Patent Application
20140044789
The present invention relates to melanin-based nanoshells and their use for protection against radiation, particularly ionizing radiation, and electronic pulses, and to methods of making materials comprising the melanin nanoshells.
Throughout this application various publications are referred to in parenthesis. Full citations for these references may be found at the end of the specification immediately preceding the claims. The disclosures of these publications are hereby incorporated by reference in their entireties into the subject application to more fully describe the art to which the subject application pertains.
Melanin is a high molecular weight pigment that is ubiquitous in nature and has a variety of biological functions (1). Melanins are found in all biological kingdoms. These pigments are among the most stable, insoluble, and resistant of biological materials (30). Melanins can have different structures depending on the biosynthetic pathway and precursor molecules. Some definitions of melanin have focused on chemical and physical properties of melanins instead of defined structures (29). Melanins can be synthesized in the laboratory by chemical means or by many living organisms. Melanins formed by the oxidative polymerization of phenolic compounds are usually dark brown or black (30). However, melanins may have other colors as illustrated by the finding that dopamine-derived melanin is reddish-brown. Fungi can make melanins from at least two major biosynthetic pathways, employing the precursor 1,8-dihydroxynapthalene (DHN melanin) or the oxidation of suitable tyrosine derivatives like dihydroxyphenylalanine (DOPA-melanin) (30). The fungus C. neoformans can make melanins from a wide variety of phenolic compounds which are oxidized by a laccase enzyme (31-33).
Melanins protect against UV light by absorbing a broad range of the electromagnetic radiation (1), and the melanin pigment is used in photo-protective creams (10). The presence of melanin is implicated in the resistance of human malignant pigmented melanoma to radiation therapy (9). Many fungi constitutively synthesize melanin (2). The ability of free-living microorganisms to make melanin may be associated with a survival advantage in the environment (3) that includes protection against solar radiation (reviewed in 4). Melanized fungi are also resistant to ionizing radiation (5). An example of such radiation resistance is provided by reports that melanized fungi colonize the walls of the damaged nuclear reactor in Chernobyl (6). The soils around the damaged reactor have blackened as the resident flora changes to include disproportionately more melanotic fungi (7). Water in nuclear reactor cooling pools is sometimes contaminated with melanized microorganisms (8). However, despite the finding of melanotic organisms in such harsh environments, the contribution of melanin to the radiation resistance of these organisms is uncertain.
The present invention is directed to nanoshells comprising melanin.
The invention also provides methods of protecting an object or a subject from radiation and/or from electronic pulses, where the methods comprise providing a material comprising melanin nanoshells between the object or subject to be protected and a source of the radiation and/or electronic pulses.
The invention further provides methods of protecting internal organs of a subject from radiation and/or from electronic pulses, where the methods comprise administering to the subject particles comprising melanin nanoshells.
The invention further provides methods of making a material comprising melanin nanoshells, where the method comprises fabricating melanin nanoshells into and/or onto the material; and materials comprising melanin nanoshells fabricated in and/or on the material.
The subject invention is directed to a nanoshell comprising melanin. Melanins are high-molecular weight pigments, arising in the course of oxidation and polymerization of phenols. The nanoshell can comprise polymerized L-dopa, epinephrine, methyldopa, a substituted phenol derivative and/or a phenolic derivative that polymerizes into melanin.
The nanoshell can comprise synthetic melanin and/or melanin isolated or derived from a biological source, such as a plant, an animal, a microorganism, and/or a melanin-containing cell, or generated by chemical synthetic process. Suitable animals include, but are not limited to, helminthes, cuttlefish and squids. The microorganism can be, e.g., a bacterium or preferably a fungus. Suitable fungi include, but are not limited to, Cryptococcus neoformans and/or Histoplasma capsulatum.
The melanin can comprise allomelanin, pheomelanin and/or eumelanin. Eumelanins are derived from the precursor tyrosine. Pheomelanin is derived from the precursors tyrosine and cysteine. Allomelanins are formed from nitrogen-free precursors such as catechol and 1,8-dihydroxynaphthalenes. In one embodiment, the nanoshell comprises pheomelanin and eumelanin, wherein the ratio of pheomelanin to eumelanin is at least 1:1. Preferably, the melanin contains divalent sulphur.
The nanoshell can comprises a nanosphere, a nanotube, a nanoellipsoid, a nanorod, a nanoball, or other suitable shape. The nanoshells can be hollow or filled with the same type of melanin as used in the shell or with a different type of melanin or with another material.
The nanoshell can have a thickness of about 10 nm to about 1,000 nm. In one embodiment, the nanoshell has a thickness of about 100 nm.
Preferably, the nanoshell has a linear attenuation coefficient for radiation that is at least 100-fold higher than that provided by powdered melanin that is not formed as a nanoparticle. More preferably, the nanoshell has a linear attenuation coefficient for radiation that is at least 1,000-fold higher than that provided by powdered melanin that is not formed as a nanoparticle. Most preferably, the nanoshell has a linear attenuation coefficient for radiation that is at least 10,000-fold higher than that provided by powdered melanin that is not formed as a nanoparticle.
Preferably, the nanoshell has a linear attenuation coefficient for radiation that is at least 10-fold higher than that provided by lead. More preferably, the nanoshell has a linear attenuation coefficient for radiation that is at least 100-fold higher than that provided by lead. Most preferably, the nanoshell has a linear attenuation coefficient for radiation that is at least 500-fold higher than that provided by lead.
The invention also provides a method of protecting an object or a subject from radiation and/or from electronic pulses, where the method comprises providing melanin nanoshells between the object or subject to be protected and a source of the radiation and/or electronic pulses. The melanin nanoshells can be fabricated in or on the source of the radiation and/or electronic pulses, and/or the melanin nanoshells can be fabricated in or on the object or subject to be protected from radiation and/or from electronic pulses.
As used herein, to protect against radiation and electronic pulses means to reduce the amount of radiation or electronic pulses reaching the object or subject to be protected, compared to the amount of radiation and electronic pulses that would reach the object or subject in the absence of the melanin nanoshells. The melanin can be internal and/or external to the object or subject. The radiation can comprise ionizing radiation. The radiation can be, for example, one or more of gamma radiation, x-ray radiation, solar radiation, cosmic radiation, electromagnetic radiation, bremsstrahlung radiation, ultraviolet radiation, and particulate radiation (e.g., α-radiation and β-radiation). The source of the radiation can be a medical isotope.
The melanin nanoshells can be, for example fabricated in a material, mixed in a material, layered in a material, or coated onto a material.
The object that is protected can be, for example, a computer, an electronic component or circuit, a printed circuit board, a cell phone, an avionic system and/or a satellite component. The subject that is protected can be an animal, a human, and/or a plant. For a human or animal subject, one or more internal organs can be protected, for example bone marrow, liver, spleen, kidneys, lungs, and/or portions or all of the gastrointestinal tract.
The melanin nanoshells can also be used to contain radiation and/or electronic pulses.
The invention further provides a method of protecting internal organs of a subject from radiation and/or from electronic pulses, where the method comprises administering to the subject particles comprising any of the melanin nanoshells described herein. The subject can be a human or an animal. The organ that is protected can be, for example, one or more of bone marrow, liver, spleen, kidneys, lungs, and gastrointestinal tract, e.g. the intestines. Preferably, bone marrow is protected. The method can further comprise administering to the subject a co-polymer of the poloxamer series, which can increase bone marrow uptake of the melanin particles. Preferably, the co-polymer of the poloxamer series is administered to the subject prior to administering the particles comprising the melanin nanoshell. Co-polymers of the poloxamer series include, for example, pluronic acid F-68, poloxamer-407 (PEG (polyethylene glycol)/PEO (polyethylene oxide), MW 13,310) (24), and poloxamine 908 (25, 28). The class of polyoxypropylene/polyoxyethylene copolymer nonionic surfactant compounds is reviewed in (27). Preferably, the particles comprising the melanin nanoshell have a diameter of about 10 nm to about 1,000 nm. The particles may be silica particles. Preferably, systemic administration such as e.g. intravenous administration is used to administer the melanin nanoshell particles and the poloxamer series co-polymer to the subject.
The invention further provides a method of making a material comprising the any of the melanin nanoshells disclosed herein, where the method comprises fabricating melanin nanoshells into and/or onto the material. The method can comprise polymerizing melanin or melanin nanoparticles onto a surface. The method can further comprise growing melanized fungi and extracting melanin nanoshells from the fungi. The fungi can be encapsulated in melanin nanospheres. The fungi can include, but are not limited to, Cryptococcus neoformans (Cn) and/or Histoplasma capsulatum (Hc). The fungi can be grown in the presence of a melanin precursor, where the melanin precursor is one or more of L-dopa (3,4-dihydroxyphenylalanin), D-dopa, catechol, 5-hydroxyindole, tyramine, dopamine, tyrosine, cysteine, m-aminophenol, o-aminophenol, p-aminophenol, 4-aminocatechol, 2-hydroxyl-1,4-naphthaquinone, 4-metholcatechol, 3,4-dihydroxynaphthalene, gallic acid, resorcinol, 2-chloroaniline, p-chloroanisole, 2-amino-p-cresol, 4,5-dihydroxynaphthalene, 1,8-dihydroxynaphthalene, 2,7-disulfonic acid, o-cresol, m-cresol, and p-cresol.
The invention also provides materials comprising melanin nanoshells fabricated in and/or on the material.
Since melanin nanoshells are negatively charged, they can be attracted or held in place with positively charged substances, or repelled using negatively charged substances.
The material, for example, can be coated with melanin nanoshells and/or encased in melanin nanoshells. The melanin nanoshells can be incorporated into the material. The material can be a plastic that is impregnated with melanin nanoshells or a surface where melanin is polymerized and/or melanin nanoshells are attached. The melanin nanoshells can be in a binder between two layers of material.
The material comprising the melanin nanoshells can be used, for example, as clothing, a protective gear, a object worn by a subject, or a packaging material. The material can be, or can be incorporated into, a wall, floor and/or ceiling of a room, building, vehicle, aircraft, ship, spacecraft, and/or submarine.
C. neoformans (Cn) and H. capsulatum (Hc).
American Type Culture Collection (ATCC, Rockville, Md.) strains Cn 24067 (serotype D) and Hc (CIB strain 1980, a gift from A. Restrepo, Medellin, Colombia) were used in all experiments. Cn was grown in Sabouraud dextrose broth (Difco laboratories, Detroit, Mich.) for 24 hrs at 30° C. with constant shaking at 150 rpm. Hc was grown with shaking at 37° C. in defined media consisting of 29.4 mM KH2PO4, 10 mM MgSO4×7H2O, 13 mM glycine, 15 mM D-glucose, 3 μM thiamine. Melanized Cn and Hc cells were generated by growing the fungi in their respective media with 1 mM 3,4-dihydroxyphenylalanin (L-dopa) for 5 days. The cells were collected by centrifugation and washed three times with PBS, pH 7.2 before radiation exposure.
Susceptibility of Cn and Hc to External Gamma Radiation.
Approximately 105 melanized or non-melanized Cn or Hc cells were placed in microcentrifuge tubes in 0.5 mL PBS and irradiated with a 137Cs source at a dose rate of 14 Gy/min. The cells were exposed to doses of up to 220 Gy. The exposures of 1,000-8,000 Gy were given by irradiating the cells at 30 Gy/min. Following radiation exposure, 103 cells from each tube were plated to determine viability as measured by colony forming units (CFU's). Alternatively, melanized or non-melanized Cn cells were plated on Sabouraud plates in air or under the nitrogen gas. The plates were irradiated at a dose rate of 14 Gy/min followed by determination of viability as measured by CFU's.
Other Sources of Melanin.
Melanin from cuttlefish Sepia officinalis was purchased from Sigma Chemical Co.
Measurement of Radiation Absorption Properties of Bulk Melanin.
A pellet of 13 mm diameter and 4 mm height with the mass of 0.71 g and density of 1.33 g/cm3 was made from Sepia melanin by applying a pressure of 6 tonn/cm2. The measuring of gamma radiation shielding properties of the pellet was performed by placing the pellet on the 3 mm in diameter opening in a lead-shielded castle inside which radioactive sources were placed. The dose rate in mrad/h at the surface of the opening was measured with and without the melanin pellet. Absorption of α- and β-radiation was evaluated by placing the melanin pellet on the point sources of 210-Polonium and 32-Phosphorus, respectively.
Transmission Electron Microscopy (TEM).
Melanized and non-melanized Cn and Hc were frozen under high pressure using a Leica EMpact High Pressure Freezer (Leica Microsystems, Austria). Frozen samples were transferred to a Leica EM AFS Freeze Substitution Unit and freeze substituted in 1% osmium tetroxide in acetone. They were brought from −90° C. to room temperature over 2-3 days, rinsed in acetone and embedded in Spurrs epoxy resin (Polysciences, Warrington, Pa.). Ultrathin sections of 70-80 nm were cut on a Reichert Ultracut UCT, stained with uranyl acetate followed by lead citrate and viewed on a JEOL (Tokyo, Japan) 1200EX transmission electron microscope at 80 kV.
Isolation and Purification of Melanins.
The cells were suspended in 1.0 M sorbitol-0.1 M sodium citrate (pH 5.5). Lysing enzymes (Sigma Chemical Co.) were added to suspension at 10 mg/mL and the suspensions were incubated overnight at 30° C. Protoplasts were collected by centrifugation and incubated in 4.0 M guanidine thiocyanate overnight at room temperature and were frequently vortexed. The resulting particulate material was collected by centrifugation, and the reaction buffer (10.0 mM tris, 1.0 mM CaCl2, 0.5% SDS) was added to the particles. Proteinase K was added to suspension at 1.0 mg/mL followed by overnight incubation at 37 (Hc) or 65° C. (Cn). The particles were boiled in 6.0 M HCl for 1 hour. Finally, resulting material was washed with PBS, dialyzed against deionized water overnight and dried in the air at 65° C. for 2 days. Approximately 1.5×1010 Cn cells and 2.2×1010 Hc cells were used. The isolation procedure yielded approximately 2.0 mg melanin per 1010 cells for Cn, and 2.3 mg per 1010 cells for Hc. The yield of melanized cells per 1 liter of medium is 2 g and the yield of purified ghosts is 0.3 g. Hollow melanin shells that remain after the treatment of melanized cells with enzymes, guanidinium isothiocyanate and 6 M HCl were dubbed “ghosts” because they preserved the shape of the cells.
Quantitative Elemental Analysis of Melanins.
Elemental analysis for carbon, hydrogen, and nitrogen was performed by Quantitative Technologies Inc. (Whitehouse, N.J.).
Oxidation of Melanins and HPLC of Oxidized Melanins.
Cn and He melanin underwent acidic permanganate oxidation using the procedure described by Ito and Fujita (16). Pyrrole-2,3,5-tricarboxylic acid (PTCA) and 1,3-thiazole-4,5-dicarboxylic acid (TDCA) were used as standard compounds. The oxidation products were analyzed by HPLC using a Shimadzu LC-600 liquid chromatograph, Hamilton PRP-1 C18 column (250×4.1 mm dimensions, 7 μm particle size), and Shimadzu SPD-6AV UV detector. The mobile phase was 0.1% trifluoroacetic acid in water (solvent A) and 0.1% trifluoroacetic acid in acetonitrile (solvent B). At 1.0 mL/min, the elution gradient was (min, % B): 0, 0; 1, 0; 12, 25; 14, 25; 16, 0. The UV detector was set at a 255 nm absorbance.
MALDI Mass Spectrometry.
The major peaks generated during chromatography of oxidized melanins were collected and analyzed by MALDI-TOF mass spectrometry in positive pressure mode on PE-Biosystems Mariner ESI TOF mass spectrometer. Peptide mixture with molecular weights of 1059.56, 1296.68 and 1672.95 in 2,5-dihydroxybenzoic acid matrix was used for calibration.
Electron Spin Resonance Spectroscopy (ESR).
The ESR of purified melanins from Cn and He cells was performed on ER 200D EPR/ENDOR spectrometer with ESP 300 upgrade (Brucker Instruments, Inc. Billerica, Mass.).
Statistical Analysis.
The slopes of the survival curves were determined by linear regression (GraphPad PRISM software, San Diego, Calif.) and a Student's test for unpaired data was performed to analyze the differences in survival. Differences were considered statistically significant when P values were <0.05.
As described herein, the ability of melanin to protect against ionizing radiation was demonstrated in two fungi capable of melanogenesis, Cryptococcus neoformans (Cn) and Histoplasma capsulatum (Hc). These fungi were chosen as model organisms because they can be grown in either melanized or non-melanized states, while fungi found in Chernobyl are constitutively melanized. Cn and He cells became encapsulated in melanin when grown with L-dopa (3,4-dihydroxyphenylalanin). Previous work (2) as well as this study showed that all melanin in the cells is concentrated in the cell wall (
Melanized and non-melanized Cn and Hc cells in phosphate buffered saline (PBS) were subjected to extremely high doses of radiation—up to 8,000 Gy. For comparison, a dose of just 5 Gy is lethal to humans. The radioprotective effect of melanin was more readily demonstrable at the higher radiation doses, as the LD90 for these organisms in non-melanized form is around 50 Gy (Cn) or 100 (Hc) Gy (11). Melanized Cn cells demonstrated reduced susceptibility to external gamma radiation (P=0.01) in the dose range of 0-220 Gy (
To compare the radioprotective properties of melanin with other materials such as lead, the linear attenuation coefficient and half value layer were calculated according to the equations:
I=I
o
e
−μx (1)
HVL=0.693/μ (2),
where Io and I are the radiation intensity before and after shielding, respectively; μ is the linear attenuation coefficient in cm−1, x is the thickness of the shield in cm, and half value layer (HVL) is the thickness of shielding necessary to reduce the intensity of radiation to half of its original value. The reduction in radiation intensity was calculated from the linear parts of survival curves assuming that a 10% increase in survival is equivalent to a 10% decrease in radiation intensity. Linear attenuation coefficient and HVL for Hc melanin were calculated to be 1.4×104 cm−1 and 0.5 μm, respectively. This melanin linear attenuation coefficient is several orders of magnitude higher than that of lead (27.1 cm−1) (13), indicating that fungal melanin in nanosphere form is a much more efficient radioprotector than lead.
To gain insights into the unusual radioprotective properties of melanin, high-pressure liquid chromatography (HPLC), matrix assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF) and elemental analysis of the fungal melanins were performed. Unlike synthetic melanins (10, 14, 15), the structures of natural melanins including fungal melanin are poorly understood. These pigments are amorphous and insoluble, characteristics that preclude a structural solution of melanins given currently available analytical tools, and have to be converted into low molecular weight fragments prior to analysis. Consequently, acidic permanganate oxidation of fungal melanins was carried out before HPLC. Two major types of melanin have been described. Eumelanin is a dark-brown to black pigment with 6-9% nitrogen and 0-1% sulphur, and is composed of 5,6-dihydroxyindole (DHI) and 5,6-dihydroxyindole-2-carboxylic acid (DHICA) monomer units (16, 17) (
C. neoformans 24067 black particulate
Since the density of melanin is only slightly greater than that of water, it cannot contribute significantly to its remarkable radioprotective properties. However, the number of electrons per gram could make a significant contribution to melanin protective properties. The number of electrons is an especially important contributor to the attenuation properties of a material at the energy levels where the Compton effect predominates (13). Thus, the higher number of electrons in oligomers of pheomelanin in comparison with eumelanin—388 versus 287, and the structure composed of electron-rich covalently linked aromatic motifs could account for better scattering properties of Hc melanin rich in pheomelanin oligomers in comparison with Cn. Secondly, pheomelanin contains divalent sulfur (
Efficient Compton scattering by melanin alone is unlikely to explain the radioprotective properties of melanin. The transfer of radiation (photon) energy to living matter occurs in a series of interactions, where energy is transferred to high-energy electrons, and then to secondary photons of progressively less energy (
In the macroscale experiment, the 4 mm thick melanin pellet made of Sepia (bulk) melanin completely absorbed α- and β-radiation from 210-Po and 32-P sources, respectively. This is better than plastic, since to stop a β-particle 7 mm of plastic (e.g., Lucite) are needed and the density of Lucite is higher than the density of the 1.33 g/cm3 melanin pellet made of Sepia melanin.
Measurement of the bulk melanin shielding effect towards gamma radiation of 122-140 keV energies showed that 4 mm of melanin cut the dose by ˜33%. Using these data, the linear attenuation coefficient (μ) for bulk melanin was calculated to be 1.01 cm−1. For comparison, at 140 keV lead has a higher μ=27.1 cm−1 but its density is 11.34 g/cm3; and aluminum has μ=0.386 cm−1 and a density of 2.7 g/cm3. It is obvious from these measurements, that melanin nanoparticles possess several orders of magnitude better radiation shielding properties than bulk melanin. Since the absorbance of radiation by matter also depends on the geometric arrangement of the photon source and the absorber, an important factor contributing to the radioprotective properties of fungal melanin can be the spatial arrangement of melanin in fungal cells. The location of melanin in the fungal cell wall outside of the plasma membrane (
To prove the contribution of the nanospherical arrangement of melanin in fungal cells to radioprotection, non-melanized C. neoformans cells were irradiated with doses of up to 400 Gy in the presence of melanin from Sepia officinalis (cuttlefish), which is not arranged in hollow spheres, in amounts equal or 20 times higher than the amount of melanin in the same number of melanized C. neoformans cells. S. officinalis melanin conferred no protection at any dose (
To further assess the shielding properties of C. neoformans melanin “ghosts”, a 96 well ELISA plate was coated with a solution of poly-lysine to make the surface of the wells positively charged in order to counteract the negative charge carried by melanin “ghosts”. The ghosts were mixed with poly-lysine solution to prepare a homogeneous suspension, and 3 different concentrations of ghosts were placed in the wells. For control different concentrations of Sepia melanin and charcoal suspensions in poly-lysine solution were used as well as lead foil of similar weights (
These results demonstrate that C. neoformans ghosts possess superior radiation shielding properties in comparison with other types of melanin (Sepia) or non-melanin carbon-based compounds (charcoal). The shielding properties of the ghosts were comparable to those of lead when one takes into consideration that the ghosts were used in the form of a suspension in poly-lysine solution, which has a lot of “gaps” between the ghosts for X-rays to penetrate without being scattered, while lead foil is a material with continuous close packing of lead atoms.
The properties of materials change dramatically when one moves from bulk materials to nanomaterials. The superior radiation shielding properties of fungal melanin nanospheres in comparison with melanin powder (bulk material) are direct consequence of principally different mechanism of radiation absorption by melanin nanoparticles—a gamma photon becomes “trapped” within a melanin nanoparticle as it is reflected several times by its inner walls and is unable to escape the particle until it transfers all of its energy to melanin.
Melanized Nanoparticles for Protection of Bone Marrow and Internal Organs from Ionizing Radiation
As bone marrow is the dose-limiting organ for both external beam radiation therapy and radioimmunotherapy, protection of bone marrow against radiation would increase safety and efficacy of these treatments. An investigation was conducted of whether melanin nanoshells administered before a dose of external radiation protect bone marrow in mice from radiation damage. It is known that, following intravenous administration of nanoparticles, 0.5-1% of the injected dose goes into bone marrow, while the majority of nanomaterial is sequestered by the mononuclear phagocytes of the liver and to a lesser degree of the spleen (24). It has been demonstrated that nanoparticles can be efficiently redirected into the bone marrow in rats by pre-treatment or co-administration of block co-polymers of the poloxamer series, for example, poloxamer-407 (PEG (polyethylene glycol)/PEO (polyethylene oxide), MW 13,310) (25), which minimizes interaction of nanoparticles with the reticuloendothelial elements of liver and spleen.
Silica nanoparticles (20 nm) were utilized in the present experiments. The surface of unmodified silica particles is covered with hydroxyl groups. Nanoparticles were melanized overnight at 35° C. in 10 nM L-Dopa solution, precipitated by lowering the pH to 1, washed from unreacted L-Dopa and transferred into deionized water. To prove that the dark color of melanized particles was due to the presence of melanin, immunofluorescence of these particles was performed with melanin-binding monoclonal antibody (mAb) 6D2 as previously described (26). 6D2 mAb bound avidly to the surface of the particles, thus proving that they were covered with a layer of melanin.
To measure the uptake of melanized particles in major organs and bone marrow with and without a co-polymer of the poloxamer series, melanized particles were radiolabeled with 188-Rhenium (188Re) by incubating 16 mg of particles per sample with 40 μL SnCl2 and Na188ReO4 for 2 hr at 37° C., separating the particles from unreacted Na188ReO4 in supernatant by centrifugation, and suspending them in Na carbonate buffer (pH=8.5). Two groups of 4 BALB/c mice were injected IV with 100 μL (1.6 mg, 50 mg/kg body weight) of melanized particles while other two groups of 4 mice were pre-injected IV with 0.13 mg/kg body weight of pluronic acid (pluronic acid F-68 is a member of the poloxamer series, and is available from Sigma as 10% solution) and 12 hr later were injected IV with the above amount of 188Re-labeled particles. The animals were sacrificed 3 and 24 hr post-injection, their major organs were removed, blotted from blood if necessary, weighed, and their radioactivity was counted in a gamma counter. The results of the biodistribution are presented in
To investigate the radiation protective properties of melanized nanoparticles (MNs), groups of 3 CD-1 mice were injected IV with MNs alone or with pluronic acid (PA)+MNs. Control groups consisted of untreated mice, mice given PA alone, non-melanized nanoparticles alone, and PA+non-melanized nanoparticles. The mice were irradiated with either 1.25 or 2.50 Gy of gamma radiation and their platelet and white blood cell (WBC) counts were monitored for 28 days post-treatment (
The protective effect of different types of melanin was evaluated on the GI tract in mice receiving lethal dose of 9 Gy at a high dose rate. CD-1 female mice were used in all experiments. Initially a check was made for potential toxicity of synthetic melanin and C. neoformans (Cn) melanin “ghosts” made from Cn strain 24067 to the GI track. Mice were fed 15 mg/kg body weight synthetic melanin or ghosts via gavage needle and their body weight and condition were monitored for 30 days. Also, 2 mice out of each group were sacrificed at 24 hr post-feeding with melanin, and their stomachs, small intestine and colon were removed and fixed in formaline-buffered PBS. The parafinized tissues were subsequently cut, stained with H&E and analyzed histologically.
There was no loss in the body weight of melanin-fed mice with all mice consistently gaining weight (
In the next experiment female CD-1 mice (10 mice per group) were fed 15 mg/kg body weight synthetic melanin or ghosts or water via gavage needle and 1 hr post feeding were subjected to whole body irradiation in 137-Cs irradiator with the total dose of 9 Gy delivered at 3 Gy per min; their body weight and survival were monitored for 22 days. At 4 hr and 24 hr 2 mice per group were sacrificed and their stomachs, small intestine and colon were removed and fixed in formalin-buffered PBS. The parafinized tissues were subsequently cut, stained with H&E and analyzed histologically. For the first 4 days post-irradiation, mice fed with ghosts were loosing less weight than mice fed with either water or synthetic melanin (
Overall, the prolongation in survival of melanin-fed mice in comparison with control water-fed mice was statistically significant by log-rank test for both synthetic and fungal melanin with synthetic melanin being a better radioprotector in the conditions of experiment. It might be possible that if the ghosts are eliciting inflammation by themselves it could increase the amount of damage sustained from radiation and this could account for less protection with the ghosts than with synthetic melanin. To avoid administration of immunogenic fungal melanin, but to use the advantage of hollow sphere shape which contributes to the radiation scattering by melanin, biodegradable particles of 200-1000 nm diameter made of poly-DL-lactic/glycolic acid (PLGA) polymer from a commercial vendor (Corpuscular Inc, Cold Spring, N.Y.) can be covered with different melanins by incubation in a solution of melanin pre-cursors during autopolymerization as described above and then dissolved the PLGA polymer with the hydrochloric acid. As melanin is extremely resistant to acid, the melanin shell will remain intact while the biodegradable core of the particle will be dissolved. The results of this study indicate that it is possible to utilize melanin for protection of the GI tract from radiation injury.
In summary, the results described herein establish that fungal melanin arranged in nanosize spheres protects against extremely high levels of ionizing radiation and suggest that the protective efficacy of this pigment is a function of its chemical structure, stable free radical presence, and spatial arrangement. In essence, melanin protects against ionizing radiation by mechanisms that are different from the radiation shielding properties of heavy metals, which depend largely on density. These results demonstrate the feasibility of designing low-density nanoshells with radiation shielding properties, which could find uses in a variety of applications by virtue of their low weight. The term “nanoshells” is used to describe nanoparticles of different shapes—e.g., nanospheres, nanotubes, nanoellipsoids and nanorods. Melanin used for manufacturing of nanoshells can be of synthetic or biological origin.
Preparation of Additional Melanin Nanoshells:
Melanin-filled nanoshells can be generated by incubating melanin such as Sepia melanin in an aerated solution of melanin precursor such as L-dopa or cysteinyl-dopa to provide the conditions for oxidative polymerization as described herein in experiments on generation of melanin-covered nanoparticles for bone marrow protection. To generate melanin-covered nanoshells filled with different materials one can use the above approach with nanoparticles of choice to cover with melanin. For generation of hollow nanospheres, biodegradable nanoparticles made of materials such as proteins or biodegradable plastics will be covered with melanin as above and then treated with concentrated acid which will dissolve the biodegradable nanoparticles but leave the melanin nanoshell intact.
Preparation of Melanin-Containing Plastics:
To make plastics impregnated with melanin nanoshells, the melanin nanoshells will be dispersed in a liquid monomer, such as diethylene glycol bis(allyl-carbonate), otherwise know as CR-39, styrene, or methylmethacrylate. Polymerization of the plastic monomer will be initiated with the help of a free-radical initiator. For example, 400 mg benzoyl peroxide will be dissolved in 10 mL of diethylene glycol bis(allyl-carbonate) (CR-39) at 50° C. Then, purified melanin nanoshells will be added, under thorough mixing, in increasing amounts starting from 30 mg until it is possible to form a homogeneous mixture. The mixture will be heated at 50° C. for one day. The mixture will be heated for two additional days at 65° C. under nitrogen, and then cured in a vacuum oven at 110° C. for 2 h.
Incorporation of Melanin Between Two Layers of Material:
Purified melanin nanoshells will be added to a binder/adhesive in the form of a suspension to achieve dispersion of melanin in the binder/adhesive. Then, a hardener will be combined with the binder/adhesive, which will then be immediately “sandwiched” between two layers of material. For example, increasing amounts of purified melanin nanoshells starting from 500 mg will be suspended in 10 mL of chloroform. This suspension will be mixed with 2 mL epoxy resin. The chloroform will then be removed by evaporation leaving melanin homogeneously dispersed in the epoxy resin. Epoxy catalyst, or hardener, will be added, and the mixture will be slowly stirred. Drops of the product will be deposited onto a material such as a plastic or glass, and an identical material will be placed on top of the melanin-epoxy suspension.
Coating Surfaces with Melanin:
As an example, purified melanin nanoshells in increasing amounts starting from 1 g will be suspended in 30 mL of water. Drops of this concentrated melanin suspension will be allowed to spread on the hydrophilized surface of a plastic or glass. The water will be allowed to evaporate leaving melanin attached to the surface of the plastic or glass. As an alternative, a melanin coating may be made on surfaces by first immobilizing on the surface the enzyme laccase which catalyzes melanin formation in fungi. Melanin coated surfaces may also be generated by autopolymerization of melanin precursors. Enzymatically-mediated generation of melanin nanoshells in situ could provide an attractive alternative for coating vulnerable surfaces with this material. Furthermore, since melanin nanoshells are negatively charged, they can be attracted to a surface that is positively charged.
Treatment of Buildings to Reduce Entry of Radon and Radiation from Radon:
Radon is a gas that forms naturally during the decay of uranium-238. Radon that occurs naturally in soil can seep from the soil into homes and other buildings. Melanin nanoshells will be added to paints, coatings, and/or building materials. Melanin-based paints and coatings applied to the foundations of buildings, and areas where pipes enter the buildings, can be used for the purpose of trapping radon when it is emitted from rocks or soil before radon enters the building. Radon decays over the course of several days to 210-Pb, which is a beta and gamma emitter and has a half-life of 22 years. Melanin should absorb 210-Pb even tighter than radon through chemosorption as melanin is known to bind two-valent metals and thus should reduce the entry not only of radon but also of radioactive lead into the environment of the building.
Protection of Subjects Against Radiation:
A sterile preparation of melanin nanospheres will be injected into an individual at risk for radiation injury. The melanin nanospheres localize to the bone marrow where they provide shielding against the cytotoxic effects of radiation on vulnerable cells. In another application an oral preparation of melanin particles will be ingested to provide protection for the gastrointestinal mucosa. Melanin nanoshells can also be used in protective clothing and gear.
Containment of Radioactively Contaminated Sites:
Melanin nanoshells will be used in environmental bioremediation. The following types of radiation are given off by radioactive material: alpha particles, beta particles, x-rays, and gamma rays. The spread of radioactive particles will be reduced by applying the melanin nanoshells to the radioactive particles. Melanin is expected to encapsulate the radioactive particles and thereby reduce their spread. Thus, melanin nanoshells may, for example, prevent the spread of radioactive contamination to ground water. Similarly, melanin nanoshells will be used to contain radiation from radioactive waste and biomedical radioactive materials. Melanin nanoshells may be used in remediation in connection with, for example, waste containers, fuel cladding, packaging containers, transport coverings for all land, air, and water vessels, and nuclear waste clean-up.
Containment of Metal Ions:
Since melanin nanoshells are negatively charged, they may be used to contain positively charged compounds, for example to act as metal chelators and to contain mercury.
Absorption of Radiation:
Melanin nanoshells may be used to absorb radiation, for example to absorb radar or radiation generated in association with NMR systems.
Industrial, Physical Buildings and Construction:
Melanin nanoshells may be used for shielding or containment in buildings, construction and containment structures in connection with, for example, concrete, plastics, steel, titanium, composites, coatings, “wafer” boards or sheeting in walls, roofs, flooring, and conduits. Melanin nanoshells may be used, for example, in shielding in connection with industrial radiation shielding; X-Ray rooms and enclosures (x-rays, gamma radiation); storage and process equipment; airport detection systems (gamma radiation); hot cells (gamma radiation); paints and pigments (alpha and beta particles); glass (alpha particles/radon); power lines (EM radiation/EM field); conductors (EM radiation/EM field); wiring (EM radiation/EM field), transformers (EM radiation/EM field); switches (EM radiation/EM field); meter boxes (EM radiation/EM field); line hardware (EM radiation/EM field); fuses (EM radiation/EM field); breakers (EM radiation/EM field); drywall (alpha particles/radon); plywood (alpha particles/radon); doors (alpha particles/radon); door frames (alpha particles/radon), window frames (alpha particles/radon); granite (alpha particles/radon); concrete (alpha particles/radon); ceramic materials (tile); commercial fertilizers (alpha particles/radium); angles (alpha particles/radon); pigs (alpha particles/radon); castings (alpha particles/radon); heat lamps (infrared radiation, UV light); road construction materials; pipes and colts (alpha particles/radon); heaters (infrared radiation); radio wave transmitters (EM radiation/radio waves); industrial radiographers (x-ray and gamma radiation); roof tiles (alpha particles/radon); metal (alpha particles/radon); steel (alpha particles/radon); titanium (alpha particles/radon); stucco (alpha particles/radon); caulk (alpha particles/radon); plastic (all types of radiation); mortar (alpha particles/radon); brick (alpha particles/radon); and VDUs (Vacuum Distillation units) (all types of radiation). This includes the use of melanin nanoshells in fossil-fuel power plants, chemical plants, paper plants, etc. and clean-up/binding of mercury and other toxic release inventory (TRI) gases/metals emissions.
Operational Equipment:
Melanin nanoshells may be used for shielding and containment in composites, coatings, or inserts in equipment with radiation exposure; for pressurized water reactors (PWRs), equipment on primary sides of plant, including, but not limited to, reactor core, reactor vessel, steam generators, pumps, conduit, electrical relay boxes; and in boiling water reactors (BWRs), primary side equipment including boilers, pumps, conduits, and also secondary side equipment including turbines, condensers, pumps, relays, and generators where radiation exists.
Airlines:
Melanin nanoshells may be used in shielding in air craft in connection with, for example, airplane materials (windows, cockpit gauges, mechanical parts, etc.) (cosmic radiation); cabinet X-ray system (x-rays); human X-ray scanner (x-rays); and blimps (cosmic radiation).
Space:
Melanin nanoshells may be used for shielding and containment in space craft in connection with, for example, astronaut jumpsuits (galactic cosmic radiation), spacecraft parts (galactic cosmic radiation), and rocket parts (engines, turbines, etc.) (galactic cosmic radiation).
Vehicles:
Melanin nanoshells may be used for shielding and containment in connection with, for example, ship parts (hull, engines, motor, etc.), vehicle parts, gauges (beta particles/tritium), and alternate fuel sources (e.g. nuclear energy).
Defense Application:
Melanin nanoshells may be used for shielding and containment in defense applications in connection with, for example, helicopter materials (cosmic radiation); submarine materials (alpha particles, beta particles, x-rays, and gamma radiation); navy carrier parts (alpha particles, beta particles, x-rays, and gamma radiation); fighter jet parts (cosmic radiation); tank parts (alpha particles, beta particles, x-rays, and gamma radiation); naval nuclear propulsion (alpha particles, beta particles, x-rays, and gamma radiation); nuclear powered vehicles; and weapon night sights (e.g., night vision goggles) (beta particles/tritium; infrared radiation). Other applications include use of melanin nanoshells in radar elusion in manned and unmanned vehicles.
Nuclear Application:
Radioactive materials in nuclear applications give off the following types of radiation: alpha particles, beta particles, x-rays, gamma rays, neutrons, protons, and heavy ions. Melanin nanoshells may be used for shielding and containment in nuclear applications in connection with, for example, power plant building materials, decay drums, waste containers, power reactors, pressurized water reactors, plant building materials, reactor core, reactor vessel, steam generators, steam turbines, pumps, electrical relay boxes, conduits, boiling water reactors, boilers, pumps, condensers, relays, respirators, neutron generators, nuclear fuel reprocessors, master-slave manipulators, nuclear batteries, radiation fallout material, and tools, gear, and equipment. In radioactive material or waste storage, including spent fuel storage, melanin nanoshells may be used for shielding and containment in building material, equipment, and fuel cladding. In transport of radioactive material or waste, melanin nanoshells may be used for shielding and containment in packaging, containers, trucks/railcars/planes/water vessels, and covering/coating/composites. In radiation contamination clean-up, melanin nanoshells may be used for stabilizing radioactive isotopes in clean-up conditions.
Homeland Security:
Melanin nanoshells may be used for shielding and containment in homeland security applications in connection with, for example, protection of buildings, equipment, computers, satellites, etc. and protection of masses of people through clothing applications, house shielding, etc. from nuclear or “dirty” bombs.
Medical/Dental:
Melanin nanoshells may be used for shielding and containment in medical and dental applications in connection with, for example, MRI machines (gamma radiation); X-Ray machines (gamma radiation); mammogram machines (gamma radiation); lasers (infrared radiation); dental crowns (gamma radiation/uranium); PET Scans (beta particles); dental porcelains (gamma radiation/uranium/thorium); external-beam radiation therapy machines (used to target localized areas of a tumor) (gamma radiation, electron beams, neutron and heavy ion beams); X-ray Tubes (gamma radiation); lab coats, coveralls, and head covers; sterilizers (gamma radiation/cobalt-60); sonogram machines (gamma radiation); radiopharmaceuticals (injectable radioisotopes) (gamma, alpha, beta (both positive and negative) and Auger electron radiation); medical diagnostic imaging; cardiac cath swing lab shielded partitions (gamma radiation); and nuclear medicine products (gamma, alpha, beta (both positive and negative) and Auger electron radiation). In medical radiation therapy, melanin nanoshells may be used in coatings to protect, for example, the following against x-ray and gamma radiation: linear accelerator swinging door systems, linear accelerator sliding door systems, H.D.R. automated swing door systems, gamma knife door systems, H.V.A.C. shielding systems, H.D.R. treatment enclosures, treatment room shielding upgrade systems, square-edge and interlocking bricks, modular vault systems, and proton therapy shielding systems.
Science Labs:
Melanin nanoshells may be used in shielding in science laboratories in connection with, for example, anodes (x-rays), atomic particle accelerators (x-rays, UV radiation), X-Ray diffraction units (x-rays), and electron microscopes (EM radiation, x-rays, and beta particles).
Consumer Products:
Melanin nanoshells may be used in shielding in consumer products in connection with, for example, protective clothes, shoes, sunglasses (EM radiation/UV light), eye glasses (EM radiation/UV light), contacts (EM radiation/UV light), make-up (EM radiation/UV light), lip gloss (EM radiation/UV light), ovens (alpha particles), toaster ovens (alpha particles), cell phone and covers (EM radiation/radio waves), televisions (alpha particles, extremely low frequency EM fields, x-rays), watches (beta particles/tritium), glow in the dark products (beta particles), light bulbs (UV radiation, infrared radiation), fire alarms (alpha particles), smoke detectors (alpha particles/americium-241, low energy gamma radiation), emergency exit signs (beta particles, tritium), tobacco (alpha particles), wireless technology, water fountains (alpha particles, radon), lantern mantles (alpha, beta, and gamma particles), lamp starters (beta particles, tritium, promethium, gamma particles, thorium), static eliminators (alpha particles/polonium-210), compasses (beta particles), batteries (beta particles/tritium), pagers (EM radiation), generators, purses, hats, gloves, shampoo and conditioner (EM radiation/UV light), hair spray (EM radiation/UV light), CRT (cathode-ray tube) monitors (x-rays), tanning bed goggles (EM radiation/UV light), cable tv wires (EM radiation), hair dryers (infrared radiation), pottery glaze (alpha, beta, and gamma particles), and food packaging materials.
Energy Production, Transmission and Distribution:
Melanin nanoshells may be used in connection with, for example, coating/composites on conductors and wiring to reduce/avoid electromagnetic field (EMF) radiation and line current losses, and coating/composites/inserts into electrical equipment and electrical working tools including, but not limited to, transformers (all sizes and types), switches, meter boxes, line hardware, fuses, and breakers, etc.
This application is a continuation-in-part of and claims priority of U.S. Provisional Patent Application No. 60/819,992, filed Jul. 10, 2006, and PCT International Patent Application No. PCT/US2005/035707, filed Oct. 3, 2005, which designates the United States of America and claims priority of U.S. Provisional Patent Application No. 60/616,056, filed Oct. 5, 2004, the contents of all of which are hereby incorporated by reference in their entirety into the subject application.
The invention disclosed herein was made with U.S. Government support under grant number R21AI52042 from the National Institutes of Health, U.S. Department of Health and Human Services. Accordingly, the U.S. Government has certain rights in this invention.
| Number | Date | Country | |
|---|---|---|---|
| 60819992 | Jul 2006 | US | |
| 60616056 | Oct 2004 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11732130 | Apr 2007 | US |
| Child | 14059960 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US05/35707 | Oct 2005 | US |
| Child | 11732130 | US |
