LUCAS VERDI ANGELOCCI
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Resumo IPEN-doc 28462 Assessing Ir-192 as an alternative to I-125 in ophthalmic treatment2020 - ANGELOCCI, L.; NOGUEIRA, B.R.; SOUZA, C.D. de; ZEITUNI, C.A.; ROSTELATO, M.E.C.M.Purpose or Objective: Brachytherapy sources for ocular melanoma usually contain Co-60, I-125, Pd-103 or Ru/Rh-106 as radionuclides. Ir-192 is not a preconized radioactive material for this purpose, although it is used for other brachytherapy applications. Higher mean energy from Ir-192 emission (ca. 380 keV) may be a reason for the preference of I-125 (35 keV) or Pd-103 (21 keV) over it, since low penetration is desired on the small structures of the human eye. This is not, however, an excluding criterion, considering Co-60 and Ru/Rh-106 have even higher mean energies. The demand in Brazil for lower-cost seeds to treat ocular melanoma lead to the development of an Ir-192 seed to make treatment more accessible, but since it is not used as an ophthalmic brachytherapy source, before its dosimetry is considered, one should care about the possibility of using it over more stablished materials. Considering this, the aim of this work is to assess the possibility of using Ir-192 seeds as ophthalmic brachytherapy sources by comparing some dosimetric parameters of a new seed model with the most stablished I-125 seed in literature, OncoSeed 6711. Material and Methods: As an initial study on the topic, this work relies only on Monte-Carlo simulations using MCNP4C transport code. Parameters analyzed are air-kerma strength, dose-rate constant and depth-dose curve, attention given to points within the human eye dimensions. The medium considered was homogeneous water, as it is a good approximation to the eye tissues in terms of composition and density and allows for future comparisons with TG-43 based calculations. OncoSeed 6711 is not produced anymore, but its long term as the reference source for dosimetry was considered. A 20 mm COMS ophthalmic applicator was also modeled and considered to be fully loaded with each seed model to compare the same parameters at a realistically clinical approach. Results: As expected, due to the higher energy of the Ir-192 emission spectrum, dose fall-off on the transversal axis of the seeds is less pronounced for the new seed model. The steeper dose gradient for I-125 is also visible on the doserate constant value. The effect of using a COMS applicator only strengthens this characteristic. Depth-dose curves were calculated up to the distance of 5 cm, both for a single seed and for an applicator fully loaded with 24 seeds. All the eye components relevant for dosimetry are located within this range, like the cells of the crystallin and the optical nerve. Conclusion: If one expects to use Ir-192 as an alternative to I-125 in ophthalmic cancer treatment, at least the dosimetry following TG-43 protocol should be carried with utmost attention, as undesirable dose to healthy nearby tissues is unavoidable. Crafting a different applicator most suited for this radionuclide is a possibility that can be taken into account. Another recommendation is to go beyond TG-43 water-based protocol and actually estimate dose to relevant eye components.Resumo IPEN-doc 26910 Efficiancy of hydrogen peroxide for cleaning production areas and equipments in the Laboratory for Brachyterapy Sources Production2017 - BAPTISTA, T.; ROSTELATO, M.C.M.; ZEITUNI, C.; PERINI, E.A.; SOUZA, C.D. de; MARQUES, J. de O.; NOGUEIRA, B.R.; ANGELOCCI, L.V.Purpose: A great challenge in the brachytherapy sources production is to fulfill the Good Manufacturing Practices (GMPs) requirements, involving the process validation and of all supporting activities such as cleaning and sanitization. The increasingly strict requirements for quality assurance system, with several norms, normative resolutions and rules that must follow both medical products and radiochemical requirements, has led to a constant validation concerns. The main goal of GMP is to reduce inherent risks such as product contamination with microorganisms and cross-contamination. Methods: In the Laboratory for Brachytherapy Sources Production it was established a cleaning program for cleanrooms and hot cells using a hydrogen peroxide solution (6%). This work aims to assess the effectiveness of this cleaning agent in reducing and/or eliminating microbial load into the cleanrooms and equipments to acceptable levels in accordance with the current legislation. Results: The analysis was conducted using the results of the environmental monitoring program with settling contact plates in cleanrooms after the cleaning procedures. Furthermore, it was possible to evaluate the action of the sanitizing agent on the microbial population at the equipment and cleanrooms’ surfaces. It was also evaluated the best way to accomplish the cleaning program considering the dosimetry factor in each production process, hence the importance of radiological contamination. All the following environmental monitoring procedures presented satisfactory results, showing that the cleaning procedures was able to reduce and maintain the acceptable levels of viable and non-viable particles for the cleanroom classification (ISO 5 and ISO 7). The cleaning process with this sanitizer (hydrogen peroxide) can be performed quickly right before the production; allowing the production of brachytherapy sources without after use residues. Conclusion: This data will help the production of a clean and reliable product.