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DOI 10.1021/acsabm.6c01682

Медицинская библиотека · ACS applied bio materials · 2026

Dexamethasone Sustained-Release Microspheres with Single-Phase Zero-Order Release Behavior for Intra-Articular Injection: Effects of Polymer Blending and Release Promoter Incorporation.

Zhang Shiman, Wang Qiuli, Jia Fucong, Zheng Kai, Zhang Shiming, Yang Xinggang

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Аннотация

Intra-articular dexamethasone injection is an effective treatment for osteoarthritis. However, the drug has a short residence time in the joint cavity, necessitating frequent administration, which results in poor patient compliance and limits its clinical use. To address these problems, dexamethasone sustained-release microspheres (Dex-MS-2) with single-phase zero-order release behavior were prepared using polymer blending combined with a release promoter. Their characteristics, in vitro release, and in vivo pharmacodynamics were evaluated. Dex-MS-2 had a slightly larger mean particle size than Dex-MS-1, but exhibited a narrower particle size distribution and good encapsulation efficiency. Compared with microspheres prepared by polymer blending alone (Dex-MS-1), the microspheres containing the release promoter exhibited no release lag and achieved zero-order release for 28 days. Following intra-articular injection in rats, Dex-MS-2 exhibited favorable anti-inflammatory activity and effectively inhibited joint swelling, with superior therapeutic efficacy to Dex-MS-1 and comparable efficacy to the marketed injection. The Dex-MS-2 developed in this study reduced the frequency of administration, improved patient compliance, and achieved sustained drug release. This formulation may effectively overcome the limitations associated with the marketed formulation.

Для цитирования: Zhang Shiman, Wang Qiuli, Jia Fucong, Zheng Kai, Zhang Shiming, Yang Xinggang. Dexamethasone Sustained-Release Microspheres with Single-Phase Zero-Order Release Behavior for Intra-Articular Injection: Effects of Polymer Blending and Release Promoter Incorporation.. ACS applied bio materials. 2026. DOI: 10.1021/acsabm.6c01682.
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