Skip to main content
Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

(R)-NODAGA-PSMA: A Versatile Precursor for Radiometal Labeling and Nuclear Imaging of PSMA-Positive Tumors

  • Eleni Gourni ,

    Current address: Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway

    Affiliations German Cancer Consortium (DKTK), Heidelberg, Germany, Department of Nuclear Medicine, University Hospital Freiburg, Freiburg, Germany, German Cancer Research Center (DKFZ), Heidelberg, Germany

  • Coline Canovas,

    Affiliation Institut de Chimie Moléculaire de l'Université de Bourgogne, UMR6302, CNRS, University Bourgogne Franche-Comté, Dijon, France

  • Victor Goncalves,

    Affiliation Institut de Chimie Moléculaire de l'Université de Bourgogne, UMR6302, CNRS, University Bourgogne Franche-Comté, Dijon, France

  • Franck Denat,

    Affiliation Institut de Chimie Moléculaire de l'Université de Bourgogne, UMR6302, CNRS, University Bourgogne Franche-Comté, Dijon, France

  • Philipp T. Meyer,

    Affiliation Department of Nuclear Medicine, University Hospital Freiburg, Freiburg, Germany

  • Helmut R. Maecke

    Affiliation Department of Nuclear Medicine, University Hospital Freiburg, Freiburg, Germany



The present study aims at developing and evaluating an urea-based prostate specific membrane antigen (PSMA) inhibitor suitable for labeling with 111In for SPECT and intraoperative applications as well as 68Ga and 64Cu for PET imaging.


The PSMA-based inhibitor-lysine-urea-glutamate-coupled to the spacer Phe-Phe-D-Lys(suberoyl) and functionalized with the enantiomerically pure prochelator (R)-1-(1-carboxy-3-carbotertbutoxypropyl)-4,7-carbotartbutoxymethyl)-1,4,7-triazacyclononane ((R)-NODAGA(tBu)3), to obtain (R)-NODAGA-Phe-Phe-D-Lys(suberoyl)-Lys-urea-Glu (CC34). CC34 was labeled with 111In, 68Ga and 64Cu. The radioconjugates were further evaluated in vitro and in vivo in LNCaP xenografts by biodistribution and PET studies. Biodistribution studies were also performed with 68Ga-HBED-CC-PSMA (HBED-CC: N,N′-bis[2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N′-diacetic acid) and 111In-PSMA-617 for comparison.


68Ga-CC34, 64Cu-CC34, and 111In-CC34 were prepared in radiochemical purity >95%. 68/natGa-CC34, 64/natCu-CC34, 111/natIn-CC34, 68/natGa-HBED-CC-PSMA, and 111/natIn-PSMA-617 exhibited high affinity for the LNCaP cells, with Kd values of 19.3±2.5 nM, 27.5±2.7 nM, 5.5±0.9 nM, 2.9±0.6 nM and 5.4±0.8 nM, respectively. They revealed comparable internalization profiles with approximately 75% of the total cell associated activity internalized after 3 h of incubation. 68Ga-CC34 showed very high stability after its administration in mice. Tumor uptake of 68Ga-CC34 (14.5±2.9% IA/g) in LNCaP xenografts at 1 h p.i. was comparable to 68Ga-HBED-CC-PSMA (15.8±1.4% IA/g) (P = 0.67). The tumor-to-normal tissue ratios at 1 and 2 h p.i of 68Ga-CC34 were also comparable to 68Ga-HBED-CC-PSMA (P>0.05). Tumor uptake of 111In-CC34 (28.5±2.6% IA/g) at 1 h p.i. was lower than 111In-PSMA-617 (52.1±6.5% IA/g) (P = 0.02). The acquisition of PET-images with 64Cu-CC34 at later time points showed wash-out from the kidneys, while tumor uptake still remained relatively high. This resulted in an increased tumor-to-kidney ratio over time.


68Ga-CC34 is comparable to 68Ga-HBED-CC-PSMA in terms of tumor uptake and tumor to normal tissue ratios. 64Cu-CC34 could enable high contrast imaging of PSMA positive tissues characterized by elevated expression of PSMA or when delayed imaging is required. 64Cu-CC34 is currently being prepared for clinical translation.


Prostate cancer is the most common malignancy found in men and the second leading cause of cancer death in the US. In 2015, it is estimated that a total of 220,800 new prostate cancer cases will be diagnosed while 27,540 prostate cancer deaths are predicted to occur [1]. Therefore, efforts to discover and evaluate new diagnostic and therapeutic biomarkers for prostate cancer continue. Prostate specific membrane antigen (PSMA) is a well-established target for diagnostic and potential therapeutic applications. PSMA is a 750 amino acid type II integral membrane glycoprotein which is primarily expressed in healthy human prostate epithelium and in non-prostatic solid tumor vasculature without being shed into the circulation [2]. It is overexpressed by almost all prostate cancers with an increased expression by a factor of about 1000 in poorly differentiated, metastatic, and hormone-refractory cases [35]. The proposed pharmacophore for PSMA active site can be divided into three parts; three carboxylic groups, a carbonyl oxygen as part of the zinc complexation and nearby aromatic residues [6].

PSMA was originally targeted by the 111In-labeled monoclonal antibody 7E11-C5 (ProstaScint®; Cytogen Corporation, Princeton, NJ) which specifically binds to the PSMA+ human adenocarcinoma cell line LNCaP [7]. 7E11-C5 only binds to the intracellular site of PSMA (amino terminus) only accessible on necrotic tumors [8], therefore this tracer did lack wide acceptance in the field of nuclear medicine for the detection of prostate cancer. Radiolabeled monoclonal antibodies which bind to the extracellular site of PSMA were further developed [913]. Their successful preclinical evaluation and promising clinical assessment justified the utility of PSMA in the diagnosis and the potential therapy of prostate cancer [14,15]. As part of the ongoing efforts of several groups to develop new PSMA-specific ligands which outperform the disadvantages of antibodies such as inadequate pharmacokinetics and tissue accessibility, several chemical scaffolds such as PSMA inhibitors of low molecular weight have been synthesized and evaluated [16]. Among them, the urea-based PSMA inhibitors, functionalized to be used for imaging with Single-Photon Emission Computed Tomography (SPECT) or Positron Emission Tomography (PET), were able to successfully image PSMA-expressing xenografted mice [1729].

Herein, the urea-based PSMA inhibitor derived from the lysine-urea-glutamate peptidomimetic structure, was coupled to the spacer Phe-Phe-D-Lys(suberoyl) and functionalized with the enantiomerically pure prochelator (R)-1-(1-carboxy-3-carbotertbutoxypropyl)-4,7-carbotartbutoxymethyl)-1,4,7-triazacyclononane ((R)-NODAGA(tBu)3), to obtain (R)-NODAGA-Phe-Phe-D-Lys(suberoyl)-Lys-urea-Glu (CC34) (Fig 1). CC34 radiolabeled with 68Ga, 64Cu and 111In. The 68Ga- 64Cu- and 111In-conjugates were further evaluated in vitro and in vivo in LNCaP tumor xenografts by biodistribution and PET imaging studies. 68Ga-HBED-CC-PSMA and 111In-PSMA-617 were also evaluated for comparison (Fig 1).

Fig 1. Schematic structures.

(R)-NODAGA-Phe-Phe-D-Lys(suberoyl-Lys-urea-Glu) (CC34), HBED-CC-PSMA and PSMA-617.

Material and Methods

The supplier information for all reagents and details of instruments used are provided in the S1 Appendix.

Synthesis of the urea-based compound CC34

The PSMA-based inhibitor, CC34, was synthesized using standard Fmoc chemistry. Description of the synthesis is given in the S2 Appendix.

Radiochemistry / Lipophilicity

For the evaluation of the 68Ga-labeling efficiency, 68Ga-CC34 and 68Ga-HBED-PSMA, were prepared within 10 min at 95°C, using the Modular-Lab PharmTracer module by Eckert & Ziegler (Berlin, Germany) (S3 Appendix).

The 64Cu- and 111In-labeled radiotracers were prepared within 30 min at 95°C and were used without any further purification (S3 Appendix).

The lipophilicity (LogD, pH 7.4) was estimated by the “shake-flask” method (S3 Appendix).

Saturation binding / Internalization studies

For receptor saturation analysis, PSMA positive LNCaP cells (metastatic lesion of human prostatic adenocarcinoma, ATCC) were seeded at a density of 0.8–1 million cells per well in 6-well poly-L-lysine PLL-coated plates and incubated overnight with medium (RPMI Medium 1640—GlutaMAX containing 1% FBS, 100 U/mL penicillin and 100 μg/mL streptomycin, sodium-pyruvat 1 mM). The next day, the medium was removed, the cells washed and incubated for 1 h at 37°C with fresh binding buffer (RPMI Medium 1640—GlutaMAX containing 1% FBS, 100 U/mL penicillin and 100 μg/mL streptomycin, 50 mM Hepes, 50 μg/mL bacitracin, 0.5% BSA). Afterwards, the plates were placed on ice for 30 min followed by incubation with increasing concentrations of either 68/natGa-CC34, 64/natCu-CC34, 111/natIn-CC34 and 111/natIn-PSMA-617 (1–100 nM) in phosphate-buffered saline binding buffer pH 7.4. After the addition of the radioligands, the cells were incubated for 120 min at 4°C. Non-specific binding was determined in the presence of 2-(phosphonomethyl)-pentanedioic acid (PMPA) at a final concentration of 1 μM. The cells were washed twice with ice-cold PBS, followed by solubilization with 1 N NaOH and the cell-associated radioactivity was measured using a gamma-counter. Specific binding was plotted against the total molar concentration of the added radiotracer. The Kd values and the concentration of the radiotracers required to saturate the receptors (Bmax) were determined by nonlinear regression using GraphPad (Prism 5 Graph Pad Software, San Diego, CA). For all the cell studies the values are normalized for 1x106 cells per well and all data are from two independent experiments with triplicates in each experiment.

For internalization experiments, LNCaP cells were seeded into 6-well plates and treated as described above. Approximately 0.25 pmol of the radiopeptides (64Cu-CC34, 68Ga-CC34, 111In-CC34, 68Ga-HBED-CC-PSMA and 111In-PSMA-617), were added to the binding buffer and the cells were incubated (in triplicates) for 0.5, 1, 2, 4 and 6 h at 37°C, 5% CO2 in case of 64Cu-CC34, 111In-CC34 and 111In-PSMA-617 and for 10, 30, 60, 90, 120 and 180 min at 37°C, 5% CO2 in case of 68Ga-CC34 and 68Ga-HBED-CC-PSMA. To determine nonspecific membrane binding and internalization, excess of PMPA (final concentration 1 μM) was added to selected wells. At each time point, the internalization was stopped by removing the medium and washing the cells twice with ice-cold PBS. To remove the receptor-bound radioligand, an acid wash was carried out twice with a 0.1 M glycine buffer pH 2.8 for 5 min on ice. Finally, cells were solubilized with 1 N NaOH. The radioactivity of the culture medium, the receptor-bound, and the internalized fractions were measured in a γ-counter.

Metabolic studies

Normal female athymic Balb/c nude mice (2) were injected with approximately 80 pmol / 9 MBq of 68Ga-CC34 in a total volume of 0.1 mL of PBS and sacrificed 15 min p.i.. Blood was collected in heparinized tubes and centrifuged (5 min, 1,700g) for plasma isolation. Sample of plasma (300 mL) was transferred to an ultrafiltration device (Vivacon 500; 30,000 molecular weight cutoff [Sartorius Stedium Biotech GmbH]), followed by centrifugation (10 min, 9,660g) for the separation of proteins. Samples from the ultrafiltrate and 68Ga-CC34 solution were analyzed by Reversed-Phase High-Performance Liquid Chromatography (RP-HPLC).

Cell line / Animal model

The PSMA+ LNCaP cell line was cultured at 37°C and 5% CO2 in (RPMI Medium 1640-GlutaMAX containing 1% FBS, 100 U/mL penicillin and 100 μg/mL streptomycin, sodium-pyruvate 1 mM.

Female athymic Balb/C nude mice (age: 4–6 weeks, weight: 17–20 g) were purchased from Janvier, France. For implantation, the tumor cells were harvested by trypsinization and 5x106 cells in 50% Matrigel (Corning Matrigel Matrix, 354230) and were inoculated subcutaneously into the right shoulder of the mice. After an average of four weeks, tumor size reached 200 to 300 mg and the animals were used for biodistribution and PET imaging studies. All animal experiments were conducted in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by the Committee on the Ethics of Animals Experiments of the University Medical Center of Freiburg, Germany (Permit Number: G-13/30).


Ten pmol of 68Ga-CC34 or 68Ga-HBED-CC-PSMA (0.7–0.8 MBq / 100 μL), 64Cu-CC34 (0.2–0.3 MBq / 100 μL), 111In-CC34 or 111In-PSMA-617 (0.09–0.1 MBq / 100 μL) in 100 μL. NaCl 0.9% were injected intravenously into the tail vein of LNCaP mice. Animals were sacrificed by isoflurane anesthesia at 1 and 2 h after injection of the 68Ga-labeled radiovectors and at 1, 4, 24 and 48 h after the injection of the 64Cu- and 111In-labeled radiovectors.

The organs of interest were dissected and weighted, and the radioactivity in tissue samples was counted in a γ-counter. Biodistribution data are given as percent of injected activity per gram of tissue (% IA/g) and are means ± SD (n = 4).

To demonstrate the specificity of binding, LNCaP mice were co-injected with 10 pmol of the radiotracers along with 20 nmol of PMPA. Animals were sacrificed at 1 h after injection by isoflurane anesthesia.

PET studies in LNCaP xenografts

For the 68Ga-labeled compounds static images were acquired for a time period of 15 min at 1 and 2 h p.i., and for 64Cu-CC34 at 1, 4, 24 and 48 h p.i. PET blocking studies of the 68Ga- and 64Cu-labeled radioconjougates, were performed as described above and static scans were obtained as previously described. PET-images were corrected for 68Ga or 64Cu decay and reconstructed with an ordered-subset expectation maximization algorithm provided by the manufacturer. PET images generated by the AMIDE software.

Tracer uptake is expressed as percentage of decay-corrected %IA/g, with a color scale set from 0% to 250% for qualitative comparison among the images.

Statistical Analysis

All data are expressed as the mean of values±standard deviation (mean±SD). Prism 5 Software (GraphPad Software) was used to determine statistical significance at the 95% confidence level, with a P value of less than 0.05 being considered significantly different.



(R)-NODAGA-Phe-Phe-D-Lys was assembled on solid phase and, after cleavage and deprotection, coupled to tBuO-(NHS-suberoyl)Lys-urea-Glu(OtBu)-OtBu. CC34 was isolated after trifluoroacetic acid (TFA) deprotection and RP-HPLC purification with an overall yield of 22% and a purity >99%, as determined by analytical RP-HPLC. Compound identity was confirmed by electrospray ionization-high-resolution mass spectrometry (ESI-HRMS): m/z = 1255.60924 [M+H]+, calculated for C59H87N10O20 1255.60926 (S1 Fig).

Radiochemistry / Lipophilicity

The PSMA urea-based conjugates were labeled with 68Ga, 64Cu and 111In with a labeling yield >98%. The specific activities were ranging between 75 and 80 MBq/nmol for the 68Ga-labeled tracers, approximately 40 MBq/nmol for 64Cu-CC34 and about 10 MBq/nmol for the 111In-labeled radioligands.

With a LogDoctanol/PBS of -4.06 ± 0.10 and -4.06 ± 0.06 68Ga-HBED-CC-PSMA and 111In-PSMA-617, respectively, show high hydrophilicity, as compared with 68Ga-CC34, 64Cu-CC34 and 111In-CC34, which showed LogDoctanol/PBS of -3.54 ± 0.06, -3.01 ± 0.06 and -3.32 ± 0.05, respectively.

Saturation binding / Internalization studies—Metabolic stability

All radiotracers exhibited high affinity for the PSMA+ LNCaP cells (Fig 2). 68/natGa-CC34, and 64/natCu-CC34 have similar affinity with Kd values of 19.3 ± 2.5 nM and 27.5 ± 2.7 nM, respectively. Both 111In-labeled PSMA-ligands, 111/natIn-CC34 and 111/natIn-PSMA-617, are more affine to PSMA with Kd values of approximately 5 nM. The Bmax values were also at the same level for all the radioconjugates (approximately 0.6 nM).

Fig 2. Saturation binding study on intact LNCaP cells.

Increasing concentrations of 68/natGa-HBED-CC-PSMA, 111/natIn-PSMA-617, 68/natGa-CC34, 111/natIn-CC34 and 64/natCu-CC34 were used, ranging from 0.1 to 1,000 nM. All radiotracers exhibited high affinity for the PSMA+ LNCaP cells. 111/natIn-CC34 and 111/natIn-PSMA-617 are more affine to PSMA Dissociation constant (Kd) and maximum number of binding sites (Bmax) were calculated from nonlinear regression analysis using GraphPad Prism.

Internalization studies showed specific internalization at 37°C and the internalized activity always exceeded the surface bound activity (Fig 3). Approximately 75% of the total cell associated activity was internalized after 3 h of incubation.

Fig 3. Internalization studies after incubation with LNCaP cells at 37°C.

Approximately 75% of the total cell associated activity internalized after 3 h of incubation with the LNCaP cells Cell uptake calculated as cell surface-bound and internalized fraction. Surface bound and receptor-specific internalization expressed as percentage of the applied radioactivity. Nonspecific binding was determined in the presence of 1 μM PMPA.

As demonstrated by RP-HPLC metabolite analysis of plasma samples 15 min p.i. of 68Ga-CC34, the remaining circulating activity exclusively consists of intact radiotracer (>95%) (Fig 4).

Fig 4. HPLC profiles.

A: formulated 68Ga-CC34, B: mouse plasma extracted from Balb/c nude mice 15 min after injection of 68Ga-CC34.

Biodistribution in LNCaP xenografts

The biodistribution data are summarized in Tables 1 to 4. 68Ga-HBED-CC-PSMA, 68Ga- and 64Cu-CC34, as well as 111In-PSMA-617 displayed rapid blood clearance with approximately 0.2% IA/g left in blood at 2 h p.i.. 111In-CC34 exhibited high blood values at early time points (8.1±0.3% IA/g and 2.0±0.8% IA/g at 1 and 2 h p.i. respectively) and slow clearance with about 0.2% IA/g remaining in blood 24 h p.i. Organs such as kidneys, spleen, lung and adrenals with elevated PSMA expression showed high and receptor mediated uptake as shown after the coinjection of 20 nmol of PMPA. 68Ga-HBED-CC-PSMA and 68Ga-CC34 exhibited similar biodistribution profile with tumor uptake of 15.8±1.4% IA/g and 14.5±2.9% IA/g at 1 h p.i. (P = 0.67). Their tumor-to-normal tissue ratios at 1 and 2 h p.i were also comparable (P>0.05). The pharmacokinetic performance of 64Cu-CC34, at later time points showed faster wash out from the PSMA positive organs compared to the tumor leading to improved tumor to background ratios over time. Both 111In-labeled tracers showed the highest tumor uptake compared to the 68Ga- and 64Cu-labeled tracers (28.5±2.6% IA/g for111In-CC34 and 52.1±6.5% IA/g for 111In-PSMA-617 at 1 h p.i.) which dropped to 16.5±1.9% IA/g and 21.2±1.6% IA/g at 48 h p.i., respectively. Compared to 64Cu-CC34 and 111In-PSMA-617, 111In-CC34 exhibited high and retained kidney uptake over time.

Table 1. Biodistribution data of 68Ga-HBED-CC-PSMA and 68Ga-CC34 in LNCaP.

PSMA tumor binding specificity was demonstrated by a reduction of the tumor uptake of about 75% in case of 68Ga-HBED-CC-PSMA and 111In-CC34 and more than 90% for 68Ga-CC34, 64Cu-CC34 and 111In-PSMA-617.

Small-animal PET studies

Representative PET images obtained upon injection of 68Ga-HBED-CC-PSMA and 68Ga-CC34 in LNCaP xenografts at 1 and 2 h p.i. (Fig 5), with specific tumor and kidney uptake, as shown by the blocking studies at 1 h p.i..

Fig 5. Maximum intensity projections (MIPs) PET images.

(A) 68Ga-HBED-CC-PSMA and (B) 68Ga-CC34 upon their injection in LNCaP tumor bearing mice at 1 h and 2 h p.i along with blocking studies at 1h p.i.. The images clearly visualized the tumors. They showed high kidney uptake at early time points and prove the specificity of the radiopeptides for the PSMA receptors, as the tumor is hardly visualized after co-injection of excess of PMPA.

The pharmacokinetics of 64Cu-CC34 was also determined by small-animal PET (Fig 6) at 1, 4, 24 and 48 h in the same animals. The radiotracer is specifically taken up by the PSMA positive organs at early time points. The PET studies of 64Cu-CC34 showed good pharmacokinetics, with gradually reduced uptake in kidneys at 24 and 48 h, respectively. The 64Cu-labeled conjugate showed low liver uptake.

Fig 6. Maximum intensity projections (MIPs) PET images of 64Cu-CC34.

The images were acquired upon the injection of 64Cu-CC34 on LNCaP tumor bearing mice at 1, 4, 24 and 48 h p.i along with blocking studies at 1h p.i.. They showed good pharmacokinetics, with clear deliniation of the tumor, gradual reduction of the kidney uptake at 24 and 48 h, respectively. The 64Cu-labeled conjugate showed low liver uptake.


Prostate cancer is a complex and biologically heterogeneous disease and therefore cannot be fully assessed with conventional imaging alone. Radionuclide molecular imaging with positron emission tomography (PET) is poised to fill this unmet need through noninvasive detection of the multiple molecular and cellular processes that are active in prostate cancer patients [30].

PSMA is primarily expressed in the human prostate epithelium, salivary and lacrimal glands as well as kidneys with enhanced expression by almost all prostate cancers and further up-regulation in poorly differentiated, metastatic and hormone-refractory carcinomas [31]. These characteristics render PSMA as promising target for prostate cancer imaging and potential therapy. Many efforts have been made especially during the last decade in regard to the development of PSMA-based imaging agents with particular focus on the low molecular weight PSMA inhibitors. A variety of chelators and spacers were introduced to the urea-based PSMA inhibitors and the derived conjugates were labeled with a series of radionuclides for SPECT and PET imaging [1729]. A representative example of this class of radiotracers is the peptidomimetic structure Lys-NH-CO-NH-Glu when coupled to the spacer 6-amino-hexanoic acid (Ahx) and functionalized with the chelator N,N′-dis [2-hydroxy-5-(carboxyethyl)benzyl] ethylenediamine-N,N′–diacetic acid (HBED-CC) to obtain HBED-CC-Ahx-Lys-NH-CO-NH-Glu (HBED-CC-PSMA). The ability to image PSMA using 68Ga-HBED-CC-PSMA shows great promise preclinically and clinically [25,32].

Our goal was to develop and evaluate a versatile probe suitable for imaging of PSMA-positive tumors. Thus, (R)-NODAGA(tBu)3 was conjugated to the well-established Lys-urea-Glu PSMA-inhibitor, through a Phe-Phe-D-Lys(suberoyl) linker [17,18,20,28]. Because of the small volume of the triazacyclononane cage and its ability to coordinate metal ions, NODAGA is particularly attractive for the rapid and stable chelation of 111In for SPECT, as well as 68Ga and 64Cu applied in PET imaging. The choice of the Phe-Phe-Lys(suberoyl) linker has already proven to be successful by Banerjee et al. [28].

CC34 was labeled with 68Ga, 64Cu and 111In, to be used for PET and SPECT imaging and intraoperative applications. Due to its availability from generator systems, the positron emitter 68Ga has gained rapidly increasing interest in the field of radiopharmaceutical chemistry [33]. 64Cu is a positron emitter with a longer half-life (12.7 h) compared to 68Ga (67.8 min) and can give PET-images at later time points with improved tumor-to-background ratios [34]. 64Cu-radiopharmaceuticals can be produced centrally and shipped to distant hospitals. 111In is used as an important SPECT label. Additionally, intraoperative gamma probes are now an important, well-established technology in the management of cancer, particularly in the detection of sentinel lymph nodes.

CC34, being labeled with 68Ga, 64Cu and 111In, showed high affinity towards PSMA on LNCaP cells, with 111/natIn-CC34 exhibiting a significantly increased affinity compared to the 68/natGa- and 64/natCu-conjugates. In our saturation binding assay, 68/natGa-HBED-CC-PSMA revealed the highest affinity towards PSMA while 111/natIn-PSMA-617 was as affine as 111/natIn-CC34.

To figure out if CC34 is subjected to in vivo metabolic degradation and to which extent, RP-HPLC metabolite analysis of plasma samples was performed. Fifteen min p.i. of 68Ga-CC34 more than 95% of the remaining circulating activity corresponds to intact radiotracer. When the Lys-NH-CO-NH-Glu peptidomimetic structure was coupled to the spacer Phe-Phe-Lysine-suberoyl (L-amino acid spacer) and functionalized with the chelator (1-(1,3-carboxy-propyl)-4,7,10(carboxymethyl)-1,4,7,10 tetraazacyclo-dodecane (DOTAGA) [23], rapid in vivo metabolization of the 68Ga-labeled radiovector was demonstrated. In the same report, the D-amino acids spacer led to an in vivo metabolic stable radiotracer. In our study we proved that only the substitution of L- with D-Lysine in the spacer, resulted in high in vivo stability of 68Ga-CC34.

The enhanced PSMA affinity, 111/natIn-CC34 and 111/natIn-PSMA-617 resulted in two- to five-fold increased internalization rate and higher but also longer tumor retention compared to 64/natCu- and 68/natGa-CC34 and 68/natGa-HBED-CC-PSMA. Although the binding affinity can be considered as the most crucial parameter which greatly influences the tumor uptake, the overall pharmacokinetic performance of a radiotracer is determined by many other factors which certainly need to be taken into consideration. In particular, parameters such as, lipophilicity, charge, plasma protein binding and molecular weight also influence the pharmacokinetic performance of a radiotracer. CC34 can be considered as a strong evidence of the above assumption. 68Ga-CC34 and 64Cu-CC34 demonstrated fast clearance from blood and normal tissues, even kidneys as proved by biodistribution and PET-studies in the case of the copper-64 labeled compounds. The superiority of NODAGA compared to HBED-CC to be efficiently labeled with 64Cu allows for the conduction of biodistribution/imaging studies at later time points and therefore the complete accomplishment of the pharmacokinetic performance of the radiotracer. 64Cu-CC34 showed faster wash out from the PSMA positive organs compared to the tumor leading to improved tumor to background ratios. The very low liver uptake of 64Cu-CC34 at all time points in combination with the short blood circulation need to be pointed out since this is a strong indication of the excellent in vivo stability of the 64Cu-NODAGA complex. Unfortunately, this was not the case for 111In-CC34. The affinity of 111/natIn-CC34 towards PSMA was higher compared to 68/natGa-CC34 and 64/natCu-CC34 by a factor of about 4 and as it was anticipated tumor uptake was higher and longer retention was also observed. Surprisingly, 111In-CC34 exhibited long blood circulation and highly retained activity in the kidneys even at 48 h p.i.. Unfortunately, this undesired in vivo profile eliminates its applicability as a SPECT imaging agent. The pharmacokinetics of the alanine-containing DOTA-conjugated PSMA inhibitor, PSMA-617, labeled with 111In, on the other hand, was excellent with impressive tumor to background ratios over time. Protein binding studies (data not shown) 15 min p.i. of 111In-CC34 and 111In-PSMA-617 in mice revealed that 83 and 53%, respectively, of the remaining circulating activity was bound to the proteins. This biodistribution profile of 111In-CC34 cannot be explained by its hydrophilicity (LogDoctanol/PBS = -3.32). NODAGA, although is not usual, might form a seven-coordinate complex with 111In, and if this is the case here, 111In-CC34 with an additional charge appears to bind strongly to proteins [35]. The seventh coordination site could be occupied by a Lys side chain of a protein. It is worth noting that 177Lu-PSMA-617, exhibited similar pharmacokinetics compared to 111In-PSMA-617, which is also characterized by high and retained tumor uptake and almost complete elimination of the radioactivity through kidneys within 24 h [26].

The chelators 1,4,8,11-tetraazabicyclo[6.6.2]-hexadecane-4,11-diacetic acid (CB2-TE2A) and 1,4,7,10-tetraazacyclododecane- N,N′,N″,N‴-tetraacetic acid (DOTA) were used for the functionalization of the Phe-Phe-L-Lys(suberoyl-Lys-urea-Glu). Significantly high in vivo stability, as evidenced by the low liver uptake and fast blood clearance was demonstrated for the 64Cu-CB2-TE2A-conjugated radiotracer with comparable tumor to blood and tumor to muscles ratios with 64Cu-CC34 at 1 h p.i.. High liver uptake and slow blood clearance for the 64Cu-DOTA-conjugated radiotracer was indicative of free Cu(II), which is accumulated in liver [29]. Kidney uptake of the 64Cu-CB2-TE2A-PSMA-based tracer was two-fold lower compared to 64Cu-CC34 and very fast wash out was demonstrated. Although the PSMA-mediated renal uptake has been shown to be specific by us and others, it is interesting that variations are observed not only in regard to the absolute kidney uptake but also as far as the renal elimination concerns.


Our data document the versatility of the (R)-NODAGA-functionalized PSMA-based radiotracer, CC34, labeled with 68Ga and 64Cu, as a highly specific targeted PET imaging agent. In particular, the favorable pharmacokinetic performance of the 64Cu-labeled radiotracer renders it a promising tracer that would enable sufficient imaging of PSMA positive tissues which are characterized by elevated expression of PSMA or in the case that delayed imaging is required. This tracer is currently prepared for clinical translation.

Supporting Information

S2 Appendix. Synthesis of the urea-based compound CC34.



We thank Yvonne Kiefer and Roswitha Toennesmann for technical assistance.

Author Contributions

Conceived and designed the experiments: EG CC VG. Performed the experiments: EG CC VG. Analyzed the data: EG. Contributed reagents/materials/analysis tools: HRM PTM FD. Wrote the paper: EG HRM PTM.


  1. 1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2015. CA Cancer J Clin. 2015;65: 5–29. pmid:25559415
  2. 2. Chang SS. Overview of prostate-specific membrane antigen. Rev Urol. 2004;6(suppl 10): 13.
  3. 3. Chang SS, Reuter VE, Heston WD, Gaudin PB. Comparison of anti-prostate-spacific membrane antigen antibodies and other immunomarkers in metastatic prostate carcinoma. Urology. 2001;57: 1179–1183. pmid:11377343
  4. 4. Wright GLJ, Grob BM, Haley C, Grossman K, Newhall K, Petrylak D, et al. Upregulation of prostate-specific membrane antigen after androgen-deprivation therapy. Urology. 1996;48: 326–334. pmid:8753752
  5. 5. Perner S, Hofer MD, Kim R, Shah RB, Li H, Moller P, et al. Prostate-specific membrane antigen expression as a predictor of prostate cancer progression. Human Pathol. 2007;38: 696–701.
  6. 6. Liu T, Toriyabe Y, Kazak M, Berkman CE. Pseudoirreversible inhibition of prostate-specific membrane antigen by phosphoramidate peptidomimetics. Biochemistry. 2008;47: 12658–12660. pmid:18983168
  7. 7. Horoszewicz JS, Kawinski E, Murphy GP. Monoclonal antibodies to a new antigenic marker in epithelial prostatic cells and serum of prostatic cancer patients. Anticancer Res. 1987;7: 927–936. pmid:2449118
  8. 8. Troyer JK, Becket ML, Wright GL. Location of prostate-specific membrane antigen in the LNCaP prostate carcinoma cell line. Prostate. 1997;30: 232–242. pmid:9111600
  9. 9. Vallabhajosula S, Kuji I, Mamacher KA, Konishi S, Kostakoglu L, Kothari PA, et al. Pharmacokinetics and biodistribution of 111In- and 177Lu-labeled J591 antibody specific for prostate-specific membrane antigen: prediction of 90Y-J591 radiation dosimetry based on 111In or 177Lu? J Nucl Med. 2005;46: 634–641. pmid:15809486
  10. 10. Holland JP, Divilov V, Bander NH, Smith-Jones PM, Larson SM, Lewis JS. 89Zr-DFO-J591 for immunoPET of prostate-specific membrane antigen expression in vivo. J Nucl Med. 2010;51: 1293–1300. pmid:20660376
  11. 11. Ruggiero A, Holland JP, Hudolin T, Shenker L, Koulova A, Bande NH et al. Targeting the internal epitope of prostate-specific membrane antigen with 89Zr-7E11 immuno-PET. J Nucl Med. 2011;52: 1608–1615. pmid:21908391
  12. 12. Elsasser-Beile U, Wolf P, Gierschner D, Buhler P, Schultze-Seemann W, Wetterauer U. A new generation of monoclonal and recombinant antibodies against cell-adherent prostate specific membrane antigen for diagnostic and therapeutic targeting of prostate cancer. Prostate. 2006;66: 1359–1370. pmid:16894535
  13. 13. Alt K, Wiehr S, Ehrlichmann W, Reischl G, Wolf P, Pichler BJ, et al. High-resolution animal PET imaging of prostate cancer xenografts with three different 64Cu-labeled antibodies against native cell-adherent PSMA. Prostate. 2010;70: 1413–1421. pmid:20687214
  14. 14. Milowsky MI, Nanus DM, Kostakoglu L, Sheehan CE, Vallabhajosula S, Goldsmith SJ, et al. Vascular targeted therapy with anti-prostate-specific membrane antigen monoclonal antibody J591 in advanced solid tumors. J Clin Oncol. 2007;25: 540–547. pmid:17290063
  15. 15. Vallabhajosula S, Goldsmith SJ, Kostakoglou L, Milowsky MI, Nanus DM, Bander NH. Radioimmunotherapy of prostate cancer using 90Y- and 177Lu-labeled J591 monoclonal antibodies: effect of multiple treatments on myelotoxicity. Clin Can Res. 2005;11: 7195–7200s.
  16. 16. Kozikowski AP, Zhang J, Nan F, Petukhov PA, Grajkowska E, Wroblewski JT, et al. Synthesis of urea-based inhibitors as active site probes of glutamate carboxypeptidase II: Efficacy as analgesic agents. J Med Chem. 2004;47: 1729–1738. pmid:15027864
  17. 17. Maresca KP, Hillier SM, Femia FL, Keith D, Barone C, Joyal JL, et al. A series of halogenated heterodimeric inhibitors of prostate-specific membrane antigen (PSMA) as radiolabeled probes for targeting prostate cancer. J Med Chem. 2009;52: 347–357. pmid:19111054
  18. 18. Chen Y, Foss CA, Byun Y, Nimmagadda S, Pullambhatla M, Fox JJ, et al. Radiohalogenated prostate-specific membrane antigen (PSMA)-based ureas as imaging agents for prostate cancer. J Med Chem. 2008;51: 7933–7943. pmid:19053825
  19. 19. Shawn MH, Maresca KP, Femia FJ, Marquis JC, Foss CA, Nguyen N, et al. Preclinical evaluation of novel-glutamate-urea-lysine analogues that target prostate-specific membrane antigen as molecular imaging pharmaceuticals for prostate cancer. Cancer Res. 2009;69: 6932–6940. pmid:19706750
  20. 20. Banerjee SR, Foss CA, Castanares M, Mease RC, Byun Y, Fox JJ, et al. Synthesis and evaluation of technetium-99m and rhenium-labeled inhibitors of the prostate-specific membrane antigen (PSMA). J Med Chem. 2008;51: 4504–4517. pmid:18637669
  21. 21. Kularatne SA, Zhou Z, Yang J, Post CB, Low PS. Design, synthesis, and preclinical evaluation of prostate-spacific membrane antigen targeted 99mTc-radioimaging agents. Mol Pharm. 2009;6: 790–800. pmid:19361232
  22. 22. Vallabhajosula S, Nikolopoulou A, Babich JW, Osborne JR, Tagawa ST, Lipai I, et al. 99mTc-labeled small-molecule inhibitors of prostate-specific membrane antigen: pharmacokinetics and biodistribution studies in healthy subjects and patients with metastatic prostate cancer. J Nucl Med. 2015;55: 1791–1798.
  23. 23. Weineisen M, Simecek J, Schottelius M, Schwaiger M, Wester HJ. Synthesis and prelinical evaluation of DOTAGA-conjugated PSMA ligands for functiona limaging and endoradiotherapy of prostate cancer. EJNMMI Research. 2014;4: 63. pmid:26116124
  24. 24. Banerjee SR, Foss CA, Pullambhatla M, Wang Y, Srinivasan S, Hobbs RF, et al. Preclinical evaluation of 86Y-labeled inhibitors of prostate-specific membrane antigen for dosimetry estimates. J Nucl Med. 2015;56: 628–634. pmid:25722448
  25. 25. Eder M, Schäfer M, Bauder-Wüst U, Hull W- E, Wängler C, Mier W, et al. 68Ga-Complex lipophilicity and the targeting property of a urea based PSMA inhibitor for PET imaging. Bioconjugate Chem. 2012;23: 688–697.
  26. 26. Benešová M, Schäfer , Bauder-Wüst U, Afshar-Oromieh A, Kratochwil C, Mier W, et al. Preclinical evauation os a tailor-made DOTA-conjugated PSMA inhibitor with optimized linker moiety for imaging and endoradiotherapy of prostate-cancer. J Nucl Med. 2015;56: 914–920. pmid:25883127
  27. 27. Weineisen M, Schottelius M, Simecek J, Baum RP, Yildiz A, Beykan S, et al. 68Ga- and 177Lu-labeled PSMA I&T: optimization of a PSMA targeted theranostic concept and first proof of concept human studies. J Nucl Med. 2015;56: 1169–1176. pmid:26089548
  28. 28. Banerjee SR, Pullambhatla M, Byun Y, Nimmagadda S, Green G, Fox JJ, et al. 68Ga-labeled inhibitors of prostate-specific membrane antigen (PSMA) for imaging prostate cancer. J Med Chem. 2010;53: 5333–5341. pmid:20568777
  29. 29. Banerjee SR, Pullambhatla M, Foss CA, Nimmagadda S, Ferdani R, Anderson CJ, et al. 64Cu-labeled inhibitors of prostate-specific membrane antigen for PET imaging of prostate cancer. J Med Chem. 2014;57: 2657–2669. pmid:24533799
  30. 30. Beer AJ, Eiber M, Souvatzoglou M, Schwaiger M, Krause BJ. Radionuclide and hybrid imaging ofrecurrent prostate cancer. Lancet Oncol. 2011;12: 181–191. pmid:20599424
  31. 31. Silver DA, Pellicer I, Fair WR, Heston WD, Cordon-Cardo C. Prostate-specific membrane antigen expression in normal and malignant human tissues. Clin Cancer Res. 1997;3: 81–85. pmid:9815541
  32. 32. Afshar-Oromieh A, Avtzi E, Giesel FL, Holland-Letz T, Linhart HG, Eder M, et al. The diagnostic value of PET/CT imaging with the (68)Ga-labelled PSMA ligand HBED-CC in the diagnosis of recurrent prostate cancer. Eur J Nucl Med Mol Imaging. 2015;42: 197–209. pmid:25411132
  33. 33. Roesch F, Riss PJ. The renaissance of the 68Ge/68Ga radionuclide generator initiates new developments in 68Ga radiopharmaceutical chemistry. Curr Top Med Chem. 2010;10: 1633–1668. pmid:20583984
  34. 34. Anderson CJ, Ferdani R. Copper-64 radiopharmaceuticals for PET imaging of cancer: advances in preclinical and clinical research. Cancer Biother Radiphar Radiopharm. 2009;24: 379–393.
  35. 35. Craig AC, Helps IM, Parker D, Adams H, Bailey NA, Williams MG, et al. Crystal and molecular structure of a seven-coordinate chloroindium(III) comple of 1,4,7-triazacyclononanetriacetic acid. Polyhedron. 1989;20: 2481–2484.