Al-Shakarchi Wejdan, Alsuraifi Ali, Curtis Anthony, Hoskins Clare
Institute of Science and Technology in Medicine, School of Pharmacy, Keele University, Keele ST5 5BG, UK.
College of Pharmacy, Mosul University, Mosul 41002, Iraq.
Pharmaceutics. 2018 May 26;10(2):63. doi: 10.3390/pharmaceutics10020063.
Liver cancer treatments are often hindered by poor drug physicochemical properties, hence there is a need for improvement in order to increase patient survival and outlook. Combination therapies have been studied in order to evaluate whether increased overall efficacy can be achieved. This study reports the combined treatment of liver cancer cells with a combination treatment of chemotherapeutic agent paclitaxel and pro-apoptotic protein cytochrome C. In order to administer both agents in a single formulation, a poly(allylamine)-based amphiphile has been fabricated with the incorporation of a hybrid iron oxide-gold nanoparticle into its structure. Here, the insoluble paclitaxel becomes incorporated into the hydrophobic core of the self-assemblies formed in an aqueous environment (256 nm), while the cytochrome C attaches irreversibly onto the hybrid nanoparticle surface via gold-thiol dative covalent binding. The self-assemblies were capable of solubilising up to 0.698 mg/mL of paclitaxel (700-fold improvement) with 0.012 mg/mL of cytochrome C also attached onto the hybrid iron oxide-gold nanoparticles (HNPs) within the hydrophobic core. The formulation was tested on a panel of liver cancer cells and cytotoxicity was measured. The findings suggested that indeed a significant improvement in combined therapy (33-fold) was observed when compared with free drug, which was double the enhancement observed after polymer encapsulation without the cytochrome C in hepatocellular carcinoma (Huh-7D12) cells. Most excitingly, the polymeric nanoparticles did result in improved cellular toxicity in human endothelian liver cancer (SK-hep1) cells, which proved completely resistant to the free drug.
肝癌治疗常常受到药物理化性质不佳的阻碍,因此需要加以改进以提高患者的生存率和预后。人们对联合疗法进行了研究,以评估是否能提高总体疗效。本研究报告了用化疗药物紫杉醇和促凋亡蛋白细胞色素C联合治疗肝癌细胞的情况。为了将这两种药物制成单一制剂,制备了一种基于聚烯丙胺的两亲物,并在其结构中掺入了杂化氧化铁-金纳米颗粒。在这里,不溶性的紫杉醇被纳入在水性环境中形成的自组装体(256纳米)的疏水核心中,而细胞色素C则通过金-硫醇配位共价键不可逆地附着在杂化纳米颗粒表面。该自组装体能溶解高达0.698毫克/毫升的紫杉醇(提高了700倍),同时有0.012毫克/毫升的细胞色素C也附着在疏水核心内的杂化氧化铁-金纳米颗粒(HNPs)上。该制剂在一组肝癌细胞上进行了测试,并测定了细胞毒性。研究结果表明,与游离药物相比,联合疗法确实有显著改善(提高了33倍),这是在肝细胞癌(Huh-7D12)细胞中没有细胞色素C的聚合物包封后观察到的增强效果的两倍。最令人兴奋的是,聚合物纳米颗粒确实提高了人内皮肝癌(SK-hep1)细胞的细胞毒性,而该细胞对游离药物完全耐药。