초록 ▼

Compositions that include fibrin microthreads are provided. The compositions can include one or more therapeutic agents including cytokines and interleukins, extracellular matrix proteins and/or biologically active fragments thereof (e.g., RGD-containing peptides), hormones, vitamins, nucleic acids,

Compositions that include fibrin microthreads are provided. The compositions can include one or more therapeutic agents including cytokines and interleukins, extracellular matrix proteins and/or biologically active fragments thereof (e.g., RGD-containing peptides), hormones, vitamins, nucleic acids, chemotherapeutics, antibiotics, and cells. Also provided are methods of making compositions that include fibrin microthreads. Also provided are methods for using the compositions to repair or ameliorate damaged or defective organs or tissues.

대표청구항 ▼

1. A method of making a fibrin microthread, the method comprising: (a) combining a first volume of fibrinogen and a second volume of a molecule capable of forming fibrin from the fibrinogen to form a mixture;(b) transferring the mixture to a lumen containing device;(c) disposing a distal end of the

1. A method of making a fibrin microthread, the method comprising: (a) combining a first volume of fibrinogen and a second volume of a molecule capable of forming fibrin from the fibrinogen to form a mixture;(b) transferring the mixture to a lumen containing device;(c) disposing a distal end of the lumen containing device into an aqueous bath;(d) moving the distal end of the lumen containing device through the aqueous bath at a first velocity;(e) extruding the mixture of the fibrinogen and the molecule through the distal end of the lumen containing device into an aqueous bath at a second velocity while moving the distal end of the lumen containing device through the aqueous bath at the first velocity, the second velocity being different than the first velocity;(f) allowing the fibrin microthread to substantially form in the aqueous bath. 2. The method of claim 1, wherein the fibrinogen is human fibrinogen or fibrinogen of a non-human primate, a domesticated animal, or a rodent. 3. The method of claim 1, wherein the fibrinogen is obtained from a naturally occurring source or is recombinantly produced. 4. The method of claim 1, wherein the molecule is a protease. 5. The method of claim 4, wherein the protease is thrombin. 6. The method of claim 1, further comprising recovering the fibrin microthread from the aqueous bath and permitting the fibrin microthread to dry. 7. The method of claim 1, further comprising providing a therapeutic agent and (a) extruding the therapeutic agent with the fibrinogen and the molecule thereby producing a fibrin microthread comprising the therapeutic agent or (b) associating the therapeutic agent with a formed fibrin microthread. 8. The method of claim 7, wherein the therapeutic agent is a growth factor, a protein, a chemotherapeutic agent, a vitamin, a mineral, an antimicrobial agent, a small organic molecule, or a biological cell. 9. The method of claim 8, wherein the growth factor is a cytokine or interleukin. 10. The method of claim 8, wherein the protein is a hormone, an extracellular matrix protein, or an antibody. 11. The method of claim 10, wherein the extracellular matrix protein is collagen, elastin, laminin, tenascin, or fibronectin. 12. The method of claim 8, wherein the antimicrobial agent is an antibacterial agent, an antiviral agent, an antifungal agent, or an antiparasitic agent. 13. The method of claim 1, further comprising the step of combining the fibrin microthread with a microthread comprising a non-fibrin polymer. 14. The method of claim 13, wherein the non-fibrin polymer is a synthetic polymer. 15. The method of claim 13, wherein the non-fibrin polymer is a natural polymer. 16. The method of claim 15, wherein the natural polymer comprises collagen or a collagen-based material, hyaluronic acid or a hyaluronic acid-based material, cellulose or a cellulose-based material, silk and combinations thereof. 17. The method of claim 1, further comprising the step of recovering the fibrin microthread from the aqueous bath and subsequently associating the fibrin microthread with a substrate. 18. The method of claim 17, wherein the substrate is a woven or non-woven mesh, a surgical pin, a surgical screw, a surgical plate, a physiologically acceptable patch, dressing, bandage, or a natural or mechanical valve. 19. A method of forming a fibrin microthread using a dispensing apparatus, the dispensing apparatus comprising a first reservoir containing fibrinogen, a second reservoir containing a molecule capable of forming fibrin from the fibrinogen, a blending connector fluidically coupled to the first reservoir and the second reservoir, and a lumen containing device fluidically coupled to the blending connector, the method comprising: transferring a first volume of fibrinogen from the first reservoir to the blending connector;transferring a second volume of the molecule capable of forming fibrin from the fibrinogen from the second reservoir to the blending connector;the first volume of fibrinogen and the second volume of the molecule forming a mixture in the blending connector;transferring the mixture from the blending connector to the lumen containing device;disposing a distal end of the lumen containing device in an aqueous bath;moving the distal end of the lumen containing device through the aqueous bath at a first velocity; andextruding the mixture from the distal end of the lumen containing device into the aqueous bath at a second velocity while moving the distal end of the lumen containing device through the aqueous bath, the ratio of the second velocity to the first velocity in the range of about 1.5 to about 6. 20. The method of claim 19, wherein the ratio of the second velocity to the first velocity is about 2. 21. The method of the claim 19, wherein an internal diameter of the lumen containing device is in the range of about 250 μm to about 1,000 μm. 22. The method of claim 19, wherein the aqueous bath is maintained at a temperature in the range of about 18 degrees Celsius to about 40 degrees Celsius. 23. The method of claim 19, further comprising; removing the fibrin microthread from the aqueous bath after a predetermined time; anddrying the fibrin microthread. 24. A method of forming a fibrin microthread comprising: combining a first volume of fibrinogen and a second volume of a molecule capable of forming fibrin from the fibrinogen to form a mixture; transferring the mixture to a lumen containing device;disposing a distal end of the lumen containing device in an aqueous bath;moving the distal end of the lumen containing device through the aqueous bath at a first velocity while extruding the mixture from the distal end of the lumen containing device into the aqueous bath at a second velocity, the second velocity being different than the first velocity;incubating the mixture in the aqueous bath for a predetermined incubation time to form the fibrin microthread. 25. The method of claim 24, wherein the incubation time is at least about 1 minute. 26. The method of claim 25, wherein the incubation time is at least about 3.5 minutes. 27. The method of claim 24, wherein the incubation time is in the range of about 1 minutes to about 30 minutes. 28. The method of claim 1, wherein the fibrin microthread has a tensile strength of at least about 4 MPa.