Lam G K
Division of Medical Physics, British Columbia Cancer Agency, Vancouver, Canada.
Bull Math Biol. 1992 Sep;54(5):813-26. doi: 10.1007/BF02459931.
Although graphic surfaces have been used routinely in the study of combined action of agents, they are mainly used for display purposes. In this paper, it is shown that useful mechanistic information can be obtained from an analytical study of these surfaces using the tools of differential geometry. From the analysis of some simple dose-effect surfaces, it is proposed that the intrinsic curvature, referred to in differential geometry as the Gaussian curvature, of a dose-effect surface can be used as a general criterion for the classification of interaction between different agents. This is analogous to the interpretation of the line curvature of a dose-effect curve as an indication of self-interaction between doses for an agent. In this framework, the dose-effect surface would have basic uniform fabric with zero curvature in the absence of interaction, tentatively referred to as null-interaction. Pictorially speaking, this fabric is distorted locally or globally like the stretching and shrinking of a rubber sheet by the presence of interaction mechanisms between different agents. Since self-interaction with dilution dummies does not generate intrinsic curvature, this criterion of null-interaction would describe the interaction between two truly different agents. It is shown that many of the published interaction mechanisms give rise to dose-effect surfaces with characteristic curvatures. This possible correlation between the intrinsic geometric curvature of dose-effect surfaces and the biophysical mechanism of interaction presents an interesting philosophical viewpoint for the study of combined action of agents.
尽管图形曲面已常规用于研究药剂的联合作用,但它们主要用于展示目的。本文表明,使用微分几何工具对这些曲面进行分析研究,可以获得有用的机理信息。通过对一些简单的剂量-效应曲面的分析,提出剂量-效应曲面的固有曲率(在微分几何中称为高斯曲率)可作为不同药剂间相互作用分类的通用标准。这类似于将剂量-效应曲线的线曲率解释为一种药剂不同剂量间自身相互作用的指标。在此框架下,剂量-效应曲面在无相互作用时将具有零曲率的基本均匀结构,暂称为零相互作用。形象地说,由于不同药剂间相互作用机制的存在,这种结构会局部或全局地像橡胶片的拉伸和收缩一样发生扭曲。由于与稀释虚拟物的自身相互作用不会产生固有曲率,这种零相互作用标准将描述两种真正不同药剂间的相互作用。结果表明,许多已发表的相互作用机制会产生具有特征曲率的剂量-效应曲面。剂量-效应曲面的固有几何曲率与生物物理相互作用机制之间的这种可能关联,为药剂联合作用的研究提供了一个有趣的哲学观点。