- freely available
Appl. Sci. 2014, 4(1), 66-78; doi:10.3390/app4010066
Published: 17 March 2014
Abstract: Two α-synuclein ligands, 3-methoxy-7-nitro-10H-phenothiazine (2a, Ki = 32.1 ± 1.3 nM) and 3-(2-fluoroethoxy)-7-nitro-10H-phenothiazine (2b, Ki = 49.0 ± 4.9 nM), were radiolabeled as potential PET imaging agents by respectively introducing 11C and 18F. The syntheses of [11C]2a and [18F]2b were accomplished in a good yield with high specific activity. Ex vivo biodistribution studies in rats revealed that both [11C]2a and [18F]2b crossed the blood-brain barrier (BBB) and demonstrated good brain uptake 5 min post-injection. MicroPET imaging of [11C]2a in a non-human primate (NHP) confirmed that the tracer was able to cross the BBB with rapid washout kinetics from brain regions of a healthy macaque. The initial studies suggested that further structural optimization of [11C]2a and [18F]2b is necessary in order to identify a highly specific positron emission tomography (PET) radioligand for in vivo imaging of α-synuclein aggregation in the central nervous system (CNS).
Although Parkinson’s disease (PD) is a degenerative neurological disorder characterized by motor symptoms, it is also known to be closely associated with dementia . The primary neuropathologic change in PD, the degeneration of dopaminergic neurons, occurs in the substantia nigra, accompanied by Lewy bodies (LB) and Lewy neurites (LN). To date, the pathogenic mechanism of PD is not fully understood . The diagnosis of PD is primarily based on the clinical symptoms, such as resting tremor, bradykinesia and rigidity. Because the current treatment for PD is to minimize the disease symptoms in the patients [1,3], a method of diagnosing PD at a very early stage would greatly help physicians to design the therapy accordingly.
α-Synuclein (α-syn) is a presynaptic terminal protein that consists of 140 amino acids; the aggregation of α-syn is considered the pathological hallmark of PD. α-Syn plays an important role in the central nervous system (CNS) in synaptic vesicle recycling; it also regulates the synthesis, storage and release of neurotransmitters . It is specifically upregulated in a discrete population of presynaptic terminals of the brain during acquisition-related synaptic rearrangement . α-Syn naturally exists in a highly soluble, unfolded state [6,7]. However, in PD brains, insoluble aggregation of misfolded fibrillar α-syn occurs in LB and LN, which may cause synaptic dysfunction and neuronal cell death [8,9,10,11]. Positron emission tomography (PET) is a non-invasive imaging modality that can provide the functional information of a living subject at the molecular and cellular level. Current diagnostic PET radioligands for PD target either the dopaminergic system (pre-synaptic and post-synaptic dopamine activity) or vesicular monoamine transporter type 2 (VMAT2) [12,13]. Unfortunately, such imaging strategies have difficulty in distinguishing PD from other parkinsonian syndromes that also result in the degeneration of nigrostriatal projections [14,15]. In addition, dopaminergic medications used for symptomatic treatment may alter striatal uptake of these agents, limiting their reliability for measuring disease progression . In contrast, α-syn is a valuable imaging target for PD, because fibrillar α-syn deposition in LB and LN distinguishes PD from other disorders and is the defining feature for post-mortem pathologic diagnosis. Thus, a small molecular PET radiotracer with high affinity and selectivity to fibrillar α-syn protein could be used to quantify the level of α-syn aggregation non-invasively. This will not only improve the diagnostic accuracy of PD, but also provide a tool to improve the understanding of disease progression and monitor the therapeutic efficacy in clinical trials.
Our group previously reported the syntheses of a class of tricyclic analogues and their in vitro binding affinities towards α-syn fibrils; several lead compounds were identified with moderate affinities for α-syn fibrils (Ki < 70 nM) (Figure 1, 2a, 2b) . Compounds 2a and 2b also displayed favorable binding selectivity to α-synuclein aggregation compared to Aβ and tau protein: for 2a, Ki-α-syn/Ki-Aβ > 3-fold and Ki-α-syn/Ki-tau > 4-fold; for 2b, Ki-α-syn/Ki-Aβ = 2.1-fold and Ki-α-syn/Ki-tau = 2.5-fold . The radioiodinated ligand, [125I]1, was synthesized to establish a methodology for screening the α-syn fibril binding affinity of new ligands using a competition binding assay . The affinities for 2a and 2b were determined using this [125I]1 assay, and the resulting Ki values (66.2 nM for 2a, 19.9 nM for 2b) were in the same range as the values obtained by the Thioflavin T assay. The 125I competition assay further confirmed the previously determined in vitro potency of 2a and 2b, which were developed as potential PET radioligands to be radiolabeled by 11C or 18F. In the current manuscript, we report the radiosyntheses of [11C]2a and [18F]2b and their validation in animal studies to determine whether [11C]2a and [18F]2b can penetrate the blood-brain barrier (BBB), have sufficient brain uptake and fast washout from the brain. Results of ex vivo biodistribution of [11C]2a and [18F]2b in Sprague-Dawley rats and microPET CNS imaging in a cynomolgus macaque of [11C]2a suggest that further structure-activity relationship (SAR) study is necessary for identifying a highly specific PET radioligand targeting α-syn aggregation.
2. Experimental Section
All reagents and chemicals were purchased from Sigma-Aldrich Corporation (Milwaukee, WI, USA) and used without further purification, unless otherwise stated. The melting points of all intermediates and final compounds were determined on a Haake-Buchler melting point apparatus and are uncorrected. 1H and 13C NMR spectra were recorded on a Varian-400 MHz spectrometer (Varian Inc. Palo Alto, CA, USA), which is maintained by the Chemistry Department of Washington University in St. Louis, MO, USA. Spectra are referenced to the deuterium lock frequency of the spectrometer. The chemical shifts (in parts per million) of residual solvents were found to be at 7.26 for CHCl3 and at 2.50 for dimethyl sulfoxide (DMSO).
2.1.2. 1-(3-Methoxy-7-nitro-10H-phenothiazin-10-yl)ethanone (3)
Acetyl chloride (360 mg, 4.59 mmol) was added into the solution of Compound 2a (420 mg, 1.53 mmol) in dichloromethane (10 mL). The reaction mixture was stirred overnight at room temperature (rt). The solvent and excess acetyl chloride was removed under reduced pressure. The residue was dissolved in ethyl acetate and washed with water and saturated sodium chloride solution. The organic extract was dried over anhydrous Na2SO4 and purified by silica gel column chromatography using ethyl acetate/hexane (1/2, v/v) as the mobile phase to yield Compound 3 as a yellow solid (267 mg, 55%). 1H NMR (CDCl3): δ 2.23 (s, 3H), 3.83 (s, 3H), 6.90 (d, J = 9.0 Hz, 1H), 6.98 (s, 1H), 7.32 (d, J = 8.7 Hz, 1H), 7.72 (d, J = 8.7 Hz, 1H), 8.18 (d, J = 8.7 Hz, 1H), 8.29 (s, 1H). 13C NMR (CDCl3): δ 22.9, 55.7, 112.7, 114.0, 122.0, 122.9, 127.4, 127.9, 130.7, 133.2, 134.3, 144.7, 145.6, 158.5, 169.2. Combustion elemental analysis (anal.) calculated (calcd.) for C15H12N2O4S: C, 56.95; H, 3.82; N, 8.86. Found: C, 56.72; H, 3.89; N, 8.70. mp 155.9–156.8 °C.
2.1.3. 1-(3-Hydroxy-7-nitro-10H-phenothiazin-10-yl)ethanone (4)
A solution of BBr3 in dichloromethane (1.0 M, 4.2 mL) was added dropwise to a solution of Compound 3 (267.3 mg, 0.84 mmol) in dichloromethane (15 mL) at −78 °C. The reaction solution was stirred overnight at rt. The solvent was removed under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic extract was dried over anhydrous Na2SO4 and purified by silica gel column chromatography using ethyl acetate/CH2Cl2 (1/10, v/v) as the mobile phase to yield Compound 4 as a yellow solid (207.4 mg, 81%). 1H NMR (DMSO-d6): δ 2.15 (s, 3H), 6.82 (d, J = 9.0 Hz, 1H), 6.93 (s, 1H), 7.47 (d, J = 9.0 Hz, 1H), 7.82 (d, J = 9.0 Hz, 1H), 8.22 (d, J = 9.0 Hz, 1H), 8.39 (s, 1H), 10.00 (br s, 1H). 13C NMR (DMSO-d6): δ 23.0, 114.3, 115.3, 122.6, 123.2, 128.4, 128.5, 129.3, 132.3, 134.2, 145.1, 145.6, 156.7, 169.1. High resolution mass spectrometry (HRMS, ESI): m/z calcd. for C14H10N2O4S [M + 1] 303.0440. Found: 303.0435. Purity: 98% (HPLC confirmed). mp 202.3–205.1 °C.
2.2.1. Radiosynthesis of [11C]2a
18.104.22.168. Production of [11C]CH3I
Briefly, [11C]CH3I was produced from [11C]CO2 using a GE PETtrace MeI Microlab (GE Healthcare, Fairfield, CT, USA). Up to 51.8 GBq of [11C]CO2 is produced from Washington University’s Japan Steel Works BC-16/8 cyclotron by irradiating a gas target of 0.2% O2 in N2 for 15–30 min with a 40 µA beam of 16 MeV protons. The GE PETtrace MeI Microlab coverts the [11C]CO2 to [11C]CH4 using a nickel catalyst (Shimalite-Ni, Shimadzu, Japan P.N.221-27719) in the presence of hydrogen gas at 360 °C; it is further converted to [11C]CH3I by reacting with iodine held in a column in the gas phase at 690 °C. Approximately 12 min after the end of bombardment (EOB), several hundred millicuries of [11C]CH3I was delivered as a gas to the hot cell, where the radiosynthesis was accomplished.
22.214.171.124. Radiosynthesis of [11C]2a
Approximately 1.2 mg of Precursor 4 was placed in the reaction vessel, and 0.20 mL of DMF was added, followed by 3.0 µL of 5 N NaOH. The mixture was thoroughly mixed on a vortex for 30 s. A stream of [11C]CH3I in helium was bubbled for 3 min into the reaction vessel. The sealed vessel was heated at 90 °C for 5 min, at which point the vessel was removed from heat and 20 µL 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in 50 µL DMF was added via syringe. The reaction mixture was heated at 90 °C for 7 min (Scheme 2); then, the reaction was quenched by adding 1.7 mL of the HPLC mobile phase, which was composed of acetonitrile/0.1 M ammonium formate buffer (60/40, v/v) and pH = 4.5. The diluted solution was purified by high performance liquid chromatography (HPLC) by injection on a Phenomenex Luna C18 reverse phase column (9.4 × 250 mm) using the mobile phase described above. The radiolabeled product was eluted using a flow rate of 4.0 mL/min, and the UV wavelength was set as 254 nm. Under these conditions, the retention time of Precursor 4 was ~7 min; the retention time of [11C]2a was ~16 min. [11C]2a was collected in a vial containing 50 mL Milli-Q water, which was then passed through a Sep-Pak Plus C18 cartridge (Waters, Milford, MA, USA). The trapped product was eluted with ethanol (0.6 mL) followed by 5.4 mL 0.9% saline. After sterile filtration, the final product was ready for quality control (QC) analysis and animal studies. QC was performed on a Phenomenex Prodigy C18 reverse phase analytic HPLC column (250 mm × 4.6 mm, 5 µA) and UV detection at a 254 nm wavelength. The mobile phase was acetonitrile/0.1 M ammonium formate buffer (80/20, v/v) using a 1.5 mL/min flow rate. Under these conditions, the retention time of [11C]2a was 4.82 min. The radioactive dose was authenticated by co-injection with the cold standard Compound 2a. Radiochemical purity was >99%; the chemical purity was >95%; the labeling yield was 35%–45% (n = 4, decay corrected to EOB), and the specific activity was >363 GBq/µmol (decay corrected to EOB, n = 4).
2.2.2. Radiosynthesis of [18F]2b
126.96.36.199. Production of [18F]fluoride
[18F]Fluoride is produced by a 18O(p, n)18F reaction through proton irradiation of enriched 18O water (95%) using Washington University’s RDS-111 cyclotron (Siemens/CTI Molecular Imaging, Knoxville, TN, USA). [18F]Fluoride is first passed through an ion-exchange resin and then eluted with 0.02 M potassium carbonate (K2CO3) solution.
A sample of approximately 5.55 GBq [18F]/fluoride was added to a reaction vessel containing Kryptofix 222 (6.5–7.0 mg). The syringe was washed with 2 × 0.4 mL of ethanol. The resulting solution was evaporated under nitrogen flow with a bath temperature of 110 °C. Acetonitrile (3 × 1.0 mL) was added to the mixture, and water was azeotropically removed by evaporation. After all the water was removed, 5.0–5.5 mg of 1,2-ethylene ditosylate was dissolved in acetonitrile (200 μL), and the solution was transferred into the reaction vessel containing [18F]fluoride/Kryptofix 222/K2CO3. The reaction vessel was capped and the reaction mixture briefly mixed and then subjected to heating in an oil bath that was preheated to 110 °C for 10 min (Scheme 2).
After heating for 10 min, the reaction mixture was diluted with 3.0 mL of the HPLC mobile phase (50/50 acetonitrile/0.1 M ammonium formate buffer, pH = 6.5) and passed through an alumina neutral Sep-Pak Plus cartridge (Waters Corporation, Milford, MA, USA). The crude product was then loaded onto an Agilent SB-C18 semi-preparative HPLC column (250 mm × 10 mm) with a UV detector set at 254 nm. The HPLC system used a 5 mL injection loop. At a 4.0 mL/min flow rate, the retention time of the product was 9.5–10 min. The retention time of the precursor was 23–24 min. The radioactivity peak observed on HPLC was collected and diluted with 50 mL sterile water and the diluted collection went through a C-18 Sep-Pak Plus cartridge to trap the 2-[18F]fluoroethyl tosylate on the Sep-Pak. The trapped product was eluted with diethyl ether (2.5 mL).
188.8.131.52. Radiosynthesis of [18F]2b
The eluted solution formed two phases: the top ether phase was transferred out, and the bottom aqueous phase was extracted with another 1-mL aliquot of ether. The combined ether extracts were passed through a set of two sodium sulfate Sep-Pak Plus dry cartridges into a reaction vessel. After ether was evaporated with a nitrogen stream at 25 °C, 1.0 mg of Precursor 4 was dissolved in 200 µL DMSO and was transferred to a vial containing 1–2 mg Cs2CO3. After vortexing for 1 min, the Cs2CO3 saturated solution was added to the reaction vessel containing the dried radioactive [18F]/F−. The tube was capped and briefly vortexed and then kept at 90 °C for 15 min. Ten microliters of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in 50 µL DMSO was added via syringe. The reaction mixture was heated at 90 °C for 15 min. The mixture was subsequently diluted with 3 mL of the HPLC mobile phase (50/50 acetonitrile/0.1 M formate buffer, pH = 4.5) and purified using a Semi-Prep HPLC system for purification. The HPLC system contains a 5-mL injection loop, an Agilent SB C-18 column, a UV detector at 254 nm and a radioactivity detector. At a 4.0 mL/min flow rate, the retention time of the product was 19–21 min, whereas the retention time of the precursor was 8–9 min. After the HPLC collection and being diluted with 50 mL sterile water, the product was trapped on a C18 Sep-Pak Plus cartridge. The product was eluted with ethanol (0.6 mL) followed by 5.4 mL 0.9% saline. After sterile filtration, the final product was ready for quality control (QC) analysis and animal studies. An aliquot was assayed by analytical HPLC (Grace Altima C18 column, 250 × 4.6 mm), UV at 276 nm, mobile phase of acetonitrile/0.1 M ammonium formate buffer (71/29, v/v), pH = 4.5. Under these conditions, the retention time for [18F]2b was approximately 4.9 min at a flow rate of 1.5 mL/min. The sample was authenticated by co-injecting with the cold standard 2b solution. The radiochemical purity was >98%; the chemical purity was >95%; the labeling yield was 55%–65% (n = 4, decay corrected), and the specific activity was >200 GBq/µmol (decay corrected to EOB, n = 4).
2.3. Biodistribution Studies
All animal experiments were conducted in compliance with the Guidelines for the Care and Use of Research Animals under protocols approved by Washington University’s Animal Studies Committee. For the biodistribution studies, 11.1–13.0 MBq of [11C]2a in 200–250 µL or 1.67–1.85 MBq of [18F]2b in 200–250 µL of saline containing 10% ethanol was injected via the tail vein into mature male Sprague-Dawley rats (175–240 g) under 2%–3% isoflurane/oxygen anesthesia. Group of rats (n = 4) were used for each time point. At 5, 30, 60 min (and 120 min for [18F]2b) post injection, the rats were anesthetized and euthanized. The whole brain was quickly removed and dissected into segments consisting of brain stem, thalamus, striatum, hippocampus, cortex and cerebellum. The remainder of the brain was also collected to determine total brain uptake. At the same time, samples of blood, heart, lung, muscle, fat, pancreas, spleen, kidney, liver (and bone for [18F]2b) were removed and counted in a Beckman Gamma 8000 well counter with a standard dilution of the injectate. Tissues were weighed, and the percent injected dose (%ID)/gram for each tissue was calculated.
2.4. MicroPET Brain Imaging Studies of [11C]2a in Cynomolgus Macaque
Following the initial evaluation in rats, the washout kinetics and ability of [11C]2a to cross the blood-brain barrier in a non-human primate (NHP) was determined on an adult male cynomolgus macaque (6−8 kg) using a microPET Focus 220 scanner (Concorde/CTI/Siemens Microsystems, Knoxville, TN). Before each scan (n = 2), the animal was fasted for 12 h and then initially anesthetized with ketamine (10 mg/kg) and glycopyrrolate (0.13 mg/kg) intramuscularly. Upon arrival at the scanner, the monkey was intubated, and a percutaneous catheter placed for tracer injection. The head was positioned supine in the adjustable head holder with the brain in the center of the field of view. Anesthesia was maintained at 0.75%−2.0% isoflurane/oxygen and the core temperature maintained at 37 °C. A 10-min transmission scan was performed to confirm positioning; this was followed by a 45-min transmission scan for attenuation correction. Subsequently, a 2-h dynamic emission scan was acquired after venous injection of 300−370 MBq of [11C]2a.
3. Results and Discussions
Compounds 2a and 2b possess a methoxy and fluoroethoxy group, respectively, enabling radiolabeling through O-alkylation of the corresponding phenol precursor. However, to avoid undesired N-alkylation product, the acetyl protected Compound 4 was used as the precursor for the radiosyntheses. As shown in Scheme 1, the synthesis of 4 was accomplished by a two-step strategy starting from 2a following our previous procedure . N-acetylation of 2a was achieved using acetyl chloride. Removing the O-methyl group of 3 with boron tribromide afforded the phenol Precursor 4, which was used in the radiosyntheses of 2a and 2b. Due to the reaction scale difference, the yields for certain reactions differ slightly from our previous report.
The radiosynthesis of [11C]2a was accomplished by a two-step approach. The reaction of the phenol Precursor 4 with [11C]CH3I was performed in DMF in the presence of NaOH [19,20,21], and the N-acetyl group of the 11C-labeled intermediate was removed by DBU following the literature procedure , as outlined in Scheme 2. [11C]2a was obtained in approximately 35%–45% overall radiochemical yield (RCY) after HPLC purification (n = 4). The radiochemical purity of [11C]2a was >99% and chemical purity was >95%. [11C]2a was identified by co-eluting with the solution of standard 2a. The entire synthetic procedure, including the production of [11C]CH3I, radiosynthesis, HPLC purification and formulation of the radiotracer for animal studies, was completed within 50–60 min. [11C]2a was obtained in a specific activity of >363 GBq/µmol at EOB (n = 4).
The radiosynthesis of [18F]2b was achieved using a three-step reaction. The radioactive intermediate, [18F]fluoroethyltosylate ([18F]FEOTs), was first synthesized through a typical fluorination of the di-tosylate substrate [23,24,25,26,27]. Treatment of ethylene glycol ditosylate using [18F]fluoride, potassium carbonate and Kryptofix 222 gave [18F]FEOTs in good yield (60%–70%, decay corrected) after HPLC purification. The intermediate was reacted with the precursor, followed by DBU hydrolysis to afford a sufficient dose of [18F]2b with the labeling yield of 55%–65% after HPLC purification (n = 4, decay corrected to EOB). The radiochemical purity of [18F]2b was >98%, and the chemical purity was >95%. [18F]2b was identified by co-eluting with the solution of standard 2b. The entire synthetic procedure, including the drying of [18F]F−, the radiosynthesis, HPLC purification and formulation of the radiotracer for in vivo studies, was completed in 3 h. Radiotracer [18F]2b was obtained in a specific activity of >200 GBq/µmol (decay corrected to EOB, n = 4).
|Table 1. Biodistribution of [11C]2a and [18F]2b in male Sprague-Dawley rats (%ID/gram).|
|Radioligand||Organ||5 min||30 min||60 min||120 min|
|[11C]2a||blood||0.506 ± 0.040||0.369 ± 0.031||0.300 ± 0.015|
|heart||0.758 ± 0.052||0.377 ± 0.046||0.245 ± 0.010|
|lung||1.149 ± 0.058||0.740 ± 0.038||0.485 ± 0.036|
|muscle||0.271 ± 0.005||0.325 ± 0.030||0.199 ± 0.016|
|fat||0.155 ± 0.023||0.241 ± 0.042||0.293 ± 0.076|
|pancreas||1.007 ± 0.262||0.506 ± 0.066||0.522 ± 0.036|
|spleen||0.659 ± 0.049||0.400 ± 0.052||0.386 ± 0.027|
|kidney||1.362 ± 0.054||0.807 ± 0.086||0.559 ± 0.053|
|liver||2.198 ± 0.111||1.349 ± 0.116||1.116 ± 0.024|
|brain||0.953 ± 0.115||0.287 ± 0.046||0.158 ± 0.013|
|[18F]2b||blood||0.553 ± 0.047||0.589 ± 0.016||0.606 ± 0.035||0.585 ± 0.046|
|heart||0.757 ± 0.033||0.505 ± 0.015||0.466 ± 0.040||0.410 ± 0.030|
|lung||0.833 ± 0.053||0.561 ± 0.021||0.491 ± 0.030||0.436 ± 0.018|
|muscle||0.430 ± 0.031||0.451 ± 0.018||0.376 ± 0.019||0.315 ± 0.015|
|fat||0.255 ± 0.037||0.425 ± 0.023||0.371 ± 0.067||0.293 ± 0.048|
|pancreas||1.004 ± 0.147||0.546 ± 0.068||0.409 ± 0.029||0.330 ± 0.021|
|spleen||0.672 ± 0.064||0.509 ± 0.022||0.446 ± 0.038||0.398 ± 0.019|
|kidney||1.070 ± 0.058||0.988 ± 0.090||0.678 ± 0.032||0.659 ± 0.027|
|liver||1.626 ± 0.221||0.847 ± 0.027||0.561 ± 0.028||0.467 ± 0.023|
|bone||0.340 ± 0.027||0.309 ± 0.020||0.407 ± 0.043||0.644 ± 0.071|
|brain||0.758 ± 0.013||0.465 ± 0.018||0.410 ± 0.030||0.359 ± 0.016|
3.3. Biodistribution in Rats
The radioactivity distribution in various organs after the injection of [11C]2a and [18F]2b in rats is summarized in Table 1. Both radiotracers displayed homogeneous distribution in the brain regions as shown in Figure 2A,B. For [11C]2a, the total brain uptake (%ID/gram) of radioactivity at five, 30 and 60 min post injection were 0.953 ± 0.115, 0.287 ± 0.046 and 0.158 ± 0.014 respectively; in the peripheral tissues, liver had the highest uptake among the tissues analyzed; the uptake (%ID/gram) in liver reached 2.198 ± 0.111 at 5 min and 1.116 ± 0.024 at 60 min. For [18F]2b, the total brain uptake (%ID/gram) at five, 30, 60 and 120 min was 0.758 ± 0.013, 0.465 ± 0.018, 0.410 ± 0.030 and 0.359 ± 0.016, respectively; At 5 min post-injection, this compound also has a high liver uptake: (%ID/gram) of 1.626 ± 0.221. However, after 30 min, the kidney has retained the highest radioactivity of all tissues that were analyzed. The bone uptake (%ID/gram) was very stable and no defluorination was observed for [18F]2b. More importantly, the ex vivo rat biodistribution data revealed that both compounds readily crossed the BBB and entered the brain. Both tracers exhibit high initial brain uptake and appropriate washout kinetics in the brain of normal rats. Rapid clearance of the radioactivity for both [11C]2a and [18F]2b was observed from brain, as well as other organs, such as lung, pancreas, spleen, kidney and liver. However, [11C]2a showed faster wash-out kinetics than [18F]2b, as shown in Figure 2. [11C]2a was chosen for subsequent microPET evaluation in an NHP.
3.4. MicroPET Studies in NHP
The representative summed images from zero to 120 min were co-registered with MRI images to accurately identify the regions of interest (Figure 3). The time-activity curve (TAC) revealed high initial uptake of [11C]2a in the brain, which peaked at 3 min post-injection; then, the radioactivity was quickly washed out from all brain regions. The summed image revealed a homogeneous distribution of radioactivity in the brain of the normal cynomolgus macaque. The microPET studies suggested that [11C]2a was able to cross the BBB and had a fast washout kinetics from the brain regions. The macaque used in the studies was a healthy young adult, and the distribution of the α-syn radioligand throughout the brain regions was homogeneous. Higher expression of α-syn protein in particular regions should not be observed in healthy subjects; thus, homogeneous distribution of the radioactivity in the macaque brain was expected. Nevertheless, PET studies of [11C]2a performed on an NHP model bearing the over-expression of α-syn aggregation will directly determine the in vivo specificity of the radiotracer.
In summary, two α-syn ligands, [11C]2a and [18F]2b, were successfully radiosynthesized by O-alkylation of the desalkyl precursor. The biodistribution studies of [11C]2a and [18F]2b were conducted in male Sprague-Dawley rats and showed that both tracers were able to cross the BBB with high initial uptake. At 5 min post-injection, the uptake (%ID/gram) reached 0.953 ± 0.115 for [11C]2a and 0.758 ± 0.013 for [18F]2b. Both [11C]2a and [18F]2b displayed a homogeneous distribution throughout the brain of healthy adult male rats with rapid washout kinetics. In vivo microPET imaging in a healthy cynomolgus macaque confirmed that [11C]2a was able to enter the brain, had homogeneous distribution and rapid washout kinetics. Further structural optimization of [11C]2a and [18F]2b may lead to a highly specific radioligand for imaging α-syn aggregation in vivo.
|CNS||central nervous system|
|EOB||end of bombardment|
|HPLC||high performance liquid chromatography|
|HRMS||high resolution mass spectrometry|
|PET||positron emission tomography|
|SUV||standardized uptake value|
|VMAT2||vesicular monoamine transporter type 2|
Financial support for these studies was provided by the National Institutes of Health under grants NS061025, NS075527, MH092797 and Barnes-Jewish Hospital Foundation/Washington University Institute of Clinical and Translational Sciences. Michael J. Fox Foundation grant supporting a Consortium to Develop an α-Synuclein Imaging Agent. Mass spectrometry was provided by the Washington University Mass Spectrometry Resource, a National Institute of Health Research Resource (grant P41RR0954). The authors gratefully thank Lynne A. Jones, William H. Margenau and Robert Dennett for their excellent assistance, as well as Joel S. Perlmutter’s research group for their assistance with the NHP microPET studies.
Conflicts of Interest
The authors declare no conflict of interest.
- Hely, M.A.; Reid, W.G.J.; Adena, M.A.; Halliday, G.M.; Morris, J.G.L. The sydney multicenter study of parkinson’s disease: The inevitability of dementia at 20 years. Mov. Disord. 2008, 23, 837–844, doi:10.1002/mds.21956.
- Hurtig, H.I.; Trojanowski, J.Q.; Galvin, J.; Ewbank, D.; Schmidt, M.L.; Lee, V.M.-Y.; Clark, C.M.; Glosser, G.; Stern, M.B.; Gollomp, S.M.; et al. Alpha-synuclein cortical lewy bodies correlate with dementia in Parkinson’s disease. Neurology 2000, 54, 1916–1921, doi:10.1212/WNL.54.10.1916.
- Jankovic, J. Parkinson’s disease: Clinical features and diagnosis. J. Neurol. Neurosurg. Psychiatry 2008, 79, 368–376, doi:10.1136/jnnp.2007.131045.
- Cheng, F.; Vivacqua, G.; Yu, S. The role of alpha-synuclein in neurotransmission and synaptic plasticity. J. Chem. Neuroanat. 2011, 42, 242–248, doi:10.1016/j.jchemneu.2010.12.001.
- George, J.M.; Jin, H.; Woods, W.S.; Clayton, D.F. Characterization of a novel protein regulated during the critical period for song learning in the zebra finch. Neuron 1995, 15, 361–372, doi:10.1016/0896-6273(95)90040-3.
- Clayton, D.F.; George, J.M. The synucleins: A family of proteins involved in synaptic function, plasticity, neurodegeneration and disease. Trends Neurosci. 1998, 21, 249–254, doi:10.1016/S0166-2236(97)01213-7.
- Uéda, K.; Fukushima, H.; Masliah, E.; Xia, Y.; Iwai, A.; Yoshimoto, M.; Otero, D.A.; Kondo, J.; Ihara, Y.; Saitoh, T. Molecular cloning of cdna encoding an unrecognized component of amyloid in alzheimer disease. Proc. Natl. Acad. Sci. USA 1993, 90, 11282–11286, doi:10.1073/pnas.90.23.11282.
- Kazantsev Ag, K.A.M. Central role of α-synuclein oligomers in neurodegeneration in Parkinson disease. Arch. Neurol. 2008, 65, 1577–1581.
- Bate, C.; Gentleman, S.; Williams, A. Alpha-synuclein induced synapse damage is enhanced by amyloid-beta1–42. Mol. Neurodegener. 2010, 5, 55, doi:10.1186/1750-1326-5-55.
- Lee, V.M.Y.; Trojanowski, J.Q. Mechanisms of Parkinson’s disease linked to pathological α-synuclein: New targets for drug discovery. Neuron 2006, 52, 33–38, doi:10.1016/j.neuron.2006.09.026.
- Kramer, M.L.; Schulz-Schaeffer, W.J. Presynaptic α-synuclein aggregates, not lewy bodies, cause neurodegeneration in dementia with lewy bodies. J. Neurosci. 2007, 27, 1405–1410, doi:10.1523/JNEUROSCI.4564-06.2007.
- Ishiwata, K.; Kimura, Y.; Oda, K.; Ishii, K.; Sakata, M.; Kawasaki, K.; Nariai, T.; Suzuki, Y.; Ishibashi, K.; Mishina, M.; et al. Development of pet radiopharmaceuticals and their clinical applications at the positron medical center. Geriatr. Gerontol. Int. 2010, 10, S180–S196.
- Chen, M.-K.; Kuwabara, H.; Zhou, Y.; Adams, R.J.; Brašić, J.R.; McGlothan, J.L.; Verina, T.; Burton, N.C.; Alexander, M.; Kumar, A.; et al. VMAT2 and dopamine neuron loss in a primate model of Parkinson’s disease. J. Neurochem. 2008, 105, 78–90, doi:10.1111/j.1471-4159.2007.05108.x.
- De la Fuente-Fernández, R. Role of datscan and clinical diagnosis in Parkinson disease. Neurology 2012, 78, 696–701, doi:10.1212/WNL.0b013e318248e520.
- Perlmutter, J.S.; Eidelberg, D. To scan or not to scan: Dat is the question. Neurology 2012, 78, 688–689, doi:10.1212/WNL.0b013e3182494c72.
- Winogrodzka, A.; Wagenaar, R.C.; Booij, J.; Wolters, E.C. Rigidity and bradykinesia reduce interlimb coordination in parkinsonian gait. Arch. Phys. Med. Rehabil. 2005, 86, 183–189, doi:10.1016/j.apmr.2004.09.010.
- Yu, L.; Cui, J.; Padakanti, P.K.; Engel, L.; Bagchi, D.P.; Kotzbauer, P.T.; Tu, Z. Synthesis and in vitro evaluation of α-synuclein ligands. Bioorg. Med. Chem. 2012, 20, 4625–4634, doi:10.1016/j.bmc.2012.06.023.
- Bagchi, D.P.; Yu, L.; Perlmutter, J.S.; Xu, J.; Mach, R.H.; Tu, Z.; Kotzbauer, P.T. Binding of the radioligand SIL23 to α-synuclein fibrils in Parkinson disease brain tissue establishes feasibility and screening approaches for developing a parkinson disease imaging agent. PLoS One 2013, 8.
- Tu, Z.; Fan, J.; Li, S.; Jones, L.A.; Cui, J.; Padakanti, P.K.; Xu, J.; Zeng, D.; Shoghi, K.I.; Perlmutter, J.S.; et al. Radiosynthesis and in vivo evaluation of [11C]MP-10 as a pet probe for imaging PDE10A in rodent and non-human primate brain. Biorg. Med. Chem. 2011, 19, 1666–1673.
- Tu, Z.; Xu, J.; Jones, L.A.; Li, S.; Mach, R.H. Carbon-11 labeled papaverine as a pet tracer for imaging PDE10A: Radiosynthesis, in vitro and in vivo evaluation. Nucl. Med. Biol. 2010, 37, 509–516, doi:10.1016/j.nucmedbio.2009.12.012.
- Kuhnast, B.; Bodenstein, C.; Wester, H.J.; Weber, W. Carbon-11 labelling of an n-sulfonylamino acid derivative: A potential tracer for mmp-2 and mmp-9 imaging. J. Labelled Compd. Radiopharm. 2003, 46, 539–553, doi:10.1002/jlcr.695.
- Chakrabarty, M.; Ghosh, N.; Khasnobis, S.; Chakrabarty, M. Dbu, a highly efficient reagent for the facile regeneration of (hetero)arylamines from their acetamides and benzamides: Influence of solvent, temperature, and microwave irradiation. Synth. Commun. 2002, 32, 265–272, doi:10.1081/SCC-120002011.
- Prabhakaran, J.; Arango, V.; Majo, V.J.; Simpson, N.R.; Kassir, S.A.; Underwood, M.D.; Polavarapu, H.; Bruce, J.N.; Canoll, P.; John Mann, J.; et al. Synthesis and in vitro evaluation of [18F](r)-FEPAQ: A potential pet ligand for VEGFR2. Bioorg. Med. Chem. Lett. 2012, 22, 5104–5107.
- Bauman, A.; Piel, M.; Schirrmacher, R.; Rosch, F. Efficient alkali iodide promoted F-18-fluoroethylations with 2-[F-18]fluoroethyl tosylate and 1-bromo-2-[F-18]fluoroethane. Tetrahedron Lett. 2003, 44, 9165–9167, doi:10.1016/j.tetlet.2003.10.034.
- Block, D.; Coenen, H.H.; Stöcklin, G. The n.C.A. Nucleophilic 18F-fluorination of 1,n-disubstituted alkanes as fluoroalkylation agents. J. Labelled Compd. Radiopharm. 1987, 24, 1029–1042, doi:10.1002/jlcr.2580240904.
- Wester, H.J.; Herz, M.; Weber, W.; Heiss, P.; Senekowitsch-Schmidtke, R.; Schwaiger, M.; Stocklin, G. Synthesis and radiopharmacology of O-(2-[F-18]fluoroethyl)-l-tyrosine for tumor imaging. J. Nucl. Med. 1999, 40, 205–212.
- Block, D.; Coenen, H.H.; Stöcklin, G. N.C.A. 18F-fluoroalkylation of h-acidic compounds. J. Labelled Compd. Radiopharm. 1988, 25, 201–216, doi:10.1002/jlcr.2580250211.
© 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).