Department of Industrial Pharmacy, Universidade Federal de Santa Maria, Av. Roraima 1000, Santa Maria, RS, 97105-900, Brazil.
PostGraduate Program in Pharmaceutical Sciences, Universidade Federal de Santa Maria, Av. Roraima 1000, Santa Maria, RS, 97105-900, Brazil.
AAPS PharmSciTech. 2019 Apr 15;20(5):165. doi: 10.1208/s12249-019-1372-5.
A promising approach to achieve a more efficient antitumor therapy is the conjugation of the active molecule to a nanostructured delivery system. Therefore, the main objective of this research was to prepare nanoparticles (NPs), with the polymer poly (ε-caprolactone) (PCL), as a carrier for the antitumor drug methotrexate (MTX). A pH-responsive behavior was obtained through conjugation of the amino acid-based amphiphile, 77KL, to the NP matrix. The NPs showed mean hydrodynamic diameter and drug entrapment efficiency of 178.5 nm and 20.52%, respectively. Owing to its pH-sensitivity, the PCL-NPs showed membrane-lytic behavior upon reducing the pH value of surrounding media to 5.4, which is characteristic of the endosomal compartments. The in vitro antitumor assays demonstrated that MTX-loaded PCL-NPs have higher antiproliferative activity than free drug in MCF-7 cells and, to a lesser extent, in HepG2 cells. This same behavior was also achieved at mildly acidic conditions, characteristic of the tumor microenvironment. Altogether, the results evidenced the pH-responsive properties of the designed NPs, as well as the higher in vitro cytotoxicity compared to free MTX, representing thus a promising alternative for the antitumor therapy.
实现更高效抗肿瘤治疗的一种有前途的方法是将活性分子与纳米结构的递药系统连接。因此,本研究的主要目的是制备纳米颗粒(NPs),载体为聚合物聚(ε-己内酯)(PCL),并将抗肿瘤药物甲氨蝶呤(MTX)包载于其中。通过将基于氨基酸的两亲分子 77KL 接枝到 NP 基质上,获得了 pH 响应行为。NPs 的平均水动力直径和药物包封效率分别为 178.5nm 和 20.52%。由于其 pH 敏感性,PCL-NPs 在周围介质的 pH 值降低至 5.4 时表现出膜裂解行为,这是内体区室的特征。体外抗肿瘤试验表明,载 MTX 的 PCL-NPs 在 MCF-7 细胞中的增殖抑制活性高于游离药物,在 HepG2 细胞中的活性稍低。在肿瘤微环境的特征性轻度酸性条件下,也观察到了这种相同的行为。总之,结果证明了设计的 NPs 的 pH 响应特性,以及与游离 MTX 相比,更高的体外细胞毒性,代表了抗肿瘤治疗的一种有前途的替代方法。