Technology development of hyperthermic pressurized intraperitoneal aerosol chemotherapy (hPIPAC)

被引:13
作者
Bachmann, C. [1 ,2 ]
Sautkin, I [1 ,2 ]
Nadiradze, G. [1 ,2 ]
Archid, R. [1 ,2 ]
Weinreich, F. J. [1 ,2 ]
Koenigsrainer, A. [1 ,2 ]
Reymond, M. A. [1 ,2 ,3 ]
机构
[1] Univ Tubingen, Dept Gen & Transplant Surg, Tubingen, Germany
[2] Univ Tubingen, Natl Ctr Pleura & Peritoneum, Tubingen, Germany
[3] Univ Hosp Tubingen, NCPP, Hoppe Seyler Str 3, D-72076 Tubingen, Germany
来源
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES | 2021年 / 35卷 / 11期
关键词
Intraperitoneal chemotherapy; Hyperthermia; Laparoscopy; Medical devices; Aerosol; SAFETY;
D O I
10.1007/s00464-021-08567-y
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Optimized drug delivery systems are needed for intraperitoneal chemotherapy. The aim of this study was to develop a technology for applying pressurized intraperitoneal aerosol chemotherapy (PIPAC) under hyperthermic conditions (hPIPAC). Methods This is an ex-vivo study in an inverted bovine urinary bladder (IBUB). Hyperthermia was established using a modified industry-standard device (Humigard). Two entry and one exit ports were placed. Warm-humid CO2 was insufflated in the IBUB placed in a normothermic bath to simulate body thermal inertia. The temperature of the aerosol, tissue, and water bath was measured in real-time. Results Therapeutic hyperthermia (target tissue temperature 41-43 degrees C) could be established and maintained over 30 min. In the first phase (insufflation phase), tissue hyperthermia was created by insufflating continuously warm-humid CO2. In the second phase (aerosolization phase), chemotherapeutic drugs were heated up and aerosolized into the IBUB. In a third phase (application phase), hyperthermia was maintained within the therapeutic range using an endoscopic infrared heating device. In a fourth phase, the toxic aerosol was discarded using a closed aerosol waste system (CAWS). Discussion We introduce a simple and effective technology for hPIPAC. hPIPAC is feasible in an ex-vivo model by using a combination of industry-standard medical devices after modification. Potential pharmacological and biological advantages of hPIPAC over PIPAC should now be evaluated.
引用
收藏
页码:6358 / 6365
页数:8
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