A novel marker design for magnetic marker monitoring in the human gastrointestinal tract.

Magnetic marker monitoring (MMM) is a technique to determine the motility of the gastrointestinal tract and to observe the dissolution of pharmaceutical compounds. Today's magnetic markers usually consist of magnetized magnetite. Because of their weak magnetic fields, highly sensitive sensor systems are required. For a wider class of applications, stronger markers and more flexible measurement setups are necessary. In this paper, a novel marker design is introduced. This marker comprises one permanent magnet and a compartment of iron powder in a magnetically unstable configuration. During dissolution of the pharmaceuticals, the powder is redistributed around the magnet, thereby altering the externally measured magnetic induction. Based on this design, magnetically marked tablets and capsules were prepared and their magnetic field during dissolution was observed. Magnetic induction values were between 16 and 0.2 µT at distances of 5-30 cm, which is considerably higher compared to the pico-Tesla range of conventional markers. During dissolution, the magnetic induction decreased by between 14% and 27%. These values could be confirmed in detailed finite element method simulations. In conclusion, the present results indicate that our novel marker design is well suited for MMM with more flexible sensor technologies, such as magnetoresistive sensors.

Dosimetry of a linear accelerator under respiratory gating.

In the present study, the impact of respiratory gating on the beam characteristics of a linear accelerator is investigated. The main focus is put on the influence of the duty cycle. Measurements were performed on a linear accelerator type Oncor (Siemens) with photon energies 6 MV and 15 MV, equipped with the Anzai gating system AZ-733V. Depth dose curves and beam profiles were found not to be significantly altered by gating even for duty cycles down to 5% for realistic respiration frequencies (dose variations all <2.5%). However, for very small duty cycles, the absolute dosimetry changes significantly (dose deviations > 10%), leading to clinically relevant underdoses. The crucial parameter for the dosimetry is the number of monitor units per gate. Our results imply that treatment planning for respiratory gating can be performed on the basis of data obtained under ungated operation if and only if the absolute gates sizes during treatment are sufficiently large. The limiting values for the gate sizes have to be determined individually for each accelerator.