Department of Medical Life Sciences, Department of Biomedicine & Health Sciences, and Catholic Photomedicine Research Institute, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea.
ACS Appl Mater Interfaces. 2021 Mar 10;13(9):10812-10821. doi: 10.1021/acsami.1c02316. Epub 2021 Feb 24.
In combination therapy, synergetic effects of drugs and their efficient delivery are essential. Herein, we screened 12 anticancer drugs for combination with photodynamic therapy (PDT) using pheophorbide a (Pba). On the basis of combination index (CI) values in cell viability tests, we selected tirapazamine (TPZ) and developed self-assembled gelatin nanoparticles (NPs) containing both Pba and TPZ. The resulting TPZ-Pba-NPs showed a synergetic effect to kill tumor cells because TPZ was activated under the hypoxic conditions that originated from the PDT with Pba and laser irradiation. After they were injected into tumor-bearing mice via the tail vein, TPZ-Pba-NPs showed 3.17-fold higher blood concentration and 4.12-fold higher accumulation in tumor tissue 3 and 24 h postinjection, respectively. Upon laser irradiation to tumor tissue, TPZ-Pba-NPs successfully suppressed tumor growth by efficient drug delivery and synergetic effects . These overall results suggest that screening of drugs based on CI values, mechanism studies in hypoxia, and real-time imaging are promising strategies in developing NPs for optimized combination therapy.
在联合治疗中,药物的协同作用及其有效传递至关重要。在此,我们使用原卟啉 IX(Pba)筛选了 12 种抗癌药物与光动力疗法(PDT)联合使用。基于细胞活力测试中的组合指数(CI)值,我们选择了替拉扎明(TPZ)并开发了含有 Pba 和 TPZ 的自组装明胶纳米颗粒(NPs)。由于 Pba 和激光照射引发的 PDT 会产生缺氧条件,从而激活 TPZ,因此所得的 TPZ-Pba-NPs 对杀死肿瘤细胞具有协同作用。将它们通过尾巴静脉注射到荷瘤小鼠中后,TPZ-Pba-NPs 在注射后 3 小时和 24 小时分别显示出 3.17 倍和 4.12 倍更高的血液浓度和肿瘤组织中的积累。对肿瘤组织进行激光照射后,TPZ-Pba-NPs 通过有效的药物传递和协同作用成功抑制了肿瘤生长。这些总体结果表明,基于 CI 值进行药物筛选、缺氧机制研究和实时成像为开发用于优化联合治疗的 NPs 提供了有前途的策略。