Claims Analysis
Total Claims: 6
Claim 1
Independent Claim
56 words
A stent for liberating TRANIRAST, which is adapted to be introduced into a vascular system such as blood vessels, comprising a stent body produced by weaving or knitting into a tubular shape a fiber containing TRANIRAST and made of a low-melting biodegradable polymer having a melting point at which no pharmacological effects of TRANIRAST are damaged.
Claim 2
Dependent Claim
56 words
A stent for liberating TRANIRAST, which is adapted to be introduced into a vascular system such as blood vessels, comprising a stent body produced by weaving or knitting into a tubular shape a fiber containing TRANIRAST and made of a low-melting biodegradable polymer having a melting point at which no pharmacological effects of TRANIRAST are damaged.
Claim 3
Dependent Claim
36 words
A stent for eluting TRANIRAST contained therein, comprising a stent body coated with a mixture composed of TRANIRAST and a low-melting biodegradable polymer having a melting point at which no pharmacological effects of TRANIRAST are damaged.
Claim 4
Dependent Claim
36 words
A stent for eluting TRANIRAST contained therein, comprising a stent body coated with a mixture composed of TRANIRAST and a low-melting biodegradable polymer having a melting point at which no pharmacological effects of TRANIRAST are damaged.
Claim 5
Dependent Claim
166 words
A stent for liberating a drug, which is adapted to be introduced into a vascular system such as blood vessels, comprising: a stent body produced by weaving or knitting into a tubular shape a composite fiber composed of fiber made of a low-melting biodegradable polymer having a melting point at which no pharmacological effects of the druq are damaged and a fiber made of a high-melting biodegradable polymer having a melting point higher than that of the fiber composed of the low-melting biodegradable polymer; wherein the low-melting biodegradable polymer exposed to an outer surface of the stent body is heat-fused to smoothen the outer surface; wherein the high-melting biodegradable polymer is at least compound selected from the group consisting of poly-lactic acid, polyglycolic acid and a copolymer thereof; wherein the melting point of the low-melting point biodegradable polymer is 80° C. or lower; and wherein the composite fiber constituting the stent body is a two folded yarn, the two folded yarn including a TRANIRAST-containing poly-ε-caprolactone fiber.
Claim 6
Dependent Claim
166 words
A stent for liberating a drug, which is adapted to be introduced into a vascular system such as blood vessels, comprising: a stent body produced by weaving or knitting into a tubular shape a composite fiber composed of fiber made of a low-melting biodegradable polymer having a melting point at which no pharmacological effects of the druq are damaged and a fiber made of a high-melting biodegradable polymer having a melting point higher than that of the fiber composed of the low-melting biodegradable polymer; wherein the low-melting biodegradable polymer exposed to an outer surface of the stent body is heat-fused to smoothen the outer surface; wherein the high-melting biodegradable polymer is at least compound selected from the group consisting of poly-lactic acid, polyglycolic acid and a copolymer thereof; wherein the melting point of the low-melting point biodegradable polymer is 80° C. or lower; and wherein the composite fiber constituting the stent body is a two folded yarn, the two folded yarn including a TRANIRAST-containing poly-ε-caprolactone fiber.