Li Yinuo, Matsumoto Yoshitaka, Chen Lili, Sugawara Yu, Oe Emiho, Fujisawa Nanami, Ebara Mitsuhiro, Sakurai Hideyuki
Department of Radiation Oncology, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba 305-8575, Japan.
Department of Radiation Oncology, Clinical Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8575, Japan.
Nanomaterials (Basel). 2023 Jan 19;13(3):414. doi: 10.3390/nano13030414.
This study aims to propose a new treatment model for glioblastoma (GBM). The combination of chemotherapy, molecular targeted therapy and radiotherapy has been achieved in a highly simultaneous manner through the application of a safe, non-toxic, locally sustained drug-releasing composite Nanofiber mesh (NFM). The NFM consisted of biodegradable poly(ε-caprolactone) with temozolomide (TMZ) and 17-allylamino-17-demethoxygeldanamycin (17AAG), which was used in radiation treatment. TMZ and 17AAG combination showed a synergistic cytotoxicity effect in the T98G cell model. TMZ and 17AAG induced a radiation-sensitization effect, respectively. The NFM containing 17AAG or TMZ, known as 17AAG-NFM and TMZ-NFM, enabled cumulative drug release of 34.1% and 39.7% within 35 days. Moreover, 17AAG+TMZ-NFM containing both drugs revealed a synergistic effect in relation to the NFM of a single agent. When combined with radiation, 17AAG+TMZ-NFM induced in an extremely powerful cytotoxic effect. These results confirmed the application of NFM can simultaneously allow multiple treatments to T98G cells. Each modality achieved a significant synergistic effect with the other, leading to a cascading amplification of the therapeutic effect. Due to the superior advantage of sustained drug release over a long period of time, NFM has the promise of clinically addressing the challenge of high recurrence of GBM post-operatively.
本研究旨在提出一种新的胶质母细胞瘤(GBM)治疗模型。通过应用一种安全、无毒、局部持续释药的复合纳米纤维网(NFM),已高度同步地实现了化疗、分子靶向治疗和放射治疗的联合应用。NFM由可生物降解的聚(ε-己内酯)与替莫唑胺(TMZ)和17-烯丙基氨基-17-去甲氧基格尔德霉素(17AAG)组成,用于放射治疗。TMZ与17AAG联合在T98G细胞模型中显示出协同细胞毒性作用。TMZ和17AAG分别诱导了放射增敏作用。含有17AAG或TMZ的NFM,即17AAG-NFM和TMZ-NFM,在35天内药物累积释放率分别为34.1%和39.7%。此外,含有两种药物的17AAG+TMZ-NFM相对于单一药物的NFM显示出协同效应。与放射联合时,17AAG+TMZ-NFM诱导出极强的细胞毒性作用。这些结果证实了NFM的应用可同时对T98G细胞进行多种治疗。每种治疗方式之间均产生了显著的协同效应,导致治疗效果呈级联放大。由于NFM具有长时间持续释药的优越优势,有望在临床上应对GBM术后高复发的挑战。