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使用脑内微透析法测定荷瘤大鼠脑内抗癌药物的药代动力学特征。

The use of intracerebral microdialysis for the determination of pharmacokinetic profiles of anticancer drugs in tumor-bearing rat brain.

作者信息

de Lange E C, de Vries J D, Zurcher C, Danhof M, de Boer A G, Breimer D D

机构信息

Leiden/Amsterdam Center for Drug Research, University of Leiden, Netherlands.

出版信息

Pharm Res. 1995 Dec;12(12):1924-31. doi: 10.1023/a:1016239822287.

Abstract

PURPOSE

The use of intracerebral microdialysis as a tool to measure the penetration of anticancer agents in brain tumor was investigated.

METHODS

Following intravenous (iv) administration of 75 mg/kg. concentration-time profiles of methotrexate (MTX) were determined in brain cortical dialysate and in plasma. The individual ratio of the area under the curve of MTX in brain dialysate over that in plasma (MTX penetration) was determined in normal brain, in tumor-bearing brain and in brain after sham tumor implantation. Individual brains were examined histologically on the presence of tumor, as well as for other factors that might influence local MTX penetration. Histological scores were related to the individual data on penetration of MTX.

RESULTS

MTX penetration values were higher in cortical brain at the site of the tumor, as compared to the levels measured in normal or sham implanted brain (mean increase to 250%). In the cortical brain contralateral to the tumor, MTX penetration values were found to be lower than in normal brain (mean reduction of 65%). Furthermore, it appeared that in the absence of tumor tissue, the presence of exudate around the probe was independently associated with increased penetration of MTX into the brain.

CONCLUSIONS

Tumor tissue appeared to be the most important parameter in changing local MTX penetration in brain after tumor implantation. In general, it is anticipated that intracerebral microdialysis combined with histological examination can be used to investigate effects of brain tumor presence on regional (periprobe) penetration of anticancer drugs into the brain.

摘要

目的

研究将脑内微透析作为一种测量抗癌药物在脑肿瘤中渗透情况的工具的应用。

方法

静脉注射75mg/kg后,测定脑皮质透析液和血浆中甲氨蝶呤(MTX)的浓度-时间曲线。在正常脑、荷瘤脑和假肿瘤植入后的脑中,测定脑透析液中MTX曲线下面积与血浆中MTX曲线下面积的个体比值(MTX渗透率)。对个体脑进行组织学检查,观察肿瘤的存在情况以及其他可能影响局部MTX渗透的因素。组织学评分与MTX渗透的个体数据相关。

结果

与正常或假植入脑相比,肿瘤部位脑皮质的MTX渗透率更高(平均增加至250%)。在肿瘤对侧的脑皮质中,MTX渗透率低于正常脑(平均降低65%)。此外,似乎在没有肿瘤组织的情况下,探针周围渗出液的存在与MTX进入脑内渗透率的增加独立相关。

结论

肿瘤组织似乎是肿瘤植入后改变脑内局部MTX渗透的最重要参数。一般而言,预计脑内微透析结合组织学检查可用于研究脑肿瘤的存在对抗癌药物向脑内区域(探针周围)渗透的影响。

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