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用(131)I标记的配体或抗体进行靶向治疗时,单细胞及微转移灶中细胞的细胞核所接受的辐射剂量。

Radiation doses to the cell nucleus in single cells and cells in micrometastases in targeted therapy with (131)I labeled ligands or antibodies.

作者信息

Hartman T, Lundqvist H, Westlin J E, Carlsson J

机构信息

The Svedberg Laboratory, Uppsala University, Uppsala, Sweden.

出版信息

Int J Radiat Oncol Biol Phys. 2000 Mar 1;46(4):1025-36. doi: 10.1016/s0360-3016(99)00476-9.

Abstract

PURPOSE

The aim of this study was to theoretically investigate how the radiation dose to cell nuclei depends on the subcellular position of (131)I. The influence of the size of the cells and crossfire irradiation in clusters of cells was also studied.

METHODS AND MATERIAL

Using data describing the dose rate around a point source of (131)I, we calculated the dose distributions inside and around cell models of different sizes. The assumed positions of (131)I were on the cellular or nuclear membrane, in the cytoplasm, in the nucleus, or spread in the whole cell. The mean doses to the nucleus of the targeted cell and to the nuclei of its neighbors were calculated using the dose distributions.

RESULTS

The dose distributions inside a single targeted cell showed very different distribution profiles depending on the subcellular position of the (131)I. Targeting the nucleus instead of the cellular membrane could increase the dose to the nucleus 10-fold. Crossfire irradiation can be the major contributor to the nuclear dose in clusters of more than six cells.

CONCLUSIONS

Dosimetry without microscopic considerations is inadequate for targeted radionuclide therapy of disseminated or clustering tumor cells exposed to (131)I. Therapeutic doses could be achieved, even in single cells, when (131)I was positioned near, or inside the cell nucleus, or when the clusters were large enough.

摘要

目的

本研究旨在从理论上探讨细胞核的辐射剂量如何取决于¹³¹I在亚细胞水平的位置。同时还研究了细胞大小和细胞簇中交叉照射的影响。

方法与材料

利用描述¹³¹I点源周围剂量率的数据,我们计算了不同大小细胞模型内部及周围的剂量分布。¹³¹I假定的位置在细胞膜或核膜上、细胞质中、细胞核内或散布于整个细胞中。利用剂量分布计算了靶向细胞的细胞核及其相邻细胞核的平均剂量。

结果

单个靶向细胞内的剂量分布根据¹³¹I在亚细胞水平的位置呈现出非常不同的分布模式。靶向细胞核而非细胞膜可使细胞核剂量增加10倍。对于超过六个细胞的细胞簇,交叉照射可能是核剂量的主要贡献因素。

结论

对于暴露于¹³¹I的播散性或聚集性肿瘤细胞的靶向放射性核素治疗,不考虑微观因素的剂量测定是不充分的。当¹³¹I位于细胞核附近或细胞核内,或细胞簇足够大时,即使在单个细胞中也能达到治疗剂量。

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