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Comparative study of cisplatin‐iodized oil suspension and emulsion for transcatheter arterial chemoembolization of rabbit VX2 liver tumors
Author(s) -
Mine Takahiko,
Murata Satoru,
Ueda Tatsuo,
Onozawa Shiro,
Onda Munehiko,
Naito Zenya,
Kumita Shinichiro
Publication year - 2012
Publication title -
hepatology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.123
H-Index - 75
eISSN - 1872-034X
pISSN - 1386-6346
DOI - 10.1111/j.1872-034x.2011.00942.x
Subject(s) - cisplatin , transcatheter arterial chemoembolization , medicine , saline , emulsion , iodized oil , chemotherapy , pharmacology , gastroenterology , hepatocellular carcinoma , chemistry , biochemistry
Aim: To evaluate the antitumor effects and hepatotoxicity of transcatheter arterial chemoembolization (TACE) with cisplatin‐iodized oil suspension and emulsion in a rabbit tumor model. Methods: Transcatheter arterial chemoembolization was performed on 12 rabbits with hepatic VX2 tumors using a cisplatin suspension (1 mg/kg cisplatin and 0.1 mL/kg iodized oil, n = 6) or emulsion (1 mg/kg cisplatin, 0.1 mL/kg of iodized oil, and 0.1 mL/kg saline solution, n = 6). Time series changes in plasma platinum concentration were compared over 24 h. All rabbits were killed at 7 days after TACE, and the growth ratio and residual viable proportion of tumors were calculated on the basis of ultrasonographic and histopathological findings. Hepatotoxicity was also evaluated. Differences between the two groups were statistically assessed with the Mann–Whitney U ‐test. The animal care committee of our institute approved this study. Results: Plasma platinum concentrations were significantly higher in the suspension group than in the emulsion group at 0.5–24 h after TACE ( P < 0.05). Growth ratios (−24.6 ± 9.98% vs. 21.4 ± 8.87%, respectively; P = 0.004) and residual viable proportions of tumors (25.8 ± 5.02% vs. 51.1 ± 11.4%, respectively; P = 0.009) were significantly lower in the suspension group than in the emulsion group. Hepatotoxicity was transient in all rabbits. Conclusion: Cisplatin‐iodized oil suspensions facilitated the slow release of cisplatin at the tumor border. A suspension is preferable to an emulsion for drug delivery and the antitumor effect during the treatment of VX2 liver tumors with TACE.