Litterst C L, Collins J M, Lowe M C, Arnold S T, Powell D M, Guarino A M
Cancer Treat Rep. 1982 Jan;66(1):157-61.
Doxorubicin was administered to rats in a simulated "belly bath" protocol. Fifty milliliters of various concentrations of drug solution was administered ip and was allowed to remain in situ for either 4 or 36 hours prior to removal. Animals were analyzed at 2, 14, and 60 days after treatment. Doses ranged from lethal (75 and 150 micrograms/ml for 4 hours; 12 and 24 micrograms/ml for 36 hours) to nontoxic (5 micrograms/ml for 4 hours). The most common lesion in surviving animals was chronic fibrosing peritonitis. Grossly, there were large volumes of peritoneal fluid in animals exposed to low concentrations (12 and 24 micrograms/ml) for 36 hours, but peritoneal adhesions were the most commonly observed finding when higher concentrations (20-150 micrograms/ml) were used for 4 hours. Commonly observed systemic toxic effects (bone marrow, gastrointestinal tract, and heart) were not seen in this study. Vehicle-treated control animals were negative for all histologic lesions and gross observations.
采用模拟“腹腔灌洗”方案给大鼠注射阿霉素。腹腔注射50毫升不同浓度的药物溶液,在取出前使其在原位保留4小时或36小时。在治疗后2天、14天和60天对动物进行分析。剂量范围从致死剂量(4小时为75和150微克/毫升;36小时为12和24微克/毫升)到无毒剂量(4小时为5微克/毫升)。存活动物中最常见的病变是慢性纤维性腹膜炎。大体观察,暴露于低浓度(12和24微克/毫升)36小时的动物腹腔内有大量腹水,但当使用较高浓度(20 - 150微克/毫升)4小时时,腹腔粘连是最常见的发现。本研究中未观察到常见的全身毒性作用(骨髓、胃肠道和心脏)。用赋形剂处理的对照动物所有组织学病变和大体观察均为阴性。