Compositions and devices of poly-4-hydroxybutyrate

Patent metadata

Field	Value
Publication number	US-9480780-B2
Application number	US-201414529217-A
Country	US
Kind code	B2
Filing date	Oct 31, 2014
Priority date	Nov 5, 2013
Publication date	Nov 1, 2016
Grant date	Nov 1, 2016

Abstract

Compositions of P4HB with high purity have been developed. The compositions are prepared by washing P4HB biomass prior to solvent extraction, and precipitating P4HB from solution. The same solvent is preferably used to wash the P4HB biomass, and as a non-solvent to precipitate the polymer from a P4HB solvent solution. The highly pure P4HB compositions are suitable for preparing implants. The implants may be used for the repair of soft and hard tissues.

First claim

We claim:

1. A composition comprising poly-4-hydroxybutyrate (P4HB) polymer, wherein the isotopes of hydrogen, carbon and/or oxygen in the polymer have optionally been enriched and wherein the P4HB polymer is obtained by a process comprising:
suspending a P4HB biomass in ethanol for a period of time effective to extract lipids into the ethanol;
separating the P4HB biomass from the ethanol by solid-liquid separation;
collecting the ethanol-washed biomass; and
extracting the P4HB polymer into a solvent.

2. The composition of claim 1 wherein the abundance of deuterium in the polymer exceeds 0.0115% of all elemental hydrogen present in the polymer, and/or the polymer contains tritium.

3. The composition of claim 1 wherein the abundance of carbon-13 in the polymer exceeds 1.07% of all elemental carbon present in the polymer, and/or the polymer contains carbon-14.

4. The composition of claim 1 wherein the abundance of oxygen-17 in the polymer exceeds 0.038% of all elemental oxygen present in the polymer, and/or the abundance of oxygen-18 in the polymer exceeds 0.205%.

5. The composition of claim 1 wherein the abundance of deuterium in the polymer exceeds 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, or 85% of the elemental hydrogen present in the polymer.

6. The composition of claim 1 wherein the composition has a lipid content of less than 100 ppm as determined by gas chromatography after butanolysis.

7. The composition of claim 1 wherein the polymer is precipitated with a non-solvent for the polymer, harvested, and dried.

8. The composition of claim 7 wherein the solvent is selected from the group consisting of methylene chloride, chloroform, tetrahydrofuran, acetone, dioxane, ethyl acetate, dimethylene carbonate, dimethyl sulfoxide, dimethyl formamide, methyl ethyl ketone, butyl acetate, butyl propionate, and diethyl carbonate, and the non-solvent is selected from the group consisting of ethanol or aqueous ethanol.

9. The composition of claim 1 wherein the weight average molecular weight of the polymer is from 50,000 to 1.2 million Da.

10. The composition of claim 1 wherein the composition further comprises a therapeutic, diagnostic or prophylactic agent.

11. The composition of claim 1 sterilized with cold ethylene oxide gas, gamma-irradiation, or electron beam irradiation.

12. The composition of claim 1 wherein the composition is used as a coating on a medical device.

13. The composition of claim 12 used for soft or hard tissue repair, regeneration or replacement.

14. The composition of claim 1 wherein the composition forms a fiber wherein the fiber has a tensile strength of greater than 126 MPa.

15. The composition of claim 14 wherein the composition is used to form a yarn wherein the tenacity of the yarn is greater than 0.5 grams per denier.

16. The composition of claim 15 formed into a suture or textile.

17. A method of manufacturing a composition comprising poly-4-hydroxybutyrate (P4HB) polymer, wherein the isotopes of hydrogen, carbon and/or oxygen-in the polymer have optionally been enriched, comprising feeding 1,4-butanediol that has been enriched in an isotope of hydrogen, carbon and/or oxygen to a microorganism comprising a gene encoding a PHA synthase, suspending the P4HB biomass in ethanol for a period of time effective to extract lipids into the ethanol;
separating the P4HB biomass from the ethanol by solid-liquid separation;
collecting the ethanol-washed biomass; and
extracting the P4HB polymer into a solvent.

18. The method of claim 17 wherein the 1,4-butanediol is fully or partially deuterated.

19. A method of monitoring the degradation of poly-4-hydroxybutyrate polymer in vivo, wherein the isotopes of hydrogen, carbon and/or oxygen in the polymer have been enriched and wherein the P4HB polymer is obtained by a process comprising:
suspending a P4HB biomass in ethanol for a period of time effective to extract lipids into the ethanol;
separating the P4HB biomass from the ethanol by solid-liquid separation;
collecting the ethanol-washed biomass; and
extracting the P4HB polymer into a solvent,
comprising detecting an isotope enriched metabolite of the polymer in a blood or urine sample.

20. The method of claim 19 wherein the metabolite is 4-hydroxybutyrate enriched with isotopes of hydrogen, carbon and/or oxygen.

21. The method of claim 19 wherein the isotope enriched metabolite is detected using mass spectroscopy in the presence of the natural 4-hydroxybutyrate metabolite.

Assignees

• Tepha Inc

Inventors

• Martin David P
• Williams Simon F

Classifications

• C08L67/04

  Polyesters derived from hydroxycarboxylic acids, e.g. lactones (C08L67/06 takes precedence) · CPC title

• A61L27/18

  obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

• A61L31/10 Primary

  Macromolecular materials · CPC title

• A61L31/06 Primary

  obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds {(A61L31/041 takes precedence)} · CPC title

• Y10T436/201666

  Carboxylic acid · CPC title