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Effects of nanoparticle size on antitumor activity of 10-hydroxycamptothecin-conjugated gold nanoparticles: in vitro and in vivo studies

机译:纳米尺寸对10-羟基喜树碱偶联金纳米颗粒抗肿瘤活性的影响:体内和体外研究

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摘要

Gold nanoparticles (AuNPs) have emerged as a promising anticancer drug delivery scaffold. However, some controversial points still require further investigation before clinical use. A complete understanding of how animal cells interact with drug-conjugated AuNPs of well-defined sizes remains poorly understood. In this study, we prepared a series of 10-hydroxycamptothecin (HCPT)-AuNP conjugates of different sizes and compared their cytotoxic effect in vitro and antitumor effect in vivo. Transmission electron micrographs showed that the NPs had a round, regular shape with a mean diameter of ~10, 25, and 50 nm. An in vitro drug release study showed that HCPT was continuously released for 120 hours. HCPT-AuNPs showed greater cytotoxic effects on the MDA-MB-231 cell line compared with an equal dose of free HCPT. Notably, HCPT-AuNPs of an average diameter of 50 nm (HCPT-AuNPs-50) had the greatest effect. Furthermore, administration of HCPT-AuNPs-50 showed the most tumor-suppressing activity against MDA-MB-231 tumor in mice among all treatment groups. The results indicate that AuNPs not only act as a carrier but also play an active role in mediating biological effects. This work gives important insights into the design of nanoscale delivery and therapeutic systems.
机译:金纳米颗粒(AuNPs)已经成为一种有前途的抗癌药物递送支架。但是,一些有争议的观点在临床使用之前仍需要进一步研究。对动物细胞如何与定义明确的大小的药物缀合的AuNP相互作用的完整理解仍然知之甚少。在这项研究中,我们制备了一系列不同大小的10-羟基喜树碱(HCPT)-AuNP共轭物,并比较了它们在体外的细胞毒性作用和体内的抗肿瘤作用。透射电子显微照片显示,NP具有圆形规则形状,平均直径约为10、25和50 nm。一项体外药物释放研究表明,HCPT持续释放120小时。与相等剂量的游离HCPT相比,HCPT-AuNPs对MDA-MB-231细胞系显示出更大的细胞毒性作用。值得注意的是,平均直径为50 nm的HCPT-AuNP(HCPT-AuNPs-50)效果最大。此外,在所有治疗组中,HCPT-AuNPs-50的给药对小鼠的MDA-MB-231肿瘤抑制作用最大。结果表明AuNPs不仅充当载体,而且在介导生物学效应中也起着积极作用。这项工作为纳米级递送和治疗系统的设计提供了重要的见识。

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