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A ceramic-based anticancer drug delivery system to treat breast cancer

机译:一种基于陶瓷的抗癌药物递送系统,可治疗乳腺癌

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摘要

Drug delivery systems offer the advantage of sustained targeted release with minimal side effect. In the present study, the therapeutic efficacy of a porous silica-calcium phosphate nanocomposite (SCPC) as a new delivery system for 5-Fluorouracil (5-FU) was evaluated in vitro and in vivo. In vitro studies showed that two formulations; SCPC50/5-FU and SCPC75/5-FU hybrids were very cytotoxic for 4T1 mammary tumor cells. In contrast, control SCPCs without drug did not show any measurable toxic effect. Release kinetics studies showed that SCPC75/ 5-FU hybrid provided a burst release of 5-FU in the first 24 h followed by a sustained release of a therapeutic dose (30.7 (μg/day) of the drug for up to 32 days. Moreover, subcutaneous implantation of SCPC75/5-FU hybrid disk in an immunocompetent murine model of breast cancer stopped 4T1 tumor growth. Blood analyses showed comparablernconcentrations of Ca, P and Si in animals implanted with or without SCPC75 disks. These results strongly suggest that SCPC/5-FU hybrids can provide an effective treatment for solid tumors with minimal side effects.
机译:药物输送系统具有持续靶向释放且副作用最小的优点。在本研究中,在体外和体内评估了多孔二氧化硅-磷酸钙纳米复合材料(SCPC)作为5-氟尿嘧啶(5-FU)新型递送系统的治疗效果。体外研究表明,有两种配方。 SCPC50 / 5-FU和SCPC75 / 5-FU杂种对4T1乳腺肿瘤细胞具有极强的细胞毒性。相反,没有药物的对照SCPC并没有表现出可测量的毒性作用。释放动力学研究表明,SCPC75 / 5-FU杂合体在最初的24小时内爆发了5-FU,随后持续释放治疗剂量(30.7(微克/天)的药物)长达32天。 ,在具有免疫能力的乳腺癌小鼠模型中皮下植入SCPC75 / 5-FU混合盘可阻止4T1肿瘤的生长,血液分析显示,植入或不植入SCPC75盘的动物中Ca,P和Si的浓度相当,这些结果强烈表明SCPC / 5-FU杂种可以为实体瘤提供有效的治疗,且副作用最小。

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  • 来源
    《Journal of materials science》 |2010年第9期|p.2701-2710|共10页
  • 作者单位

    Department of Mechanical Engineering and Engineering Science, DCH 177, The University of North Carolina at Charlotte, 9201 University City Blvd., Charlotte,NC 28223, USA;

    rnDepartment of Mechanical Engineering and Engineering Science, DCH 177, The University of North Carolina at Charlotte, 9201 University City Blvd., Charlotte,NC 28223, USA;

    rnCellular and Molecular Biology Division, Department of Biology, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA;

    rnCellular and Molecular Biology Division, Department of Biology, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA;

    rnCellular and Molecular Biology Division, Department of Biology, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA;

    rnCellular and Molecular Biology Division, Department of Biology, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA;

    rnDepartment of Pharmacology, School of Pharmacy, University of Kentucky, 740 South Limestone Street, Lexington, KY 40536-0001, USA;

    rnDepartment of Medicine, Medical School, University of Louisville, Louisville, KY 40292, USA;

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