Intranasal absorption of sumatriptan and naratriptan: no evidence of local transfer from the nasal cavities to the brain arterial blood in male rats

IF 2 4区 医学 Q3 PHARMACOLOGY & PHARMACY Biopharmaceutics & Drug Disposition Pub Date : 2001-11-19 DOI:10.1002/bdd.281
Niels Einer-Jensen, Lise Larsen, Stephanie Deprez, Elaine Starns, Sheila Schwartz
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引用次数: 8

Abstract

Nasal administration to rats of small molecules (tritiated water, tyrosine, and propanol) results in a higher concentration in the brain arterial blood than in other arteries. The preferential distribution is based on a counter current transfer, which takes place between nasal vein blood and brain arterial blood in the cavernous sinus-carotid artery complex. This model was used to investigate whether the antimigraine 5HT1B/1D receptor agonists sumatriptan and naratriptan may also be transferred by the system. The ratio of ‘head’:‘heart’ plasma concentrations obtained from two carotid catheters after intranasal administration was not different from 1.00 for either compound, and thus, there was no experimental evidence of a preferential local transfer of drug from the nose to the carotid artery circulation. However, plasma concentrations increased from the first minute after intranasal dosing suggesting that sumatriptan and naratriptan are absorbed into the general systemic circulation from the nasal cavity in rats in a first-order fashion with no lag time. This is consistent with the clinical onset of efficacy of sumatriptan after an intranasal dose which occurs as early as 15 min post dose. Copyright © 2001 John Wiley & Sons, Ltd.

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舒马曲坦和纳曲坦的鼻内吸收:雄性大鼠没有从鼻腔局部转移到脑动脉血的证据
给大鼠鼻腔注射小分子(氚化水、酪氨酸和丙醇)会导致其在脑动脉血液中的浓度高于其他动脉。这种优先分布是基于在海绵状窦-颈动脉复区的鼻静脉血液和脑动脉血液之间发生的逆流转移。该模型用于研究抗偏头痛5HT1B/1D受体激动剂舒马匹坦和纳曲普利坦是否也可以通过系统转移。两种化合物经鼻给药后,从两根颈动脉导管获得的“头”:“心”血浆浓度比与1.00没有差异,因此,没有实验证据表明药物从鼻子优先局部转移到颈动脉循环。然而,从鼻内给药后的第一分钟起,血浆浓度增加,这表明舒马曲坦和纳曲坦从大鼠鼻腔以一级方式进入全身循环,没有滞后时间。这与舒马曲坦在鼻内给药后最早在给药后15分钟出现疗效的临床发作是一致的。版权所有©2001 John Wiley &儿子,有限公司
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
35
审稿时长
6-12 weeks
期刊介绍: Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes: - animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites, - in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man - studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition, - simulation and modeling in drug discovery and development - theoretical treatises - includes themed issues and reviews and exclude manuscripts on - bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation - analytical methods
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