The present invention provides a modified fibroin fiber having a shrinkage history of being irreversibly shrunk after spinning, the modified fibroin fiber containing modified fibroin, wherein a fiber diameter of a raw material fiber before being irreversibly shrunk exceeds 25 μm.

The present invention provides a modified fibroin fiber having a shrinkage history of being irreversibly shrunk after spinning, the modified fibroin fiber containing modified fibroin, wherein a fiber diameter of a raw material fiber before being irreversibly shrunk exceeds 25 μm.

According to an embodiment of the disclosure, a method of creating an object with a conduit is disclosed. A material is deposited on a sacrificial collector; and, the sacrificial collector is then removed to create the object with the conduit. Both the object and the sacrificial collector can approximate the shape of desired blood vessel. The method can also include a 3-D printing of the desired shape of the mold and utilization of Gallium as the sacrificial collector. The sacrificial object is created by insertion of the gallium in the mold. After removal of the gallium from the mold, fibers are electrospun onto the gallium. The gallium is removed through melting—leaving a scaffold, the object with the conduit. In addition to the gallium, an extra sacrificial layer of a water-soluble material may be utilized.

According to an embodiment of the disclosure, a method of creating an object with a conduit is disclosed. A material is deposited on a sacrificial collector; and, the sacrificial collector is then removed to create the object with the conduit. Both the object and the sacrificial collector can approximate the shape of desired blood vessel. The method can also include a 3-D printing of the desired shape of the mold and utilization of Gallium as the sacrificial collector. The sacrificial object is created by insertion of the gallium in the mold. After removal of the gallium from the mold, fibers are electrospun onto the gallium. The gallium is removed through melting—leaving a scaffold, the object with the conduit. In addition to the gallium, an extra sacrificial layer of a water-soluble material may be utilized.

The present invention relates to a fibrous 3-dimensional porous scaffold obtained by electro-spinning for tissue regeneration and a method for preparing the same.

The present invention relates to a fibrous 3-dimensional porous scaffold obtained by electro-spinning for tissue regeneration and a method for preparing the same.

A method of producing carbon nanofibers is disclosed that substantially impacts the carbon nanofibers' chemical and physical properties. Such carbon nanofibers include a semi-graphitic carbon material characterized by wavy graphite planes ranging from 0.1 nm to 1 nm and oriented parallel to an axis of a respective carbon nanofiber, the semi-graphitic carbon material also being characterized by an inclusion of 4 to 10 atomic percent of nitrogen heteroatoms, the nitrogen heteroatoms including a combined percentage of quaternary and pyridinic nitrogen groups equal to or greater than 60% of the nitrogen heteroatoms. The method of manufacture includes, for example, preparing a Polyacrylonitrile (PAN) based precursor solution, providing the PAN-based precursor solution to a spinneret and then performing an electro-spinning operation on the PAN-based precursor solution to create the one or more PAN-based nanofibers. The electro-spinning operation includes passing the PAN-based precursor solution from the spinneret to a collector at a distance between 1 cm to 30 cm while providing an Alternating Current (AC) voltage between the spinneret and the collector, the AC voltage including a frequency ranging from 20 Hz to 100,000 Hz and either a Peak-to-Peak (P-P) voltage ranging from 100 V to 30,000 V or a Root-Mean-Square (RMS) voltage ranging from 100 V to 30,000 V. Afterwards, post-electro-spinning operations, stabilizing treatments and pyrolysis treatments are performed.

A method of producing carbon nanofibers is disclosed that substantially impacts the carbon nanofibers' chemical and physical properties. Such carbon nanofibers include a semi-graphitic carbon material characterized by wavy graphite planes ranging from 0.1 nm to 1 nm and oriented parallel to an axis of a respective carbon nanofiber, the semi-graphitic carbon material also being characterized by an inclusion of 4 to 10 atomic percent of nitrogen heteroatoms, the nitrogen heteroatoms including a combined percentage of quaternary and pyridinic nitrogen groups equal to or greater than 60% of the nitrogen heteroatoms. The method of manufacture includes, for example, preparing a Polyacrylonitrile (PAN) based precursor solution, providing the PAN-based precursor solution to a spinneret and then performing an electro-spinning operation on the PAN-based precursor solution to create the one or more PAN-based nanofibers. The electro-spinning operation includes passing the PAN-based precursor solution from the spinneret to a collector at a distance between 1 cm to 30 cm while providing an Alternating Current (AC) voltage between the spinneret and the collector, the AC voltage including a frequency ranging from 20 Hz to 100,000 Hz and either a Peak-to-Peak (P-P) voltage ranging from 100 V to 30,000 V or a Root-Mean-Square (RMS) voltage ranging from 100 V to 30,000 V. Afterwards, post-electro-spinning operations, stabilizing treatments and pyrolysis treatments are performed.

A method of producing carbon nanofibers is disclosed that substantially impacts the carbon nanofibers' chemical and physical properties. Such carbon nanofibers include a semi-graphitic carbon material characterized by wavy graphite planes ranging from 0.1 nm to 1 nm and oriented parallel to an axis of a respective carbon nanofiber, the semi-graphitic carbon material also being characterized by an inclusion of 4 to 10 atomic percent of nitrogen heteroatoms, the nitrogen heteroatoms including a combined percentage of quaternary and pyridinic nitrogen groups equal to or greater than 60% of the nitrogen heteroatoms. The method of manufacture includes, for example, preparing a Polyacrylonitrile (PAN) based precursor solution, providing the PAN-based precursor solution to a spinneret and then performing an electro-spinning operation on the PAN-based precursor solution to create the one or more PAN-based nanofibers. The electro-spinning operation includes passing the PAN-based precursor solution from the spinneret to a collector at a distance between 1 cm to 30 cm while providing an Alternating Current (AC) voltage between the spinneret and the collector, the AC voltage including a frequency ranging from 20 Hz to 100,000 Hz and either a Peak-to-Peak (P-P) voltage ranging from 100 V to 30,000 V or a Root-Mean-Square (RMS) voltage ranging from 100 V to 30,000 V. Afterwards, post-electro-spinning operations, stabilizing treatments and pyrolysis treatments are performed.

A method of producing carbon nanofibers is disclosed that substantially impacts the carbon nanofibers' chemical and physical properties. Such carbon nanofibers include a semi-graphitic carbon material characterized by wavy graphite planes ranging from 0.1 nm to 1 nm and oriented parallel to an axis of a respective carbon nanofiber, the semi-graphitic carbon material also being characterized by an inclusion of 4 to 10 atomic percent of nitrogen heteroatoms, the nitrogen heteroatoms including a combined percentage of quaternary and pyridinic nitrogen groups equal to or greater than 60% of the nitrogen heteroatoms. The method of manufacture includes, for example, preparing a Polyacrylonitrile (PAN) based precursor solution, providing the PAN-based precursor solution to a spinneret and then performing an electro-spinning operation on the PAN-based precursor solution to create the one or more PAN-based nanofibers. The electro-spinning operation includes passing the PAN-based precursor solution from the spinneret to a collector at a distance between 1 cm to 30 cm while providing an Alternating Current (AC) voltage between the spinneret and the collector, the AC voltage including a frequency ranging from 20 Hz to 100,000 Hz and either a Peak-to-Peak (P-P) voltage ranging from 100 V to 30,000 V or a Root-Mean-Square (RMS) voltage ranging from 100 V to 30,000 V. Afterwards, post-electro-spinning operations, stabilizing treatments and pyrolysis treatments are performed.