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Anticancer activity of drug-loaded calcium phosphate nanocomposites against human osteosarcoma

机译:载药磷酸钙纳米复合材料对人骨肉瘤的抗癌活性

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BackgroundCalcium phosphate (CaP) based nanoparticles are considered to be ideal drug carriers for delivery of anticancer drugs because of their excellent biocompatibility and pH responsiveness. However, CaP nanoparticles have the problems of limited drug load capacity, initial burst release, and short-term release. Thus, we prepared the CaP nanocomposites containing anticancer drug such as caffeic acid (CA-NP), chlorogenic acid (CG-NP), or cisplatin (CP-NP) in the presence of alginate as a polymer template to control the release rate of drugs. ResultsThe drug-loaded CaP nanocomposites exhibited spherical shape with a size of under 100?nm and the size of nanocomposites was hardly affected by the addition of drug. UV-visible spectroscopic analysis confirmed the insertion of drug into the CaP nanocomposites. These nanocomposites showed an initial burst release of drug, followed by a prolonged release, in which the release profile of drugs was depended on the solution pH. In addition, the drug-loaded CaP nanocomposites revealed anticancer activity on human osteosarcoma in a manner dependent on concentration of drugs and time. ConclusionsThe drug-loaded CaP nanocomposites can contribute to the development of a new generation of controlled drug release carriers for chemotherapy of cancers.
机译:背景技术基于磷酸钙(CaP)的纳米颗粒由于其出色的生物相容性和pH响应性,被认为是抗癌药物的理想药物载体。然而,CaP纳米粒子具有受限的药物负载能力,初始爆发释放和短期释放的问题。因此,我们在藻酸盐作为聚合物模板的情况下,制备了包含抗癌药(例如咖啡酸(CA-NP),绿原酸(CG-NP)或顺铂(CP-NP))的CaP纳米复合材料,以控制其释放速率。毒品。结果载药的CaP纳米复合材料呈球形,尺寸小于100nm,并且纳米复合材料的尺寸几乎不受添加药物的影响。紫外可见光谱分析证实了将药物插入CaP纳米复合材料中。这些纳米复合材料显示出药物的初始爆发释放,然后是长时间释放,其中药物的释放曲线取决于溶液的pH值。此外,载药的CaP纳米复合材料以依赖于药物浓度和时间的方式对人骨肉瘤显示出抗癌活性。结论载药的CaP纳米复合材料可有助于开发用于癌症化疗的新一代控释药物载体。

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