Candelaria Ines Camara , Caterina Ricci , Laura Bertocchi , Rosaria Bassi , Annalisa Bianchera , Ruggero Bettini , Elena Del Favero
{"title":"Hyaluronic acid-based nanoparticles for pulmonary delivery of poorly soluble drugs","authors":"Candelaria Ines Camara , Caterina Ricci , Laura Bertocchi , Rosaria Bassi , Annalisa Bianchera , Ruggero Bettini , Elena Del Favero","doi":"10.1016/j.colcom.2025.100868","DOIUrl":null,"url":null,"abstract":"<div><div>The delivery of poorly soluble drugs poses significant challenges in pharmacotherapy, particularly for corticosteroids. This study investigates the development of hyaluronic acid-based nanoparticles to enhance the solubility and bioavailability of dexamethasone. Hyaluronic acid-dexamethasone formulations, (HAm 15–30 kDa and HAl 750–1000 kDa), were produced as stable powders to be resuspended. We characterized the nanoparticles formed after resuspension by laser-light and X-ray scattering. Nanoparticles showed nanometric size, good stability, a core-shell arrangement, and muco-inert properties. We evaluated the interaction of nanoparticles with lung surfactant models, by nebulization of formulations on DPPC Langmuir monolayers to mimic their effects on alveolar interfaces when administered via nebulization. They showed good biocompatibility and enhanced anti-inflammatory response, as assessed by pro-inflammatory cytokine TNF-α release in LPS-stimulated macrophages. The favorable structural and biopharmaceutical characteristics of HA-based formulations can be exploited to improve the delivery of poorly soluble drugs to the lungs by inhalation.</div></div>","PeriodicalId":10483,"journal":{"name":"Colloid and Interface Science Communications","volume":"70 ","pages":"Article 100868"},"PeriodicalIF":6.7000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloid and Interface Science Communications","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2215038225000524","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/6 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The delivery of poorly soluble drugs poses significant challenges in pharmacotherapy, particularly for corticosteroids. This study investigates the development of hyaluronic acid-based nanoparticles to enhance the solubility and bioavailability of dexamethasone. Hyaluronic acid-dexamethasone formulations, (HAm 15–30 kDa and HAl 750–1000 kDa), were produced as stable powders to be resuspended. We characterized the nanoparticles formed after resuspension by laser-light and X-ray scattering. Nanoparticles showed nanometric size, good stability, a core-shell arrangement, and muco-inert properties. We evaluated the interaction of nanoparticles with lung surfactant models, by nebulization of formulations on DPPC Langmuir monolayers to mimic their effects on alveolar interfaces when administered via nebulization. They showed good biocompatibility and enhanced anti-inflammatory response, as assessed by pro-inflammatory cytokine TNF-α release in LPS-stimulated macrophages. The favorable structural and biopharmaceutical characteristics of HA-based formulations can be exploited to improve the delivery of poorly soluble drugs to the lungs by inhalation.
期刊介绍:
Colloid and Interface Science Communications provides a forum for the highest visibility and rapid publication of short initial reports on new fundamental concepts, research findings, and topical applications at the forefront of the increasingly interdisciplinary area of colloid and interface science.