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

S. Poh
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Abstract

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.
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可还原热敏纳米颗粒释放抗炎肽抑制促炎细胞因子反应
活化的巨噬细胞在炎性疾病如骨关节炎的发展中起着关键作用。使用多肽药物治疗炎症性疾病可能通过促进抗炎作用而有效。然而,较差的生物利用度和潜在的肽抗原性可能导致不必要的免疫反应,从而限制了其商业应用。因此,为了提高多肽药物的疗效,必须寻求替代的给药途径。为此,我们设计了一种可还原的热敏性生物相容性聚(n -异丙基丙烯酰胺)(pNIPAm)聚合物作为药物载体,以保护多肽免受酶降解,从而提高多肽的半衰期和功效。这些研究表明,pNIPAm纳米颗粒可以成为治疗骨关节炎离体模型的有效替代工具。
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