Centre for Molecular Nanometrology, Department of Pure and Applied Chemistry, Thomas Graham Building, University of Strathclyde, 295 Cathedral Street, G1 1XL Glasgow, United Kingdom.
J Am Chem Soc. 2010 Apr 7;132(13):4678-84. doi: 10.1021/ja908117a.
The platinum-based anticancer drugs cisplatin, carboplatin, and oxaliplatin are an important component of chemotherapy but are limited by severe dose-limiting side effects and the ability of tumors to develop resistance rapidly. These drugs can be improved through the use of drug-delivery vehicles that are able to target cancers passively or actively. In this study, we have tethered the active component of the anticancer drug oxaliplatin to a gold nanoparticle for improved drug delivery. Naked gold nanoparticles were functionalized with a thiolated poly(ethylene glycol) (PEG) monolayer capped with a carboxylate group. [Pt(1R,2R-diaminocyclohexane)(H(2)O)(2)]2NO(3) was added to the PEG surface to yield a supramolecular complex with 280 (+/-20) drug molecules per nanoparticle. The platinum-tethered nanoparticles were examined for cytotoxicity, drug uptake, and localization in the A549 lung epithelial cancer cell line and the colon cancer cell lines HCT116, HCT15, HT29, and RKO. The platinum-tethered nanoparticles demonstrated as good as, or significantly better, cytotoxicity than oxaliplatin alone in all of the cell lines and an unusual ability to penetrate the nucleus in the lung cancer cells.
基于铂的抗癌药物顺铂、卡铂和奥沙利铂是化疗的重要组成部分,但由于严重的剂量限制副作用和肿瘤迅速产生耐药性的能力而受到限制。这些药物可以通过使用能够被动或主动靶向癌症的药物输送载体来改善。在这项研究中,我们将抗癌药物奥沙利铂的活性成分连接到金纳米颗粒上,以提高药物递送效率。裸露的金纳米颗粒用带有羧酸盐基团的巯基化聚乙二醇(PEG)单层功能化。将[Pt(1R,2R-二氨基环己烷)(H(2)O)(2)]2NO(3)添加到 PEG 表面,得到每个纳米颗粒有 280(+/-20)个药物分子的超分子复合物。研究了铂键合纳米颗粒在 A549 肺上皮癌细胞系以及结肠癌细胞系 HCT116、HCT15、HT29 和 RKO 中的细胞毒性、药物摄取和定位。与单独使用奥沙利铂相比,铂键合纳米颗粒在所有细胞系中均表现出相当或更好的细胞毒性,并且具有在肺癌细胞中穿透细胞核的异常能力。
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