Abstract
Background: Oxaliplatin-based hyperthermic intraperitoneal chemotherapy (HIPEC) involves mixing oxaliplatin with 5% dextrose solution (5DW) to prevent the structural degradation of oxaliplatin in chloride-containing fluids. This study evaluated oxaliplatin degradation in carrier fluids containing different chloride ion concentrations to determine a carrier fluid that is optimal for use in oxaliplatin-based HIPEC. Methods: Five types of carrier fluids (normal saline, half saline, 5DW, Dianeal PD-2 peritoneal dialysis solution, and non-chloride Dianeal solution) were compared. An in vitro study was performed that monitored an oxaliplatin concentration of 1 ml (2 mg/ml) oxaliplatin mixed in 24 ml of each carrier fluid during 3 days to evaluate the rate of oxaliplatin degradation in each carrier fluid. An in vivo study, which subjected Sprague-Dawley rats to HIPEC for 60 min, also was performed. The efficacy of each carrier fluid for preserving oxaliplatin was evaluated using area under the curve (AUC) ratios between peritoneal fluid and plasma. Results: The degradation rate of oxaliplatin in non-chloride fluids was significantly lower than in chloride-containing fluids. However, the rate was less than 10 to 15% at 30 min. The in vivo study indicated that oxaliplatin concentrations in peritoneal fluids did not differ significantly, whereas those in plasma did differ. The AUC ratios of both normal saline and Dianeal were higher than those of 5DW and non-Cl– Dianeal solutions. Conclusions: Chloride-containing fluids, such as normal saline or Dianeal, which display high absorption rates of oxaliplatin and acceptable degradation rates, may be more beneficial for use in oxaliplatin-based HIPEC than 5DW.
Original language | English |
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Pages (from-to) | 8583-8592 |
Number of pages | 10 |
Journal | Annals of surgical oncology |
Volume | 29 |
Issue number | 13 |
DOIs | |
Publication status | Published - 2022 Dec |
Bibliographical note
Funding Information:This study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT (NRF-2018R1A6A1A03023718, NRF-2019R1I1A1A01058889, NRF-2021R1A2C1012853, NRF-2022R1A2C1013201) and the Research Grant from Gangnam Severance Hospital, Yonsei University College of Medicine (3-2020-0315). We thank Jee Eun Lee for aiding with the in vitro study and Hye Sun Lee for performing the statistical analyses.
Publisher Copyright:
© 2022, Society of Surgical Oncology.
All Science Journal Classification (ASJC) codes
- Surgery
- Oncology