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药物不良反应如何在创新药物研究中发挥作用。

How adverse drug reactions can play a role in innovative drug research.

作者信息

Rikken F, Vos R

机构信息

Groningen Institute for Drug Studies (GIDS), University Center for Pharmacy, The Netherlands.

出版信息

Pharm World Sci. 1995 Nov 24;17(6):195-200. doi: 10.1007/BF01870611.

Abstract

We describe how adverse drug reactions (ADRs) can play an important role in pharmaceutical research and drug development. Not only do ADRs represent the risks and drawbacks associated with drugs but they can also be related to other knowledge available in pharmaceutical and medical research. We offer a model that can be used to systematically map the pathways through which ADRs can lead to innovative research. These pathways include chemical, therapeutic or pathophysiological steps that can be taken to arrive at new knowledge based on ADRs. We used the development of angiotensin-converting enzyme inhibitors, especially captopril, as a case study. The similarity between the ADR profiles of captopril and penicillamine was a starting point for further innovation. Historical analysis shows that in several instances research in the field of angiotensin-converting enzyme inhibitors has been triggered by ADRs. The model presented here might be applicable to other areas of innovative drug research.

摘要

我们描述了药物不良反应(ADR)如何在药物研究和药物开发中发挥重要作用。药物不良反应不仅代表了与药物相关的风险和弊端,还可能与药物和医学研究中的其他现有知识相关。我们提供了一个模型,可用于系统地描绘药物不良反应导致创新研究的途径。这些途径包括化学、治疗或病理生理步骤,可据此基于药物不良反应获得新知识。我们以血管紧张素转换酶抑制剂尤其是卡托普利的研发为例进行了研究。卡托普利和青霉胺的药物不良反应谱之间的相似性是进一步创新的起点。历史分析表明,在多个实例中,血管紧张素转换酶抑制剂领域的研究都是由药物不良反应引发的。此处提出的模型可能适用于创新药物研究的其他领域。

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