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亲骨性放射性药物给药后胃肠道的活性。小鼠实验研究。

Activity in the gastrointestinal tract after administration of bone-seeking radiopharmaceuticals. Experimental studies in mice.

作者信息

Cronhjort M, Jonsson C, Nilsson S O, Garmelius B, Jacobsson H

机构信息

Department of Diagnostic Radiology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Acta Radiol. 1996 Sep;37(5):785-90. doi: 10.1177/02841851960373P271.

Abstract

PURPOSE

To test the possibility that (radio)activity of non-pertechnetate nature is excreted into the gastrointestinal tract at bone scintigraphy.

MATERIAL AND METHODS

The distribution of a bone-seeking radiopharmaceutical (99mTc-HDP) was studied in an experimental mouse system by dissecting different organs and assessing their activity with a gamma-counter.

RESULTS

A comparison of the activity of the submandibular glands, which are assumed to accumulate only pertechnetate, and the gastrointestinal tract showed that a significant fraction of the activity excreted into the gastrointestinal tract did not consist of pertechnetate. Part of the excretion took place in the stomach. It was not connected to a specific bone-seeking agent or 99Mo/99mTc generator. Nor did it increase with time between make-up and injection. The excretion of the non-pertechnetate activity was reduced by cimetidine and omeprazole. These gastric-secretion blocking drugs did not reduce excretion of pertechnetate or significantly affect the general distribution of the radiopharmaceutical.

CONCLUSION

There is a significant excretion of non-pertechnetate activity in the gastrointestinal tract. Part of this may be caused by excretion of the undegraded radiopharmaceutical by the stomach mucosa.

摘要

目的

检测在骨闪烁显像时非高锝酸盐性质的(放射性)活性物质排泄到胃肠道的可能性。

材料与方法

通过解剖不同器官并用γ计数器评估其活性,在实验小鼠系统中研究一种亲骨性放射性药物(99mTc-HDP)的分布。

结果

对假定仅蓄积高锝酸盐的下颌下腺与胃肠道的活性进行比较,结果显示排泄到胃肠道的活性物质中有很大一部分并非高锝酸盐。部分排泄发生在胃中。它与特定的亲骨剂或99Mo/99mTc发生器无关。在配制与注射之间的时间内它也没有增加。西咪替丁和奥美拉唑可减少非高锝酸盐活性物质的排泄。这些胃分泌阻断药物不会减少高锝酸盐的排泄,也不会显著影响放射性药物的总体分布。

结论

胃肠道中存在大量非高锝酸盐活性物质的排泄。其中一部分可能是由于胃黏膜排泄未降解的放射性药物所致。

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