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在载体中以高盐浓度给药的顺铂在小鼠体内的抗肿瘤活性降低。

Reduced antineoplastic activity in mice of cisplatin administered with high salt concentration in the vehicle.

作者信息

Aamdal S, Fodstad O, Kaalhus O, Pihl A

出版信息

J Natl Cancer Inst. 1984 Sep;73(3):743-52.

PMID:6590919
Abstract

The effect of high NaCl concentration in the vehicle on the toxic and antineoplastic activities of cisplatin [cis-dichloro-diammineplatinum(II)] (CDDP) was reinvestigated in mice. The toxicity, as measured by the survival of mice given CDDP iv, was reduced by 50-60% when the NaCl concentration in the vehicle was raised from 0.9 to 4%. In ascitic P388 leukemia the antineoplastic activity of CDDP given ip was not reduced significantly. However, in all other systems studied the antitumor activity was reduced when the CDDP was dissolved in high NaCl solution. The tumor models studied included systemic P388 and L1210 leukemias, Lewis lung carcinoma, and 5 human tumor xenografts. The human tumors were studied by the subrenal capsule assay. In the case of a malignant melanoma and a malignant fibrous histiocytoma, the effect also was demonstrated in the subcutaneous nude mouse model. In one of the malignant melanomas a 50% increase in the CDDP dose did not compensate for the reduced antitumor activity caused by the high NaCl concentration in the vehicle. These results, which stand in contrast to current views, question the experimental basis for the use of high-NaCl vehicles in the "high-dose" CDDP regimens.

摘要

在小鼠中重新研究了载体中高氯化钠浓度对顺铂[顺 - 二氯 - 二氨合铂(II)](CDDP)的毒性和抗肿瘤活性的影响。当载体中的氯化钠浓度从0.9%提高到4%时,通过静脉注射CDDP的小鼠存活率来衡量的毒性降低了50 - 60%。在腹水型P388白血病中,腹腔注射CDDP的抗肿瘤活性没有显著降低。然而,在所有其他研究的系统中,当CDDP溶解在高氯化钠溶液中时,其抗肿瘤活性降低。所研究的肿瘤模型包括全身性P388和L1210白血病、Lewis肺癌以及5种人肿瘤异种移植模型。通过肾包膜下测定法研究人肿瘤。在恶性黑色素瘤和恶性纤维组织细胞瘤的情况下,在皮下裸鼠模型中也证实了这种效果。在其中一种恶性黑色素瘤中,CDDP剂量增加50%并不能弥补载体中高氯化钠浓度导致的抗肿瘤活性降低。这些结果与当前观点相反,对在“高剂量”CDDP方案中使用高氯化钠载体的实验依据提出了质疑。

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