SILK FIBROIN BIOINKS AND RELATED USE FOR 3D BIOPRINTING

20240226377

18/278082

February 24, 2022

The present invention relates to silk fibroin bioinks specifically formulated for use in 3D bioprinting and the production of ex-vivo models capable of supporting hematopoiesis and the production of platelets and blood cells.

1. A bioink formulation comprising: a silk fibroin in an amount of 0.5%-35% w/v; a gelatin or derivatives thereof in an amount of 5-20% w/v; an alginic acid or derivatives thereof in an amount of 0.5-2% w/v; a glucose or analogue thereof in an amount of 3-4% w/v; a controlled density solution in an amount of 1-3% w/v; a buffer in an amount of 4-6% w/v; and a saline buffer solution up to 100% w/v; wherein the gelatin and alginic acid or derivatives thereof are present in a reciprocal ratio ranging from about 10:1 to about 20:1; wherein the silk fibroin and gelatin are present in a reciprocal ratio ranging from about 1:5 to about 1:0.5; wherein said glucose or analogue thereof is selected from the group consisting of disaccharides, stereoisomers, isomers, epimers, alditols or acids of glucose, precursors or products deriving from the glucose metabolism, capable of entering the cell via glucose transporters to be part of the glycolysis cycle; suitable for extrusion with hematopoietic lineage cells.

2. The bioink formulation according to claim 1, further comprising a cell component selected from the group consisting of progenitor cells of the myeloid or lymphoid lineage, stem cells or differentiated cells of the hematopoietic lineage selected from the group consisting of monocytes, macrophages, granulocytes, neutrophils, basophils, eosinophils, red cells, megacaryocytes, platelets, dendritic cells, T lymphocytes, B lymphocytes, NK cells, fibroblasts, mesenchymal stem cells, endothelial cells.

3. The bioink formulation according to claim 1, wherein said cells are present at a concentration within the range of 0.5-4×106 cells/ml, preferably 1×106 cells/ml.

4. The bioink formulation according to claim 1, wherein the gelatin is type A or type B.

5. The bioink formulation according to claim 1, wherein the derivatives of alginic acid are salts with alkaline and alkaline earth metals selected from the group consisting of sodium alginate, calcium alginate, magnesium alginate, potassium alginate and alginate methacrylate.

6. The bioink formulation according to claim 1, wherein the controlled density solution is a defined density solution selected from the group consisting of colloidal silica, copolymers, hydrophilic polysaccharides or synthetic high-molecular-weight polymers.

7. The bioink formulation according to claim 1, wherein the buffer is organic or mineral selected from the group consisting of: HEPES, MES, ADA, ACES, PIPES, MOPSO, Bis-6Tris Propane, BES, MOPS, TES, DIPSO, MOBS, TAPSO, HEPPSO, POPSO, EPPS (HEPPS), Tricine, Gly-Gly, Bicine, HEPBS, TAPS, AMPD, TABS, AMPSO, CHES, CAPSO, AMP, CAPS and CABS.

8. The bioink formulation according to claim 1, further comprising at least one of a fluorescent marker, a contrast agent, a luminescent agent, a radiopaque agent, a radioactive element or combinations thereof.

9. The bioink formulation according to claim 1, wherein the formulation is sterile.

10. The bioink formulation according to claim 1, further characterized in that it is at a temperature of 37° C.

11. A method of bioprinting comprising applying of a bioink formulation according to claim 1.

12. A method for the production of scaffolds comprising progenitor cells of the myeloid or lymphoid lineage, stem cells or differentiated cells of the hematopoietic lineage comprising applying the bioink formulation of claim 1.

13. A method for the production of a 3D scaffold, comprising: a) bioprinting of the bioink formulation according to claim 1 through a nozzle having a caliber ranging from 18 G to 27 G at an extrusion pressure within the range of 5-200 kPa and a printing rate within the range of 5-1,000 mm/min on a substrate to obtain a mono- or multi-layer 3D scaffold; b) soaking the 3D scaffold obtained according to step a) in a reticulating solution; c) adding the cell culture medium to the scaffold and optionally growth factors to promote cell differentiation.

14. The method for the production of a 3D scaffold according to claim 13, wherein the extrusion pressure ranges from 5 kPa to 20 kPa and the printing rate is within the range of 400-1,000 mm/min.

15. A scaffold obtained by a bioprinting method of the bioink formulation according to claim 1.

16. A scaffold obtained by a bioprinting method of the bioink formulation according to claim 13.

17. The scaffold according to claim 15, wherein the bioink formulation further comprises one or more molecules selected from the group consisting of: components of the extracellular matrix such as proteoglycans, hyaluronic acid, collagens, elastin, fibronectin, fibrin, fibrinogen, laminin, thrombospondin; growth factors, cytokines and chemokins, preferably hematopoietic, such as interleukins, CSF-1, G-CSF, GM-CSF, SCF, FLT3-L, TPO, EPO, SDF-1α; TGF-β1, TNFα, VEGF, FGF, Notch ligands, WNT, Angiopoietin-1, BMP, IGF-2 and fragments or variants thereof; antigens, conjugated or unconjugated antibodies, or their fragments such as CDRs or epitopes; hormones, such as insulin, glucagon, triiodothyronine, thyroxine, or their antagonists; drugs or prodrugs, such as TPO mimetics, TPO receptor agonists, tyrosine kinase receptor agonists, tyrosine kinase receptor inhibitors, Rho kinase inhibitors (ROCK), kinase inhibitors, aryl hydrocarbon receptor antagonists, chemotherapeutic agents; nucleic acids, such as DNA, RNA, siRNA, RNAi and microRNA, plasmids, lentiviruses, CRISPR; enzymes and/or intermediates of enzymatic reactions; and toxins.

18. A method for dissolving the scaffold obtained from a bioprinting method of the bioink formulation according to claim 1, wherein the method comprises preparing the scaffold by means of the method of claim 13, and further comprises using a dissolution solution of the scaffold comprising sodium citrate, collagenase, alginate lyase and a source of glucose.

19. The method according to claim 18, wherein the dissolution solution of the scaffold comprises: sodium citrate in an amount of 15 mM collagenase in an amount of 10 U/mL alginate lyase in an amount of 5 U/mL 5 mM glucose a saline buffer solution.

20. A method of supporting hematopoiesis or for the production of platelets and blood cells comprising using the scaffold according to claim 15 as an ex vivo model.

21. A method of supporting in vivo hematopoiesis or the production of platelets and blood cells comprising using the scaffold of claim 15 as a surgical implant.

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edspap.20240226377