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首页> 外文期刊>RSC Advances >pH-sensitive CAP/SiO2 composite for efficient co-delivery of doxorubicin and siRNA to overcome multiple drug resistance
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pH-sensitive CAP/SiO2 composite for efficient co-delivery of doxorubicin and siRNA to overcome multiple drug resistance

机译:pH敏感盖/ SiO2复合材料,用于高效共递送多柔比星和siRNA,以克服多种耐药性

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摘要

Long-term administration of chemotherapeutic agents often leads to multiple drug resistance (MDR), which greatly impairs the treatment outcome. To overcome this problem, a biodegradable nanocarrier based on an acid-sensitive calcium phosphate/silica dioxide (CAP/SiO _(2) ) composite was constructed for the codelivery of drug and siRNA. Anticancer drug doxorubicin (DOX) was encapsulated into the composite scaffold by interacting with the exposed Ca ~(2+) of CAP/SiO _(2) to achieve high drug loading (180 μg mg ~(?1) ). With further decoration of siRNA, the nanocarrier was applied to enhance the therapeutic efficacy by silencing MDR-relevant genes (P-gp) of DOX-resistance K562/ADR cancer cells. Benefiting from the intrinsic acid degradability of CAP/SiO _(2) , the nanocomposite demonstrated pH-responsive release behavior, favoring drug/siRNA release within acidic endo-/lysosomes. Consequently, due to the drug and gene effects, this biodegradable nanomedicine demonstrated enhanced therapeutic efficiency, providing a novel strategy for cancer therapy.
机译:长期施用化学治疗剂通常导致多种耐药性(MDR),这极大地损害了治疗结果。为了克服该问题,构建基于酸敏感磷酸钙/二氧化硅(Cap / SiO_(2))复合材料的可生物降解的纳米载体用于药物和siRNA的编码。通过与盖子/ SiO_(2)的暴露的Ca〜(2)相互作用以实现高药物载荷(180μgmg〜(α1)),将抗癌药物多柔比蛋白(DOX)包封到复合支架中。利用siRNA的进一步装饰,纳米载体被扫描以增强DOx抗性K562 / ADR癌细胞的MDR相关基因(P-GP)来增强治疗效果。受益于帽/ SiO_(2)的内在酸可降解性,纳米复合材料显示pH-响应释放行为,最有利于酸性内核/溶酶体中的药物/ siRNA释放。因此,由于药物和基因效应,这种可生物降解的纳米医生证明了增强的治疗效率,为癌症治疗提供了新的策略。

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