丙酸氟替卡松
生物相容性
药物输送
材料科学
鼻腔给药
生物医学工程
纳米技术
化学工程
化学
药理学
医学
皮质类固醇
外科
工程类
冶金
作者
Laura Nižić Nodilo,Mirna Perkušić,Ivo Ugrina,Drago Špoljarić,Cvijeta Jakobušić Brala,Daniela Amidžić Klarić,Jasmina Lovrić,Vesna Saršon,Maša Safundžić Kučuk,Dijana Zadravec,Livije Kalogjera,Ivan Pepić,Anita Hafner
标识
DOI:10.1016/j.ejpb.2022.04.009
摘要
In this work we present the development of in situ gelling nanosuspension as advanced form for fluticasone propionate nasal delivery. Drug nanocrystals were prepared by wet milling technique. Incorporation of drug nanocrystals into polymeric in situ gelling system with pectin and sodium hyaluronate as constitutive polymers was fine-tuned attaining appropriate formulation surface tension, viscosity and gelling ability. Drug nanonisation improved the release profile and enhanced formulation mucoadhesive properties. QbD approach combining formulation and administration parameters resulted in optimised nasal deposition profile, with 51.8% of the dose deposited in the middle meatus, the critical region in the treatment of rhinosinusitis and nasal polyposis. Results obtained in biocompatibility and physico-chemical stability studies confirmed the leading formulation potential for safe and efficient nasal corticosteroid delivery.
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