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低药物负载量下螺哌啶醇和溴螺哌啶醇的体内结合

In vivo binding of spiroperidol and bromospiroperidol at low drug loadings.

作者信息

DeJesus O T, Revenaugh J R, Dinerstein R J, Friedman A M

出版信息

Life Sci. 1984 Nov 19;35(21):2165-8. doi: 10.1016/0024-3205(84)90517-4.

Abstract

The binding of spiroperidol and bromospiroperidol, in vivo, was studied over a wide range of drug dosages. It was found that while spiroperidol and bromospiroperidol bind selectively in vivo to tissues known to be high in dopamine receptor binding sites, this specificity of binding does not persist at very low doses. Such anomalous binding behavior can have implications for the non-invasive imaging of these drugs.

摘要

在广泛的药物剂量范围内研究了螺哌啶醇和溴螺哌啶醇在体内的结合情况。结果发现,虽然螺哌啶醇和溴螺哌啶醇在体内选择性地与已知多巴胺受体结合位点含量高的组织结合,但这种结合的特异性在非常低的剂量下并不持续。这种异常的结合行为可能对这些药物的非侵入性成像有影响。

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