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A prototype single-port device for pressurized intraperitoneal aerosol chemotherapy. Technical feasibility and local drug distribution
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.
  • Seitenfus, Rafael; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Ferreira, Paulo Roberto Walter; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Santos, Gabriel Oliveira dos; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Alves, Rafael José Vargas; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Kalil, Antonio Nocchi; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Barros, Eduardo Dipp de; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Glehen, Olivier; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Casagrande, Thaís Andrade Costa; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Bonin, Eduardo Aimoré; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
  • Silva Junior, Edison Martins da; Santa Casa de Misericórdia de Porto Alegre. Hospital Santa Rita. Department of Surgical Oncology. BR
Acta cir. bras ; 32(12): 1056-1063, Dec. 2017. tab, graf
Article in English | LILACS | ID: biblio-886194
ABSTRACT
Abstract

Purpose:

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).

Methods:

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.

Results:

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.

Conclusions:

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.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Peritoneal Neoplasms / Drug Delivery Systems / Aerosols Type of study: Prognostic study Limits: Animals Language: English Journal: Acta cir. bras Journal subject: General Surgery / Procedimentos Cir£rgicos Operat¢rios Year: 2017 Type: Article Affiliation country: Brazil Institution/Affiliation country: Santa Casa de Misericórdia de Porto Alegre/BR

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Full text: Available Index: LILACS (Americas) Main subject: Peritoneal Neoplasms / Drug Delivery Systems / Aerosols Type of study: Prognostic study Limits: Animals Language: English Journal: Acta cir. bras Journal subject: General Surgery / Procedimentos Cir£rgicos Operat¢rios Year: 2017 Type: Article Affiliation country: Brazil Institution/Affiliation country: Santa Casa de Misericórdia de Porto Alegre/BR