CC BY
2
bcutaneous Tumor Xenograft Sources Efficiency
esearcher, Fluorescent Bioimaging Laboratory, Research Institute
.N. Druzkova
_..,jerimental Oncology and Biomedical Technologies1 A. Pakhomova, Student2
of !
Medicine1
N.I. Ignatova, PhD, Associate Professor, Department of Epidemiology, Microbiology and Evidence-Based Suleymanova, Student1;
.V. Maslennikova, MD, DSc, Head of the Department of Oncology, Radiation Therapy and Radiology1
1Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Square, Nizhny Novgorod, 603005, Russia; 2National Research Lobachevsky State University of Nizhny Novgorod, 23 Prospekt Gagarina, Nizhny Novgorod, 603022, Russia
Boron neutron capture therapy (BNCT), due to its high biological efficiency, is one of the most promising methods of radiation therapy for malignant tumors. Currently, research in this area has received momentum due to the emergence of fundamentally new compact neutron sources suitable for clinical use.
The aim of the investigation was to study L-boronphenylalanine (L-BPA) biodistribution in the organs of experimental animals with subcutaneous tumor xenografts, and evaluate the application of the experimental model to assess the effectiveness of new neutron sources.
Materials and Methods. The experiments were carried out on BALB/c mice with subcutaneous xenograft of mouse adenocarcinoma CT26. L-boronphenylalanine in a molar excess of fructose was administered intravenously at a dose of 350 mg/kg, the organs under study were taken 1.5, 3, 6, and 24 h after drug administration. The content of the 10B isotope was analyzed using inductively coupled plasma mass spectroscopy (ICP-MS). The absence of toxic effects was verified pathomorphologically.
Results. The maximum L-BPA content in the tumor was 142.0±4.41 ig/g 1.5 h after drug administration. The minimum therapeutic concentration of L-BPA in the tumor persists up to 5.4 h after drug administration. Among normal organs, the maximum content was observed in the kidneys, it is most likely being associated with the structural and functional features of the organ rather than the true content of L-BPA in the tissues. Histological studies revealed no structural disorders and dystrophic changes in tissues against the background of L-BPA introduction.
Conclusion. The results of the study demonstrate the feasibility of the studied tumor model to evaluate the efficiency of new neutron sources for BNCT. The L-borophenylalanine content in the tumor and the time of maintaining the minimum therapeutic concentration appeared to be sufficient for effective BNCT. The high contrast of 10B accumulation relative to non-pathological tissues minimizes the possible side effects of BNCT.
Key words: boron neutron capture therapy; L-boronphenylalanine; biodistribution; radiation therapy.
L-BPA; inductively coupled plasma mass spectroscopy;
How to cite: Druzkova I.N., Pakhomova A.A., Ignatova N.I., Suleymanova A.R., Maslennikova A.V. L-boronphenylalanine biodistribution dynamics in the organs of mice with subcutaneous tumor xenograft is a model to assess neuron sources efficiency in boron neutron capture therapy. Sovremennye tehnologii v medicine 2023; 15(6): 14, https://doi.org/10.17691/stm2023.15.6.02
This is an open access article under the CC BY 4.0 license (https://creativecommons.org/licenses/by/4.0/).
Introduction
Boron neutron capture therapy (BNCT) is a kind of binary radiotherapy, and one of the most effective and promising methods to treat malignancies as of today. The method is based on making use of the reactions occurring
between 10B isotope nuclei and a flow of neutrons, their energy being in the range of 5-10-3—5-104 eV.
One of the major problems hindering the large-scale clinical BNCT implementation is the lack of compact neutron radiation sources, which can be installed in a radiotherapy clinic. From the beginning of BNCT
Corresponding author: Irina N. Druzkova, e-mail: danirin@ya.ru
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epoch, nuclear reactors were used to obtain thermal and epithermal neutron beams, and it drastically limited the implementation of the method in clinical practice. Beams were obtained on the basis of self-sustaining chain nuclear reaction of uranium-235 degradation. The spectrum of such neutrons has the energy up to 10 MeV, the average energy being about 2 MeV [1, 2]. However, currently, there have already appeared the prototypes of compact accelerating sources of various modifications; the prototypes enable to obtain neutron beams with energy close to that required for clinical use [3-9]. Along with that, the prototypes of D-D-neutron generators have been developed, which enable to obtain neutron beams with density, which appears to be record for compact systems [10, 11]. Thus, currently, BNCT has been given a new lease of life and is relevant again to solve the biological problems related to its implementation.
Boron preparations containing 10B atoms are the second component in BNCT. At present, there are only two preparations certified for clinical use: L-p-dixydroxy-boro-nanilphenylalanine (4-(dihydroxyboranyl)-L-phenylalanine, L-BPA) and sodium mercaptoundecahydro-closo-dodecaborate (sodium borocaptate, BSH), their structural formulas are given in Figure 1.
Preparation L-BPA is an amino acid, which is capable of relatively selectively (maximum contrast 2:1) accumulating in a tumor due to the more effective transport system of L-amino acids in its cells compared to normal ones [12, 13]. The compound contains only one boron atom, although due to the low toxicity of the compound in general it enables to accumulate a sufficient for therapy amount of boron in the tumor cells. In BSH, there are 12 boron atoms, which enables with a great probability to achieve the necessary therapeutic concentration (24-35 jg/g) in tumor cells [14]; however, it has less accumulation contrast (1.1-1.8:1) compared to L-BPA [15].
It follows that the control over isotope 10B accumulation efficiency in a target-tumor, as well as in surrounding healthy tissues, is of great importance for BNCT development.
The highest accuracy of 10B isotope content estimate is achieved by using direct methods such as gamma ray spectroscopy [16-18], inductively coupled plasma mass spectrometry (ICP-MS) [19, 20], high-resolution alpha-radiography, alpha-ray spectroscopy, neutron capture radiography [21, 22], secondary neutral mass-spectrometry [23], spectroscopy of characteristic electronic energy loss [24], ion trap mass spectrometry [25]. Using the mentioned techniques, we received the data on 10B isotope accumulated in a tumor and in some tissues and organs. However, there are no detailed studies on 10B isotopes content dynamics in a tumor and vital organs, which can become a target for neutrons.
The selection of an adequate tumor model to assess BNCT effect is a critical task.
The aim of the investigation. The present study offers a model of a tumor subcutaneous
Figure 1. Structural formulas of L-BPA (L-p-dixydroxy-boronanilphenylalanine, 4-(dihydroxyboranyl)-L-phenyl-alanine) and BSH (sodium mercaptoundecahydro-closo-dodecaborate, sodium borocaptate) certified for clinical use as boron-containing agents
xenograft obtained from a cell line of CT26 intestinal adenocarcinoma in BALB/c mice as a potential model to assess the effectiveness of new neutron sources. The biodistribution of L-boronphenylalanine in organs and tissues of experimental animals was studied in dynamics by ICP-MS method and the prospects of using the presented model to evaluate the efficiency of new neutron sources application were determined.
Materials and Methods
Preparation of L-boronphenylalanine solution in molar fructose excess. L-BPA preparation for the experiments was given by the staff members of Budker Institute of Nuclear Physics of Siberian Branch Russian Academy of Sciences (Novosibirsk, Russia). The preparation solution in molar fructose excess was made according to the protocol by Coderre et al. [26]: we prepared weighed L-BPA portion to obtain the solution, its final concentration being 35 mg/ml, and fructose weighed portion at the rate of L-BPA:fructose=1:1.1. Weighed portion of L-BPA was dissolved in water purified using MilliQ system (Milliport, Germany) resulted in obtaining cloudy solution, its initial pH was 4.5-6.0. Then, using 10N of NaOH solution, pH was made to reach 9.0-10.5. The resulted solution was stirred for 20 min till it became clear by adding a fructose portion and stirring for at least 10 min to form a complex of L-BPA and fructose. Subsequently, using concentrated 1 M HCl, pH was gradually made to reach the value of 7.4 avoiding solution precipitation. The prepared solution was used on the day of preparation or stored at 4°C for no more than 12 days. Before use, the solution was filtered using an antibacterial filter, its pore diameter was 0.2 |jm.
The experiments on animals. The experiments were carried out on BALB/c line mice. A subcutaneous tumor was induced in the animals by CT26 cell suspension, the concentration was 5-105 cells in 100 jl of phosphate buffer solution, which was injected in the right thigh area. When a tumor grew up to about 50 mm3, L-BPA
L-BPA Biodistribution is a Novel Model to Assess Neutron Sources CTM J 2023 J vol. 15 J No.6 15
preparation in a saturated fructose solution in a dose of 350 mg/kg body mass was administered intravenously to the animal's lateral caudal vein. The study was approved by the Ethical Committee of Privolzhsky Research Medical University (Nizhny Novgorod, Russia), protocol No.19 dated December 9, 2022.
For tissue retrieval, the animals were sacrificed by a mixture of Zoletil (a dose of 40 mg/kg) and 2% Rometar (a dose of 10 mg/kg) followed by the euthanasia by cervical dislocation. The animal tissue samples of liver, kidneys, spleen, intestine, lungs, tumor, skin, muscular tissue, and blood were withdrawn 1.5, 3, 6, and 24 h after the L-BPA administration, at least 100 mg in volume. The samples were kept in labelled test tubes and stored at -80°C before the investigation. At every time point, tissue samples were withdrawn from three animals (n=12). By analogy, we analyzed L-BPA biodistribution in tumor-free animals (n=12). The study involved totally 24 animals.
Determination of 10B isotope content using inductively coupled plasma mass spectroscopy.
This study part was performed in the Institute of Microelectronics Technology and High-Purity Materials of Russian Academy of Sciences (Chernogolovka, Russia).
Decomposition of tissue samples. The procedure was performed in an autoclave decomposition system with resistance heating. Weighed portions of the samples under study, their mass being from 60 to 200 mg, were put into Teflon autoclave reaction tanks, added 2 ml of concentrated nitric acid — HNO3, 65% (Merk, Germany), and kept for 20 min at 160°C and for 1 h at 200°C.
Inductively coupled plasma mass spectroscopic analysis. The content of 10B and 11B isotopes, as well as 9Be and 115In (used as internal standards to account temporal variations of mass-spectrometer sensitivity and consider a matrix effect) in the samples was determined using XSeries 2 mass-spectrometer (Thermo Fisher
Scientific, USA), it has the following parameters: generator output capability of 1350 W; concentric PolyCon (Glass Expansion) as a dispenser; spraying chamber — quartz cooled (3°C); plasma-forming argon flow consumption of 13 L/min; auxiliary argon flow consumption — 0.89 L/min; studied sample consumption — 0.8 ml/min; resolution of 0.8 M.
The isotopes were determined in the samples by using external calibration by calibrating solutions containing from 1 to 500 jg/L of analytes; among them, there were multiple-element standard solution ICP-MS-68; solution A; multiple-element standard solution ICP-AM-6A; certified reference material "Traces of metals in drinking water", Standard B CRM-TMDW-B (all solutions manufactured by High-Purity Standards, USA).
Statistical data processing. The data were presented as an arithmetic mean by three dimensions ± mean root square deviation. The tumor-blood and tumor-organs concentration ratio (accumulation contrast) was calculated as the ratio of tumor 10B content to its content in the studied organs and tissues (blood). When calculating the time of achieving minimal therapeutic concentration for a curve of 10B content decrease in a tumor, there was developed a trend line with max R2 (power dependence), t (time) was calculating by the formula:
f=[Cmin/252.41][1/(-1-394)l,
where Cmin — minimal therapeutic concentration, equal to 24 |jg/g.
Results
In the course of our work in order to reveal L-BPA biodistribution, we studied isotope 10B content using ICP-MS in the following animal tissues and organs: liver, kidneys, spleen, intestine, lungs, skin, muscular tissue,
Ta bl e 1
10B isotope content in the organs and tissues of the animals with induced tumor after L-boronphenylalanine administration
Organ/tissue 10B content (|ig/g)
1.5 h 3 h 6 h 24 h
Tumor 142.0±4.41 59.30±3.63 18.67±4.0 3.10±0.01
Lung 45.0±1.40 18.90±1.16 6.57±1.41 <DL
Liver 31.50±0.98 15.13±0.93 5.33±1.14 <DL
Kidney 107.30±3.34 35.70±2.19 11.60±2.49 0.82±0.01
Spleen 50.77±1.58 25.13±1.54 6.90±1.48 <DL
Intestine 39.73±1.24 30.57±1.87 7.87±1.69 0.59±0.01
Muscle 67.40±2.10 25.37±1.55 7.50±1.61 0.75±0.01
Skin 73.17±2.27 28.70±1.76 9.70±2.08 <DL
Blood 32.17±1.0 16.33±1.0 4.67±1.0 <DL
Note: DL — determination limit.
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16 CTM | 2023 | V0l. 15 | N0.6 I.N. Druzkova, A.A. Pakhomova, N.I. Ignatova, A.R. Suleymanova, A.V. Maslennikova
180 160 140 120 100 80 60 40 20 0
20 25
Time (h)
#v
Figure 2. 10B isotope content in the organs and tissues of the animals with induced tumor after L-boronphenylalanine administration:
(a) 10B content decrease dynamics in a tumor; (b) 10B distribution in animal organs 1.5 h after L-boronphenylalanine administration
b
a
blood, and tumor (if any). Organ and blood samples were taken 1.5, 3, 6, and 24 h after intravenous L-BPA infusion.
Biodistribution of L-boronphenylalanine in the organs of the animals with induced tumor. Table 1 presents the mean 10B isotope in the studied tissues in the animals with induced tumor.
Figure 2 demonstrates the curve showing 10B isotope content decrease in a tumor depending on a time-point after drug infusion, also the diagram demonstrating 10B isotope concentration in the organs and tissues 1.5 h after the drug administration.
1.5 h after L-BPA administration, tumor-blood concentration ratio of 10B isotope was 4.4, while concentration ratios of tumor and normal tissues were from 1.3 to 4.5 (Table 2). Whereas 10B isotope content in a tumor significantly exceeded the required (according to literature data) therapeutic concentration (24-35 jg/g).
In approximation of the 10B isotope content decrease curve in a tumor and non-pathological organs, we
Blood 4.41 3.63 1.0 1.0
Table 3
10B isotope content in the organs and tissues
of the animals without tumor
after L-boronphenylalanine administration
Organ/tissue 10B content (|jg/g)
1.5 h 3 h 6 h 24 h
Lung 45.20±7.10 13.53±3.04 3.73±1.45 <DL
Liver 27.80±3.97 12.05±2.09 3.40±1.22 <DL
Kidney 59.73±4.16 28.80±9.43 9.27±4.37 <DL
Spleen 46.83±1.38 19.77±4.72 5.13±2.18 <DL
Intestine 36.37±5.06 14.87±3.13 3.93±1.27 <DL
Muscle 39.20±6.75 17.87±9.21 3.10±1.76 <DL
Skin 76.93±17.24 22.0±8.69 4.53±2.23 <DL
Blood 27.37±3.15 11.13±1.86 3.03±1.26 <DL
Note: DL — determination limit.
calculated the time to reach minimal required therapeutic concentration (24 ^g/g). Minimal concentration in a tumor was found to be achieved 5.4 h after the L-BPA administration, while for most inner organs except skin and kidneys this time appeared to be from 1.0 to 2.6 h. Therefore, the optimal time for tumor irradiation was estimated in the range from 1.5 to 5.5 h after the drug administration.
Biodistribution of L-boronphenylalanine in the organs of the animals without tumor. The study of L-BPA biodistribution in the organs and tissues of the animals without tumor showed 10B isotope content 1.5 h after the drug administration was the same as in the animals with tumor; however, the decreasing of 10B isotope concentration was slightly faster. Table 3 demonstrates mean 10B isotope content in the organs of the tumor-free animals.
Table 2
10B isotope contrast accumulation in a tumor
Organ/tissue In relation to an organ In relation to blood
1.5 h 3 h 1.5 h 3 h
Tumor 1.0 1.0 4.41 3.63
Lung 3.15 3.14 1.40 1.16
Liver 4.51 3.92 0.98 0.93
Kidney 1.32 1.66 3.34 2.19
Spleen 2.80 2.10 1.58 1.54
Intestine 3.57 1.94 1.24 1.87
Muscle 2.11 2.34 2.10 1.55
Skin 1.94 2.10 2.27 1.76
L-BPA Biodistribution is a Novel Model to Assess Neutron Sources CTM j 2023 j vol. 15 j No.6 17
Figure 3. Representative histological images of the mice organs and tumor:
(a) no L-BPA administration; (b) after L-BPA administration. Bar — 200 jm for all images, the area marked by dotted line was photographed with higher magnification (on the right panel)
Histological study. We collected the samples of some organs and tissues to verify the absence of L-BPA-related toxic effect in mice organs. Pathomorphological study revealed neither structural disturbances nor cell degeneration signs in the tissues and organs of the animals with subcutaneous tumor xenograft after L-BPA administration compared to the control animals, who were not injected with L-BPA (Figure 3).
Discussion
Using ICP-MS, maximal content of 10B isotope in a tumor (142.0±4.41 Mg/g) was determined 1.5 h after L-BPA administration, tumor-blood concentration ratio of 10B isotope was 4.4, while concentration ratios of tumor and normal tissues were from 1.3 to 4.5. The required therapeutic concentration of 10B isotope in a tumor persisted up to 5.5 h after the drug administration, the accumulation contrast sustaining 3.63 in relation to blood and 1.66-3.92 in relation to other organs.
The present characteristics are one of the highest values represented in literature. In the study by Seo et al. [27] for a model of subcutaneous heterotopic tumor U87 (human glioma) in intravenous L-BPA administration at a dose of 500 Mg/kg, 10B isotope content 1 h after injection was 23.7±5.1 Mg/g, the tumor-blood concentration ratio being 2.8. For a model DLD-1 (colorectal cancer) in the retroperitoneal space in intra-abdominal injection of L-BPA at a dose of 250 mg/kg, the accumulation in a tumor reached its maximum 4 h after the injection and was 123.6±29.9 Mg/g, the tumor-blood concentration ratio was 8.69±3.24 [28]. In the study by Yoshimura et al. [29], when forming lymphoma in the murine brain after intratumoral injection of L-BPA, 24 mg/kg, 10B content in a tumor was 9.9±1.6 Mg/g, the tumor-blood concentration ratio being 0.7. Tsygankova et al. [30] studied the model of subcutaneous glioma U87: L-BPA was administered at a dose of 350 mg/kg in the retro-orbital sinus; 10B isotope content in the tumor 2 h after the injection was 11.0±2.0 Mg/g, the tumor-
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18 CTM I 2023 I V0l. 15 I N0.6 I.N. Druzkova, A.A. Pakhomova, N.I. Ignatova, A.R. Suleymanova, A.V. Maslennikova
blood concentration ratio being 1.6. Lee et al. [31] had the same experimental model; 1 h after intravenous injection, 10B isotope content was determined as being 152.2±12.1 pg/g. These data have proved higher efficiency of intravenous administration compared to that injected in the retro-orbital sinus. However, this study did not show 10B isotope biodistribution in other animal organs.
It should be noted that higher isotope 10B content compared to other healthy tissues was found in kidneys; however, it was likely to be related to functional and structural characteristics of kidneys as a filtering organ, since filter structures comprise the most of the parenchyma: tubules filtering the apparatus (Bowman's capsule), as well as renal pelvises, where primary filtrate accumulates, which is in fact blood plasma. The values show 10B isotope content in biological fluids rather than in tissues. Relatively high 10B isotope content was also found in skin that is related, in particular, to active absorption of L-BPA by melanocytes, since its chemical structure is similar to tyrosine, which is necessary for melanogenesis [32].
Thus, in our research we studied for the first time L-BPA biodistribution in the organs of the animals with induced tumor, the dynamics was up to 24-h follow-up. The findings demonstrate a model tumor can be exposed to irradiation 1.5 h after the drug administration, when 10B isotope content in the tumor is about 140 pg/g; and irradiation is possible to last within at least 4 h. At the same time, throughout the radiation period in a tumor a minimal required concentration of 10B isotope will persist to perform BNCT, while accumulation contrast in relation to blood will be maintained at the level of 4.4-3.5, which will make it possible to achieve a therapeutic effect.
Conclusion
The obtained results of L-boronphenylalanine biodistribution dynamics demonstrate the tumor model (subcutaneous xenograft of CT26 in BALB/c mice) feasibility to assess the efficiency of new neutron sources for boron neutron capture therapy. L-boronphenylalanine was found to sufficiently accumulate in a tumor needed for performing effective treatment and sustaining minimal therapeutic concentration within long time period, with good accumulation contrast in relation to non-pathological organs that enables to minimize possible side effects of boron neutron capture therapy.
Study funding. The study was funded by the research work "The study of neutron D-D-generator efficiency for boron neutron capture therapy" as a part of Federal scientific and technical program "Development of synchrotron and neutron studies and research infrastructure".
Acknowledgements. The authors appreciate the staff members of Budker Institute of Nuclear Physics of Siberian Branch Russian Academy of Sciences
(Novosibirsk, Russia): S.Yu. Taskaev, D.A. Kasatov, A.I. Kasatova for providing L-BPA preparation, and the researchers of the Institute of Microelectronics Technology and High-Purity Materials of Russian Academy of Sciences (Chernogolovka, Russia): V.K. Karandyshev, V.A. Khvostikov, T.V. Orlova for performing the analysis of boron content in the samples of biological tissues using ICP-MS method.
Conflicts of interest. The authors declare no conflicts of interest related to the present study.
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I.N. Druzkova, A.A. Pakhomova, N.I. Ignatova, A.R. Suleymanova, A.V. Maslennikova
