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

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2024-12-01 Epub Date: 2024-07-11 DOI:10.1080/10717544.2024.2372279
Katarzyna Krzeminska, Malgorzata Sznitowska, Magdalena Wroblewska, Eliza Wolska, Katarzyna Winnicka
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引用次数: 0

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.

抗生素在自乳化油中的悬浮液是一种新方法,可用于配制含有在水环境中会水解的物质的滴眼液。
本研究旨在开发含有头孢呋辛钠(CEF)或盐酸万古霉素(VAN)的眼药水,这些抗生素在水中不稳定。建议使用无水自乳化油(SEO)作为载体,悬浮抗生素。在与泪液接触时,制剂应转化为乳液,抗生素可快速溶解。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)溶于 Miglyol、蓖麻油或橄榄油制备而成的 SEO 载体中。对含有或不含柠檬酸钠(2% w/w)的配方进行了比较。在 40 °C 下进行了 6 个月或 1 年的稳定性测试。使用高效液相色谱法评估了 CEF 和 VAN 的含量,并使用琼脂扩散法评估了抗生素的效力。在与水接触时,悬浮在 SEO 中的药物颗粒迅速溶解并形成水包油型乳液。在 40 °C 下放置 1 年后,降解产物的含量在 CEF 制剂中最多为 0.5%,在 VAN 制剂中最多为 4.0%。琼脂扩散试验表明,SEO 中添加的 CEF 和 VAN 对敏感微生物的效力与水溶液相当。因此,SEO 可用作活性物质的新型载体,这些活性物质可能不需要提高溶解性或吸收性,但需要防潮。这种制剂可以进行工业化生产,不受稳定性或药物浓度的限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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