Introduction

Within the past decades, magnetic resonance imaging (MRI) has become an indispensable tool for medical diagnostics. Because of its low sensitivity, however, the only nucleus used in clinical routine is hydrogen (1H), which is the most abundant element in vivo (∼80 M) and holds the greatest gyromagnetic ratio of all stable nuclei (42 × 2π MHz T−1). But even for 1H, the polarization, which is the fraction of all spins contributing to the MR signal, does not exceed 3 p.p.m. in a magnetic field of 1 T. All other stable nuclei have a lower polarization and much lower abundance in vivo.

Still, the need for a non-invasive tool for chemical analysis in vivo, for example to measure the metabolism and treatment response of tumors1, is great. It appears that this need is precisely met by magnetic resonance (MR) spectroscopy, which is very successful for chemical analysis in vitro. However, low sensitivity makes its use in clinical routines very limited2. Nuclear hyperpolarization (HP) promises to overcome this hurdle and has enabled MR signal enhancement by several orders of magnitude3. The MR signal of most X-nuclei (nuclei other than protons) in vivo is low and thus both distribution and metabolism of magnetically labelled or hyperpolarized X-nuclei can be observed without significant background, similar to positron emission tomography. The first human studies of this method have shown very promising results4,5 and more are underway.

The most prominent techniques for the production of hyperpolarized 13C-tracers are dissolution dynamic nuclear polarization (dDNP)6 and parahydrogen (pH2) and synthesis allows dramatically enhanced nuclear alignment (PASADENA)7, also known as pH2-induced polarization (PHIP)8. dDNP achieves liquid-state polarization by transferring polarization from electrons to nuclei in the solid state at a temperature of a few K and in a strong magnetic field of a few T, followed by rapid dissolution. PHIP, in contrast, is the only technique to date that allows polarization to take place in the liquid state, either by hydrogenation7 or reversible exchange with pH2 (ref. 9). While dDNP is the only technique commercially available and used for human applications, it is associated with rather high cost, a relatively low output and long polarization cycles, although many promising attempts are being pursued to overcome these shortcomings10,11,12. PHIP, in contrast, is more cost efficient, very fast and requires less hardware. A hitherto substantial drawback of this technique—its limited portfolio of tracers—may have been overcome by the discovery of new agents13,14,15 and side-arm hydrogenation PHIP (PHIP-SAH), which has enabled the polarization of acetate and pyruvate16. Both methods share the disadvantage that the HP-tracer has to be produced in a dedicated polarizing device (polarizer) outside of the MRI system3,6,17,18,19,20,21,22,23,24,25,26,27,28,29. During the ensuing transfer through varying magnetic fields to the application site, inevitably, some of the polarization is lost to the T1 decay towards thermal equilibrium.

Here, we present a new method that achieves 13C-HP in excess of 20% in aqueous solution within seconds in the bore of a commercial MRI system. No external polarizer is needed—the only items that are required, in addition to an MRI scanner, are pH2, a reaction chamber, some valves and a digital output to control the process. By Synthesis Amid the Magnet Bore, A Dramatically Enhanced Nuclear Alignment (SAMBADENA) is obtained. By producing a sterile HP-tracer in situ, within the bore of an MRI, at the application site and at high field, this new method addresses some of the aforementioned shortcomings of dDNP and PHIP.

Results

SAMBADENA produces high and reproducible in-bore 13C-HP

A maximum theoretical polarization yield of 48.7% was simulated for 1-13C hydroxyenthyl-propionate (HEP), a tracer that was previously used for in vivo angiography2730. The corresponding evolution intervals for the spin-order-transfer (SOT) sequence l-PH-INEPT+ (longitudinal-para-hydrogen-insensitive nuclei enhancement by polarization transfer) were t1=69.8 ms and t2=38.9 ms (total 108.7 ms). Several other polarization maxima were found but required longer evolution intervals (Fig. 1). The polarization yield was found to be relatively stable with respect to errors of J-couplings, pulses and evolution times (Fig. 1).

Figure 1: Simulated stability and intervals of l-PHINEPT for SAMBADENA.
figure 1

The resulting polarization of the SOT sequence l-PH-INEPT+ (longitudinal-parahydrogen-insensitive nuclei enhancement by polarization transfer) was simulated as function of erroneous J-couplings and flip angles (a) and as function of the evolution intervals (b). J represents the J-couplings of the simplified 3-spin-½ system of the tracer and α represents the flip angle of the pulses of the sequence; both values were varied by±15%. The values of t1 and t2 denote the free evolution intervals between the effective pulses of the SOT sequence (see Fig. 8).

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Experimentally, HP was produced within an MRI system by using the available hardware of the system itself (Fig. 2). The signal that was directly produced by the PH-INEPT+ sequence was quantified and corresponded to a nuclear polarization of P=24%, approximately half of the theoretical maximum. This polarization level corresponds to an enhancement factor of η≈40,000 for 13C at 7 T (hydrogenation time th=4s, 5.54 mM HEP in H2O; Fig. 3).

Figure 2: HP without a polarizer:
figure 2

Schematic view of the experimental setup, where the HP-tracer is produced in situ within the MRI close to the application site. The essential components comprise the reaction chamber, valves, tubing, pH2 and the MRI system. The latter is used to transfer the spin order and to detect the hyperpolarized signal.

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Figure 3: 13C-HP generated inside an MRI system.
figure 3

Non-localized 13C-spectra of thermally polarized acetone at natural abundance (red) and 13C-HEP in aqueous solution (black) hyperpolarized by SAMBADENA within an MRI system. The polarization yield was quantified to ∼24%, which corresponds to a ∼40,000-fold enhancement of the thermal 13C-polarization which amounts to∼6 p.p.m. at 7 T.

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The inter-day yield and reproducibility of SAMBADENA was quantified in nine experiments to P≈(21±2) % with 5.54 mM HEP in H2O (Fig. 4).

Figure 4: SAMBADENA reproducibility:
figure 4

A mean polarization of P=(21±2) % was achieved in nine experiments on 2 days. Error bars correspond to the s.d. of the respective day or, in case of the mean, all experiments (reaction temperature T≈80 °C, hydrogenation time th=4 s, concentration of substrate cHEP=5.54 mM).

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Production of longitudinal hyperpolarization by l-PH-INEPT+

While a polarization of the order of few per cent is sufficient for biomedical use3,31, the short-lived transversal polarization generated by the PH-INEPT+ sequence is not suited for in vivo application—longitudinal magnetization is required instead. As predicted by Bär et al.32, the l-PH-INEPT+ sequence enabled the production of longitudinal magnetization hyperpolarized to a similar level, P=(19±2) % (detected 2 s after generation, for 5.54 mM HEP in D2O) (Fig. 5). This magnetization decayed much slower with T1 (instead of T2) and enabled other experiments as described in the following.

Figure 5: The lifetime of the polarization is long at high field.
figure 5

The decay of one sample of hyperpolarized 13C-HEP was monitored by acquiring 12 non-localized spectra with a repetition time of TR=15 s and a small flip angle of 9° (squares). A mono-exponential decay function (line) was fitted to the data and yielded T1∼(79±2) s. A correction factor—described in the methods—was applied to each data point to compensate for the fact that each measurement pulse consumes a finite amount of the magnetization. The T1 determined from the low flip angle measurement correlates well to the polarizations that were detected by full, 90° excitations 0, 20 and 120 s after the HP. For each time point, the mean of three measurements (bars) is shown, and error bars indicate the s.d. The tracer concentration was 5.54 mM in D2O.

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SAMBADENA enables magnetization storage at high field

The T1 of HEP dissolved in D2O was measured to (79±2) s at 7 T (Fig. 5), which is more than the 70 s reported at 4.7 T (ref. 26). In degassed and deionized H2O, the T1 of HEP at 7 T was measured to (75±5) s, which is less than (101±7) s reported at 48 mT (ref. 19). These long relaxation times are advantageous with respect of the further use of the tracer. If, for example, 20 s were to be used for the injection of the tracer in vivo, only about one fifth of the initial polarization would be lost.

Optimized reaction conditions

As expected and reported before18, the hydrogenation time had a strong impact on the HP yield: the highest polarizations were observed between th=4–8 s (Fig. 6). Note that considerable polarization, about half of the maximum, was observed after hydrogenation periods th as long as 15 s. The slow decay is likely attributed to the decay of the para-order of the hydrogens that were added to the tracer. Note that no refocusing or decoupling pulses were applied during th.

Figure 6: Hydrogenation time affects polarization.
figure 6

Mean 13C-HP (columns) and s.d. (error bars) of HEP (1-13C HEP) as a function of hydrogenation time (th) and fit (line). In agreement with earlier reports18, the optimum th was between 4–8 s. The time constants for the catalytic hydrogenation reaction, Tcat=(1.6±0.9) s, and the para-order relaxation, Tpara=(16±6) s, were extracted from a model fitted to the data. The model is described in Methods (equation (2)). Each time point was measured three times.

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The apparent build-up hydrogenation time constant of the catalysis (Tcat) and para-order relaxation constant (Tpara) were estimated to Tcat=(1.6±0.9) s and Tpara=(16±6) s, respectively, by fitting a model to the experimental data (equation (2) in Methods). The onset of the hydrogenation reaction (t0) extracted from the fit was t0=(1.0±0.5) s. This value reflects the finite time required for the hydrogen being delivered to the reactor, to enter the solution, to build-up pressure and to start the reaction. It is supported by a high-speed video of the hydrogenation reaction, where the bubbling came to a stop ∼1 s after the injection, indicating an equilibration of the pressure (Supplementary Movie 1). Disregarding the contribution of relaxation, the asymptotic maximum polarization level extracted from the fit was (27±5) % (goodness of the fit: R2=0.7, concentrations of HEP and catalyst of cHEP=5.5 mM and ccat=2.1 mM). The deviation to the theoretical maximum may be attributed to noise in the data, relaxation before and during the SOT-sequence itself or experimental imperfections.

This data indicates that after th=4 s, (85±18) % of all molecules are hydrogenated. Since 100% hydrogenation is assumed for the quantification of the polarization yield, it is likely that the reported polarization is underestimated. Note that Tcat, Tpara, maximum polarization level and the optimal th are expected to be dependent on concentrations of the precursor and catalyst.

Hyperpolarization at elevated tracer concentrations

For any biomedical application, highly concentrated, highly hyperpolarized samples are needed to achieve sufficient signal. By variation of th, the catalyst concentration (ccat) and reaction pressure (p), the polarization achieved for 80 mM tracer was increased from 3.4 to 7.1% and eventually∼13% (Table 1 and Supplementary Fig. 1). It must be noted, though, that the last measurement could not be repeated because the pressure exceeded the specifications of the current instrumentation and caused damage to the equipment. In addition, P≈17% was readily achieved in a sample of 22 mM, 3.5 cm off the isocentre of the magnet.

Table 1 Experimental parameters and corresponding polarization yields.
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SAMBADENA and ex vivo13C-MRI

To demonstrate the feasibility of simultaneous HP and MRI, HEP was hyperpolarized by SAMBADENA within seconds, injected into a rat post mortem and 13C-MRI was acquired (rattus rattus, 7 days old). The rat was placed next to the reaction chamber and positioned in the sensitive volume of the coil within the magnet (Fig. 7a,b). In contrast to all other experiments, in this setting, the reaction chamber was not in the isocentre, but at a distance of 3.5 cm along the z axis of the magnet. At this position, the SOT sequence was still efficient, as demonstrated by an HP of 17% that was achieved for 22 mM HEP in 700 μl aqueous solution in the reactor (Table 1).

Figure 7: Simultaneous 13C-HP and ex vivo imaging:
figure 7

The compact design of the setup enabled SAMBADENA next to a small rat post mortem in the sensitive volume of the magnet (a,b). Within seconds, the 13C-tracer HEP was polarized to ∼17% at a concertation of 22 mM. Without leaving the magnet, ∼330 μl of the tracer were injected into the rat, and strong 13C signal with a maximum SNR of 113 was observed by MRI acquired in 0.5 s (c). Subsequently, a T2-weighted 1H-MRI (d) and 1H Zero-Echo-Time (ZTE) MRI were recorded. Co-registration of 1H and 13C-data revealed the location of the tracer, in the reaction chamber and surrounding the heart of the animal (e,f). The isocenter of the magnet is the center of the images. R, reactor; FOV, field of view; M, Model Solution M3; 1, 2, 3: lines for pressure relieve, pH2 supply and pH2 injection, respectively.

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For ex vivo MRI, a catheter was connected to the outlet of the reaction chamber and inserted into the thorax of the rat. The HP-experiment was repeated and ∼330 μl of the hyperpolarized tracer were injected through the catheter into the rat without leaving the magnet. Sub-second 13C-MRI was acquired and strong, hyperpolarized signal was observed (Fig. 7c). The co-registration with a T2-weighted 1H-MRI (Fig. 7d,e) showed that the 13C-signal was localized around the heart of the animal and within the reaction chamber, with a maximum 13C-signal-to-noise ratio (SNR) of 113 and 111, respectively (Supplementary Fig. 2 and Supplementary Table 1). In the same scan, the SNR in the model solution was quantified to 9. A Zero-Echo-Time (ZTE) MRI33 was acquired afterwards to depict the entire setup (Fig. 7f).

Discussion

SAMBADENA enables the HP of 13C-labelled tracers to high levels, in aqueous solution, within seconds and within the magnet bore next to the application site. For the first time, high 13C-HP was achieved without a dedicated polarizer—the hardware of an MRI system was used instead. This method circumvents some of the shortcomings that are associated with current 13C-HP methods, foremost the need of a dedicated, expensive and complex external polarizer and lengthy transfer of the sample. Other challenges persist and are discussed in the following.

Obtaining a pure solution devoid of the catalyst is a persisting challenge for all pH2-based HP methods, although strong progress was reported recently by using either heterogeneous catalysts34,35,36,37 or a biphasic approach38. The latter appears to be particularly promising with respect to the implementation in the presented setup, and heterogeneous catalysts are currently being investigated in our laboratory.

Whereas other HP methods require an extra polarizer device whose complexity, operation and cost can exceed that of the MRI scanner itself, the additional equipment needed here is very little. The only extra component that is needed inside the magnet is a reaction chamber. In the experiments presented here, the bulk reactor occupies less than one-third of the imaging field of view (FOV). A significant reduction in size appears feasible because the actual inner volume of the reactor is less than 1/100 of the FOV (2 cm3 versus 342 cm3). The only requirement for the MRI system is a 13C channel, which is necessary for 13C-MRI in general.

A relatively large volume transmitter is advantageous to enable simultaneous application of the SOT and MRI sequence. A dedicated pickup coil at the region of interest (ROI) may assure a high sensitivity while the homogeneous excitation of the large volume coil (covering both chamber and animal) would be maintained. To improve the accuracy of the applied pulse sequences, two different shim settings were used; one for the HP and one for the imaging.

SAMBADENA may be simplified further by using the digital outputs of the MRI system to control the valves; its implementation on any commercial multinuclear MRI system appears feasible. Other pH2-based approaches are much less cost intensive than dDNP, but still require an external polarizer device with the associated cost and complexity17,18,19,21,22,23,26,27,29,29.

While the actual HP process is executed with a single button, the production of pH2 and precursor solution requires some training. In the future, both pH2 and solution may be prepared elsewhere and shipped to the application site. At this stage, the catalyst–substrate solution is filled manually into the reactor outside the scanner. We envision that future implementations will feature in-bore loading, automatic heating and likely automated injection18.

Any preparation of the hyperpolarized tracer, such as cooling or quality control, would take place at the elevated field of the host MRI system where the T1 is long (here:∼80 s). Note, however, that any human application would require fast and comprehensive testing of the solution before injection, to ensure the safety of the patient, which is challenging especially in the magnet bore.

The HP levels reached −∼20% for a tracer concentration of 6 and 22 mM, and 13% for 80 mM—are likely sufficient for a meaningful in vivo application, in particular because no lengthy transfer of the tracer through varying magnetic fields is necessary.

The SOT-sequence l-PH-INEPT+ was implemented for the first time, and about half of the theoretically achievable polarization yield was observed (P=(19±2) %). Other sequences with a higher theoretical yield appear feasible and may improve the polarization as well.

Fast hydrogenation at elevated temperature and high pressure was found to be essential for a high polarization (Fig. 2 and Supplementary Fig. 1). The catalytic hydrogenation time constant extracted from experimental data indicated that (85±18) % of a 5.5 mM precursor solution were hydrogenated after a 4 s reaction at 15 bar and∼80 °C. Especially with respect to a high substrate concentration, an even higher pressure and temperature is expected to improve the yield further (see Supplementary Fig. 1).

Polarization losses may be attributed to relaxation before, during and after the polarization transfer, imperfect pulses, timings (or erroneous J-coupling constants) and incomplete hydrogenation. We observed that the reaction chamber distorted the line shape of a model solution, which may also cause polarization loss (see Supplementary Figs 3 and 4). Note that 100% hydrogenation and pH2 enrichment was assumed for the quantification, which results in some underestimation of the reported polarization.

The technical feasibility of using the MRI simultaneously for the HP and subsequent imaging was demonstrated by an ex vivo experiment (Fig. 7). Although there appears to be no fundamental hurdle for a preclinical in vivo application, the following aspects have to be taken into account: First, the equipment to support the animal (anaesthesia, vital sign monitoring, heating) have to fit into the bore along with the animal and the reactor. This issue may be addressed by employing a smaller reactor designed to be used with a commercial animal bed. Second, the injection needs to be well controlled regarding flow, pressure and total volume. An automated injection system for dDNP that was already described and evaluated positively in many in vivo experiments39 may be used here. Third, unwanted heating of the animal (by the reactor) should be avoided, and the HP-solution needs to be cooled to temperature that is acceptable for injection. This first implementation was not designed with an in vivo demonstration in mind, but the temperature at the position of the animal is close to the required range (measured as 42 to 37 °C as a function of distance from the outside wall of the reactor, see Supplementary Fig. 5). The temperature at the position of the animal may be reduced further by adding insulation and/or using a different method of heating. As for the temperature of the solution, an elevated temperature is required only at the time of the hydrogenation (to provide fast catalysis, a high polarization yield and sterilize the tracer solution, see Supplementary Note 1). The temperature of the tracer exiting the catheter used in vitro was measured to (43±3)°C and was further reduced to (32±3)°C by guiding the catheter through iced water (Supplementary Table 2). Thus, it appears feasible to reach an acceptable temperature within seconds. Current work focuses on adapting SAMBADENA for the HP of biomolecules to conduct metabolic studies in vivo.

A major limitation of pH2-based methods was the hitherto restricted portfolio of relevant tracers. However, this hurdle may have been overcome by the HP of pyruvate and acetate16, phospholactate13,14,15, and (diethyl-) succinate1,40,41,42,43 with pH2. Current work focuses on adapting SAMBADENA to these tracers.

Compared with other methods, the HP of a liquid-state tracer next to the application site may enable the delivery of higher polarization in vivo at the time of detection, especially for agents with short relaxation time T1 (such as glucose), and enable better resolution of metabolites with hitherto low SNR.

Given its simplicity, its high polarization yield, fast production and low cost, SAMBADENA may have an important impact on the research of HP tracers, which hold the potential to revolutionize the use of MRI in modern diagnostics.

Methods

Parahydrogen production

pH2 was enriched to ∼95% similar as descried previously and stored in aluminium bottle to be used on demand44.

Experimental setup

Measurements were performed using a 7 T preclinical small animal MRI system (Biospec 7/20, PV5.1, Bruker, Germany), using a dual-resonant 1H–13C transmit-receive volume coil (Rapid, Germany; Fig. 2).

A reaction chamber with an inner volume of ∼2 ml was custom-made from polysulfone (PSU 1000) to allow a high hydrogenation temperature (∼80 °C) and pressure (∼15 bar). Tubes were connected to the inlet at the bottom (1/8” × 1/16”, PTFE, SCP GmbH, Germany) and outlet at the top (1/16” × 0.75 mm, PTFE, SCP GmbH, Germany) to inject and release pH2, respectively. Both tubes were connected to magnetic valves (type 0124, Bürkert, Germany) outside of the MR system. The valves were controlled by a custom-written software (MATLAB, MathWorks, USA) using the digital outputs of a data acquisition board (DAQ 6125, National Instruments, USA). A second reactor was used for hydrogenation experiments (Fig. 6) and ex vivo MRI experiments, where an additional outlet at the bottom served to inject the tracer into the animal (Fig. 7).

Preparation of the samples

A rhodium-based catalyst was prepared fresh by mixing a biphosphine ligand (1,4-bis-[(phenyl-3-propane sulfonate) phosphine] butane disodium salt, Q36333, MW=562.53 g mol−1, Sigma Aldrich, MO, USA) with a rhodium complex (bis(norbornadiene)rhodium (I) tetrafluoroborate, MW=373.99 g mol−1, CAS 36620-11-8, StremChemicals, MA, USA) in degassed D2O (Deuterium oxide, 99.9 atom % D, CAS 7789-20-0, Sigma Aldrich, MO, USA) or degassed and deionized H2O (ref. 17).

In contrast to previous reports17,26, the rhodium moiety was dissolved in warm H2O/D2O (∼60 °C) instead of acetone.

1-13C, 2,3,3-2H3-hydroxyethyl-acrylate (HEA, 99% 13C, MW=120.13 g mol−1, CAS: 1216933-17-3, Sigma Aldrich, USA) was added to the solution. During the HP experiment, pH2 was added to HEA and 1-13C, 2,3,3-2H3-HEP was formed (Fig. 8).

Figure 8: Schematic view of the HP method:
figure 8

The tracer to-be-hyperpolarized is formed by catalytic addition of pH2 to an unsaturated precursor molecule (a, here: hydroxyethyl-acrylate forms the angiography-tracer27,30 HEP). Next, a pulse sequence is applied subsequently to transfer the spin order (grey bars, here: PH-INEPT+ (ref. 45)), and the enhanced 13C signal is recorded (c). In b, refocusing pulses are shown in light grey. (c) Real 13C-data in the time domain acquired after one HP experiment.

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To achieve a high hydrogenation temperature, but to avoid degeneration of the catalyst18, a stock solution containing catalyst and substrate at high concentrations was prepared and kept at room temperature (concentrations: crhodium=21 mM, cligand=23 mM, cHEA=55.4 mM). The reaction chamber was heated in a water bath to ∼90–95 °C. Shortly before the experiment, one part (100 μl) of the stock and nine parts of hot H2O or D2O (∼90 °C) were filled into the reaction chamber and placed in the MRI scanner. Unless otherwise indicated, the final concentration was 2.1 mM for the catalyst (with 10% excess of the ligand) and 5.54 mM of HEA.

For the experiment with elevated tracer concentrations, the required amount of HEA was added to the reactor afterwards (for example 9 mg to reach 80 mM in 1 ml solvent).

This procedure permitted obtaining a high hydrogenation temperature of >80 °C, while keeping the catalyst at room temperature for most of the time18.

Spin order transfer

Both PH-INEPT+ (ref. 45) and l-PH-INEPT+ (ref. 31) sequences were implemented on the MRI system. The PH-INEPT+ sequence, which consists of three excitation pulses (45°y-1H, 90°y-1H and 90°x-13C) interleaved by two refocusing pulses (180° on 1H and 13C), was used to transform the para-spin order into hyperpolarized transversal 13C magnetization (Fig. 8). The transversal magnetization generated by this method is short-lived and decays with T2*. The l-PH-INEPT+ (ref. 31) sequence, instead, generates long-lasting longitudinal magnetization by the addition of an extra 90°y-13C pulse to PH-INEPT+. Note that the evolution intervals between the pulses of the sequences (t1 and t2) depend on the hydrogen-hydrogen- and hydrogen-carbon J-couplings of the target molecule.

Quantum mechanical simulations were carried out to optimize t1 and t2 and to determine the theoretical polarization yield. The simulations were performed using the product operator and density matrix formalism in a reduced spin system containing the two para-hydrogens and the target nucleus 13C (J-couplings: JH-H=7.57 Hz, JH1-C=7.24 Hz JH2-C=−5.62 Hz)46. It was assumed that only longitudinal spin order survives the hydrogenation process, and that evolution takes place under the isotropic liquid-state Hamiltonian. The optimal timings with respect to the highest polarization yield were obtained by numerical optimization. Relaxation was neglected and rotation operators were applied to mimic the effect of radio frequency pulses. To assess the effect of erroneous intervals, flip angles and J-couplings, these parameters were varied31,47.

MR settings

For in vitro experiments, 1 ml of H2O was filled into the reactor and placed in the isocentre of the scanner (referred to as position 1) to match and tune the coil and to adjust the frequency and field homogeneity (iterative first-order shim). The 1H frequency was manually set to ∼2.8 p.p.m. The 13C frequency was set to ∼185 p.p.m., the chemical shift of 1-13C HEP, using the 13CO-resonance of acetone (referred to as model solution M1, 1.1 atom % natural abundance of carbon-13, 8 ml, concentration of ∼14 M, chemical shift of the 13CO resonance 210 p.p.m.).

The 13C flip angle was calibrated manually using free induction decays with varying pulse power and an 8 ml sample of ethanol at natural abundance (reference pulse gains for a 1 ms, 90° pulse of 53.6 W (17.2 dB) for 1H and 163.5 W (8.2 dB) for 13C).

For the imaging experiments, the reactor was placed at a distance of 3.5 cm to the isocentre (referred to as position 2). The 1H and 13C flip angles were calibrated using a model solution containing 667 mg 1-13C sodium acetate in 2 ml deionized H2O (denoted as model solution M2, longitudinal relaxation time T1=(22±1) s (see Supplementary Fig. 6), 99 atom % 13C, MW=83.03 g mol−1, c=4 M, CAS 23424-28-4, Sigma Aldrich, USA) in a cutoff 10 mm nuclear magnetic resonance (NMR) tube that was placed within the reaction chamber. Compared with the flip angles measured at position 1, deviations of 1% for 1H and 18% for 13C were found (reference pulse gains of 54.2 W (17.1 dB) for 1H and 190.5 W (7.1 dB) for 13C (Supplementary Fig. 7).

Before HP, the first-order shims and frequencies were adjusted for the reactor and the rat using a PRESS48 localization. Both settings were saved and loaded before HP or imaging was conducted.

The receiver gain was set to 64 dB for all 13C-experiments.

Hyperpolarization

After the reactor was filled with the precursor solution, closed and placed in the magnet, the automated HP procedure was started, consisting of the following steps: First, the hydrogenation reaction was initialized by injecting pH2 at 15 bar (unless indicated otherwise) for a period of 2 s, followed by a variable delay of 1–12 s, yielding a total hydrogenation time of th=3–14 s. Next, the SOT-sequence was executed (∼100 ms). If the PH-INEPT+ sequence was used, the 13C signal was detected directly at the end of t2; if l-PH-INEPT+ was applied, the magnetization was read out after another delay td, either by non-localized spectroscopy or imaging. Note that ∼300 μl of the solution was flushed into the outlet tube during the hydrogenation.

Longitudinal relaxation time T1

After an l-PH-INEPT+ experiment, the T1 of HEP in D2O and H2O was measured by probing the decaying longitudinal magnetization with small-angle acquisitions of 9°, interleaved by 15 s (D2O) or 5 s (H2O). T1 was extracted from an exponential decay function S(t)=S0·exp(−t/T1)·cos(α)n−1, where S(t) is the acquired signal, S0 is the signal at t=0, α the flip angle (9°) and n the number of the pulse of the series. The absolute polarization of this scan was estimated using the signal of the first acquisition and α. Note, that the data points in Fig. 5 were corrected for polarization loss induced by the previous excitations by dividing the measured signals by cos(α)n−1.

Quantification of HP

The absolute polarization yield P was quantified with respect to the signal of a thermally polarized sample (M1) for the in vitro experiments, and a model solution containing 333 mg 1-13C sodium acetate dissolved in 1.2 ml deionized H2O (denoted as model solution M3, concentration of sodium acetate of c=3.3 M) for the ex vivo experiments:

where HP and ref indicate a value of the hyperpolarized sample and the reference model solution, N is the number of summated scans (1 for all HP experiments), F13C is the atomic fraction of the 13C isotope, c is the concentration of the molecule, V is the volume of the sample, S the measured 13C-NMR signal and α the excitation flip angle, Ptherm is the thermal 13C-polarization at 7T and room temperature (∼6 p.p.m.). Note that 100% pH2 enrichment and complete hydrogenation was assumed, which results in an underestimation of the HP that was actually achieved.

The NMR signals were numerically integrated after multiplication with an exponential function (10 Hz), Fourier-transformation and automated phase and baseline correction (Topspin 2.0, Bruker, Germany).

Hydrogenation

The quantification of the hydrogenation yield by NMR of the samples after HP is problematic because the hydrogenation reaction continues after HP. Indeed, complete conversion was found in all samples investigated. Attempts to monitor the conversion during the reaction failed because of low signal (localized spectroscopy, PRESS at 9.4T and∼100 mM substrate concentration) or strong distortions of the resonances (non-localized spectroscopy).

Instead, the HP yield (P) was recorded as a function of the hydrogenation time th at otherwise identical conditions. From the resulting data, an apparent para-order relaxation time Tpara and a hydrogenation constant Tcat were obtained: we hypothesize that P is governed by a saturated growth described by Tcat and a mono-exponential decay of the para-order (Tpara) after the hydrogenation occurred. By solving the differential equations describing the chemical kinetics, an analytical expression for P(th) was derived and fitted to the experimental data. The function P(th) reads:

The coefficients b and t0 allow the maximum polarization level to be adjusted and a time delay between the application of pH2 pressure and the onset of the hydrogenation reaction, respectively.

Ex vivo experiments

An ex vivo rat (rattus rattus, 35 g, 7 cm, 7 days old) and model solution M3 were placed next to the reaction chamber. An injection hose (42 cm, 1/16’’, PTFE, SCP GmbH, Germany) was connected to the outlet of the reactor and inserted into the thorax of the rat. The setup was positioned in the coil within the MRI system. The reactor was at a distance of 3.5 cm from the isocentre (position 2). The field homogeneity was optimized for two volumes, the position of the reactor and the entire rat. The settings were saved and loaded when needed. After the HP, pH2 pressure was released, and a manual valve (V in Fig. 7) was actuated to inject the HP-tracer directly into the rat without leaving the magnet.

Two-dimensional single-shot RARE (rapid acquisition with relaxation enhancement)49 images were acquired before, as well as∼10 s and ∼41 s after the HP was generated (90/180°, RARE factor 38, partial Fourier factor 1.7778, 38·96 matrix, FOV (8.4 cm)2, zero-filled to 128·128, (0.65 mm)2 in-plane resolution, 6-cm-slice thickness, acquisition time/TR=0.487 s, TE=79 ms, acquisition time 487 ms, bandwidth 10 kHz, centred in the isocentre).

Subsequently, a T2-weighted, two-dimensional, 1H-Turbo-RARE sequence was acquired with the same in-plane FOV for anatomical reference (90/180°, RARE factor 8, bandwidth 46.9 kHz, matrix 2562, in-plane resolution (328 μm)2, TR=2.5 s, TE=33 ms, acquisition time 80 s, 15 slices 1 mm thick, 1.5 mm apart, centred in the isocenter).

A ZTE MRI was acquired to display the reaction chamber and rat simultaneously (2.3°, matrix 1283, FOV 16.8 cm, TR=4 ms, acquisition time 208 s, bandwidth 300 kHz, 51,896 projections, centred in the isocentre).

The SNR was calculated by dividing the maximum signal intensity of a chosen ROI by the standard deviation of the noise (paravision 5.1, Bruker, Germany) (Supplementary Fig. 2 and Supplementary Table 1). For the co-registration, black was set transparent in the 13C image (Fig. 7) (GNU image manipulation program). The ZTE data are shown as a max. intensity projection (imageJ50). The images were composed with Inkscape.

Data availability

The authors declare that all relevant data presented here are available from the corresponding author upon reasonable request.

Additional information

How to cite this article: Schmidt, A. B. et al. Liquid-state carbon-13 hyperpolarization generated in an MRI system for fast imaging. Nat. Commun. 8, 14535 doi: 10.1038/ncomms14535 (2017).

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