Balázová E, Koza I
Cancer Research Institute, Slovak Academy of Sciences, Bratislava, Czechoslovakia.
Neoplasma. 1988;35(6):725-8.
Optimal schedules of benzaldehyde (50-100 mg kg-1 intraperitoneally) on day 1 or on several days after inoculation of 10(5) P388 leukemia cells to DBA 2J mice increased survival by 70-100%. No significant prolongation of survival was observed between the various schedules of benzaldehyde treatment. Significantly longer survival was observed on day 30 after benzaldehyde treatment with 100 mg kg-1 on day 1 or 50 mg kg-1 on days 1-4 as compared to untreated controls, but no cure was achieved with any schedule and dose of benzaldehyde. No or minimal activity of benzaldehyde on L1210 and L5178Y leukemias, Ehrlich adenocarcinoma and Yoshida sarcoma was observed.
在给DBA 2J小鼠接种10⁵个P388白血病细胞后的第1天或接种后的数天,腹腔注射苯甲醛(50 - 100毫克/千克)的最佳给药方案可使小鼠存活率提高70% - 100%。不同苯甲醛治疗方案之间未观察到存活时间的显著延长。与未治疗的对照组相比,在第1天给予100毫克/千克苯甲醛或在第1 - 4天给予50毫克/千克苯甲醛治疗后第30天观察到存活时间显著延长,但任何苯甲醛给药方案和剂量均未实现治愈。未观察到苯甲醛对L1210和L5178Y白血病、艾氏腺癌和吉田肉瘤有活性或仅有最小活性。