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阿替洛尔、噻吗洛尔和倍他洛尔混合物在兔眼部的局部药代动力学和生物利用度

Topical ocular pharmacokinetics and bioavailability for a cocktail of atenolol, timolol and betaxolol in rabbits.

作者信息

Fayyaz Anam, Ranta Veli-Pekka, Toropainen Elisa, Vellonen Kati-Sisko, Valtari Annika, Puranen Jooseppi, Ruponen Marika, Gardner Iain, Urtti Arto, Jamei Masoud, Del Amo Eva M

机构信息

Certara UK, Simcyp Division, Level 2-Acero, 1 Concourse Way, Sheffield, S1 2BJ, United Kingdom; University of Eastern Finland, School of Pharmacy, Biopharmaceutics, Yliopistonranta 1, Kuopio 70210, Finland.

University of Eastern Finland, School of Pharmacy, Biopharmaceutics, Yliopistonranta 1, Kuopio 70210, Finland.

出版信息

Eur J Pharm Sci. 2020 Dec 1;155:105553. doi: 10.1016/j.ejps.2020.105553. Epub 2020 Sep 16.

Abstract

Ocular bioavailability after eye drops administration is an important, but rarely determined, pharmacokinetic parameter. In this study, we measured the pharmacokinetics of a cocktail of three beta blockers after their topical administration into the albino rabbit eye. Samples from aqueous humour were analysed with LC-MS/MS. The pharmacokinetic parameters were estimated using compartmental and non-compartmental analyses. The ocular bioavailability was covering broad range of values: atenolol (0.07 %), timolol (1.22%, 1.51%) and betaxolol (3.82%, 4.31%). Absolute ocular bioavailability presented a positive trend with lipophilicity and the values showed approximately 60-fold range. The generated data enhances our understanding for ocular pharmacokinetics of drugs and may be utilized in pharmacokinetic model building in ophthalmic drug development.

摘要

滴眼液给药后的眼部生物利用度是一个重要但很少测定的药代动力学参数。在本研究中,我们测量了三种β受体阻滞剂混合液经局部给药进入白化兔眼后的药代动力学。房水样本用液相色谱-串联质谱法进行分析。药代动力学参数采用房室分析和非房室分析进行估算。眼部生物利用度涵盖了广泛的值范围:阿替洛尔(0.07%)、噻吗洛尔(1.22%,1.51%)和倍他洛尔(3.82%,4.31%)。绝对眼部生物利用度随亲脂性呈正趋势,其值显示出约60倍的范围。所生成的数据增进了我们对药物眼部药代动力学的理解,并可用于眼科药物开发中的药代动力学模型构建。

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