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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Synthesis of temperature/pH dual-sensitive supramolecular micelles from beta-cyclodextrin-poly(N-isopropylacrylamide) star polymer for drug delivery
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Synthesis of temperature/pH dual-sensitive supramolecular micelles from beta-cyclodextrin-poly(N-isopropylacrylamide) star polymer for drug delivery

机译:来自β-环糊精 - 聚(N-异丙基丙烯酰胺)星聚合物的温度/ pH双敏胶质胶束的合成用于药物递送

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摘要

In this paper, temperature and pH dual-sensitive supramolecular micelles were constructed from star polymer beta-cyclodextrin-poly(N-isopropylacrylamide) (beta-CD-PNIPAM) and benzimidazole terminated poly(epsilon-caprolactone) (BM-PCL). The supramolecular micelles were formed based on the reversible host-guest recognition between beta-CD and BM. The size of supramolecular micelles was about 50-100 nm and the LCST was about 30.5 degrees C. The drug loading efficiency of supramolecular micelles for DOX was high due to the hydrophobic micelles core of PCL and hydrophobic cavity of beta-CD. The release of drugs from supramolecular micelles was suppressed at neutral solution and room temperature but accelerated at acidic solution and 37 degrees C. The drug loaded supramolecular micelles exhibited higher anti-cancer activity than free drugs. These temperature and pH dual-sensitive supra molecular micelles might possess potential applications for anticancer drug delivery.
机译:在本文中,温度和pH双敏感的超分子胶束由Star聚合物β-环糊精 - 聚(N-异丙基丙烯酰胺)(β-CD-PNIPAM)和苯并咪唑封端的聚(ε-己内酯)(BM-PCL)构成。 基于β-CD和BM之间的可逆宿主访客识别来形成超分子胶束。 超分子胶束的尺寸约为50-100nm,LCST为约30.5℃。由于β-CD的PCL和疏水性腔的疏水胶束核心,对DOX的超分子胶束的药物负载效率高。 在中性溶液和室温下抑制来自超分子胶束的药物,但在酸性溶液中加速,37℃。药物负载的超分子胶束表现出比游离药物更高的抗癌活性。 这些温度和pH双敏感的Supra分子胶束可能具有抗癌药物递送的潜在应用。

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