Medical device comprising polyhydroxyalkanoate having pyrogen removed
View Patent ↗Polyhydroxyalkanoates (PHAs) from which pyrogen has been removed are provided for use in numerous biomedical applications. PHAs which have been chemically modified to enhance physical and/or chemical properties, for targeting or to modify biodegradability or clearance by the reticuloendothelial system (RES), are described. Methods for depyrogenating PHA polymers prepared by bacterial fermentation processes are also provided, wherein pyrogens are removed from the polymers without adversely impacting the polymers' inherent chemical structures and physical properties. PHAs with advantageous processing characteristics, including low melting points and/or solubility in non-toxic solvents, are also described. PHAs are provided which are suitable for use in vivo applications such as in tissue coatings, stents, sutures, tubing, bone and other prostheses, bone or tissue cements, tissue regeneration devices, wound dressings, drug delivery, and for diagnostic and prophylactic uses. Properties which are selected for include degradability, elasticity, inclusion of functional groups or derivatized groups, which can in turn be used to attach targeting agents, and bioadhesion.
1. A biocompatible medical device comprising a polyhydroxyalkanoate which is prepared using a process which introduces a pyrogen into the polyhydroxyalkanoate, wherein the pyrogen is removed from the polyhydroxyalkanoate to produce a pyrogen level of less than 20 endotoxin units (EU) per device, and wherein the device is sterilized by exposure to ethylene oxide gas.
2. The device of claim 1 wherein the pyrogen is removed by treatment with an oxidizing agent, hydrolysis, or a combination thereof.
3. The device of claim 1 wherein the device is in a form selected from the group consisting of stents, coatings on prosthetic devices, sutures, staples, and tubing.
4. The device of claim 1 wherein the device is in a form selected from the group consisting of tissue regeneration devices, cell culture devices, vascular grafts, wound dressings, and cell or tissue coatings.
5. The device of claim 1 wherein the device is in a form selected from the group consisting of drug, diagnostic or prophylactic delivery devices.
6. The device of claim 1 wherein the device is a porous membrane.
7. The device of claim 1 wherein the device is in the form of microparticles or nanoparticles.
8. The device of claim 5 wherein the device comprises a material selected from the group consisting of therapeutic, prophylactic and diagnostic agents.
9. The device of claim 8 wherein the device comprises a therapeutic or diagnostic agent selected from the group consisting of peptides and proteins, nucleic acids, saccharides and polysaccharides, lipids, synthetic drug molecules, and imaging agents.
10. The device of claim 5 wherein the device is formulated for administration to a mucosal surface.
11. The device of claim 1 wherein the polyhydroxyalkanoate is a polymer blend or copolymer.
12. The device of claim 7 wherein molecules selected from the group consisting of molecules which are bioactive, molecules which can be detected, targeting molecules, and molecules affecting charge, lipophilicity or hydrophilicity, are bound to the particles.
13. The device of claim 1 wherein the device is for tissue engineering further comprising cells seeded onto or within the device.
14. The device of claim 1 wherein the device is formed into a bone prosthesis.
15. The device of claim 1 further comprising structural and adhesive materials to form a bone cement.
16. The device of claim 1 in the form of a heart prosthetic selected from the group consisting of heart valves, heart leaflets, and heart annulus.
17. The device of claim 1 in the form of a periodontal graft.
18. The device of claim 1 in the form of a pericardial patch.