Complexes of myo-inositol-hexakisphosphate (InsP6) with zinc or lanthanum to enhance excretion of radioactive strontium from the body

Kazuma Ogawa; Miho Aoki; Sumi Kadono; Akira Odani

doi:10.1371/journal.pone.0195067

Abstract

⁹⁰Sr, which was released into the atmosphere and the ocean following the Chernobyl and Fukushima Daiichi nuclear power plant disasters, is an important nuclear fission element. Compounds that inhibit the absorption of ⁹⁰Sr into the bloodstream and enhance its elimination can be beneficial in decreasing the absorbed radiation dose in people exposed to ⁹⁰Sr. Recently, we prepared complexes of myo-inositol-hexakisphosphate (InsP6) with zinc or lanthanum as decorporation agents. These complexes, called Zn-InsP6 and La-InsP6 respectively, are insoluble in water and can potentially chelate additional metal cations. Hypothesizing that these complexes can assist the excretion of ⁹⁰Sr from the body, we evaluated them using ⁸⁵Sr instead of ⁹⁰Sr. In in vitro binding experiments, Zn-InsP6 showed higher strontium adsorption capacity than La-InsP6. We then performed in vivo biodistribution experiments of Zn-InsP6 in mice after oral administration of ⁸⁵SrCl₂. Mice treated with Zn-InsP6 showed significantly lower bone accumulation of radioactivity than mice in a non-treatment control group. Zn-InsP6 adsorbed radiostrontium in the gastrointestinal tract, inhibited this ion’s absorption into the bloodstream, and enhanced its excretion in the feces. Therefore, Zn-InsP6 appears to be a promising ⁹⁰Sr “decorporation” agent.

Citation: Ogawa K, Aoki M, Kadono S, Odani A (2018) Complexes of myo-inositol-hexakisphosphate (InsP6) with zinc or lanthanum to enhance excretion of radioactive strontium from the body. PLoS ONE 13(4): e0195067. https://doi.org/10.1371/journal.pone.0195067

Editor: Chunhua Song, Pennsylvania State University, UNITED STATES

Received: November 13, 2017; Accepted: March 15, 2018; Published: April 3, 2018

Copyright: © 2018 Ogawa et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: All relevant data are within the paper.

Funding: The authors received no specific funding for this work.

Competing interests: The authors have declared that no competing interests exist.

Introduction

Strontium, an alkaline earth metal, acts as a calcium mimic and highly accumulates in bone [1]. Different types of radiostrontium exist. ⁸⁹Sr (t_1/2 = 50.5 d) as ⁸⁹SrCl₂ has been administered as a pain palliation for patients with bone metastases of cancer [2]. Following the intravenous injection of ⁸⁹SrCl₂ solution, ⁸⁹Sr²⁺ is incorporated into collagen mineralization during new bone formation, so accumulates at high levels at the sites of bone metastases. Consequently, the intense pain associated with bone cancer is diminished by the radiation emitted by ⁸⁹Sr. On the other hand, ⁹⁰Sr (t_1/2 = 29.1 y) is one of the most important nuclear fission elements. After the nuclear power plant disasters of Chernobyl and Fukushima Daiichi, ⁸⁹Sr and ⁹⁰Sr were released into the atmosphere and the ocean [3–6]. ⁹⁰Sr is more harmful to humans than ⁸⁹Sr, because ⁹⁰Sr has a much longer half-life, and its daughter radionuclide, ⁹⁰Y (t_1/2 = 64.1 h), emits high-energy beta particles. It has been reported that internal exposure to ⁹⁰Sr could be associated with the development of leukemia and osteosarcoma [7,8]. Therefore, compounds inhibiting the absorption of radiostrontium from the gastrointestinal tract into the bloodstream and enhancing its elimination after intake can decrease the absorbed radiation dose of people exposed to radiostrontium. Indeed, basic research has shown that alginate can promote the excretion of ⁹⁰Sr [9,10].

Myo-inositol-hexakisphosphate (phytic acid: InsP6, Fig 1) is a natural compound that abounds in plants, especially in whole grains, cereals, legumes, seeds, and nuts [11]. Due to its structure, InsP6 exhibits high chelation potential with many kinds of metal cations [12,13]. Recently, we prepared complexes of InsP6 with zinc or lanthanum ions (Zn-InsP6 and La-InsP6, respectively) and evaluated them as radiocesium “decorporation” agents, because both complexes are insoluble in water and are spacious enough to potentially accommodate additional metal cations coordinated by chelation. In fact, InsP6 is soluble in water, but chelation with zinc or lanthanum ions decreases the solubility in water, and thereby reduces the absorption in the intestinal tract.

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Fig 1. The structure of myo-inositol-hexakisphosphate (InsP6).

https://doi.org/10.1371/journal.pone.0195067.g001

In this study, we hypothesized that Zn-InsP6 and La-InsP6 can work as ⁹⁰Sr decorporation agents and evaluated their potential in vitro and in vivo. Experiments using normal mice were performed to evaluate the influence of Zn-InsP6 on the biodistribution of radiostrontium. In these experiments, we replaced ⁹⁰Sr with ⁸⁵Sr (T_1/2 = 64.8 d) because ⁸⁵Sr emits gamma rays, which are easy to measure.

Materials and methods

Materials

⁸⁵SrCl₂ (> 111 GBq/g) was purchased from PerkinElmer (Waltham, MA, USA). InsP6 was purchased from Sigma-Aldrich (St. Louis, MO, USA) as phytic acid sodium salt hydrate, InsP6•6Na⁺•6H₂O. Other reagents were of reagent grade and used as received. All sections of this report adhere to the ARRIVE Guidelines for reporting animal research [14]. A completed ARRIVE guidelines checklist is included in supporting information (S1 File).

In vitro adsorption of ⁸⁵Sr to La-InsP6 and Zn-InsP6

La-InsP6 and Zn-InsP6 were prepared by the method previously reported [15]. La-InsP6 (La: InsP6 = 2: 1) and Zn-InsP6 (Zn: InsP6 = 2: 1) were used for in vitro and in vivo experiments. La-InsP6 and Zn-InsP6 samples (10 mg/mL) containing various concentrations of Sr and 10 kBq/mL of ⁸⁵Sr, in 20 mM HEPES buffer (pH 7.4) containing 10 mM Na⁺, were prepared. After shaking at 1,000 rpm and 37°C for 1 h, the samples were centrifuged at 10,000g and room temperature for 10 min. The radioactivity of the supernatant was measured using an auto-well gamma counter (ARC-380; Hitachi healthcare, Ltd., Tokyo, Japan), and the counts were corrected for background radiation. Control experiments were performed using the same procedure but without M-InsP6 (M = Zn or La). The binding ratios were determined as follows:

Effects of cations (Na⁺ or Ca²⁺) on the in vitro adsorption of ⁸⁵Sr to M-InsP6 (M = Zn or La)

Sr solutions (300 ppm at final concentration) containing 10 kBq/mL of ⁸⁵Sr in 20 mM HEPES buffer (pH 7.4) containing 10 mM Na⁺, 20 mM Na⁺, 50 mM Na⁺, 10 mM Na⁺ + 10 mM Ca²⁺, and 10 mM Na⁺ + 40 mM Ca²⁺ were prepared by dissolution of NaCl or CaCl₂. M-InsP6 samples (10 mg) were suspended in 1 mL of each Sr solution. After shaking the suspensions at 1,000 rpm and 37°C for 1 h, the binding ratio of each sample to M-InsP6 was determined using the methods described above.

Biodistribution experiments after oral administration of ⁸⁵Sr with pretreatment of Zn-InsP6

Experiments with all animals (N = 59) were conducted in strict accordance with the Guidelines for the Care and Use of Laboratory Animals of Kanazawa University. The animal experimental protocols used were approved by the Committee on Animal Experimentation of Kanazawa University. The animals were housed (4 mice in one polycarbonate cage) under conventional conditions with free access to food and water at 23°C with a 12-hour alternating light/dark schedule. Autoclaved wood chips were applied as bedding material. The behavior of the mice during the experimental period was normal.

Mice were randomly divided into three groups. In a Zn-InsP6 administration group (N = 16), Zn-InsP6 suspension in 5% glucose aqueous solution (30 mg / 0.5 mL) was orally administered into 6-week-old male ddY mice (23–30 g, Japan SLC, Inc., Hamamatsu, Japan) using disposable flexible-type animal-feeding-needles (Fuchigami, Muko, Japan).

In an InsP6 administration group (N = 18), InsP6 solution in 5% glucose aqueous solution (20 mg / 0.5 mL) was orally administered. In a control group (N = 25), 0.5 mL of 5% glucose aqueous solution was orally administered. The number of mice of each group was optimized for ethical reasons, balancing between the number of animals required for statistical reasons for analysis and minimizing the number of mice. Then, just after administration of either Zn-InsP6 suspension, InsP6 solution, or glucose aqueous solution, saline solution of ⁸⁵SrCl₂ (37 kBq / 100 μL) was orally administered. All animals showed no signs of illness following the administration of the compounds. Mice were sacrificed by decapitation at 1, 4, 24, and 48 h post-administration. Tissues of interest were removed and weighed, and radioactivity counts were determined. From 12 h pre-administration to 24 h post-administration, the fasting was carried out. No animal died prematurely (i.e. besides euthanasia) due to the experimental procedures.

Radiation dose estimates for ⁹⁰Sr

Radiation dose was calculated from the data of the biodistribution experiments using ⁸⁵Sr as described previously [16]. Namely, for estimation of the radiation dose absorbed by the bone marrow, the percent dose of radioactivity per gram tissue in the bone marrow was assumed to be 30% of the percent dose of radioactivity per gram tissue in the blood. The red marrow mass was assumed to be 25% of blood volume. The blood, bone, and muscle mass of mice were assumed to be 8%, 5%, and 48% of body weight, respectively. According to the International Commission on Radiological Protection (ICRP), an equal distribution of the radionuclide to trabecular and cortical bone was assumed [17]. The non-decay-corrected activity from each source organ was converted to a percentage of the injected radioactivity. The area under each organ’s activity curve from time zero to infinity was calculated by extrapolation of the biodistribution data. To correct for the different ratios of organ to total body weights in mouse and in human, we used the following organ correction factor (CR): According to the values, the radiation doses for ⁹⁰Sr were calculated for an adult male patient using OLINDA 1.0 software (Vanderbilt University) [18].

Statistical evaluation

A one-way analysis of variance (ANOVA) followed by Dunnett’s post hoc test compared to the control group was used for experiments of cation effects on the in vitro adsorption and biodistribution experiments.

Results were considered statistically significant at p < 0.05.

Results

Experiments of in vitro ⁸⁵Sr adsorption by Zn-InsP6 and La-InsP6 (Langmuir adsorption model)

Adsorption capacity of Zn-InsP6 and La-InsP6 for strontium (Sr) was evaluated by the Langmuir model. The Langmuir equation is expressed as: (1) where q (mg / g) represents Sr binding per Zn-InsP6 and La-InsP6, C_eq (mg / L) is the equilibrium concentration of Sr, q_max (mg / g) is the maximum sorption capacity, and a (L / mg) is the sorption constant.

As shown in Fig 2, the amount of strontium bound to Zn-InsP6 and La-InsP6 increased linearly at low strontium concentrations, and plateaued at high strontium concentrations, indicating saturation of the adsorption sites. These data meet the requirements of the Langmuir adsorption model, indicating the correctness of the assumption that the adsorbate acts as a uniform surface with finite identical binding sites characterized by monolayer adsorption of the adsorbate. The maximum sorption capacity of Zn-InsP6 and La-InsP6 was estimated as 133.7 and 6.4 mg Sr/g, respectively.

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Fig 2. Langmuir model.

Adsorption capacity of (A) Zn-InsP6 and (B) La-InsP6 to strontium. Data are expressed as the mean ± SD of three samples.

https://doi.org/10.1371/journal.pone.0195067.g002

Effects of cations (Na⁺ or Ca²⁺) on in vitro adsorption of ⁸⁵Sr²⁺ by Zn-InsP6 and La-InsP6

Fig 3 shows how other cations affect the binding of strontium to Zn-InsP6 and La-InsP6. The presence of Na⁺ decreased the amount of strontium bound to La-InsP6, but not the amount bound to Zn-InsP6. On the other hand, the presence of Ca²⁺ substantially decreased the amount of strontium bound to both complexes, and this effect depended on the Ca²⁺ concentration.

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Fig 3. Adsorption of ⁸⁵Sr to IP6 complexes in the presence of cations.

Binding ratios of ⁸⁵Sr²⁺ to (A) Zn-InsP6 and (B) La-InsP6 in the presence of Na⁺ or Ca²⁺. Zero additional metal concentration (white columns) means using HEPES buffer containing 10 mM Na⁺. Data are expressed as the mean ± SD of three samples. Significance was determined using one-way ANOVA followed by Dunnett’s post hoc test (*p < 0.05 vs. Control (HEPES buffer containing 10 mM Na⁺)).

https://doi.org/10.1371/journal.pone.0195067.g003

Biodistribution experiments

To evaluate whether Zn-InsP6 can enhance the elimination of ⁸⁵Sr from the body in vivo, ⁸⁵SrCl₂ was orally administrated to mice in “treatment groups” just after oral administration of Zn-InsP6 suspension or InsP6 solution. The biodistribution of radioactivity in the mice after 1, 4, 24, and 48 h of oral administration of ⁸⁵SrCl₂, with or without pretreatment with Zn-InsP6 or InsP6, are reported in Tables 1–4. Pretreatment with Zn-InsP6 significantly decreased the accumulation of radioactivity in the bone and the blood at the early time points after oral administration of ⁸⁵SrCl₂, relative to the non-treatment control group. These results indicate that Zn-InsP6 inhibited the absorption of ⁸⁵Sr²⁺ from the intestine into the bloodstream and enhanced the excretion of ⁸⁵Sr²⁺ in the feces. At 48 h after administration of ⁸⁵SrCl₂, the radioactivity levels in all study groups were low in all tissues except bone.

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Table 1. Biodistribution of radioactivity in mice at 1 h after oral administration of ⁸⁵SrCl₂ with pretreatment of 5% glucose aqueous solution (control), InsP6 in 5% glucose aqueous solution, or Zn-InsP6 in 5% glucose aqueous solution.

https://doi.org/10.1371/journal.pone.0195067.t001

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Table 2. Biodistribution of radioactivity in mice at 4 h after oral administration of ⁸⁵SrCl₂ with pretreatment of 5% glucose aqueous solution (control), InsP6 in 5% glucose aqueous solution, or Zn-InsP6 in 5% glucose aqueous solution.

https://doi.org/10.1371/journal.pone.0195067.t002

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Table 3. Biodistribution of radioactivity in mice at 24 h after oral administration of ⁸⁵SrCl₂ with pretreatment of 5% glucose aqueous solution (control), InsP6 in 5% glucose aqueous solution, or Zn-InsP6 in 5% glucose aqueous solution.

https://doi.org/10.1371/journal.pone.0195067.t003

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Table 4. Biodistribution of radioactivity in mice at 48 h after oral administration of ⁸⁵SrCl₂ with pretreatment of 5% glucose aqueous solution (control), InsP6 in 5% glucose aqueous solution, or Zn-InsP6 in 5% glucose aqueous solution.

https://doi.org/10.1371/journal.pone.0195067.t004

Dosimetry

The absorbed radiation dose of ⁹⁰Sr was extrapolated from the data of the ⁸⁵Sr biodistribution experiments, because ⁹⁰Sr should behave identically to ⁸⁵Sr in vivo. Table 5 shows the estimated absorbed radiation doses after oral intake of ⁹⁰SrCl₂ over a one-month period, with and without pretreatment with Zn-InsP6 or InsP6. The Zn-InsP6 treatment decreased the effective dose equivalent of radiation by approximately one half, relative to the non-treatment group. However, the effective dose equivalent was not decreased by treatment with InsP6 (in the absence of the zinc ion).

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Table 5. Absorbed dose estimates in human after oral intake of ⁹⁰SrCl₂ with pretreatment of InsP6 or Zn-InsP6, or non-treatment control.

https://doi.org/10.1371/journal.pone.0195067.t005

Discussion

We recently synthesized complexes of La-InsP6 and Zn-InsP6 as radiocesium decorporation agents. We expected that these insoluble complexes can chelate cesium ions in the gastrointestinal tract, inhibiting their absorption into the bloodstream and enhancing the excretion of radioactive Cs⁺ in the feces. According to the experimental results, Zn-InsP6 and La-InsP6 bind Cs⁺ in vitro but were ineffective as decorporation agents in vivo, because their binding to Cs⁺ was neither strong nor selective enough [15]. In an in vitro study, binding of Cs⁺ by La-InsP6 and Zn-InsP6 was inhibited in the presence of Na⁺, K⁺, or Ca²⁺. Among these inhibiting cations, Ca²⁺ most detrimentally affected the binding of La-InsP6 and Zn-InsP6 to Cs⁺. Since InsP6 is known to have a high binding affinity for Ca²⁺ [19], and given the similar chemical properties of Ca²⁺ and Sr²⁺, we assumed that InsP6 can bind a strontium ion more strongly than a cesium ion. Thus, we hypothesized that La-InsP6 and Zn-InsP6 could work as decorporation agents for radioactive strontium.

In the in vitro binding experiments, Zn-InsP6 showed higher strontium ion adsorption capacity than La-InsP6 (Fig 2). This difference may derive from the inherent characteristics of the two ions, La³⁺ and Zn²⁺, when forming chelation complexes with InsP6. Whereas Zn²⁺ can form tetracoordinate and hexacoordinate chelation complexes, La³⁺ can only form hexacoordinate complexes. It is speculated that La-InsP6, which should be a strong polymer complex with a dense structure formed by hexacoordination, has limited room for accommodating chelated Sr²⁺. In contrast, Zn-InsP6 has a flexible structure formed by tetracoordination, with more space available for Sr²⁺ binding. These scenarios might explain the higher adsorption capacity of Zn-InsP6 as compared to La-InsP6. Based on the results of the in vitro experiments, we performed in vivo experiments using Zn-InsP6 alone.

In the Zn-InsP6 treatment group, much lower radioactivity was observed in the blood 1 h after ⁸⁵Sr²⁺ administration when compared to the untreated control group (Table 1). This evidence suggests that Zn-InsP6 prominently inhibited absorption of ⁸⁵Sr²⁺ into the bloodstream from the intestine, due to the adsorption of ⁸⁵Sr²⁺ by the insoluble Zn-InsP6 complex. Since ⁸⁵Sr²⁺ transported by blood preferably accumulates into bone in the whole body, mice in the Zn-InsP6-treated group showed much lower radioactivity in their femurs than mice in the non-treatment control group. Therefore, Zn-InsP6 may be a promising ⁹⁰Sr decorporation agent. Bone accumulation of high-energy beta-particle-emitting radionuclides such as ⁹⁰Sr greatly affect the radiation dose in bone marrow. Moreover, as the biological half-life of strontium in bone tissue is extremely long, strontium accumulated in bone maintains its detrimental effects over a long period [20]. Thus, ⁹⁰Sr bone accumulation is the most important factor determining the effective dose of radiation (Tables 4 and 5).

As InsP6 can bind Sr²⁺, InsP6 alone may also work as a strontium decorporation agent. To test this idea, we performed the biodistribution experiment on an additional control group that had been pre-treated with InsP6. According to the results, InsP6 seemed to inhibit the absorption of ⁸⁵Sr²⁺ into the bloodstream and the accumulation of radioactivity in bone because mice treated with InsP6 displayed lower radioactivity in their blood and bone in the early time points than mice in the non-treatment control group. However, 48 h after administration of ⁸⁵Sr²⁺, the radioactivity biodistributions were almost identical in the InsP6-treated mice and the non-treated mice (Table 4). This evidence indicates that InsP6 alone delayed the movement of ⁸⁵Sr²⁺ along the gastrointestinal tract, but did not prevent its absorption into the bloodstream. In other words, the water-soluble InsP6 (without metal ions) failed as a strontium decorporation agent.

In a previous report, we evaluated Chlorella—a genus of single-cell green algae that grow in fresh water—as a decorporation agent for radioactive strontium [21]. In that study, the maximum strontium sorption capacity of Chlorella was estimated as 9.06 mg Sr/g. In biodistribution experiments after oral administration of ⁸⁵SrCl₂ in mice, pretreatment with Chlorella significantly decreased the accumulation of radioactivity in bone compared to the control group, but the effects of Chlorella showed less than expected ability to inhibit strontium absorption into the bloodstream from the gastrointestinal tract. The efficacies of Zn-InsP6 and Chlorella are not easily comparable because the appropriate maximum dose for each compound is not understood. Nevertheless, adsorption of radiostrontium in the intestine and inhibition of its absorption into the bloodstream were anticipated to occur through similar mechanisms by both species. The maximum adsorption capacity of Zn-InsP6 was estimated as 133.7 mg Sr/g, much higher than that of Chlorella. This result was reflected in the data of in vivo mouse experiments: pretreatment with Zn-InsP6 prominently decreased the accumulation of radioactivity in mouse bones, whereas the inhibitory effects of Chlorella were not very pronounced. Since Chlorella is a health food, and its safety is highly guaranteed, we cannot simply conclude that Zn-InsP6 is a better option than Chlorella. However, Zn-InsP6 is certainly an effective decorporation agent.

In conclusion, these results indicate that the insoluble Zn-InsP6 complex adsorbs radioactive strontium in the gastrointestinal tract, inhibits its absorption into the bloodstream, and enhances its excretion in the feces. Consequently, extrapolating from the results of the biodistribution experiments conducted in mice, the estimated effective dose of ⁹⁰Sr radiation in a human treated with Zn-InsP6 is approximately half of that of the control group. Therefore, Zn-InsP6 presents as a promising ⁹⁰Sr decorporation agent.

Supporting information

S1 File. ARRIVE check list.

https://doi.org/10.1371/journal.pone.0195067.s001

(DOCX)

Acknowledgments

The authors would like to thank Enago for the English language review.

References

1. Davis J, Cook ND, Pither RJ (2000) Biologic mechanisms of 89SrCl2 incorporation into type I collagen during bone mineralization. J Nucl Med 41: 183–188. pmid:10647622
- View Article
- PubMed/NCBI
- Google Scholar
2. Ogawa K, Washiyama K (2012) Bone target radiotracers for palliative therapy of bone metastases. Curr Med Chem 19: 3290–3300. pmid:22664247
- View Article
- PubMed/NCBI
- Google Scholar
3. Brumfiel G, Cyranoski D (2011) Fukushima deep in hot water. Nature 474: 135–136. pmid:21654773
- View Article
- PubMed/NCBI
- Google Scholar
4. Kanai Y (2012) Monitoring of aerosols in Tsukuba after Fukushima Nuclear Power Plant incident in 2011. J Environ Radioact 111: 33–37. pmid:22071363
- View Article
- PubMed/NCBI
- Google Scholar
5. Evangeliou N, Balkanski Y, Cozic A, Moller AP (2014) Global and local cancer risks after the Fukushima Nuclear Power Plant accident as seen from Chernobyl: a modeling study for radiocaesium (¹³⁴Cs &¹³⁷Cs). Environ Int 64: 17–27. pmid:24361922
- View Article
- PubMed/NCBI
- Google Scholar
6. Yablokov AV, Nesterenko VB (2009) 1. Chernobyl contamination through time and space. Ann N Y Acad Sci 1181: 5–30. pmid:20002040
- View Article
- PubMed/NCBI
- Google Scholar
7. Dungworth DL, Goldman M, Switzer J, McKelvie DH (1969) Development of a myeloproliferative disorder in beagles continuously exposed to ⁹⁰Sr. Blood 34: 610–632. pmid:5260601
- View Article
- PubMed/NCBI
- Google Scholar
8. Barnes DW, Carr TE, Evans EP, Loutit JF (1970) ⁹⁰Sr-induced osteosarcomas in radiation chimaeras. Int J Radiat Biol Relat Stud Phys Chem Med 18: 531–537. pmid:4925187
- View Article
- PubMed/NCBI
- Google Scholar
9. Haratake M, Hatanaka E, Fuchigami T, Akashi M, Nakayama M (2012) A strontium-90 sequestrant for first-aid treatment of radiation emergency. Chem Pharm Bull (Tokyo) 60: 1258–1263.
- View Article
- Google Scholar
10. Sutton A (1967) Reduction of strontium absorption in man by the addition of alginate to the diet. Nature 216: 1005–1007. pmid:6072965
- View Article
- PubMed/NCBI
- Google Scholar
11. Graf E (1983) Applications of phytic acid. Journal of the American Oil Chemists’ Society 60: 1861–1867.
- View Article
- Google Scholar
12. Szkudelski T (2005) Phytic acid-induced metabolic changes in the rat. J Anim Physiol Anim Nutr (Berl) 89: 397–402.
- View Article
- Google Scholar
13. Graf E, Eaton JW (1990) Antioxidant functions of phytic acid. Free Radic Biol Med 8: 61–69. pmid:2182395
- View Article
- PubMed/NCBI
- Google Scholar
14. Kilkenny C, Browne WJ, Cuthill IC, Emerson M, Altman DG (2010) Improving bioscience research reporting: the ARRIVE guidelines for reporting animal research. PLoS Biol 8: e1000412. pmid:20613859
- View Article
- PubMed/NCBI
- Google Scholar
15. Ogawa K, Aoki M, Fukuda T, Kadono S, Kiwada T, Odani A (2017) Complexes of myo-Inositol-Hexakisphosphate (IP6) with Zinc or Lanthanum for the Decorporation of Radiocesium. Chem Pharm Bull (Tokyo) 65: 261–267.
- View Article
- Google Scholar
16. Ogawa K, Kawashima H, Shiba K, Washiyama K, Yoshimoto M, Kiyono Y, et al. (2009) Development of ⁹⁰Y-DOTA-conjugated bisphosphonate for treatment of painful bone metastases. Nucl Med Biol 36: 129–135. pmid:19217524
- View Article
- PubMed/NCBI
- Google Scholar
17. Liepe K, Hliscs R, Kropp J, Runge R, Knapp FF Jr., Franke WG (2003) Dosimetry of ¹⁸⁸Re-hydroxyethylidene diphosphonate in human prostate cancer skeletal metastases. J Nucl Med 44: 953–960. pmid:12791825
- View Article
- PubMed/NCBI
- Google Scholar
18. Stabin MG, Sparks RB, Crowe E (2005) OLINDA/EXM: the second-generation personal computer software for internal dose assessment in nuclear medicine. J Nucl Med 46: 1023–1027. pmid:15937315
- View Article
- PubMed/NCBI
- Google Scholar
19. Simpson CJ, Wise A (1990) Binding of zinc and calcium to inositol phosphates (phytate) in vitro. Br J Nutr 64: 225–232. pmid:2400762
- View Article
- PubMed/NCBI
- Google Scholar
20. Harrison JE, McNeill KG, Finlay JM, Sheppard RH, Mortimer DC (1966) A preliminary study of human calcium metabolism using long-term whole body tracer measurements. Can Med Assoc J 94: 1092–1097. pmid:5933055
- View Article
- PubMed/NCBI
- Google Scholar
21. Ogawa K, Fukuda T, Han J, Kitamura Y, Shiba K, Odani A (2016) Evaluation of Chlorella as a Decorporation Agent to Enhance the Elimination of Radioactive Strontium from Body. PLoS One 11: e0148080. pmid:26828430
- View Article
- PubMed/NCBI
- Google Scholar

[ref1] 1. Davis J, Cook ND, Pither RJ (2000) Biologic mechanisms of 89SrCl2 incorporation into type I collagen during bone mineralization. J Nucl Med 41: 183–188. pmid:10647622
View Article
PubMed/NCBI
Google Scholar

[2] View Article

[3] PubMed/NCBI

[4] Google Scholar

[ref2] 2. Ogawa K, Washiyama K (2012) Bone target radiotracers for palliative therapy of bone metastases. Curr Med Chem 19: 3290–3300. pmid:22664247
View Article
PubMed/NCBI
Google Scholar

[6] View Article

[7] PubMed/NCBI

[8] Google Scholar

[ref3] 3. Brumfiel G, Cyranoski D (2011) Fukushima deep in hot water. Nature 474: 135–136. pmid:21654773
View Article
PubMed/NCBI
Google Scholar

[10] View Article

[11] PubMed/NCBI

[12] Google Scholar

[ref4] 4. Kanai Y (2012) Monitoring of aerosols in Tsukuba after Fukushima Nuclear Power Plant incident in 2011. J Environ Radioact 111: 33–37. pmid:22071363
View Article
PubMed/NCBI
Google Scholar

[14] View Article

[15] PubMed/NCBI

[16] Google Scholar

[ref5] 5. Evangeliou N, Balkanski Y, Cozic A, Moller AP (2014) Global and local cancer risks after the Fukushima Nuclear Power Plant accident as seen from Chernobyl: a modeling study for radiocaesium (¹³⁴Cs &¹³⁷Cs). Environ Int 64: 17–27. pmid:24361922
View Article
PubMed/NCBI
Google Scholar

[18] View Article

[19] PubMed/NCBI

[20] Google Scholar

[ref6] 6. Yablokov AV, Nesterenko VB (2009) 1. Chernobyl contamination through time and space. Ann N Y Acad Sci 1181: 5–30. pmid:20002040
View Article
PubMed/NCBI
Google Scholar

[22] View Article

[23] PubMed/NCBI

[24] Google Scholar

[ref7] 7. Dungworth DL, Goldman M, Switzer J, McKelvie DH (1969) Development of a myeloproliferative disorder in beagles continuously exposed to ⁹⁰Sr. Blood 34: 610–632. pmid:5260601
View Article
PubMed/NCBI
Google Scholar

[26] View Article

[27] PubMed/NCBI

[28] Google Scholar

[ref8] 8. Barnes DW, Carr TE, Evans EP, Loutit JF (1970) ⁹⁰Sr-induced osteosarcomas in radiation chimaeras. Int J Radiat Biol Relat Stud Phys Chem Med 18: 531–537. pmid:4925187
View Article
PubMed/NCBI
Google Scholar

[30] View Article

[31] PubMed/NCBI

[32] Google Scholar

[ref9] 9. Haratake M, Hatanaka E, Fuchigami T, Akashi M, Nakayama M (2012) A strontium-90 sequestrant for first-aid treatment of radiation emergency. Chem Pharm Bull (Tokyo) 60: 1258–1263.
View Article
Google Scholar

[34] View Article

[35] Google Scholar

[ref10] 10. Sutton A (1967) Reduction of strontium absorption in man by the addition of alginate to the diet. Nature 216: 1005–1007. pmid:6072965
View Article
PubMed/NCBI
Google Scholar

[37] View Article

[38] PubMed/NCBI

[39] Google Scholar

[ref11] 11. Graf E (1983) Applications of phytic acid. Journal of the American Oil Chemists’ Society 60: 1861–1867.
View Article
Google Scholar

[41] View Article

[42] Google Scholar

[ref12] 12. Szkudelski T (2005) Phytic acid-induced metabolic changes in the rat. J Anim Physiol Anim Nutr (Berl) 89: 397–402.
View Article
Google Scholar

[44] View Article

[45] Google Scholar

[ref13] 13. Graf E, Eaton JW (1990) Antioxidant functions of phytic acid. Free Radic Biol Med 8: 61–69. pmid:2182395
View Article
PubMed/NCBI
Google Scholar

[47] View Article

[48] PubMed/NCBI

[49] Google Scholar

[ref14] 14. Kilkenny C, Browne WJ, Cuthill IC, Emerson M, Altman DG (2010) Improving bioscience research reporting: the ARRIVE guidelines for reporting animal research. PLoS Biol 8: e1000412. pmid:20613859
View Article
PubMed/NCBI
Google Scholar

[51] View Article

[52] PubMed/NCBI

[53] Google Scholar

[ref15] 15. Ogawa K, Aoki M, Fukuda T, Kadono S, Kiwada T, Odani A (2017) Complexes of myo-Inositol-Hexakisphosphate (IP6) with Zinc or Lanthanum for the Decorporation of Radiocesium. Chem Pharm Bull (Tokyo) 65: 261–267.
View Article
Google Scholar

[55] View Article

[56] Google Scholar

[ref16] 16. Ogawa K, Kawashima H, Shiba K, Washiyama K, Yoshimoto M, Kiyono Y, et al. (2009) Development of ⁹⁰Y-DOTA-conjugated bisphosphonate for treatment of painful bone metastases. Nucl Med Biol 36: 129–135. pmid:19217524
View Article
PubMed/NCBI
Google Scholar

[58] View Article

[59] PubMed/NCBI

[60] Google Scholar

[ref17] 17. Liepe K, Hliscs R, Kropp J, Runge R, Knapp FF Jr., Franke WG (2003) Dosimetry of ¹⁸⁸Re-hydroxyethylidene diphosphonate in human prostate cancer skeletal metastases. J Nucl Med 44: 953–960. pmid:12791825
View Article
PubMed/NCBI
Google Scholar

[62] View Article

[63] PubMed/NCBI

[64] Google Scholar

[ref18] 18. Stabin MG, Sparks RB, Crowe E (2005) OLINDA/EXM: the second-generation personal computer software for internal dose assessment in nuclear medicine. J Nucl Med 46: 1023–1027. pmid:15937315
View Article
PubMed/NCBI
Google Scholar

[66] View Article

[67] PubMed/NCBI

[68] Google Scholar

[ref19] 19. Simpson CJ, Wise A (1990) Binding of zinc and calcium to inositol phosphates (phytate) in vitro. Br J Nutr 64: 225–232. pmid:2400762
View Article
PubMed/NCBI
Google Scholar

[70] View Article

[71] PubMed/NCBI

[72] Google Scholar

[ref20] 20. Harrison JE, McNeill KG, Finlay JM, Sheppard RH, Mortimer DC (1966) A preliminary study of human calcium metabolism using long-term whole body tracer measurements. Can Med Assoc J 94: 1092–1097. pmid:5933055
View Article
PubMed/NCBI
Google Scholar

[74] View Article

[75] PubMed/NCBI

[76] Google Scholar

[ref21] 21. Ogawa K, Fukuda T, Han J, Kitamura Y, Shiba K, Odani A (2016) Evaluation of Chlorella as a Decorporation Agent to Enhance the Elimination of Radioactive Strontium from Body. PLoS One 11: e0148080. pmid:26828430
View Article
PubMed/NCBI
Google Scholar

[78] View Article

[79] PubMed/NCBI

[80] Google Scholar

Figures

Abstract

Introduction

Materials and methods

Materials

In vitro adsorption of 85Sr to La-InsP6 and Zn-InsP6

Effects of cations (Na+ or Ca2+) on the in vitro adsorption of 85Sr to M-InsP6 (M = Zn or La)

Biodistribution experiments after oral administration of 85Sr with pretreatment of Zn-InsP6

Radiation dose estimates for 90Sr

Statistical evaluation

Results

Experiments of in vitro 85Sr adsorption by Zn-InsP6 and La-InsP6 (Langmuir adsorption model)

Effects of cations (Na+ or Ca2+) on in vitro adsorption of 85Sr2+ by Zn-InsP6 and La-InsP6

Biodistribution experiments

Dosimetry

Discussion

Supporting information

S1 File. ARRIVE check list.

Acknowledgments

References

In vitro adsorption of ⁸⁵Sr to La-InsP6 and Zn-InsP6

Effects of cations (Na⁺ or Ca²⁺) on the in vitro adsorption of ⁸⁵Sr to M-InsP6 (M = Zn or La)

Biodistribution experiments after oral administration of ⁸⁵Sr with pretreatment of Zn-InsP6

Radiation dose estimates for ⁹⁰Sr

Experiments of in vitro ⁸⁵Sr adsorption by Zn-InsP6 and La-InsP6 (Langmuir adsorption model)

Effects of cations (Na⁺ or Ca²⁺) on in vitro adsorption of ⁸⁵Sr²⁺ by Zn-InsP6 and La-InsP6