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长春新碱与依托泊苷联合使用:给药顺序的评估

Combination vincristine and VP-16-213: evaluation of drug sequence.

作者信息

Jackson D V, Long T R, Rice D G, Morgan T M

出版信息

Cancer Biochem Biophys. 1986 Oct;8(4):265-75.

PMID:3802048
Abstract

The combination of vincristine and VP-16-213 has been found to have synergistic antitumor activity in a murine system in vivo when the sequence of drug administration was vincristine followed by VP-16-213. To investigate the potential influence of drug scheduling on this synergistic combination, the reverse sequence of drug administration was evaluated. DBA/2 mice were inoculated with 10(6) P-388 murine leukemia cells, after which saline only, VP-16-213 only, vincristine only, or VP-16-213 followed at various time intervals by vincristine, were administered. Probable cure (survival greater than 60 days) was observed in 0/20, 0/20, 0/120, and 46/115 (40%), respectively (p less than 0.001). The proportion of animals attaining probable cure was greatest in the group receiving vincristine 4-72 hours after VP-16-213 (40-50%). Similar results had been obtained previously with the reverse drug sequence. In this animal model, the synergistic antitumor activity of vincristine and VP-16-213 does not appear to be schedule-dependent with respect to the sequence of drug administration.

摘要

在小鼠体内系统中,当给药顺序为长春新碱后接VP - 16 - 213时,已发现长春新碱与VP - 16 - 213联合具有协同抗肿瘤活性。为研究给药时间安排对这种协同联合的潜在影响,评估了相反的给药顺序。给DBA/2小鼠接种10(6)个P - 388小鼠白血病细胞,之后分别给予仅生理盐水、仅VP - 16 - 213、仅长春新碱,或在不同时间间隔后给予长春新碱的VP - 16 - 213。可能治愈(存活超过60天)的比例分别为0/20、0/20、0/120和46/115(40%)(p小于0.001)。在VP - 16 - 213后4 - 72小时接受长春新碱的组中,达到可能治愈的动物比例最高(40 - 50%)。先前用相反的给药顺序也获得了类似结果。在这个动物模型中,长春新碱与VP - 16 - 213的协同抗肿瘤活性似乎在给药顺序方面不依赖于给药时间安排。

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