[On the history of barbiturates].

Dansk medicinhistorisk arbog Pub Date : 2015-01-01
Svend Norn, Henrik Permin, Edith Kruse, Poul R Kruse
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Abstract

Throughout the history of humanity, numerous therapeutic agents have been employed for their sedative and hypnotic properties such as opium, henbane (Hyoscyamus niger) and deadly nightshade (Atropa belladonna), but also alcohol and wine. In the 19th century potassium bromide was introduced as a sedative - and antiepileptic drug and chloral hydrate as sedative-hypnotics. A new era was reached by the introduction of barbiturates. The story started with the chemist Adolf von Baeyer. His breakthrough in the synthesis of new agents as barbituric acid and indigo and his education of young chemists was of great importance for the science of organic chemistry and the development of the dye and medicine industry in the late 19th century. The next important step was the development of barbiturates. The pioneers were Josef von Mering and Emil Fischer. Using the Grimaux-method they synthesized various barbiturates. It was von Mering who got the idea of introducing ethyl groups in the inactive barbituric acid to obtain sedatives, but the synthesis was succeeded by the chemist Emil Fischer. Experiments with dogs clearly showed sedative and hypnotic effect of the barbiturates and the oral administration of barbital (Veronal) confirmed the effect in humans. Barbital was commercialized in 1903 and in 1911 phenobarbital (Luminal) was introduced in the clinic, and this drug showed hypnotic and antiepileptic effects. Thereafter a lot of new barbiturates appeared. Dangerous properties of the drugs were recognized as abuse, addiction, and poisoning. An optimum treatment of acute barbiturate intoxication was obtained by the "Scandinavian method", which was developed in the Poison Centre of the Bispebjerg Hospital in Copenhagen. The centre was established by Carl Clemmesen in 1949 and the intensive care treatment reduced the mortality of the admitted persons from 20% to less than 2%. To-day only a few barbiturates are used in connection with anaesthesia and for the treatment of epilepsy, and chemists are focusing on drugs with more selective effects.

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[关于巴比妥类药物的历史]。
纵观人类历史,许多治疗药物因其镇静和催眠的特性而被使用,如鸦片、天仙子(Hyoscyamus niger)和致命的龙葵(Atropa belladonna),还有酒精和葡萄酒。在19世纪,溴化钾作为镇静和抗癫痫药物被引入,水合氯醛作为镇静催眠剂被引入。巴比妥酸盐的引入开创了一个新时代。这个故事要从化学家阿道夫·冯·拜尔说起。他在合成巴比妥酸和靛蓝等新试剂方面的突破,以及他对年轻化学家的教育,对19世纪后期有机化学科学以及染料和医药工业的发展具有重要意义。下一个重要的步骤是巴比妥酸盐的开发。先驱者是约瑟夫·冯·埃林和埃米尔·费舍尔。他们用格里莫法合成了各种巴比妥酸盐。冯·埃林提出了在非活性巴比妥酸中引入乙基以获得镇静剂的想法,但化学家埃米尔·费舍尔继承了这一合成。对狗进行的实验清楚地显示了巴比妥类药物的镇静和催眠作用,而口服巴比妥类药物也证实了这种作用。巴比妥于1903年商业化,1911年苯巴比妥(Luminal)被引入临床,该药具有催眠和抗癫痫作用。此后出现了许多新的巴比妥类药物。这些药物的危险特性被认为是滥用、成瘾和中毒。“斯堪的纳维亚方法”是治疗急性巴比妥酸盐中毒的最佳方法,该方法是在哥本哈根比斯贝尔格医院的中毒中心开发的。该中心由卡尔·克莱门森于1949年建立,重症监护治疗将入院患者的死亡率从20%降低到不到2%。今天,只有少数巴比妥类药物用于麻醉和治疗癫痫,化学家们正在集中精力研究具有更选择性作用的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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