Studenovský Martin, Rumlerová Anna, Kostka Libor, Etrych Tomáš
Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovský Sq. 2, 162 06 Prague 6, Czech Republic.
Polymers (Basel). 2021 Jul 30;13(15):2530. doi: 10.3390/polym13152530.
Recently, the antitumor potential of benzimidazole anthelmintics, such as mebendazole and its analogues, have been reported to have minimal side effects, in addition to their well-known anti-parasitic abilities. However, their administration is strongly limited owing to their extremely poor solubility, which highly depletes their overall bioavailability. This study describes the design, synthesis, and physico-chemical properties of polymer-mebendazole nanomedicines for drug repurposing in cancer therapy. The conjugation of mebendazole to water-soluble and biocompatible polymer carrier was carried out via biodegradable bond, relying on the hydrolytic action of lysosomal hydrolases for mebendazole release inside the tumor cells. Five low-molecular-weight mebendazole derivatives, differing in their inner structure, and two polymer conjugates differing in their linker structure, were synthesized. The overall synthetic strategy was designed to enable the modification and polymer conjugation of most benzimidazole-based anthelmintics, such as albendazole, fenbendazole or albendazole, besides the mebendazole. Furthermore, the described methodology may be suitable for conjugation of other biologically active compounds with a heterocyclic N-H group in their molecules.
最近,有报道称苯并咪唑驱虫药(如甲苯咪唑及其类似物)除了具有众所周知的抗寄生虫能力外,其抗肿瘤潜力的副作用极小。然而,由于其溶解性极差,严重降低了其整体生物利用度,其给药受到极大限制。本研究描述了用于癌症治疗中药物重新利用的聚合物 - 甲苯咪唑纳米药物的设计、合成及物理化学性质。甲苯咪唑与水溶性且生物相容性良好的聚合物载体通过可生物降解键进行偶联,依靠溶酶体水解酶的水解作用使甲苯咪唑在肿瘤细胞内释放。合成了五种内部结构不同的低分子量甲苯咪唑衍生物以及两种连接子结构不同的聚合物偶联物。整体合成策略旨在能够对大多数基于苯并咪唑的驱虫药(如阿苯达唑、芬苯达唑或甲苯咪唑)进行修饰和聚合物偶联,除了甲苯咪唑之外。此外,所描述的方法可能适用于将其他分子中含有杂环N - H基团的生物活性化合物进行偶联。