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首页> 外文期刊>Online journal of biological sciences >Employing New Mathematical Models and Equations to Evaluate Risk-Benefit Criteria of Clinical Therapeutics | Science Publications
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Employing New Mathematical Models and Equations to Evaluate Risk-Benefit Criteria of Clinical Therapeutics | Science Publications

机译:应用新的数学模型和方程式评估临床治疗的风险-获益标准科学出版物

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> Current preclinical and clinical evaluation of a drugs or therapy is at first to find out a maximum toxicity tolerance, which is overall fixed. The potential therapeutic dosage will be ranged just lower or within the periphery of these maximum tolerant data. A hidden acceptance among general researchers lies as the toxicity concentration of a drug is always the same and can be referred as a fixed data. However, practical therapeutics is not very strictly following this doctrine. Even using many strict well-formed mathematical models and toxicity evaluating systems, the disputes and lawsuits of some newly-developed drugs are increasing dramatically nowadays. In this work, a mathematical equation and a dynamic parameter  are generated to help improving this situation. This new mathematic model combines and integrates effective, toxicity and no effective data as a whole, which fits to evaluate the risk-benefits of therapeutics in dynamic and changeable states. We need no more to deduce therapeutic dosage from fixed tolerance data regardless different therapeutic modes of action and toxicity of drugs acting on different organs and physiological systems. We hypothesize and equation that risk-benefit ratios are varied with drug dosages. It is a new start to help the understanding of effects and toxicities of therapeutic same time in a single clinical practice and well compliment with previous mathematical models.
机译: >当前对一种药物或疗法的临床前和临床评估首先是要找出最大的毒性耐受性,这是总体固定的。潜在的治疗剂量将在这些最大耐受数据的较低范围内或范围之内。在一般研究人员中,一个隐藏的观点是,药物的毒性浓度始终相同,可以称为固定数据。但是,实际的治疗方法并非严格遵循该原则。即使使用许多严格的格式正确的数学模型和毒性评估系统,当今一些新开发药物的争议和诉讼也在急剧增加。在这项工作中,将生成一个数学方程式和一个动态参数来帮助改善这种情况。这种新的数学模型将有效,毒性和无有效数据作为一个整体进行整合和整合,适合评估处于动态和多变状态的治疗药物的风险收益。无论采用何种治疗方式和作用于不同器官和生理系统的药物毒性,我们都不再需要从固定的耐受性数据中得出治疗剂量。我们假设风险方程式随药物剂量的变化而变化。这是一个新的开始,可帮助您在单一临床实践中同时了解治疗的效果和毒性,并很好地补充了先前的数学模型。

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