BACKGROUND:
75Se (
120 days,
215 keV) offers advantages over
192Ir (
74 days,
360 keV) as a high dose rate brachytherapy source due to its lower gamma energy and longer half-life. Despite its widespread use in industrial gamma radiography, a
75Se brachytherapy source has yet to be manufactured.
PURPOSE: A novel
75Se-based source design with a vanadium diselenide core, titled the SeCure source, was proposed. This study aimed to evaluate the feasibility of this source design for dosimetry and manufacturability purposes and to develop an activated prototype source.
METHODS: The source was modeled and integrated into the Monte Carlo-based treatment planning system RapidBrachyMCTPS, where its TG-43U1 parameters, photon spectrum, and broad beam first half-value layers (HVL
1) and tenth-value layers (TVL
1) in lead, tungsten, and concrete were calculated. A prototype source was manufactured, and the vanadium diselenide content of the capsule was verified with neutron radiography. The source was then activated to a nominal activity of
mCi at the McMaster Nuclear Reactor. The activity was measured with two separate dose calibrators. Gamma spectroscopy was used to characterize any activated radioactive contaminants in the source, and wipe testing was performed to check for any leakage of
75Se from the encapsulation.
RESULTS: The SeCure source's TG-43U1 parameters were computed, showing that
times the activity of
75Se is required relative to
192Ir to achieve the same dose rate in water at (1 cm, 90
). The mean spectral energy of the source is
keV, resulting in reduced first half-value and tenth-value layers relative to
192Ir in attenuating materials. For example, the
was reduced from
mm to
mm in lead, from
mm to
mm in tungsten, and from
mm to
mm in concrete. The activated source achieved the desired activity, indicated as
mCi and
mCi at the end of irradiation on the two dose calibrators. All identified radionuclide contaminants decaying below
of the
75Se activity after 5 days post-irradiation. Wipe testing only identified radioactive contaminants present in activated titanium, with only
mCi of
detected 72 h post-irradiation, indicating that the integrity of the encapsulation was maintained.
CONCLUSIONS: The SeCure design possesses the dosimetric, spectral, and physical properties necessary for a feasible high dose rate brachytherapy source. Next, manufacturing of a high-activity SeCure source will be pursued.