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将抗生素混悬于自乳化油中作为一种新方法来制备在水相环境中易发生水解的物质的滴眼剂。

Suspensions of antibiotics in self-emulsifying oils as a novel approach to formulate eye drops with substances which undergo hydrolysis in aqueous environment.

机构信息

Department of Pharmaceutical Technology, Faculty of Pharmacy, Medical University of Gdansk, Gdansk, Poland.

Department of Pharmaceutical Technology, Faculty of Pharmacy, Medical University of Bialystok, Bialystok, Poland.

出版信息

Drug Deliv. 2024 Dec;31(1):2372279. doi: 10.1080/10717544.2024.2372279. Epub 2024 Jul 11.

DOI:10.1080/10717544.2024.2372279
PMID:38992340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11249160/
Abstract

The aim of this study was to develop eye-drops with cefuroxime (CEF) sodium or vancomycin (VAN) hydrochloride, antibiotics that are instable in water. Anhydrous self-emulsifying oils (SEO) are proposed as a carrier and antibiotics are suspended. In the contact with tear fluid, the formulation should transform into emulsion, with fast dissolution of an antibiotic. CEF or VAN (5% w/w) was suspended in SEO carriers prepared by dissolving surfactants (Tween 20 or Span 80 5% w/w) in Miglyol, castor oil, or olive oil. Formulations with or without sodium citrate (2% w/w) were compared. Six-months or 1-year stability tests were carried out at 40 °C. The content of CEF and VAN was evaluated using HPLC and the potency of the antibiotic was assessed with agar diffusion method. In contact with water, drug particles suspended in SEO dissolved rapidly and o/w emulsion was formed. After 1-year at 40 °C, the content of degradation products was at most 0.5% in CEF and 4.0% in VAN formulations. The agar diffusion assay has shown that CEF and VAN loaded into SEO retained its potency against the sensitive microorganisms comparable to an aqueous solution. Therefore, SEO can be used as a novel carrier for the active substances which may not require improved solubility or absorption but need to be protected from moisture. This is a formulation that can be produced on industrial scale, with no limitation of stability or drug concentration.

摘要

本研究旨在开发含有头孢呋辛(CEF)钠或盐酸万古霉素(VAN)的眼药水,这两种抗生素在水中不稳定。无水自乳化油(SEO)被提议作为载体来悬浮抗生素。在与泪液接触时,制剂应转化为乳液,使抗生素快速溶解。将 CEF 或 VAN(5%w/w)悬浮在由表面活性剂(吐温 20 或司盘 80,5%w/w)溶解于 Miglyol、蓖麻油或橄榄油中制成的 SEO 载体中。比较了含有或不含有柠檬酸钠(2%w/w)的制剂。在 40°C 下进行了 6 个月或 1 年的稳定性测试。采用 HPLC 法测定 CEF 和 VAN 的含量,采用琼脂扩散法评价抗生素的效价。与水接触时,SEO 中悬浮的药物颗粒迅速溶解,并形成 o/w 乳液。在 40°C 下放置 1 年后,CEF 制剂中降解产物的含量最高为 0.5%,VAN 制剂中降解产物的含量最高为 4.0%。琼脂扩散试验表明,负载于 SEO 中的 CEF 和 VAN 保持了对敏感微生物的效价,与水溶液相当。因此,SEO 可用作活性物质的新型载体,这些物质可能不需要提高溶解度或吸收性,但需要防止水分。这是一种可以在工业规模生产的制剂,不受稳定性或药物浓度的限制。

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