The Czech Academy of Sciences, Institute of Chemical Process Fundamentals, Rozvojová 135, 165 02 Prague, Czech Republic.
Faculty of Science, University of Jan Evangelista Purkyně in Ústí nad Labem, Pasteurova 1, 400 96 Ústí nad Labem, Czech Republic.
Biomacromolecules. 2022 Jan 10;23(1):276-290. doi: 10.1021/acs.biomac.1c01264. Epub 2021 Dec 20.
The complexity of drug delivery mechanisms calls for the development of new transport system designs. Here, we report a robust synthetic procedure toward stable glycodendrimer (glyco-DDM) series bearing glucose, galactose, and oligo(ethylene glycol)-modified galactose peripheral units. In vitro cytotoxicity assays showed exceptional biocompatibility of the glyco-DDMs. To demonstrate applicability in drug delivery, the anticancer agent doxorubicin (DOX) was encapsulated in the glyco-DDM structure. The anticancer activity of the resulting glyco-DDM/DOX complexes was evaluated on the noncancerous (BJ) and cancerous (MCF-7 and A2780) cell lines, revealing their promising generation- and concentration-dependent effect. The glyco-DDM/DOX complexes show gradual and pH-dependent DOX release profiles. Fluorescence spectra elucidated the encapsulation process. Confocal fluorescence microscopy demonstrated preferential cancer cell internalization of the glyco-DDM/DOX complexes. The conclusions were supported by computer modeling. Overall, our results are consistent with the assumption that novel glyco-DDMs and their drug complexes are very promising in drug delivery and related applications.
药物输送机制的复杂性要求开发新的传输系统设计。在这里,我们报告了一种稳健的合成方法,用于制备稳定的糖基树状大分子(glyco-DDM)系列,其具有葡萄糖、半乳糖和聚(乙二醇)修饰的半乳糖外围单元。体外细胞毒性试验表明糖基 DDM 具有出色的生物相容性。为了证明在药物输送中的适用性,将抗癌药物阿霉素(DOX)封装在糖基 DDM 结构中。所得糖基 DDM/DOX 复合物对非癌细胞(BJ)和癌细胞(MCF-7 和 A2780)系的抗癌活性进行了评估,显示出其具有代际和浓度依赖性的潜力。糖基 DDM/DOX 复合物显示出逐渐且 pH 依赖性的 DOX 释放曲线。荧光光谱阐明了封装过程。共聚焦荧光显微镜显示了糖基 DDM/DOX 复合物对癌细胞的优先内化。计算机建模支持了这些结论。总体而言,我们的结果与假设一致,即新型糖基 DDM 及其药物复合物在药物输送和相关应用中非常有前途。