Theranostics 2017; 7(3):562-572. doi:10.7150/thno.16895
Tracking Perfluorocarbon Nanoemulsion Delivery by 19F MRI for Precise High Intensity Focused Ultrasound Tumor Ablation
1. Molecular Imaging & Therapy Branch, Division of Precision Medicine, National Cancer Center, Goyang, Korea;
2. Dept. of Radiology, Seoul National University Hospital, Seoul, Korea
Shin SH, Park EJ, Min C, Choi SI, Jeon S, Kim YH, Kim D. Tracking Perfluorocarbon Nanoemulsion Delivery by 19F MRI for Precise High Intensity Focused Ultrasound Tumor Ablation. Theranostics 2017; 7(3):562-572. doi:10.7150/thno.16895. Available from https://www.thno.org/v07p0562.htm
Perfluorocarbon nanoemulsions (PFCNEs) have recently been undergoing rigorous study to investigate their ability to improve the therapeutic efficacy of tumor ablation by high intensity focused ultrasound (HIFU). For precise control of PFCNE delivery and thermal ablation, their accumulation and distribution in a tumor should be quantitatively analyzed. Here, we used fluorine-19 (19F) magnetic resonance imaging (MRI) to quantitatively track PFCNE accumulation in a tumor, and analyzed how intra-tumoral PFCNE quantities affect the therapeutic efficacy of HIFU treatment. Ablation outcomes were assessed by intra-voxel incoherent motion analysis and bioluminescent imaging up to 14 days after the procedure. Assessment of PFCNE delivery and treatment outcomes showed that 2-3 mg/mL of PFCNE in a tumor produces the largest ablation volume under the same HIFU insonation conditions. Histology showed varying degrees of necrosis depending on the amount of PFCNE delivered. 19F MRI promises to be a valuable platform for precisely guiding PFCNE-enhanced HIFU ablation of tumors.
Keywords: Perfluorocarbon nanoemulsion (PFCNE), 19F MRI, High Intensity Focused Ultrasound (HIFU), Tumor Ablation, Diffusion MR
High intensity focused ultrasound (HIFU) is a promising non-invasive therapy that thermally and/or mechanically ablates tumors. This procedure has been approved by the United States Food and Drug Administration for the treatment of uterine fibroids, prostate cancer and for palliative care in bone metastasis patients . Preclinical and clinical studies for treating other types of tumors including breast, brain, and liver are also underway [2-5]. Because of the long treatment time, microbubbles (MBs) are being investigated for their potential to reduce the acoustic energy and treatment time required for ablation of tumors. However, MBs have a short half-life in the bloodstream (an order of minutes), and their micron-scale sizes preclude their extravasation and accumulation in the tumor interstitium through the enhanced permeation and retention (EPR) effect.
Nano-sized droplets and emulsions composed of perfluorocarbon (PFC) molecules have been highlighted as an alternative of MBs [6-8]. Upon HIFU insonation, PFC nanoemulsions (PFCNE) rapidly vaporize to MBs through a process called acoustic droplet vaporization and initiate cavitation activity. These PFCNEs show significantly longer circulation time and are smaller in size (~200 nm), making them suitable for improved extravasation through the leaky vasculature of a tumor. Owing to such advantages, PFCNEs are also currently being assessed as ultrasound-triggered drug carriers that can synergistically treat tumors in conjunction with HIFU [9-11].
Considering the heterogeneous nature of a tumor microenvironment, the amount of PFCNEs delivered to a tumor can be highly variable even if delivery parameters, such as nanoemulsion formulation, injection dosage, and delivery route, remain constant . For efficient and reproducible HIFU treatment, the delivery of PFCNEs to a tumor should be visualized in a quantitative fashion so that their amount and distribution can be correlated with the treatment outcome. With this information, PFCNE formulation and HIFU conditions can be optimized for each tumor, leading to precise, safe and rapid ablation of tumors.
Currently, HIFU treatment is usually guided by either ultrasonography (US) or magnetic resonance imaging (MRI) to monitor the treatment procedure and outcome. US directly detects the cavitation activity of PFCNE upon HIFU insonation on a real-time basis; however, the quantification of PFCNE load and distribution in a tumor is difficult. In case of MRI, MBs and PFCNEs can be visualized by incorporating contrast agents such as iron oxide or manganese oxide-based nanoparticles [13-15]. Once these nanoparticles are involved, however, multi-parametric analyses including thermometry cannot be performed as nearby proton spins are perturbed, losing the primary advantage of MR-guided HIFU.
We hypothesized that introducing fluorine-19 (19F) MRI during HIFU treatment would enhance the quality of such treatment by non-invasively quantifying PFCNE delivery to tumors without interfering with MR-based parametric analyses of treatment procedures and outcomes. Aside from its role as a precursor of MBs, PFCNE has been widely used as a tracer agent of 19F MRI, especially for tracking cellular therapeutics and host macrophages in inflammatory disease models [16-19]. The lack of fluorine atoms in biological tissues allows unambiguous detection of signals from PFCNEs as 'hot spots' . As 19F MRI directly detects fluorine atoms, the relationship between the amount of fluorine and corresponding MR signal intensity is linear, enabling facile signal quantification.
In this study, we used 19F MRI to monitor the accumulation of PFCNE in a mouse tumor model. Different PFCNE dosages were administered to mice through intravenous injection to achieve a wide range of PFCNE concentrations in tumors, followed by HIFU treatment with the same acoustic conditions. Intra-voxel incoherent motion (IVIM) analysis and bioluminescence imaging (BLI) were performed to assess the therapeutic efficacy of HIFU treatment, which were confirmed by histology.
Materials & Methods
PFCNE Formulation and Characterization
PFCNEs were formulated using a previous protocol with a subtle modification [21, 22]. In brief, 60 mg/mL of Lutrol F68 (BASF, Ludwigshafen, Germany), 4 μL/mL 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI; Molecular Probes, Eugene, OR, USA) and 60% w/v perfluoro-15-crown-5-ether (PCE; Matrix Scientific, Columbia, SC, USA) were mixed in phosphate buffered saline (PBS; Gibco, Waltham, MA, USA). The mixture was emulsified by sonication for 10 minutes in ice-cold water in pulsed mode (2 s on/2 s off) at 1.5 W power using a Sonicator 3000 (Misonix, Farmingdale, NY, USA). The resulting emulsions were filter-sterilized (0.2 μm; Sartorius Stedim, Aubagne, France) and kept at 4˚C until use. The size and polydispersity index (PDI) of the PFCNEs were measured by dynamic light scattering (Malvern Zetasizer, Worcestershire, UK), and cytotoxicity was measured using a trypan blue exclusion assay in HCT116 human colon cancer cells. PFCNE morphologies were observed via transmission electron microscopy at an accelerating voltage of 120 kV (JEM-2010; JEOL Ltd., Tokyo, Japan).
Ex Vivo Simulation of HIFU
For ex vivo simulation of HIFU treatment, egg white-based phantoms were prepared . Briefly, 35% v/v egg white, 31.4% v/v degassed deionized water, 33% acrylamide-bisacrylamide (Sigma Aldrich, St. Louis, MO, USA), 0.5% v/v ammonium persulfate (Sigma Aldrich), 0.1% v/v tetramethylethylenediamine (TEMED, Sigma Aldrich), and either 0.1, 0.5, or 1% v/v of PFCNE were mixed, degassed, and cross-linked. The resulting phantom was insonated with HIFU (f = 1.05 MHz) in a continuous mode for 15 s at peak-negative pressures of 2.51 MPa, 3.01 MPa, 3.52 MPa, or 4.27 MPa. The volumes of the resulting lesions were optically measured using the following formula: volume = w2hπ/6, where h and w refer to the height and width of a lesion, respectively.
All animal experiments were performed under Institutional Animal Care and Use Committee (IACUC; Approval number: NCC-15-249) guidelines provided by the National Cancer Center, Korea. For a subcutaneous tumor model, HCT116 cells expressing luciferase were cultured in RPMI-1640 media (HyClone, Logan, UT, USA) supplemented with 10% fetal bovine serum (Cellgro, Tewksbury, MA, USA) and 1% antibiotics (Gibco, Grand Island, NY, USA) at 37˚C in a 5% CO2 incubator. Six-week old female BALB/c-nu mice were subcutaneously injected into the left flank with 5 × 106 cells suspended in 100 μL of 5 mg/mL Matrigel (Corning, Corning, NY, USA) in PBS. Tumors were grown for 2 weeks until attaining a volume of 150-200 mm3 before HIFU treatment.
In vivo Study Design
Forty-eight hours before the first MRI and BLI, mice were intravenously injected with 50 μL (n = 5; PFC50+), 100 μL (n = 4; PFC100+), or 200 μL (n = 4; PFC200+) of PFCNE through their tail veins. The 48-hour time point was chosen upon considering the blood half-life of similar PFCNEs in previous studies, and allowed for maximum accumulation in tumors [24, 25]. For the group receiving 400 μL of PFCNE (n = 6; PFC400+), the injection was administered over 2 days (48 and 24 hours before the first MR scan) using 200 μL per day to allow mice to adapt to increased circulation volume. Untreated mice (n = 5; control) and a group treated without PFCNE (n = 5; PFC-) were also included. MRI and BLI were performed up to 2 weeks following the HIFU insonation. A schematic illustration describing the in vivo experimental procedure is shown in Fig. 1.
In vivo MRI
MR images were acquired using a 7T scanner (BioSpec 70/20 USR; Bruker, Billerica, MA, USA) and a custom-made 1H/19F-double tune 35 mm volume coil. Mice were anesthetized with 2% isoflurane gas, and their respiration rates were monitored during the scans. For proton anatomical images, rapid acquisition with relaxation enhancement (RARE) sequence was used with the following parameters: repetition time (TR)/echo time (TE) = 2600/30 ms, number of average (NA) = 2, RARE factor = 4, matrix = 256 × 192, slice thickness (ST) = 1.25 mm, and field of view = 4 × 3 cm. Diffusion-weighted images (DWIs) and 19F images were also acquired (DWI: Spin Echo, TR/TE = 2000 / 26 ms, matrix = 192 × 128, b-values = 0, 45, 350, 1000, and 2000 s/mm2; 19F: FLASH, TR/TE = 50/2.5 ms, matrix = 64 × 48, NA = 512, receive bandwidth = 25 kHz, echo position = 30%, ST = 2.5 mm). For 19F imaging, a reference tube with 5 mg/mL of PFCNE in acrylamide gel was placed adjacent to a mouse for signal quantification purpose. Before signal quantification, raw 19F images were corrected for Rician noise distribution as previously described . The processed images were rendered in a pseudo-color scale and superimposed on corresponding proton images.
Schematic illustration showing the usage of 19F MRI for efficient and reproducible perfluorocarbon nanoemulsion (PFCNE)-enhanced high intensity focused ultrasound (HIFU) tumor ablation. Owing to the heterogeneous tumor microenvironment, the accumulation of PFCNE in a tumor can be highly variable, leading to unpredictable therapeutic outcomes after HIFU treatment. Using 19F MRI, the concentration of PFCNE in a tumor can be quantified via imaging along by using a reference containing a known concentration of PFCNE. HIFU treatment can be performed after the quantification process, followed by evaluation of therapeutic outcomes. Afterwards, the PFCNE concentration in a tumor, as measured by 19F MRI, can be correlated with therapeutic outcomes. This information will enable the prediction of the therapeutic outcomes at given concentrations of PFCNE, as well as the optimization of the parameters involved in PFCNE accumulation in a tumor (such as PFCNE formulation and delivery route) for efficient HIFU tumor ablation.(Click on the image to enlarge.)
in which S0 = signal intensity at the b-value of 0; Sb = signal intensity at a given b-value other than 0; f = microvascular volume fraction; Dt = true diffusion coefficient of water molecule; and Dp = pseudo-diffusion coefficient due to microcirculation. A custom-written program based on Interactive Data Language (IDL 8.2.2; Exelis Visual Information Solutions, Inc., Boulder, CO, USA) was used for the fitting process. The region of interest (ROI) was manually drawn over a tumor, and pixels with Dt values higher than 150% of the median of untreated tumors (7.5 × 10-4 mm2/s) were analyzed for delineation of lesions formed by HIFU ablation.
Mice were anesthetized with 2% isoflurane gas during imaging; 150 mg/kg body weight of D-luciferin (Gold Biotechnology Inc., St. Louis, MO, USA) was injected into the peritoneal cavities of mice and imaged 20 minutes after the injection using a Xenogen IVIS Spectrum (Perkin Elmer, Waltham, MA, USA). Acquired images were processed with Living Image 2.6 software (Perkin Elmer). ROIs with the same area were placed on tumors for signal measurement.
Ex Vivo Fluorescence Imaging
Three additional mice from each group injected with PFCNE were sacrificed without HIFU treatment after confirming the accumulation of PFCNE in tumors via 19F MRI. Tumors were excised and imaged using the Xenogen IVIS Spectrum system with a DsRed filter (excitation passband: 500-550 nm; emission passband: 575-650 nm). Acquired images were processed with Living Image 2.6 software, and the signals from the tumors were quantified.
Each mouse was placed on a degassed water bath beneath which a single-element transducer (diameter: 4 cm, focal distance: 3.5 cm) was positioned. Mice were subjected to a single-shot HIFU (f = 1.05 MHz) for 15 s in a continuous mode at the peak-negative pressure of 3.52 MPa. The focal size (-3 dB) was 0.87 mm in diameter and 5.4 mm in length.
Immediately after HIFU treatment, 3 additional mice from each HIFU-treated group were sacrificed. Tumors were excised and fixed in 4% paraformaldehyde for 24 hours. Fixed tumors were embedded in paraffin blocks, and 4-μm thick sections were made for hematoxylin and eosin (H&E) staining. H&E-stained sections were imaged with Aperio Scan Scope XT (Leica Biosystems, Heidelberg, Germany) at 200× magnification.
All statistical analyses were performed using GraphPad Prism 5 (GraphPad Software, La Jolla, CA, USA) and Microsoft Excel 2010 (Microsoft, Seattle, WA, USA). For multi-group comparisons, one-way ANOVA was performed followed by Bonferroni correction. Pearson's test was performed for correlation analyses. Two-tailed p-values less than 0.05 were considered statistically significant. All data values are represented as the mean ± standard error of the mean unless otherwise indicated.
Characterization of PFCNEs
The average PFCNE diameter was 159 ± 2.7 nm and PDI was 0.08 ± 0.02 after production (Fig. 2D). The size and dispersity of PFCNEs remained stable at 4˚C for up to 3 weeks, while sizes increased with time at 25˚C and 37˚C (Fig. 2E). Stability was not significantly affected by serum (Fig. 2F). The viability of HCT116 cells was not affected by PFCNEs in the culture media at increasing concentrations up to 30 mg/mL (Fig. 2G). To validate the 19F MR signal quantification, a fluorescent dye was incorporated into PFCNEs. MR and fluorescence images of PFCNE-incorporated phantoms were acquired, and signals from these modalities showed significant correlation (R2 = 0.954, P = 0.0002; Fig. 2H, I).
HIFU Simulation in Phantoms
To investigate the effect of PFCNE concentration on HIFU treatment, egg white-based phantoms with different PFCNE concentrations were insonated using different powers of focused ultrasound with constant mode (continuous wave) and duration (15 s). Under the same HIFU conditions, phantoms with 0.6 mg/mL PFCNE showed the largest lesion volumes, with the exception of the 2.51 MPa HIFU condition (Fig. 3). Higher concentrations of PFCNEs produced smaller lesion volumes that were comparable to lesions generated in phantoms without PFCNEs.
In vitro characterization of perfluorocarbon nanoemulsions (PFCNEs). Chemical structures of (A) perfluoro-15-crown-5-ether and (B) Lutrol F68. (C) Transmission electron microscopy image of PFCNE (scale bar = 800 nm for low magnification and 100 nm for the inset). (D) Size distribution of PFCNEs immediately after formulation. (E) Long term tracking of PFCNE size while subjected to 3 different temperatures for up to 3 weeks. (F) Serum stability of PFCNE incubated at 37˚C. (G) HCT116 cell viability after PFCNE treatment. (H) Correlation of fluorescence signal and 19F MR signal intensity of PFCNE. (I) Fluorescence image (top row) and 19F MR images (bottom row) of reference tubes with various PFCNE concentrations.(Click on the image to enlarge.)
Ex vivo simulation of high intensity focused ultrasound (HIFU) ablation. (A) Volumes of lesions formed by HIFU of different peak-negative pressures in tissue phantoms with various perfluorocarbon nanoemulsion (PFCNE) concentrations. (B) Photographs of lesions formed in the phantoms.(Click on the image to enlarge.)
In vivo 19F magnetic resonance imaging (MRI) and signal quantification. (A-D) 1H/19F merged images of mice injected with 50 μL (A), 100 μL (B), 200 μL (C), and 400 μL (D) of perfluorocarbon nanoemulsion (PFCNE). PFCNE is mostly accumulated in the tumor rim (arrowhead). (E) Quantification of PFCNE accumulated in tumor. A significant increase in accumulation is observed when the dosage increases from 100 μL to 200 μL. (F) Fluorescence images of excised tumors from mice injected with 50, 100, 200, and 400 μL of PFCNE (left to right). (G) Correlation of fluorescence intensity and 19F MR signal intensity from excised tumors (green: 50 μL; blue: 100 μL; yellow: 200 μL; red: 400 μL).(Click on the image to enlarge.)
In Vivo MR Tracking of PFCNE
Before HIFU treatment, 19F MR images of mice with a reference tube were acquired to visualize the distribution of PFCNEs and quantify them in tumors. With increasing dosage, higher accumulation of PFCNEs was detected in the tumor rims, as expected by the size of PFCNEs as well as the EPR effect (Fig. 4A-D). In the PFC400+ group, 19F MR signal was also detected in the tumor core, which may be attributed to the migration of splenic macrophages that had engulfed the injected PFCNEs. The amount of PFCNE in a tumor was quantified based on the signal intensity of the reference tube. Upon injection of 50, 100, 200, or 400 μL volumes, intra-tumoral PFCNE concentrations were found to be 0.52 ± 0.34, 0.84 ± 0.56, 2.83 ± 3.54, and 3.25 ± 2.74 mg/mL, respectively (Fig. 4E). To verify these quantities, tumors were excised and fluorescence images were acquired (Fig. 4F). Significant correlation between fluorescence and 19F MR signal intensity was observed (R2 = 0.874, P < 0.0001).
Lesion Delineation by IVIM Mapping
HIFU-ablated lesions were clearly delineated by elevated levels of diffusion coefficients (Fig. 5A). In all HIFU-treated groups, Dt values in lesions rapidly increased after HIFU treatment from ~5 × 10-4 mm2/s to ~1 × 10-3 mm2/s and remained stable up to day 14 (Fig. 5B). The sustained increase of Dt may be explained by chronic inflammation accompanied by edema. The PFC200+ group showed the largest increase throughout the experimental period, but was not significantly higher than the other HIFU-treated groups. In the PFC200+ group, lesion volume decreased on day 1, but rapidly increased by day 7 (24.3±14.8 mm3) while the volumes of the other groups remained constant or increased slowly (Fig. 5C). By day 7, the average lesion volume of the PFC200+ group was significantly higher than that of the PFC- group (Fig. 5C). Comparison of PFCNE amounts and Dt in lesions showed a correlation in that increasing the PFCNE concentration up to 3 mg/mL caused a greater increase in Dt; however, the increase in Dt was smaller with PFCNE concentrations above 3 mg/mL (Fig. 5D). Correlation of lesion volume and PFCNE concentration in a tumor also suggests that approximately 3 mg/mL of PFCNE in a tumor generates the largest lesion volume (Fig. 5E).
Immediately after HIFU insonation, a significant decrease of the BLI signal was observed from all HIFU-treated groups (Fig. 6A). In particular, the PFC200+ group showed the most significant decrease in the BLI signal, which was reduced by 76.4 ± 8.88% (Fig. 6B). In all HIFU-treated groups, the BLI signal dropped on day 1 and gradually recovered to the original level before HIFU treatment by day 14 (Fig. 6B, C). Similar to the results observed with IVIM, increasing PFCNE concentration up to 2-3 mg/mL generated a larger BLI signal reduction. PFCNE concentrations above 3 mg/mL produced a smaller BLI signal reduction (Fig. 6D).
Intra-voxel incoherent motion (IVIM) analysis of ablated lesions. (A) Longitudinal Dt maps of mice before and after high intensity focused ultrasound (HIFU) treatment. Ablated lesions are marked by increased Dt values. (B) Dt values of lesions over time beginning immediately after HIFU treatment (day 0). The black line indicates the median Dt of tumors before HIFU treatment, and the dashed lines indicate the standard deviation. (C) Lesion volume changes over time beginning immediately after HIFU treatment (day 0) as a function of perfluorocarbon nanoemulsion (PFCNE) volume (*P < 0.05 vs. PFC-). (D) Correlation of the maximum lesion Dt increase and tumor PFCNE concentration. The dashed line indicates the trend of the data. (E) Correlation of lesion volume and PFCNE concentration in tumor, measured on day 7. The dashed line indicates the trend of the data.(Click on the image to enlarge.)
Ablated lesions were clearly visible in H&E stained sections of all groups treated with HIFU (Fig. 7). Ballooning degeneration was commonly observed in the peripheral zones of lesions from all groups, forming a borderline between the lesion and non-ablated viable zone. The central zone of the lesion was highly variable among the groups. Red coloration by hemorrhage was observed in the PFC- group, and the PFC50+ group showed small necrotic regions scattered in the central zone. The PFC100+ group showed dilated blood vessels due to the heat generated by HIFU treatment. The PFC200+ group showed the most severe effect with complete necrosis and few cellular remnants. The central zones of lesions in the PFC400+ group did not show marked differences from the viable regions.
Longitudinal bioluminescence imaging (BLI). (A) BLI of mice before and after high intensity focused ultrasound (HIFU) treatment. (B) BLI signal intensity measurements after HIFU treatment. (C) Comparison of BLI signal intensities of animal groups measured immediately after HIFU treatment (◆: P < 0.05 vs. control; ●: P < 0.05 vs. PFC-; ■: P < 0.05 vs. PFC50+). (D) Correlation of BLI signal reduction and PFCNE concentration in a tumor. The dashed line indicates the trend of the data.(Click on the image to enlarge.)
In this study, we demonstrated the feasibility of combining HIFU treatment with 19F MRI for precise and efficient ablation of tumors through quantitative tracking of PFCNEs. PFCNEs maintained appropriate size and stability with minimum cytotoxicity while enhancing thermal ablation in a tissue phantom. The accumulation of PFCNE in the tumor rim was clearly visible and quantifiable through 19F MRI. The effects of PFCNE on tumor ablation were non-invasively determined using IVIM analysis and BLI, and were subsequently confirmed by histological examination.
PFCNEs are widely studied as enhancers of HIFU tumor ablation. Yet, the correlation between their amounts in tumors and the efficiency of HIFU ablation remains undetermined. To estimate the effects of PFCNE amounts in HIFU tumor ablation, we used egg white phantoms incorporating various concentrations of PFCNE. Through applying HIFU with different acoustic pressures, we established a relationship between PFCNE concentration and lesion volume made in an egg white phantom (Fig. 3A); the largest lesion was produced with 0.6 mg/mL of PFCNE, concentrations above which lesion sizes decreased. Similar trends were observed in vivo; in both IVIM (Fig. 5C, E) and BLI (Fig. 6D) settings, peak ablation was achieved at 2-3 mg/mL of PFCNE. The decreased ablation at higher concentrations of PFCNE may be due to PFCNE coalescence, as the frequency of HIFU at which the PFCNE initiates cavitation activity is highly dependent on its size . Further investigation is required to clarify the underlying mechanism.
Not only can the amount of PFCNE in a tumor be confirmed by 19F MRI and correlated with therapeutic efficacy of HIFU, but the distribution of PFCNE in a tumor can be determined as well. We administered PFCNE through intravenous injection to mimic the drug administration method used in the clinic. This method of delivery caused most PFCNEs to accumulate only in the periphery of a tumor; therefore, direct intra-tumoral injection may be a more favorable method for achieving various patterns of intra-tumoral distribution of PFCNEs. Although direct injection is a clinically limited approach, it may facilitate controlling the distribution of PFCNE as well as observing the effect of PFCNE cavitation more clearly at a lower dosage.
IVIM served as a proof-of-principle that MR parametric analysis can be simultaneously performed with 19F MRI . Although no significant difference was observed among HIFU-insonated groups in terms of Dt value increase in lesions (Fig. 5B), the volumes of lesions in the PFC200+ group dramatically increased up to day 7, and were significantly larger than those observed in the PFC- group (Fig. 5C). The lesion volume development over time may be associated with inflammatory edema. While IVIM provides information on changes in water diffusion due to cellular and nuclear membrane disruption, other physiological responses to HIFU ablation, such as protein denaturation and halted metabolism, can also be assessed through alternative parametric MR analyses (amide proton transfer imaging, MR spectroscopy, etc.) that are also compatible with 19F MRI. [31, 32]. Performing these parametric analyses along with 19F MRI will provide a thorough understanding of the effects of PFCNE in HIFU treatment.
Histology of tumors after high intensity focused ultrasound (HIFU) treatment. HIFU-ablated regions are clearly visible in low magnification (10×) overview (dashed lines). Higher magnification images (200×, scale bar: 100 μm) were acquired in the central zone (yellow box) and peripheral zone (white box) of ablated lesions. All groups show ballooning degeneration in the peripheral zone of the ablated lesions; the PFC50+ group additionally shows dilated blood vessels (green arrows). Different degrees of necrosis and histological features were observed in the central zone depending on the amount of PFCNE injection (PFC-: hemorrhage; PFC50+: scattered necrotic zones [white arrows]; PFC100+: dilated blood vessels [white arrowheads]; PFC200+: complete necrosis with few cell remnants; PFC400+: no significant changes observed).(Click on the image to enlarge.)
BLI showed a significant decrease of tumor viability immediately after HIFU treatment (Fig. 6). This decrease was observed on day 1, although recovery was observed beginning on day 3 and was complete by day 14. This indicates that the tumors were not completely ablated and were able to recur. While the cause of relapse was not investigated at a molecular level, immunohistochemistry and/or flow cytometry can be performed in the future to evaluate whether candidate molecules such as hypoxia-inducible factor 1-alpha and M2-phenotype tumor-associated macrophages are involved in tumor cell changes after HIFU treatment [33, 34]. For now, we treated each mouse with a single shot of HIFU to clearly distinguish an ablated lesion from any viable tumor portions. We postulate that repeated treatment with HIFU may completely ablate tumors and suppress their growth, leading to clearer differentiation of the effect of PFCNEs on HIFU ablation as determined by both IVIM mapping and BLI.
To increase the therapeutic efficiency and suppress tumor recurrence, anti-cancer drugs can be loaded onto PFCNEs so that tumors are ablated not only by the thermal dose from PFCNE cavitation but also by drugs released from these same PFCNEs. In many cases, sensitive tissues surrounding a tumor hinder complete ablation and leave viable tumor margins. It was previously shown that concurrent therapy with HIFU plus anti-cancer drugs suppresses tumor growth more effectively by destroying the tumor margins; this cannot be accomplished by HIFU alone . Therefore, 19F MRI ought to play a significant role in such synergistic therapies, as the amount of drug delivered to a tumor can be quantified if the drug loading efficiency is calculated.
We used PCE for formulating PFCNEs, although other PFCs with lower boiling points such as perfluoropentane (PFP) and perfluorohexane are more widely used for HIFU ablation . We chose PCE because it has 20 equivalent 19F atoms that generate a strong single nuclear magnetic resonance peak without any chemical shifts upon imaging. The echogenicity of PCE is also comparable to that of PFP; hence, nanoemulsions formulated with PCE also significantly increase the thermal dose . Still, it may be more advantageous in terms of therapeutic efficiency to use low boiling point-PFCs, and the feasibility of imaging such PFCs with 19F MRI should therefore be tested.
Up to 400 μL of PFCNE was injected into mice to achieve a high intra-tumoral concentration. While similar or even larger quantities of PFCNE were injected in previous studies to ensure MR visibility, such doses may be too large and might cause spleen engorgement and leakage into the small intestine through the bile duct [37-39]. Thus, the low sensitivity of 19F MRI must be overcome so that the injection dosage of PFCNE is kept to a minimum to alleviate safety issues. Improvements in 19F MR sensitivity are being made by using pulse sequences that generate a high signal-to-noise ratio (SNR). Such improvements include using balanced steady state free precession sequence  and adopting advanced image reconstruction techniques, such as compressed sensing algorithms that were shown to accelerate 19F MR scanning time 8-fold without compromising the SNR and spatial resolution . Considering these improvements and a recent clinical trial involving cell therapy , 19F MRI is highly expected to enter clinical trials for guiding precise HIFU tumor ablation in the future.
In this study, we showed that 19F MRI is a useful platform for guiding HIFU ablation of tumors by quantitatively tracking PFCNE accumulation. PFCNE accumulation in the tumor periphery was clearly visible and quantifiable, and was confirmed by fluorescence imaging. IVIM analysis was performed not only to assess therapeutic outcomes but also to demonstrate the feasibility of multi-parametric analysis along with 19F MR tracking of PFCNE delivery. Increased water diffusion was observed in the ablated lesions, indicating cellular and nuclear membrane disruptions as well as inflammatory edema. BLI was also performed to measure tumor viability after HIFU treatment. Both IVIM analysis and BLI showed that 2-3 mg/mL of PFCNE in a tumor produces optimal ablation, with a similar trend observed in phantom experiments. Going forward, 19F MRI will be a valuable tool for non-invasively optimizing the use of PFCNE in HIFU ablation, enabling more precise and robust HIFU treatment in future.
19F: fluorine-19; ANOVA: analysis of variance; BLI: bioluminescence imaging; DWI: diffusion-weighted image; EPR: enhanced permeation and retention; HIFU: high intensity focused ultrasound; H&E: hematoxylin and eosin; IVIM: intra-voxel incoherent motion; MB: microbubble; MRI: magnetic resonance imaging; NA: number of average; PCE: perfluoro-15-crown-5-ether; PDI: polydispersity index; PFC: perfluorocarbon; PFCNE: perfluorocarbon nanoemulsion; PFP: perfluoropentane; RARE: rapid acquisition with relaxation enhancement; ROI: region of interest; SNR: signal-to-noise ratio; ST: slice thickness; TE: echo time; TEMED: tetramethylethylenediamine; TR: repetition time; US: ultrasonography.
The authors are grateful to the Molecular Imaging Core in the National Cancer Center, Korea, for experimental support. This research was supported by a Grant from the National Cancer Center (NCC-1510030).
Ethics Committee Approval
This study was reviewed and approved by the Institutional Animal Care and Use Committee (IACUC) of the National Cancer Center Research Institute. The Institute is an Association for Assessment and Accreditation of Laboratory Animal Care International-accredited facility that abides by the Institute of Laboratory Animal Resources guide.
The authors have declared that no competing interest exists.
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Corresponding author: Daehong Kim, Ph.D. National Cancer Center, Molecular Imaging & Therapy Branch, Division of Precision Medicine, Research Bldg., Ilsanro-323, Ilsandong-gu, Goyang, Korea, 10408; Phone: +82-31-920-2513; E-mail: dkimre.kr. Eun-Joo Park, Ph.D. Seoul National University Hospital, Dept. of Radiology, 101 Daehak-ro, Jongno-gu, Seoul, Korea, 03080; Phone: +82-2-2072-4358; E-mail: ejparkorg.