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A pH-sensitive drug delivery system based on folic acid-targeted HBP-modified mesoporous silica nanoparticles for cancer therapy

机译:一种基于叶酸靶向HBP改性的介孔二氧化硅纳米粒子癌治疗的pH敏感药物递送系统

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Mesoporous silica nanoparticles with folic acid (MSN-COOH-Tet-HBP-FA) are able to mediate targeting and have a pH stimulation response character, and therefore have been successfully synthesized as vectors for antitumor drug delivery. The model drug is tetrandrine (Tel). The chemical structure and properties of these NPs were characterized through systematic characterization analyses. Their drug loading capacity was significantly improved through carboxy modification (26.86 % in max), and they exhibited pH-dependent drug release profiles("zero pre-release" within 20 h in a normal physiological environment). In vitro cytotoxicity and cell uptake of the as-synthesized NPs in Hela and A549 cells were also evaluated, and exhibited high cytotoxicity and cell-targeted uptake capacity. It was concluded that MSN - COOH-Tet-HBP-FA could be used as a promising drug delivery system for cancer therapy.
机译:具有叶酸(MSN-COOH-TET-HBP-FA)的中孔二氧化硅纳米颗粒能够介导靶向并具有pH刺激响应特征,因此已成功地合成为抗肿瘤药物递送的载体。 模型药物是Tetrandrine(Tel)。 通过系统表征分析来表征这些NP的化学结构和性质。 通过羧基改性(最大值26.86%)显着提高了它们的药物负载能力,并且它们在正常生理环境中显示出pH依赖性药物释放曲线(“零预释放”)。 还评估了HeLa和A549细胞中的体外细胞毒性和细胞吸收,并且表现出高细胞毒性和细胞靶向摄取能力。 得出结论,MSN - CoOH-TET-HBP-FA可用作癌症治疗的有希望的药物递送系统。

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