首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >The effect of infinitesimal drug dilutions on the pharmacokinetics of nalidixic acid and atenolol.
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The effect of infinitesimal drug dilutions on the pharmacokinetics of nalidixic acid and atenolol.

机译:极小的药物稀释液对萘啶酸和阿替洛尔药代动力学的影响。

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摘要

1. Ten healthy subjects received two treatments: a single 1 g oral dose of nalidixic acid (NA) followed 1 h later by either an infinitesimal dilution of the drug (NA 7CH) or by succussed water which served as placebo. The study was repeated 18 months later in 10 different subjects. 2. A further 10 healthy subjects received three treatments: a single 100 mg oral dose of atenolol (AT) followed 3 h later by either placebo or a dilution of AT (AT 7CH) or of bisoprolol (BI 7CH). The homoeopathic preparations were administered by the sublingual route. 3. In the first NA experiment NA 7CH significantly shortened the elimination half-life of NA from 8.6 +/- 2.2 (placebo) to 6.4 +/- 1.6 h (NA 7CH). In the second NA experiment none of the pharmacokinetic parameters was modified significantly by the administration of NA 7CH. Neither AT 7CH nor BI 7CH modified the pharmacokinetics of AT.
机译:1.十名健康受试者接受了两种治疗:口服1克萘啶酸(NA)单次剂量,然后在1小时后无限次稀释该药物(NA 7CH)或加入作为安慰剂的水。 18个月后,在10个不同的受试者中重复了该研究。 2.另有10名健康受试者接受了三种治疗:口服100 mg阿替洛尔(AT),然后在3小时后服用安慰剂或AT(AT 7CH)或比索洛尔(BI 7CH)稀释液。通过舌下途径施用同种疗法制剂。 3.在第一个NA实验中,NA 7CH将NA的消除半衰期从8.6 +/- 2.2(安慰剂)显着缩短至6.4 +/- 1.6 h(NA 7CH)。在第二个NA实验中,通过使用NA 7CH并未显着改变任何药代动力学参数。 AT 7CH和BI 7CH均未改变AT的药代动力学。

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