Seitenfus Rafael, Ferreira Paulo Roberto Walter, Santos Gabriel Oliveira Dos, Alves Rafael José Vargas, Kalil Antonio Nocchi, Barros Eduardo Dipp de, Glehen Olivier, Casagrande Thaís Andrade Costa, Bonin Eduardo Aimoré, Silva Junior Edison Martins da
MD, Surgical Oncologist, Department of Surgical Oncology, Hospital Santa Rita, Santa Casa de Misericórdia de Porto Alegre, RS, Brazil. Intellectual, scientific, conception and design of the study; acquisition, analysis and interpretation of data; technical procedures; manuscript preparation and writing; final approval.
MSc, Assistant Professor, Graduate Program in Engineering, Innovation and Entrepreneurship, Faculdade de Desenvolvimento do Rio Grande do Sul (FADERGS), Porto Alegre-RS, Brazil; and Research, Development and Innovation Manager, Bhio Supply, Esteio-RS, Brazil. Intellectual, scientific, conception and design of the study; analysis and interpretation of data; manuscript preparation, final approval.
Acta Cir Bras. 2017 Dec;32(12):1056-1063. doi: 10.1590/s0102-865020170120000007.
To evaluate the technical feasibility and homogeneity of drug distribution of pressurized intraperitoneal aerosol chemotherapy (PIPAC) based on a novel process of intraperitoneal drug application (multidirectional aerosolization).
This was an in vivo experimental study in pigs. A single-port device was manufactured at the smallest diameter possible for multidirectional aerosolization of the chemotherapeutic drug under positive intraperitoneal pressure. Four domestic pigs were used in the study, one control animal that received multidirectional microjets of 9 mL/sec for 30 min and three animals that received multidirectional aerosolization (pig 02: 9 mL/sec for 30 min; pigs 03 and 04: 3 mL/sec for 15 min). Aerosolized silver nitrate solution was applied for anatomopathological evaluation of intraperitoneal drug distribution.
Injection time was able to maintain the pneumoperitoneum pressure below 20 mmHg. The rate of moderate silver nitrate staining was 45.4% for pig 01, 36.3% for pig 02, 36.3% for pig 03, and 72.7% for pig 04.
Intra-abdominal drug distribution had a broad pattern, especially in animals exposed to the drug for 30 min. Our sample of only four animals was not large enough to demonstrate an association between aerosolization and a higher silver nitrate concentration in the stained abdominal regions.
基于一种新型腹腔内给药方法(多向雾化)评估加压腹腔内气溶胶化疗(PIPAC)的技术可行性和药物分布的均匀性。
这是一项在猪身上进行的体内实验研究。制造了一个单端口装置,其直径尽可能小,以便在腹腔内正压下对化疗药物进行多向雾化。该研究使用了4头家猪,1头对照动物接受9毫升/秒的多向微喷射30分钟,3头动物接受多向雾化(猪02:9毫升/秒,30分钟;猪03和猪04:3毫升/秒,15分钟)。应用雾化硝酸银溶液对腹腔内药物分布进行解剖病理学评估。
注射时间能够将气腹压力维持在20 mmHg以下。猪01的中度硝酸银染色率为45.4%,猪02为36.3%,猪03为36.3%,猪04为72.7%。
腹腔内药物分布具有广泛的模式,特别是在接触药物30分钟的动物中。我们仅4只动物的样本量不足以证明雾化与染色腹部区域中较高的硝酸银浓度之间存在关联。