Search

This study evaluated the performance of tissue equivalent polymer gel dosimetry as a tool for 3-dimensional dose quality assurance to using Magnetic Resonance Imaging (MRI) measure the dose characteristics of therapeutic radiation using and applying it to intensity modulated radiation therapy (IMRT). The polymer gel under normoxic conditions was synthesized using Gelatin, methyacrylic acid (MAA), hydroquinone (HQ) and tetrakis hydroxymethyl phosphonium chloride (THPC), and a polymer gel dosimeter was fabricated by placing the gel into each phantom appropriate for experimental use. The dose reaction experiment employed Co gamma-rays and a 6-MV photon beam with a dose range of 0 ∼ 14 Gy. The dose characteristics of the polymer gel were compared with those of an ion chamber, Gafchromic EBT2 film, by using MRI. The linear correlations coefficient for the polymer gel, the ion chamber and the film were r = 0.970, r = 0.999, and r = 0.972, respectively. The percentage depth doses at a depth of 50 mm were 85.8% and 84.6% for the polymer gel and the ion chamber, respectively, giving a difference of 1.2%. On the other hand, the percentage depth dose at the depth of 100 mm was 66.2% and 63.7% for the polymer gel and the ion chamber, respectively, indicating a 2.5% gap. The flatness and the symmetry of the gel dosimeter on the cross plane were 3.80% and 3.58%, respectively. The gel dosimeter was applied to an IMRT. The doses measured in the 100% dose domain of the therapeutic plan was 96.2%, 103.0%, and 100% for the axial, sagittal and coronal planes, respectively, highlighting the applicability of the gel dosimeter as a 3-dimensional dosimeter.

This study developed a portable respiratory training device to improve breathing stability, which is an important element in using the CyberKnife Synchrony respiratory tracking device, one of the typical Stereotactic Radiation Therapy (SRT) devices. It produced an interface for users to be able to select one of two displays, a graph type and a bar type, supported an auditory system that helps them expect next respiration by improving a sense of rhythm of their respiratory period, and provided comfortable respiratory inducement. By targeting 5 applicants and applying individual respiratory period detected through a self-developed program, it acquired signal data of 'guide respiration' that induces breathing through signal data gained from 'free respiration' and an auditory system, and evaluated the usability by comparing deviation average values of respiratory period and respiratory amplitude. It could be identified that respiratory period decreased 55.74±0.14% compared to free respiration, and respiratory amplitude decreased 28.12±0.10% compared to free respiration, which confirmed the consistency and stability of respiratory. SBRT, developed based on these results, using the portable respiratory training device, for liver cancer or lung cancer, is evaluated to be able to help reduce delayed treatment time due to respiratory instability and improve treatment accuracy, and if it could be applied to developing respiratory training applications targeting an android-based portable device in the future, even use convenience and economic efficiency are expected.