the film being torn when the stent is bent, an additional connection wire is not required, the process of manufacturing the stent is simple, and the costs required for the manufacture of the stent are not high.

Abstract: The present invention relates to a drug-releasing biodegradable stent. The drug-releasing biodegradable stent includes: a first stent structure configured to have a plurality of cells by means of the wire crossing pattern of a woven structure and be provided in a hollow cylindrical shape by weaving a metal wire made of a shape-memory alloy in a specific pattern on a jig; and a second stent structure formed as a 3D print that is provided to have a plurality of cells by means of the wire crossing pattern of a printed structure and also have a hollow cylindrical shape by performing 3D printing using a printing material including a biodegradable polymer and a drug, and disposed such that it covers the outer circumferential surface of the first stent structure or the outer circumferential surface thereof is covered with the first stent structure.

Abstract: The present invention relates to a connection stent and a method of manufacturing the stent. The connection stent includes: a body configured to form a plurality of cells through the intersection of wires, and provided in a hollow cylindrical shape; an upper head formed to extend from one end of the body to have a diameter larger than that of the body; and a lower head formed to extend from a remaining end of the body to have a diameter larger than that of the body. The upper head and the lower head are respectively placed to come into contact with insides of heterogeneous tissues. Accordingly, according to the present invention, there can be manufactured a stent which can connect heterogeneous tissues and form a bypass and which can provide sufficient expansion force and minimum axial force for the maintenance of the bypass formed as described above.

Abstract: The present invention relates to a method for manufacturing a stent, the method using a jig in which detachable protruding pins are installed at all respective location points at which circumference division lines and length division lines intersect each other, the method forming cells through intersection of wire by setting any one of the location points as a start point and repeatedly bending and moving the wire from the start point upward and downward to pass over the protruding pins located in diagonal directions, wherein a first stent woven such that intersection portions formed through the intersection of a wire are spaced apart from each other in a diagonal direction and arranged one for each length division line and a second stent woven to maintain the structural stability of the first stent and to prevent the first stent from being twisted can be provided as a single stent.

Abstract: The present invention relates to a stent and a method for manufacturing the same. The stent includes: a first hollow cylindrical body portion formed by weaving a metal wire; a second hollow cylindrical body portion formed by weaving a metal wire, and configured to surround the first body portion; an integral portion configured to form two adjacent ends of the first body portion and the second body portion integrally; and a membrane inserted between the first body portion and the second body portion, and configured to surround the outside of the first body portion. According to the present invention, there is no risk of the film being torn when the stent is bent, an additional connection wire is not required, the process of manufacturing the stent is simple, and the costs required for the manufacture of the stent are not high.

Abstract: The present invention relates to: a paper-based surface-enhanced Raman scattering (SERS) substrate comprising metal nanoparticles, which are uniformly distributed and adsorbed on a designed pattern and have a diameter of 1 nm to 100 nm; a point-of-care (POC) diagnostic kit, comprising the paper-based SERS substrate; and a method for preparing the paper-based SERS substrate.

Abstract: The present invention relates to a connection stent and a method of manufacturing the stent. The connection stent includes: a body configured to form a plurality of cells through the intersection of wires, and provided in a hollow cylindrical shape; an upper head formed to extend from one end of the body to have a diameter larger than that of the body; and a lower head formed to extend from a remaining end of the body to have a diameter larger than that of the body. The upper head and the lower head are respectively placed to come into contact with insides of heterogeneous tissues. Accordingly, according to the present invention, there can be manufactured a stent which can connect heterogeneous tissues and form a bypass and which can provide sufficient expansion force and minimum axial force for the maintenance of the bypass formed as described above.

Abstract: The present invention relates to a drug-releasing biodegradable stent. The drug-releasing biodegradable stent includes: a first stent structure configured to have a plurality of cells by means of the wire crossing pattern of a woven structure and be provided in a hollow cylindrical shape by weaving a metal wire made of a shape-memory alloy in a specific pattern on a jig; and a second stent structure formed as a 3D print that is provided to have a plurality of cells by means of the wire crossing pattern of a printed structure and also have a hollow cylindrical shape by performing 3D printing using a printing material including a biodegradable polymer and a drug, and disposed such that it covers the outer circumferential surface of the first stent structure or the outer circumferential surface thereof is covered with the first stent structure.

Abstract: The present invention relates to a multi-hole stent for digestive organs, the multi-hole stent including: a body configured to form a plurality of cells through the intersection of wires and to be provided in a hollow cylindrical shape; and a film configured to be installed in contact with the inner surface of the body; wherein one or more discharge holes are formed in the film. The multi-hole stent for digestive organs is placed in a stenotic region in a biliary track, and can thus secure a discharge path by restoring a narrowed diameter. Furthermore, the film is installed on the inner surface of the body, and can thus prevent the entry of a lesion into the stent and re-stenosis attributable to the growth of the lesion and can thus provide discharge paths for body fluids generated from side branches through the discharge holes formed in the film.

Abstract: The present invention relates to a stent and a method for manufacturing the same. The stent includes: a first hollow cylindrical body portion formed by weaving a metal wire; a second hollow cylindrical body portion formed by weaving a metal wire, and configured to surround the first body portion; an expanded portion configured to form two adjacent ends of the first body portion and the second body portion integrally; and a membrane inserted between the first body portion and the second body portion, and configured to surround the outside of the first body portion. According to the present invention, there is no risk of the film being torn when the stent is bent, an additional connection wire is not required, the process of manufacturing the stent is simple, and the costs required for the manufacture of the stent are not high.

Abstract: The present invention relates to a connection stent and a method of manufacturing the stent. The connection stent includes: a body configured to form a plurality of cells through the intersection of wires, and provided in a hollow cylindrical shape; an upper head formed to extend from one end of the body to have a diameter larger than that of the body; and a lower head formed to extend from a remaining end of the body to have a diameter larger than that of the body. The upper head and the lower head are respectively placed to come into contact with insides of heterogeneous tissues. Accordingly, according to the present invention, there can be manufactured a stent which can connect heterogeneous tissues and form a bypass and which can provide sufficient expansion force and minimum axial force for the maintenance of the bypass formed as described above.

Abstract: The present invention relates to a method for manufacturing a stent, the method using a jig in which detachable protruding pins are installed at all respective location points at which circumference division lines and length division lines intersect each other, the method forming cells through intersection of wire by setting any one of the location points as a start point and repeatedly bending and moving the wire from the start point upward and downward to pass over the protruding pins located in diagonal directions, wherein a first stent woven such that intersection portions formed through the intersection of a wire are spaced apart from each other in a diagonal direction and arranged one for each length division line and a second stent woven to maintain the structural stability of the first stent and to prevent the first stent from being twisted can be provided as a single stent.

Abstract: The present invention relates to: a paper-based surface-enhanced Raman scattering (SERS) substrate comprising metal nanoparticles, which are uniformly distributed and adsorbed on a designed pattern and have a diameter of 1 nm to 100 nm; a point-of-care (POC) diagnostic kit, comprising the paper-based SERS substrate; and a method for preparing the paper-based SERS substrate.

Abstract: The present invention relates to a catheter for a stent operation. The catheter for a stent operation according to the present invention comprises: a solid bar of which one end is coupled to the side of a handle; an outer tube into which the solid bar is inserted, having an insertion hole through which a guide wire can be inserted from the outside to the inside, and of which one end is coupled to the side of the body; a guide tip coupled to the side of the solid bar, and guiding the guide wire by having a through-hole through which the guide wire passes; a connection tube for connecting and coupling the guide tip to the solid bar, wherein the solid bar has an accommodation groove, for preparing a space capable of accommodating the guide wire, formed in a predetermined section of a region to be connected to the connection tube, such that the guide wire can be accommodated inside of the outer tube.

Abstract: Disclosed herein is an X-ray source having cooling and shielding functions. The X-ray source includes an X-ray generation unit (100) which has one or more insulation columns (160) and emits X-rays in a vacuum; a cooling unit (180) which is provided around a periphery of the X-ray generation unit and removes heat generated from the X-ray generation unit; and a shielding unit (190) which is provided around a periphery of the cooling unit and shields an area exposed to X-rays other than the areas related to the emission of the X-rays.

Abstract: The present invention relates to a method for providing information on the presence of viral infection, comprising: a first step of preparing a dried tear sample on a substrate; a second step of measuring a Raman spectrum from the dried tear sample; a third step of extracting Gaussian sub-peaks by deconvolution of the measured Raman spectrum; a fourth step of deriving a log value for the relative intensity ratio of a peak corresponding to an amide III ?-sheet and a peak corresponding to C—H deformation; and a fifth step of determining the sample as normal if the derived value is positive and as infected if the derived value is negative.

Abstract: The present invention discloses a digital X-ray source.

Abstract: The present invention provides a hybrid stent for a blood vessel, the stent including: a plurality of first wires configured to form a plurality of rows in one direction and maintain the shape thereof inside a human body; a plurality of second wires configured to intersect the first wires and form a plurality of rows; and connectors configured to connect portions where the first wires and the second wires intersect each other; wherein a plurality of hollow holes are formed by the first wires and the second wires, and one or more of the plurality of second wires are degraded inside the human body after a predetermined period of time. Accordingly, the effect of enabling the stent to be easily removed can be expected because the second wires made of the biodegradable polymer are gradually degraded by body fluids.

Abstract: The present invention relates to a stent and a method for manufacturing the same. The stent includes: a first hollow cylindrical body portion formed by weaving a metal wire; a second hollow cylindrical body portion formed by weaving a metal wire, and configured to surround the first body portion; an expanded portion configured to form two adjacent ends of the first body portion and the second body portion integrally; and a membrane inserted between the first body portion and the second body portion, and configured to surround the outside of the first body portion. According to the present invention, there is no risk of the film being torn when the stent is bent, an additional connection wire is not required, the process of manufacturing the stent is simple, and the costs required for the manufacture of the stent are not high.