Wang Jun, Zhang Zongyong, Ai Yilong, Liu Fang, Chen Min-Min, Liu Dahai
Department of Basic Medicine and Biomedical Engineering, School of Medicine, Foshan University, Foshan, 528000, Guangdong, PR China.
College of Materials and Chemical Engineering, Ningbo University of Technology, Ningbo, 315211, Zhejiang, PR China.
Carbohydr Res. 2021 Mar;501:108275. doi: 10.1016/j.carres.2021.108275. Epub 2021 Feb 26.
In order to achieve efficient delivery of methotrexate (MTX), thymine-chitosan nanoparticles (Thy-Cs NPs) were prepared, and further decorated with lactobionic acid (LA) to obtain tumor-targeting nanoparticles (LA-Thy-Cs NPs). These nanoparticles possessed a regular spherical structure with the average size about 190-250 nm and narrow size distribution, which were kinetically stable in the physiological environment. Due to electrostatic interactions and multiple hydrogen-bonding interactions between MTX and carriers, MTX was loaded into Thy-Cs NPs with high drug loading content (~20%). MTX release from Thy-Cs NPs was significantly accelerated in the mildly acidic environment due to the destruction of two types of non-covalent interactions. In vitro cell experiments demonstrated that LA-Thy-Cs NPs could be efficiently internalized into hepatoma carcinoma cells, leading to higher cytotoxicity. Moreover, MTX-loaded LA-Thy-Cs NPs performed an enhanced growth inhibition in three-dimensional multicellular tumor spheroids. Thus, the LA decorated thymine-chitosan nanocarriers can be a promising candidate for efficient delivery of MTX.
为了实现甲氨蝶呤(MTX)的高效递送,制备了胸腺嘧啶-壳聚糖纳米颗粒(Thy-Cs NPs),并进一步用乳糖酸(LA)修饰以获得肿瘤靶向纳米颗粒(LA-Thy-Cs NPs)。这些纳米颗粒具有规则的球形结构,平均尺寸约为190-250nm,尺寸分布窄,在生理环境中动力学稳定。由于MTX与载体之间的静电相互作用和多重氢键相互作用,MTX以高载药量(约20%)载入Thy-Cs NPs。由于两种非共价相互作用的破坏,MTX从Thy-Cs NPs的释放在轻度酸性环境中显著加速。体外细胞实验表明,LA-Thy-Cs NPs能够有效地内化进入肝癌细胞,导致更高的细胞毒性。此外,负载MTX的LA-Thy-Cs NPs在三维多细胞肿瘤球状体中表现出增强的生长抑制作用。因此,LA修饰的胸腺嘧啶-壳聚糖纳米载体有望成为MTX高效递送的候选者。