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细胞毒性药物在人肿瘤球体中的渗透、结合及平均浓度之间的关系。

Relations between the penetration, binding and average concentration of cytostatic drugs in human tumour spheroids.

作者信息

Erlanson M, Daniel-Szolgay E, Carlsson J

机构信息

Department of Oncology, University of Umeå, Sweden.

出版信息

Cancer Chemother Pharmacol. 1992;29(5):343-53. doi: 10.1007/BF00686002.

Abstract

A penetration assay based on freeze-drying and vapour fixation was applied to show the spatial distribution of non-bound and bound cytostatic drugs in cellular spheroids. Several studies have proposed that peripheral binding of drugs correlates with limited penetration. We showed that granular accumulation, mainly at the peripheral part of spheroids, might occur in parallel with good penetration. For example, this was the case in human glioma spheroids after incubation with Adriamycin for 15-30 min. Following treatment with actinomycin D, colon carcinoma spheroids exhibited rather good penetration but also showed granular accumulation mainly in their peripheral regions. Ara-C accumulated largely and homogeneously in the peripheral regions of colon carcinoma spheroids and this severely delayed penetration. It took about 1 h for ara-C in the central regions of the spheroids to reach the same concentration as in the culture medium. In contrast, ara-C easily penetrated glioma spheroids without accumulating noticeably at the periphery. Retention tests involving washing and further incubation in drug-free culture medium revealed that the areas demonstrating extensive accumulation most often retained the drug, indicating binding, whereas the concentration of drug in other areas decreased. The oil-centrifugation method, which was used for rapid separation of the spheroids from the drug-containing medium, showed that the average concentration of daunomycin in the spheroids exceeded that in the culture medium as early as after 15 min, by which time only limited penetration had occurred. We found that good penetration of ara-C correlated with a low average concentration in glioma spheroids, whereas limited penetration correlated with a high average concentration in colon carcinoma spheroids. The latter finding was attributable to the high accumulation of drug at the spheroid periphery. Thus, there was an inverse relationship between penetration and binding and between penetration and average drug concentration. It seemed that binding delayed or prevented penetration, whereas little, if any binding resulted in better penetration. Granular binding such as that observed Adriamycin and actinomycin D gave intermediately good penetration.

摘要

一种基于冷冻干燥和蒸汽固定的渗透试验被用于展示细胞球体中未结合和结合的细胞抑制药物的空间分布。多项研究表明,药物的外周结合与有限的渗透相关。我们发现,颗粒状积累(主要在球体的外周部分)可能与良好的渗透同时发生。例如,人胶质瘤球体在用阿霉素孵育15 - 30分钟后就是这种情况。在用放线菌素D处理后,结肠癌球体表现出相当好的渗透,但也主要在其外周区域显示出颗粒状积累。阿糖胞苷在结肠癌球体的外周区域大量且均匀地积累,这严重延迟了渗透。球体中心区域的阿糖胞苷大约需要1小时才能达到与培养基中相同的浓度。相比之下,阿糖胞苷很容易穿透胶质瘤球体,且在外周没有明显积累。涉及洗涤和在无药物培养基中进一步孵育的保留试验表明,显示广泛积累的区域最常保留药物,表明存在结合,而其他区域的药物浓度降低。用于从含药培养基中快速分离球体的油离心法表明,早在15分钟后,球体中柔红霉素的平均浓度就超过了培养基中的浓度,此时只发生了有限的渗透。我们发现,阿糖胞苷的良好渗透与胶质瘤球体中的低平均浓度相关,而有限的渗透与结肠癌球体中的高平均浓度相关。后一发现归因于药物在球体外周的高积累。因此,渗透与结合之间以及渗透与平均药物浓度之间存在反比关系。似乎结合延迟或阻止了渗透,而几乎没有(如果有的话)结合则导致更好的渗透。如在阿霉素和放线菌素D中观察到的颗粒状结合给出了中等良好的渗透。

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