Patent Application
20160220709
This application claims the benefit of priority of Singapore patent application No. 201306889-5 filed on 12 Sep. 2013, the content of which is incorporated herein by reference in its entirety for all purposes.
The invention relates to photoacoustic contrast agent compositions.
Photoacoustic imaging (PAI) is a non-invasive imaging technique which generally involves flashing a laser at low energy onto a target area or region on a subject's body. The laser at low energy may penetrate deeply into the body to create a large radiated area for more detailed imaging. Rapid absorption of laser energy may expand the tissue through transient thermo-elastic expansion. This expansion creates ultrasonic acoustic waves that may be detected using ultrasound detectors of appropriate sensitivity, such as ultrasound transducers. The transducer readings may be processed and interpreted using mathematical algorithms to create two dimensional or three dimensional images of the target area to depict the tissue structure.
Researches have been carried out in search for suitable contrast agents to assist in generating images using PAI. Examples of contrast agents include organic based contrast agents, such as cyanine dyes, nanoparticles, polyhydroxy-fullerene and carbon nanotubes. However, the photoacoustic contrast that is achieved using the contrast agents may be low, resulting in poor spatial resolution of the images.
In view of the above, there is a need for photoacoustic contrast agents that are able to exhibit improved photoacoustic contrasts.
In a first aspect, a photoacoustic imaging contrast agent composition is provided. The composition comprises a metal carbonyl cluster compound having the general formula (I)
M3(CO)xL12-x (I)
wherein M at each occurrence denotes a metal selected from Group 6 to Group 11 of the Periodic Table of Elements; x is an integer from 10 to 12; and each L is independently selected from the group consisting of —H and -A-(CH2)n—COO−Y+, wherein A is selected from the group consisting of S, O, C and N; n is an integer from 1 to 10; and Y is any cation.
In a second aspect, use of a photoacoustic imaging contrast agent composition according to the first aspect in photoacoustic imaging is provided.
The invention will be better understood with reference to the detailed description when considered in conjunction with the non-limiting examples and the accompanying drawings, in which:
Photoacoustic imaging is based on the mechanism that electromagnetic waveforms, such as radio frequency (rf) or optical waves, may be absorbed by a material, to result in local heating and thermoelastic expansion. The thermoelastic expansion may, in turn, produce megahertz ultrasonic waves in the material, thereby generating a photoacoustic signal. Accordingly, the term “photoacoustic imaging” as used herein refers to signal generation caused by an electromagnetic pulse, with absorption and expansion of a photoacoustic imaging contrast agent, followed by acoustic detection, where the photoacoustic imaging contrast agent absorbs the light energy and converts it to thermal energy that generates the photoacoustic signal.
The invention refers in a first aspect to a photoacoustic imaging contrast agent composition comprising a metal carbonyl cluster compound. Advantageously, the metal carbonyl cluster compound offers multiple sites for attachment of various ligands as property modifiers. Further, by conjugation to a myriad of bioactive agents such as proteins, antibodies, and drugs, molecular imaging and therapeutic monitoring may be carried out.
As used herein, the term “metal carbonyl cluster” refers to metal cluster compounds comprising carbon monoxide in complex combination with metal atoms, wherein the metal atoms in the metal carbonyl cluster are held together entirely or at least substantially by bonds between metal atoms.
The metal carbonyl cluster compound has general formula (I)
M3(CO)xL12-x (I),
wherein M at each occurrence denotes a metal selected from Group 6 to Group 11 of the Periodic Table of Elements; x is an integer from 10 to 12; and each L is independently selected from the group consisting of —H and -A-(CH2)n—COO−Y+, wherein A is selected from the group consisting of S, O, C and N; n is an integer from 1 to 10; and Y is any cation. CO in formula (I) denotes a carbonyl ligand.
M at each occurrence denotes a metal selected from Group 6 to Group 11 of the Periodic Table of Elements. In various embodiments, M is independently selected from the group consisting of chromium (Cr), molybdenum (Mo), tungsten (W), manganese (Mn), technetium (Tc), rhenium (Re), iron (Fe), ruthenium (Ru), osmium (Os), cobalt (Co), rhodium (Rh), iridium (Ir), nickel (Ni), palladium (Pd), platinum (Pt), copper (Cu), silver (Ag), and gold (Au). In specific embodiments, M is independently selected from the group consisting of Fe, Ru, and Os. In one embodiment, M is Os.
The metal carbonyl cluster compound may comprise more than one metal. For example, M in the general formula M3(CO)xL12-x mentioned above may be represented by (Ma)2Mb, Ma(Mb)2, (Mb)2Mc, Mb(Mc)2, (Ma)2Mc, Ma(Mc)2, or MaMbMc, where Ma, Mb and Mc denote different metals. In such embodiments, the metal carbonyl compound may have general formula MaMbMc(CO)xL12-x, wherein Ma, Mb, and Mc denote different metals, and CO, L, and x having the same definitions as that mentioned above.
In general formula (I), x is an integer from 10 to 12, such as 10, 11, or 12. In various embodiments, x is 10.
The metal carbonyl cluster compound may contain one or more different ligands besides carbonyl ligands, as represented by L in general formula (I). Each L is independently selected from the group consisting of —H and -A-(CH2)—COO−Y+, wherein A is selected from the group consisting of S, O, C and N; n is an integer from 1 to 10; and Y is any cation.
In various embodiments, A is S.
In various embodiments, n is an integer from 1 to 6, such as 1, 2, 3, 4, 5, or 6. In specific embodiments, n is 2.
In various embodiments, Y is selected from the group consisting of an alkali metal and NH4. For example, Y may be lithium (Li), sodium (Na), potassium (K), rubidium (Rb), cesium (Cs), or NH4. In some embodiments, Y is selected from the group consisting of Na and K. In specific embodiments, Y is Na.
In specific embodiments, the metal carbonyl cluster compound is Os3(CO)10(μ-H)μ-S(CH2)2COO−Na+. In the formula, the symbol “μ” is used to denote a bridging atom. Hence, in the compound Os3(CO)10(μ-H)μ-S(CH2)2COO−Na+, H and S are bridging atoms.
The metal carbonyl cluster compound may be conjugated or attached to a bioactive agent. As used herein, the term “bioactive agent” is defined as those organic molecules having an effect in a biological system, whether such system is in vitro, in vivo, or in situ. Biologically active molecules may include, but are not limited to growth factors, cytokines, antiseptics, antibiotics, anti-inflammatory agents, analgesics, anesthetics, chemotherapeutic agents, clotting agents, metabolites, chemoattractants, hormones, steroids, and other drugs, or cell attachment molecules.
In various embodiments, the bioactive agent is a protein, an antibody, an antibody fragment, an antibody like molecules, or a drug.
For instance, the bioactive agent may be a proteinaceous molecule, such as an antibody, for example a monoclonal or polyclonal antibody, which immunologically binds to a target analyte at a specific determinant or epitope. The term “antibody” is used in the broadest sense and specifically covers monoclonal antibodies as well as antibody variants, fragments or antibody like molecules, such as for example, Fab, F(ab′)2, scFv, Fv diabodies and linear antibodies, so long as they exhibit the desired binding activity.
In some embodiments, the bioactive agent is a monoclonal antibody. The term “monoclonal antibody” as used herein refers to an antibody obtained from a population of substantially homogeneous antibodies, i.e., the individual antibodies comprising the population are identical except for possible naturally occurring mutations that may be present in minor amounts. Monoclonal antibodies are highly specific, being directed against a single antigenic site. Furthermore, in contrast to conventional (polyclonal) antibody preparations which typically include different antibodies directed against different determinants (epitopes), each monoclonal antibody is directed against a single determinant on the antigen. In addition to their specificity, the monoclonal antibodies are advantageous in that they may be synthesized by the hybridoma culture, uncontaminated by other immunoglobulins. The modifier “monoclonal” indicates the character of the antibody as being obtained from a substantially homogeneous population of antibodies, and is not to be construed as requiring production of the antibody by any particular method. The monoclonal antibodies may include “chimeric” antibodies and humanized antibodies. A “chimeric” antibody is a molecule in which different portions are derived from different animal species, such as those having a variable region derived from a murine mAb and a human immunoglobulin constant region.
In some embodiments, the bioactive molecule is a polyclonal antibody. “Polyclonal antibodies” refer to heterogeneous populations of antibody molecules derived from the sera of animals immunized with an antigen, or an antigenic functional derivative thereof. For the production of polyclonal antibodies, host animals such as rabbits, mice and goats, may be immunized by injection with an antigen or hapten-carrier conjugate optionally supplemented with adjuvants.
“Peptide” generally refers to a short chain of amino acids linked by peptide bonds. Typically peptides comprise amino acid chains of about 2-100, more typically about 4-50, and most commonly about 6-20 amino acids. “Polypeptide” generally refers to individual straight or branched chain sequences of amino acids that are typically longer than peptides. “Polypeptides” usually comprise at least about 20 to 1000 amino acids in length, more typically at least about 100 to 600 amino acids, and frequently at least about 200 to about 500 amino acids. Included are homo-polymers of one specific amino acid, such as for example, poly-lysine. “Proteins” include single polypeptides as well as complexes of multiple polypeptide chains, which may be the same or different.
Multiple chains in a protein may be characterized by secondary, tertiary and quaternary structure as well as the primary amino acid sequence structure, may be held together, for example, by disulfide bonds, and may include post-synthetic modifications such as, without limitation, glycosylation, phosphorylation, truncations or other processing.
Antibodies such as IgG proteins, for example, are typically comprised of four polypeptide chains (i.e., two heavy and two light chains) that are held together by disulfide bonds. Furthermore, proteins may include additional components such associated metals (e. g., iron, copper and sulfur), or other moieties. The definitions of peptides, polypeptides and proteins includes, without limitation, biologically active and inactive forms; denatured and native forms; as well as variant, modified, truncated, hybrid, and chimeric forms thereof.
In the context of the invention, the term “drug” generally means a therapeutic or pharmaceutical agent which may be included/mixed into the photoacoustic imaging contrast agent composition, or conjugated or attached to the metal carbonyl cluster compound comprised in the photoacoustic imaging contrast agent composition.
Examples of a drug include, but are not limited to: antiproliferative/antimitotic agents including natural products such as vinca alkaloids (e.g. vinblastine, vincristine, and vinorelbine), paclitaxel, epidipodophyllotoxins (e.g. etoposide, teniposide), antibiotics (dactinomycin (actinomycin D) daunorubicin, doxorubicin and idarubicin), anthracyclines, mitoxantrone, bleomycins, plicamycin (mithramycin) and mitomycin, enzymes (L-asparaginase which systemically metabolizes L-asparagine and deprives cells which do not have the capacity to synthesize their own asparagine); antiproliferative/antimitotic alkylating agents such as nitrogen mustards (such as mechlorethamine, cyclophosphamide and analogs, melphalan, chlorambucil), ethylenimines and methylmelamines (hexamethylmelamine and thiotepa), alkyl sulfonates-busulfan, nirosoureas (carmustine (BCNU) and analogs, streptozocin), trazenes-dacarbazinine (DTIC); antiproliferative/antimitotic antimetabolites such as folic acid analogs (methotrexate), pyrimidine analogs (fluorouracil, floxuridine, and cytarabine), purine analogs and related inhibitors (mercaptopurine, thioguanine, pentostatin and 2-chlorodeoxyadenosine (cladribine)); platinum coordination complexes (cisplatin, carboplatin), procarbazine, hydroxyurea, mitotane, amino glutethimide; hormones (e.g. estrogen); anticoagulants (heparin, synthetic heparin salts and other inhibitors of thrombin); fibrinolytic agents (such as tissue plasminogen activator, streptokinase and urokinase); antiplatelet (such as aspirin, dipyridamole, ticlopidine, clopidogrel, abciximab); antimigratory; antisecretory (such as breveldin); antiinflammatory: such as adrenocortical steroids (Cortisol, cortisone, fludrocortisone, prednisone, prednisolone, 6-alpha-methylprednisolone, triamcinolone, betamethasone, and dexamethasone), non-steroidal agents (such as salicylic acid derivatives e.g. aspirin); para-aminophenol derivatives (e.g. acetaminophen); indole and indene acetic acids (such as indomethacin, sulindac, and etodalac), heteroaryl acetic acids (such as tolmetin, diclofenac, and ketorolac), arylpropionic acids (such as ibuprofen and derivatives), anthranilic acids (such as mefenamic acid, and meclofenamic acid), enolic acids (such as piroxicam, tenoxicam, phenylbutazone, and oxyphenthatrazone), nabumetone, gold compounds (such as auranofin, aurothioglucose, gold sodium thiomalate); immunosuppressive (such as cyclosporine, tacrolimus (FK-506), sirolimus (rapamycin), azathioprine, mycophenolate mofetil); angiogenic such as vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF); nitric oxide donors; anti-sense oligo nucleotides and combinations thereof.
The invention refers in a second aspect to use of a photoacoustic imaging contrast agent composition according to the first aspect in photoacoustic imaging.
Radio frequency and optical waves are used in photoacoustic imaging because of their desirable physical properties, such as deeper tissue penetration and better absorption by contrast agents. Advantageously, it is able to provide higher spatial resolutions with high intrinsic contrasts, as compared to most optical imaging techniques. As different biological tissues exhibit different absorption coefficients, by applying photoacoustic imaging on biological samples, measuring the acoustic signals generated with ultrasonic transducers allows rebuilding of the distribution of optical energy deposition, and ultimately to obtain images of the biological tissues.
The photoacoustic imaging may be a laser-based photoacoustic imaging. The photoacoustic imaging may be carried out at a wavelength in the range of about 400 nm to about 900 nm, which correspond to the visible range (400 nm to 750 nm) and near infrared region of the spectrum (750 nm to 900 nm). In various embodiments, the photoacoustic imaging is carried out at a wavelength in the visible range. In specific embodiments, the photoacoustic imaging is carried out at a wavelength of about 410 nm.
In various embodiments, the photoacoustic imaging is photoacoustic microscopy. For example, the photoacoustic microscopy may include laser pulse generation, delivery of the laser pulse to a subject under study, reception of photoacoustic signal generated from the subject, image reconstruction, and display of the image. Exemplary illustrations of how photoacoustic microscopy may be carried out are provided in the examples disclosed herein.
Hereinafter, the present invention will be described more fully with reference to the accompanying drawings, in which exemplary embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the exemplary embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. In the drawings, lengths and sizes of layers and regions may be exaggerated for clarity.
As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof.
The invention illustratively described herein may suitably be practiced in the absence of any element or elements, limitation or limitations, not specifically disclosed herein. Thus, for example, the terms “comprising”, “including”, “containing”, etc. shall be read expansively and without limitation. Additionally, the terms and expressions employed herein have been used as terms of description and not of limitation, and there is no intention in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments and optional features, modification and variation of the inventions embodied therein herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention.
The invention has been described broadly and generically herein. Each of the narrower species and subgeneric groupings falling within the generic disclosure also form part of the invention. This includes the generic description of the invention with a proviso or negative limitation removing any subject matter from the genus, regardless of whether or not the excised material is specifically recited herein.
Other embodiments are within the following claims and non-limiting examples. In addition, where features or aspects of the invention are described in terms of Markush groups, those skilled in the art will recognize that the invention is also thereby described in terms of any individual member or subgroup of members of the Markush group.
In this study, feasibility of osmium carbonyl clusters as a reliable PA contrast agent was explored and its performance in imaging the PA signal changes of the contrast agent at the superior sagittal sinus (SSS) in anaesthetized rat brain was demonstrated. Advantageously, osmium carbonyl clusters are oxygen-stable and moisture-stable. Further, they are suitable for biomedical imaging, and some of their derivatives have potential to interact with various biomolecules.
All manipulations for chemical synthesis were carried out using standard Schlenk techniques under an argon or nitrogen atmosphere. Os3(CO)12 was purchased from Oxkem; all other chemicals were purchased from other commercial sources and used as supplied. IR spectra were obtained using a Bruker Alpha Fourier transform infrared spectrometer. NMR spectra were recorded in CDCl3 on a JEOL ECA400 or ECA400SL spectrometer and were referenced to residual solvent resonances.
Os3(CO)10(NCCH3)2 (200 mg, 0.22 mmol) was stirred with thioglycolic acid (48 mg, 0.22 mmol) in dichloromethane (30 ml) at room temperature for 12 h. After the reaction, the solvent was removed in vacuo and the residue purified by column chromatography using hexane/DCM as the eluant to yield a yellow solid. Yield: 57%.
IR (CH2Cl2): νCO 2106 (w), 2066 (s), 2057(s), 2020 (s), 1997 (w).
1H NMR (CDCl3): δ 2.58-2.69 (m, 4H, CH2CH2), −17.40 (s, 1H, OsHOs)
To Os3(CO)10(μ-H)μ-S(CH2)2COOH (100 mg, 0.09 mmol) in methanol (20 ml) was added sodium carbonate (18.7 mg, 0.19 mmol). The mixture was refluxed for 1 h, cooled to room temperature, and the excess sodium carbonate filtered off. The solvent was removed under reduced pressure to afford 2 as a water-soluble, yellow solid. Yield: 95%.
IR (KBr): νCO 2110 (w), 2061 (s), 2009 (s), 1928 (w).
1H NMR (300 MHz, D2O): δ 2.47-2.69 (m, 4H, CH2CH2), −17.11 (s, 1H, OsHOs) ESI (m/z): 957.1 [M−]
The 50-MHz dark-field confocal fPAM system used and the experimental set-up for in vivo imaging, is depicted below.
The microscopy system consists of laser pulse generation and delivery, PA signal reception, and image reconstruction and display. Laser pulses, 4 ns wide, were generated at a frequency of 10 Hz by using an optical parametric oscillator (Surlite OPO Plus, Continuum, USA). The laser was pumped by a frequency-tripled Nd:YAG Q-switched laser (Surlite II-10, Continuum, USA). The incident wavelength was set at 410 nm. The custom-made 50-MHz ultrasonic transducer (Acoustic Sensor, Taiwan) has a −6 dB fractional bandwidth of 57.5%, focal length of 9 mm, and a 6 mm active element, offering an axial resolution of 32 μm and a lateral resolution of 61 μm.
Laser energy was delivered using a 1-mm multimodal fiber. The fiber tip was coaxially aligned with a convex lens, an axicon, a plexiglass mirror, and an ultrasonic transducer on an optical bench, forming dark-field illumination that was confocal with the focal point of the ultrasonic transducer. The incident energy density on the sample surface was well within American National Standards Institute (ANSI) safety limits. The transducer was immersed in an acrylic water tank during the imaging process, and the hole at the bottom of the tank was sealed with a piece of 15-van thick polyethylene film. A thin layer of ultrasonic gel was applied as a PA conductive medium, which was then attached to the thin polyethylene film to ensure reliable coupling of the PA waves with the water tank. The PA signals received by the ultrasonic transducer were pre-amplified by a low-noise amplifier (noise
Fluctuations in the laser energy were monitored with a photodiode (DET36A/M, Thorlabs, USA). The recorded photodiode signals were measured prior to the experiment to compensate for PA signal variations caused by laser-energy instability. The achievable penetration depth of the current PA microscopy system was 3 mm with approximately 18-dB SNR, where SNR is defined as the ratio of the signal peak value to the root-mean-square value of the noise. Three scan types can be provided by this system: A-line (i.e., one-dimensional images where the axis represents the imaging depth), B-scan (i.e., two-dimensional images where one axis is the lateral scanning distance and the other is the imaging depth), and C-scan (i.e., projection images from the three-dimensional images). The amplitude of the envelope-detected PA signals was used in the subsequent functional imaging analysis.
For both in vivo and in vitro imaging, the laser was pulsed with a pulse repetition rate of 10 Hz and coupled by a lens to an optical fiber to illuminate the ROI. A window at the bottom of the water container was sealed with an optically and ultrasonically transparent, disposable polyethylene film. After a commercially available ultrasound gel was applied to the brain for acoustic coupling, the brain was placed between the water container and the custom-made stereotaxic apparatus for imaging.
The trinuclear carbonyl clusters of the group 8 metals, viz., M3(CO)12 (1, M=Fe (a), Ru (b) or Os(c)) are all readily available and variedly coloured.
Consistent with their electronic spectra, 1c exhibited the highest PA signal among the three carbonyl clusters (
All the PA images in this study were acquired at 410 nm without any need for signal averaging, and yet the contrast quality of the PA images is high.
The compounds 1 a-c were dissolved in a water/ethanol (60:40, v/v) mixture. The compound 1c, however, has low water solubility. The water-soluble cluster [Os3(CO)10(μ-H)(μ-S(CH2)2COO)]−Na+(2) was thus synthesized, and its cytoxicity was evaluated. An MTS cytotoxicity assay shows that 2 poses little effect on the viability of cells (
Cortical vasculature of the rat was in vivo imaged at 32×61 μm resolution, with a designed 50-MHz dark-field confocal PA microscopy system (
Some of the optical techniques can monitor intrinsic changes of SSS based on detection of light diffusively scattered from a target tissue, like Near-infrared spectroscopy (NIRS). However, NIRS measures only volume-averaged of brain tissue and cannot distinguish between venous, capillary, and arterial blood. In contrast, PA imaging can see venous, capillary, and arterial blood. However, it was found that the SSS was not satisfactorily visualized in the projected PA C-scan image. Although the SSS could be seen in the PA B-scan images, the detected PA signals from the SSS were weaker than those from other cortical vessels. This weaker SSS signals may result from the frequency of the PA signals generated by the SSS may be out of the detection bandwidth of the transducer. Moreover, sensing with spherical geometric focusing inherently prefers point-like PA sources, which is not the case of for the large sized SSS, thus weakening the detection of PA signals from the SSS. That is, probing the changes of SSS via the designed contrast agents provide a novel insight for optical imaging technique to study the SSS related neuroscience issues. Compared to the brain PA B-scan image obtained from the intrinsic optical contrast, the image acquired 20 min after the administration of a solution of 2 showed the brain vasculature with greater clarity, especially the SSS (
Five thousand oral squamous cell carcinoma (OSCC) cells were seeded in a 96-well plate for 24 h before a solution of 2 in DMEM (1 mL) with the indicated concentrations (0.01-30 μM) was introduced into each well. After incubation for 24 h, 10 μL of CCK8 (cell counting kit-8, Sigma-Aldrich) was added to each well. Cell absorbance was measured with a SpectraMax 384 Plus spectral analyser after 4 h, with 450 nm excitation.
A polyethylene tubing (about 20 cm in length) was filled with the sample solution and then positioned at the focus of the transducer, i.e. at a depth of 9 mm with respect to the transducer in the water tank. The system was maintained in a 25° C. water bath throughout the experiment. Imaging was carried out with the PA microscopy system at 32×61-μm resolution, with a scanning step size of 20 μm for each B-scan.
Six male Wistar rats (NUS-CARE, Singapore), weighing 250-300 grams, were used. Animal experiments were conducted in accordance with guidelines from Institutional Animal Care and Use Committee (IACUC) at the National University of Singapore. The rats were fasted for 24 h prior to the imaging experiments, but were given water ad libitum. They were anesthetized with isoflurane (2 to 3% in 100% O2), mounted in a dorsal position over a custom-made acrylic stereotaxic holder, and the skin and muscle on the skull were removed to expose the bregma landmark. The anteroposterior (AP) distance between the bregma and the interaural line was directly surveyed. The bregma was 9.3±0.12 mm (mean±standard deviation [SD]) anterior to the interaural line.
A craniotomy was also performed for each animal, and a bilateral cranial window of approximately 6 (horizontal)×4 (vertical) mm size was made with a high-speed drill. After the rat was secured to the stereotaxic frame and placed on the bed pallet, the pallet was moved to position at the bregma, which was 9 mm anterior to an imaginary line drawn between the centers of each ear bar (the interaural line). The interaural and bregma references were then used to position the heads in the PAM system. After bregma positioning, a PA C-scan (projection image from the three-dimensional images) was performed to acquire reference images of the cortical vasculature, at λ410. 200 μL of 2 at 30 μM was administered via retro-orbital injection prior to imaging.
We have shown in this study that organometallic carbonyl cluster compounds may be safe contrast agents for use in laser-based photoacoustic imaging. As demonstrated herein, a water-soluble osmium carbonyl cluster was used for the in vivo imaging of the rat cerebral vasculature, with high spatial resolution and satisfactory sensitivity. Use of an exogenous contrast agent may potentially provide a method to monitor intra- or extravascular blood flow in biological tissues. This is important for an accurate assessment of acute ischaemic stroke, lesion development, thermal injury, neovascularization, tumor angiogenesis, tumor necrosis, hepatic function and regional blood flow response. Choice of the osmium carbonyl clusters rests primarily because on their well-studied chemistry, and also on the fact that they offer multiple sites for attachment of various ligands as property modifiers. Through conjugation to bioactive materials such as proteins, antibodies, and drugs, molecular imaging and therapeutic monitoring may also be carried out.
While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present invention as defined by the following claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201306889-5 | Sep 2013 | SG | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/SG2014/000423 | 9/9/2014 | WO | 00 |
