钝化
车辆段
骨关节炎
PLGA公司
化学
生物利用度
原位
镁
炎症
乙醇酸
材料科学
药理学
乳酸
生物化学
医学
内科学
病理
有机化学
体外
生物
细菌
考古
替代医学
历史
图层(电子)
遗传学
作者
Wei‐Lin Wan,Yu‐Jung Lin,Po‐Chien Shih,Yu‐Ru Bow,Qinghua Cui,Yen Chang,Wei‐Tso Chia,Hsing‐Wen Sung
标识
DOI:10.1002/anie.201806159
摘要
Inflammation is involved in many human pathologies, including osteoarthritis (OA). Hydrogen (H2 ) is known to have anti-inflammatory effects; however, the bioavailability of directly administered H2 gas is typically poor. Herein, a local delivery system that can provide a high therapeutic concentration of gaseous H2 at inflamed tissues is proposed. The delivery system comprises poly(lactic-co-glycolic acid) microparticles that contain magnesium powder (Mg@PLGA MPs). Mg@PLGA MPs that are intra-muscularly injected close to the OA knee in a mouse model can act as an in situ depot that can evolve gaseous H2 continuously, mediated by the cycle of passivation/activation of Mg in body fluids, at a concentration that exceeds its therapeutic threshold. The analytical data that are obtained in the biochemical and histological studies indicate that the proposed Mg@PLGA MPs can effectively mitigate tissue inflammation and prevent cartilage from destruction, arresting the progression of OA changes.
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