Patent Grant
7682539
The invention relates to the process of spinning fibers of silk and silk-like proteins from an admixture of solubilized silk or silk-like protein in an ionic liquid solvent.
Artificial spinning methods for silk fibroin have typically fallen into the categories of wet spinning and electrospinning. Wet spinning has the advantage of producing reelable fiber that can be drawn and tested for mechanical properties. Electrospinning can produce extremely fine fibers in the form of a non-woven mat, however mechanical testing of individual fibers is not feasible. These electrospun mats can be used as scaffolds for biomedical applications.
In previously reported results, spin dopes have been formed with silk fibroin dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) (U.S. Pat. No. 5,252,285), hexafluoroacetone (HFA), formic acid, trifluoroacetic acid (TFA), and water mixed with polyethylene oxide (PEO). All of these spin dopes require a time-consuming, multistep process, where the silk fibroin is first washed of the glue-like sericin covering the fiber, dissolved in a salt based solvent, dialysed, and dried to eliminate the β-sheet crystal structure before the fibroin is soluble in the spinning solvent. It has been shown previously that silk fibroin is directly soluble in organic-based ionic liquids, both with or without the sericin present, as in U.S. patent application Ser. No. 11/326,678, incorporated herein by reference. These ionic liquid silk solutions were used to cast films of silk. As a spin dope, ionic liquids exhibit several advantages over the aforementioned spin dopes, such as negligible volatility and ease of solvent recovery.
The approach to wet spinning of silk fibroin from the silkworm Bombyx mori has varied in terms of equipment, i.e. a syringe pump with a hypodermic needle, a cylinder pressurized with N2 gas to force the spin dopes through a spinneret, and a syringe pump with a tapered spinneret etched in silicon to better control the fiber crystallite orientation. These spinning techniques typically utilize a methanol coagulation bath to remove the spinning solvent and induce crystallization in the fibers. Subsequent post-spin fiber drawing is typically conducted after soaking the fibers overnight in a methanol bath while the fibers were wet with methanol or water. Some fibers have been steam annealed. The drawing and annealing improve both the maximum modulus and the strain to break of the fibers.
The present invention relates to a process of forming fibers of silk and silk-like proteins in a solution with a solvent consisting of a pure ionic liquid, an ionic liquid mixture, an ionic liquid mixed with one or more cosolvents, or an ionic liquid mixture mixed with one or more cosolvents. A solution is extruded through a spinneret orifice to form a fiber. The spinneret is either directly immersed in the coagulation bath or the spinneret is surrounded by a noncoagulating medium (i.e., air or other inert fluid) and the extruded fiber is subsequently immersed in a coagulation bath. Fibers may also be formed by extruding a fiber directly from a reservoir of solution into a noncoagulating, inert medium and then immersing the extruded fibers into a coagulation bath to rinse the fiber of ionic liquid.
Silk and silk-like proteins are readily soluble in ionic liquid solvents. See, e.g., U.S. patent application Ser. No. 11/326,678, filed on Dec. 29, 2005, incorporated herein by reference. These silk in ionic liquid solutions can be used as spin dopes to form fibers. The present invention allows for custom diameters of silk and silk-like fibers to be formed via wet spinning, dry-jet wet spinning, drawing or extrusion. For natural silk proteins, the present invention allows for diameters and properties that are not found in nature.
As used herein the term “ionic liquid” refers to a liquid that is comprised of anions and cations. Ionic liquids are attractive solvents as they are non-volatile, non-flammable, have a high thermal stability, are relatively inexpensive to manufacture, are environmentally friendly, and can be used to provide greater control and flexibility in the overall processing methodology. Ionic liquids of interest exist as liquids well below room temperature up to a temperature as high as 200° C. U.S. patent application Ser. No. 11/326,678, filed on Dec. 29, 2005, referred to above, contains numerous examples of suitable ionic liquid solvents for dissolving silk and silk-like proteins.
Viscosity can become an issue with ionic liquid solutions as the silk content is increased. To be useful as a spin dope, the solution must flow and must have a high enough silk or silk-like protein concentration to allow the molecules to hydrogen bond during the spinning process. A typical spin dope contains about 20% (w/w) of silk or silk-like protein loading. To reduce the viscosity, the temperature can be increased to near the neat ionic liquid melting temperature or a compatible cosolvent can be added. Both means are feasible, however prolonged exposure to elevated temperature can degrade the silk or silk-like protein.
A desirable cosolvent that is miscible with the ionic liquid can be used to lower the solution viscosity without causing the silk or silk-like protein to crash from the solution. It is desirable to have the cosolvent poise the solution for crashing so that the spinning process induces aligned crystallization within the fiber without the aid of a coagulation bath or post-spin drawing. Compatible cosolvents include but are not limited to water, methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, 2-methyl-1-propanol, 2-methyl-2-propanol, or acetonitrile or mixtures thereof.
The spinnable solution may then be spun into fibers using elements known in the art. These processes include, for example, wet spinning, dry-jet wet spinning, and extrusion/drawing. The choice of the ionic liquid and cosolvent makes the spin dope solutions highly tunable to be compatible with the various spinning methods.
In the wet spinning process, the spinning solution is extruded through a spinneret directly into a coagulating bath. The coagulant may be any fluid wherein the ionic liquid and cosolvent(s) are soluble, but wherein the silk or silk-like protein is not. Examples of suitable fluids include but are not limited to water, methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, 2-methyl-1-propanol, 2-methyl-2-propanol, or acetonitrile or mixtures thereof. Methanol is a preferred coagulant because in addition to removing the ionic liquid from the fiber, it induces crystalline β-sheet formation within the fibers. The fibers can be cold drawn while still wet with the coagulant to modify their mechanical properties. Preferably, the fibers are dried while under tension to improve their tensile properties.
In dry-jet wet spinning, the spinning solution is extruded through a spinneret; attenuated and stretched in an inert, noncoagulating medium; and then immersed into a coagulating medium in a fashion similar to wet jet spinning. Care must be taken with the choice of medium when using ionic liquids. For example, humidity in the air can be absorbed into the spun fiber and possibly cause the silk or silk-like protein to redissolve. This can lead to fiber breakage.
In extrusion/drawing, the fiber is pulled directly from a reservoir of spin dope; attenuated and stretched in an inert, noncoagulating medium; and then immersed into a coagulating medium in a fashion similar to dry-jet wet spinning. As in dry-jet wet spinning, care must be taken with the choice of medium when using ionic liquids.
The following examples further describe the invention but should not be construed as limiting the scope of the invention.
For this work, the spin dope was prepared from silkworm cocoon silk dissolved in the ionic liquid 1-ethyl-3-methylimidazolium chloride (EMIC). The silk for this work was grown in house with silkworms raised on a diet consisting exclusively of Silkworm Chow (Mulberry Farms, Fallbrook, Calif.). The cocoons were harvested between two and seven days of spinning by cutting the cocoons to release the pupae unharmed, which reduces the contaminants in the silk. To remove the sericin, the cocoons were boiled in a 50 mM Na2CO3 and 50 mM Na2EDTA solution, thoroughly rinsed in distilled, deionized water, and lyophilized. The dried silk was mixed with the dry EMIC to make a 10% (w/w) spin dope solution. To dissolve the silk, the spin dope was heated at 95° C. and stirred while exposed to ambient air with a 20% RH. The water content of the final spin dope cooled to room temperature was 1.62±2.00% (w/w) as determined via headspace analysis using a Mettler Toledo DL39 Karl Fischer coulometer connected to a Stromboli® oven sample changer. Spin dope was also prepared under a dry N2 atmosphere, however, the dry spin dope was glassy at room temperature and unusable in our spinning apparatus.
For the spinning equipment, applicants used a glass syringe fitted with a 26 gauge, blunt tip needle with an inside diameter of 0.26 mm and an overall length of 23 mm. The spin dope was placed into the syringe while hot, and the air was removed. The spinning was performed by extruding the spin dope at a rate of approximately 3 m/min across a 50 mm air gap into a coagulation bath. The extruded fiber swelled to a diameter of about 1 mm before entering the coagulation bath.
a Only a small amount of silk remained in a fiber skeleton.
b The ionic liquid was immiscible with the coagulation solvent.
Several solvents were tested as coagulation baths. The coagulation bath solvent effects for the spun fibers are listed in Table 1. The methanol bath formed clear, solid fibers, the acetonitrile bath formed crusted, white fibers, and the water bath appeared to form fibers similar to the methanol bath. The remaining baths of ethyl acetate, acetone, and hexanes all resulted in rapid droplet formation from the extruded spin dope; these droplets were immiscible with the bath solvents and did not coagulate. In cases where fibers persisted, the fibers were allowed to remain in their respective coagulation baths overnight to remove the residual EMIC.
For the methanol, acetonitrile, and water coagulation baths, only the fibers from the methanol bath could be handled. Sections of the methanol bath fibers were hand drawn to twice (2×) their as spun length. Both the as spun and 2× methanol rinsed fibers were allowed to air dry to remove the bath solvent. The acetonitrile bath fibers adhered to the bottom of the coagulation bath tank and fractured during attempts to remove them. The water bath fibers broke and collapsed when removed from the bath.
The diameters of the undrawn and 2× draw ratio methanol bath fibers were 250 and 150 μm, respectively. The crystallite alignment of the fibers was further examined by wide angle X-ray scattering (WAXS). The WAXS data for the 2× draw ratio fiber show crystallite alignment along the fiber axis and the peaks for the β-sheet form of silk fibroin. The'crystallite alignment is critical to the strength and toughness of natural Bombyx mori silk cocoon fibers.
For this work, the spin dope was prepared from silkworm cocoon silk dissolved in the ionic liquid 1-butyl-3-methylimidazolium chloride (BMIC). The silk for this work was obtained commercially. To remove the sericin and any sizing agents, the cocoons were boiled heating in 30 times(v/w) of 8M aqueous urea containing 0.04 M Tris-SO4 (pH 7) and 0.5M mercaptoethanol. The stripped silk was rinsed 10 times with deionized water to remove any sericin residue and lyophilized. The dried silk was combined with the dry BMIC to make a 25% (w/w) silk mixture. To dissolve the silk, the spin dope was heated at 110° C. and stirred with a centrifugal mixer under a dry N2 atmosphere. The temperature was reduced to 95° C. after the silk dissolved. A cosolvent of water was added to the admixture in 1% (w/w) increments to a total of 5% (w/w) water to establish a liquid admixture at room temperature. The final admixture was 9.5% (w/w) silk, 85.5% (w/w) BMIC, and 5% (w/w) water.
Silk fibers were formed by forcing the room temperature admixture through a 100 μm nickel spinneret submerged in a 100% methanol coagulation bath. The pressure drop for the spinneret was 7500 psig for a 75 μl/min flow rate. The formed fibers were loosely collected onto a submerged reel and soaked in the methanol bath overnight. The fibers were subsequently transferred to a water bath for a day and then air dried. No post spin drawing was conducted. The mechanical properties of the fibers are listed in Table 2.
For this work, the spin dope was prepared from silkworm cocoon silk dissolved in the ionic liquid 1-butyl-3-methylimidazolium chloride (BMIC). The silk for this work was obtained commercially. To remove the sericin and any sizing agents, the cocoons were boiled heating in 30 times (v/w) of 8M aqueous urea containing 0.04 M Tris-SO4 (pH 7) and 0.5M mercaptoethanol. The stripped silk was rinsed 10 times with deionized water to remove any sericin residue and lyophilized. The dried silk was combined with the dry BMIC to make a 20% (w/w) silk mixture. To dissolve the silk, the spin dope was heated at 110° C. and stirred with a centrifugal mixer under a dry N2 atmosphere. Although the solution solidified when cooled to room temperature, they could be easily reheated without separation.
Silk fibers were formed by placing a reservoir of the spin dope under a dry N2 atmosphere and heating it to 60° C. The fiber drawing was conducted by touching a glass rod to the reservoir surface and pulling a fiber. The pulled fibers were immediately immersed into a coagulation bath of methanol to rinse the ionic liquid from the fibers. The average fiber diameter obtained from this method is 10 μm.
This application claims priority of the filing date of Provisional Application Ser. No. 60/762,212, filed on Jan. 11, 2006.
The invention described herein may be manufactured and used by or for the Government of the United States for all governmental purposes without the payment of any royalty.
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| Number | Date | Country | |
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| 60762212 | Jan 2006 | US |
