[Retracted] The Copper Radioisotopes: A Systematic Review with Special Interest to <sup>64</sup>Cu

Niccoli Asabella, Artor; Cascini, Giuseppe Lucio; Altini, Corinna; Paparella, Domenico; Notaristefano, Antonio; Rubini, Giuseppe

doi:https://doi.org/10.1155/2014/786463

BioMed Research International

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Radiopharmaceuticals in Nuclear Medicine: Recent Developments for SPECT and PET Studies

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Volume 2014 | Article ID 786463 | https://doi.org/10.1155/2014/786463

[Retracted] The Copper Radioisotopes: A Systematic Review with Special Interest to ⁶⁴Cu

Artor Niccoli Asabella,¹Giuseppe Lucio Cascini,²Corinna Altini,¹Domenico Paparella,¹Antonio Notaristefano,¹and Giuseppe Rubini¹

Academic Editor: Gianluca Valentini

Received23 Dec 2013

Accepted18 Apr 2014

Published07 May 2014

Abstract

Copper (Cu) is an important trace element in humans; it plays a role as a cofactor for numerous enzymes and other proteins crucial for respiration, iron transport, metabolism, cell growth, and hemostasis. Natural copper comprises two stable isotopes, ⁶³Cu and ⁶⁵Cu, and 5 principal radioisotopes for molecular imaging applications (⁶⁰Cu, ⁶¹Cu, ⁶²Cu, and ⁶⁴Cu) and in vivo targeted radiation therapy (⁶⁴Cu and ⁶⁷Cu). The two potential ways to produce Cu radioisotopes concern the use of the cyclotron or the reactor. A noncopper target is used to produce noncarrier-added Cu thanks to a chemical separation from the target material using ion exchange chromatography achieving a high amount of radioactivity with the lowest possible amount of nonradioactive isotopes. In recent years, Cu isotopes have been linked to antibodies, proteins, peptides, and nanoparticles for preclinical and clinical research; pathological conditions that influence Cu metabolism such as Menkes syndrome, Wilson disease, inflammation, tumor growth, metastasis, angiogenesis, and drug resistance have been studied. We aim to discuss all Cu radioisotopes application focusing on ⁶⁴Cu and in particular its form ⁶⁴CuCl₂ that seems to be the most promising for its half-life, radiation emissions, and stability with chelators, allowing several applications in oncological and nononcological fields.

1. Introduction

Copper (Cu) is a transition metal with atomic number 29, known since ancient times. It is an important trace element for most organisms in all kingdoms. In humans, copper plays a role as a cofactor for numerous enzymes, such as Cu/Zn-superoxide dismutase, cytochrome c oxidase, tyrosinase, ceruloplasmin, and other proteins, crucial for respiration, iron transport and metabolism, cell growth, and hemostasis [1, 2].

In the last decades, the scientific knowledge and the technological development permitted to overcome the limit of the morphological imaging and to move in the way of biometabolic imaging. This new approach creates further opportunities for clinical research, diseases diagnosis, and treatment. It allows physicians to generate high-resolution images of the human body noninvasively, diagnose illness, and choose treatment regimens based upon them [3].

New radioisotopes in Nuclear Medicine can be used in their simple form or bound with carrier molecules for the production of complex radiopharmaceutical, creating new opportunities for different metabolic imaging of several organs and systems.

For widespread use in medicine of any radioisotope, two factors are essential: availability of the isotope and a stable and effective mode of binding with an appropriate chemical carrier [4].

Selection of the proper radionuclide in radiopharmaceutical design is critical and depends upon several factors. The half-life of the radionuclide should allow sufficient uptake and distribution to yield considerable contrast and quality images. The energies of the radionuclide emission should be appropriate for proper detection by the equipment, while cost and availability are also important considerations [3].

With the progress in medical sciences, copper has gained a lot of attention.

Natural copper comprises two stable isotopes, ⁶³Cu (69.17%) and ⁶⁵Cu (30.83%), and 27 known radioisotopes, five of them are particularly interesting for molecular imaging applications (⁶⁰Cu, ⁶¹Cu, ⁶²Cu, and ⁶⁴Cu), and in vivo targeted radiation therapy (⁶⁴Cu and ⁶⁷Cu) [4].

Copper radionuclides offer a varying range of half-lives and decay modes [3].

2. Production of Cu Radioisotopes

One of the major challenges is the production of radionuclides with high specific activity, that is, a high amount of radioactivity with the lowest possible amount of nonradioactive isotopes.

Preparing high specific activity Cu radionuclides is an even bigger challenge, since Cu is ubiquitous in the environment. For all of the Cu isotopes, a noncopper target is used to produce noncarrier-added Cu. In using a target, having a different atomic number, a chemical separation of the copper radionuclide from the target material is possible. In addition, the experimental conditions for preparing the target and separating the copper radionuclides from it must be as metal-free as possible [3].

The following fundamental step is the extraction of each Cu radioisotope from the target, performed using ion exchange chromatography [5].

The two potential ways to produce Cu radioisotopes concern the use of the cyclotron or the reactor. At the state of the art, the cyclotron production is the most studied.

The main characteristics of the Cu radioisotopes of medical interest and their most common ways of production are reported on Table 1.

2.1. ⁶⁰Cu

⁶⁰Cu is a emitter with decay properties making it possible candidate tracer for positron emission tomography (PET), even it has the disadvantage of emissions [4]. ⁶⁰Cu is a proton-rich nuclide that decays to its stable Ni isotopes through a combination of positron decay and electron capture processes. It can be produced on a medical cyclotron at relatively low costs using proton or deuteron induced reactions on enriched ⁶⁰Ni targets [5, 6]. Other ways of production have been recently developed (e.g. + ³He, + a) [7, 8].

2.2. ⁶¹Cu

⁶¹Cu isotope can be produced from zinc, nickel, or cobalt targets on a medical cyclotron using proton or deuteron or alpha particles induced reactions. Necessity of highly enriched Ni and Zn targets or high-energy particle beams limited accessibility of ⁶¹Cu for biomedical use, until more economic production methods from natural Zn or Co will be developed [9, 10]. Half-life longer than that of ⁶⁰Cu and ⁶²Cu makes ⁶¹Cu better choice for prolonged imaging of processes with slower kinetics. This isotope, however, is much less popular in today’s biomedical studies than other copper radioisotopes [4, 8, 11–14].

2.3. ⁶²Cu

⁶²Cu has unique properties being almost pure emitter (98%) with short half-life of 9.7 min. ⁶²Cu is a proton-rich nuclide that decays to its stable Ni isotope through a combination of positron decay and electron capture processes. It can be produced on a medical cyclotron using proton or deuteron induced reactions on enriched ⁶²Ni targets. ⁶²Cu can also be produced indirectly through its parent ⁶²Zn in a ⁶²Zn/⁶²Cu generator system. This is the preferred option, reducing the levels of radioactivity that need to be manipulated and allowing ⁶²Cu to be eluted as required [5].

Current ⁶²Zn/⁶²Cu generators can start with ⁶²Zn activities of 5-6 GBq, 93% of this activity being released as ⁶²Cu in the first 3.2 mL of eluate; however relatively short half-life of parent ⁶²Zn makes these generators operable for not more than three days.

Currently the proton induced reactions on natural copper is the method of choice for the production of the mother nuclide ⁶²Zn. Recently, ⁶²Cu production was also investigated via + p reactions [15, 16].

This isotope is currently the most intensively studied copper radioisotope besides ⁶⁴Cu [4].

2.4. ⁶⁴Cu

⁶⁴Cu is a highly unusual isotope because it decays by three processes, namely, positron, electron capture, and beta decays. This property allows either cyclotron or reactor production, with the latter route resulting in either low specific activity (n,) or high specific activity (n,p) products [5].

At present, the most common production method for ⁶⁴Cu utilizes the ⁶⁴Ni(p,n)⁶⁴Cu reaction [17, 18].

The production of noncarrier-added ⁶⁴Cu via the ⁶⁴Ni(p,n)⁶⁴Cu reaction on a biomedical cyclotron was proposed by Szelecsenyi et al. Subsequent studies by McCarthy et al. were performed, and this method is now used to provide ⁶⁴Cu to researchers throughout the United States [17, 19].

The target for producing ⁶⁴Cu is enriched ⁶⁴Ni (99.6%). The ⁶⁴Ni (typically 10–50 mg) is prepared and electroplated onto a gold disk using a procedure modified from Piel et al. [20].

The target is bombarded on the cyclotron. Recently, Obata et al. reported the production of ⁶⁴Cu on a 12 MeV cyclotron, which is more representative of the modern cyclotrons currently in operation [21].

After bombardment, the ⁶⁴Cu is separated from the target nickel in a one-step procedure using an ion exchange column. Typically, 18.5 GBq of ⁶⁴Cu are produced with a 40 mg ⁶⁴Ni target and a bombardment time of 4 h. The specific activity of the ⁶⁴Cu ranges from 47.4 to 474 GBq/μmol (1280 to 12,800 mCi/μmol). The typical yields for ⁶⁴Cu productions are 0.2 mCi/μA·h per mg ⁶⁴Ni. The enriched ⁶⁴Ni can be 85–95% recovered as previously described and reused for future bombardments, which contributes to the cost-efficiency of this method of ⁶⁴Cu production [3].

Another method of ⁶⁴Cu production is the ⁶⁴Zn(n,p)⁶⁴Cu reaction in a nuclear reactor [22, 23].

Most reactor-produced radionuclides are produced using thermal neutron reactions, or (n,) reactions, where the thermal neutron is of relatively low energy, and the target material is of the same element as the product radionuclide.

For producing high specific activity ⁶⁴Cu, fast neutrons are used to bombard the target in a (n,p) reaction [22–26].

Unfortunately, one of the byproducts of producing ⁶⁴Cu with a natural Zn target was ⁶⁵Zn ( d), which limits the practicality of production by this method [27].

Smith et al. separated large amounts of ⁶⁴Cu by product from cyclotron production of ⁶⁷Ga via the ⁶⁸Zn(p,2n)⁶⁷Ga reaction at the National Medical Cyclotron, Sydney, Australia [28]. This method of production has the advantage of being very economical and allows for the production of very large amounts (>111 GBq (>3 Ci)) of reasonably high specific activity material (~31.8 TBq/mmol (~860 Ci/mmol)). The disadvantage is that on-demand production would be problematic, since the major radionuclide produced is long-lived ⁶⁷Ga ( h).

The production of ⁶⁷Ga, which has identical gamma energies to ⁶⁷Cu, makes activity measurements prior to separation difficult. In addition, isotopes of nickel, cobalt, manganese, and chromium have been observed that while being relatively easy to separate add complexity to the required separation scheme [5].

Although the proton induced reaction on enriched ⁶⁴Ni plays a key role for practical production, recently the deuteron induced reactions are also intensively studied and seem to be very promising [29].

2.5. ⁶⁷Cu

This isotope of copper, owning to interesting decay properties, is potentially useful for radioimmunotherapy, but due to limited availability, researches that actually use this isotope are few, compared to other Cu isotopes [30, 31].

Dynamic growth of radioimmunotherapy can increase demand for this isotope. Medvedev et al. reported an attempt to produce ⁶⁷Cu in a larger scale, which gives perspectives for wider commercial availability of the isotope in the near future [32].

⁶⁷Cu is the longest living copper radioisotope and also one of the most difficult to produce, since it requires fast neutron flux reactor or high-energy proton beams and costly ⁶⁸Zn target [33]. Therapeutic amounts of ⁶⁷Cu can be produced via several reactions on Zn. The production by the reaction ⁶⁸Zn(p,2p)⁶⁷Cu is the largest contributor of ⁶⁷Cu in North America. Providing a reliable supply of ⁶⁷Cu by this method requires dedicated proton beam and chemistry station that are rarely possible at one of these multipurpose facilities [34, 35].

The ⁶⁸Zn(p,2p)⁶⁷Cu reaction requires increasing proton energy, from 20 to 70 MeV, according to Stoll et al. (which includes data from two other studies) [36].

Due to the nature of the spallation process, there will always be a variety of products in the target and enriched targets are seldom used except to determine the reaction cross section. Targets are mainly zinc metal foils which allow for greater heat dissipation and have a higher density than zinc oxide [34, 36].

A small subset of the literature involves the use of a low energy proton beam, 20 MeV, driving a reaction on ⁷⁰Zn(p,a)⁶⁷Cu. The presence of ⁶⁷Ga complicates gamma counting of the sample until after a radiochemical separation. Large amounts of ⁶⁵Zn are also expected to accumulate in any recycled target due to its 244-day half-life. A demonstration with a larger target mass will determine if this method of production is comparable to other techniques. In contrast to other production methods, the ⁷⁰Zn(p,a)⁶⁷Cu reaction does not coproduce large amounts of other radioisotopes due to the low energy protons used [34, 37].

The production of ⁶⁷Cu in a nuclear reactor by the reaction ⁶⁷Zn(n,p)⁶⁷Cu has been pursued in part due to its simplicity. One only needs to place a suitably contained zinc target in a commercial or research reactor to produce a usable amount of ⁶⁷Cu. However, access to reactors, waste concerns, and undesirable side reactions complicate the use of this reaction for extended productions and medical applications. In the literature the production of ⁶⁷Cu by the reaction ⁶⁸Zn(,p)⁶⁷Cu is also reported. Linear accelerators producing 30–60 MeV electrons were focused on a convertor plate, usually tungsten or tantalum, which produces photons with a similar energy range [34].

However, the best yield for the (,p) reaction on an enriched target only used a few milligrams of zinc; a demonstration with a larger target is required to produce a more accurate yield and validate this method [34].

3. Clinical Application

Nuclear medicine imaging provides information about function and structure, using safe, not invasive, and cost-effective techniques for diagnosis and therapy [38].

This discipline is of great importance to medical specialties such as cardiology, neurology, oncology, orthopedics, endocrinology, hematology, nephrology, and pulmonology [38–43].

Copper radioisotopes can have a “conventional role” as radioactive markers that can be added to carrier molecules, conferring all the biological targeting specificity that is needed; furthermore, they can be used as “real tracers,” when directed at the in vivo study of the Cu metabolism itself.

As molecular imaging continues to advance, PET and single photon emission computed tomography (SPECT) techniques are nowadays an integral part of the molecular imaging toolbox; among all the available molecular imaging strategies, PET and SPECT allow targeting of extracellular, cell surface, intracellular proteins, and nucleic acids.

Availability of Cu isotopes for preclinical and clinical research has greatly improved in recent years, also because many potential chelators were developed during over past 20–30 years [4, 44, 45].

The well-established coordination chemistry of Cu allows for its reaction with a wide variety of chelator systems that can potentially be linked to antibodies, proteins, peptides, and other biologically relevant small molecules [3].

Cu metabolism varies from individual to individual. Physiological and pathological conditions that influence Cu metabolism include inherited copper metabolic defects, such as Menkes syndrome and Wilson disease, and acquired copper metabolism disorder or imbalance caused by pregnancy, inflammation, and tumor growth, metastasis, angiogenesis, and drug resistance [46–48].

All Cu radioisotopes are currently investigated for clinical applications but at the state-of- art ⁶⁴Cu, and, in particular, its form ⁶⁴CuCl₂ seems to be the most promising for its half-life, radiation emissions, and stability with chelators.

3.1. The Role of Cu in Oncology

In the last years, many preclinical studies have demonstrated an effect of Cu on cancer development. In fact, in comparison with normal human subjects, significantly higher copper levels have been measured in serum and tumor cells of patients with cancer including prostate, breast, and brain cancer [49].

⁶⁴CuCl₂ is the most widely isotope studied, for its potential role in PET imaging and therapy; it has been bound to several carrier that can be applied to monitor copper metabolism status and guide personalized copper chelator treatment in cancer patients [50].

3.1.1. Cu-Labeled Antibodies and Peptides for Tumor Targeting

Monoclonal antibodies (mAbs) are a vast group of biotechnologically produced proteins, with constantly rising number of applications in immunotherapy, targeted drug delivery, and in vivo/in vitro diagnostics. ⁶⁴Cu-labeled antibodies for PET imaging are trastuzumab (breast cancers expressing human epidermal growth factor receptor 2 or HER2), cetuximab (targeting EGFR-epidermal growth-factor receptor expressing tumors), TRC105-Fab (targeting CD105), and etaracizumab (antibody against human integrin) [4].

Radiolabeling of trastuzumab as well as related fragments and antibodies have been investigated for both diagnostic and radiotherapeutic applications [51].

EGFR expression is increased in many human tumors such as breast cancer, squamous-cell carcinoma of the head and neck, and prostate cancer. At present mAbs, which block the binding of EGF to the extracellular ligand-binding domain of the receptor, have shown promise from a therapeutic standpoint. Cetuximab (C225; Erbitux, Bristol-Myers Squibb, New York, NY) was the first mAb targeted against the EGFR approved by the U.S. Food and Drug Administration (FDA) for the treatment of patients with EGFR-expressing, metastatic colorectal carcinoma [52].

The growth and metastasis of most solid tumors depend on angiogenesis, without which they cannot grow beyond a few millimeters in size. The most widely studied angiogenesis-related targets include CD105 (i.e., endoglin), integrin , and vascular endothelial growth factor receptors (VEGFRs) [53].

CD105 immunohistochemistry is now the accepted standard approach for identifying actively proliferating tumor vessels; it has several advantages over the other targets, including high levels of expression in a wide variety of solid malignancies, independence from its expression on neoplastic cells, lack of tumor histotype specificity, and immediate accessibility of malignant lesions through the bloodstream. With high affinity/specificity for CD105, radiolabeled TRC105-Fab demonstrated its potential in several preclinical tumor models to serve as a promising diagnostic agent for PET imaging. [54].

3.1.2. Cu Labeled Peptides for Tumor Angiogenesis

⁶⁴Cu labeled peptides for targeted cancer therapy/imaging are one of the largest groups of copper radiopharmaceuticals currently researched. They are built of a targeting peptide such as bombesin or octreotide analogue, a linker, and a bifunctional chelator (BFC), commonly tetraazamacrocycle derivate, like TETA or DOTA. The peptide binds to a specific receptor expressed by cancer cells, while copper isotope-BFC moiety allows localization of the tumor by positron emission detection. Attractiveness of peptides for targeted radiotherapy, in comparison to monoclonal antibodies, comes from their good tissue distribution, fast clearance, low immunogenicity, and inexpensive, automated production [4].

It was also observed that copper salts were the simplest angiogenic component of the tumor extract, acting through a stimulation of the migration of the endothelial cells [49].

Alpha beta 3 () is one of the most widely studied integrins, since it is upregulated in endothelial cells involved in active angiogenesis but not in quiescent endothelial cells, making it an ideal biomarker for angiogenesis and tumor imaging. Tumors where is found to be highly expressed include glioblastomas, breast and prostate tumors, malignant melanomas, and ovarian carcinomas. The integrin binds to extracellular proteins through a specific binding pocket that recognizes the three-amimo-acid sequence, arginine-glycine-aspartic acid (Arg-Gly-Asp or RGD).

Sprague et al. conjugated c (RGDyK) to a different chelator, CB-TE2A, and found that the corresponding ⁶⁴Cu complex was taken up specifically by osteoclasts, which are upregulated in osteolytic lesions and bone metastases. These investigations open the possibility of other applications for imaging in diseases, such as osteoarthritis or osteoporosis, as well as imaging osteolytic bone metastases [52, 54].

Hao et al. found ⁶¹Cu-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA)-human serum albumin to be good blood pool imaging agent and suggested its application in antiangiogenic therapy monitoring [55].

⁶⁷Cu is one of the best-suited isotopes for radioimmunotherapy, because its half-life is long enough to allow good biodistribution within tumor (similar to biological half-life of many mAbs), relatively low gamma radiation abundance (lower whole body dose for patient and safer for medical personnel), higher tumor uptake (compared to iodine-131), and simple radiolabeling procedure. Examples of ⁶⁷Cu labelled mAbs are chCE7, an anti-L1-cell adhesion molecule antibody for neuroblastoma, ovarian, and some renal carcinoma therapy, Lym-1 for non-Hodgkin’s lymphoma, C595 an anti-MUC1 mucin antibody for bladder cancer treatment [4].

3.1.3. Cu Labeled Somatostatin Analogs for Targeting Neuroendocrine Tumors

Somatostatin is a 14-amino-acid peptide involved in the regulation and release of several hormones.

Somatostatin receptors (SSRs) are present in many different normal organ systems, such as the central nervous system (CNS), the gastrointestinal tract, the exocrine, and endocrine pancreas, breast, and lung, making it a viable disease target [52].

Targeting of SSRs in tumors has been a goal in cancer treatment and diagnosis since the 1980s, labeling octreotide (OC) with 123I, 111In, and ⁶⁷Ga [52].

In the first-in-humans study, Pfeifer et al. found ⁶⁴Cu-DOTATATE PET useful for clinical somatostatin receptor imaging. Compared with ¹¹¹In-DTPA-octreotride SPECT, ⁶⁴Cu-DOTATATE PET provided superior image quality, detected more true-positive lesions, and was associated with a lower radiation burden [56].

3.1.4. Imaging Tumor Hypoxia

It is well established that hypoxia is an important determinant of the overall tumor response to conventional therapy. Hypoxia can result in an increase in tumor aggressiveness, failure of local control, and activation of transcription factors that support cell survival and migration [57].

The ability to locate and quantify the extent of hypoxia within solid tumors by using noninvasive nuclear imaging would facilitate early diagnosis and help clinicians select the most appropriate treatment for each individual patient [52].

Diacetyl-2,3-bis(-methyl-3-thiosemicarbazone) (ATSM) seems to be an innovative compound for hypoxia imaging which could be labeled with copper positron emitter radioactive isotopes like ^60/61/62/64Cu. The metabolism and pharmacological pathway of Cu-ATSM complex is the same for all the copper isotopes, and the choice for clinical use between these isotopes is based on physical properties. ⁶⁰Cu-ATSM was clinically studied for monitoring tumor hypoxia in lung and cervical cancer and found to be feasible for prediction of tumor response to therapy [57, 58]. Chao et al. suggested that PET images obtained with ⁶⁰Cu-ATSM can be used for intensity-modulated radiation therapy of head and neck cancer [59].

⁶¹Cu-2-acetylpyridine thiosemicarbazone (⁶¹Cu-APTS) complex, for PET imaging of cancer, was proposed by Belicchi-Ferrari et al. Using APTS as a ligand can give additional antiproliferative activity to the compound, which was previously observed by other authors [60].

⁶²Cu-pyruvaldehyde-bis(-methylthiosemicarbazone) (⁶²Cu-PTSM) can be used together with ⁶²Cu-ATSM to obtain complementary data on tumor hypoxia and blood circulation in a single PET session [4, 61].

⁶⁴Cu presents the best compromise between adapted physical properties (sufficiently long half-life, better intrinsic image resolution with low maximal energy) and good production yield (reasonable production costs) [57].

Similar to ^60/61/62Cu isotopes, ⁶⁴Cu-ATSM is subject of many ongoing researches as selective tumor hypoxia imaging agent. Phase II clinical trials of ⁶⁴Cu-ATSM PET/CT are monitoring therapeutic progress in patients with cervical cancer. Similar compound, ⁶⁴Cu-diacetyl-bis( ethylthiosemicarbazone) (⁶⁴Cu-ATSE), has wider tissue-oxygenation level specificity than ⁶⁴Cu-ATSM. In various clinical trials, ⁶⁴Cu-ATSM provided images of tumor hypoxia that improved the clinical outcome of patients submitted to external beam radiotherapy [57].

In conclusion, ⁶⁴Cu-ATSM has several advantages over other radiopharmaceuticals used for PET of hypoxia, including a simple and rapid method for radiolabeling, faster clearance from normoxic tissues (allowing a short time between injection and imaging), a simple method for quantification, and very good image quality [57].

3.1.5. Chemotherapy Resistance

The chemotherapeutic agent Cisplatin (DDP) is a highly polar molecule not readily diffusible across lipid membranes. In many cell types, DDP triggers, as the Cu, a rapid degradation of human copper transporter 1 (hCtr1). This DDP action is obtained at much lower concentrations and more rapidly respect to copper. hCtr1 expression decreases with the acquisition of a DDP resistance, so, in accordance with this phenomenon, a reduced Cu intracellular uptake should be observed in presence of a DDP resistance [49].

In particular, ⁶⁴CuCl₂ can be used to test the drug resistance to therapeutic schemes based on DDP, as in patients affected by breast, ovarian, or colon cancer [49].

3.1.6. Prostate Cancer

In view of the fact that human tumor tissues contain high concentrations of copper, Peng et al. hypothesized that human prostate cancers express high levels of hCtr1 and can be detected by ⁶⁴Cu PET. hCtr1 is a high-affinity copper transporter that mediates cellular uptake of copper in humans and is highly expressed in the liver [62].

The hCtr1 expression level may be related to the aggressiveness or prognosis of the prostate cancer and to the response of prostate cancer to cisplatin chemotherapy because hCtr1 was recently reported to be able to mediate cellular uptake of cisplatin [62].

On the ⁶⁴Cu PET images, there was less background activity in the urinary bladder region because ⁶⁴CuCl₂ was cleared mainly by the hepatobiliary pathway, instead of renally as ¹⁸F-FDG [62].

3.2. The Role of Cu in Neurology

It was assumed that Wilson Disease (WD) patient will have increased uptake of copper in brain tissue and pathologic analysis of the brain may show gliosis and neuronal loss in association with increased Cu deposition. Some WD patients have copper accumulation in the brain and show neurological disorder, while others do not [63].

Diagnosis of WD can be challenging as symptoms mimic other diseases and may gradually appear over time. In addition, the presence of many different mutations in Atp7b gene makes it difficult to screen and diagnose WD by genetic testing. ⁶⁴CuCl₂ PET may change the management of WD patients because it could reflect the symptoms variation of WD and thus affect the treatment strategy. With more detailed information and a SUV cut-off value obtained from further validation of the methodology, ⁶⁴CuCl₂ PET could serve as a simple, straightforward, and noninvasive method for WD diagnosis [63].

Diagnosis of Alzheimer’s disease has been investigated using imaging agent that targets amyloid plaque burden, but new approach highlights altered copper homeostasis. A bis-(thiosemicarbazonato) complex radiolabeled with ⁶⁴Cu can be used for a new and alternative method for the noninvasive diagnosis of Alzheimer’s disease using PET. This approach has the potential to offer complementary information to other diagnostic procedures that elucidate plaque burden [64].

Furthermore, studies in Parkinson’s patients and cerebral perfusion preclinical studies have been performed in freely moving subjects using ^60/61/62/64Cu-PTSM and later ⁶²Cu-ethylglyoaxal bis(thiosemicarbazone) (⁶²Cu-ETS), suggesting their potential application to clinical neurology or neuropsychiatry [65–68].

3.3. Other Potential Roles

Studies over the last 20 years investigated the usefulness of Cu radioisotopes complexed with ATSM for the detection of myocardial perfusion. ⁶²Cu-ATSM complex is widely researched for PET imaging of myocardial ischaemia; ⁶⁴Cu-ATSM seems to be useful to study myocardial hypoxia [69–72].

Furthermore, 5,13-dioximino-6,9,9,12-tetramethyl-7,11-diazaheptadeca-6,11-diene complex of ⁶⁴Cu synthesized by Packard et al. can be potentially used as myocardial perfusion imaging agent and PECAM-1 antibody conjugated with DOTA and labeled with ⁶⁴Cu was successfully performed to evaluate induced myocardial infarction in mouse model [70].

Novel approach for therapy of multinodular goitre, using human chorionic gonadotropin (hCG) directly labeled with ionic Cu emitters was proposed by Maiti et al. [73]. Initial studies indicate that copper-hCG complex half-life is shorter than that of a hCG-TSH (thyroid stimulating hormone) receptor complex, thus hyperactive thyroid cells can be destroyed before internalization of the receptor occurs. More in vitro and in vivo studies are required to assess usefulness of this purpose [4].

Interesting perspectives for copper imaging with PET could be related to the analysis of inflammatory conditions [49].

Nanoparticles labeled with ⁶⁴Cu were used to detect macrophages in atherosclerotic plaques showing high sensitivity and direct correlation with CD68 expression [74].

Locke et al. showed in mouse model that ⁶⁴Cu labeled peptides targeting the formil peptide receptor on neutrophil in vitro accumulate at sites of inflammation in vivo, suggesting that new radiolabeled peptides may prove to be a useful tool to probe inflammation [75].

4. Conclusions

Copper isotopes are gaining a worthy role in the PET radionuclide scenario. Versatility of copper isotopes gives them a strong position in development of new pharmaceuticals. Currently, there are few applications in medicine but numerous ongoing studies will most likely result in novel use in the future.

The longer half-life allows ⁶⁴Cu to be produced at regional or national cyclotron facilities and distributed to local nuclear medicine departments. In addition, ⁶⁴Cu longer half-life is compatible with the time scales required for the ability to create complex radiopharmaceutical, optimal biodistribution of slower clearing agents, such as monoclonal antibodies (mAbs), nanoparticles, and higher molecular weight polypeptides requiring longer imaging times allowing several applications in oncological and nononcological fields.

Conflict of Interests

The authors have no potential conflict of interests to disclose. All authors have no financial or nonfinancial relationships to disclose.

References

S. Puig and D. J. Thiele, “Molecular mechanisms of copper uptake and distribution,” Current Opinion in Chemical Biology, vol. 6, no. 2, pp. 171–180, 2002.
View at: Publisher Site | Google Scholar
I. Bertini, G. Cavallaro, and K. S. McGreevy, “Cellular copper management-a draft user's guide,” Coordination Chemistry Reviews, vol. 254, no. 5-6, pp. 506–524, 2010.
View at: Publisher Site | Google Scholar
T. J. Wadas, E. H. Wong, G. R. Weisman, and C. J. Anderson, “Copper chelation chemistry and its role in copper radiopharmaceuticals,” Current Pharmaceutical Design, vol. 13, no. 1, pp. 3–16, 2007.
View at: Publisher Site | Google Scholar
P. Szymański, T. Frączek, M. Markowicz, and E. Mikiciuk-Olasik, “Development of copper based drugs, radiopharmaceuticals and medical materials,” Biometals, vol. 25, pp. 1089–1112, 2012.
View at: Publisher Site | Google Scholar
H. A. Williams, S. Robinson, P. Julyan, J. Zweit, and D. Hastings, “A comparison of PET imaging characteristics of various copper radioisotopes,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 32, no. 12, pp. 1473–1480, 2005.
View at: Publisher Site | Google Scholar
D. W. McCarthy, L. A. Bass, P. D. Cutler et al., “High purity production and potential applications of copper-60 and copper-61,” Nuclear Medicine and Biology, vol. 26, no. 4, pp. 351–358, 1999.
View at: Publisher Site | Google Scholar
F. Szelecsényi, Z. Kovács, K. Suzuki, K. Okada, T. Fukumura, and K. Mukai, “Formation of ⁶⁰Cu and ⁶¹Cu via Co + ³He reactions up to 70 MeV: production possibility of ⁶⁰Cu for PET studies,” Nuclear Instruments and Methods in Physics Research B: Beam Interactions with Materials and Atoms, vol. 222, no. 3-4, pp. 364–370, 2004.
View at: Publisher Site | Google Scholar
F. Szelecsényi, K. Suzuki, Z. Kovács, M. Takei, and K. Okada, “Production possibility of ^60,61,62Cu radioisotopes by alpha induced reactions on cobalt for PET studies,” Nuclear Instruments and Methods in Physics Research B: Beam Interactions with Materials and Atoms, vol. 187, no. 2, pp. 153–163, 2002.
View at: Publisher Site | Google Scholar
P. Rowshanfarzad, M. Sabet, A. R. Jalilian, and M. Kamalidehghan, “An overview of copper radionuclides and production of ⁶¹Cu by proton irradiation of ${}^{nat}{Zn}$ at a medical cyclotron,” Applied Radiation and Isotopes, vol. 64, no. 12, pp. 1563–1573, 2006.
View at: Publisher Site | Google Scholar
S. S. Das, S. Chattopadhyay, L. Barua, and M. K. Das, “Production of ⁶¹Cu using natural cobalt target and its separation using ascorbic acid and common anion exchange resin,” Applied Radiation and Isotopes, vol. 70, no. 2, pp. 365–368, 2012.
View at: Publisher Site | Google Scholar
T. Fukumura, K. Okada, F. Szelecsényi, Z. Kovács, and K. Suzuki, “Practical production of ⁶¹Cu using natural Co target and its simple purification with a chelating resin for⁶¹CU-ATSM,” Radiochimica Acta, vol. 92, no. 4–6, pp. 209–214, 2004.
View at: Publisher Site | Google Scholar
F. Szelecsényi, Z. Kovács, K. Suzuki et al., “Production possibility of ⁶¹Cu using proton induced nuclear reactions on zinc for PET studies,” Journal of Radioanalytical and Nuclear Chemistry, vol. 263, pp. 539–546, 2005.
View at: Publisher Site | Google Scholar
A. H. Asada, S. V. Smith, S. . Chana et al., “Cyclotron production of ⁶¹Cu using natural Zn & enriched ⁶⁴Zn targets,” in Proceedings of the 14th International Workshop on Targetry and Target Chemistry, vol. 1509 of AIP Conference Proceedings, pp. 91–95, 2012.
View at: Publisher Site | Google Scholar
F. Szelecsényi, G. F. Steyn, Z. Kovács, T. N. van der Walt, and K. Suzuki, “Comments on the feasibility of ⁶¹Cu production by proton irradiation of ${}^{nat}{Zn}$ on a medical cyclotron,” Applied Radiation and Isotopes, vol. 64, no. 7, pp. 789–791, 2006.
View at: Publisher Site | Google Scholar
F. Szelecsényi, Z. Kovács, T. N. van der Walt, G. F. Steyn, K. Suzuki, and K. Okada, “Investigation of the ${}^{nat}{Zn}$ (p,x)⁶²Zn nuclear process up to 70 MeV: a new ⁶²Zn/⁶²Cu generator,” Applied Radiation and Isotopes, vol. 58, no. 3, pp. 377–384, 2003.
View at: Publisher Site | Google Scholar
T. Fukumura, K. Okada, H. Suzuki et al., “An improved ⁶²Zn/⁶²Cu generator based on a cation exchanger and its fully remote-controlled preparation for clinical use,” Nuclear Medicine and Biology, vol. 33, no. 6, pp. 821–827, 2006.
View at: Publisher Site | Google Scholar
D. W. McCarthy, R. E. Shefer, R. E. Klinkowstein et al., “Efficient production of high-specific-activity ⁶⁴Cu using a biomedical cyclotron,” Nuclear Medicine and Biology, vol. 24, no. 1, pp. 35–43, 1997.
View at: Publisher Site | Google Scholar
C. Alliot, N. Michel, A.-C. Bonraisin et al., “One step purification process for no-carrier-added ⁶⁴Cu produced using enriched nickel target,” Radiochimica Acta, vol. 99, no. 10, pp. 627–630, 2011.
View at: Publisher Site | Google Scholar
F. Szelecsenyi, G. Blessing, and S. M. Qaim, “Excitation functions of proton induced nuclear reactions on enriched ⁶¹Ni and ⁶⁴Ni: possibility of production of No-carrier-added ⁶¹Cu and ⁶⁴Cu at a small cyclotron,” Applied Radiation and Isotopes, vol. 44, no. 3, pp. 575–580, 1993.
View at: Google Scholar
H. Piel, S. M. Qaim, and G. Stocklin, “Excitation functions of (p, xn)-reactions on ${}^{nat}{Ni}$ and highly enriched ⁶²Ni: possibility of production of medically important radioisotope ⁶²Cu on a small cyclotron,” Radiochimica Acta, vol. 57, pp. 1–5, 1992.
View at: Google Scholar
A. Obata, S. Kasamatsu, D. W. McCarthy et al., “Production of therapeutic quantities of ⁶⁴Cu using a 12 MeV cyclotron,” Nuclear Medicine and Biology, vol. 30, no. 5, pp. 535–539, 2003.
View at: Publisher Site | Google Scholar
K. R. Zinn, T. R. Chaudhuri, T.-P. Cheng, J. S. Morris, and W. A. Meyer Jr., “Production of no-carrier-added ⁶⁴Cu from zinc metal irradiated under boron shielding,” Cancer, vol. 73, pp. 774–778, 1994.
View at: Google Scholar
K. V. Vimalnath, A. Rajeswari, V. Chirayil et al., “Studies on preparation of ⁶⁴Cu using (n,γ) route of reactor production using medium flux research reactor in India,” Journal of Radioanalytical and Nuclear Chemistry, vol. 290, no. 1, pp. 221–225, 2011.
View at: Publisher Site | Google Scholar
F. Szelecsényi, G. F. Steyn, K. Suzuki et al., “Application of Zn+p reactions for production of copper radioisotopes for medical studies,” in Proceedings of the International Conference on Nuclear Data for Science and Technology (ND '07), O. Bersillon, F. Gunsing, E. Bange et al., Eds., pp. 1395–1398, 2007.
View at: Publisher Site | Google Scholar
A. H. Al Rayyes and Y. Ailouti, “Routine simultaneous production of no-carrier-added high purity ⁶⁴Cu and ⁶⁷Ga,” Nukleonika, vol. 56, no. 4, pp. 259–262, 2011.
View at: Google Scholar
S. G. Dolley, T. N. van der Walt, G. F. Steyn, F. Szelecsényi, and Z. Kovács, “The production and isolation of Cu-64 and Cu-67 from zinc target materialand other radionuclides,” Czechoslovak Journal of Physics, vol. 56, no. 4, pp. D539–D544, 2006.
View at: Publisher Site | Google Scholar
S. Monica and C. J. Anderson, “Molecular imaging of cancer with copper-64 radiopharmaceuticals and positron emission tomography (PET),” Accounts of Chemical Research, vol. 42, no. 7, pp. 832–841, 2009.
View at: Publisher Site | Google Scholar
S. V. Smith, D. J. Waters, and N. di Bartolo, “Separation of ⁶⁴Cu from ⁶⁷Ga waste products using anion exchange and low acid aqueous/organic mixtures,” Radiochimica Acta, vol. 75, no. 2, pp. 65–68, 1996.
View at: Google Scholar
P. J. Kozempel, K. Abbas, F. Simonelli et al., “Preparation of ⁶⁷Cu via deuteron irradiation of ⁷⁰Zn,” Radiochimica Acta, vol. 100, pp. 419–423, 2012.
View at: Publisher Site | Google Scholar
S. C. Srivastava, “Paving the way to personalized medicine: production of some promising theragnostic radionuclides at Brookhaven national laboratory,” Seminars in Nuclear Medicine, vol. 42, no. 3, pp. 151–163, 2012.
View at: Publisher Site | Google Scholar
D. A. Ehst, N. A. Smith, D. L. Bowers et al., “Copper-67 production on electron Linacs-Photonuclear technology development,” in Proceedings of the 14th International Workshop on Targetry and Target Chemistry, vol. 1509 of AIP Conference Proceedings, pp. 157–161.
View at: Publisher Site | Google Scholar
D. G. Medvedev, L. F. Mausner, G. E. Meinken et al., “Development of a large scale production of ⁶⁷Cu from ⁶⁸Zn at the high energy proton accelerator: closing the ⁶⁸Zn cycle,” Applied Radiation and Isotopes, vol. 70, no. 3, pp. 423–429, 2012.
View at: Publisher Site | Google Scholar
T. Katabuchi, S. Watanabe, N. S. Ishioka et al., “Production of ⁶⁷Cu via the ⁶⁸Zn(p,2p)⁶⁷Cu reaction and recovery of ⁶⁸Zn target,” Journal of Radioanalytical and Nuclear Chemistry, vol. 277, no. 2, pp. 467–470, 2008.
View at: Publisher Site | Google Scholar
N. A. Smith, D. L. Bowers, and D. A. Ehst, “The production, separation, and use of ⁶⁷Cu for radioimmunotherapy: a review,” Applied Radiation and Isotopes, vol. 70, no. 10, pp. 2377–2383, 2012.
View at: Publisher Site | Google Scholar
F. Szelecsényi, G. F. Steyn, S. G. Dolley, Z. Kovács, C. Vermeulen, and T. N. van der Walt, “Investigation of the ⁶⁸Zn(p, 2p)⁶⁷Cu nuclear reaction: new measurements up to 40 MeV and compilation up to 100 MeV,” Nuclear Instruments and Methods in Physics Research B: Beam Interactions with Materials and Atoms, vol. 267, no. 11, pp. 1877–1881, 2009.
View at: Publisher Site | Google Scholar
T. Stoll, S. Kastleiner, Y. N. Shubin, H. H. Coenen, and S. M. Qaim, “Excitation functions of proton induced reactions on ⁶⁸Zn from threshold up to 71 MeV, with specific reference to the production of ⁶⁷Cu,” Radiochimica Acta, vol. 90, no. 6, pp. 309–313, 2002.
View at: Google Scholar
J. Kozempel, K. Abbas, F. Simonelli et al., “A novel method for n.c.a. ⁶⁴Cu production by the ⁶⁴Zn(d, 2p)⁶⁴Cu reaction and dual ion-exchange column chromatography,” Radiochimica Acta, vol. 95, no. 2, pp. 75–80, 2007.
View at: Publisher Site | Google Scholar
C. D. Gadaleta, L. Solbiati, V. Mattioli et al., “Unresectable lung malignancy: combination therapy with segmental pulmonary arterial chemoembolization with drug-eluting microspheres and radiofrequency ablation in 17 patients,” Radiology, vol. 267, no. 2, pp. 627–637, 2013.
View at: Publisher Site | Google Scholar
M. M. Ciccone, A. Niccoli-Asabella, P. Scicchitano et al., “Cardiovascular risk evaluation and prevalence of silent myocardial ischemia in subjects with asymptomatic carotid artery disease,” Vascular Health and Risk Management, vol. 7, pp. 129–134, 2011.
View at: Google Scholar
A. Niccoli-Asabella, A. Notaristefano, M. G. Garribba, D. Rubini, C. Ferrari, and G. Rubini, “The PET/CT with ¹⁸F-fluorocholine in the diagnosis of gliomatosis cerebri type 2,” Recenti Progressi in Medicina, vol. 104, no. 2, pp. 73–75, 2013.
View at: Google Scholar
A. Niccoli-Asabella, C. Altini, A. Notaristefano et al., “A retrospective study comparing contrast-enhanced computed tomography with ¹⁸F-FDG-PET/CT in the early follow-up of patients with retroperitoneal sarcomas,” Nuclear Medicine Communications, vol. 34, no. 1, pp. 32–39, 2013.
View at: Publisher Site | Google Scholar
D. Cafagna, G. Rubini, F. Iuele et al., “Whole-body MR-DWIBS vs. [¹⁸F]-FDG-PET/CT in the study of malignant tumors: a retrospective study,” La Radiologia Medica, vol. 117, no. 2, pp. 293–311, 2012.
View at: Publisher Site | Google Scholar
A. Niccoli-Asabella, A. Cimmino, C. Altini, A. Notaristefano, and G. Rubini, “¹⁸F-FDG positron emission tomography/computed tomography and ${}^{99m}{Tc}$ -MDP skeletal scintigraphy in a case of Erdheim-Chester disease,” Hellenic Journal of Nuclear Medicine, vol. 14, no. 3, pp. 311-312, 2011.
View at: Google Scholar
D. Ma, F. Lu, T. Overstreet, D. E. Milenic, and M. W. Brechbiel, “Novel chelating agents for potential clinical applications of copper,” Nuclear Medicine and Biology, vol. 29, no. 1, pp. 91–105, 2002.
View at: Publisher Site | Google Scholar
X. Sun, M. Wuest, G. R. Weisman et al., “Radiolabeling and in vivo behavior of copper-64-labeled cross-bridged cyclam ligands,” Journal of Medicinal Chemistry, vol. 45, no. 2, pp. 469–477, 2002.
View at: Publisher Site | Google Scholar
A. Donsante, P. Johnson, L. A. Jansen, and S. G. Kaler, “Somatic mosaicism in Menkes disease suggests choroid plexus-mediated copper transport to the developing brain,” American Journal of Medical Genetics A, vol. 152, no. 10, pp. 2529–2534, 2010.
View at: Publisher Site | Google Scholar
K.-I. Inoue, H. Takano, A. Shimada, and M. Satoh, “Metallothionein as an anti-inflammatory mediator,” Mediators of Inflammation, vol. 2009, Article ID 101659, 7 pages, 2009.
View at: Publisher Site | Google Scholar
H. Wang and X. Chen, “Visualization of copper metabolism by ⁶⁴CuCl₂-PET,” Molecular Imaging and Biology, vol. 14, no. 1, pp. 14–16, 2012.
View at: Publisher Site | Google Scholar
L. Evangelista, L. Mansi, and G. L. Cascini, “New issues for copper-64: from precursor to innovative pet tracers in clinical oncology,” Current Radiopharmaceuticals, vol. 6, no. 3, pp. 117–123, 2013.
View at: Publisher Site | Google Scholar
C. N. Hancock, L. H. Stockwin, B. Han et al., “A copper chelate of thiosemicarbazone NSC 689534 induces oxidative/ER stress and inhibits tumor growth in vitro and in vivo,” Free Radical Biology and Medicine, vol. 50, no. 1, pp. 110–121, 2011.
View at: Publisher Site | Google Scholar
C. L. Ferreira, D. T. T. Yapp, S. Crisp et al., “Comparison of bifunctional chelates for ⁶⁴Cu antibody imaging,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 37, no. 11, pp. 2117–2126, 2010.
View at: Publisher Site | Google Scholar
C. J. Anderson and R. Ferdani, “Copper-64 radiopharmaceuticals for PET imaging of cancer: advances in preclinical and clinical research,” Cancer Biotherapy and Radiopharmaceuticals, vol. 24, no. 4, pp. 379–393, 2009.
View at: Publisher Site | Google Scholar
Y. Zhang, H. Hong, H. Orbay et al., “PET imaging of CD105/endoglin expression with a ^61/64Cu-labeled Fab antibody fragment,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 40, no. 5, pp. 759–767, 2013.
View at: Publisher Site | Google Scholar
J. E. Sprague, H. Kitaura, W. Zou et al., “Noninvasive imaging of osteoclasts in parathyroid hormone-induced osteolysis using a ⁶⁴Cu-labeled RGD peptide,” Journal of Nuclear Medicine, vol. 48, no. 2, pp. 311–318, 2007.
View at: Google Scholar
G. Hao, T. Fukumura, R. Nakao et al., “Cation exchange separation of ⁶¹Cu²⁺ from ${}^{nat}{Co}$ targets and preparation of ⁶¹Cu-DOTA-HSA as a blood pool agent,” Applied Radiation and Isotopes, vol. 67, no. 4, pp. 511–515, 2009.
View at: Publisher Site | Google Scholar
A. Pfeifer, U. Knigge, J. Mortensen et al., “Clinical PET of neuroendocrine tumors using ⁶⁴Cu-DOTATATE: First-in-Humans study,” Journal of Nuclear Medicine, vol. 53, pp. 1207–1215, 2012.
View at: Publisher Site | Google Scholar
M. Bourgeois, H. Rajerison, F. Guerard et al., “Contribution of [⁶⁴Cu]-ATSM PET in molecular imaging of tumour hypoxia compared to classical [¹⁸F] -MISO—a selected review,” Nuclear Medicine Review, vol. 14, no. 2, pp. 90–95, 2011.
View at: Publisher Site | Google Scholar
F. Dehdashti, M. A. Mintun, J. S. Lewis et al., “In vivo assessment of tumor hypoxia in lung cancer with ⁶⁰Cu-ATSM,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 30, no. 6, pp. 844–850, 2003.
View at: Google Scholar
K. S. C. Chao, W. R. Bosch, S. Mutic et al., “A novel approach to overcome hypoxic tumor resistance: Cu-ATSM-guided intensity-modulated radiation therapy,” International Journal of Radiation Oncology Biology Physics, vol. 49, no. 4, pp. 1171–1182, 2001.
View at: Publisher Site | Google Scholar
M. Belicchi-Ferrari, F. Bisceglie, C. Casoli et al., “Copper(II) and cobalt(III) pyridoxal thiosemicarbazone complexes with nitroprusside as counterion: syntheses, electronic properties, and antileukemic activity,” Journal of Medicinal Chemistry, vol. 48, no. 5, pp. 1671–1675, 2005.
View at: Publisher Site | Google Scholar
Y. Fujibayashi, H. Taniuchi, Y. Yonekura, H. Ohtani, J. Konishi, and A. Yokoyama, “Copper-62-ATSM: a new hypoxia imaging agent with high membrane permeability and low redox potential,” Journal of Nuclear Medicine, vol. 38, no. 7, pp. 1155–1160, 1997.
View at: Google Scholar
F. Peng, X. Lu, J. Janisse, O. Muzik, and A. F. Shields, “PET of human prostate cancer xenografts in mice with increased uptake of ⁶⁴CuCl₂,” Journal of Nuclear Medicine, vol. 47, no. 10, pp. 1649–1652, 2006.
View at: Google Scholar
I. Subramanian, Z. F. Vanek, and J. M. Bronstein, “Diagnosis and treatment of Wilson’s disease,” Current Neurology and Neuroscience Reports, vol. 2, no. 4, pp. 317–323, 2002.
View at: Publisher Site | Google Scholar
M. T. Fodero-Tavoletti, V. L. Villemagne, B. M. Paterson et al., “Bis (thiosemicarbazonato) Cu-64 complexes for positron emission tomography imaging of Alzheimer's disease,” Journal of Alzheimer's Disease, vol. 20, no. 1, pp. 49–55, 2010.
View at: Publisher Site | Google Scholar
M. Ikawa, H. Okazawa, T. Kudo, M. Kuriyama, Y. Fujibayashi, and M. Yoneda, “Evaluation of striatal oxidative stress in patients with Parkinson's disease using [⁶²Cu]ATSM PET,” Nuclear Medicine and Biology, vol. 38, no. 7, pp. 945–951, 2011.
View at: Publisher Site | Google Scholar
M. Ikawa, H. Okazawa, K. Arakawa et al., “PET imaging of redox and energy states in stroke-like episodes of MELAS,” Mitochondrion, vol. 9, no. 2, pp. 144–148, 2009.
View at: Publisher Site | Google Scholar
D. P. Holschneider and J.-M. I. Maarek, “Mapping brain function in freely moving subjects,” Neuroscience and Biobehavioral Reviews, vol. 28, no. 5, pp. 449–461, 2004.
View at: Publisher Site | Google Scholar
N. E. Basken, C. J. Mathias, A. E. Lipka, and M. A. Green, “Species dependence of [⁶⁴Cu]Cu-Bis(thiosemicarbazone) radiopharmaceutical binding to serum albumins,” Nuclear Medicine and Biology, vol. 35, no. 3, pp. 281–286, 2008.
View at: Publisher Site | Google Scholar
Y. Fujibayashi, C. S. Cutler, C. J. Anderson et al., “Comparative studies of Cu-64-ATSM and C-11-acetate in an acute myocardial infarction model: ex vivo imaging of hypoxia in rats,” Nuclear Medicine and Biology, vol. 26, no. 1, pp. 117–121, 1999.
View at: Publisher Site | Google Scholar
A. B. Packard, J. F. Kronauge, E. Barbarics, S. Kiani, and S. T. Treves, “Synthesis and biodistribution of a lipophilic ⁶⁴Cu-labeled monocationic copper(II) complex,” Nuclear Medicine and Biology, vol. 29, no. 3, pp. 289–294, 2002.
View at: Publisher Site | Google Scholar
N. Takahashi, Y. Fujibayashi, Y. Yonekura et al., “Copper-62 ATSM as a hypoxic tissue tracer in myocardial ischemia,” Annals of Nuclear Medicine, vol. 15, no. 3, pp. 293–296, 2001.
View at: Google Scholar
M. Isozaki, Y. Kiyono, Y. Arai et al., “Feasibility of ⁶²Cu-ATSM PET for evaluation of brain ischaemia and misery perfusion in patients with cerebrovascular disease,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 38, no. 6, pp. 1075–1082, 2011.
View at: Publisher Site | Google Scholar
M. Maiti, K. Sen, S. Sen, and S. Lahiri, “Studies on stabilities of some human chorionic gonadotropin complexes with β-emitting radionuclides,” Applied Radiation and Isotopes, vol. 69, no. 2, pp. 316–319, 2011.
View at: Publisher Site | Google Scholar
M. Nahrendorf, H. Zhang, S. Hembrador et al., “Nanoparticle PET-CT imaging of macrophages in inflammatory atherosclerosis,” Circulation, vol. 117, no. 3, pp. 379–387, 2008.
View at: Publisher Site | Google Scholar
L. W. Locke, M. D. Chordia, Y. Zhang et al., “A novel neutrophil-specific PET imaging agent: cFLFLFK-PEG-⁶⁴Cu,” Journal of Nuclear Medicine, vol. 50, no. 5, pp. 790–797, 2009.
View at: Publisher Site | Google Scholar

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