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Suppression of Pro-Inflammatory Cytokine Response by Anti-Inflammatory Peptide Release from Reducible Thermosensitive Nanoparticles

机译:通过从还原热敏纳米粒子释放抗炎肽释放的促炎细胞因子响应的抑制

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Activated macrophages constitute key players in the development of inflammatory disease such as osteoarthritis. Treatment of inflammatory disorders using peptide drugs may be effective by promoting anti-inflammatory effects. However, poor bioavailability and potential peptide antigenicity may result in unwanted immune responses thus limit its commercial applications. Therefore, in order to improve the efficacy of the peptide drug, alternative delivery approaches must be sought. For this purpose, we designed a reducible thermosensitive biocompatible poly(N-isopropylacrylamide) (pNIPAm) polymer as a drug carrier to protect the peptide from enzymatic degradation, thus increasing the half-life and efficacy of the peptide. The studies presented suggest pNIPAm nanoparticles can be an effective alternative tool for treatment of osteoarthritis ex-vivo model.
机译:活化的巨噬细胞构成炎症疾病如骨关节炎的开发中的关键球员。使用肽药物治疗炎性疾病可以通过促进抗炎作用来有效。然而,差的生物利用度和潜在的肽抗原可能导致不希望的免疫反应,从而限制其商业应用。因此,为了提高肽药物的功效,必须寻求替代递送方法。为此目的,我们设计了一种可还原的热敏生物相容性聚(N-异丙基丙烯酰胺)(N-异丙基丙烯酰胺)(PNIPAM)聚合物,为药物载体,以保护肽免受酶促劣化,从而增加肽的半衰期和功效。提出的研究表明肺脂纳米颗粒可以是用于治疗骨关节炎前体内模型的有效替代工具。

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