Nucleus Pulposus Filler
Abstract
The present invention provides a nucleus pulposus filler or the like which is to be packed into an area in deformed intervertebral disc wherein normal nucleus should be located and can be stabley maintained for a long time. More preferably, the present invention provides a nucleus pulposus filler comprising a crosslinked chondroitin sulfate as an active ingredient. The photocrosslinked chondroitin sulfate is preferably the following one: a photocrosslinked chondroitin sulfate obtainable by freezing a photoreactive chondroitin sulfate-containing solution comprising: a photoreactive chondroitin sulfate to which a photoreactive group is bound; an aqueous solvent capable of dissolving the photoreactive chondroitin sulfate; and any one substance selected from the group consisting of an alcohol having aqueous solvent miscibility, a surfactant, and a cheleting agent; irradiating the resulting frozen product with light; and then melting the frozen product. The filler can be provided as a kit by packing it into a container from which the filler can be pushed out.
Claims
exact text as granted — not AI-modified1 . A nucleus pulposus filler comprising a crosslinked chondroitin sulfate as an active ingredient.
2 . The nucleus pulposus filler according to claim 1 , wherein said crosslinking is photocrosslinking.
3 . The nucleus pulposus filler according to claim 2 , wherein the photocrosslinked chondroitin sulfate is the following one:
a photocrosslinked chondroitin sulfate obtainable by freezing a photoreactive chondroitin sulfate-containing solution comprising: a photoreactive chondroitin sulfate to which a photoreactive group is bound; an aqueous solvent capable of dissolving the photoreactive chondroitin sulfate; and any one substance selected from the group consisting of an alcohol having aqueous solvent miscibility, a surfactant, and a cheleting agent; irradiating the resulting frozen product with light; and then melting the frozen product.
4 . The nucleus pulposus filler according to claim 3 , wherein the alcohol is an alcohol having a property of keeping a frozen state at a temperature of −7° C. or lower in the case that the alcohol is added to the aqueous solvent solution of the photoreactive chondroitin sulfate, the whole is frozen to obtain a frozen body, and then the temperature is elevated.
5 . The nucleus pulposus filler according to claim 3 , wherein the alcohol is one represented by the following formula (I):
R—OH (1) wherein R is selected from the group consisting of: a linear alkyl having 1 to 10 carbon atoms, a branched alkyl having 3 to 10 carbon atoms, —CH 2 —(CHOH) l —CH 2 OH, wherein 1 is an integer of 0 to 5,
wherein m is an integer of 3 to 5, and
—(CH 2 CH 2 O) n —H, wherein n is an integer of 3 to 70.
6 . The nucleus pulposus filler according to claim 3 , wherein the surfactant is a nonionic surfactant or an anionic surfactant.
7 . The nucleus pulposus filler according to claim 6 , wherein the nonionic surfactant is polyethylene glycol, and the anionic surfactant is an alkyl sulfate salt.
8 . The nucleus pulposus filler according to claim 3 , wherein the cheleting agent is an oxycarboxylic acid or a polyaminocarboxylic acid.
9 . The nucleus pulposus filler according to claim 8 , wherein the oxycarboxylic acid is citric acid or a salt thereof, and the polyaminocarboxylic acid is ethylenediamine tetraacetic acid.
10 . The nucleus pulposus filler according to any one of claim 1 , wherein the chondroitin sulfate has a weight average molecular weight of 10,000 to 100,000.
11 . The nucleus pulposus filler according to any one of claim 3 , wherein the photoreactive group in the photoreactive chondroitin sulfate is bound to a carboxyl group of the chondroitin sulfate.
12 . The nucleus pulposus filler according to any one of claim 3 , wherein the photoreactive chondroitin sulfate is contained in an amount of 1 to 20% by weight in the photoreactive chondroitin sulfate-containing solution.
13 . The nucleus pulposus filler according to any one of claim 1 , wherein the crosslinked chondroitin sulfate has the following properties:
viscosity measured under conditions of 20° C. and standard corn 0 degree) by means of a rotary viscosimeter is from 300 to 30,000 mPa·S and the chondroitin sulfate shows a gel form.
14 . The nucleus pulposus filler according to any one of claim 1 , wherein the filler is administrated by injection.
15 . The nucleus pulposus filler according to any one of claim 1 , which is used for regeneration of nucleus pulposus.
16 . A nucleus pulposus filler kit comprising the filler according to claim 1 and a container from which the filler can be pushed out, wherein the filler is packed into the container.Join the waitlist — get patent alerts
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