I. INTRODUCTION
Nuclear technology has found many applications in medical diagnosis and disease treatment, such as the X/γ-CT, X/γ-cure, and positron emission computed tomography (PET), etc. In radiation therapy, the side effects, most of which are predictable and expected, are avoidable in the patient’s normal tissue. It is desirable to understand the origination of side effects and ways to reduce the unwanted side effects. Besides the complex biochemical effects [1-3] of γ rays on molecules, mainly through ionization and Compton scattering [4], γ rays can induce a nuclear reaction through positron-electron pair production and photon activation reactions. Though the possibility is quite low, the high energy γ rays (Eγ > ∼10 MeV) can also induce nuclear activation reactions and activate the stable nucleus into radioactive nucleus. It is well known that around γ = 15 MeV, the nucleus has a strong γ-absorption (γ-emission) rate because of the giant dipole resonance [5, 6, 7, 8], in which stable nuclei can be activated to unstable ones via (γ, n) or (γ, p) reactions. In particular, for nuclei with small mass numbers, the (γ, n) cross section may form a peak below 15 MeV, for example, 13C [8], 17O [9], 18O [10] and 29Si [11]. The energy of γ rays used in γ cure can be larger than 10 MeV, which potentially can induce γ-activation reactions. The residue nucleus of γ-activation reactions in potential can be one kind of inner radioactivity and harmful to normal tissue if it has a long half-life. It is interesting to study the γ-induced reactions on the elements forming the human body in the energy range of γ-cure. Motivated by this reason, in this article, the γ-induced reactions on the isotopes of essential elements of the human body will be investigated. Meanwhile, the possible nuclear activation reactions for these isotopes will be discussed.
II. METHODS
The γ induced reactions on the nucleus are called photon-nucleus reactions, which have attracted much attention in nuclear physics. A lot of γ induced reactions on various isotopes have been measured for different purposes. The optical model is very successful in predicting the γ induced reactions for outgoing particles. In the Talys toolkit [12], the ECIS-06 code has been implanted as a subroutine to deal with the optical model calculations [13, 14]. The Talys toolkit is usually used in the analysis of experiments and generating of nuclear data. With different adjustable parameters, the Talys toolkit can reproduce the neutron induced reactions on the nuclei with a mass of A > 30. While for a nucleus of A < 30, the parameters in Talys should be adjusted to coincide with the experimental results [14, 15]. Talys version 1.4 is adopted in this work. We will not describe the model since the aim of this work is not to introduce the physics of Talys. The complete description of Talys1.4 can be found in the user manual [12]. The long half-life time radioactive nuclei produced from stable nuclei by γ-activation reactions will be the focus. The (γ, n) and (γ, p) channels will be calculated by considering whether the residue nucleus is unstable or not, and whether the residue nucleus has a long half-life time. The calculated results are also compared to the experimental results, which are extracted from the EXFOR library [16]. The default parameters in Talys1.4 are adopted, since we do not aim to exactly reproduce the measured data, which requires the careful adjustment of parameters. All the natural abundance data and the half-life time of the isotopes are taken from the National Nuclear Data Center (NNDC) [17]. The knowledge about human elements in the following discussion is extracted from the website of the Micronutrient Information Center of Linus Pauling Institute (MICLPI) [18].
III. RESULTS AND DISCUSSION
In medical experimentation, the samples of blood and hair are generally inspected. In this work, we study the γ induced reactions on the isotopes of Na, Cl, Ca, K, and Mg, which have a relatively large weight in the human body. The γ induced reactions on the isotopes of important microelements will also be studied, such as Fe, which has a long retention time in the body.
A. 23Na(γ, n)22Na
Sodium has only one stable isotope, 23Na. For an adult, sodium accounts for 0.15% of the human body, most of which exists in bones (about 40–47%), extracellular fluids (about 44–50%), and blood (about 9–10%).The function of sodium is to maintain the balance of osmotic pressures and moisture inside and outside the cell and to assist in the normal operation of the nerves, heart, muscles, and other physiological functions [19]. The retention time of sodium is short in the body, and is discharged mainly by sweat and the renal system. The normal level of Na+ in blood is 136–146 mmol/L.
For the 23Na(γ, n)22Na reaction, the residue 22Na is a radioactive nucleus, which decays to 22Ne via positron emissions with a half-life time of 2.60 y. 22Na is used to create test-objects and point-sources for positron emission tomography. In nuclear accidents, the sodium isotopes are also indicators to estimate exposure to neutron radiation [15].
The cross section (σ) of 23Na(γ, n)22Na is plotted in Fig. 1. The calculated threshold energy (Eth) for 23Na(γ, n)22Na is 12.50 MeV, which agrees with the measured results. The measured σ for the (γ, n) reaction by Alvarez et al. [20] and Veyssiere et al. [21] are consistent. When Eγ > Eth, the measured σ increases quickly with Eγ, but forms a plateau when Eγ > 16 MeV. The calculated results overestimate the measured ones in 12.5 MeV < Eγ < 16 MeV. The measured σ for 23Na(γ, n)22Na within the range of 16 MeV < Eγ < 23 MeV is around 10 mb. It could be necessary to track the 22Na in body after the γ cure since it has a long half-life and sodium accounts for a relatively large percentage of body weight.
-201503/1001-8042-26-03-016/alternativeImage/1001-8042-26-03-016-F001.jpg)
B. 42Ca(γ, n)41Ca, 43Ca(γ, p)42K, and 44Ca(γ, p)43K
Calcium is the most abundant mineral in the human body. About 99% of the calcium in the body is in bones and teeth, with the other 1% in the blood and soft tissues. Calcium is deposited in body and kept for a long time. The normal level of calcium in the blood is 1.55–2.10 mmol/L.
For the γ + Ca reaction, the three isotopes 42Ca, 43Ca, and 44Ca (with the natural abundance 0.647%, 0.135%, and 2.08%, respectively), are considered. For the 42Ca(γ, n)41Ca, 43Ca(γ, p)42K and 44Ca(γ, p)43K channels, 41Ca decays into 41K via electron capture with a half-life of 1.02×105 a; 42K decays to 42Ca and 43K decays into 43Ca, both via electron emission with the half-lifes of 12.32 h and 22.30 h, respectively. There are no natural 42K and 43K isotopes.
No measured data was found for the 42Ca(γ, n)41Ca, 43Ca(γ, p)42K and 44Ca(γ, p)43K reactions. The calculated results are plotted in Fig. 2. The calculated Eth for the 42Ca(γ, n)41Ca, 43Ca(γ, p)42K and 44Ca(γ, p)43K channels are 11.48, 10.68 and 12.16 MeV, respectively. The distributions of the cross section form peaks around 19.80, 19.40 and 20.60 MeV, respectively. Since these reactions have Eth around 10 MeV, and the residue nuclei have relatively long half-life, it is necessary to track the decays of 41Ca, 42K, and 43K after the γ therapy.
-201503/1001-8042-26-03-016/alternativeImage/1001-8042-26-03-016-F002.jpg)
C. 25Mg(γ, p)24Na
Magnesium accounts for about 0.05% of the weight of an adult. Magnesium is an essential mineral and a cofactor for hundreds of enzymes. It is also one of the main components of bone and an essential mineral element in the human body. The normal value of magnesium levels in blood is 0.6–0.95 mmol/L.
The natural abundance of 25Mg is about 10%. For the 25Mg(γ, p)24Na reaction, 24Na is unstable, which allows it to decay to 24Mg via electron emission with a half-life of 15.00 h. The calculated results are plotted in Fig. 2. The Eth is 12.06 MeV. The cross sections form a peak around 21 MeV and the largest cross section is 6.25 mb, which is very small compared to the other elements.
The results for the γ induced reactions on isotopes of the human essential elements have been summarized in Table 1. The cross sections for the reactions are very low, with the maximum values no larger than 100 mb. From Table 1, it can be seen that 23Na, 37Cl, and 42Ca can be activated by γ with σ> 10 mb. At the same time, the radioactive residue nuclei have a long half-life. By considering the weight percentages that the elements account for and the importance of them in body, it is suggested to track the 22Na, 42,43K, and 41Ca after γ therapy.
Reaction | 23Na(γ, n)22Na | 25Mg(γ, p)24Na | 37Cl(γ, n)36Cl | 42Ca(γ, n)41Ca | 43Ca(γ, p)42K | 44Ca(γ, p)43K |
---|---|---|---|---|---|---|
Eth(MeV) | 12.50 | 12.06 | 10.31 | 11.48 | 10.68 | 12.16 |
Decay mode | e+ | e- | e- | EC | e- | e- |
Half-life time | 2.6027 y | 15.00 h | 3.01×105 y | 1.02×105 a | 12.32 h | 22.30 h |
Final residue | 22Ne | 24Mg | 36Ar | 41K | 42Ca | 43Ca |
aMax. of σ | 10.58 | 6.25 | 37.14 | 34.47 | 6.83 | 4.42 |
bHigh σ range | 19.6–21.2 | — | 11–23.5 | 14.2–23 | — | — |
IV. SUMMARY
In this article, the γ induced activated reactions on the stable nuclei of human essential elements have been presented. The possible changes of nuclei are discussed. In γ therapy, the radioactive nucleus produced by the γ induced activated reactions can potentially be one kind of inner radioactivity. The Talys1.4 toolkit was used to predict the cross sections of the reactions. By considering whether the residue nucleus is radioactive or not and whether it has a long half-life, the γ induced reactions on 23Na, 25Mg, 37Cl, and 42, 43,44Ca are investigated, which include the (γ, n) and (γ, p) channels. The cross sections for the reactions are very low, with the maximum values no larger than 100 mb. By considering the threshold energies, the half-life of the residue nucleus, the percentages of the elements accounting for weight and the importance of them in body, it is suggested to track the 22Na, 42,43K, and 41Ca after γ therapy.
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