不同途径给药阿霉素对埃利希腹水肿瘤细胞的影响

Hatice Gümüşhan, D. Musa
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引用次数: 6

摘要

阿霉素(ADR)是一种抗肿瘤药物,从peucetius变种caesius链霉菌中分离出来,具有细胞毒性。它通过插入结合DNA并抑制复制和转录。临床上,ADR用于静脉注射和静脉注射。埃利希腹水瘤(Ehrlich as腹水瘤,EAT)起源于小鼠乳腺癌。它以固体和腹水的形式生长。本研究的目的是通过比较给药途径,探讨不良反应对进食小鼠的影响。0.01毫克。g -1 ADR通过腹腔、静脉和皮下给药给药。实验第0天,每只小鼠接种3 × 10 5个EAT细胞。在给药后第2、4、6、8天,分别抽取腹腔腹水,计数活细胞数和有丝分裂数。对数据进行统计学评价。在治疗特性方面,观察到最有效的是第一组,其中不良反应通过腹腔给药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Adriamycin Administered via Different Routes on Ehrlich Ascites Tumor Cells
Adriamycin (ADR) is an antineoplastic drug, isolated from Streptomyces peucetius var. caesius , and has cytotoxic features. It binds DNA by intercalation and inhibits replication and transcription. Clinically, ADR is used intravenously and intravesically. Ehrlich ascites tumor (EAT) was originated from breast carcinoma in a mouse. It grows in solid and ascitic forms. The aim of our study is to investigate the effectiveness of ADR on mice bearing EAT by comparing its administration routes. 0.01 mg.g -1 ADR was administered mice bearing EAT via intraperitoneal, intravenous and subcutaneous. On day 0 each mouse in the experiment was inoculated with 3x10 5 EAT cells. On the 2 nd , 4 th , 6 th , 8 th days after administration, number of viable cells and mitosis number were counted from each animal by drainage the ascites fluid from the peritoneal cavity of each mouse. Data were evaluated statistically. The most efficient in respect of curing properties was observed in group I in which ADR administered via intraperitoneal.
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