Patent Application
20140213764
Embodiments of the present invention generally relate to nanocellulose and, more particularly, to methods of preparing nanocellulose foam containing one or more active ingredients.
Wound dressings may be comprised of films, gels, hydrocolloids and foams. Foam wound dressings may include polyurethane foams, foams of cellulose derivatives and bacterial foams and gels. The inventors have deduced that incorporating one or more active ingredients, such as antibacterial agents and antimicrobial agents, into nanocellulose foams, also referred to as cellulose nanofibril foams, should help promote wound healing.
Therefore, the inventors have provided improved nanocellulose foams containing one or more active ingredients and methods of preparing such nanocellulose foams containing one or more active ingredients.
Embodiments of the present invention relate to methods of preparing nanocellulose foam containing one or more active ingredients. In some embodiments, a method of forming a nanocellulose structure may include forming a liquid mixture of nanocellulose, wherein the nanocellulose is dispersed, suspended and/or gelled in the liquid mixture; drying the liquid mixture of nanocellulose to form a nanocellulose foam; and mixing one or more active ingredients into at least one of the liquid mixture of nanocellulose or the nanocellulose foam.
In some embodiments, a nanocellulose structure may include a nanocellulose foam comprising at least one of a carboxylate group, a hydroxyl group, or a sulfate group bonded to an active ingredient.
Other and further embodiments of the invention are described in more detail below.
So that the manner in which the above recited features of the present invention can be understood in detail, a more particular description of the invention, briefly summarized above, may be had by reference to embodiments, some of which are illustrated in the appended drawings. It is to be noted, however, that the appended drawings illustrate only typical embodiments of this invention and are therefore not to be considered limiting of its scope, for the invention may admit to other equally effective embodiments.
a through 5d depict the results of zone of inhibition antimicrobial tests of the nanocellulose hydrogel (a and c) and nanocellulose-Ag hydrogel (b and d) against (a-b) Escherichia coli and (c-d) Staphylococcus aureus.
Embodiments of the present invention include nanocellulose foams containing one or more active ingredients as well as methods of preparing such nanocellulose foams containing one or more active ingredients. Nanocellulose foams in accordance with embodiments of the present invention may advantageously have high surface area, porosity, and absorption and adsorption properties, as well, as biocompatibility and flexible mechanical properties.
The nanocellulose produced by TEMPO oxidation is surface functionalized with carboxylate groups. The nanocellulose produced by sulfuric acid hydrolysis is surface functionalized with sulfate groups. The carboxylate groups or sulfate groups or hydroxyl groups of cellulose advantageously allow for the incorporation of a variety of active ingredients to provide a variety of functionalities, as discussed below.
At 104, the liquid mixture of nanocellulose is dried to form a nanocellulose foam. In some embodiments, the liquid mixture of nanocellulose is dried using a freeze drying process. For example, in some embodiments, the liquid mixture is frozen in an ethanol/dry ice bath then freeze dried at a pressure of 0.1 mbar. The freeze dried nanocellulose foam has an average pore size diameter of about 1 μm to about 100 μm. The pore sizes may vary from one side of the foam to another side of the foam (e.g., opposing sides). For example, a foam may be formed to have an average pore size of about 50 μm on one side and about 10 μm on another side. Alternatively, the mixture of nanocellulose can be dried using one of a super-critical carbon dioxide (CO2) drying process or a liquid carbon dioxide (CO2) drying process. The nanocellulose foam prepared by super-critical or liquid carbon dioxide drying comprises a pore size in the sub-micron range and a high surface area of about 200 m2/g to about 400 m2/g.
At 106, one or more active ingredients may be added to the nanocellulose. The active ingredient may be mixed into at least one of the liquid mixture of nanocellulose prior to drying 104 (discussed above) or into the nanocellulose foam after drying at 104. As used herein, an active ingredient is any chemical element, compound or other substance that can be coupled to the nanocellulose to provide additional activity that the bulk nanocellulose does not normally provide, for example pharmaceutical activity or antimicrobial activity. Some suggested active ingredients are described below in detail. In some embodiments, the active ingredient is coupled to the nanocellulose by a physical interaction, such as adhesion, or by a chemical interaction, such as covalent bonding, ionic bonding, or hydrogen bonding, or by a self-assembly process or a by vapor deposition process, or by a layer by layer process.
In some embodiments, additional materials, such as binders, proteins, surfactants, preservatives, fillers or colorants, may be added to the nanocellulose foam. Such materials can be added to the liquid mixture of nanocellulose prior to drying or to the dried nanocellulose foam. These materials can be coupled to the nanocellulose by physical or chemical interaction.
In some embodiments, as depicted in
In some embodiments, the structure of nanocellulose foam is enhanced by hydrogelation of nanocellulose dispersion with cations before drying process. A few examples of these cations include, but are not limited to, Ca2+, Zn2+, Cu2+, Al3+ and Fe3+, among which Ca2+ and Fe3+ are biocompatible. Nanocellulose hydrogels are produced by addition of a metal salt solution to the top of nanocellulose aqueous dispersion. The moduli of thus formed hydrogels correlate well with binding strength of cations with surface carboxylate groups on nanocellulose, as provided in Table 1.
To include the active ingredients in cation-induced hydrogels, active ingredients can be either added to the liquid dispersion prior to hydrogelation or added to hydrogels after gel formation. For example, proteins that promote wound healing are chemically attached or physically absorbed to the surface of cation-induced hydrogels.
In some embodiments, nanocellulose gels can be functionalized with chitosan. In one example, nanocellulose beads with chitosan are generated by dropping nanocellulose dispersion into CaCl2 or other aqueous salt solution, followed by hardening and rinsing with water. Then the nanocellulose beads were incubated with chitosan. In another example, nanocellulose dispersion was dropped into chitosan/CaCl2 or other aqueous salt solution to form nanocellulose/chitosan beads.
In some embodiments, the liquid mixture of nanocellulose can be functionalized with silver (Ag) to form a hydrogel. For example, in some embodiments, the hydrogel is generated by adding silver nitrate (AgNO3) to the liquid mixture of nanocellulose. In an exemplary embodiment, a sufficient amount of silver nitrate (AgNO3) is added to the liquid mixture of nanocellulose to ensure complete saturation of carboxylate groups with silver ions. The addition of silver nitrate (AgNO3) results in the gelation of the liquid mixture of nanocellulose. The hydrogel is allowed to sit for a desired period of time in order to promote the slow reduction from silver ions (Ag+) to silver (Ag) nanoparticles. The hydrogel may be immersed in water to rinse off any unattached silver (Ag) species.
In some embodiments, to form an aerogel, silver nitrate (AgNO3) is introduced to the liquid mixture of nanocellulose in quantities to remain below the gelation threshold. The functionalized liquid mixture of nanocellulose is then degassed under vacuum to remove air bubbles and freeze dried as described above. To reduce silver ions (Ag+) to silver (Ag) nanoparticles, the top and bottom sides of the dried aerogels are exposed under a UV lamp for 30 minutes each.
In other embodiments, as depicted in
For example, in some embodiments, a nanocellulose foam is prepared by adding an acid, such as hydrochloric acid (HCl), to a liquid mixture of nanocellulose resulting in the gelation of the liquid mixture. The non-functionalized nanocellulose hydrogel is removed from the hydrochloric acid (HCl) solution and washed with water several times. The hydrogel can then be dipped in a liquid solution containing an active ingredient, such as silver, and dried as described above to form a functionalized nanocellulose foam 206A.
Alternatively, for example, the nanocellulose foam is an aerogel formed by degassing the liquid mixture of nanocellulose under vacuum to remove air bubbles. The liquid mixture of nanocellulose is then freeze dried as described above. The freeze dried nanocellulose aerogel can then be loaded with an active ingredient such as silver ions or silver nanoparticles. In some embodiments, the foam can be particle or bead shapes or in sheet forms.
In some embodiments, the nanocellulose foam is used as a wound dressing and the selected active ingredient has at least one of antimicrobial properties, antiviral properties, or hemostatic properties. In some embodiments, the nanocellulose foam can have a high porosity, for example, greater than about 99%, such that upon application to the wound, the nanocellulose foam can absorb large amounts of wound fluid exudates. As the nanocellulose foam absorbs fluid, it releases the active ingredient to the wound. For example, in some embodiments, the active ingredient is at least one of a silver species, a copper species, chitosan, an antimicrobial drug, an antibiotic, a pharmaceutical, a vitamin, a mineral, or a diagnostic agent.
A variety of active ingredients can be added to the liquid mixture of nanocellulose suitable for use in a variety of industries, such as biomedical, cosmetic, and pharmaceutical. In some embodiments, the active ingredient is advantageously selected to promote a variety of properties, such as adsorption of external materials, permeability of matter or energy, conductivity, catalysis, biological activity, reactivity, electrochemical reactions, or mechanical properties.
For example, in some embodiments, the nanocellulose foam is a tissue scaffold and the active ingredient is selected to provide stability and attachment for cell growth. In such embodiments, the active ingredient is at least one of collagen, chitosan, hyaluronic acid, or proteins.
In some embodiments, the active ingredient has high adsorption or absorption properties, which can be useful in applications such as wound dressings or diapers.
In some embodiments, the active ingredient is selected to bind, trap, or filter target materials in liquid or gas phase effluent, which is useful in applications such as air purification, water sanitization or wastewater treatment.
In some embodiments, the active ingredient has a high electrical conductivity, which is useful in a variety of applications including but not limited to electronics or protection against stray current (e.g., lightning strike). In such embodiments, the active ingredient is, for example, a metal species such as copper, silver, gold, or platinum, or an electrically conducting polymer, such as polypyrrole, polyaniline, or poly(3,4-ethylenedioxythiophene). In some embodiments, the active ingredient has high electrical resistivity, which is useful in a variety of applications including but not limited to electrical shielding or electronics.
In some embodiments, the active ingredient has either thermally conductive properties, such as silver, copper or aluminum oxide, or has thermal insulation properties, such as rubber, silica, or polyethylene. Such properties are useful in a variety of applications including but not limited to insulation or thermoelectrics.
In some embodiments, the active ingredient provides acoustic dampening properties which are useful in a variety of applications including but not limited to sound insulation in buildings.
In some embodiments, the active ingredient is a non-linear optical material, such as lead pthalocyanine and related derivatives.
In some embodiments, the active ingredient interacts with electromagnetic waves. In some embodiments, the active ingredient reflects energy in the form of electromagnetic waves, sound, or heat so as to provide a waveguide through the nanostructure, which is useful in a variety of applications.
In some embodiments, the active ingredient can store energy, which is useful in a variety of applications including but not limited to electrochemical batteries or capacitors. In some embodiments, the active ingredient can undergo oxidative or reductive changes to store ionic or electric charge. In such embodiments, the active ingredient is at least one of a redox-active polymer, such as polyaniline or polypyrrole, a transition metal, such as lithium, cobalt oxide, lithium manganese oxide, or lithium iron phosphate, carbon, such as graphite or carbon nanotubes, silicon, tin, lithium, sodium, lead, or other electrode materials.
In some embodiments, the active ingredient has chemically active properties. In some embodiments, the active ingredient has catalytic properties. In some embodiments, the active ingredient is a gas-phase catalyst and is selected from a group consisting of a noble metal or a metal alloy catalyst. In some embodiments, the active ingredient is a liquid-phase catalyst and is selected from a group consisting of a noble metal or a metal alloy catalyst.
In some embodiments, the active ingredient reacts with chemical or biological agents to render them inert, for example, titanium oxide.
In some embodiments, the active ingredient can react with an external stimulus, such as increased temperature or an applied voltage to generate a detectable chemical, mechanical, or electrical signal, which is useful in a variety of sensor applications.
In some embodiments, the active ingredient has mechanical properties that change based on external stimuli.
In some embodiments, the active ingredient has magnetic properties, which is useful in a variety of applications including but not limited to electric generators or data recording. In such embodiments, the active ingredient is, for example, at least one of a ferrite or a rare-earth-element-based complex such as samarium-cobalt or an alloy of neodymium, iron and boron.
Nanocellulose-Ag hydrogels were generated by addition of AgNO3 aqueous solution to an aqueous dispersion of carboxylated nanocellulose followed by reduction. Typically, nanocellulose dispersion was put into a container. An equal volume of 50 mM AgNO3 solution was added dropwise along the sidewall into the 1 wt % nanocellulose dispersion without stirring. Gelation occurred rapidly upon the addition of AgNO3. The gel sat for five days to allow for slow reduction of Ag+ to Ag nanoparticles. UV reduction as an alternative method could also be used to convert Ag+ to Ag nanoparticles. A brown gel thus formed was removed from the AgNO3 solution, and immersed into water several times to rinse off the unattached Ag species.
A freeze-drying method was used to prepare nanocellulose-Ag aerogels. The molar amount of AgNO3 added to the 1 wt % nanocellulose dispersion was calculated on the basis of the dried nanocellulose weight. Low quantities were desired to remain below the gelation threshold. To 40 g of nanocellulose aqueous dispersion, the calculated amount of AgNO3 corresponding to 0.2 mmol or 0.5 mmol Ag+ per gram of dried nanocellulose was dissolved in 1 mL of H2O and added dropwise under vigorous stirring. After continuously stirring for 30 min, the aqueous dispersion was degassed quickly under vacuum. 8 grams of each sample were put in a glass freeze-drying vial and immersed in an ethanol/dry ice bath. An ethanol/dry ice bath was preferred over liquid N2 for freezing the NFC dispersion as it was found to generate fewer cracks in the aerogel structures. The frozen dispersion was then freeze-dried at a pressure of 0.1 mbar in a FreeZone freeze dry system. The drying was typically finished within 12-24 h. To reduce Ag+ to Ag nanoparticles, the dried aerogels were exposed under a UV lamp (λ=320-395 nm) 30 min each for the top side and the bottom side.
Nanocellulose hydrogels were produced by addition of a metal salt solution to the top of aqueous dispersion of carboxylated nanocellulose. A certain weight of 1 wt % nanocellulose dispersion was put in a container. An equal weight of a 50 mM aqueous solution of metal salt, such as CaCl2 or FeCl3, was added dropwise along the wall of the container into the CNF dispersion without stirring. Gelation occurs upon the addition of the metal salt solution. After standing for overnight, the metal salt solution was decanted, the resulting hydrogel was soaked and rinsed with water several times to remove unbounded metal ions. For the hydrogel generated with FeCl3, a yellow gel formed after addition of 50 mM FeCl3. t, the gel of CNF—Fe3+ was rinsed with water of pH 3 before rinsing with neutral water.
The hydrogels in example 1 and 3 were dried either by freeze-drying using similar conditions as described in example 2 or by sc-CO2 drying after solvent exchanged with acetone.
1 wt % nanocellulose dispersion was pumped through a syringe into a gelling bath that contained an aqueous solution of 50 mM CaCl2 solution. The gel beads were allowed to harden in the gelling bath for 1 hour, and then rinsed with water. The gel beads were then incubated with buffered chitosan solution for overnight.
Other details and/or embodiments may be described in a journal article titled” Hydrogel, aerogel and film of cellulose nanofibrils functionalized with silver nanoparticles” Carbohydrate Polymers 95 (2013 760-767) which is hereby incorporated by reference.
While the foregoing is directed to embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof.
This application claims benefit of U.S. patent application Ser. No. 61/657,259, filed Jun. 8, 2012, entitled, “Nanofibrillated cellulose foam containing one or more active ingredients for wound dressing, catalysis, active filtration, and/or other applications,” which is herein incorporated by reference in its entirety.
Governmental Interest—The invention described herein may be manufactured, used and licensed by or for the U.S. Government.
| Number | Date | Country | |
|---|---|---|---|
| 61657259 | Jun 2012 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13912743 | Jun 2013 | US |
| Child | 14231666 | US |
