Micro-collimators fabricated by chemical etching of thin polyallyldiglycol carbonate polymer films exposed to oxygen ions
Introduction
Studies on biological effects of α particles are important because (1) α particle irradiation is ubiquitous in our natural environment, which arise from our inhalation of radon progeny [1], [2], [3], [4], [5] and (2) α particles have large linear energy transfer (LET) values and are efficient in causing DNA double strand breaks (DSBs) [6], [7], [8], [9]. In α particle radiobiological experiments where the targets (such as cultured cells or other organisms) are irradiated with α particles, it is necessary to determine the dose absorbed by the targets, which requires the accurate positions and incident energies of α particle hits on the targets.
There are different approaches to determine the number and energy of α particles actually incident on the targets. The first one is to make use of versatile microbeam facilities in which the hit positions and the energies of the incident ions can be precisely controlled but will involve sophisticated equipment and instrumentation [10], [11], [12], [13], [14], [15]. Columbia’s group also developed a stand-alone microbeam without a conventional accelerator as a source of energetic ions, but focused α particles from an α emitter using a compound magnetic lens consisting of 24 permanent magnets arranged in two quadrupole triplets [16].
Another approach is to make use of a radioactive α particle source such as 241Am without focusing. However, due to the statistical nature of radioactivity and the random direction of α particle emission, both the hit positions and the energies of the α particles cannot be controlled. For this method, researchers have made use of solid-state nuclear track detectors (SSNTDs) as support substrates of the targets, which can record the hit positions of α particles and reveal these on subsequent chemical etching, to help determine the hit positions retrospectively (see Refs. [17], [18], [19], [20], [21], [22], [23], [24], [25], [26], [27], [28]). A review on SSNTDs was given by Nikezic and Yu [29]. The targets are irradiated with α particles, which pass through the SSNTD substrate to strike the targets in contact with the substrate. However, the incident angle of the α particles on the substrate will vary due to the random direction of α particle emission. Excessively oblique incidence will make accurate determination of hit positions difficult and at the same time will necessitate tedious procedures to determine the resultant energy of the α particles incident onto the target. To tackle this problem, Choi et al. [30] recently proposed the use of a micro-collimator to screen out those α particles insufficiently close to normal incidence with respect to the surface of the support substrate. The micro-collimator was an etched polyallyldiglycol carbonate (PADC) film, which was an SSNTD and commercially sometimes available as the CR-39 detector. PADC films have become popular support substrates for cell culture with track registration capability in that they are transparent, biocompatible [31] and are not dissolved in the alcohol used for sterilizing the substrate.
The micro-collimator fabricated by Choi et al. [30] was 15 μm thick; so the energy loss of α particles while traveling through the air columns in the collimator was minimized. By approximating an air channel as a frustum of a cone, the semi-cone angle was found to be ∼23°. As commented by Choi et al. [30], it is desirable to fabricate mirco-collimators with more cylindrical bores, i.e., those with smaller semi-cone angles, so that the α particles passing through the collimators will be closer to normal incidence. With the help of surfactants (5% DOWFAX 2A1) in the etchant, Choi et al. [30] succeeded to fabricate mirco-collimators with semi-cone angles of ∼20°. In the present paper, we proposed an alternative method to fabricate micro-collimators to restrict passing α particles to those even closer to normal incidence with respect to the substrate surface by making use of the high-energy heavy ions generated from the heavy-ion medical accelerator in Chiba (HIMAC). The fabricated micro-collimators were characterized and the results were discussed.
Section snippets
Preparation of PADC films
In the present work, PADC films with thicknesses of both 1 mm and 100 μm commercially available from Page Mouldings (Pershore) Limited, Worcestershire, were employed.
Here we first describe our use of the 100 μm PADC films. For different purposes, thin PADC films with different thicknesses smaller than 100 μm were prepared using the method proposed by Chan et al. [22]. Briefly, they were chemically etched in a 1 N NaOH/ethanol solution at 40 °C, for which the bulk etch rate was about 10 μm h−1 [32].
Relationship between track length and etching period
As described in Section 2.3, five pieces of rectangular films with a length of 1.8 cm, a width of ∼0.36 cm and a thickness of 74 μm PADC film, which were irradiated with 4.83 MeV/n oxygen ions, were used to study the relationship between the track length and the etching time. These films were etched separately in 6.25 N NaOH/water at 70 °C for different etching periods, such as, 0.5, 1.0, 1.5, 2.0 and 2.5 h, and were then embedded in resin. The resin embedding an etched PADC film was cut into two
Conclusions
In the present paper, we proposed a method to fabricate micro-collimators to restrict α particles to those with deviations from normal incidence with respect to the collimator surface. Commercially available PADC films with a thickness of 100 μm were first etched to a thickness of 70 μm, which were then irradiated by 4.83 MeV/n oxygen ions. These were chemically etched for at least 2.7 h to achieve etched-through air channels to form the micro-collimators. An experimental setup was employed to test
Acknowledgments
This study was supported by the research project with heavy ions (19-B413) at NIRS-HIMAC. We would like to thank Ms. Mayu Isono from Metropolitan University Tokyo for helping set up the beam line and with irradiation in HIMAC-MEXP and Ms. Kumiko Kodama for assistance with ion fluence analysis.
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