Injectable biopolymer compositions and associated systems and methods
Injectable biopolymer compositions and associated systems and methods are disclosed herein. In some embodiments, a biopolymer composition for treating an aneurysm is provided. The biopolymer composition can include an injectable hydrogel including: a biopolymer; a chemical crosslinker forming covalent bonds with the biopolymer; and a stabilizer configured to inhibit ex vivo precipitation of the biopolymer. The injectable hydrogel can have an ex vivo storage modulus of at least 100 Pa at 37° C. over a linear viscoelastic region of the injectable hydrogel. The ex vivo storage modulus can be greater than an ex vivo loss modulus of the injectable hydrogel over the linear viscoelastic region of the injectable hydrogel.
1. A biopolymer composition for treating an aneurysm, the biopolymer composition comprising:
an injectable hydrogel comprising:
at least 2% w/v chitosan, wherein the chitosan has a weight average molecular weight of at least 100 kDa;
a chemical crosslinker comprising genipin, wherein the genipin forms covalent bonds between different chains of the chitosan; and
at least 1% w/v hydroxyethyl cellulose, wherein the hydroxyethyl cellulose interacts noncovalently with the chitosan to inhibit ex vivo precipitation of the chitosan, wherein the hydroxyethyl cellulose has a weight average molecular weight of at least 500 kDa, wherein the hydroxyethyl cellulose comprises a viscosity of at least 2000 Pa-s when measured as a 1% w/v solution at 20° C. and a shear rate of 1/s, and wherein the hydroxyethyl cellulose does not form covalent bonds with the genipin,
wherein the injectable hydrogel comprises an ex vivo storage modulus of at least 100 Pa at 37° C. over a linear viscoelastic region of the injectable hydrogel, and
wherein the injectable hydrogel is configured to occlude the aneurysm without undergoing a phase transition.
2. The biopolymer composition of claim 1 , wherein the injectable hydrogel does not undergo a phase transition upon exposure to in vivo conditions.
3. The biopolymer composition of claim 1 , wherein the chitosan comprises a viscosity of at least 50 Pa-s when measured as a 1% w/v solution at 20° C. and a shear rate of 1/s.
4. The biopolymer composition of claim 1 , wherein the injectable hydrogel comprises at least 2% w/v and no more than 9% w/v of the chitosan.
5. The biopolymer composition of claim 1 , wherein the hydroxyethyl cellulose is configured to inhibit ex vivo precipitation of the chitosan over a period of at least 1 month.
6. The biopolymer composition of claim 1 , wherein the injectable hydrogel comprises at least 1% w/v and no more than 5% w/v of the hydroxyethyl cellulose.
7. The biopolymer composition of claim 1 , wherein the injectable hydrogel comprises a contrast agent.
8. The biopolymer composition of claim 1 , wherein the injectable hydrogel comprises a physical crosslinker forming noncovalent interactions with the chitosan.
9. A biopolymer composition for treating an aneurysm, the biopolymer composition comprising:
an injectable hydrogel comprising:
at least 2% w/v chitosan, wherein the chitosan has a weight average molecular weight of at least 100 kDa;
a chemical crosslinker comprising genipin, wherein the genipin forms covalent bonds with the chitosan; and
at least 1% w/v hydroxyethyl cellulose, wherein the hydroxyethyl cellulose interacts noncovalently with the chitosan to inhibit ex vivo phase separation of the chitosan, wherein the hydroxyethyl cellulose has a weight average molecular weight of at least 500 kDa, wherein the hydroxyethyl cellulose comprises a viscosity of at least 2000 Pa-s when measured as a 1% w/v solution at 20° C. and a shear rate of 1/s, and wherein the hydroxyethyl cellulose does not form covalent bonds with the genipin,
wherein the injectable hydrogel comprises an ex vivo storage modulus that is greater than an ex vivo loss modulus of the injectable hydrogel over a linear viscoelastic region of the injectable hydrogel, and
wherein the injectable hydrogel is configured to be delivered into the aneurysm without undergoing a phase transition.
10. The biopolymer composition of claim 9 , wherein the injectable hydrogel comprises a preformed, ex vivo state that is configured to be stable at room temperature over a storage period of at least 1 month.
11. The biopolymer composition of claim 10 , wherein the ex vivo storage modulus of the injectable hydrogel varies by no more than 25% over the storage period.
12. The biopolymer composition of claim 9 , wherein the hydroxyethyl cellulose is configured to form an interpenetrating network with the chitosan.
13. The biopolymer composition of claim 9 , wherein the hydroxyethyl cellulose is configured to space apart hydrophobic groups on the chitosan.
14. The biopolymer composition of claim 9 , wherein the hydroxyethyl cellulose is configured to inhibit ex vivo phase separation of the chitosan after the injectable hydrogel has undergone heat sterilization.
15. The biopolymer composition of claim 1 , wherein the injectable hydrogel comprises from 0.005% w/v to 0.01% w/v of the genipin.
16. The biopolymer composition of claim 7 , wherein the contrast agent comprises one or more of the following: iohexol, iodixanol, iopamidol, diatrizoate, iothalamate, iopromide, ioversol, ioxilan, iothalamate/meglumine, ioxaglate/meglumine, diatrizoate/meglumine, iodomide sodium, or metrizamide.