Polymeric electrospun embolization device and methods of use
An embolization device may include a fiber section having a plurality of polymeric electrospun fibers and, optionally, a contrast agent. An embolization device may further include a plurality of fiber sections, wherein each fiber section is separated by a linker. A method of deploying such an embolization device may include inserting the embolization device into a vessel. The method may further include applying an electrical current to one or more of the linkers, applying electrothermal heat to at least a portion of the device, or applying force to at least a portion of a delivery vehicle for the device. A method of manufacturing the device may include electrospinning a fiber section, and processing the fiber section by straining, twisting, heating, or shaping it.
1. A coil embolization device for treatment of an aneurysm, the coil embolization device comprising:
a plurality of fiber sections having a plurality of polymeric electrospun fibers, wherein the fiber section excludes a core structure and comprises a twisted sheet of the polymeric electrospun fibers; and
a plurality of electrolytically degradable linkers, wherein each of the plurality of fiber sections is separated by one of the plurality of electrolytically degradable linkers, and wherein the plurality of electrolytically degradable linkers are configured to degrade and separate from an adjacent fiber section in response to an electrical current being applied thereto;
wherein the plurality of electrolytically degradable linkers comprise a first metal having a first galvanic potential, and a second metal having a second galvanic potential different from the first galvanic potential;
wherein the coil embolization device is configured to be placed within and conform to a shape of the aneurysm.
2. The coil embolization device of claim 1 , wherein the plurality of fiber sections comprise from about 200 twists per meter to about 4000 twists per meter.
3. The coil embolization device of claim 1 , wherein the plurality of fiber sections excludes a metal or polymer core structure within the plurality of fiber sections.
4. The coil embolization device of claim 1 , wherein the electrolytically degradable linkers comprise an electrically conductive polymer.
5. The coil embolization device of claim 1 , wherein the fiber sections and the electrolytically degradable linkers comprise different levels of radio-opacity.
6. The coil embolization device of claim 1 , wherein the plurality of fiber sections comprise a contrast agent.
7. The coil embolization device of claim 1 , wherein the polymeric electrospun fibers are spun from a polymer solution comprising tantalum in an amount of about 1000 wt %.
8. The coil embolization device of claim 1 , wherein the coil embolization device is configured to be able to achieve a packing density of between 59% to 79%.
9. The coil embolization device of claim 1 , wherein the coil embolization device comprises a framing component and a filling component, the framing component being a relatively long and stiff component and the filling component being a relatively short and soft component.
10. The coil embolization device of claim 1 , wherein the plurality of fiber sections comprise a thickness within a range from about 15 μm to about 500 μm.
11. The coil embolization device of claim 1 , further comprising a delivery device comprising a resistive or heating element, wherein at least a portion of the delivery device is releasably couplable to at least a portion of the coil embolization device with an adhesive, and wherein at least a portion of the adhesive is configured to melt in response to heat applied from the resistive or heating element to at least one of the coil embolization device portion or the delivery device portion to release the coil embolization device from the delivery device.
12. The coil embolization device of claim 1 , further comprising a delivery device, the delivery device comprising an inner wire and an outer sheath, the inner wire offset from the central axis of the outer sheath by a distance of about 1 mm to about 10 mm, wherein at least a portion of the plurality of fiber sections are configured to be positioned within the outer sheath and further configured to be released from the outer sheath as a result of a mechanical force applied to at least a portion of the delivery device.
13. The coil embolization device of claim 12 , wherein the outer sheath comprises at least one crimped portion configured to stabilize the fiber section portion within the delivery device when the fiber section portion is positioned within the crimped portion of the outer sheath, and wherein the fiber section portion is configured to be released from the crimped portion of the outer sheath due to the mechanical force.
14. The coil embolization device of claim 1 , wherein a shape of the plurality of fiber sections is set by application of heat at a temperature from about 150 degrees F. to about 400 degrees F.
15. The coil embolization device of claim 1 , wherein the plurality of fiber sections comprise a stiffened fiber section obtained by application of a strain between about 25% to about 50% of an original length of the plurality of fiber sections.
16. The coil embolization device of claim 1 , wherein the plurality of fiber sections further comprise an anti-proliferative drug or an anti-inflammatory drug.
17. The coil embolization device of claim 1 , wherein the plurality of fiber sections comprise a deflection stiffness from about 0.05 g to about 0.3 g.
18. The coil embolization device of claim 1 , wherein the plurality of fiber sections comprise a diameter from about 100 μm to about 1000 μm.