Carbon Nanotube Based Imaging Agents

Compositions and methods related to carbon Nanotubes are provided. More particularly, imaging agents comprising carbon Nanotubes internally loaded with a contrast agent and associated methods are provided. One example of a method may involve a method for imaging comprising: providing an imaging agent comprising a carbon Nanotube loaded with contrast agent; introducing the imaging agent into a cell; and imaging the cell to detect the presence of the imaging agent.

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Description
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of International Application No. PCT/US2007/069459, filed May 22, 2007, which claims the benefit of U.S. Provisional Application Ser. No. 60/747,874, filed May 22, 2006, both of which are incorporated in this application by reference.

BACKGROUND

The discovery of the “buckyball” by Smalley et al. at Rice in 1985 and its cousin the single-walled carbon Nanotube (SWNT) by Sumio Iijima in 1991 has sparked two decades of intense research on possible applications of these novel Nanostructures. SWNTs have useful properties, such as high tensile strength, low density, high electrical conductivity, and high thermal conductivity. SWNTs have demonstrated the ability to translocate into cells opening the possibility of intracellular diagnostic and therapeutic applications.

One such application, computed tomography (CT), sometimes known as computed axial tomography (CAT), is a powerful diagnostic imaging tool utilized in thousands of diagnoses annually. In CT, imaging is achieved by measuring the attenuation of an X-ray, defined as the loss of energy of the radiant beam due to absorption, scattering, and beam divergence as it propagates through a medium. X-ray slice data is generated by rotating an X-ray source around an object. Detectors opposite the source measure the intensity of the exiting X-ray, which is directly proportional to the radiodensity of the scanned object. The X-ray slices can then be reconstructed into a three-dimensional image for interpretation. Naturally radiodense objects, such as bone, can be easily distinguished from fatty tissue using unenhanced CT. However, for objects with similar radiodensities, such as cancerous tissue compared to healthy tissue, a contrast agent usually needs to be employed to achieve the correct diagnosis.

The majority of existing commercial CT contrast agents are iodine-based because of two factor: iodine is an effective X-ray scatterer due to its large number of electrons (atomic number 53) and current clinical CT X-ray sources operate at 33 keV, an energy which is also absorbed by the iodine atoms; thereby improving the overall performance of the contrast agent. The increase in attenuation at 33 keV for iodine is due to the photoelectric absorption of X-rays at that specific energy by iodine inner-shell electrons.

Many existing CT contrast agents consist of a 1,3,5 tri-iodo benzene backbone with the other three positions on the benzene ring consisting of water-solubilizing groups containing alcohol, amine, amide, and carbonyl functional groups. The major difference between the various contrast agents on the market is the structure of the water-solubilizing groups, but the tri-iodo benzene backbone is nearly universal. These CT agents contain between 25 and 50 percent by mass iodine, have high water solubility, on the order of 150 mg/mL, and are known as blood pool agents. This means the agent circulates in the blood pool, but does not translocate into the interior of cells. Sufficient contrast is achieved solely because abnormal tissues, such as cancerous tumors, require increased blood flow to sustain their growth, resulting in higher local concentrations of contrast agent. Current CT contrast agents are generally not targeted to specific cell types which lead to limitations in the detection of diseases such as vulnerable plaque in the coronary artery.

SUMMARY

The present disclosure relates to compositions and methods related to carbon Nanotubes. More particularly, the present disclosure relates to an imaging agent comprising carbon Nanotubes internally loaded with a contrast agent and associated methods of preparation and use.

The hollow structure of SWNTs may be used as a capsule to deliver diagnostic and/or therapeutic agents to specific cell-types of interest, such as cancers.

Existing CT technology lacks the ability to non-invasively diagnose critical diseases, such as coronary artery disease vulnerable plaque. The imaging agents of the present disclosure may be used as blood pool CT contrast agents, with long circulation times, avoiding the use of a catheter during x-ray angiography.

By using a carbon Nanotube as the base structure of the imaging agent, toxic contrast agents, such as I2 may be sequestered within the interior of the Nanotube. This may be advantageous for in vivo applications, to ensure the iodine toxicity is completely sequestered within the interior of the carbon Nanotube. The exterior of the Nanotube may be substituted with peptides, water-solubilizing groups, and the like, to enhance the ability of the nanotube to be internalized by cells.

The features and advantages of the present disclosure will be readily apparent to those skilled in the art upon a reading of the description of the embodiments that follows.

DRAWINGS

Some specific example embodiments of the disclosure may be understood by referring, in part, to the following description and the accompanying drawings.

FIG. 1 shows the three species of I2 present in I2-loaded full-length SWNTs: (A) physisorbed to the outside of a Nanotube bundle, (B) contained within the interior of the Nanotube, and (C) intercalated within the interstitial spaces of a Nanotube bundle.

FIG. 2 shows thermal gravimetric analysis of raw SWNTs (blue) and I2-SWNTs (red).

FIG. 3 shows a Raman spectrum of (a) raw SWNTs and (b) I2-SWNTs.

FIG. 4 is a TEM image of raw SWNTs (left) and I2-SWNTs (right).

FIG. 5 shows an I 3d5/2 XPS spectrum (left) and X-ray induced Auger emission spectrum (right) of I2-SWNTs.

FIG. 6 shows a C 1s XPS spectrum for I2-SWNTs

FIG. 7 shows an AFM image of raw HiPco SWNTs (left) and reduced HiPco SWNTs (right).

FIG. 8 shows AFM height measurements for raw HiPco SWNTs.

FIG. 9 shows AFM height measurements for Na°/THF reduced HiPco SWNTs.

FIG. 10 shows a Raman spectrum of (a) raw HiPco SWNTs and (b) Na°/THF reduced HiPco SWNTs.

FIG. 11 shows a) I 3d5/2 XPS spectrum of I2-SWNTs (black) and I2@SWNTs (red) reduced by the Na°/THF reaction and then quenched by water. b) X-ray induced Auger emission spectrum over the I MNN region for I2-SWNTs (black) and I2@SWNTs (red) reduced by the Na°/THF reaction and then quenched by water. The peaks due to externally-adsorbed I2 are denoted by an asterisk.

FIG. 12 shows a) Variable-temperature XPS study of I2-SWNTs under high vacuum and b) X-ray induced Auger emission spectrum of I2-SWNTs at room temperature (black), at 100° C. (green), at 200° C. (blue), at 300° C. (red), and reduced by the Na°/THF reduction reaction (yellow). All spectra were acquired under high vacuum. Possible instrument error is +10° C. and +0.1% Iodine.

FIG. 13 shows an I 3d5/2 XPS spectrum for twice-Na°/THF-reduced I2-SWNTs.

FIG. 14 shows an x-ray induced Auger emission spectrum over the I MNN region for twice-Na°/THF-reduced I2-SWNTs

FIG. 15 shows a) Raman spectrum of raw (a) raw SWNTs, (b) I2-SWNTs, (c) Na°/THF reduced I2-SWNTs, (d) I2-SWNTs heated to 400° C., and (e) I2-SWNTs heated to 1000° C. b) The low energy region of a) magnified. The ν (I-I) stretching mode peak is denoted by an asterisk.

FIG. 16 shows micro CT images of (a) raw SWNTs, (b) I2-SWNTs, and (c) Na0/THF reduced I2@SWNTs.

FIG. 17 shows AFM image of US-tubes. Only 20-40 nm in length, the US-tubes are seen as bright dots in a 2 μm2 image.

FIG. 18 shows AFM height measurements for US-tubes.

FIG. 19 shows a Raman spectrum of (a) raw SWNTs and (b) US-tubes.

FIG. 20 shows AFM height measurements for Na°/THF reduced US-tubes

FIG. 21 shows Raman spectrum of I2-US-tubes.

FIG. 22 shows an XPS spectrum (left) and X-ray induced Auger emission spectrum (right) of I2-US-tubes. In the Auger emission spectrum, the peaks assigned previously to external I2 for full-length I2-SWNTs are denoted by asterisks.

FIG. 23 shows a Raman spectrum of Na°/THF reduced I2-US-tubes.

FIG. 24 shows a micro CT images of (a) empty US-tubes, (b) I2-US-tubes, and (c) Na°/THF reduced I2-US-tubes. The calculated radiodensities are 4366 HU, 43,716 HU, and 4395 HU respectively.

FIG. 25 shows a) Variable-temperature XPS study of I2-US-tubes under high vacuum and b) X-ray induced Auger emission spectrum of I2-US-tubes at room temperature (black), at 100° C. (green), at 200° C. (blue), and at 300° C. (red). All spectra were acquired under high vacuum. Possible instrument error is ±10° C. and ±0.1% iodine.

FIG. 26 shows a Raman spectrum of (a) Na°/THF reduced I2-US-tubes, (b) NaH reduced I2@US-tubes, and (c) Na°/THF reduced I2@SWNTs. The region of interest is enlarged in the right image.

FIG. 27 shows an I 3d5/2 XPS spectrum (left) and X-ray induced Auger emission spectrum (right) of NaH reduced I2@US-tubes.

FIG. 28 shows a reaction scheme for the synthesis of PEG-US-tubes.

FIG. 29 shows an alternative reaction scheme for PEG-US-tubes.

FIG. 30 shows a reaction scheme for serinol amide-US-tubes.

FIG. 31 shows molecular structure of amphifullerene, AF1.

FIG. 32 shows CT image of 50 mg of unloaded SWNTs (left) and an equal amount of I2@SWNTs (right) as solids. The lines beneath the samples are a support material for the sample holders.

FIG. 33 shows an I 3d5/2 XPS spectrum of I2 loaded US-tubes substituted with serinol after NaH reduction. The position of the peak is 619 eV, consistent with all previous measurements.

FIG. 34 shows an XAES spectrum of I2 loaded US-tube substituted with serinol (black), I2 loaded US-tube substituted with serinol after EtOH washing (blue), and I2 loaded US-tube substituted with serinol after 10 mins NaH reduction (red). The black and blue spectra have all 3 I2 peaks, meaning they contain both internal and external I2. Only after the NaH reduction is all external I2 removed.

The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

While the present disclosure is susceptible to various modifications and alternative forms, specific example embodiments have been shown in the figures and are herein described in more detail. It should be understood, however, that the description of specific example embodiments is not intended to limit the invention to the particular forms disclosed, but on the contrary, this disclosure is to cover all modifications and equivalents as illustrated, in part, by the appended claims.

DESCRIPTION

The present disclosure relates to compositions and methods related to carbon Nanotubes. More particularly, the present disclosure relates to an imaging agent comprising carbon Nanotubes internally loaded with a contrast agent and associated methods of preparation and use.

In one embodiment, the present disclosure relates to imaging agents comprising a carbon Nanotube and a contrast agent. As used herein, the term “contrast agent” refers to any agent which is detectable by any means. As used herein, the term “carbon nanotube” refers to a type of fullerene having an elongated, tube-like shape of fused five-membered and six-membered rings that is approximately 1 nm in diameter. Examples of carbon Nanotubes that may be used in conjunction with the methods of the present disclosure include, but are not limited to, single walled carbon Nanotubes (SWNTs) and ultra-short carbon Nanotubes (US-tubes).

SWNTs, also known as single walled tubular fullerenes, are cylindrical molecules consisting essentially of sp2 hybridized carbons. In defining the size and conformation of single-walled carbon Nanotubes, the system of nomenclature described by Dresselhaus et al., Science of Fullerenes and Carbon Nanotubes, Ch. 19, ibid. will be used. Single walled tubular fullerenes are distinguished from each other by a double index (x,y), where x and y are integers that describe how to cut a single strip of hexagonal graphite such that its edges join seamlessly when the strip is wrapped onto the surface of a cylinder. When x=y, the resultant tube is said to be of the “arm-chair” or (x,x) type, since when the tube is cut perpendicularly to the tube axis, only the sides of the hexagons are exposed and their pattern around the periphery of the tube edge resembles the arm and seat of an arm chair repeated n times. When y=0, the resultant tube is said to be of the “zig-zag” or (x,0) type, since when the tube is cut perpendicular to the tube axis, the edge is a zig zag pattern. Where x≠y and y≠0, the resulting tube has chirality. The electronic properties of the Nanotube are dependent on the conformation, for example, arm-chair tubes are metallic and have extremely high electrical conductivity. Other tube types are metallic, semi-metals or semi-conductors, depending on their conformation. Regardless of tube type, all SWNTs have extremely high thermal conductivity and tensile strength. The SWNT may be a cylinder with two open ends, a cylinder with one closed end, or a cylinder with two closed ends. Generally, an end of an SWNT can be closed by a hemifullerene, e.g. a (10, 10) carbon Nanotube can be closed by a 30-carbon hemifullerene. If the SWNT has one or two open ends, the open ends can have any valences unfilled by carbon-carbon bonds within the single wall carbon Nanotube filled by bonds with hydrogen, hydroxyl groups, carboxyl groups, or other groups. SWNTs can also be cut into ultra-short pieces, thereby forming US-tubes. As used herein, the term “US tubes” refers to ultra short carbon Nanotubes with lengths from about 20 nm to about 100 nm.

Generally, the carbon Nanotubes, more particularly, the SWNTs may be produced by the HiPco process or by electric arc discharge. Virtually all previous research about loading SWNT samples was performed with electric-arc discharge-produced SWNTs as opposed to other SWNT production methods, such as high-pressure carbon monoxide (HiPco), because arc-produced SWNTs have a larger diameter than HiPco SWNTs (1.4 nm average diameter for arc vs. 1.0 nm diameter for HiPco) and arc SWNTs are generally believed to contain more sidewall defects than HiPco SWNTs, thereby facilitating loading. For medical applications, however, the uniformity and purity of HiPco SWNTs is advantageous. Suitable commercially available carbon Nanotubes may be obtained from Carbon Nanotechnologies Inc., Houston, Tex.

Current methods known in the art to produce US tubes from SWNTs require full-length SWNTs to be cut into short pieces by a four-step process. First, residual iron catalyst particles are removed by oxidation via exposure to wet-air or SF6 followed by a strong acid (HCl) treatment to extract the oxidized iron particles. The purified SWNTs are then fluorinated by a gaseous mixture of 1% F2 in He at elevated temperatures for up to 2 hours and cut into short pieces by pyrolysis under argon at 900° C. The fluorination reaction produces F-SWNTs, with a stoichiometry of CFx (x<0.2), which consist of bands of flurorinated-SWNT separated by regions of pristine SWNT. Pyrolysis under Ar liberates volatile fluorocarbons, thereby cutting the SWNTs into pieces with lengths corresponding to the areas of pristine SWNT. While this method known in the art is effective at producing cut SWNTs, improvements can be made; specifically, the separate purification step is unnecessary and can be eliminated.

To overcome the inefficiencies of current methods to produce US tubes, a three-step process may be used to produce US tubes. First, as produced HiPco SWNTs are fluorinated in a monel steel apparatus by a mixture of 1% F2 in He at 100° C. for 2 hours. During this process, both the SWNTs and the iron catalyst particles become fluorinated. Subsequent exposure to concentrated HCl removes the fluorinated catalyst particles without affecting the F-SWNTs, which have a stoichiometry of ˜C10F after the acid treatment. The, now-purified, F-SWNTs are cut into US-tubes by pyrolysis under Ar at 900° C. The resulting US-tubes have lengths ranging from 20-80 nm, with the majority being ˜40 nm in length. Utilizing this method, the amount of iron catalyst is reduced from ˜25 mass percent in raw SWNTs to ˜1 mass percent for US-tubes. Therefore, this method is ideal for the purification of SWNTs, but only as a precursor to producing US-tubes. This is because the fluorine remaining, after the HCl acid treatment, is very hard to remove, making the F-SWNTs only viable for subsequent cutting. Furthermore, the time to produce US tubes from SWNTs using this method is significantly reduced.

Typically, carbon Nanotubes are of micron-length. Such lengths may reduce the ability of the carbon Nanotubes to internalize into the cells. The carbon Nanotubes of the present disclosure may be of a length of about 100 nm to about 5 μm, alternatively 100 nm or less, alternatively of about 50 nm or less, and alternatively from about 20 nm to about 50 nm. Generally, carbon Nanotubes of Nano-length may be suited for internalization by cells. In certain embodiments, the carbon Nanotubes used in the compositions of the present disclosure may comprise US tubes of length in the range of about 20 nm to about 80 nm. In certain embodiments, the carbon Nanotubes used in the compositions of the present disclosure may comprise SWNTs of a length of less than 100 nm.

The carbon Nanotube can be substituted or unsubstituted. By “substituted” it is meant that a group of one or more atoms is covalently linked to one or more atoms of the carbon Nanotube. Generally, Bingel chemistry may be used to substitute the Nanotube with appropriate groups. Examples of groups suitable for use include, but are not limited to, malonate groups, serinol malonates, groups derived from malonates, serinol groups, serinol amide, carboxylic acid, dicarboxyilic acid, polyethyleneglycol (PEG), and the like. In certain embodiments, the carbon Nanotube is substituted with one or more water-solubilizing groups. Water-solubilizing groups are polar groups (that is, groups having a net dipole moment) that render the generally hydrophobic Nanotube soluble in water. Such groups may allow for greater biocompatibility of the carbon Nanotube and enhanced diffusion through the cell membrane. In certain embodiments, the carbon Nanotube may be substituted before loading of the contrast agent within the tube. For example, in certain embodiments using US tubes, the US tubes may be substituted with serinol groups prior to loading of a contrast agent within the tube. The degree of lipophilicity of the substituted Nanotube should roughly parallel the degree of lipophilicity of the groups covalently linked to the surface of the nanotube.

The imaging agents of the present disclosure also comprise a contrast agent. In certain embodiments, the contrast agent is I2. In other embodiments, the contrast agent may be any iodine moiety. In other embodiments, the contrast agent may be magnetic metallic particles, such as Gd3+. Examples of contrast agents include, but are not limited to, MRI contrast agents (e.g. magnetic metal particles), CT contrast agents (e.g. hyperpolarized gas), X-ray contrast agents, nucleosan contrast agents, and ultrasonic contrast agents, among others.

The contrast agents of the present disclosure are generally sequestered within the carbon Nanotube. Generally all or a portion of the carbon Nanotube may be loaded with contrast agent. The carbon Nanotubes may be loaded through the ends of the carbon nanotubes and/or through the side wall defects. Examples of suitable methods that may be used to load the carbon Nanotubes with contrast agent include, but are not limited to, solution phase method, molten phase method, and sublimation. One of ordinary skill in the art, with the benefit of the disclosure will realize what method would be suitable for loading the carbon Nanotube based on the properties of the contrast agent to be loaded.

To prepare the imaging agents of the present invention, loading by sublimation may be effective when using materials that sublime at relatively low temperatures, such as I2. In certain embodiments, carbon Nanotubes are loaded with I2 in high yields via sublimation. In certain embodiments, HiPco SWNTs are loaded with a contrast agent, such as I2. Typically, HiPco SWNTs are not used for loading experiments because the interior of the HiPco SWNT was thought to be inaccessible for loading due to the lack of sidewall defects and the presence of the iron catalyst particle, which blocks the open end of the SWNT. However, such HiPco produced tubes do load with I2 without exposure to strong acids, known to create sidewall defects in the Nanotube that would facilitate loading. It may be possible for I2 to react with the iron catalyst particle to remove it from the end of the SWNT, thus allowing loading through the open end of the SWNT. US tubes may also be loaded in the same manner as SWNTs.

Though the Nanotubes are able to be loaded, exterior adsorbed I2 must be removed. In certain embodiments, a chemical reduction procedure may be performed to debundle carbon Nanotubes after loading with the contrast agent to ensure that the contrast agent is completely sequestered within the carbon Nanotubes. In particular, procedures useful for debundling SWNTs are known in the art. One such procedure, a Na0/THF reduction reaction, results in the SWNTs becoming highly charged (˜10 electrons/nm), which creates an electrostatic repulsion resulting in the debundling of the Nanotubes into mostly individual SWNTs. In the case of I2 loaded SWNTs, this debundling would allow for any I2 intercalated within the surface spaces of a SWNT bundle to be chemically reduced to I− and washed away. In other embodiments, the I2 loaded SWNTs may be heated to 300° C. without reduction to remove I2 adsorbed to the exterior surface of the Nanotube. In these embodiments, the resulting loaded Nanotubes are stable and loaded contrast agent will not be lost even after further reduction steps or additional heating.

In certain embodiments, the carbon Nanotubes are US tubes and such reduction methods for SWNTs result in the unloading of contrast agent, I2, from the interior of the US tubes. In these embodiments, the US tubes may be reduced using NaH. Such reduction methods, however, are time-dependent. The length the reaction is allowed to proceed will depend on the presence or absence of internally loaded I2. Generally, in these embodiments, when reduction reactions are performed on carbon Nanotubes loaded with contrast agents, the reaction should not proceed for longer than one hour to ensure that contrast agent remains loaded within the tubes. In other embodiments, the removal of externally adsorbed I2 may occur by heating the loaded Nanotubes to 400° C.

In certain other embodiments, the imaging agents of the present disclosure may comprise carbon Nanotubes that are US tubes. In these embodiments, the US tubes may be substituted with serinol groups prior to loading with contrast agent. The contrast agent may be I2 and may be loaded after the US tubes have been substituted via sublimation. To remove the any exterior adsorbed contrast agent, the US tubes may be reduced using NaH to form a substituted and loaded US tube imaging agent.

In certain embodiments, the imaging agents of the present disclosure may be enclosed within a buckysome. As used herein, the term “buckysome” refers to amphifullerenes, AF1, (FIG. 31) that have self assembled into unilamellar vesicles which resemble unilamellar liposomes. As used herein, the term “unilamellar” refers to having only one bilayer around an aqueous core. The imaging agents of the present disclosure may be entrapped within the fullerene cage of the buckysome. Buckysomes have been found to be temperature and pH sensitive. In certain embodiments, under high temperature and pH, the imaging agents may be released at much higher rates than at low temperature and low pH. This pH dependent release is due to the protonation and deprotonation of the carboxylic acid groups of the individual AF1 groups. Upon deprotonation, the carboxylic acid moieties become negatively charged and may repel one another, resulting in a more fluid structure which increases the release of imaging agent from the vesicles. An acidic environment results in a more tightly packed structure. Additionally, the AF1 molecule has potential for an almost unlimited degree of further derivatization of its structure, which gives it “tunability” with respect to imaging agent release.

In certain embodiments, the imaging agents of the present disclosure may be used to diagnose diseases. Examples of such diseases include, but are not limited to, coronary heart disease resulting from vulnerable plaque, intracranial hemorrhages, acute and chronic lung conditions such as cancer, emphysema, or pneumonia, and several abdominal conditions such as kidney stones or appendicitis. In these embodiments, the imaging agents may be internalized by cells of interest. Imaging techniques known in the art may be used to detect the presence of imaging agent after internalization by the cells. Such imaging techniques include, but are not limited to, CT, MRI, X-Ray, and the like.

To facilitate a better understanding of the present disclosure, the following examples of certain aspects of some embodiments are given. In no way should the following examples be read to limit, or define, the entire scope of the invention.

EXAMPLES Example 1 Synthesis of I2 Loaded SWNTs (Hereinafter I2-SWNTs)

A raw Nanotube sample of SWNTs, produced by the HiPco process, with an average diameter of 1.0 nm and containing 25% by weight iron catalyst impurities was obtained from Carbon Nanotechnologies Inc. The, as received, SWNT sample was not purified by exposure to a strong acid treatment which is known to create additional defects in the sidewalls. Loading of raw, full-length SWNTs with contrast agent, I2 was accomplished via sublimation of I2 (˜100° C.) in the presence of SWNTs for one hour in a closed glass vessel. In all cases, SWNTs and I2 were kept separate to ensure loading was via I2 sublimation and not via molten iodine. In a typical experiment, 50 mg of raw SWNTs were used and the SWNT sample gained approximately 80% mass during the loading process (total mass after loading was 90 mg). However, not all of this mass gain is due to internally-loaded I2; in fact, a central question surrounding loaded SWNTs is whether the loading material is contained within the interior of the SWNT or adsorbed to its exterior surface. Nanotubes aggregate into large bundles which are difficult to separate (˜1 eV/nm binding energy) and hydrophobic molecules, e.g. I2, can become intercalated in the surface spaces within a SWNT bundle. As shown in FIG. 1, there are actually 3 possible I2 species present; I2 adsorbed to the exterior of a Nanotube bundle, I2 intercalated within the surface spaces of a nanotube bundle, but not loaded within any one SWNT, and I2 loaded within the interior of a SWNT.

Example 2 Thermal Gravimetric Analysis of I2-SWNTs

Thermal gravimetric analysis (TGA) in air measures the mass loss of the I2-SWNTs as a function of temperature (FIG. 2). Raw SWNTs, with no loaded I2, exhibit very little loss of mass until temperatures greater than 400° C. are reached, at which point the SWNTs combust. For I2-SWNTs, mass loss is observed much earlier, around 150° C., as I2 is liberated. The total mass lost from 150° C. to 400° C., when the SWNTs again combust, is approximately 35%, which is in good agreement with the observed mass gain from the loading process. However, no distinction can be made as to which species of I2 is liberated and only a quantification of the total amount of iodine removed can be made. For raw SWNTs, the mass remaining at 600° C. is iron oxide residue from iron catalyst particles present in raw SWNTs; 19 mass percent of iron oxide remaining corresponds to an initial iron content of 25% by mass. In the case of the I2-SWNTs, only 7 mass percent remains at 600° C. This is not necessarily because iron is being removed during the loading process. The added iodine mass due to the loading process results in a lower overall mass percent of iron in the I2-SWNTs.

Example 3 Raman Spectroscopy of I2-SWNTs

Raman spectroscopy provides additional structural information about the I2-SWNTs but is also unable to distinguish the multiple species of I2 present. Comparative Raman spectra of raw SWNTs and I2-SWNTs are shown in FIG. 3. Characteristic SWNT bands at 1590 cm−1 (sp2 hybridized carbon), 1350 cm−1 (sp3 hybridized carbon), and in the region of 100-300 cm−1 (radial breathing modes for SWNTs of various diameters) are present in both the raw SWNT and I2-SWNT samples. However, the I2-SWNTs exhibit an additional band at 159 cm−1 which is not present in the raw SWNT spectrum. This peak disappears when the I2-SWNTs are heated to 1000° C. and reappears after a second I2 sublimation treatment, therefore it can confidently be assigned to the ν(I-I) stretching mode. The position of this ν(I-I) band for I2-SWNTs, 159 cm−1, is somewhat surprising, because it does not correspond with either the ν(I-I) stretching mode observed at 178 cm−1 for crystalline I2 or at 211 cm−1 for gaseous I2. Thus, the interior of a SWNT or SWNT bundle is a unique chemical environment. While this is interesting information, Raman spectroscopy alone is not able to identify or quantify the multiple species of I2 present; thus other techniques, such as electron microscopy, must be explored.

Example 4 Transmission Electron Microscopy of I2-SWNTs

High-resolution transmission electron microscopy (HRTEM) has thus far been the method of choice for characterizing loaded SWNT samples. While HRTEM is a powerful technique and is able to visualize individual atoms of loading material, HRTEM does have several disadvantages. The long acquisition time, inability to characterize bulk samples, and inability to quantify each species present of HRTEM indicate that better techniques are needed for complete characterization. Perhaps the greatest disadvantage of the HRTEM used in the previous work is its uniqueness; very few labs in the world have the equipment and software necessary to perform this type of HRTEM analysis. Due to the limited availability of the equipment, only regular TEM could be performed on the I2-SWNTs. In addition to the disadvantages experienced by HRTEM, the resolution of regular TEM is too low to visualize individual I2 molecules. In fact, very little difference can be seen between raw SWNTs and I2-SWNTs (FIG. 4). Energy Dispersive X-ray spectroscopy (EDAX) does confirm the presence of iodine loaded in the I2-SWNTs and the absence of iodine in raw SWNTs, but certainly this method cannot be used to identify or quantify the multiple species of I2 present.

Example 4 X-Ray Photoelectron Spectroscopy of I2-SWNTs

After loading, the I2-SWNTs contained 5.3 atomic % of iodine by XPS (36% by mass) which agrees well with the mass gain observed during the loading process. The position of the I-3d5/2 peak in the XPS spectrum (FIG. 5) at 619.5±0.2 eV is consistent with accepted values for I2 (as opposed to polyiodide chains such as I3− and I5−), indicating that I2 does not react with SWNTs to form C—I bonds. This is also confirmed by the absence of a second peak in the C 1s spectrum (FIG. 6), which would also indicate C—I bond formation, for the I2-SWNT sample. However, only one peak is observed in the I-3d5/2 region and no shoulders are visible which would indicate the presence of a hidden second peak. Therefore, it would appear that XPS cannot distinguish between the I2 species. However, inspection of the X-ray-induced Auger emissions reveals several features of interest (FIG. 5). For I2-SWNTs, the X-ray induced Auger emission spectrum exhibits peaks at kinetic energies of 507.5±0.2 eV and 519.0±0.2 eV. Additionally, there is a prominent shoulder observed on the 507.5 eV peak, with a maximum at ˜510 eV. The 507.5 and 510.0 eV peaks stem from I-M5N45N45 emissions, whereas the 519.0 peak stems from I-M4N45N45 emissions. Unfortunately, despite lengthy efforts curve-fitting the various peaks in the X-ray induced Auger emission spectrum; no conclusive discrimination of individual I2 species could be made. It became obvious that the only method to definitively identify any single I2 species was to debundle the SWNTs; this would result in the intercalated I2 becoming accessible to an organic solvent or a reactive species, leading to the removal of this unwanted, external I2 species.

Example 5 Chemical Reduction of SWNTs

A method of debundling SWNTs via chemical reduction in tetrahydrofuran (THF) was published by Petit et al. 50 milligrams of raw SWNTs were added to a dry 250 mL round bottom flask with a 2:1 molar excess of sodium metal (100 mg). Then, 150 mL of dry THF was added to the flask, and the flask was purged with N2(g), capped, and bath sonicated for one hour. After one hour, the reduction reaction was quenched with DI water and the sample was isolated using a glass frit filter (Pyrex #36060). Atomic force microscopy (AFM) confirmed the debundling of the SWNTs by the Na°/THF reduction reaction into mostly individuals (FIG. 7). The AFM image was acquired before the addition of water, although the SWNTs are likely quenched via exposure to the atmosphere. Height measurements taken for several points in the reduced SWNT sample measure 1 nm, corroborating individual SWNTs (FIGS. 8 and 9).

2. Example 6 Raman Spectroscopy of Na0/THF Reduced SWNTs

Raman spectroscopy was used to assess structural changes in the SWNTs as a result of the Na0/THF reduction reaction. Such changes could be either residual delocalized negative charge not quenched by the addition of water as suggested in the original work, or protonation (similar to the Birch reaction) of the charged SWNTs upon quenching by water. As shown in FIG. 10, the Raman spectrum before and after the Na°/THF reduction is nearly identical, with the exception of a small increase in the disorder band at ˜1300 cm−1. This band is indicative of sp3-hybridized carbon which suggests that some degree of protonation of the SWNTs has occurred. This was confirmed by an elemental analysis performed by Galbraith Laboratories which showed increased hydrogen content in the Na0/THF reduced SWNTs, with a C:H ratio of ˜20:1 measured for Na°/THF reduced SWNTs as opposed to a C:H ratio of >150:1 measured for raw SWNTs (Table 1). Once the effects of the Na°/THF reduction reaction on raw SWNTs were understood, a Na°/THF reduction was performed on I2-SWNTs under the same reaction conditions to determine if removal of intercalated I2 was achieved.

TABLE 1 Carbon and hydrogen elemental analysis of raw HiPco SWNTs and Na°/THF reduced HiPco SWNTs Atomic Percent Sample Carbon Hydrogen Raw HiPco SWNTs 69.49 <0.5 Na0/THF reduced HiPco SWNTs 67.91 3.21

Example 6 XPS of Na0/THF Reduced I2-SWNTs

After an I2-SWNT sample was reduced by the Na0/THF reaction, 2.8 atomic % or 22% by weight I2 remained in the sample, which approximates to be 3.1 atoms of iodine/nm of SWNT. A slight shift of the I-3d5/2 peak to a lower binding energy (619.1±0.2 eV) is observed in the reduced I2@SWNT sample; however, the shift is within experimental error and is not large enough to provide conclusive evidence as to the removal of exterior-adsorbed I2. Additionally, this value is still within those accepted for I2, which indicates the remaining I2 in the sample has not been reduced to some polyiodide form (I3− or I5−) as a result of the Na°/THF reaction. This would likely occur only if the remaining I2 was sequestered within the interior of the hydrophobic Nanotube and therefore, inaccessible to chemical reduction.

Inspection of the X-ray induced iodine Auger emission spectrum reveals significant differences between the I2-SWNT sample and the Na0/THF reduced I2@SWNTs. As described above, the unreduced I2-SWNT sample exhibits peaks at kinetic energies of 507.5±0.2 eV and 519.0±0.2 eV, with a prominent shoulder observed on the 507.5 eV peak (maximum at ˜510 eV). The reduced I2@SWNT sample, on the other hand, exhibits a single peak at 510.0±0.2 eV with a shoulder at approximately 517 eV. This shoulder is initially hidden in the I2-SWNT spectrum by the I2 peak at 519 eV and is likely also due to internal I2. This phenomenon is also observed in the Auger temperature studies discussed below (red trace in FIG. 12b). Representative spectra comparing the iodine photoelectron and X-ray induced Auger emissions for the I2-SWNT (black) and reduced I2@SWNT (red) samples are shown in FIG. 11. As discussed above, the 507.5 and 510.0 eV peaks stem from I-M5N45N45 emissions, whereas the 519.0 peak stems from I-M4N45N45 emissions. This allows for the calculation of Auger parameters for each peak, a valuable tool in deriving chemical state information.

Since the I-M4N45N45 emissions appear at 11.5 eV lower kinetic energy than I-M5N45N45 emissions, addition of this value allows for Auger parameters to be derived. Such parameters are an effective method of deriving additional chemical state information. Auger parameters are derived by adding the I-3d5/2 peak binding energy to the I-M4N45N45 kinetic energy, or by adding the I-3d5/2 peak binding energy to the I-M5N45N45 kinetic energy plus 11.5 eV. For the unreduced I2-SWNT sample, Auger parameter values of 1138.5 eV for the 507.5 eV peak, 1141.0 eV for the 510.0 eV shoulder, and 1138.5 eV for the 519.0 eV peak are derived. A value of 1141.0 eV is derived for the peak at 510.0 eV in the Na0/THF reduced I2@SWNT sample.

The Auger peak at 510.0 eV is thus assigned to internally-loaded I2, while those at 507.5 eV and 519.0 eV are attributed to externally-adsorbed I2. The difference in the kinetic energies of these Auger emissions represents a definitive method of distinguishing between internal and external I2. Auger parameters of 1138 eV are consistent with I2, confirming once again that the external-adsorbed iodine is I2, not a polyiodide or a C—I species. The shift observed in the Auger parameter, from 1138.5 eV to 1141 eV, for internal I2, is likely due to the unique chemical environment experienced by I2 confined within the interior of a SWNT.

Example 7 Inductively-Coupled Plasma Analysis

The removal of iodine from the I2-SWNTs during the Na0/THF reduction reaction was also confirmed by inductively-coupled plasma/atomic emission detector (ICP-AE) analysis of the THF/water filtrate. After the Na°/THF reaction was quenched with water, the reduced I2@SWNTs were isolated by a glass frit filter. The THF/water filtrate was heated to remove the THF, and ICP-AE confirmed the presence of iodine (present as NaI) in the filtrate after the reduction reaction. A 20 mL sample contained 550 mg/L of I-, which corresponds to 10 mg of I2 removed from the I2-SWNT sample during the reduction reaction. This is consistent with the change observed in the atomic % of I2 by XPS.

To confirm the stability of the internal I2 with respect to chemical reduction, a second Na0/THF reaction was performed on the already reduced I2-SWNTs (hereinafter I2@SWNTs) under the same conditions. After a second Na°/THF reduction, 2.3 atomic % of iodine remained which is unchanged (within error) from the amount of I2 present in the I2-SWNT sample after the first reduction. Additionally, the peak positions for iodine in the XPS and X-ray induced Auger emission spectra were unchanged from the peak positions after the first reduction (FIGS. 13 and 14) ICP-AE also confirmed that no iodine (as NaI) was present in the filtrate after the second reduction. These results establish that internal I2 is truly sequestered within the interior of the Nanotube (I2@SWNTs) and is impervious to chemical reduction by Na°/THF.

Example 8 Variable-Temperature XPS Studies

Variable-temperature XPS analysis was performed on an I2-SWNT sample to assess the thermal stability of the internal I2 vs. external I2. A sample of the unreduced I2-SWNTs was heated from room temperature to 800° C. under high vacuum. During this process, a mass spectrum analysis indicated I2+ (254 amu) and I+ (127 amu) were the only positive ion species liberated from the I2-SWNT sample in the temperature range of 200° C.-800° C. XPS spectra and X-ray induced Auger emission spectra were acquired every 100° C. As shown in FIG. 12a, a linear loss of iodine is observed by XPS from room temperature until 300° C. From 300° C. to 500° C., the iodine content remains constant, and above 500° C. linear loss of iodine is again observed. The atomic % of iodine remaining at 400° C. is ˜2.0%, a value consistent with the amount of internally-loaded I2 from the reduction experiments. As also shown in FIG. 12b, the X-ray induced Auger emission spectra of the I2-SWNTs at room temperature (black), 100° C. (green), 200° C. (blue), 300° C. (red), and after the Na0/THF reduction reaction (yellow) confirm that the decrease in the atomic % of iodine observed by XPS is due to the removal of exterior-adsorbed I2. The Auger peaks at 507.5 eV and 519.0 eV, assigned above to externally-adsorbed I2, decrease in intensity from room temperature until their disappearance at ˜300° C. This is illustrated by the shift from an unresolved doublet in the 505-510 eV region at room temperature (black trace in FIG. 9b, maxima at 507.5 eV and 510 eV) to a single peak at 300° C. (red trace in FIG. 12b, maximum at 510 eV). As discussed above, a shoulder is once again observed at ˜517 eV after the external I2 is removed from the SWNT sample (red trace in FIG. 12b). The Auger peak at 510.0 eV, assigned to internal I2, is largely unchanged during the temperature study. The Auger emission spectrum of I2-SWNTs at 300° C. (red trace in FIG. 12b) and the spectrum for reduced I2@SWNTs (yellow trace in FIG. 12b) are identical with respect to the features at 507.5 and 519.0 eV. Heating to 300° C. thus provides an alternative method for removing externally-adsorbed I2. It is possible to also remove the interior I2 from the SWNT sample, but temperatures upwards of 800° C. are required.

3. Example 8 Raman Spectroscopy of Na0/THF Reduced I2-SWNTs

Raman spectroscopy is used to characterize changes in the I-I stretching mode present in the I2-SWNT sample as a result of the removal of external I2, either by heating or Na°/THF reduction. As discussed above and shown in FIG. 15, there is an additional band at 159 cm−1 in the Raman spectrum of I2-SWNTs (FIG. 15b), which is not present in the raw SWNT spectrum (FIG. 15a). This band is therefore assigned to the ν(I-I) stretching mode. Interestingly, this ν(I-I) stretching mode decreases significantly when the I2-SWNTs are reduced by the Na°/THF reduction reaction or heated to 400° C. (FIGS. 15c and 15d respectively). Upon heating to 1000° C., which removes all I2, the 159 cm−1 band completely disappears (FIG. 15e) and the Raman spectrum is once again identical to that for the raw SWNT sample (FIG. 15a). Thus, Raman spectroscopy can also be used to discriminate between internal and external I2, by way of the relative intensities of the ν(I-I) stretching mode, but only in conjunction with XPS spectral data.

Example 9 Micro Computed Tomography (MicroCT)

Finally, MicroCT experiments confirm that I2@SWNTs are functional computed tomography contrast agents. Solid samples of raw SWNTs, I2-SWNTs, and Na°/THF reduced I2@SWNTs were placed in a cylindrical polyethylene holder and analyzed by a Skyscan 1172 microcomputed tomography scanner. The raw SWNTs, as expected, exhibit very little X-ray attenuation; qualitatively, raw SWNTs appear similar to the polyethylene holder. The attenuation for raw SWNTs, which contain no iodine, is most likely due to the presence of iron catalyst particles which also scatter X-rays, although not nearly as effectively as iodine (26 electrons for iron compared to 57 for iodine). The I2-SWNTs, on the other hand, display extremely high attenuation. I2@SWNTs, as expected, demonstrate much higher attenuation than the raw SWNTs, but not as high as the I2-SWNTs. This is, of course, because I2-SWNTs contain both internal and external I2 (5.3 atomic %) whereas I2@SWNTs contain only internal I2 (2.8 atomic %). Comparative 2-D MicroCT images for raw SWNTs, I2-SWNTs, and I2@SWNTs are shown in FIGS. 16 and 32.

To quantify the performance of each sample, Hounsfield Units (HU) were calculated. The Hounsfield scale, established by Sir Godfrey Hounsfield, one of the developers of computed tomography, is a quantitative way of describing radiodensity. Specifically, distilled water is defined as 0 HU and air is defined as −1000 HU. Using these values, Hounsfield units of 14,927 HU, 46,438 HU, and 28,400 HU were calculated for raw SWNTs, I2-SWNTs and I2@SWNTs, respectively.

Example 10 Modified Approach Using Fluorination for Purification

US-tubes, with lengths ranging from 20-80 nm, were prepared via a modification of a known process. Currently, full-length SWNTs are cut into short pieces by a four-step process. First, residual iron catalyst particles are removed by oxidation via exposure to wet-air or SF6 followed by a strong acid (HCl) treatment to extract the oxidized iron particles. The purified SWNTs are then fluorinated by a gaseous mixture of 1% F2 in He at elevated temperatures for up to 2 hours and cut into short pieces by pyrolysis under argon at 900° C. The fluorination reaction produces F-SWNTs, with a stoichiometry of CFx (x<0.2), which consist of bands of flurorinated-SWNT separated by regions of pristine SWNT. Pyrolysis under Ar liberates volatile fluorocarbons, thereby cutting the SWNTs into pieces with lengths corresponding to the areas of pristine SWNT. While this method is effective at producing cut SWNTs, improvements can be made; specifically, the separate purification step is unnecessary and can be eliminated.

US-tubes were prepared via a three-step process. First, as produced HiPco SWNTs are fluorinated in a monel steel apparatus by a mixture of 1% F2 in He at 100° C. for 2 hours. During this process, both the SWNTs and the iron catalyst particles become fluorinated. Subsequent exposure to concentrated HCl removes the fluorinated catalyst particles without affecting the F-SWNTs, which have a stoichiometry of ˜C10F after the acid treatment. The, now-purified, F-SWNTs are cut into US-tubes by pyrolysis under Ar at 900° C. The resulting US-tubes have lengths ranging from 20-80 nm, with the majority being ˜40 nm in length. Utilizing this method, the amount of iron catalyst is reduced from ˜25 mass percent in raw SWNTs to ˜1 mass percent for US-tubes. Therefore, this method is ideal for the purification of SWNTs, but only as a precursor to producing US-tubes. This is because the fluorine remaining, after the HCl acid treatment, is very hard to remove, making the F-SWNTs only viable for subsequent cutting.

Example 11 Atomic Force Microscopy of US-Tubes

Atomic force microscopy (AFM) analysis of the US-tubes illustrates the effectiveness of the cutting process. Shown in FIG. 17, all US-tubes are between 20 and 80 nm in length, with the majority being ˜40 nm. No evidence of SWNTs longer than TOO nm can be found. Height measurements (FIG. 18) confirm that the US-tubes exist as small bundles, with heights between 3 and 7 nm.

Example 12 Raman Spectroscopy of US-Tubes

Raman spectroscopy evaluates the structural changes to the SWNT resulting from the cutting procedure. The increase in the band at 1350 cm−1, indicative of sp3-hybridized carbon, confirms additional sidewall defects are created as a result of the cutting process. Comparative Raman spectra for SWNTs and US-tubes are shown in FIG. 19.

Atomic force microscopy also confirms that the Na°/THF reduction reaction debundles empty US-tubes into individuals. Shown in FIG. 20, height measurements substantiate individual US-tubes (diameters of ˜1 nm). This is a significant result because it represents the first example of individual US-tubes in suspension. This is critical to the sidewall functionalization of US-tubes.

Example 13 Loading Procedures for US-Tubes

The loading and characterization procedures of US-tubes are taken directly from the full-length SWNT model system. Loading of US-tubes is again accomplished via sublimation of I2 in a closed glass vessel at 100° C. The mass gain observed for US-tubes is slightly higher than that observed for full-length SWNTs; typically a 50 mg sample of US-tubes increases 100-120% by mass during the loading process (final mass=100-110 mg) as opposed to the 80% mass increase observed for full-length SWNTs. This is likely due to the increased surface area of the US-tubes as compared to full-length SWNTs. XPS also confirms that I2-US-tubes contain a greater amount of iodine than do I2-SWNTs. Values of 8-9 atomic % iodine (˜57% iodine by mass) are obtained for I2-US-tubes in contrast to 5.3 atomic % for I2-SWNTs (36% iodine by mass). This increase in atomic percent iodine is once again consistent with the mass increase observed during the I2 sublimation process. The Raman spectrum for I2-US-tubes, shown in FIG. 21, displays the peak, at 159 cm−1, proven to be the ν(I-I) stretching mode, once more confirming the presence of I2.

Example 14 XPS of I2-US-Tubes

The I 3d5/2 peak position, shown in FIG. 22, for I2-US-tubes is 619.2±0.2 eV, consistent with both the I2-SWNT data and accepted values for I2 from the literature. The X-ray induced Auger emission spectrum for I2-US-tubes, also shown in FIG. 22, again shows the same general features as I2-SWNTs. Peaks are once again observed at 507.5 eV and 519 eV, with a shoulder at 510 eV. Thus, US-tubes and full-length SWNTs behave identically with respect to the loading process; however, the stability of the internal I2 is dramatically reduced for I2-US-tubes.

In the case of full-length SWNTs, the internal I2 is remarkably stable with respect to either chemical reduction or elevated temperatures. In contrast, the internal I2 in I2-US-tubes is completely removed by either the Na0/THF reduction reaction or temperatures above 300° C. This is likely a consequence of the sidewall defects created during the cutting process, which allows Na° (Na°→Na++e−) access to the US-tube interior and permits escape of internal I2 from the US-tube at elevated temperatures.

Example 15 Raman Spectroscopy of Na°/THF Reduced I2-US-Tubes

I2-US-tubes were reduced via the Na°/THF reaction using the same conditions described previously for I2-SWNTs. The Raman spectrum of the Na°/THF reduced I2-US-tubes, shown in FIG. 19, exhibits no peak in the vicinity of 159 cm−1, indicating complete removal of I2. XPS analysis confirms no iodine present in the Na°/THF reduced I2-US-tubes. Therefore, the Na0/THF reduction of I2-US-tubes to remove external I2 is not a viable option, because the reduction also removes the internal I2.

Comparing empty US-tubes (FIG. 16a) and empty SWNTs (FIG. 11a); it is apparent that empty SWNTs demonstrate higher X-ray attenuation. This is because iron catalyst particles, which scatter X-rays, are present in raw SWNTs but are removed during the preparation of US-tubes. Thus, US-tubes are very poor at attenuating X-rays and have a radiodensity of only 4366 HU. In stark contrast, I2-US-tubes, which contain 57 mass % iodine by XPS, exhibit extraordinary X-ray attenuation. The radiodensity of I2-US-tubes, again as a solid, is 43,716 HU. Even though this value is actually less than that of I2-SWNTs (FIG. 11b, radiodensity=46,438 HU), I2-US-tubes are likely superior X-ray attenuators due to their greater amount of iodine. In these experiments, the radiodensities of I2-SWNTs and I2-US-tubes are similar only because both attenuate the X-ray beam the maximum that can be measured.

I2-US-tubes which have been reduced by the Na°/THF reaction are shown in FIG. 16c. As expected based on the previous XPS and Raman results, very little X-ray attenuation is demonstrated because all I2 has been removed by the Na0/THF reduction reaction. The radiodensity of the Na°/THF reduced I2-US-tubes is only 4395 HU as opposed to the 28,400 HU obtained for Na°/THF reduced I2-SWNTs (FIG. 14c).

Example 16 Variable-Temperature XPS Study on I2-US-Tubes

An XPS temperature study demonstrates that elevated temperatures also result in the removal of internal I2 from I2-US-tubes. The atomic percent of iodine in I2-US-tubes, as shown in FIG. 21, decreases much more rapidly with respect to temperature as compared to I2-SWNTs. By 300° C., a temperature at which 2.8 atomic % of internal I2 still remains in I2-SWNTs, nearly all I2 has been removed from I2-US-tubes. The X-ray induced Auger emission temperature study, also shown in FIG. 18, does provide encouraging results. The same behavior exhibited by I2-SWNTs, the disappearance of the X-ray induced Auger peaks at 507.5 and 519 eV as external I2 is removed and the relative stability of the internal I2 peak at 510 eV, is also demonstrated by I2-US-tubes, albeit at lower temperatures. Thus, in spite of the sidewall defects present in US-tubes, the internal I2 is more stable than external I2, at least with respect to temperature.

While careful heating could provide a method of producing internally-loaded I2@US-tubes, a chemical reduction method that does not remove internal I2 would seem more advantageous, particularly with respect to functionalization of the I2@US-tubes. US-tubes, even more so than full-length SWNTs, are very difficult to suspend in any solvent. Full-length SWNTs can be suspended, as individual tubes, in aqueous solvents via surfactant wrapping and, in both organic and aqueous solvents via Na°/THF reduction, thereby allowing functionalization reactions to take place on individual SWNTs as opposed to bundled SWNTs. US-tubes, in contrast, can not be suspended via surfactant wrapping and, as illustrated above, the Na°/THF reaction can not be used to suspend I2-US-tubes. Therefore, it is imperative that an alternate chemical reduction method be found that does not remove the internal I2 from I2-US-tubes.

Example 17 NaH Reduction of I2-US-Tubes

Fortunately, experimentation with NaH, a reducing agent used as the first step in the Bingel cyclopropanation reaction, suggests that I2 remains in the I2-US-tubes after exposure to NaH for 1 hour. In a typical experiment, 10 mg I2-US-tubes are added to a round bottom flask containing 20 mL toluene in a dry box. Then, 20 mg dimethylsulfoxide, DMSO, and 40 mg NaH are added to the flask and the reaction is allowed to proceed for one hour. After one hour, the reaction is quenched by the careful addition of ethanol. The reduced I2@US-tubes are then isolated by filtration on a glass frit filter, washed with three 10 mL portions of EtOH and dried overnight at 40° C.

Example 18 Raman Spectroscopy of NaH Reduced I2-US-Tubes

Raman analysis reveals that I2 remains after the NaH reduction. Shown in FIG. 23 are comparative Raman spectra for (a) Na°/THF reduced I2-US-tubes, (b) NaH reduced I2@US-tubes, and (c) Na°/THF reduced full-length I2@SWNTs containing only internal I2. The spectrum for the NaH reduced I2@US-tubes exhibits a similar peak at 159 cm−1 as the Na0/THF reduced I2@SWNTs. The Na0/THF reduced I2-US-tubes, in contrast, exhibit no such peak. Thus, Raman spectroscopy indicates that I2, most likely internal I2, survives a 1 hour NaH reduction reaction.

Example 19 Micro CT of Na0/THF Reduced I2-US-Tubes

Micro computed tomography (MicroCT) experiments illustrate the extremely high X-ray attenuation of I2-US-tubes and the low X-ray attenuation of Na0/THF reduced I2-US-tubes which, as a result of the Na0/THF reduction, no longer contain I2. Shown in FIG. 24 are MicroCT images of a) empty US-tubes, b) I2-US-tubes, and c) Na0/THF reduced I2-US-tubes.

Comparing empty US-tubes (FIG. 24a) and empty SWNTs (FIG. 14a); it is apparent that empty SWNTs demonstrate higher X-ray attenuation. This is because iron catalyst particles, which scatter X-rays, are present in raw SWNTs but are removed during the preparation of US-tubes. Thus, US-tubes are very poor at attenuating X-rays and have a radiodensity of only 4366 HU. In stark contrast, I2-US-tubes, which contain 57 mass % iodine by XPS, exhibit extraordinary X-ray attenuation. The radiodensity of I2-US-tubes, again as a solid, is 43,716 HU. Even though this value is actually less than that of I2-SWNTs (FIG. 14b, radiodensity=46,438 HU), I2-US-tubes are likely superior X-ray attenuators due to their greater amount of iodine. In these experiments, the radiodensities of I2-SWNTs and I2-US-tubes are similar only because both attenuate the X-ray beam the maximum that can be measured.

I2-US-tubes which have been reduced by the Na°/THF reaction are shown in FIG. 24c. As expected based on the previous XPS and Raman results, very little X-ray attenuation is demonstrated because all I2 has been removed by the Na°/THF reduction reaction. The radiodensity of the Na°/THF reduced I2-US-tubes is only 4395 HU as opposed to the 28,400 HU obtained for Na°/THF reduced I2-SWNTs (FIG. 16c).

Example 20 Variable-Temperature XPS Study on I2-US-Tubes

An XPS temperature study demonstrates that elevated temperatures also result in the removal of internal I2 from I2-US-tubes. The atomic percent of iodine in I2-US-tubes, as shown in FIG. 251, decreases much more rapidly with respect to temperature as compared to I2-SWNTs. By 300° C., a temperature at which 2.8 atomic % of internal I2 still remains in I2-SWNTs, nearly all I2 has been removed from I2-US-tubes. The X-ray induced Auger emission temperature study, also shown in FIG. 25, does provide encouraging results. The same behavior exhibited by I2-SWNTs, the disappearance of the X-ray induced Auger peaks at 507.5 and 519 eV as external I2 is removed and the relative stability of the internal I2 peak at 510 eV, is also demonstrated by I2-US-tubes, albeit at lower temperatures. Thus, in spite of the sidewall defects present in US-tubes, the internal I2 is more stable than external I2, at least with respect to temperature.

Example 21 NaH Reduction of I2-US-Tubes

Fortunately, experimentation with NaH, a reducing agent used as the first step in the Bingel cyclopropanation reaction, suggests that I2 remains in the I2-US-tubes after exposure to NaH for 1 hour. In a typical experiment, 10 mg I2-US-tubes are added to a round bottom flask containing 20 mL toluene in a dry box. Then, 20 mg dimethylsulfoxide, DMSO, and 40 mg NaH are added to the flask and the reaction is allowed to proceed for one hour. After one hour, the reaction is quenched by the careful addition of ethanol. The reduced I2@US-tubes are then isolated by filtration on a glass frit filter, washed with three 10 mL portions of EtOH and dried overnight at 40° C.

Example 22 Raman Spectroscopy of NaH Reduced I2-US-Tubes

Raman analysis reveals that I2 remains after the NaH reduction. Shown in FIG. 26 are comparative Raman spectra for (a) Na°/THF reduced I2-US-tubes, (b) NaH reduced I2@US-tubes, and (c) Na°/THF reduced full-length I2@SWNTs containing only internal I2. The spectrum for the NaH reduced I2 US-tubes exhibits a similar peak at 159 cm−1 as the Na0/THF reduced I2@SWNTs. The Na°/THF reduced I2-US-tubes, in contrast, exhibit no such peak. Thus, Raman spectroscopy indicates that I2, most likely internal I2, survives a 1 hour NaH reduction reaction.

Example 23 XPS of NaH Reduced I2-US-Tubes

This indication is confirmed by XPS and X-ray induced Auger spectral analysis. XPS analysis verifies that 1.3 atomic % iodine remains in the NaH reduced I2@US-tubes. The position of the I 3d5/2 peak in the XPS spectrum of NaH reduced I2@US-tubes is 619.2±0.2 eV, consistent with all previous measurements (FIG. 27). The X-ray induced Auger emission spectrum of NaH reduced I2@US-tubes contains one peak, at 510 eV, with a visible shoulder at ˜515 eV as shown in FIG. 27. This is consistent with the X-ray induced Auger emission spectrum, shown in FIG. 11, of Na0/THF reduced I2@SWNTs which contain only internal I2; thus, the NaH reduced I2@US-tubes also contain only internal I2. The I 3d5/2 XPS spectrum and X-ray induced Auger emission spectrum of NaH reduced I2@US-tubes are shown in FIG. 23. Unfortunately, unlike I2@SWNTs, which do not lose additional I2 with repeated reduction treatments or extended exposure to the reduction reagent, the internal I2 stability of I2@US-tubes is short-lived. As described above, the NaH reduction reaction is quenched after one hour and, under these conditions, I2 remains. However, if the reaction is allowed to proceed for 24 hours, all I2 is removed. Therefore, given enough time, the internal I2 in I2@US-tubes is accessible to the NaH reduction. This result has important consequences for I2@US-tube sidewall functionalization reactions.

Example 24 I2 Loading Before PEG Functionalization

The first attempt at synthesizing PEG-I2@SWNTs involves first loading US-tubes with I2 followed by sidewall functionalization of the I2-US-tubes with PEG using the reaction scheme shown in FIG. 28. This would be the ideal method of producing PEG-I2@US-tubes because it would unequivocally ensure that any I2 present in the final product is contained within the interior of the US-tube. The first step of this method, the attachment of diethyl malonate, requires the presence of NaH which also removes all external I2. Thus, there would be no risk of I2 interfering with subsequent reactions or reacting with PEG itself Unfortunately, the attachment of the diethyl malonate requires overnight exposure to NaH and, this results in the complete removal of all I2. A one hour reaction, which does leave some internal I2, is insufficient and does not result derivatization with diethyl malonate groups. XPS measurements confirm that no iodine is seen in the final product using this method. To counteract the removal of all I2 by NaH, an alternate method of diethyl malonate attachment can be used, as shown in FIG. 29.

Example 25 I2 Loading Before Alternate PEG Functionalization

This method circumvents the problem of 24 hour exposure of I2@US-tubes to NaH by utilizing an alternate functionalization method. In this method, initial attachment of the diethyl malonate groups is achieved by a reaction with carbon tetrabromide (CBr4) and 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU), a strong organic base, in THF. For this method, US-tubes are again loaded with I2 prior to any functionalization reactions. Unfortunately, as mentioned previously, US-tubes are extremely difficult to suspend in any solvent. In fact, the only known method of suspending US-tubes in THF, or any organic solvent for that matter, is, of course, chemical reduction, which cannot be performed on I2-US-tubes without removal of all I2. Sonication of the I2-US-tubes for 1 hour in several organic solvents, without the presence of a reducing agent, did not result in suspension of the I2-US-tubes, therefore the diethyl malonate reaction could not occur.

This method was also attempted with US-tubes which were first reduced by the Na0/THF reaction prior to I2 loading, but this was also unsuccessful. While empty US-tubes are usually able to be resuspended after the Na0/THF reduction and subsequent drying, US-tubes which were Na0/THF reduced, then loaded with I2 did not resuspended in organic solvents with sonication. It is unclear, but likely, that the I2 loading process resulted in the inability to resuspended the reduced I2-US-tubes. Regardless, these attempts illustrate that I2 is not stable enough within the interior of a US-tube to survive Bingel reaction conditions. Therefore, even though I2 loading after the PEGylation of the US-tubes is not the ideal scenario, the instability of the internal I2 necessitates this approach.

Example 26 I2 Loading After Complete PEG Functionalization

The I2 loading of PEG-US-tubes is not an ideal method for three reasons. First, the PEG groups are bulky and may prevent I2 from entering the SWNT. Second, since I2 loading is the last step in this process, additional washing steps and characterization must be performed to ensure that any I2 present is contained within the SWNT and not adsorbed to the exterior. Finally, experiments must be developed to make certain that I2 does not react with the PEG itself Nevertheless, US-tubes were first functionalized with PEG via the Bingel reactions (FIG. 28). The PEG-US-tubes were then isolated using a glass frit filter and dried overnight. Solid PEG-US-tubes were then subjected to I2 loading conditions as described previously and washed with three 20 mL portions of ethanol to remove excess I2. The first two ethanol washings produced a dark orange and pale yellow color, respectively, indicative of I2. The third ethanol washing did not produce any color, indicating excess I2 removal was complete. However, XPS of the PEG-I2-US-tubes indicated no iodine present. Therefore, it can be concluded that the PEG groups prevent I2 access to the US-tube interior. It can also be deduced that I2 does not react with the hydroxyl groups in PEG, which is important for future experiments involving serinol amide-I2@US-tubes. These three methods demonstrate that I2 loading cannot be either the first or last step in the PEG functionalization process. Therefore, the only logical choice remaining is I2 loading between steps of the Bingel reactions.

Example 27 I2 Loading After Diethyl Malonate Reaction

Since this reaction scheme (FIG. 28) is a three step process and previous attempts have illustrated that I2 loading cannot occur either before the first step or after the last step, only two choices remain; I2 loading after the attachment of diethyl malonate or after conversion of the diethyl malonate to acid chloride. Because taking an acid chloride to dryness is generally a bad idea, only one logical choice remains. Thus the fourth and final attempt to synthesize PEG-I2@US-tubes involves performing the diethyl malonate functionalization on empty US-tubes, followed by I2 loading. After I2 loading, excess I2 is removed by washing with ethanol then the acid chloride and PEGylation reactions are performed.

First, US-tubes are functionalized with diethyl malonate via Reaction 1 in FIG. 28. The resulting product is again isolated using a glass frit filter, dried overnight, then loaded with I2 via sublimation. XPS confirms that these diethyl malonate-US-tubes load with I2, unlike PEG-US-tubes; 5.6 atomic % iodine is present after the loading process. However, after three washings with 20 mL portions of ethanol, 0 atomic % iodine is measured by XPS. It is unclear whether the iodine present after the loading of diethyl malonate-US-tubes is all externally-adsorbed, which would explain its easy removal, or if I2 is contained within the diethyl malonate-US-tubes, but removed by ethanol washing. Regardless, the I2 does not survive the remaining reactions and XPS confirms no iodine remaining in the PEG-US-tubes utilizing this method.

Example 28 I2 loaded US Tubes Substituted with Serinol Groups

I2 loaded US-tubes substituted with serinol groups have been made by performing the serinol functionalization on empty US-tubes as shown by the reaction scheme in FIG. 30. Then the functionalized US-tubes are filled with I2 via sublimation as described above. External I2 is removed by a very short (10 minute) exposure to NaH. XPS and XAES analyses confirm that iodine remains after the reduction, that it is only internal I2, and that the serinol moieties are not affected. The final product contains 1.2 atomic % iodine, or about 10% by weight.

The XPS and XAES spectra (FIGS. 33 and 34) which give the atomic % iodine and prove that it is only internally-loaded I2 due to the disappearance of the XAES peaks at 507.5 eV and 519 eV, which illustrates the removal of external I2. The peak at 510 eV is due to internal I2. The nitrogen % in the XPS data is due to the serinol amide moiety.

Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contain certain errors necessarily resulting from the standard deviation found in their respective testing measurements.

Therefore, the present invention is well adapted to attain the ends and advantages mentioned as well as those that are inherent therein. While numerous changes may be made by those skilled in the art, such changes are encompassed within the spirit of this invention as illustrated, in part, by the appended claims.

Claims

1. An imaging agent comprising a carbon Nanotube and a contrast agent, the contrast agent being disposed within the carbon Nanotube.

2. The imaging agent of claim 1 wherein the carbon Nanotube is an ultra short carbon nanotube.

3. The imaging agent of claim 1 wherein the Nanotube is substituted with serinol groups.

4. The imaging agent of claim 1 further comprising a buckysome, wherein the imaging agent is disposed within the buckysome.

5. The imaging agent of claim 1 wherein the contrast agent is I2 or a molecule having an iodine moiety.

6. A method of preparing ultra short carbon Nanotubes comprising:

providing a plurality of single walled carbon Nanotubes produced by HiPco;
fluorinating the tubes;
purifying the tubes with concentrated HCl; and
cutting the tubes using pyrolysis.

7. A method of loading Nanotubes with contrast agent comprising:

providing ultra short carbon Nanotubes and a contrast agent; and
allowing the contrast agent to sublime thereby loading the ultra short carbon nanotubes.

8. The method of claim 7 wherein the contrast agent is I2.

9. The method of claim 7 further comprising reducing the loaded tubes using NaH.

10. A method for imaging comprising:

providing an imaging agent comprising a carbon Nanotube loaded with contrast agent;
introducing the imaging agent into a cell; and
imaging the cell to detect the presence of the imaging agent.

11. The method of claim 10 wherein the cell is imaged using computed tomography.

12. The method of claim 10 wherein the contrast agent is I2.

13. The method of claim 10 wherein the imaging agent is disposed within a buckysome.

14. The method of claim 10 wherein the carbon Nanotube is a single walled carbon nanotube.

15. The method of claim 10 wherein the carbon Nanotube is an ultra short carbon nanotube.

16. The method of claim 10 wherein the carbon Nanotube is substituted.

17. The method of claim 10 wherein the carbon Nanotube is unsubstituted.

Patent History
Publication number: 20090136987
Type: Application
Filed: Nov 19, 2008
Publication Date: May 28, 2009
Inventors: Lon J. Wilson (Houston, TX), Kyle Ryan Kissell (Manvel, TX), Keith Bennett Hartmann (Houston, TX)
Application Number: 12/274,174
Classifications
Current U.S. Class: Involving Viable Micro-organism (435/29); Fiber, Fabric, Or Textile (423/447.1); Of Radiant Energy (977/954); Carbon Nanotubes (cnts) (977/742)
International Classification: C12Q 1/02 (20060101); D01F 9/12 (20060101);