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PHRM-02. DELIVERY OF CHEMOTHERAPEUTICS TO PEDIATRIC BRAIN TUMORS USING CITRATE-CAPPED GOLD NANOPARTICLES

机译:PHRM-02。枸RATE酸包覆金纳米粒子将化学治疗药物递送至小儿脑肿瘤

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摘要

Medulloblastomas and gliomas account for nearly 28% of primary tumors and about 80% of malignant tumors in children. Many of the chemo-drugs that are found effective in killing tumor cells perform well in laboratory settings but fail to cross the blood-brain barrier in humans in direct clinical applications. This problem is overcome by using carriers which could deliver the drugs across the blood-brain barrier. To increase the efficacy of drugs in targeting different tumors, different nanoparticles have been used as carriers in the recent past. Some drugs, including AZD-1775 and Gemcitabine, have been shown by researchers to be effective in multiple brain tumors but have not been adequately utilized alone and/or in combination in pediatric brain tumor patients. In our study, we have conjugated AZD-1775 and Gemcitabine to citrate-capped gold nanoparticles (AuNPs). Cells have been treated with a drug alone, or AuNP alone and AuNP conjugated with drugs for 72 hours. Cell viability assays, cell cycle analysis and western blotting have been used to evaluate the delivery of drug to cells. Both the drugs and their AuNP-conjugates inhibited the growth of cells tested. AuNPs conjugated with the drugs showed more effective delivery of the drugs to cells than drugs alone at the same concentrations, as measured by tumor cell growth. Also, our initial in vivo study shows prolonged survival of mice bearing brain tumors treated with AuNP-conjugated AZD-1775 than those treated with AZD-1775 alone. These results confirm that AuNPs are a suitable platform to deliver chemotherapeutics to brain tumors.
机译:儿童髓母细胞瘤和神经胶质瘤占原发肿瘤的近28%,恶性肿瘤约占80%。被发现有效杀死肿瘤细胞的许多化学药物在实验室环境下表现良好,但在直接的临床应用中却无法穿越人类的血脑屏障。通过使用可以将药物跨血脑屏障传递的载体克服了这个问题。为了提高药物靶向不同肿瘤的功效,最近已经使用了不同的纳米颗粒作为载体。研究人员显示,包括AZD-1775和吉西他滨在内的一些药物在多发性脑肿瘤中有效,但在儿科脑肿瘤患者中并未单独和/或联合使用。在我们的研究中,我们将AZD-1775和吉西他滨偶联到了柠檬酸盐封端的金纳米颗粒(AuNPs)。已经用单独的药物或单独的AuNP和与药物缀合的AuNP处理细胞72小时。细胞活力测定,细胞周期分析和蛋白质印迹已用于评估药物向细胞的递送。药物及其AuNP共轭物均抑制测试细胞的生长。通过肿瘤细胞生长测定,与相同浓度的药物结合的AuNPs比相同浓度的单独药物更有效地将药物递送至细胞。同样,我们的初始体内研究显示,与单独使用AZD-1775相比,用AuNP偶联的AZD-1775处理的带有脑瘤的小鼠的存活期更长。这些结果证实AuNPs是将化学治疗剂递送至脑肿瘤的合适平台。

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