Spinal disc regenerative composition and method of manufacture and use
The present invention provides a novel way to replenish the disc using retooled disc compositions to repair degenerative discs. There is no better source of proteoglycans than the actual disc material ( 6 ) itself. To this end, there has been developed a technique to remove the nucleus pulposus and retool the morphology of the nucleus pulposus to create a powder material ( 10 ) that is dry and can be stored at room temperature for long periods of time. This powder ( 10 ) can then be reconstituted with a variety of fluids, the most suitable being normal saline or lactated ringers to form a flowable mixture ( 20 ).
1. A composition consisting of:
(a) a syringe or injectable device which is capable of being inserted into a damaged disc to be treated; and
(b) a hydrated composition comprising hypothermically dried micronized nucleus pulposus in a fluid, produced by a method consisting of:
(i) providing normal human cadaveric intervertebral discs;
(ii) separating the nucleus pulposus from the annulus fibrosus of the normal human cadaveric intervertebral disc;
(iii) drying the nucleus pulposus;
(iv) micronizing the dried nucleus pulposus by pulverizing in a cryomill at low temperature into particles sized less than 400 microns;
(v) hypothermically drying the nucleus pulposus, wherein said hypothermically drying occurs during step (iii), and/or between steps (iii) and (iv), and/or during step (iv), and/or between steps (iv) and step (vi); and then
(vi) mixing the hypothermically dried micronized nucleus pulposus with a fluid, thereby producing the hydrated composition;
wherein the (b) hydrated composition is contained within the (a) syringe or injectable device, and
wherein the (b) hydrated composition has a viscosity which permits it to flow through a cannula.
2. The composition of claim 1 wherein step (i) providing normal human cadaveric intervertebral discs involves aseptically recovering multiple intervertebral disc segments recovered from cadaveric spine segments from T9 to L5 by cutting between cancellous bone and vertebral endplate junctions.
3. The composition of claim 1 wherein the fluid used in step (vi) rehydrating is selected from the group consisting of normal saline, lactated ringers solution, blood, platelet rich plasma, and combinations thereof.
4. The composition of claim 1 wherein the (b) hydrated composition has a viscosity that permits the composition to flow through a 22 gauge or finer bore cannula.
5. The composition of claim 1 wherein the step (v) hypothermically drying of the nucleus pulposus occurs prior to step (iv) micronizing.
6. The composition of claim 1 wherein the step (v) hypothermically drying of the nucleus pulposus occurs after step (iv) micronizing.
7. A composition consisting of:
(a) a syringe or injectable device which is capable of being inserted into a damaged disc to be treated; and
(b) a hydrated composition consisting of hydrated hypothermically dried micronized nucleus pulposus in a fluid, produced by a method consisting of:
(i) providing normal human cadaveric intervertebral discs;
(ii) separating the nucleus pulposus from the annulus fibrosus of the normal human cadaveric intervertebral discs;
(iii) drying the nucleus pulposus;
(iv) micronizing the dried nucleus pulposus by placing the dried material in a cryomill at low temperature and pulverizing the dried nucleus pulposus into particles sized less than 400 microns;
(v) hypothermically drying the nucleus pulposus, wherein said hypothermically drying occurs during step (iii), and/or between steps (iii) and (iv), and/or during step (iv), and/or between steps (iv) and step (vi); and then
(vi) aseptically rehydrating the hypothermically dried micronized nucleus pulposus with a fluid, thereby producing the hydrated composition;
wherein the (b) hydrated composition is contained within the (a) syringe or injectable device; and
wherein the (b) hydrated composition has a viscosity which permits it to flow through a cannula.
8. The composition of claim 7 wherein the fluid used in step (vi) rehydrating is selected from the group consisting of normal saline, lactated ringers solution, blood, platelet rich plasma, and combinations thereof.
9. The composition of claim 7 wherein the (b) hydrated composition has a viscosity that permits the composition to flow through a 22 gauge or finer bore cannula.
10. The composition of claim 7 wherein the step (v) hypothermically drying of the nucleus pulposus occurs prior to step (iv) micronizing.
11. The composition of claim 7 wherein the step (v) hypothermically drying of the nucleus pulposus occurs after step (iv) micronizing.
12. A composition consisting of:
(a) a syringe or injectable device which is capable of being inserted into a damaged disc to be treated; and
(b) a hydrated composition comprising hypothermically dried micronized nucleus pulposus in a fluid, produced by a method consisting of:
(i) providing normal human cadaveric intervertebral discs;
(ii) separating the nucleus pulposus from the annulus fibrosus of the normal human cadaveric intervertebral disc;
(iii) drying the nucleus pulposus;
(iv) micronizing the dried nucleus pulposus by pulverizing in a cryomill at low temperature into particles sized less than 400 microns;
(v) hypothermically drying the nucleus pulposus, wherein said hypothermically drying occurs during step (iii), and/or between steps (iii) and (iv), and/or during step (iv), and/or between steps (iv) and step (vi), thereby forming a powdered hypothermically dried micronized nucleus pulposus;
(vi) mixing the powdered hypothermically dried micronized nucleus pulposus with a fluid; and
(vii) mixing one or more of stem cells that are derived from marrow, fat, blood or interspinous ligaments; micronized amnion; platelet rich plasma; and/or growth factors encapsulated in pharmacologically active microspheres with the powdered hypothermically dried micronized nucleus pulposus, wherein step (vii) occurs before, during and/or after step (vi), thereby producing the hydrated composition;
wherein the (b) hydrated composition is contained within the (a) syringe or injectable device, and wherein the (b) hydrated composition has a viscosity which permits it to flow through a cannula.