Faculty of Pharmaceutical Sciences , Sojo University , Ikeda 4-22-1, Nishi-ku , Kumamoto 860-0082 , Japan.
Institute of Macromolecular Chemistry , Czech Academy of Sciences , Heyrovsky Sq. 2 , 162 06 Prague 6 , Czech Republic.
Mol Pharm. 2019 Aug 5;16(8):3452-3459. doi: 10.1021/acs.molpharmaceut.9b00248. Epub 2019 Jul 11.
-(2-Hydroxypropyl)methacrylamide copolymer conjugates of pirarubicin (THP), P-THP, accumulates selectively in solid tumor tissue by the enhanced permeability and retention (EPR) effect. Despite of high accumulation in solid tumors, some macromolecular antitumor agents show poor therapeutic outcome because of poor tissue diffusion into the tumor as well as obstructed tumor blood flow. Here, we confirmed that cellular uptake of P-THP was 25 times less than that of free THP at 1-4 h incubation time . The passage of P-THP through the confluent tight-monolayer cells junction was 12 times higher than free THP, and P-THP penetrated deeper into the tumor cell spheroid (1.3-1.7-fold) than free THP in 4 h. In addition, P-THP showed cytotoxicity comparable to that of free THP to tumor-cells in spheroid form, despite of 7 times lower cytotoxicity of P-THP to the monolayer cells to that of free THP . These results indicate that P-THP administration can exhibit deeper diffusion into the tumor cell spheroid than free THP. As a consequence, P-THP exhibits more efficient antitumor activity than free THP , which is also supported by better pharmacokinetics and tumor accumulation of P-THP than free THP.
-(2-羟丙基)甲基丙烯酰胺共聚物与吡柔比星(THP)的缀合物(P-THP)通过增强的通透性和保留(EPR)效应选择性地积聚在实体瘤组织中。尽管在实体瘤中有很高的积累,但一些高分子抗肿瘤剂由于组织向肿瘤内扩散不良以及肿瘤血流受阻而表现出较差的治疗效果。在这里,我们证实 P-THP 的细胞摄取量在 1-4 小时孵育时间内比游离 THP 低 25 倍。P-THP 通过紧密单层细胞连接的通透性比游离 THP 高 12 倍,并且 P-THP 在 4 小时内比游离 THP更深地渗透到肿瘤细胞球体中(1.3-1.7 倍)。此外,尽管 P-THP 对单层细胞的细胞毒性比游离 THP 低 7 倍,但 P-THP 对球体形式的肿瘤细胞的细胞毒性与游离 THP 相当。这些结果表明,与游离 THP 相比,P-THP 可以更深地扩散到肿瘤细胞球体中。因此,P-THP 表现出比游离 THP 更高的抗肿瘤活性,这也得到了 P-THP 比游离 THP 更好的药代动力学和肿瘤积累的支持。