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速发型西地那非舌下给药系统:家兔体外评价及体内药代动力学研究

Rapid-Onset Sildenafil Sublingual Drug Delivery Systems: In Vitro Evaluation and In Vivo Pharmacokinetic Studies in Rabbits.

作者信息

Sheu Ming-Thau, Hsieh Chien-Ming, Chen Ray-Neng, Chou Po-Yu, Ho Hsiu-O

机构信息

School of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei 110, Taiwan, ROC.

Department of Cosmetic Science, Providence University, Taichung City, Taiwan, ROC.

出版信息

J Pharm Sci. 2016 Sep;105(9):2774-2781. doi: 10.1016/j.xphs.2016.01.015. Epub 2016 Mar 15.

Abstract

The aim of the present study was to prepare sublingual delivery systems for sildenafil and evaluate its relative bioavailability after sublingual administration in rabbits to attain a rapid onset of action with good efficacy at lower doses. For sublingual application, sildenafil and its citrate were formulated in 2 different dosage forms: the first was a sublingual spray consisting of sildenafil in 2 microemulsion systems, oleic acid or propylene glycol (PG), and the second was sublingual tablets prepared with various granulated sublingual sprays adsorbed onto a silicate adsorbant (Florite(®) R), binders (Cyclocel(®) or EMDEX(®)), and disintegrants (Ac-Di-Sol(®) or Kollidon(®) CL). Results showed that sublingual absorption of sildenafil spray prepared with PG was fairly rapid. At a 0.5-mg dose, the mean onset of action was 1.3 ± 0.6 min and lasted for about 1.5 h according to the pharmacokinetic studies. In vivo studies also showed that for sublingual tablets formulated with sildenafil in PG adsorbed onto Florite(®) R at a 1:1 weight ratio then mixed with Cycloel(®) and Ac-Di-Sol(®), the onset action was fast at 1.9 ± 0.4 min and lasted for about 1 h at 0.5 mg. These findings suggest the potential for the sublingual delivery of sildenafil instead of the conventional oral administration.

摘要

本研究的目的是制备西地那非的舌下给药系统,并评估其在兔体内舌下给药后的相对生物利用度,以实现快速起效且在较低剂量下具有良好疗效。对于舌下应用,西地那非及其柠檬酸盐被制成两种不同剂型:第一种是舌下喷雾剂,由西地那非在两种微乳体系(油酸或丙二醇(PG))中组成;第二种是舌下片剂,用吸附在硅酸盐吸附剂(Florite(®) R)上的各种颗粒状舌下喷雾剂、粘合剂(Cyclocel(®) 或 EMDEX(®))和崩解剂(Ac-Di-Sol(®) 或 Kollidon(®) CL)制备。结果表明,用PG制备的西地那非喷雾剂舌下吸收相当迅速。根据药代动力学研究,在0.5毫克剂量下,平均起效时间为1.3±0.6分钟,持续约1.5小时。体内研究还表明,对于以1:1重量比将PG中的西地那非吸附在Florite(®) R上,然后与Cycloel(®) 和 Ac-Di-Sol(®) 混合制成的舌下片剂,在0.5毫克剂量下起效迅速,为1.9±0.4分钟,持续约1小时。这些发现表明西地那非舌下给药替代传统口服给药的潜力。

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